Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84263 |
| ensemblid | ENSG00000119471.15 |
| hgncid | 18572 |
| symbol | HSDL2 |
| name | hydroxysteroid dehydrogenase like 2 |
| refseq_nuc | NM_032303.5 |
| refseq_prot | NP_115679.2 |
| ensembl_nuc | ENST00000398805.8 |
| ensembl_prot | ENSP00000381785.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 112380108 |
| end | 112472405 |
| strand | + |
| ver | v1.2 |
| region | chr9:112380108-112472405 |
| region5000 | chr9:112375108-112477405 |
| regionname0 | HSDL2_chr9_112380108_112472405 |
| regionname5000 | HSDL2_chr9_112375108_112477405 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 418 | 365 | 86 | 63 | 166 | 12 | 36 | 132 | HSDL2_chr9_112375108_112477405 | HSDL2 | MLPNT others(413): Show |
chr9 | 112375108 | 112477405 |
| a0002 | 0/0 | 418 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | MLPNT others(413): Show |
chr9 | 112375108 | 112477405 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1254 | 345 | 86 | 63 | 146 | 12 | 36 | HSDL2_chr9_112375108_112477405 | HSDL2 | ATGTT others(1249): Show |
chr9 | 112375108 | 112477405 | ||
| a0001c0002 | 0/0 | 1254 | 20 | 0 | 0 | 20 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | ATGTT others(1249): Show |
chr9 | 112375108 | 112477405 | ||
| a0002c0003 | 0/0 | 1254 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | ATGTT others(1249): Show |
chr9 | 112375108 | 112477405 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3174 | 185 | 46 | 31 | 86 | 7 | 13 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3169): Show |
chr9 | 112375108 | 112477405 |
| a0001c0001t0002 | 0/0 | 3174 | 108 | 26 | 19 | 39 | 5 | 19 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3169): Show |
chr9 | 112375108 | 112477405 |
| a0001c0001t0003 | 0/0 | 3174 | 13 | 3 | 6 | 4 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3169): Show |
chr9 | 112375108 | 112477405 |
| a0001c0001t0004 | 0/0 | 3174 | 7 | 1 | 4 | 0 | 0 | 2 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3169): Show |
chr9 | 112375108 | 112477405 |
| a0001c0001t0005 | 0/0 | 3173 | 7 | 0 | 0 | 7 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3168): Show |
chr9 | 112375108 | 112477405 |
| a0001c0001t0006 | 0/0 | 3174 | 6 | 6 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3169): Show |
chr9 | 112375108 | 112477405 |
| a0001c0001t0007 | 0/0 | 3174 | 3 | 0 | 0 | 3 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3169): Show |
chr9 | 112375108 | 112477405 |
| a0001c0001t0008 | 0/0 | 3174 | 2 | 0 | 0 | 2 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3169): Show |
chr9 | 112375108 | 112477405 |
| a0001c0001t0009 | 0/0 | 3174 | 2 | 0 | 0 | 0 | 0 | 2 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3169): Show |
chr9 | 112375108 | 112477405 |
| a0001c0001t0010 | 0/0 | 3174 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3169): Show |
chr9 | 112375108 | 112477405 |
| a0001c0001t0011 | 0/0 | 3174 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3169): Show |
chr9 | 112375108 | 112477405 |
| a0001c0001t0012 | 0/0 | 3174 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3169): Show |
chr9 | 112375108 | 112477405 |
| a0001c0001t0013 | 0/0 | 3174 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3169): Show |
chr9 | 112375108 | 112477405 |
| a0001c0001t0014 | 0/0 | 3174 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3169): Show |
chr9 | 112375108 | 112477405 |
| a0001c0001t0015 | 0/0 | 3162 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3157): Show |
chr9 | 112375108 | 112477405 |
| a0001c0001t0016 | 0/0 | 3174 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3169): Show |
chr9 | 112375108 | 112477405 |
| a0001c0001t0017 | 0/0 | 3174 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3169): Show |
chr9 | 112375108 | 112477405 |
| a0001c0001t0018 | 0/0 | 3174 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3169): Show |
chr9 | 112375108 | 112477405 |
| a0001c0001t0019 | 0/0 | 3140 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3135): Show |
chr9 | 112375108 | 112477405 |
| a0001c0001t0020 | 0/0 | 3174 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3169): Show |
chr9 | 112375108 | 112477405 |
| a0001c0001t0021 | 0/0 | 3173 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3168): Show |
chr9 | 112375108 | 112477405 |
| a0001c0002t0002 | 0/0 | 3174 | 20 | 0 | 0 | 20 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3169): Show |
chr9 | 112375108 | 112477405 |
| a0002c0003t0002 | 0/0 | 3174 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | AGCTC others(3169): Show |
chr9 | 112375108 | 112477405 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0003 | 1/0 | 3 | 0 | 1 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0005g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0006g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0007g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0007g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0008g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0008g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0009g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0009g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0010g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0011g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0012g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0013g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0014g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0015g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0016g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0017g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0018g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0019g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0020g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0001t0021g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| a0002c0003t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0193 | EUR | GBR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0124 | EUR | GBR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | FIN | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0287 | EUR | FIN | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | FIN | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | CHS | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | CHS | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0322 | EAS | CHS | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | CHS | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | CHS | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00673 | hp1 | a0001 | c0001 | t0010 | g0214 | EAS | CHS | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0207 | EAS | CHS | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00741 | hp1 | a0001 | c0001 | t0013 | g0095 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG00741 | hp2 | a0001 | c0001 | t0020 | g0121 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0342 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01099 | hp2 | a0002 | c0003 | t0002 | g0089 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0235 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0233 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0230 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | CLM | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01433 | hp1 | a0001 | c0001 | t0018 | g0023 | AMR | CLM | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0247 | EUR | IBS | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0293 | EUR | IBS | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | ACB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01891 | hp2 | a0001 | c0001 | t0012 | g0088 | AFR | ACB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0323 | AMR | PEL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PEL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PEL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0130 | AMR | PEL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0324 | AMR | PEL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0232 | AMR | PEL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PEL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02027 | hp2 | a0001 | c0001 | t0019 | g0199 | EAS | KHV | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | KHV | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0328 | EAS | KHV | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | KHV | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | KHV | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0242 | EAS | KHV | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | KHV | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | CDX | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02155 | hp2 | a0001 | c0001 | t0005 | g0040 | EAS | CDX | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | CDX | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CDX | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | ACB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | ACB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0349 | AFR | ACB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0325 | AMR | PEL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0346 | AFR | ACB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | KHV | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | GWD | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02630 | hp2 | a0001 | c0001 | t0011 | g0258 | AFR | GWD | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | GWD | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0234 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0332 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0338 | AFR | GWD | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02738 | hp1 | a0001 | c0001 | t0009 | g0184 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0326 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | GWD | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0090 | AFR | GWD | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | ESN | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | ESN | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | ESN | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0343 | AFR | ESN | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0066 | AFR | ESN | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0067 | AFR | GWD | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03098 | hp1 | a0001 | c0001 | t0014 | g0031 | AFR | MSL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0337 | AFR | ESN | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0064 | AFR | ESN | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0340 | AFR | ESN | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | MSL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | MSL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | MSL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | MSL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | ESN | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | GWD | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03540 | hp2 | a0001 | c0001 | t0017 | g0021 | AFR | GWD | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0262 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0264 | SAS | STU | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | STU | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0231 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | BEB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0261 | SAS | BEB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | BEB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03942 | hp2 | a0001 | c0001 | t0009 | g0180 | SAS | BEB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0280 | SAS | BEB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | STU | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | STU | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | YRI | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | YRI | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | CHB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | CHB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | CHB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0341 | AFR | YRI | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18948 | hp1 | a0001 | c0001 | t0007 | g0026 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18951 | hp1 | a0001 | c0001 | t0015 | g0057 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18969 | hp1 | a0001 | c0001 | t0016 | g0092 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18972 | hp2 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18975 | hp2 | a0001 | c0001 | t0021 | g0051 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0210 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0053 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0050 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19012 | hp1 | a0001 | c0001 | t0008 | g0015 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | LWK | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | LWK | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | LWK | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0295 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0348 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19076 | hp2 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19081 | hp1 | a0001 | c0001 | t0005 | g0054 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19082 | hp1 | a0001 | c0001 | t0007 | g0029 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19085 | hp2 | a0001 | c0001 | t0008 | g0014 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | YRI | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0339 | AFR | YRI | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ASW | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ASW | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0309 | EUR | TSI | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0321 | EUR | TSI | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | GIH | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | GIH | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | CLM | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0065 | AFR | ACB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0347 | AFR | ACB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | ACB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | ACB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | USA | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | USA | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0345 | AFR | USA | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0294 | AFR | USA | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | LWK | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | LWK | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0112 | REF | REF | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0003 | REF | REF | HSDL2_chr9_112375108_112477405 | HSDL2 | chr9 | 112375108 | 112477405 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:112405714 | A | T | 1 | a0002 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.272A>T | p.Lys91Ile | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/11 | 328/3174 | 272/1257 | 91/418 | chr9 | 112405714 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:112454041 | A | G | 1 | a0001c0002 | 20 | HG00621.hp1 HG00673.hp2 HG02129.hp2 others(17): Show |
synonymous_variant | LOW | c.894A>G | p.Lys298Lys | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/11 | 950/3174 | 894/1257 | 298/418 | chr9 | 112454041 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:112470554 | TA | T | 2 | a0001c0001t0005 a0001c0001t0021 |
8 | HG02155.hp2 NA18975.hp2 NA18982.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*19delA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 19 | INFO_REALIGN_3_PRIME | chr9 | 112470554 | |||||
| chr9:112470840 | G | A | 1 | a0001c0001t0010 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*296G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 296 | chr9 | 112470840 | ||||||
| chr9:112470900 | G | T | 1 | a0001c0001t0020 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*356G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 356 | chr9 | 112470900 | ||||||
| chr9:112470931 | T | A | 1 | a0001c0001t0007 | 3 | NA18948.hp1 NA18972.hp2 NA19082.hp1 |
3_prime_UTR_variant | MODIFIER | c.*387T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 387 | chr9 | 112470931 | ||||||
| chr9:112470938 | C | A | 1 | a0001c0001t0011 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*394C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 394 | chr9 | 112470938 | ||||||
| chr9:112471019 | A | T | 1 | a0001c0001t0009 | 2 | HG02738.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*475A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 475 | chr9 | 112471019 | ||||||
| chr9:112471117 | C | G | 1 | a0001c0001t0003 | 13 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*573C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 573 | chr9 | 112471117 | ||||||
| chr9:112471237 | CCTTAGAA others(27): Show |
C | 1 | a0001c0001t0019 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*694_*727delCTTAGA others(28): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 694 | chr9 | 112471237 | ||||||
| chr9:112471319 | T | C | 1 | a0001c0001t0012 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*775T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 775 | chr9 | 112471319 | ||||||
| chr9:112471349 | A | G | 1 | a0001c0001t0018 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*805A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 805 | chr9 | 112471349 | ||||||
| chr9:112471406 | A | G | 1 | a0001c0001t0017 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*862A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 862 | chr9 | 112471406 | ||||||
| chr9:112471633 | G | C | 1 | a0001c0001t0021 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1089G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 1089 | chr9 | 112471633 | ||||||
| chr9:112471634 | C | G | 1 | a0001c0001t0021 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1090C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 1090 | chr9 | 112471634 | ||||||
| chr9:112471893 | C | T | 1 | a0001c0001t0008 | 2 | NA19012.hp1 NA19085.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1349C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 1349 | chr9 | 112471893 | ||||||
| chr9:112472114 | G | C | 1 | a0001c0001t0004 | 7 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1570G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 1570 | chr9 | 112472114 | ||||||
| chr9:112472195 | C | A | 1 | a0001c0001t0006 | 6 | HG02109.hp2 HG02486.hp2 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1651C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 1651 | chr9 | 112472195 | ||||||
| chr9:112472224 | G | A | 1 | a0001c0001t0013 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1680G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 1680 | chr9 | 112472224 | ||||||
| chr9:112472323 | T | C | 1 | a0001c0001t0014 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1779T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 1779 | chr9 | 112472323 | ||||||
| chr9:112472330 | C | T | 1 | a0001c0001t0016 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1786C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 1786 | chr9 | 112472330 | ||||||
| chr9:112472331 | G | A | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(5): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*1787G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 1787 | chr9 | 112472331 | ||||||
| chr9:112472375 | GAATCGCT others(5): Show |
G | 1 | a0001c0001t0015 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1834_*1845delTCGC others(8): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 11/11 | 1834 | INFO_REALIGN_3_PRIME | chr9 | 112472375 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:112380281 | G | A | 24 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(21): Show |
25 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(22): Show |
intron_variant | MODIFIER | c.17+101G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112380281 | |||||||
| chr9:112380297 | C | T | 1 | a0001c0001t0001g0349 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.17+117C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112380297 | |||||||
| chr9:112380309 | C | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.17+129C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112380309 | |||||||
| chr9:112380648 | G | C | 1 | a0001c0002t0002g0037 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.17+468G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112380648 | |||||||
| chr9:112380662 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.17+482G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112380662 | |||||||
| chr9:112380663 | AT | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0043 others(20): Show |
25 | HG00558.hp2 HG00621.hp1 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.17+492delT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112380663 | ||||||
| chr9:112380713 | A | G | 1 | a0001c0001t0003g0348 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.17+533A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112380713 | |||||||
| chr9:112380850 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG02615.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.17+670G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112380850 | |||||||
| chr9:112380953 | G | T | 3 | a0001c0001t0002g0345 a0001c0001t0002g0346 a0001c0001t0002g0347 |
3 | HG02280.hp2 HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.17+773G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112380953 | |||||||
| chr9:112381088 | T | TACACAC | 8 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0227 others(5): Show |
8 | HG01109.hp2 HG01891.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.17+932_17+937dupCA others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112381088 | ||||||
| chr9:112381088 | T | TACACACA others(1): Show |
35 | a0001c0001t0001g0001 a0001c0001t0001g0044 a0001c0001t0001g0045 others(32): Show |
37 | HG00558.hp2 HG01167.hp1 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.17+930_17+937dupCA others(6): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112381088 | ||||||
| chr9:112381088 | T | TACACACA others(3): Show |
42 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(39): Show |
44 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.17+928_17+937dupCA others(8): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112381088 | ||||||
| chr9:112381088 | T | TACACACA others(5): Show |
55 | a0001c0001t0001g0033 a0001c0001t0001g0120 a0001c0001t0001g0134 others(52): Show |
56 | HG00408.hp1 HG01070.hp2 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.17+926_17+937dupCA others(10): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112381088 | ||||||
| chr9:112381088 | T | TACACACA others(7): Show |
21 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0036 others(18): Show |
21 | HG00099.hp2 HG00735.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.17+924_17+937dupCA others(12): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112381088 | ||||||
| chr9:112381088 | T | TACACACA others(9): Show |
52 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(49): Show |
56 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.17+922_17+937dupCA others(14): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112381088 | ||||||
| chr9:112381088 | T | TACACACA others(11): Show |
10 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
10 | HG01167.hp2 HG01169.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.17+920_17+937dupCA others(16): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112381088 | ||||||
| chr9:112381088 | T | TACACACA others(13): Show |
7 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(4): Show |
7 | HG02132.hp2 NA18941.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.17+918_17+937dupCA others(18): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112381088 | ||||||
| chr9:112381088 | T | TACACACA others(15): Show |
1 | a0001c0001t0001g0068 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.17+916_17+937dupCA others(20): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112381088 | ||||||
| chr9:112381088 | TAC | T | 4 | a0001c0001t0002g0250 a0001c0001t0002g0251 a0001c0001t0002g0252 others(1): Show |
4 | HG00558.hp1 HG02165.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.17+936_17+937delCA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112381088 | ||||||
| chr9:112381094 | C | CACACACA others(5): Show |
1 | a0001c0001t0001g0254 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.17+925_17+926insTA others(10): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112381094 | ||||||
| chr9:112381096 | C | CACACACA others(11): Show |
4 | a0001c0001t0006g0064 a0001c0001t0006g0065 a0001c0001t0006g0066 others(1): Show |
4 | HG02109.hp2 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.17+933_17+934insAA others(16): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112381096 | ||||||
| chr9:112381096 | C | CACACACA others(3): Show |
13 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(10): Show |
13 | HG01261.hp2 HG02602.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.17+925_17+926insTA others(8): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112381096 | ||||||
| chr9:112381098 | C | CACACACA others(1): Show |
83 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(80): Show |
88 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.17+925_17+926insTA others(6): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112381098 | ||||||
| chr9:112381118 | T | C | 24 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0062 others(21): Show |
24 | HG01109.hp2 HG01891.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.17+938T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112381118 | |||||||
| chr9:112381188 | ATTCT | A | 10 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.17+1015_17+1018del others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112381188 | ||||||
| chr9:112381233 | A | G | 173 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0068 others(170): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.17+1053A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112381233 | |||||||
| chr9:112381403 | C | T | 8 | a0001c0001t0001g0181 a0001c0001t0002g0073 a0001c0001t0002g0119 others(5): Show |
8 | HG01070.hp2 HG02735.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.17+1223C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112381403 | |||||||
| chr9:112381605 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.17+1425C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112381605 | |||||||
| chr9:112381634 | G | A | 10 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.17+1454G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112381634 | |||||||
| chr9:112381907 | T | C | 95 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0038 others(92): Show |
98 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.17+1727T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112381907 | |||||||
| chr9:112381978 | C | G | 25 | a0001c0001t0001g0034 a0001c0001t0001g0177 a0001c0001t0002g0171 others(22): Show |
25 | HG00621.hp2 HG00673.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.17+1798C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112381978 | |||||||
| chr9:112382175 | C | T | 10 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.17+1995C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112382175 | |||||||
| chr9:112382191 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.17+2011C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112382191 | |||||||
| chr9:112382209 | G | A | 3 | a0001c0001t0002g0345 a0001c0001t0002g0346 a0001c0001t0002g0347 |
3 | HG02280.hp2 HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.17+2029G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112382209 | |||||||
| chr9:112382219 | C | T | 18 | a0001c0001t0002g0132 a0001c0002t0002g0037 a0001c0002t0002g0168 others(15): Show |
18 | HG00673.hp2 HG03831.hp1 NA18942.hp1 others(15): Show |
intron_variant | MODIFIER | c.17+2039C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112382219 | |||||||
| chr9:112382251 | T | A | 23 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(20): Show |
24 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(21): Show |
intron_variant | MODIFIER | c.17+2071T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112382251 | |||||||
| chr9:112382281 | A | G | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02145.hp1 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.17+2101A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112382281 | |||||||
| chr9:112382301 | C | T | 339 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(336): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.17+2121C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112382301 | |||||||
| chr9:112382609 | T | C | 183 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0034 others(180): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.17+2429T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112382609 | |||||||
| chr9:112382639 | C | T | 1 | a0001c0001t0002g0343 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.17+2459C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112382639 | |||||||
| chr9:112382640 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0043 others(19): Show |
24 | HG00558.hp2 HG00621.hp1 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.17+2460G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112382640 | |||||||
| chr9:112382642 | A | G | 23 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(20): Show |
24 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(21): Show |
intron_variant | MODIFIER | c.17+2462A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112382642 | |||||||
| chr9:112382788 | T | A | 4 | a0001c0001t0002g0250 a0001c0001t0002g0251 a0001c0001t0002g0252 others(1): Show |
4 | HG00558.hp1 HG02165.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.17+2608T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112382788 | |||||||
| chr9:112382941 | CT | C | 125 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0044 others(122): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.17+2776delT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112382941 | ||||||
| chr9:112383178 | G | A | 216 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(213): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.17+2998G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112383178 | |||||||
| chr9:112383324 | C | T | 23 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(20): Show |
24 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(21): Show |
intron_variant | MODIFIER | c.17+3144C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112383324 | |||||||
| chr9:112383355 | G | T | 10 | a0001c0001t0001g0032 a0001c0001t0001g0185 a0001c0001t0001g0223 others(7): Show |
10 | HG01109.hp2 HG01891.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.17+3175G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112383355 | |||||||
| chr9:112383470 | A | AT | 2 | a0001c0001t0001g0004 a0001c0001t0001g0344 |
4 | HG02109.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.17+3297dupT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112383470 | ||||||
| chr9:112383470 | A | ATT | 95 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0038 others(92): Show |
98 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.17+3296_17+3297dup others(2): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112383470 | ||||||
| chr9:112383637 | C | T | 53 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(50): Show |
54 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.17+3457C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112383637 | |||||||
| chr9:112383663 | G | A | 10 | a0001c0001t0001g0032 a0001c0001t0001g0185 a0001c0001t0001g0223 others(7): Show |
10 | HG01109.hp2 HG01891.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.17+3483G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112383663 | |||||||
| chr9:112383709 | A | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.17+3529A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112383709 | |||||||
| chr9:112383773 | T | G | 210 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(207): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.17+3593T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112383773 | |||||||
| chr9:112383825 | C | T | 177 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0034 others(174): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.17+3645C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112383825 | |||||||
| chr9:112383879 | T | A | 1 | a0001c0001t0001g0035 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.17+3699T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112383879 | |||||||
| chr9:112383978 | G | T | 10 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.17+3798G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112383978 | |||||||
| chr9:112383991 | C | G | 4 | a0001c0001t0006g0064 a0001c0001t0006g0065 a0001c0001t0006g0066 others(1): Show |
4 | HG02109.hp2 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.17+3811C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112383991 | |||||||
| chr9:112384004 | A | T | 1 | a0001c0001t0001g0342 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.17+3824A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112384004 | |||||||
| chr9:112384205 | T | TG | 36 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0032 others(33): Show |
36 | HG00621.hp2 HG00733.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.17+4029dupG | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112384205 | ||||||
| chr9:112384243 | T | TTAGTAAA others(10): Show |
8 | a0001c0001t0001g0185 a0001c0001t0001g0223 a0001c0001t0001g0227 others(5): Show |
8 | HG01109.hp2 HG01891.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.17+4063_17+4064ins others(17): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112384243 | |||||||
| chr9:112384246 | C | T | 8 | a0001c0001t0001g0185 a0001c0001t0001g0223 a0001c0001t0001g0227 others(5): Show |
8 | HG01109.hp2 HG01891.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.17+4066C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112384246 | |||||||
| chr9:112384247 | T | TAAAA | 8 | a0001c0001t0001g0185 a0001c0001t0001g0223 a0001c0001t0001g0227 others(5): Show |
8 | HG01109.hp2 HG01891.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.17+4067_17+4068ins others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112384247 | |||||||
| chr9:112384609 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.17+4429G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112384609 | |||||||
| chr9:112384991 | G | A | 1 | a0001c0001t0002g0133 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.17+4811G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112384991 | |||||||
| chr9:112385087 | T | G | 5 | a0001c0001t0002g0173 a0001c0001t0002g0174 a0001c0001t0002g0175 others(2): Show |
5 | HG01243.hp2 HG02723.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.17+4907T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112385087 | |||||||
| chr9:112385099 | A | C | 1 | a0001c0001t0002g0221 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.17+4919A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112385099 | |||||||
| chr9:112385109 | C | CACA | 337 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(334): Show |
351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.17+4945_17+4947dup others(3): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112385109 | ||||||
| chr9:112385183 | G | A | 317 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(314): Show |
329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.17+5003G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112385183 | |||||||
| chr9:112385448 | C | A | 4 | a0001c0001t0002g0173 a0001c0001t0002g0174 a0001c0001t0002g0175 others(1): Show |
4 | HG02723.hp1 HG03225.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.17+5268C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112385448 | |||||||
| chr9:112385495 | A | AT | 237 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(234): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.17+5329dupT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112385495 | ||||||
| chr9:112385495 | A | ATT | 57 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(54): Show |
58 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.17+5328_17+5329dup others(2): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112385495 | ||||||
| chr9:112385525 | T | C | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02145.hp1 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.17+5345T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112385525 | |||||||
| chr9:112385578 | T | C | 303 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(300): Show |
315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.17+5398T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112385578 | |||||||
| chr9:112385594 | A | G | 4 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(1): Show |
4 | HG02132.hp1 HG02155.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.17+5414A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112385594 | |||||||
| chr9:112385596 | T | TCTC | 303 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(300): Show |
315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.17+5418_17+5419ins others(3): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112385596 | ||||||
| chr9:112385643 | C | T | 8 | a0001c0001t0001g0265 a0001c0001t0002g0260 a0001c0001t0002g0261 others(5): Show |
8 | HG02602.hp1 HG03654.hp1 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.17+5463C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112385643 | |||||||
| chr9:112385653 | A | AT | 7 | a0001c0001t0001g0165 a0001c0001t0001g0332 a0001c0001t0006g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.17+5486dupT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112385653 | ||||||
| chr9:112385837 | C | G | 2 | a0001c0002t0002g0210 a0001c0002t0002g0211 |
2 | NA18975.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.17+5657C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112385837 | |||||||
| chr9:112385945 | T | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(18): Show |
22 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.17+5765T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112385945 | |||||||
| chr9:112385953 | T | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0043 others(19): Show |
24 | HG00558.hp2 HG00621.hp1 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.17+5773T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112385953 | |||||||
| chr9:112385993 | T | C | 1 | a0001c0001t0001g0017 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.17+5813T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112385993 | |||||||
| chr9:112385994 | C | T | 1 | a0001c0001t0001g0017 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.17+5814C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112385994 | |||||||
| chr9:112385995 | A | C | 1 | a0001c0001t0001g0017 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.17+5815A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112385995 | |||||||
| chr9:112386112 | G | A | 1 | a0001c0001t0002g0347 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.17+5932G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112386112 | |||||||
| chr9:112386169 | C | T | 4 | a0001c0001t0006g0064 a0001c0001t0006g0065 a0001c0001t0006g0066 others(1): Show |
4 | HG02109.hp2 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.17+5989C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112386169 | |||||||
| chr9:112386303 | G | T | 1 | a0001c0001t0002g0198 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.17+6123G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112386303 | |||||||
| chr9:112386560 | T | A | 1 | a0001c0001t0013g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.17+6380T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112386560 | |||||||
| chr9:112386618 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.17+6438C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112386618 | |||||||
| chr9:112386619 | C | CA | 137 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0063 others(134): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.17+6448dupA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112386619 | ||||||
| chr9:112386619 | C | CAAA | 52 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(49): Show |
53 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.17+6446_17+6448dup others(3): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112386619 | ||||||
| chr9:112386629 | T | A | 339 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(336): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.17+6449T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112386629 | |||||||
| chr9:112386810 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.17+6630C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112386810 | |||||||
| chr9:112387519 | T | C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0255 a0001c0001t0001g0256 others(3): Show |
6 | HG01261.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.17+7339T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112387519 | |||||||
| chr9:112387569 | A | G | 25 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(22): Show |
26 | HG01261.hp2 HG01433.hp1 HG02273.hp1 others(23): Show |
intron_variant | MODIFIER | c.17+7389A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112387569 | |||||||
| chr9:112387639 | G | A | 50 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(47): Show |
51 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.17+7459G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112387639 | |||||||
| chr9:112387774 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(152): Show |
163 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.17+7594A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112387774 | |||||||
| chr9:112387830 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.17+7650G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112387830 | |||||||
| chr9:112387856 | T | C | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG01261.hp2 HG02630.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.17+7676T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112387856 | |||||||
| chr9:112387923 | C | A | 1 | a0001c0001t0001g0268 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.17+7743C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112387923 | |||||||
| chr9:112387953 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.17+7773A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112387953 | |||||||
| chr9:112388015 | T | C | 10 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.17+7835T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112388015 | |||||||
| chr9:112388085 | G | A | 9 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(6): Show |
9 | HG02615.hp2 HG02622.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.17+7905G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112388085 | |||||||
| chr9:112388113 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(96): Show |
107 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.17+7933T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112388113 | |||||||
| chr9:112388116 | A | AC | 28 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(25): Show |
29 | HG01433.hp1 HG02258.hp2 HG02273.hp1 others(26): Show |
intron_variant | MODIFIER | c.17+7938dupC | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112388116 | ||||||
| chr9:112388150 | G | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.17+7970G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112388150 | |||||||
| chr9:112388160 | G | GA | 21 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(18): Show |
22 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.17+7987dupA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112388160 | ||||||
| chr9:112388164 | A | AC | 9 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(6): Show |
9 | HG02615.hp2 HG02622.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.17+7984_17+7985ins others(1): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112388164 | |||||||
| chr9:112388172 | C | CA | 31 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(28): Show |
32 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(29): Show |
intron_variant | MODIFIER | c.17+8001dupA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112388172 | ||||||
| chr9:112388182 | C | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(27): Show |
31 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(28): Show |
intron_variant | MODIFIER | c.17+8002C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112388182 | |||||||
| chr9:112388182 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.17+8002C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112388182 | |||||||
| chr9:112388332 | G | A | 123 | a0001c0001t0001g0034 a0001c0001t0001g0165 a0001c0001t0001g0166 others(120): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.17+8152G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112388332 | |||||||
| chr9:112388354 | G | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(18): Show |
22 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.17+8174G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112388354 | |||||||
| chr9:112388417 | C | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG01261.hp2 HG02630.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.17+8237C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112388417 | |||||||
| chr9:112388460 | CA | C | 114 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(111): Show |
118 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.17+8300delA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112388460 | ||||||
| chr9:112388460 | CAA | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(159): Show |
171 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.17+8299_17+8300del others(2): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112388460 | ||||||
| chr9:112388460 | CAAA | C | 34 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(31): Show |
35 | HG01891.hp1 HG01943.hp2 HG02273.hp1 others(32): Show |
intron_variant | MODIFIER | c.17+8298_17+8300del others(3): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112388460 | ||||||
| chr9:112388709 | G | A | 1 | a0001c0001t0002g0073 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.17+8529G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112388709 | |||||||
| chr9:112388726 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.17+8546C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112388726 | |||||||
| chr9:112388732 | C | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0113 a0001c0001t0001g0114 others(2): Show |
5 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.17+8552C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112388732 | |||||||
| chr9:112388736 | T | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(26): Show |
30 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(27): Show |
intron_variant | MODIFIER | c.17+8556T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112388736 | |||||||
| chr9:112388736 | T | C | 310 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(307): Show |
323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.17+8556T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112388736 | |||||||
| chr9:112388737 | G | A | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG01261.hp2 HG02630.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.17+8557G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112388737 | |||||||
| chr9:112388798 | G | GCAGACTG others(294): Show |
6 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0083 others(3): Show |
6 | HG02615.hp2 HG02976.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.17+8633_17+8634ins others(301): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112388798 | ||||||
| chr9:112388798 | G | GCAGACTG others(294): Show |
2 | a0001c0001t0001g0084 a0001c0001t0001g0120 |
2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.17+8633_17+8634ins others(301): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112388798 | ||||||
| chr9:112388798 | G | GCAGACTG others(288): Show |
1 | a0001c0001t0001g0085 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.17+8633_17+8634ins others(295): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112388798 | ||||||
| chr9:112388798 | G | GCAGACTG others(288): Show |
20 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(17): Show |
21 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.17+8633_17+8634ins others(295): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112388798 | ||||||
| chr9:112388954 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0097 others(3): Show |
7 | NA18960.hp1 NA18971.hp2 NA18988.hp2 others(4): Show |
intron_variant | MODIFIER | c.17+8774G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112388954 | |||||||
| chr9:112389026 | C | CT | 37 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(34): Show |
38 | HG01433.hp1 HG02083.hp2 HG02129.hp1 others(35): Show |
intron_variant | MODIFIER | c.17+8859dupT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112389026 | ||||||
| chr9:112389026 | C | CTT | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
17 | HG00621.hp1 HG02155.hp2 NA18943.hp1 others(14): Show |
intron_variant | MODIFIER | c.17+8858_17+8859dup others(2): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112389026 | ||||||
| chr9:112389223 | C | G | 2 | a0001c0001t0006g0006 a0001c0001t0006g0067 |
3 | HG02486.hp2 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.17+9043C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112389223 | |||||||
| chr9:112389223 | CTA | C | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
17 | HG00621.hp1 HG02155.hp2 NA18943.hp1 others(14): Show |
intron_variant | MODIFIER | c.17+9045_17+9046del others(2): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112389223 | ||||||
| chr9:112389244 | C | T | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG01109.hp2 HG02145.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.17+9064C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112389244 | |||||||
| chr9:112389285 | T | C | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
17 | HG00621.hp1 HG02155.hp2 NA18943.hp1 others(14): Show |
intron_variant | MODIFIER | c.17+9105T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112389285 | |||||||
| chr9:112389410 | T | C | 5 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(2): Show |
5 | NA18747.hp2 NA18945.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.17+9230T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112389410 | |||||||
| chr9:112389412 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(26): Show |
30 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(27): Show |
intron_variant | MODIFIER | c.17+9232G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112389412 | |||||||
| chr9:112389433 | A | C | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
17 | HG00621.hp1 HG02155.hp2 NA18943.hp1 others(14): Show |
intron_variant | MODIFIER | c.17+9253A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112389433 | |||||||
| chr9:112389458 | A | G | 339 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(336): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.17+9278A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112389458 | |||||||
| chr9:112389460 | AT | A | 36 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(33): Show |
37 | HG01433.hp1 HG01891.hp1 HG02273.hp1 others(34): Show |
intron_variant | MODIFIER | c.17+9288delT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112389460 | ||||||
| chr9:112389578 | C | A | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
17 | HG00621.hp1 HG02155.hp2 NA18943.hp1 others(14): Show |
intron_variant | MODIFIER | c.17+9398C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112389578 | |||||||
| chr9:112389789 | G | T | 1 | a0001c0001t0002g0341 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.17+9609G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112389789 | |||||||
| chr9:112389790 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.17+9610C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112389790 | |||||||
| chr9:112389849 | G | A | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
17 | HG00621.hp1 HG02155.hp2 NA18943.hp1 others(14): Show |
intron_variant | MODIFIER | c.17+9669G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112389849 | |||||||
| chr9:112389852 | C | G | 46 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
47 | HG00621.hp1 HG01433.hp1 HG02155.hp2 others(44): Show |
intron_variant | MODIFIER | c.17+9672C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112389852 | |||||||
| chr9:112389933 | C | T | 5 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(2): Show |
5 | NA18747.hp2 NA18945.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.17+9753C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112389933 | |||||||
| chr9:112389934 | G | A | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
17 | HG00621.hp1 HG02155.hp2 NA18943.hp1 others(14): Show |
intron_variant | MODIFIER | c.17+9754G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112389934 | |||||||
| chr9:112389952 | G | C | 46 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
47 | HG00621.hp1 HG01433.hp1 HG02155.hp2 others(44): Show |
intron_variant | MODIFIER | c.17+9772G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112389952 | |||||||
| chr9:112390065 | A | AAAAT | 112 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0034 others(109): Show |
117 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.17+9917_17+9920dup others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112390065 | ||||||
| chr9:112390065 | A | AAAATAAA others(1): Show |
33 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0022 others(30): Show |
33 | HG00621.hp2 HG01109.hp2 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.17+9913_17+9920dup others(8): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112390065 | ||||||
| chr9:112390065 | A | AAAATAAA others(5): Show |
48 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0038 others(45): Show |
49 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.17+9909_17+9920dup others(12): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112390065 | ||||||
| chr9:112390065 | A | AAAATAAA others(9): Show |
45 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(42): Show |
49 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.17+9905_17+9920dup others(16): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112390065 | ||||||
| chr9:112390065 | A | AAAATAAA others(13): Show |
3 | a0001c0001t0001g0329 a0001c0001t0003g0013 a0001c0001t0003g0328 |
4 | HG01070.hp1 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.17+9901_17+9920dup others(20): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112390065 | ||||||
| chr9:112390065 | A | AAAGT | 18 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(15): Show |
18 | HG01891.hp1 HG02027.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.17+9887_17+9888ins others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112390065 | ||||||
| chr9:112390065 | AAAATAAA others(1): Show |
A | 21 | a0001c0001t0002g0132 a0001c0001t0010g0214 a0001c0002t0002g0037 others(18): Show |
21 | HG00673.hp1 HG00673.hp2 HG02129.hp2 others(18): Show |
intron_variant | MODIFIER | c.17+9913_17+9920del others(8): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112390065 | ||||||
| chr9:112390068 | A | G | 44 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(41): Show |
45 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.17+9888A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112390068 | |||||||
| chr9:112390101 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(26): Show |
30 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(27): Show |
intron_variant | MODIFIER | c.17+9921G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112390101 | |||||||
| chr9:112390255 | T | A | 334 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(331): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.17+10075T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112390255 | |||||||
| chr9:112390401 | C | T | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
17 | HG00621.hp1 HG02155.hp2 NA18943.hp1 others(14): Show |
intron_variant | MODIFIER | c.17+10221C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112390401 | |||||||
| chr9:112390461 | T | A | 1 | a0001c0001t0002g0193 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.17+10281T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112390461 | |||||||
| chr9:112390465 | T | C | 1 | a0001c0001t0002g0347 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.17+10285T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112390465 | |||||||
| chr9:112390486 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0006g0067 |
2 | HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.17+10306G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112390486 | |||||||
| chr9:112390538 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.17+10358C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112390538 | |||||||
| chr9:112390555 | GCAAT | G | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
17 | HG00621.hp1 HG02155.hp2 NA18943.hp1 others(14): Show |
intron_variant | MODIFIER | c.17+10377_17+10380d others(6): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112390555 | ||||||
| chr9:112390604 | C | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(26): Show |
30 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(27): Show |
intron_variant | MODIFIER | c.17+10424C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112390604 | |||||||
| chr9:112390704 | C | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): Show |
103 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.17+10524C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112390704 | |||||||
| chr9:112390850 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.17+10670G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112390850 | |||||||
| chr9:112391178 | A | AAATAAT | 16 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(13): Show |
16 | HG00621.hp1 HG02155.hp2 NA18943.hp1 others(13): Show |
intron_variant | MODIFIER | c.17+11017_17+11022d others(8): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112391178 | ||||||
| chr9:112391178 | A | AAATAATA others(2): Show |
53 | a0001c0001t0001g0008 a0001c0001t0001g0060 a0001c0001t0001g0068 others(50): Show |
54 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.17+11014_17+11022d others(11): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112391178 | ||||||
| chr9:112391178 | A | AAATAATA others(5): Show |
9 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(6): Show |
9 | HG01256.hp1 HG01496.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.17+11011_17+11022d others(14): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112391178 | ||||||
| chr9:112391178 | A | AAATAATA others(8): Show |
3 | a0001c0001t0001g0131 a0001c0001t0001g0185 a0001c0001t0014g0031 |
3 | HG00738.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.17+11008_17+11022d others(17): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112391178 | ||||||
| chr9:112391271 | G | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0185 a0001c0001t0001g0192 others(4): Show |
7 | HG01891.hp1 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.17+11091G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112391271 | |||||||
| chr9:112391296 | TC | T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(26): Show |
30 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(27): Show |
intron_variant | MODIFIER | c.17+11124delC | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112391296 | ||||||
| chr9:112391303 | C | G | 1 | a0001c0001t0001g0018 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.17+11123C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112391303 | |||||||
| chr9:112391304 | C | A | 56 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(53): Show |
57 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.17+11124C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112391304 | |||||||
| chr9:112391349 | C | T | 81 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0035 others(78): Show |
82 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.17+11169C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112391349 | |||||||
| chr9:112391437 | C | G | 1 | a0001c0001t0001g0326 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.17+11257C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112391437 | |||||||
| chr9:112391549 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.17+11369A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112391549 | |||||||
| chr9:112391570 | G | A | 1 | a0001c0001t0001g0301 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.17+11390G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112391570 | |||||||
| chr9:112391572 | A | G | 1 | a0001c0001t0002g0154 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.17+11392A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112391572 | |||||||
| chr9:112391613 | C | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0185 a0001c0001t0001g0192 others(4): Show |
7 | HG01891.hp1 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.17+11433C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112391613 | |||||||
| chr9:112391643 | T | A | 1 | a0001c0001t0001g0186 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.17+11463T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112391643 | |||||||
| chr9:112391766 | G | T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(26): Show |
30 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(27): Show |
intron_variant | MODIFIER | c.17+11586G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112391766 | |||||||
| chr9:112391800 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0349 |
3 | HG02258.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.17+11620G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112391800 | |||||||
| chr9:112391808 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.17+11628C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112391808 | |||||||
| chr9:112391812 | C | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG01261.hp2 HG02630.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.17+11632C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112391812 | |||||||
| chr9:112391886 | C | CA | 26 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0033 others(23): Show |
26 | HG00621.hp1 HG02155.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.17+11718dupA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112391886 | ||||||
| chr9:112391886 | C | CAA | 29 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(26): Show |
30 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(27): Show |
intron_variant | MODIFIER | c.17+11717_17+11718d others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112391886 | ||||||
| chr9:112391897 | AAG | A | 7 | a0001c0001t0001g0058 a0001c0001t0001g0077 a0001c0001t0001g0099 others(4): Show |
7 | HG00558.hp2 HG01167.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.17+11719_17+11720d others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112391897 | ||||||
| chr9:112391898 | AG | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(145): Show |
154 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.17+11719delG | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112391898 | |||||||
| chr9:112391899 | G | A | 184 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(181): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.17+11719G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112391899 | |||||||
| chr9:112391900 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.17+11720A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112391900 | |||||||
| chr9:112391984 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.17+11804A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112391984 | |||||||
| chr9:112392151 | G | T | 1 | a0001c0001t0001g0277 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.18-11844G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112392151 | |||||||
| chr9:112392162 | A | G | 1 | a0001c0001t0017g0021 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.18-11833A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112392162 | |||||||
| chr9:112392218 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(96): Show |
104 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.18-11777T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112392218 | |||||||
| chr9:112392296 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0017g0021 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.18-11699A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112392296 | |||||||
| chr9:112392316 | T | C | 7 | a0001c0001t0001g0018 a0001c0001t0001g0255 a0001c0001t0001g0256 others(4): Show |
7 | HG01261.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.18-11679T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112392316 | |||||||
| chr9:112392386 | C | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG01261.hp2 HG02630.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-11609C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112392386 | |||||||
| chr9:112392443 | G | A | 20 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(17): Show |
21 | HG01433.hp1 HG02273.hp1 NA18944.hp1 others(18): Show |
intron_variant | MODIFIER | c.18-11552G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112392443 | |||||||
| chr9:112392502 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0017g0021 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.18-11493G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112392502 | |||||||
| chr9:112392778 | A | G | 21 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(18): Show |
22 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.18-11217A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112392778 | |||||||
| chr9:112392830 | A | G | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.18-11165A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112392830 | |||||||
| chr9:112392909 | C | T | 2 | a0001c0001t0003g0339 a0001c0001t0003g0340 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.18-11086C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112392909 | |||||||
| chr9:112392964 | T | C | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.18-11031T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112392964 | |||||||
| chr9:112392984 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
203 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.18-11011T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112392984 | |||||||
| chr9:112393022 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
203 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.18-10973T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393022 | |||||||
| chr9:112393041 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(99): Show |
108 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.18-10954G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393041 | |||||||
| chr9:112393048 | T | C | 57 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(54): Show |
58 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.18-10947T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393048 | |||||||
| chr9:112393094 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0076 |
2 | NA18941.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.18-10901C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393094 | |||||||
| chr9:112393144 | A | G | 21 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(18): Show |
22 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.18-10851A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393144 | |||||||
| chr9:112393145 | T | A | 1 | a0001c0001t0001g0269 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.18-10850T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393145 | |||||||
| chr9:112393155 | C | G | 1 | a0001c0001t0002g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.18-10840C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393155 | |||||||
| chr9:112393203 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.18-10792C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393203 | |||||||
| chr9:112393223 | T | C | 7 | a0001c0001t0001g0032 a0001c0001t0001g0185 a0001c0001t0001g0192 others(4): Show |
7 | HG01891.hp1 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.18-10772T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393223 | |||||||
| chr9:112393255 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0344 |
4 | HG02109.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-10740A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393255 | |||||||
| chr9:112393255 | A | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(18): Show |
22 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.18-10740A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393255 | |||||||
| chr9:112393274 | C | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(18): Show |
22 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.18-10721C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393274 | |||||||
| chr9:112393275 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.18-10720G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393275 | |||||||
| chr9:112393308 | G | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(18): Show |
22 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.18-10687G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393308 | |||||||
| chr9:112393372 | T | C | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.18-10623T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393372 | |||||||
| chr9:112393401 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.18-10594C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393401 | |||||||
| chr9:112393460 | C | T | 1 | a0001c0002t0002g0209 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.18-10535C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393460 | |||||||
| chr9:112393670 | G | A | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.18-10325G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393670 | |||||||
| chr9:112393758 | T | G | 57 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(54): Show |
58 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.18-10237T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393758 | |||||||
| chr9:112393759 | C | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(166): Show |
176 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.18-10236C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393759 | |||||||
| chr9:112393770 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.18-10225T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393770 | |||||||
| chr9:112393902 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.18-10093A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393902 | |||||||
| chr9:112393983 | T | A | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.18-10012T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393983 | |||||||
| chr9:112393987 | T | G | 1 | a0001c0001t0001g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.18-10008T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112393987 | |||||||
| chr9:112394050 | A | G | 6 | a0001c0001t0003g0013 a0001c0001t0003g0130 a0001c0001t0003g0322 others(3): Show |
7 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.18-9945A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112394050 | |||||||
| chr9:112394109 | C | T | 57 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(54): Show |
58 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.18-9886C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112394109 | |||||||
| chr9:112394110 | G | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(18): Show |
22 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.18-9885G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112394110 | |||||||
| chr9:112394266 | T | C | 23 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(20): Show |
26 | HG01433.hp1 HG02109.hp1 HG02273.hp1 others(23): Show |
intron_variant | MODIFIER | c.18-9729T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112394266 | |||||||
| chr9:112394427 | A | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0081 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.18-9568A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112394427 | |||||||
| chr9:112394505 | A | G | 123 | a0001c0001t0001g0034 a0001c0001t0001g0165 a0001c0001t0001g0166 others(120): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.18-9490A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112394505 | |||||||
| chr9:112394538 | A | T | 1 | a0001c0001t0002g0264 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.18-9457A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112394538 | |||||||
| chr9:112394592 | T | C | 1 | a0001c0001t0002g0158 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.18-9403T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112394592 | |||||||
| chr9:112394672 | C | T | 1 | a0001c0001t0001g0033 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.18-9323C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112394672 | |||||||
| chr9:112394713 | G | A | 123 | a0001c0001t0001g0034 a0001c0001t0001g0165 a0001c0001t0001g0166 others(120): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.18-9282G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112394713 | |||||||
| chr9:112394716 | A | G | 6 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0120 others(3): Show |
6 | HG02622.hp1 HG02976.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.18-9279A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112394716 | |||||||
| chr9:112394728 | CAGACTTG others(13): Show |
C | 6 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0120 others(3): Show |
6 | HG02622.hp1 HG02976.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.18-9265_18-9246del others(20): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112394728 | ||||||
| chr9:112394751 | A | G | 2 | a0001c0001t0003g0339 a0001c0001t0003g0340 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.18-9244A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112394751 | |||||||
| chr9:112394798 | T | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0349 |
3 | HG02258.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.18-9197T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112394798 | |||||||
| chr9:112394849 | C | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0185 a0001c0001t0001g0192 others(4): Show |
7 | HG01891.hp1 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.18-9146C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112394849 | |||||||
| chr9:112394914 | G | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(18): Show |
22 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.18-9081G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112394914 | |||||||
| chr9:112395167 | T | C | 6 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0120 others(3): Show |
6 | HG02622.hp1 HG02976.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.18-8828T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112395167 | |||||||
| chr9:112395330 | T | C | 339 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(336): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.18-8665T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112395330 | |||||||
| chr9:112395391 | G | A | 1 | a0001c0001t0001g0283 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.18-8604G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112395391 | |||||||
| chr9:112395401 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0017g0021 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.18-8594C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112395401 | |||||||
| chr9:112395650 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0344 |
4 | HG02109.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-8345A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112395650 | |||||||
| chr9:112395749 | G | T | 339 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(336): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.18-8246G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112395749 | |||||||
| chr9:112395766 | C | CTTCCCTG others(3): Show |
1 | a0001c0001t0002g0266 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.18-8227_18-8218dup others(10): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112395766 | ||||||
| chr9:112396094 | G | A | 1 | a0001c0001t0001g0243 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.18-7901G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112396094 | |||||||
| chr9:112396117 | T | C | 1 | a0001c0001t0014g0031 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.18-7878T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112396117 | |||||||
| chr9:112396139 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(99): Show |
108 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.18-7856C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112396139 | |||||||
| chr9:112396218 | A | G | 3 | a0001c0001t0002g0224 a0001c0001t0002g0225 a0001c0001t0002g0226 |
3 | HG02647.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.18-7777A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112396218 | |||||||
| chr9:112396351 | A | G | 57 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(54): Show |
58 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.18-7644A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112396351 | |||||||
| chr9:112396409 | A | G | 6 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0120 others(3): Show |
6 | HG02622.hp1 HG02976.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.18-7586A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112396409 | |||||||
| chr9:112396642 | T | G | 18 | a0001c0001t0001g0181 a0001c0001t0002g0073 a0001c0001t0002g0119 others(15): Show |
18 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.18-7353T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112396642 | |||||||
| chr9:112396718 | C | T | 57 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(54): Show |
58 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.18-7277C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112396718 | |||||||
| chr9:112396765 | T | C | 57 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(54): Show |
58 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.18-7230T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112396765 | |||||||
| chr9:112396767 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0344 |
4 | HG02109.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-7228G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112396767 | |||||||
| chr9:112396789 | C | G | 1 | a0001c0001t0002g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.18-7206C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112396789 | |||||||
| chr9:112396887 | G | T | 1 | a0001c0001t0001g0281 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.18-7108G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112396887 | |||||||
| chr9:112396950 | T | C | 4 | a0001c0001t0001g0083 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG02976.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-7045T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112396950 | |||||||
| chr9:112396958 | T | G | 57 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(54): Show |
58 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.18-7037T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112396958 | |||||||
| chr9:112396961 | G | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(18): Show |
22 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.18-7034G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112396961 | |||||||
| chr9:112397000 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.18-6995G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112397000 | |||||||
| chr9:112397027 | C | T | 21 | a0001c0001t0002g0132 a0001c0001t0014g0031 a0001c0002t0002g0037 others(18): Show |
21 | HG00673.hp2 HG02129.hp2 HG03098.hp1 others(18): Show |
intron_variant | MODIFIER | c.18-6968C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112397027 | |||||||
| chr9:112397225 | A | G | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.18-6770A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112397225 | |||||||
| chr9:112397239 | C | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): Show |
102 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.18-6756C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112397239 | |||||||
| chr9:112397413 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
203 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.18-6582T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112397413 | |||||||
| chr9:112397442 | A | G | 1 | a0001c0001t0001g0349 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18-6553A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112397442 | |||||||
| chr9:112397482 | C | T | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.18-6513C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112397482 | |||||||
| chr9:112397522 | T | G | 6 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0120 others(3): Show |
6 | HG02622.hp1 HG02976.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.18-6473T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112397522 | |||||||
| chr9:112397567 | C | G | 2 | a0001c0001t0001g0018 a0001c0001t0017g0021 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.18-6428C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112397567 | |||||||
| chr9:112397624 | C | T | 2 | a0001c0001t0002g0156 a0001c0001t0002g0157 |
2 | HG02257.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.18-6371C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112397624 | |||||||
| chr9:112397625 | G | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(18): Show |
22 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.18-6370G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112397625 | |||||||
| chr9:112397668 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0120 |
2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.18-6327C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112397668 | |||||||
| chr9:112397758 | A | G | 4 | a0001c0001t0001g0034 a0001c0001t0002g0212 a0001c0001t0002g0218 others(1): Show |
4 | HG00621.hp2 HG00673.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-6237A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112397758 | |||||||
| chr9:112397886 | C | T | 1 | a0001c0001t0001g0283 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.18-6109C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112397886 | |||||||
| chr9:112397887 | G | A | 1 | a0001c0001t0005g0047 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.18-6108G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112397887 | |||||||
| chr9:112397935 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
203 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.18-6060A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112397935 | |||||||
| chr9:112397936 | C | T | 6 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0120 others(3): Show |
6 | HG02622.hp1 HG02976.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.18-6059C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112397936 | |||||||
| chr9:112397957 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.18-6038C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112397957 | |||||||
| chr9:112397997 | C | T | 57 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(54): Show |
58 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.18-5998C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112397997 | |||||||
| chr9:112398025 | G | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(187): Show |
198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.18-5970G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112398025 | |||||||
| chr9:112398037 | A | G | 6 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0120 others(3): Show |
6 | HG02622.hp1 HG02976.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.18-5958A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112398037 | |||||||
| chr9:112398092 | G | A | 4 | a0001c0001t0001g0282 a0001c0001t0001g0284 a0001c0001t0001g0285 others(1): Show |
4 | NA18957.hp2 NA18977.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.18-5903G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112398092 | |||||||
| chr9:112398176 | C | A | 1 | a0001c0001t0002g0132 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.18-5819C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112398176 | |||||||
| chr9:112398261 | C | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): Show |
102 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.18-5734C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112398261 | |||||||
| chr9:112398322 | A | C | 1 | a0001c0001t0001g0321 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.18-5673A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112398322 | |||||||
| chr9:112398335 | T | C | 1 | a0001c0001t0001g0045 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.18-5660T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112398335 | |||||||
| chr9:112398400 | T | G | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG01109.hp2 HG02145.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.18-5595T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112398400 | |||||||
| chr9:112398426 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(109): Show |
118 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.18-5569C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112398426 | |||||||
| chr9:112398445 | A | G | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG01109.hp2 HG02145.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.18-5550A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112398445 | |||||||
| chr9:112398498 | A | G | 1 | a0002c0003t0002g0089 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.18-5497A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112398498 | |||||||
| chr9:112398579 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0344 |
4 | HG02109.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-5416C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112398579 | |||||||
| chr9:112398612 | A | T | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.18-5383A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112398612 | |||||||
| chr9:112398640 | T | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
203 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.18-5355T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112398640 | |||||||
| chr9:112398661 | C | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(18): Show |
22 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.18-5334C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112398661 | |||||||
| chr9:112398777 | T | G | 7 | a0001c0001t0001g0177 a0001c0001t0002g0171 a0001c0001t0002g0215 others(4): Show |
7 | HG02280.hp2 HG02486.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.18-5218T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112398777 | |||||||
| chr9:112398872 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.18-5123C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112398872 | |||||||
| chr9:112398933 | A | G | 1 | a0001c0001t0001g0320 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.18-5062A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112398933 | |||||||
| chr9:112398973 | T | A | 57 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(54): Show |
58 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.18-5022T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112398973 | |||||||
| chr9:112399007 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.18-4988G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399007 | |||||||
| chr9:112399045 | C | T | 20 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0043 others(17): Show |
20 | HG00621.hp1 HG02155.hp2 NA18943.hp1 others(17): Show |
intron_variant | MODIFIER | c.18-4950C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399045 | |||||||
| chr9:112399068 | A | AAAAG | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
203 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.18-4926_18-4923dup others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112399068 | ||||||
| chr9:112399192 | C | T | 1 | a0001c0001t0001g0319 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.18-4803C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399192 | |||||||
| chr9:112399201 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
203 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.18-4794T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399201 | |||||||
| chr9:112399202 | G | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(20): Show |
26 | HG01433.hp1 HG02109.hp1 HG02273.hp1 others(23): Show |
intron_variant | MODIFIER | c.18-4793G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399202 | |||||||
| chr9:112399223 | C | T | 2 | a0001c0001t0006g0064 a0001c0001t0006g0065 |
2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.18-4772C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399223 | |||||||
| chr9:112399269 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): Show |
102 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.18-4726A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399269 | |||||||
| chr9:112399423 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(99): Show |
108 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.18-4572A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399423 | |||||||
| chr9:112399476 | G | A | 1 | a0001c0001t0002g0191 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.18-4519G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399476 | |||||||
| chr9:112399499 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0017g0021 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.18-4496A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399499 | |||||||
| chr9:112399502 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): Show |
102 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.18-4493A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399502 | |||||||
| chr9:112399568 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(99): Show |
108 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.18-4427A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399568 | |||||||
| chr9:112399616 | C | T | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.18-4379C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399616 | |||||||
| chr9:112399617 | G | A | 1 | a0001c0001t0003g0338 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.18-4378G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399617 | |||||||
| chr9:112399634 | C | G | 4 | a0001c0001t0002g0216 a0001c0001t0002g0224 a0001c0001t0002g0225 others(1): Show |
4 | HG01884.hp1 HG02647.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.18-4361C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399634 | |||||||
| chr9:112399705 | G | T | 2 | a0001c0001t0001g0318 a0001c0001t0001g0320 |
2 | NA18612.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.18-4290G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399705 | |||||||
| chr9:112399714 | G | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
203 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.18-4281G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399714 | |||||||
| chr9:112399721 | G | A | 2 | a0001c0001t0006g0006 a0001c0001t0006g0067 |
3 | HG02486.hp2 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.18-4274G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399721 | |||||||
| chr9:112399772 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(99): Show |
108 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.18-4223G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399772 | |||||||
| chr9:112399805 | G | T | 1 | a0001c0001t0001g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.18-4190G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399805 | |||||||
| chr9:112399826 | T | C | 28 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(25): Show |
29 | HG01433.hp1 HG01891.hp1 HG02273.hp1 others(26): Show |
intron_variant | MODIFIER | c.18-4169T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399826 | |||||||
| chr9:112399872 | CAT | C | 21 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(18): Show |
22 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.18-4122_18-4121del others(2): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112399872 | |||||||
| chr9:112400059 | G | A | 19 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(16): Show |
19 | HG00621.hp1 HG02155.hp2 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.18-3936G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112400059 | |||||||
| chr9:112400083 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0344 |
4 | HG02109.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-3912C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112400083 | |||||||
| chr9:112400089 | C | A | 11 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
11 | HG00099.hp2 HG00639.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.18-3906C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112400089 | |||||||
| chr9:112400249 | C | G | 1 | a0001c0001t0017g0021 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.18-3746C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112400249 | |||||||
| chr9:112400262 | G | A | 1 | a0002c0003t0002g0089 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.18-3733G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112400262 | |||||||
| chr9:112400386 | A | T | 1 | a0001c0001t0003g0325 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.18-3609A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112400386 | |||||||
| chr9:112400476 | G | A | 56 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(53): Show |
57 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.18-3519G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112400476 | |||||||
| chr9:112400483 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0349 a0001c0001t0017g0021 |
3 | HG02258.hp2 HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.18-3512T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112400483 | |||||||
| chr9:112400521 | C | T | 1 | a0001c0002t0002g0169 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.18-3474C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112400521 | |||||||
| chr9:112400539 | G | A | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
17 | HG00621.hp1 HG02155.hp2 NA18943.hp1 others(14): Show |
intron_variant | MODIFIER | c.18-3456G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112400539 | |||||||
| chr9:112400578 | T | A | 123 | a0001c0001t0001g0034 a0001c0001t0001g0165 a0001c0001t0001g0166 others(120): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.18-3417T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112400578 | |||||||
| chr9:112400584 | T | G | 123 | a0001c0001t0001g0034 a0001c0001t0001g0165 a0001c0001t0001g0166 others(120): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.18-3411T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112400584 | |||||||
| chr9:112400786 | C | T | 56 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(53): Show |
57 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.18-3209C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112400786 | |||||||
| chr9:112400787 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
202 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.18-3208A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112400787 | |||||||
| chr9:112400891 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.18-3104C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112400891 | |||||||
| chr9:112400915 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.18-3080A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112400915 | |||||||
| chr9:112401010 | C | T | 1 | a0001c0001t0006g0065 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.18-2985C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112401010 | |||||||
| chr9:112401066 | G | A | 1 | a0001c0001t0001g0349 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18-2929G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112401066 | |||||||
| chr9:112401188 | A | C | 20 | a0001c0001t0002g0132 a0001c0002t0002g0037 a0001c0002t0002g0168 others(17): Show |
20 | HG00673.hp2 HG02129.hp2 HG03831.hp1 others(17): Show |
intron_variant | MODIFIER | c.18-2807A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112401188 | |||||||
| chr9:112401317 | G | T | 3 | a0001c0002t0002g0169 a0001c0002t0002g0208 a0001c0002t0002g0209 |
3 | NA18948.hp2 NA19076.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.18-2678G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112401317 | |||||||
| chr9:112401419 | G | T | 56 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(53): Show |
57 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.18-2576G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112401419 | |||||||
| chr9:112401441 | CA | C | 124 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0042 others(121): Show |
128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.18-2527delA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112401441 | ||||||
| chr9:112401441 | CAA | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(98): Show |
107 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.18-2528_18-2527del others(2): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112401441 | ||||||
| chr9:112401441 | CAAA | C | 62 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(59): Show |
63 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.18-2529_18-2527del others(3): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112401441 | ||||||
| chr9:112401441 | CAAAAA | C | 20 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(17): Show |
21 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.18-2531_18-2527del others(5): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112401441 | ||||||
| chr9:112401530 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.18-2465T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112401530 | |||||||
| chr9:112401719 | G | T | 3 | a0001c0001t0001g0181 a0001c0001t0002g0073 a0001c0001t0002g0222 |
3 | HG02735.hp1 HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.18-2276G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112401719 | |||||||
| chr9:112401776 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0344 |
4 | HG02109.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-2219T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112401776 | |||||||
| chr9:112401777 | G | C | 123 | a0001c0001t0001g0034 a0001c0001t0001g0165 a0001c0001t0001g0166 others(120): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.18-2218G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112401777 | |||||||
| chr9:112402035 | T | C | 10 | a0001c0001t0001g0034 a0001c0001t0002g0158 a0001c0001t0002g0179 others(7): Show |
10 | HG00621.hp2 HG00673.hp1 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.18-1960T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112402035 | |||||||
| chr9:112402039 | C | G | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.18-1956C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112402039 | |||||||
| chr9:112402102 | T | A | 1 | a0001c0001t0001g0186 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.18-1893T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112402102 | |||||||
| chr9:112402550 | T | TAA | 183 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
193 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.18-1432_18-1431dup others(2): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112402550 | ||||||
| chr9:112402562 | A | AAG | 8 | a0001c0001t0001g0032 a0001c0001t0001g0185 a0001c0001t0001g0192 others(5): Show |
8 | HG01891.hp1 HG02630.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.18-1432_18-1431ins others(2): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112402562 | ||||||
| chr9:112402579 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.18-1416A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112402579 | |||||||
| chr9:112402793 | C | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.18-1202C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112402793 | |||||||
| chr9:112402811 | C | T | 1 | a0001c0001t0002g0317 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.18-1184C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112402811 | |||||||
| chr9:112402815 | GGAGGCTG others(17): Show |
G | 1 | a0001c0001t0002g0133 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18-1158_18-1135del others(24): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112402815 | ||||||
| chr9:112402827 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.18-1168A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112402827 | |||||||
| chr9:112402887 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.18-1108T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112402887 | |||||||
| chr9:112402958 | C | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(186): Show |
197 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.18-1037C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112402958 | |||||||
| chr9:112402960 | C | A | 8 | a0001c0001t0001g0032 a0001c0001t0001g0185 a0001c0001t0001g0192 others(5): Show |
8 | HG01891.hp1 HG02630.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.18-1035C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112402960 | |||||||
| chr9:112402960 | C | T | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.18-1035C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112402960 | |||||||
| chr9:112402975 | A | AAC | 2 | a0001c0001t0001g0004 a0001c0001t0001g0344 |
4 | HG02109.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-1008_18-1007dup others(2): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112402975 | ||||||
| chr9:112403067 | G | A | 6 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0120 others(3): Show |
6 | HG02622.hp1 HG02976.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.18-928G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112403067 | |||||||
| chr9:112403134 | G | A | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
17 | HG00621.hp1 HG02155.hp2 NA18943.hp1 others(14): Show |
intron_variant | MODIFIER | c.18-861G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112403134 | |||||||
| chr9:112403142 | T | C | 8 | a0001c0001t0001g0032 a0001c0001t0001g0185 a0001c0001t0001g0192 others(5): Show |
8 | HG01891.hp1 HG02630.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.18-853T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112403142 | |||||||
| chr9:112403199 | C | CT | 192 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
202 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.18-793dupT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 112403199 | ||||||
| chr9:112403235 | G | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0060 a0001c0001t0001g0069 others(35): Show |
39 | HG01167.hp2 HG01169.hp2 HG02080.hp2 others(36): Show |
intron_variant | MODIFIER | c.18-760G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112403235 | |||||||
| chr9:112403285 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.18-710T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112403285 | |||||||
| chr9:112403419 | T | C | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.18-576T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112403419 | |||||||
| chr9:112403443 | G | A | 56 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(53): Show |
57 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.18-552G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112403443 | |||||||
| chr9:112403541 | G | T | 1 | a0001c0001t0004g0234 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.18-454G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112403541 | |||||||
| chr9:112403644 | C | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0344 |
4 | HG02109.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-351C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112403644 | |||||||
| chr9:112403719 | T | G | 20 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(17): Show |
21 | HG01433.hp1 HG02273.hp1 NA18944.hp1 others(18): Show |
intron_variant | MODIFIER | c.18-276T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1/10 | chr9 | 112403719 | |||||||
| chr9:112404322 | G | A | 22 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(19): Show |
23 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.181+164G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 2/10 | chr9 | 112404322 | |||||||
| chr9:112404386 | G | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0344 a0001c0001t0011g0258 |
5 | HG02109.hp1 HG02630.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.181+228G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 2/10 | chr9 | 112404386 | |||||||
| chr9:112404520 | C | T | 1 | a0001c0001t0002g0263 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.181+362C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 2/10 | chr9 | 112404520 | |||||||
| chr9:112404557 | C | G | 7 | a0001c0001t0002g0260 a0001c0001t0002g0261 a0001c0001t0002g0262 others(4): Show |
7 | HG02602.hp1 HG03654.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.181+399C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 2/10 | chr9 | 112404557 | |||||||
| chr9:112404855 | T | C | 6 | a0001c0001t0001g0181 a0001c0001t0002g0073 a0001c0001t0002g0119 others(3): Show |
6 | HG01070.hp2 HG02735.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.181+697T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 2/10 | chr9 | 112404855 | |||||||
| chr9:112404866 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(93): Show |
101 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.181+708T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 2/10 | chr9 | 112404866 | |||||||
| chr9:112404921 | CAG | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(188): Show |
199 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.182-702_182-701del others(2): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 2/10 | chr9 | 112404921 | |||||||
| chr9:112405089 | A | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
203 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.182-535A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 2/10 | chr9 | 112405089 | |||||||
| chr9:112405610 | A | G | 2 | a0001c0001t0001g0316 a0001c0001t0001g0329 |
2 | HG01192.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.182-14A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 2/10 | chr9 | 112405610 | |||||||
| chr9:112405893 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(69): Show |
77 | HG00323.hp1 HG00558.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.280+171G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112405893 | |||||||
| chr9:112405977 | A | C | 6 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0120 others(3): Show |
6 | HG02622.hp1 HG02976.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.280+255A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112405977 | |||||||
| chr9:112406166 | GA | G | 56 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0035 others(53): Show |
59 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.280+458delA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 112406166 | ||||||
| chr9:112406175 | A | G | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.280+453A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112406175 | |||||||
| chr9:112406179 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(131): Show |
141 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.280+457A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112406179 | |||||||
| chr9:112406181 | G | A | 3 | a0001c0001t0002g0224 a0001c0001t0002g0225 a0001c0001t0002g0226 |
3 | HG02647.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.280+459G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112406181 | |||||||
| chr9:112406332 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.280+610G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112406332 | |||||||
| chr9:112406399 | T | C | 316 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(313): Show |
330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.280+677T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112406399 | |||||||
| chr9:112406416 | GT | G | 29 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(26): Show |
30 | HG01433.hp1 HG01891.hp1 HG02273.hp1 others(27): Show |
intron_variant | MODIFIER | c.280+695delT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112406416 | |||||||
| chr9:112406530 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.280+808G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112406530 | |||||||
| chr9:112406531 | C | T | 5 | a0001c0001t0006g0006 a0001c0001t0006g0064 a0001c0001t0006g0065 others(2): Show |
6 | HG02109.hp2 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.280+809C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112406531 | |||||||
| chr9:112406539 | C | T | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG01109.hp2 HG02145.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+817C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112406539 | |||||||
| chr9:112406573 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.280+851C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112406573 | |||||||
| chr9:112406709 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.280+987C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112406709 | |||||||
| chr9:112406767 | C | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(28): Show |
35 | HG01433.hp1 HG02109.hp1 HG02109.hp2 others(32): Show |
intron_variant | MODIFIER | c.280+1045C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112406767 | |||||||
| chr9:112406903 | A | G | 32 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(29): Show |
36 | HG01433.hp1 HG02109.hp1 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.280+1181A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112406903 | |||||||
| chr9:112406986 | T | TGTGAGGG others(17): Show |
21 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(18): Show |
22 | HG01433.hp1 HG02273.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.280+1265_280+1288d others(26): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 112406986 | ||||||
| chr9:112407026 | A | C | 27 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(24): Show |
29 | HG01433.hp1 HG02109.hp2 HG02273.hp1 others(26): Show |
intron_variant | MODIFIER | c.280+1304A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112407026 | |||||||
| chr9:112407121 | T | C | 5 | a0001c0001t0006g0006 a0001c0001t0006g0064 a0001c0001t0006g0065 others(2): Show |
6 | HG02109.hp2 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.280+1399T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112407121 | |||||||
| chr9:112407124 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(93): Show |
101 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.280+1402A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112407124 | |||||||
| chr9:112407228 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.280+1506C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112407228 | |||||||
| chr9:112407417 | C | CT | 54 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(51): Show |
55 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.281-1480dupT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 112407417 | ||||||
| chr9:112407504 | C | T | 5 | a0001c0001t0006g0006 a0001c0001t0006g0064 a0001c0001t0006g0065 others(2): Show |
6 | HG02109.hp2 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.281-1403C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112407504 | |||||||
| chr9:112407694 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(303): Show |
320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.281-1213A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112407694 | |||||||
| chr9:112407823 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.281-1084T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112407823 | |||||||
| chr9:112407857 | A | G | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.281-1050A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112407857 | |||||||
| chr9:112407983 | G | T | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(4): Show |
7 | HG02027.hp2 NA18941.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-924G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112407983 | |||||||
| chr9:112407993 | A | C | 126 | a0001c0001t0001g0034 a0001c0001t0001g0165 a0001c0001t0001g0166 others(123): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.281-914A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112407993 | |||||||
| chr9:112408033 | G | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(90): Show |
98 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.281-874G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112408033 | |||||||
| chr9:112408182 | T | G | 17 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0083 others(14): Show |
17 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.281-725T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112408182 | |||||||
| chr9:112408295 | A | G | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG01109.hp2 HG02145.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-612A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112408295 | |||||||
| chr9:112408476 | A | G | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.281-431A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112408476 | |||||||
| chr9:112408607 | A | T | 1 | a0001c0001t0001g0329 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.281-300A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112408607 | |||||||
| chr9:112408782 | T | C | 345 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(342): Show |
360 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.281-125T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3/10 | chr9 | 112408782 | |||||||
| chr9:112409029 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0036 others(2): Show |
7 | HG02109.hp1 HG02258.hp2 HG02818.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.395+8T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112409029 | |||||||
| chr9:112409053 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0270 |
2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.395+32A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112409053 | |||||||
| chr9:112409133 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.395+112A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112409133 | |||||||
| chr9:112409245 | A | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0268 |
3 | NA18951.hp2 NA18963.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.395+224A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112409245 | |||||||
| chr9:112409293 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.395+272G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112409293 | |||||||
| chr9:112409698 | A | G | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.395+677A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112409698 | |||||||
| chr9:112409706 | T | G | 313 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(310): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.395+685T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112409706 | |||||||
| chr9:112409746 | A | C | 54 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(51): Show |
55 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.395+725A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112409746 | |||||||
| chr9:112409795 | A | G | 1 | a0001c0001t0002g0253 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.395+774A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112409795 | |||||||
| chr9:112409971 | G | A | 1 | a0001c0001t0014g0031 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.395+950G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112409971 | |||||||
| chr9:112410006 | A | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0270 |
2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.395+985A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112410006 | |||||||
| chr9:112410019 | G | A | 9 | a0001c0001t0002g0153 a0001c0001t0002g0191 a0001c0001t0004g0090 others(6): Show |
9 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.395+998G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112410019 | |||||||
| chr9:112410021 | T | TA | 20 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(17): Show |
20 | HG00621.hp1 HG02155.hp2 HG03139.hp1 others(17): Show |
intron_variant | MODIFIER | c.395+1013dupA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 112410021 | ||||||
| chr9:112410157 | T | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
9 | HG01891.hp1 HG02109.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.395+1136T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112410157 | |||||||
| chr9:112410379 | A | G | 7 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
9 | HG01891.hp1 HG02109.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.395+1358A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112410379 | |||||||
| chr9:112410520 | TA | T | 7 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0185 others(4): Show |
7 | HG02622.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+1500delA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112410520 | |||||||
| chr9:112410654 | T | C | 1 | a0001c0001t0002g0135 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.395+1633T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112410654 | |||||||
| chr9:112410659 | GCTCATGC others(8): Show |
G | 146 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(143): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.395+1640_395+1654d others(17): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 112410659 | ||||||
| chr9:112410695 | G | T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0084 others(6): Show |
9 | HG02622.hp1 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.395+1674G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112410695 | |||||||
| chr9:112410705 | T | C | 59 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(56): Show |
60 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.395+1684T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112410705 | |||||||
| chr9:112410736 | A | G | 20 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(17): Show |
21 | HG01433.hp1 HG02273.hp1 NA18944.hp1 others(18): Show |
intron_variant | MODIFIER | c.395+1715A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112410736 | |||||||
| chr9:112410799 | C | T | 1 | a0001c0001t0017g0021 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.395+1778C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112410799 | |||||||
| chr9:112410995 | T | A | 59 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(56): Show |
60 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.395+1974T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112410995 | |||||||
| chr9:112411216 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.395+2195C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112411216 | |||||||
| chr9:112411289 | T | C | 1 | a0001c0001t0001g0296 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.395+2268T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112411289 | |||||||
| chr9:112411291 | G | A | 1 | a0001c0001t0006g0006 | 2 | HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.395+2270G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112411291 | |||||||
| chr9:112411301 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0344 |
4 | HG02109.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.395+2280G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112411301 | |||||||
| chr9:112411307 | C | T | 1 | a0001c0001t0002g0315 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.395+2286C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112411307 | |||||||
| chr9:112411367 | C | A | 1 | a0001c0001t0020g0121 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.395+2346C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112411367 | |||||||
| chr9:112411410 | C | T | 7 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0185 others(4): Show |
7 | HG02622.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+2389C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112411410 | |||||||
| chr9:112411442 | A | G | 5 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(2): Show |
5 | HG01109.hp2 HG02145.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.395+2421A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112411442 | |||||||
| chr9:112411496 | G | A | 8 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(5): Show |
8 | HG01261.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.395+2475G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112411496 | |||||||
| chr9:112411607 | G | A | 146 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(143): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.395+2586G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112411607 | |||||||
| chr9:112411654 | A | G | 339 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(336): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.395+2633A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112411654 | |||||||
| chr9:112412006 | A | C | 4 | a0001c0001t0001g0083 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG02976.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.395+2985A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112412006 | |||||||
| chr9:112412100 | C | T | 8 | a0001c0001t0001g0030 a0001c0001t0001g0186 a0001c0001t0001g0270 others(5): Show |
9 | HG02109.hp2 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.395+3079C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112412100 | |||||||
| chr9:112412113 | A | G | 1 | a0001c0001t0014g0031 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.395+3092A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112412113 | |||||||
| chr9:112412131 | T | G | 1 | a0001c0002t0002g0169 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.395+3110T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112412131 | |||||||
| chr9:112412210 | A | G | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG01109.hp2 HG02145.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.395+3189A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112412210 | |||||||
| chr9:112412252 | T | A | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | HG03927.hp1 NA18994.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.395+3231T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112412252 | |||||||
| chr9:112412289 | TA | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): Show |
100 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.395+3269delA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112412289 | |||||||
| chr9:112412322 | A | G | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG01109.hp2 HG02145.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.395+3301A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112412322 | |||||||
| chr9:112412328 | T | C | 139 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(136): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.395+3307T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112412328 | |||||||
| chr9:112412368 | A | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): Show |
100 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.395+3347A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112412368 | |||||||
| chr9:112412416 | T | C | 12 | a0001c0001t0001g0030 a0001c0001t0001g0083 a0001c0001t0001g0186 others(9): Show |
13 | HG02109.hp2 HG02486.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.395+3395T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112412416 | |||||||
| chr9:112412532 | T | C | 7 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
9 | HG01891.hp1 HG02109.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.395+3511T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112412532 | |||||||
| chr9:112412624 | C | T | 4 | a0001c0001t0001g0083 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG02976.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.395+3603C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112412624 | |||||||
| chr9:112412749 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.395+3728G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112412749 | |||||||
| chr9:112412841 | C | T | 2 | a0001c0001t0001g0316 a0001c0001t0001g0329 |
2 | HG01192.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.395+3820C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112412841 | |||||||
| chr9:112412842 | G | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
9 | HG01891.hp1 HG02109.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.395+3821G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112412842 | |||||||
| chr9:112412943 | A | T | 5 | a0001c0001t0001g0254 a0001c0001t0001g0276 a0001c0001t0001g0277 others(2): Show |
5 | HG02027.hp1 NA18956.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.396-3898A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112412943 | |||||||
| chr9:112413232 | A | C | 4 | a0001c0001t0001g0083 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG02976.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.396-3609A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112413232 | |||||||
| chr9:112413249 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.396-3592C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112413249 | |||||||
| chr9:112413250 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.396-3591G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112413250 | |||||||
| chr9:112413269 | G | T | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.396-3572G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112413269 | |||||||
| chr9:112413295 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): Show |
100 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.396-3546A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112413295 | |||||||
| chr9:112413298 | G | C | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.396-3543G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112413298 | |||||||
| chr9:112413341 | G | A | 12 | a0001c0001t0001g0030 a0001c0001t0001g0083 a0001c0001t0001g0186 others(9): Show |
13 | HG02109.hp2 HG02486.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.396-3500G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112413341 | |||||||
| chr9:112413381 | G | A | 63 | a0001c0001t0001g0170 a0001c0001t0002g0002 a0001c0001t0002g0007 others(60): Show |
67 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.396-3460G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112413381 | |||||||
| chr9:112413386 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0344 |
4 | HG02109.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.396-3455A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112413386 | |||||||
| chr9:112413495 | GA | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): Show |
100 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.396-3338delA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 112413495 | ||||||
| chr9:112413499 | A | G | 4 | a0001c0001t0001g0083 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG02976.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.396-3342A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112413499 | |||||||
| chr9:112413499 | AAAAAG | A | 138 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(135): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.396-3328_396-3324d others(7): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 112413499 | ||||||
| chr9:112413500 | A | G | 1 | a0001c0001t0002g0220 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.396-3341A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112413500 | |||||||
| chr9:112413504 | G | A | 1 | a0001c0001t0002g0220 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.396-3337G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112413504 | |||||||
| chr9:112413504 | G | T | 4 | a0001c0001t0001g0083 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG02976.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.396-3337G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112413504 | |||||||
| chr9:112413509 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): Show |
100 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.396-3332G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112413509 | |||||||
| chr9:112413550 | G | T | 1 | a0001c0001t0001g0334 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.396-3291G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112413550 | |||||||
| chr9:112413565 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(163): Show |
173 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.396-3276C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112413565 | |||||||
| chr9:112413737 | A | G | 12 | a0001c0001t0001g0030 a0001c0001t0001g0083 a0001c0001t0001g0186 others(9): Show |
13 | HG02109.hp2 HG02486.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.396-3104A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112413737 | |||||||
| chr9:112413792 | A | G | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.396-3049A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112413792 | |||||||
| chr9:112413859 | G | A | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(4): Show |
7 | HG02027.hp2 NA18941.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-2982G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112413859 | |||||||
| chr9:112413929 | G | A | 5 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0084 others(2): Show |
5 | HG02258.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.396-2912G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112413929 | |||||||
| chr9:112414035 | C | A | 339 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(336): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.396-2806C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112414035 | |||||||
| chr9:112414110 | A | G | 59 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(56): Show |
60 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.396-2731A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112414110 | |||||||
| chr9:112414482 | A | T | 2 | a0001c0001t0002g0122 a0001c0001t0002g0125 |
2 | HG01109.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.396-2359A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112414482 | |||||||
| chr9:112414596 | A | AG | 153 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(150): Show |
159 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.396-2243dupG | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 112414596 | ||||||
| chr9:112414604 | C | T | 12 | a0001c0001t0001g0030 a0001c0001t0001g0083 a0001c0001t0001g0186 others(9): Show |
13 | HG02109.hp2 HG02486.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.396-2237C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112414604 | |||||||
| chr9:112414741 | T | C | 1 | a0001c0001t0002g0224 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.396-2100T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112414741 | |||||||
| chr9:112414818 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0014g0031 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.396-2023C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112414818 | |||||||
| chr9:112414891 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.396-1950G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112414891 | |||||||
| chr9:112414957 | G | GA | 172 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(169): Show |
179 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.396-1874dupA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 112414957 | ||||||
| chr9:112415071 | A | C | 1 | a0001c0001t0001g0016 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.396-1770A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112415071 | |||||||
| chr9:112415101 | C | T | 4 | a0001c0001t0001g0083 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG02976.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.396-1740C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112415101 | |||||||
| chr9:112415106 | T | A | 1 | a0001c0002t0002g0202 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.396-1735T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112415106 | |||||||
| chr9:112415191 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0270 |
2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.396-1650G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112415191 | |||||||
| chr9:112415402 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.396-1439A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112415402 | |||||||
| chr9:112415565 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.396-1276A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112415565 | |||||||
| chr9:112415749 | C | A | 147 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(144): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.396-1092C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112415749 | |||||||
| chr9:112415788 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.396-1053C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112415788 | |||||||
| chr9:112415951 | A | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0349 |
3 | HG02258.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.396-890A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112415951 | |||||||
| chr9:112415976 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0014g0031 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.396-865C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112415976 | |||||||
| chr9:112416105 | C | CA | 54 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0068 others(51): Show |
55 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.396-721dupA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 112416105 | ||||||
| chr9:112416105 | CA | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(99): Show |
107 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.396-721delA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 112416105 | ||||||
| chr9:112416105 | CAAA | C | 5 | a0001c0001t0006g0006 a0001c0001t0006g0064 a0001c0001t0006g0065 others(2): Show |
6 | HG02109.hp2 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.396-723_396-721del others(3): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 112416105 | ||||||
| chr9:112416252 | G | GA | 18 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG00621.hp1 HG02155.hp2 NA18943.hp1 others(15): Show |
intron_variant | MODIFIER | c.396-579dupA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 112416252 | ||||||
| chr9:112416260 | A | C | 1 | a0001c0001t0002g0133 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.396-581A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112416260 | |||||||
| chr9:112416439 | A | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(151): Show |
160 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.396-402A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112416439 | |||||||
| chr9:112416440 | AAACAAAC | A | 9 | a0001c0001t0001g0030 a0001c0001t0001g0083 a0001c0001t0001g0187 others(6): Show |
10 | HG02109.hp2 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.396-398_396-392del others(7): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 112416440 | ||||||
| chr9:112416443 | C | A | 2 | a0001c0001t0002g0219 a0001c0001t0002g0221 |
2 | NA18956.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.396-398C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112416443 | |||||||
| chr9:112416482 | C | T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0084 others(6): Show |
9 | HG02622.hp1 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.396-359C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112416482 | |||||||
| chr9:112416515 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0349 |
3 | HG02258.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.396-326G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112416515 | |||||||
| chr9:112416574 | C | G | 3 | a0001c0001t0002g0086 a0001c0001t0002g0248 a0001c0001t0012g0088 |
3 | HG01891.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.396-267C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112416574 | |||||||
| chr9:112416588 | T | TA | 119 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(116): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.396-237dupA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 112416588 | ||||||
| chr9:112416588 | TA | T | 55 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(52): Show |
56 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.396-237delA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 112416588 | ||||||
| chr9:112416630 | GTGC | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(162): Show |
172 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.396-207_396-205del others(3): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 112416630 | ||||||
| chr9:112416729 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.396-112G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112416729 | |||||||
| chr9:112416811 | A | C | 1 | a0001c0001t0001g0117 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.396-30A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 4/10 | chr9 | 112416811 | |||||||
| chr9:112417036 | A | AT | 95 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): Show |
100 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.499+93dupT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 112417036 | ||||||
| chr9:112417167 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(151): Show |
160 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.499+223G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | chr9 | 112417167 | |||||||
| chr9:112417249 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0270 |
2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.499+305T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | chr9 | 112417249 | |||||||
| chr9:112417477 | T | TA | 18 | a0001c0001t0001g0011 a0001c0001t0001g0048 a0001c0001t0001g0076 others(15): Show |
20 | HG00597.hp1 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.499+551dupA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 112417477 | ||||||
| chr9:112417477 | TA | T | 143 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(140): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.499+551delA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 112417477 | ||||||
| chr9:112417556 | T | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(309): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.499+612T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | chr9 | 112417556 | |||||||
| chr9:112417713 | C | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0120 |
2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.499+769C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | chr9 | 112417713 | |||||||
| chr9:112417781 | T | TA | 58 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(55): Show |
59 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.499+851dupA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 112417781 | ||||||
| chr9:112417781 | T | TAA | 11 | a0001c0001t0001g0030 a0001c0001t0001g0083 a0001c0001t0001g0187 others(8): Show |
12 | HG02109.hp2 HG02486.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+850_499+851dup others(2): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 112417781 | ||||||
| chr9:112417815 | T | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.499+871T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | chr9 | 112417815 | |||||||
| chr9:112417883 | G | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0060 others(1): Show |
4 | NA18951.hp2 NA18957.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+939G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | chr9 | 112417883 | |||||||
| chr9:112417918 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0344 |
4 | HG02109.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.500-942A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | chr9 | 112417918 | |||||||
| chr9:112417923 | C | T | 53 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(50): Show |
54 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.500-937C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | chr9 | 112417923 | |||||||
| chr9:112417981 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): Show |
100 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.500-879G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | chr9 | 112417981 | |||||||
| chr9:112418168 | CAAATATT | C | 3 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0125 |
3 | HG01109.hp1 HG01175.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.500-690_500-684del others(7): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 112418168 | ||||||
| chr9:112418169 | AAAT | A | 137 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(134): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.500-689_500-687del others(3): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 112418169 | ||||||
| chr9:112418188 | T | C | 1 | a0001c0001t0004g0234 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.500-672T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | chr9 | 112418188 | |||||||
| chr9:112418532 | G | A | 2 | a0001c0001t0002g0179 a0001c0001t0002g0220 |
2 | NA18983.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.500-328G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | chr9 | 112418532 | |||||||
| chr9:112418542 | C | T | 1 | a0001c0001t0001g0320 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.500-318C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | chr9 | 112418542 | |||||||
| chr9:112418562 | C | CA | 153 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(150): Show |
158 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.500-283dupA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 112418562 | ||||||
| chr9:112418562 | C | CAA | 23 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0035 others(20): Show |
27 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.500-284_500-283dup others(2): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 112418562 | ||||||
| chr9:112418649 | T | A | 4 | a0001c0001t0001g0083 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG02976.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.500-211T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | chr9 | 112418649 | |||||||
| chr9:112418696 | TATATGTA others(25): Show |
T | 1 | a0001c0001t0004g0232 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.500-150_500-119del others(32): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 112418696 | ||||||
| chr9:112418850 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0270 |
2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.500-10G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 5/10 | chr9 | 112418850 | |||||||
| chr9:112419097 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.598+139C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112419097 | |||||||
| chr9:112419175 | A | AT | 339 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(336): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.598+222dupT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112419175 | ||||||
| chr9:112419255 | T | C | 1 | a0001c0001t0002g0142 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.598+297T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112419255 | |||||||
| chr9:112419256 | G | A | 1 | a0001c0001t0002g0142 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.598+298G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112419256 | |||||||
| chr9:112419270 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.598+312C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112419270 | |||||||
| chr9:112419419 | A | G | 18 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG00621.hp1 HG02155.hp2 NA18943.hp1 others(15): Show |
intron_variant | MODIFIER | c.598+461A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112419419 | |||||||
| chr9:112419633 | C | A | 1 | a0002c0003t0002g0089 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.598+675C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112419633 | |||||||
| chr9:112419719 | A | G | 1 | a0001c0001t0003g0328 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.598+761A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112419719 | |||||||
| chr9:112419933 | T | C | 140 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(137): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.598+975T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112419933 | |||||||
| chr9:112419969 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.598+1011C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112419969 | |||||||
| chr9:112420017 | A | G | 4 | a0001c0001t0001g0083 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG02976.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+1059A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112420017 | |||||||
| chr9:112420059 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.598+1101C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112420059 | |||||||
| chr9:112420137 | T | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0349 |
3 | HG02258.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.598+1179T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112420137 | |||||||
| chr9:112420249 | G | A | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.598+1291G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112420249 | |||||||
| chr9:112420273 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.598+1315C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112420273 | |||||||
| chr9:112420332 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(150): Show |
159 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.598+1374T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112420332 | |||||||
| chr9:112420435 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): Show |
100 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.598+1477C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112420435 | |||||||
| chr9:112420446 | T | TGGGA | 5 | a0001c0001t0001g0032 a0001c0001t0001g0185 a0001c0001t0001g0192 others(2): Show |
5 | HG02630.hp1 HG03098.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+1491_598+1494d others(6): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112420446 | ||||||
| chr9:112420506 | TA | T | 7 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(4): Show |
7 | HG01261.hp2 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+1559delA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112420506 | ||||||
| chr9:112420516 | A | AC | 140 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(137): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.598+1558_598+1559i others(3): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112420516 | |||||||
| chr9:112420516 | A | C | 7 | a0001c0001t0001g0083 a0001c0001t0001g0187 a0001c0001t0001g0188 others(4): Show |
7 | HG01952.hp1 HG02976.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+1558A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112420516 | |||||||
| chr9:112420524 | C | A | 12 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0032 others(9): Show |
12 | HG02559.hp2 HG02622.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.598+1566C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112420524 | |||||||
| chr9:112420526 | A | C | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.598+1568A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112420526 | |||||||
| chr9:112420711 | T | C | 5 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(2): Show |
5 | HG01109.hp2 HG02145.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+1753T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112420711 | |||||||
| chr9:112420801 | A | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0185 a0001c0001t0001g0192 others(2): Show |
5 | HG02630.hp1 HG03098.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+1843A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112420801 | |||||||
| chr9:112420854 | A | T | 1 | a0001c0001t0004g0090 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.598+1896A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112420854 | |||||||
| chr9:112420940 | G | A | 53 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(50): Show |
54 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.598+1982G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112420940 | |||||||
| chr9:112420947 | A | AT | 171 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(168): Show |
178 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.598+2000dupT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112420947 | ||||||
| chr9:112421070 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.598+2112T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112421070 | |||||||
| chr9:112421147 | T | G | 1 | a0001c0001t0001g0186 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.598+2189T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112421147 | |||||||
| chr9:112421326 | C | G | 1 | a0001c0001t0002g0294 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.598+2368C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112421326 | |||||||
| chr9:112421332 | C | G | 1 | a0001c0001t0001g0321 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.598+2374C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112421332 | |||||||
| chr9:112421448 | T | G | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(4): Show |
7 | HG02027.hp2 NA18941.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+2490T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112421448 | |||||||
| chr9:112421476 | G | A | 20 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(17): Show |
20 | HG00621.hp1 HG01192.hp1 HG02155.hp2 others(17): Show |
intron_variant | MODIFIER | c.598+2518G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112421476 | |||||||
| chr9:112421555 | A | T | 339 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(336): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.598+2597A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112421555 | |||||||
| chr9:112421556 | A | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): Show |
100 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.598+2598A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112421556 | |||||||
| chr9:112421656 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): Show |
100 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.598+2698C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112421656 | |||||||
| chr9:112421762 | C | T | 5 | a0001c0001t0006g0006 a0001c0001t0006g0064 a0001c0001t0006g0065 others(2): Show |
6 | HG02109.hp2 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.598+2804C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112421762 | |||||||
| chr9:112421864 | T | G | 345 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(342): Show |
360 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.598+2906T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112421864 | |||||||
| chr9:112421912 | C | T | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.598+2954C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112421912 | |||||||
| chr9:112421926 | T | C | 5 | a0001c0001t0006g0006 a0001c0001t0006g0064 a0001c0001t0006g0065 others(2): Show |
6 | HG02109.hp2 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.598+2968T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112421926 | |||||||
| chr9:112421961 | G | T | 4 | a0001c0001t0001g0083 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG02976.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+3003G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112421961 | |||||||
| chr9:112422113 | G | A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0270 a0001c0001t0006g0006 others(4): Show |
8 | HG02109.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.598+3155G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112422113 | |||||||
| chr9:112422144 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0270 |
2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.598+3186C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112422144 | |||||||
| chr9:112422145 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.598+3187T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112422145 | |||||||
| chr9:112422459 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0058 a0001c0001t0001g0306 |
5 | HG00558.hp2 HG02056.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+3501G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112422459 | |||||||
| chr9:112422627 | A | T | 1 | a0001c0001t0002g0197 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.598+3669A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112422627 | |||||||
| chr9:112422636 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.598+3678C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112422636 | |||||||
| chr9:112422737 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.598+3779T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112422737 | |||||||
| chr9:112422747 | A | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(309): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.598+3789A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112422747 | |||||||
| chr9:112422940 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.598+3982C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112422940 | |||||||
| chr9:112423021 | T | C | 53 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(50): Show |
54 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.598+4063T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112423021 | |||||||
| chr9:112423047 | G | A | 1 | a0001c0001t0002g0220 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.598+4089G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112423047 | |||||||
| chr9:112423333 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0344 |
4 | HG02109.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+4375T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112423333 | |||||||
| chr9:112423364 | G | A | 1 | a0001c0001t0002g0315 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.598+4406G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112423364 | |||||||
| chr9:112423372 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.598+4414G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112423372 | |||||||
| chr9:112423404 | T | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(309): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.598+4446T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112423404 | |||||||
| chr9:112423644 | T | C | 5 | a0001c0001t0006g0006 a0001c0001t0006g0064 a0001c0001t0006g0065 others(2): Show |
6 | HG02109.hp2 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.598+4686T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112423644 | |||||||
| chr9:112423695 | T | C | 11 | a0001c0001t0001g0030 a0001c0001t0001g0083 a0001c0001t0001g0187 others(8): Show |
12 | HG02109.hp2 HG02486.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.598+4737T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112423695 | |||||||
| chr9:112423783 | A | G | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.598+4825A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112423783 | |||||||
| chr9:112423796 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.598+4838C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112423796 | |||||||
| chr9:112423838 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.598+4880C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112423838 | |||||||
| chr9:112423842 | T | C | 1 | a0001c0001t0016g0092 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.598+4884T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112423842 | |||||||
| chr9:112423860 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.598+4902C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112423860 | |||||||
| chr9:112423870 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): Show |
100 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.598+4912C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112423870 | |||||||
| chr9:112423871 | G | A | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.598+4913G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112423871 | |||||||
| chr9:112423875 | A | G | 64 | a0001c0001t0001g0170 a0001c0001t0002g0002 a0001c0001t0002g0007 others(61): Show |
68 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.598+4917A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112423875 | |||||||
| chr9:112423983 | G | A | 1 | a0001c0002t0002g0241 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.598+5025G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112423983 | |||||||
| chr9:112423991 | A | G | 339 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(336): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.598+5033A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112423991 | |||||||
| chr9:112424196 | C | T | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.598+5238C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112424196 | |||||||
| chr9:112424295 | G | A | 140 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(137): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.598+5337G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112424295 | |||||||
| chr9:112424312 | T | G | 1 | a0001c0001t0006g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.598+5354T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112424312 | |||||||
| chr9:112424320 | C | CA | 67 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0186 others(64): Show |
71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.598+5378dupA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112424320 | ||||||
| chr9:112424320 | C | CAA | 52 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(49): Show |
53 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.598+5377_598+5378d others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112424320 | ||||||
| chr9:112424337 | T | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.598+5379T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112424337 | |||||||
| chr9:112424486 | A | T | 1 | a0001c0001t0001g0321 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.598+5528A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112424486 | |||||||
| chr9:112424509 | G | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
9 | HG01891.hp1 HG02109.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.598+5551G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112424509 | |||||||
| chr9:112424811 | A | T | 11 | a0001c0001t0001g0030 a0001c0001t0001g0083 a0001c0001t0001g0187 others(8): Show |
12 | HG02109.hp2 HG02486.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.598+5853A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112424811 | |||||||
| chr9:112425109 | G | A | 1 | a0001c0001t0002g0007 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.598+6151G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112425109 | |||||||
| chr9:112425122 | CA | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0349 |
3 | HG02258.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.598+6165delA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112425122 | |||||||
| chr9:112425161 | G | A | 140 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(137): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.598+6203G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112425161 | |||||||
| chr9:112425199 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.598+6241A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112425199 | |||||||
| chr9:112425433 | T | C | 2 | a0001c0001t0002g0122 a0001c0001t0002g0125 |
2 | HG01109.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.598+6475T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112425433 | |||||||
| chr9:112425549 | C | T | 1 | a0001c0001t0006g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.598+6591C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112425549 | |||||||
| chr9:112425597 | G | T | 11 | a0001c0001t0001g0030 a0001c0001t0001g0083 a0001c0001t0001g0187 others(8): Show |
12 | HG02109.hp2 HG02486.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.598+6639G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112425597 | |||||||
| chr9:112425604 | CCTTTGAG others(10): Show |
C | 147 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(144): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.598+6650_598+6666d others(19): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112425604 | ||||||
| chr9:112425729 | T | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0349 |
3 | HG02258.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.598+6771T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112425729 | |||||||
| chr9:112425734 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.598+6776T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112425734 | |||||||
| chr9:112425906 | T | TTG | 96 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(93): Show |
101 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.598+6954_598+6955d others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112425906 | ||||||
| chr9:112425914 | A | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(309): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.598+6956A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112425914 | |||||||
| chr9:112426020 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.598+7062C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112426020 | |||||||
| chr9:112426064 | C | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0270 |
2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.598+7106C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112426064 | |||||||
| chr9:112426165 | C | T | 61 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0068 others(58): Show |
62 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.598+7207C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112426165 | |||||||
| chr9:112426234 | C | CT | 12 | a0001c0001t0001g0030 a0001c0001t0001g0069 a0001c0001t0001g0071 others(9): Show |
12 | HG02559.hp2 HG02630.hp2 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.598+7295dupT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112426234 | ||||||
| chr9:112426234 | C | CTT | 47 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0070 others(44): Show |
48 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.598+7294_598+7295d others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112426234 | ||||||
| chr9:112426234 | CT | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(227): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.598+7295delT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112426234 | ||||||
| chr9:112426234 | CTT | C | 7 | a0001c0001t0001g0281 a0001c0001t0004g0233 a0001c0002t0002g0200 others(4): Show |
7 | HG01168.hp2 NA18959.hp1 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.598+7294_598+7295d others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112426234 | ||||||
| chr9:112426329 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): Show |
100 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.598+7371G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112426329 | |||||||
| chr9:112426427 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.598+7469G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112426427 | |||||||
| chr9:112426433 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0134 |
2 | NA19000.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.598+7475G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112426433 | |||||||
| chr9:112426565 | T | C | 2 | a0001c0001t0002g0074 a0001c0001t0002g0172 |
2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.598+7607T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112426565 | |||||||
| chr9:112426884 | A | G | 7 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
9 | HG01891.hp1 HG02109.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.598+7926A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112426884 | |||||||
| chr9:112426922 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): Show |
100 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.598+7964A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112426922 | |||||||
| chr9:112426927 | G | A | 5 | a0001c0001t0006g0006 a0001c0001t0006g0064 a0001c0001t0006g0065 others(2): Show |
6 | HG02109.hp2 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.598+7969G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112426927 | |||||||
| chr9:112427073 | G | A | 5 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(2): Show |
5 | NA18747.hp2 NA18945.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+8115G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112427073 | |||||||
| chr9:112427132 | G | A | 1 | a0001c0001t0002g0193 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.598+8174G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112427132 | |||||||
| chr9:112427184 | A | T | 3 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 |
3 | NA18977.hp1 NA18991.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.598+8226A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112427184 | |||||||
| chr9:112427242 | A | G | 1 | a0001c0001t0002g0197 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.598+8284A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112427242 | |||||||
| chr9:112427506 | C | A | 1 | a0001c0001t0001g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.598+8548C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112427506 | |||||||
| chr9:112427936 | T | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0058 a0001c0001t0001g0306 |
5 | HG00558.hp2 HG02056.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+8978T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112427936 | |||||||
| chr9:112427972 | A | G | 1 | a0001c0001t0006g0067 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.598+9014A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112427972 | |||||||
| chr9:112428042 | G | A | 53 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(50): Show |
54 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.598+9084G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112428042 | |||||||
| chr9:112428325 | T | C | 347 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(344): Show |
362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.598+9367T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112428325 | |||||||
| chr9:112428367 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(90): Show |
98 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.598+9409C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112428367 | |||||||
| chr9:112428371 | A | T | 1 | a0001c0001t0001g0094 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.598+9413A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112428371 | |||||||
| chr9:112428373 | G | T | 1 | a0001c0001t0001g0094 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.598+9415G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112428373 | |||||||
| chr9:112428428 | T | G | 1 | a0001c0001t0002g0143 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.598+9470T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112428428 | |||||||
| chr9:112428429 | G | T | 1 | a0001c0001t0002g0143 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.598+9471G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112428429 | |||||||
| chr9:112428431 | G | A | 9 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0084 others(6): Show |
9 | HG02622.hp1 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.598+9473G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112428431 | |||||||
| chr9:112428566 | G | A | 1 | a0001c0001t0001g0249 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.598+9608G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112428566 | |||||||
| chr9:112428685 | G | C | 11 | a0001c0001t0001g0070 a0001c0001t0001g0078 a0001c0001t0001g0080 others(8): Show |
11 | HG02083.hp2 HG02129.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.598+9727G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112428685 | |||||||
| chr9:112428795 | T | C | 2 | a0001c0001t0001g0316 a0001c0001t0001g0329 |
2 | HG01192.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.599-9636T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112428795 | |||||||
| chr9:112428939 | C | A | 1 | a0001c0001t0001g0268 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.599-9492C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112428939 | |||||||
| chr9:112429062 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.599-9369C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112429062 | |||||||
| chr9:112429192 | C | T | 4 | a0001c0001t0001g0083 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG02976.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-9239C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112429192 | |||||||
| chr9:112429206 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.599-9225C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112429206 | |||||||
| chr9:112429399 | A | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0187 a0001c0001t0001g0188 others(3): Show |
8 | HG02109.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.599-9032A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112429399 | |||||||
| chr9:112429461 | G | A | 17 | a0001c0002t0002g0168 a0001c0002t0002g0169 a0001c0002t0002g0200 others(14): Show |
17 | HG00673.hp2 HG02129.hp2 NA18948.hp2 others(14): Show |
intron_variant | MODIFIER | c.599-8970G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112429461 | |||||||
| chr9:112429714 | T | G | 1 | a0001c0001t0002g0337 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.599-8717T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112429714 | |||||||
| chr9:112429752 | C | A | 6 | a0001c0001t0001g0084 a0001c0001t0001g0120 a0001c0001t0001g0165 others(3): Show |
6 | HG01109.hp2 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.599-8679C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112429752 | |||||||
| chr9:112429758 | C | A | 6 | a0001c0001t0001g0084 a0001c0001t0001g0120 a0001c0001t0001g0165 others(3): Show |
6 | HG01109.hp2 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.599-8673C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112429758 | |||||||
| chr9:112429900 | T | C | 1 | a0001c0001t0006g0006 | 2 | HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.599-8531T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112429900 | |||||||
| chr9:112429916 | A | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0120 |
2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.599-8515A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112429916 | |||||||
| chr9:112429927 | A | G | 6 | a0001c0001t0001g0084 a0001c0001t0001g0120 a0001c0001t0001g0165 others(3): Show |
6 | HG01109.hp2 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.599-8504A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112429927 | |||||||
| chr9:112430033 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.599-8398G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112430033 | |||||||
| chr9:112430046 | T | C | 179 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0048 others(176): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.599-8385T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112430046 | |||||||
| chr9:112430083 | C | CA | 6 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(3): Show |
7 | HG01256.hp2 HG01258.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.599-8335dupA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112430083 | ||||||
| chr9:112430098 | A | G | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG01109.hp2 HG02145.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.599-8333A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112430098 | |||||||
| chr9:112430223 | G | A | 5 | a0001c0001t0006g0006 a0001c0001t0006g0064 a0001c0001t0006g0065 others(2): Show |
6 | HG02109.hp2 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.599-8208G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112430223 | |||||||
| chr9:112430314 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.599-8117A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112430314 | |||||||
| chr9:112430357 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0349 |
3 | HG02258.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.599-8074G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112430357 | |||||||
| chr9:112430607 | G | T | 1 | a0001c0001t0002g0267 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.599-7824G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112430607 | |||||||
| chr9:112430700 | T | C | 21 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0030 others(18): Show |
23 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.599-7731T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112430700 | |||||||
| chr9:112430886 | G | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.599-7545G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112430886 | |||||||
| chr9:112431043 | T | G | 18 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0030 others(15): Show |
20 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.599-7388T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112431043 | |||||||
| chr9:112431051 | CA | C | 62 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0018 others(59): Show |
66 | HG00408.hp2 HG00597.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.599-7359delA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112431051 | ||||||
| chr9:112431051 | CAA | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(205): Show |
216 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.599-7360_599-7359d others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112431051 | ||||||
| chr9:112431051 | CAAA | C | 12 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(9): Show |
13 | HG00099.hp2 HG01943.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.599-7361_599-7359d others(5): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112431051 | ||||||
| chr9:112431054 | A | G | 1 | a0001c0001t0001g0296 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.599-7377A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112431054 | |||||||
| chr9:112431072 | A | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0120 |
2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.599-7359A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112431072 | |||||||
| chr9:112431072 | AT | A | 3 | a0001c0001t0002g0019 a0001c0001t0002g0025 a0001c0001t0002g0028 |
3 | NA18999.hp1 NA19001.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.599-7356delT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112431072 | ||||||
| chr9:112431075 | T | A | 6 | a0001c0001t0001g0062 a0001c0001t0001g0131 a0001c0001t0001g0186 others(3): Show |
6 | HG00733.hp2 HG00738.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.599-7356T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112431075 | |||||||
| chr9:112431076 | A | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0030 others(11): Show |
16 | HG02109.hp1 HG02559.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.599-7355A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112431076 | |||||||
| chr9:112431249 | G | T | 54 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(51): Show |
55 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.599-7182G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112431249 | |||||||
| chr9:112431283 | T | A | 1 | a0001c0001t0001g0307 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.599-7148T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112431283 | |||||||
| chr9:112431429 | TAGGAAGA others(4): Show |
T | 1 | a0001c0001t0003g0325 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.599-6988_599-6978d others(13): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112431429 | ||||||
| chr9:112431467 | C | T | 4 | a0001c0001t0001g0285 a0001c0001t0007g0020 a0001c0001t0007g0026 others(1): Show |
4 | NA18948.hp1 NA18972.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-6964C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112431467 | |||||||
| chr9:112431483 | T | G | 282 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(279): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.599-6948T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112431483 | |||||||
| chr9:112431513 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.599-6918C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112431513 | |||||||
| chr9:112431576 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0344 |
4 | HG02109.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-6855T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112431576 | |||||||
| chr9:112431651 | A | G | 5 | a0001c0001t0006g0006 a0001c0001t0006g0064 a0001c0001t0006g0065 others(2): Show |
6 | HG02109.hp2 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.599-6780A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112431651 | |||||||
| chr9:112431701 | T | G | 1 | a0001c0001t0001g0185 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.599-6730T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112431701 | |||||||
| chr9:112431790 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(264): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.599-6641T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112431790 | |||||||
| chr9:112431806 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.599-6625G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112431806 | |||||||
| chr9:112431874 | CT | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
287 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.599-6539delT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112431874 | ||||||
| chr9:112431874 | CTT | C | 54 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(51): Show |
55 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.599-6540_599-6539d others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112431874 | ||||||
| chr9:112431940 | T | C | 347 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(344): Show |
362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.599-6491T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112431940 | |||||||
| chr9:112431941 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(95): Show |
104 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.599-6490G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112431941 | |||||||
| chr9:112431987 | C | A | 1 | a0001c0002t0002g0241 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.599-6444C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112431987 | |||||||
| chr9:112432030 | C | A | 1 | a0001c0001t0002g0225 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.599-6401C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112432030 | |||||||
| chr9:112432070 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.599-6361C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112432070 | |||||||
| chr9:112432188 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.599-6243T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112432188 | |||||||
| chr9:112432303 | C | G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0032 others(9): Show |
14 | HG02109.hp1 HG02622.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.599-6128C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112432303 | |||||||
| chr9:112432320 | C | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.599-6111C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112432320 | |||||||
| chr9:112432321 | C | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0030 others(11): Show |
16 | HG02109.hp1 HG02258.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.599-6110C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112432321 | |||||||
| chr9:112432355 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.599-6076C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112432355 | |||||||
| chr9:112432432 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.599-5999G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112432432 | |||||||
| chr9:112432548 | T | A | 1 | a0001c0001t0002g0145 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.599-5883T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112432548 | |||||||
| chr9:112433064 | C | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0030 others(11): Show |
16 | HG02109.hp1 HG02258.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.599-5367C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112433064 | |||||||
| chr9:112433434 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.599-4997A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112433434 | |||||||
| chr9:112433634 | C | T | 54 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(51): Show |
55 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.599-4797C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112433634 | |||||||
| chr9:112433830 | T | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | NA18972.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.599-4601T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112433830 | |||||||
| chr9:112433834 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(96): Show |
104 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.599-4597T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112433834 | |||||||
| chr9:112433893 | C | T | 1 | a0001c0001t0002g0143 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.599-4538C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112433893 | |||||||
| chr9:112433894 | G | A | 2 | a0001c0001t0001g0270 a0001c0001t0011g0258 |
2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.599-4537G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112433894 | |||||||
| chr9:112434094 | G | A | 1 | a0001c0001t0002g0271 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.599-4337G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112434094 | |||||||
| chr9:112434096 | C | T | 1 | a0001c0001t0001g0349 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.599-4335C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112434096 | |||||||
| chr9:112434136 | G | A | 340 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(337): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.599-4295G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112434136 | |||||||
| chr9:112434278 | A | G | 169 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0030 others(166): Show |
177 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.599-4153A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112434278 | |||||||
| chr9:112434605 | G | A | 1 | a0001c0001t0002g0142 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.599-3826G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112434605 | |||||||
| chr9:112434614 | C | T | 2 | a0001c0001t0001g0342 a0001c0001t0020g0121 |
2 | HG00741.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.599-3817C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112434614 | |||||||
| chr9:112434615 | G | A | 7 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(4): Show |
7 | HG02083.hp2 HG02129.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-3816G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112434615 | |||||||
| chr9:112434629 | G | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0268 |
3 | NA18951.hp2 NA18963.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.599-3802G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112434629 | |||||||
| chr9:112434776 | T | C | 1 | a0001c0001t0001g0349 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.599-3655T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112434776 | |||||||
| chr9:112434804 | CTTAAGAC others(2899): Show |
C | 2 | a0001c0001t0001g0032 a0001c0001t0014g0031 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.599-3548_599-643de others(1): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112434804 | ||||||
| chr9:112435098 | C | G | 1 | a0001c0001t0002g0176 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.599-3333C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112435098 | |||||||
| chr9:112435177 | G | T | 54 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(51): Show |
55 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.599-3254G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112435177 | |||||||
| chr9:112435376 | T | G | 2 | a0001c0001t0002g0195 a0001c0001t0002g0197 |
2 | HG01261.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.599-3055T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112435376 | |||||||
| chr9:112435636 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.599-2795A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112435636 | |||||||
| chr9:112435703 | TTTTTA | T | 54 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(51): Show |
55 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.599-2715_599-2711d others(7): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112435703 | ||||||
| chr9:112435754 | A | T | 145 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0009 others(142): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.599-2677A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112435754 | |||||||
| chr9:112435911 | T | A | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.599-2520T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112435911 | |||||||
| chr9:112436066 | C | T | 54 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(51): Show |
55 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.599-2365C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112436066 | |||||||
| chr9:112436110 | A | G | 54 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(51): Show |
55 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.599-2321A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112436110 | |||||||
| chr9:112436242 | C | CA | 43 | a0001c0001t0001g0049 a0001c0001t0001g0060 a0001c0001t0001g0068 others(40): Show |
44 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.599-2164dupA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112436242 | ||||||
| chr9:112436242 | CA | C | 29 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(26): Show |
30 | HG01175.hp1 HG01515.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.599-2164delA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112436242 | ||||||
| chr9:112436242 | CAA | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(86): Show |
93 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.599-2165_599-2164d others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112436242 | ||||||
| chr9:112436284 | A | AT | 3 | a0001c0001t0001g0185 a0001c0001t0001g0192 a0001c0001t0001g0223 |
3 | HG03471.hp2 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.599-2142dupT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112436284 | ||||||
| chr9:112436291 | G | A | 3 | a0001c0001t0001g0185 a0001c0001t0001g0192 a0001c0001t0001g0223 |
3 | HG03471.hp2 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.599-2140G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112436291 | |||||||
| chr9:112436412 | C | T | 1 | a0001c0001t0002g0019 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.599-2019C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112436412 | |||||||
| chr9:112436827 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.599-1604G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112436827 | |||||||
| chr9:112436960 | C | CT | 12 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0001g0109 others(9): Show |
13 | HG01167.hp2 HG01169.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.599-1454dupT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112436960 | ||||||
| chr9:112436960 | C | CTTT | 116 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0009 others(113): Show |
121 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.599-1456_599-1454d others(5): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112436960 | ||||||
| chr9:112436960 | C | CTTTT | 14 | a0001c0001t0002g0125 a0001c0001t0002g0135 a0001c0001t0002g0137 others(11): Show |
14 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.599-1457_599-1454d others(6): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112436960 | ||||||
| chr9:112436960 | C | CTTTTT | 7 | a0001c0001t0002g0019 a0001c0001t0002g0025 a0001c0001t0002g0028 others(4): Show |
7 | HG02523.hp2 HG04184.hp1 NA18999.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-1458_599-1454d others(7): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112436960 | ||||||
| chr9:112436960 | C | CTTTTTT | 7 | a0001c0001t0002g0260 a0001c0001t0002g0261 a0001c0001t0002g0262 others(4): Show |
7 | HG02602.hp1 HG03654.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.599-1459_599-1454d others(8): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112436960 | ||||||
| chr9:112436977 | TG | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0030 others(6): Show |
11 | HG02109.hp1 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.599-1453delG | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112436977 | |||||||
| chr9:112436978 | G | T | 2 | a0001c0001t0001g0185 a0001c0001t0001g0192 |
2 | HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.599-1453G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112436978 | |||||||
| chr9:112437012 | A | T | 220 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(217): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.599-1419A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112437012 | |||||||
| chr9:112437212 | G | A | 1 | a0001c0001t0002g0009 | 2 | NA18944.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.599-1219G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112437212 | |||||||
| chr9:112437227 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
172 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.599-1204C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112437227 | |||||||
| chr9:112437238 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0344 |
4 | HG02109.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-1193G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112437238 | |||||||
| chr9:112437412 | C | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0084 others(7): Show |
12 | HG02109.hp1 HG02622.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.599-1019C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112437412 | |||||||
| chr9:112437451 | C | A | 1 | a0001c0001t0002g0142 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.599-980C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112437451 | |||||||
| chr9:112437455 | A | G | 167 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0030 others(164): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.599-976A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112437455 | |||||||
| chr9:112437545 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(94): Show |
102 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.599-886G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112437545 | |||||||
| chr9:112437562 | A | T | 1 | a0001c0001t0002g0220 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.599-869A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112437562 | |||||||
| chr9:112437566 | ATG | A | 143 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0009 others(140): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.599-860_599-859del others(2): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 112437566 | ||||||
| chr9:112437571 | T | C | 2 | a0001c0001t0002g0345 a0001c0001t0002g0346 |
2 | HG02280.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.599-860T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112437571 | |||||||
| chr9:112437571 | T | G | 1 | a0001c0001t0005g0295 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.599-860T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112437571 | |||||||
| chr9:112437575 | T | C | 164 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0030 others(161): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.599-856T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112437575 | |||||||
| chr9:112437883 | T | C | 168 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0030 others(165): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.599-548T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112437883 | |||||||
| chr9:112437986 | G | T | 2 | a0001c0001t0002g0261 a0001c0001t0002g0264 |
2 | HG03688.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.599-445G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112437986 | |||||||
| chr9:112438022 | C | T | 4 | a0001c0001t0002g0086 a0001c0001t0002g0248 a0001c0001t0002g0341 others(1): Show |
4 | HG01891.hp2 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-409C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112438022 | |||||||
| chr9:112438094 | T | A | 1 | a0001c0001t0001g0274 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.599-337T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 6/10 | chr9 | 112438094 | |||||||
| chr9:112438660 | G | A | 1 | a0001c0001t0001g0349 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.793+35G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112438660 | |||||||
| chr9:112438729 | T | C | 1 | a0001c0001t0005g0295 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.793+104T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112438729 | |||||||
| chr9:112438775 | C | G | 1 | a0001c0001t0002g0149 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.793+150C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112438775 | |||||||
| chr9:112438835 | G | GAT | 18 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(15): Show |
19 | HG01433.hp1 HG02273.hp1 NA18944.hp1 others(16): Show |
intron_variant | MODIFIER | c.793+230_793+231dup others(2): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 112438835 | ||||||
| chr9:112438835 | GATAT | G | 212 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0068 others(209): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.793+228_793+231del others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 112438835 | ||||||
| chr9:112438835 | GATATAT | G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0032 others(9): Show |
14 | HG02109.hp1 HG02622.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.793+226_793+231del others(6): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 112438835 | ||||||
| chr9:112439551 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.793+926T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112439551 | |||||||
| chr9:112439555 | C | T | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.793+930C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112439555 | |||||||
| chr9:112439572 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.793+947T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112439572 | |||||||
| chr9:112439580 | C | T | 1 | a0001c0001t0002g0178 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.793+955C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112439580 | |||||||
| chr9:112439722 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(94): Show |
102 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.793+1097A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112439722 | |||||||
| chr9:112439770 | C | G | 12 | a0001c0001t0003g0013 a0001c0001t0003g0046 a0001c0001t0003g0130 others(9): Show |
13 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.793+1145C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112439770 | |||||||
| chr9:112439788 | G | A | 146 | a0001c0001t0001g0186 a0001c0001t0002g0002 a0001c0001t0002g0007 others(143): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.793+1163G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112439788 | |||||||
| chr9:112439991 | G | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
6 | NA18960.hp1 NA18971.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.793+1366G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112439991 | |||||||
| chr9:112440208 | C | T | 1 | a0001c0001t0001g0349 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.794-1491C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112440208 | |||||||
| chr9:112440215 | G | A | 5 | a0001c0001t0006g0006 a0001c0001t0006g0064 a0001c0001t0006g0065 others(2): Show |
6 | HG02109.hp2 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-1484G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112440215 | |||||||
| chr9:112440330 | G | A | 222 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(219): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.794-1369G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112440330 | |||||||
| chr9:112440352 | T | A | 1 | a0001c0001t0001g0331 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.794-1347T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112440352 | |||||||
| chr9:112440401 | G | C | 340 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(337): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.794-1298G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112440401 | |||||||
| chr9:112440703 | T | C | 1 | a0001c0001t0001g0349 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.794-996T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112440703 | |||||||
| chr9:112440735 | A | G | 224 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(221): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.794-964A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112440735 | |||||||
| chr9:112440859 | G | T | 340 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(337): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.794-840G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112440859 | |||||||
| chr9:112441029 | A | T | 159 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0001g0186 others(156): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.794-670A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112441029 | |||||||
| chr9:112441030 | T | A | 159 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0001g0186 others(156): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.794-669T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112441030 | |||||||
| chr9:112441041 | T | C | 19 | a0001c0002t0002g0037 a0001c0002t0002g0168 a0001c0002t0002g0169 others(16): Show |
19 | HG00673.hp2 HG02129.hp2 NA18942.hp1 others(16): Show |
intron_variant | MODIFIER | c.794-658T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112441041 | |||||||
| chr9:112441074 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.794-625C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112441074 | |||||||
| chr9:112441187 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0228 a0001c0001t0001g0344 |
5 | HG02109.hp1 HG02818.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-512G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112441187 | |||||||
| chr9:112441280 | A | G | 56 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(53): Show |
57 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.794-419A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112441280 | |||||||
| chr9:112441296 | A | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0058 a0001c0001t0001g0306 |
5 | HG00558.hp2 HG02056.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-403A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112441296 | |||||||
| chr9:112441410 | T | C | 2 | a0001c0001t0001g0270 a0001c0001t0011g0258 |
2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.794-289T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 7/10 | chr9 | 112441410 | |||||||
| chr9:112441927 | A | G | 1 | a0001c0001t0002g0182 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.865+157A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112441927 | |||||||
| chr9:112442011 | C | T | 4 | a0001c0001t0002g0179 a0001c0001t0002g0219 a0001c0001t0002g0220 others(1): Show |
4 | NA18956.hp1 NA18966.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.865+241C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112442011 | |||||||
| chr9:112442082 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.865+312C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112442082 | |||||||
| chr9:112442091 | G | A | 54 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(51): Show |
55 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.865+321G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112442091 | |||||||
| chr9:112442263 | T | C | 1 | a0001c0001t0001g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.865+493T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112442263 | |||||||
| chr9:112442268 | C | CA | 21 | a0001c0001t0001g0060 a0001c0001t0001g0115 a0001c0001t0001g0166 others(18): Show |
21 | HG00621.hp1 HG01123.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.865+524dupA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112442268 | ||||||
| chr9:112442268 | CA | C | 132 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0032 others(129): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.865+524delA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112442268 | ||||||
| chr9:112442268 | CAA | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0270 a0001c0001t0001g0344 others(2): Show |
7 | HG02109.hp1 HG02258.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.865+523_865+524del others(2): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112442268 | ||||||
| chr9:112442291 | AAAAG | A | 47 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0070 others(44): Show |
48 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.865+524_865+527del others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112442291 | ||||||
| chr9:112442525 | T | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(94): Show |
102 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.865+755T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112442525 | |||||||
| chr9:112442558 | C | A | 1 | a0001c0001t0001g0245 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.865+788C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112442558 | |||||||
| chr9:112442631 | A | T | 12 | a0001c0001t0003g0013 a0001c0001t0003g0046 a0001c0001t0003g0130 others(9): Show |
13 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.865+861A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112442631 | |||||||
| chr9:112442762 | T | G | 223 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(220): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.865+992T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112442762 | |||||||
| chr9:112442763 | C | T | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | HG03927.hp1 NA18994.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.865+993C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112442763 | |||||||
| chr9:112443079 | A | G | 1 | a0001c0001t0002g0263 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.865+1309A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112443079 | |||||||
| chr9:112443246 | T | C | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.865+1476T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112443246 | |||||||
| chr9:112443443 | T | G | 1 | a0001c0001t0001g0223 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.865+1673T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112443443 | |||||||
| chr9:112443545 | T | A | 2 | a0001c0001t0001g0018 a0001c0001t0017g0021 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.865+1775T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112443545 | |||||||
| chr9:112443752 | A | T | 54 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(51): Show |
55 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.865+1982A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112443752 | |||||||
| chr9:112443928 | T | C | 54 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(51): Show |
55 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.865+2158T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112443928 | |||||||
| chr9:112443990 | A | G | 7 | a0001c0001t0002g0260 a0001c0001t0002g0261 a0001c0001t0002g0262 others(4): Show |
7 | HG02602.hp1 HG03654.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.865+2220A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112443990 | |||||||
| chr9:112444143 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.865+2373C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112444143 | |||||||
| chr9:112444295 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(96): Show |
104 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.865+2525A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112444295 | |||||||
| chr9:112444404 | C | G | 1 | a0001c0001t0002g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.865+2634C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112444404 | |||||||
| chr9:112444422 | G | GT | 52 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(49): Show |
53 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.865+2662dupT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112444422 | ||||||
| chr9:112444422 | GT | G | 168 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0030 others(165): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.865+2662delT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112444422 | ||||||
| chr9:112444461 | G | C | 5 | a0001c0001t0006g0006 a0001c0001t0006g0064 a0001c0001t0006g0065 others(2): Show |
6 | HG02109.hp2 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.865+2691G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112444461 | |||||||
| chr9:112444601 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.865+2831G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112444601 | |||||||
| chr9:112444623 | A | C | 1 | a0001c0001t0001g0301 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.865+2853A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112444623 | |||||||
| chr9:112444753 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0229 |
2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.865+2983C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112444753 | |||||||
| chr9:112444834 | G | GT | 155 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0083 others(152): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.865+3084dupT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112444834 | ||||||
| chr9:112444834 | G | GTT | 19 | a0001c0001t0001g0030 a0001c0001t0001g0084 a0001c0001t0001g0120 others(16): Show |
20 | HG01109.hp1 HG01346.hp2 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.865+3083_865+3084d others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112444834 | ||||||
| chr9:112444834 | GT | G | 71 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0043 others(68): Show |
72 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.865+3084delT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112444834 | ||||||
| chr9:112444944 | C | A | 1 | a0001c0001t0001g0056 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.865+3174C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112444944 | |||||||
| chr9:112444962 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.865+3192T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112444962 | |||||||
| chr9:112444980 | A | G | 1 | a0001c0001t0002g0151 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.865+3210A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112444980 | |||||||
| chr9:112445007 | T | C | 2 | a0001c0001t0001g0270 a0001c0001t0011g0258 |
2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.865+3237T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112445007 | |||||||
| chr9:112445080 | T | C | 1 | a0001c0001t0001g0017 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.865+3310T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112445080 | |||||||
| chr9:112445267 | C | G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0083 a0001c0001t0001g0270 others(2): Show |
5 | HG02258.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.865+3497C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112445267 | |||||||
| chr9:112445276 | G | A | 9 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0084 others(6): Show |
9 | HG02622.hp1 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.865+3506G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112445276 | |||||||
| chr9:112445350 | T | C | 2 | a0001c0001t0001g0270 a0001c0001t0011g0258 |
2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.865+3580T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112445350 | |||||||
| chr9:112445477 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(116): Show |
124 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(121): Show |
intron_variant | MODIFIER | c.865+3707G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112445477 | |||||||
| chr9:112445511 | G | GT | 18 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0032 others(15): Show |
20 | HG02109.hp1 HG02258.hp2 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.865+3752dupT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112445511 | ||||||
| chr9:112445543 | T | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0058 a0001c0001t0001g0306 |
5 | HG00558.hp2 HG02056.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.865+3773T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112445543 | |||||||
| chr9:112445588 | G | C | 12 | a0001c0001t0001g0038 a0001c0001t0001g0096 a0001c0001t0001g0272 others(9): Show |
12 | HG00323.hp1 HG00639.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.865+3818G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112445588 | |||||||
| chr9:112445614 | G | T | 320 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(317): Show |
334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.865+3844G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112445614 | |||||||
| chr9:112445832 | A | AT | 148 | a0001c0001t0001g0030 a0001c0001t0001g0186 a0001c0001t0002g0002 others(145): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.865+4071dupT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112445832 | ||||||
| chr9:112445895 | A | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.865+4125A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112445895 | |||||||
| chr9:112445897 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.865+4127A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112445897 | |||||||
| chr9:112446002 | C | T | 1 | a0001c0001t0016g0092 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.865+4232C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112446002 | |||||||
| chr9:112446111 | A | AT | 273 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
286 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.865+4351dupT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112446111 | ||||||
| chr9:112446203 | C | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.865+4433C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112446203 | |||||||
| chr9:112446290 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.865+4520C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112446290 | |||||||
| chr9:112446311 | C | T | 5 | a0001c0001t0001g0075 a0001c0001t0001g0091 a0001c0001t0001g0108 others(2): Show |
5 | HG02080.hp2 NA18969.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.865+4541C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112446311 | |||||||
| chr9:112446403 | T | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.865+4633T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112446403 | |||||||
| chr9:112446407 | C | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0016 others(35): Show |
40 | HG01168.hp1 HG01255.hp2 HG01433.hp1 others(37): Show |
intron_variant | MODIFIER | c.865+4637C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112446407 | |||||||
| chr9:112446473 | T | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.865+4703T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112446473 | |||||||
| chr9:112446492 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.865+4722G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112446492 | |||||||
| chr9:112446891 | T | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.865+5121T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112446891 | |||||||
| chr9:112446930 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.865+5160G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112446930 | |||||||
| chr9:112446996 | A | G | 8 | a0001c0002t0002g0041 a0001c0002t0002g0168 a0001c0002t0002g0201 others(5): Show |
8 | HG00621.hp1 HG00673.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.865+5226A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112446996 | |||||||
| chr9:112447028 | T | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(94): Show |
102 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.865+5258T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112447028 | |||||||
| chr9:112447256 | A | G | 5 | a0001c0001t0006g0006 a0001c0001t0006g0064 a0001c0001t0006g0065 others(2): Show |
6 | HG02109.hp2 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.865+5486A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112447256 | |||||||
| chr9:112447393 | C | A | 155 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(152): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.865+5623C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112447393 | |||||||
| chr9:112447418 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.865+5648C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112447418 | |||||||
| chr9:112447666 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.865+5896A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112447666 | |||||||
| chr9:112447692 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.865+5922T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112447692 | |||||||
| chr9:112447704 | A | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.865+5934A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112447704 | |||||||
| chr9:112447706 | T | C | 1 | a0001c0001t0001g0349 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.865+5936T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112447706 | |||||||
| chr9:112447817 | TAAAC | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.865+6051_865+6054d others(6): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112447817 | ||||||
| chr9:112447847 | C | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.865+6077C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112447847 | |||||||
| chr9:112447957 | C | T | 11 | a0001c0001t0002g0119 a0001c0001t0002g0152 a0001c0001t0002g0158 others(8): Show |
11 | HG00621.hp2 HG00673.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-6056C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112447957 | |||||||
| chr9:112448013 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0255 a0001c0001t0014g0031 |
3 | HG01261.hp2 HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.866-6000C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112448013 | |||||||
| chr9:112448126 | A | ACAT | 3 | a0001c0001t0006g0064 a0001c0001t0006g0065 a0001c0001t0006g0066 |
3 | HG02109.hp2 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.866-5883_866-5881d others(5): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112448126 | ||||||
| chr9:112448261 | A | G | 6 | a0001c0001t0002g0002 a0001c0001t0002g0190 a0001c0001t0002g0193 others(3): Show |
8 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.866-5752A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112448261 | |||||||
| chr9:112448305 | CTATTT | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(261): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.866-5700_866-5696d others(7): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112448305 | ||||||
| chr9:112448507 | TCTTTCTT others(9): Show |
T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-5490_866-5475d others(18): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112448507 | ||||||
| chr9:112448548 | CTCT | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-5463_866-5461d others(5): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112448548 | ||||||
| chr9:112448584 | C | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-5429C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112448584 | |||||||
| chr9:112448614 | T | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-5399T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112448614 | |||||||
| chr9:112448634 | G | A | 6 | a0001c0001t0002g0171 a0001c0001t0002g0215 a0001c0001t0002g0343 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.866-5379G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112448634 | |||||||
| chr9:112448679 | G | C | 1 | a0001c0001t0013g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.866-5334G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112448679 | |||||||
| chr9:112448703 | C | G | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG02976.hp1 HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.866-5310C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112448703 | |||||||
| chr9:112448711 | AT | A | 320 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(317): Show |
334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.866-5291delT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112448711 | ||||||
| chr9:112448721 | T | A | 1 | a0001c0001t0001g0032 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.866-5292T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112448721 | |||||||
| chr9:112448722 | T | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-5291T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112448722 | |||||||
| chr9:112448758 | C | T | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.866-5255C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112448758 | |||||||
| chr9:112449011 | T | TAA | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-5002_866-5001i others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112449011 | |||||||
| chr9:112449080 | GT | G | 9 | a0001c0001t0001g0030 a0001c0001t0001g0083 a0001c0001t0001g0094 others(6): Show |
9 | HG01256.hp1 HG01943.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.866-4914delT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112449080 | ||||||
| chr9:112449080 | GTT | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(277): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.866-4915_866-4914d others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112449080 | ||||||
| chr9:112449080 | GTTT | G | 34 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(31): Show |
36 | HG00673.hp1 HG01167.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.866-4916_866-4914d others(5): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112449080 | ||||||
| chr9:112449139 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0008g0014 a0001c0001t0008g0015 |
3 | NA18993.hp2 NA19012.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.866-4874C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112449139 | |||||||
| chr9:112449174 | C | T | 264 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(261): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.866-4839C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112449174 | |||||||
| chr9:112449220 | A | G | 1 | a0001c0001t0004g0090 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.866-4793A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112449220 | |||||||
| chr9:112449445 | T | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.866-4568T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112449445 | |||||||
| chr9:112449582 | G | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-4431G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112449582 | |||||||
| chr9:112449592 | G | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-4421G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112449592 | |||||||
| chr9:112449643 | T | C | 1 | a0001c0001t0002g0239 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.866-4370T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112449643 | |||||||
| chr9:112449654 | C | T | 8 | a0001c0001t0002g0074 a0001c0001t0002g0086 a0001c0001t0002g0087 others(5): Show |
8 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.866-4359C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112449654 | |||||||
| chr9:112449680 | A | G | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.866-4333A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112449680 | |||||||
| chr9:112449700 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.866-4313C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112449700 | |||||||
| chr9:112449716 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.866-4297T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112449716 | |||||||
| chr9:112449729 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.866-4284G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112449729 | |||||||
| chr9:112449732 | G | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0305 a0001c0001t0001g0311 others(1): Show |
5 | HG01255.hp2 HG02280.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.866-4281G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112449732 | |||||||
| chr9:112449827 | A | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-4186A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112449827 | |||||||
| chr9:112449929 | G | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-4084G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112449929 | |||||||
| chr9:112450027 | A | G | 2 | a0001c0001t0001g0270 a0001c0001t0011g0258 |
2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.866-3986A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112450027 | |||||||
| chr9:112450136 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.866-3877A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112450136 | |||||||
| chr9:112450146 | C | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-3867C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112450146 | |||||||
| chr9:112450261 | C | CCCCCG | 30 | a0001c0001t0001g0084 a0001c0001t0001g0120 a0001c0001t0001g0227 others(27): Show |
31 | HG00408.hp1 HG00597.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.866-3749_866-3748i others(7): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112450261 | ||||||
| chr9:112450261 | C | CCCCG | 228 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(225): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.866-3749_866-3748i others(6): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112450261 | ||||||
| chr9:112450261 | C | CCCG | 55 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(52): Show |
56 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.866-3750_866-3749i others(5): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112450261 | ||||||
| chr9:112450274 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.866-3739A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112450274 | |||||||
| chr9:112450358 | C | T | 1 | a0001c0001t0001g0349 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.866-3655C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112450358 | |||||||
| chr9:112450359 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0003g0348 |
2 | HG02622.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.866-3654G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112450359 | |||||||
| chr9:112450417 | G | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-3596G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112450417 | |||||||
| chr9:112450420 | G | A | 1 | a0001c0001t0020g0121 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.866-3593G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112450420 | |||||||
| chr9:112450485 | C | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-3528C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112450485 | |||||||
| chr9:112450536 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(90): Show |
98 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.866-3477C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112450536 | |||||||
| chr9:112450544 | G | A | 1 | a0001c0001t0002g0140 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.866-3469G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112450544 | |||||||
| chr9:112450584 | A | G | 1 | a0001c0001t0002g0007 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.866-3429A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112450584 | |||||||
| chr9:112450587 | C | T | 146 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0009 others(143): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.866-3426C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112450587 | |||||||
| chr9:112450591 | T | C | 1 | a0001c0001t0002g0039 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.866-3422T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112450591 | |||||||
| chr9:112450626 | C | CAA | 66 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(63): Show |
67 | HG00280.hp1 HG00558.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.866-3372_866-3371d others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112450626 | ||||||
| chr9:112450626 | C | CAAA | 240 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(237): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.866-3373_866-3371d others(5): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112450626 | ||||||
| chr9:112450626 | C | CAAAA | 8 | a0001c0001t0001g0018 a0001c0001t0001g0186 a0001c0001t0001g0254 others(5): Show |
8 | HG02622.hp2 HG02630.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.866-3374_866-3371d others(6): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112450626 | ||||||
| chr9:112450626 | C | CAAAAA | 7 | a0001c0001t0001g0270 a0001c0001t0006g0006 a0001c0001t0006g0064 others(4): Show |
8 | HG02109.hp2 HG02486.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.866-3375_866-3371d others(7): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112450626 | ||||||
| chr9:112450655 | T | A | 2 | a0001c0001t0001g0278 a0001c0001t0002g0294 |
2 | HG04184.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.866-3358T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112450655 | |||||||
| chr9:112450982 | T | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-3031T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112450982 | |||||||
| chr9:112451019 | G | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-2994G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112451019 | |||||||
| chr9:112451230 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.866-2783A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112451230 | |||||||
| chr9:112451422 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(77): Show |
85 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.866-2591G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112451422 | |||||||
| chr9:112451680 | G | A | 2 | a0001c0001t0001g0270 a0001c0001t0011g0258 |
2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.866-2333G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112451680 | |||||||
| chr9:112451846 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0117 |
2 | NA19066.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.866-2167T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112451846 | |||||||
| chr9:112452121 | A | T | 1 | a0001c0001t0001g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.866-1892A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112452121 | |||||||
| chr9:112452155 | A | T | 1 | a0001c0001t0002g0212 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.866-1858A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112452155 | |||||||
| chr9:112452361 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.866-1652G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112452361 | |||||||
| chr9:112452384 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(106): Show |
116 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.866-1629C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112452384 | |||||||
| chr9:112452468 | C | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-1545C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112452468 | |||||||
| chr9:112452521 | T | G | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG01109.hp2 HG02145.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.866-1492T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112452521 | |||||||
| chr9:112452522 | G | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(15): Show |
19 | HG01433.hp1 HG02273.hp1 NA18944.hp1 others(16): Show |
intron_variant | MODIFIER | c.866-1491G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112452522 | |||||||
| chr9:112452639 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.866-1374C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112452639 | |||||||
| chr9:112452685 | G | A | 1 | a0001c0001t0002g0124 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.866-1328G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112452685 | |||||||
| chr9:112452695 | G | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-1318G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112452695 | |||||||
| chr9:112452804 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.866-1209C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112452804 | |||||||
| chr9:112452834 | G | T | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.866-1179G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112452834 | |||||||
| chr9:112452844 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(106): Show |
116 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.866-1169T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112452844 | |||||||
| chr9:112453014 | A | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-999A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112453014 | |||||||
| chr9:112453017 | G | A | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.866-996G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112453017 | |||||||
| chr9:112453093 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0259 |
2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.866-920A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112453093 | |||||||
| chr9:112453160 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.866-853G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112453160 | |||||||
| chr9:112453209 | T | G | 2 | a0001c0001t0001g0270 a0001c0001t0011g0258 |
2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.866-804T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112453209 | |||||||
| chr9:112453240 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.866-773T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112453240 | |||||||
| chr9:112453441 | G | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-572G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112453441 | |||||||
| chr9:112453454 | G | A | 55 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(52): Show |
56 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.866-559G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112453454 | |||||||
| chr9:112453525 | T | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-488T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112453525 | |||||||
| chr9:112453574 | G | C | 1 | a0001c0001t0001g0302 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.866-439G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112453574 | |||||||
| chr9:112453674 | T | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-339T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112453674 | |||||||
| chr9:112453840 | G | A | 5 | a0001c0001t0006g0006 a0001c0001t0006g0064 a0001c0001t0006g0065 others(2): Show |
6 | HG02109.hp2 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.866-173G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112453840 | |||||||
| chr9:112453942 | GATTA | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.866-63_866-60delAA others(2): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 112453942 | ||||||
| chr9:112453977 | A | G | 1 | a0001c0001t0001g0342 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.866-36A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 8/10 | chr9 | 112453977 | |||||||
| chr9:112454210 | G | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0185 others(4): Show |
7 | HG02622.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1015+48G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112454210 | |||||||
| chr9:112454313 | A | G | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG02976.hp1 HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1015+151A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112454313 | |||||||
| chr9:112454484 | C | T | 56 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0009 others(53): Show |
60 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.1015+322C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112454484 | |||||||
| chr9:112454485 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1015+323G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112454485 | |||||||
| chr9:112454489 | G | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1015+327G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112454489 | |||||||
| chr9:112454547 | T | C | 1 | a0001c0001t0002g0317 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1015+385T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112454547 | |||||||
| chr9:112454582 | G | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1015+420G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112454582 | |||||||
| chr9:112454668 | C | T | 2 | a0001c0001t0001g0275 a0001c0001t0001g0297 |
2 | HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1015+506C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112454668 | |||||||
| chr9:112454671 | T | C | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
17 | HG02155.hp2 NA18943.hp1 NA18951.hp2 others(14): Show |
intron_variant | MODIFIER | c.1015+509T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112454671 | |||||||
| chr9:112454736 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1015+574C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112454736 | |||||||
| chr9:112454759 | G | A | 1 | a0001c0002t0002g0242 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1015+597G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112454759 | |||||||
| chr9:112454793 | C | A | 1 | a0001c0001t0003g0338 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1015+631C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112454793 | |||||||
| chr9:112454874 | T | G | 1 | a0001c0001t0002g0251 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1015+712T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112454874 | |||||||
| chr9:112455190 | A | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0034 |
4 | NA18954.hp1 NA18969.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015+1028A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112455190 | |||||||
| chr9:112455250 | T | A | 1 | a0001c0001t0001g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1015+1088T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112455250 | |||||||
| chr9:112455255 | G | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1015+1093G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112455255 | |||||||
| chr9:112455276 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1015+1114G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112455276 | |||||||
| chr9:112455318 | AC | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1015+1158delC | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 112455318 | ||||||
| chr9:112455334 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(94): Show |
102 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.1015+1172G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112455334 | |||||||
| chr9:112455381 | C | G | 1 | a0001c0001t0001g0312 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1015+1219C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112455381 | |||||||
| chr9:112455534 | T | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1015+1372T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112455534 | |||||||
| chr9:112455558 | C | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1015+1396C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112455558 | |||||||
| chr9:112455559 | T | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1015+1397T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112455559 | |||||||
| chr9:112455597 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1015+1435A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112455597 | |||||||
| chr9:112455751 | T | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0185 a0001c0001t0001g0192 others(2): Show |
5 | HG02630.hp1 HG03098.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1015+1589T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112455751 | |||||||
| chr9:112455897 | G | A | 146 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0009 others(143): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1015+1735G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112455897 | |||||||
| chr9:112456108 | T | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1015+1946T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112456108 | |||||||
| chr9:112456450 | T | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1015+2288T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112456450 | |||||||
| chr9:112456594 | T | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1015+2432T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112456594 | |||||||
| chr9:112456632 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1015+2470C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112456632 | |||||||
| chr9:112456649 | G | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1015+2487G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112456649 | |||||||
| chr9:112456737 | G | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1015+2575G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112456737 | |||||||
| chr9:112456770 | G | GT | 4 | a0001c0001t0001g0162 a0001c0001t0002g0158 a0001c0001t0002g0252 others(1): Show |
4 | HG00558.hp1 NA18972.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015+2615dupT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 112456770 | ||||||
| chr9:112456800 | G | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1015+2638G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112456800 | |||||||
| chr9:112456861 | T | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1016-2588T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112456861 | |||||||
| chr9:112457062 | C | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1016-2387C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112457062 | |||||||
| chr9:112457083 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0017g0021 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1016-2366G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112457083 | |||||||
| chr9:112457089 | G | A | 1 | a0001c0001t0002g0271 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1016-2360G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112457089 | |||||||
| chr9:112457103 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1016-2346G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112457103 | |||||||
| chr9:112457159 | G | GA | 5 | a0001c0001t0006g0006 a0001c0001t0006g0064 a0001c0001t0006g0065 others(2): Show |
6 | HG02109.hp2 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1016-2281dupA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 112457159 | ||||||
| chr9:112457199 | C | A | 5 | a0001c0001t0006g0006 a0001c0001t0006g0064 a0001c0001t0006g0065 others(2): Show |
6 | HG02109.hp2 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1016-2250C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112457199 | |||||||
| chr9:112457338 | C | A | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG02976.hp1 HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1016-2111C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112457338 | |||||||
| chr9:112457338 | C | T | 1 | a0001c0001t0002g0150 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1016-2111C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112457338 | |||||||
| chr9:112457339 | T | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(261): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.1016-2110T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112457339 | |||||||
| chr9:112457353 | C | T | 2 | a0001c0001t0001g0275 a0001c0001t0001g0297 |
2 | HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1016-2096C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112457353 | |||||||
| chr9:112457605 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1016-1844A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112457605 | |||||||
| chr9:112457632 | A | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1016-1817A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112457632 | |||||||
| chr9:112457665 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1016-1784A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112457665 | |||||||
| chr9:112457712 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1016-1737C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112457712 | |||||||
| chr9:112457787 | A | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1016-1662A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112457787 | |||||||
| chr9:112457904 | A | G | 2 | a0001c0001t0001g0270 a0001c0001t0011g0258 |
2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1016-1545A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112457904 | |||||||
| chr9:112457908 | C | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1016-1541C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112457908 | |||||||
| chr9:112457958 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0017g0021 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1016-1491G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112457958 | |||||||
| chr9:112458103 | GTT | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1016-1336_1016-133 others(6): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 112458103 | ||||||
| chr9:112458120 | C | A | 5 | a0001c0001t0006g0006 a0001c0001t0006g0064 a0001c0001t0006g0065 others(2): Show |
6 | HG02109.hp2 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1016-1329C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112458120 | |||||||
| chr9:112458285 | G | A | 1 | a0001c0001t0001g0301 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1016-1164G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112458285 | |||||||
| chr9:112458299 | A | G | 5 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(2): Show |
5 | NA18747.hp2 NA18945.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.1016-1150A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112458299 | |||||||
| chr9:112458320 | C | G | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1016-1129C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112458320 | |||||||
| chr9:112458320 | CT | C | 18 | a0001c0001t0001g0030 a0001c0001t0001g0042 a0001c0001t0001g0043 others(15): Show |
18 | HG02155.hp2 HG02559.hp2 NA18943.hp1 others(15): Show |
intron_variant | MODIFIER | c.1016-1113delT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 112458320 | ||||||
| chr9:112458321 | T | TTTC | 318 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(315): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.1016-1126_1016-112 others(7): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 112458321 | ||||||
| chr9:112458389 | G | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(18): Show |
22 | HG01168.hp1 HG01433.hp1 HG02273.hp1 others(19): Show |
intron_variant | MODIFIER | c.1016-1060G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112458389 | |||||||
| chr9:112458418 | A | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1016-1031A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112458418 | |||||||
| chr9:112458690 | A | C | 3 | a0001c0001t0001g0181 a0001c0001t0001g0273 a0001c0001t0001g0310 |
3 | HG01099.hp1 HG01978.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1016-759A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112458690 | |||||||
| chr9:112458703 | C | T | 2 | a0001c0001t0002g0248 a0001c0001t0002g0341 |
2 | HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1016-746C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112458703 | |||||||
| chr9:112458747 | C | T | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG02976.hp1 HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1016-702C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112458747 | |||||||
| chr9:112458762 | AC | A | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG02976.hp1 HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1016-686delC | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112458762 | |||||||
| chr9:112458936 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0270 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1016-513G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112458936 | |||||||
| chr9:112458938 | G | A | 55 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(52): Show |
56 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.1016-511G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112458938 | |||||||
| chr9:112459006 | C | CA | 315 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(312): Show |
329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.1016-437dupA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 112459006 | ||||||
| chr9:112459008 | AAAAAC | A | 7 | a0001c0001t0002g0260 a0001c0001t0002g0261 a0001c0001t0002g0262 others(4): Show |
7 | HG02602.hp1 HG03654.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.1016-436_1016-432d others(7): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 112459008 | ||||||
| chr9:112459203 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1016-246C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 9/10 | chr9 | 112459203 | |||||||
| chr9:112459764 | G | C | 57 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0069 others(54): Show |
58 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.1144+187G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112459764 | |||||||
| chr9:112459782 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1144+205T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112459782 | |||||||
| chr9:112459851 | G | A | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG02976.hp1 HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1144+274G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112459851 | |||||||
| chr9:112459858 | C | T | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+281C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112459858 | |||||||
| chr9:112459953 | T | C | 1 | a0001c0001t0016g0092 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1144+376T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112459953 | |||||||
| chr9:112460032 | G | T | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+455G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112460032 | |||||||
| chr9:112460465 | T | C | 2 | a0001c0001t0005g0050 a0001c0001t0005g0295 |
2 | NA18998.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1144+888T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112460465 | |||||||
| chr9:112460475 | C | A | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+898C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112460475 | |||||||
| chr9:112460485 | G | A | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+908G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112460485 | |||||||
| chr9:112460536 | C | T | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+959C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112460536 | |||||||
| chr9:112460537 | C | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0228 a0001c0001t0001g0344 |
5 | HG02109.hp1 HG02818.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1144+960C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112460537 | |||||||
| chr9:112460604 | T | G | 2 | a0001c0002t0002g0241 a0001c0002t0002g0242 |
2 | HG02129.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1144+1027T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112460604 | |||||||
| chr9:112460738 | C | CCT | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+1161_1144+116 others(6): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112460738 | |||||||
| chr9:112460760 | T | C | 1 | a0001c0001t0002g0271 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1144+1183T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112460760 | |||||||
| chr9:112461018 | G | A | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+1441G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112461018 | |||||||
| chr9:112461079 | GA | G | 3 | a0001c0001t0001g0083 a0001c0001t0001g0094 a0001c0001t0001g0186 |
3 | HG01256.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1144+1504delA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112461079 | ||||||
| chr9:112461081 | A | C | 2 | a0001c0001t0001g0270 a0001c0001t0011g0258 |
2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1144+1504A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112461081 | |||||||
| chr9:112461081 | A | T | 318 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(315): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.1144+1504A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112461081 | |||||||
| chr9:112461098 | C | T | 155 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(152): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.1144+1521C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112461098 | |||||||
| chr9:112461328 | C | T | 1 | a0001c0001t0001g0330 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1144+1751C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112461328 | |||||||
| chr9:112461375 | G | A | 3 | a0001c0001t0001g0094 a0001c0001t0001g0104 a0001c0001t0001g0131 |
3 | HG00738.hp2 HG01256.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1144+1798G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112461375 | |||||||
| chr9:112461428 | A | G | 2 | a0001c0001t0002g0345 a0001c0001t0002g0346 |
2 | HG02280.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1144+1851A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112461428 | |||||||
| chr9:112461656 | G | A | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1144+2079G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112461656 | |||||||
| chr9:112461694 | G | A | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+2117G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112461694 | |||||||
| chr9:112461810 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1144+2233G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112461810 | |||||||
| chr9:112461929 | G | C | 7 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0185 others(4): Show |
7 | HG02622.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1144+2352G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112461929 | |||||||
| chr9:112461983 | T | C | 1 | a0001c0001t0001g0301 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1144+2406T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112461983 | |||||||
| chr9:112462026 | G | A | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+2449G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112462026 | |||||||
| chr9:112462119 | T | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+2542T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112462119 | |||||||
| chr9:112462140 | G | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+2563G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112462140 | |||||||
| chr9:112462270 | C | T | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+2693C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112462270 | |||||||
| chr9:112462425 | C | T | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+2848C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112462425 | |||||||
| chr9:112462444 | C | T | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+2867C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112462444 | |||||||
| chr9:112462462 | C | CA | 17 | a0001c0001t0001g0016 a0001c0001t0001g0071 a0001c0001t0001g0284 others(14): Show |
18 | HG00597.hp1 HG01070.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.1144+2899dupA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112462462 | ||||||
| chr9:112462462 | C | CAA | 295 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1144+2898_1144+289 others(6): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112462462 | ||||||
| chr9:112462462 | C | CAAA | 9 | a0001c0001t0001g0017 a0001c0001t0001g0120 a0001c0001t0002g0125 others(6): Show |
10 | HG01175.hp2 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1144+2897_1144+289 others(7): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112462462 | ||||||
| chr9:112462513 | C | A | 1 | a0001c0001t0001g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1144+2936C>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112462513 | |||||||
| chr9:112462600 | A | ATG | 13 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0044 others(10): Show |
14 | HG00597.hp2 HG02155.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1144+3063_1144+306 others(6): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112462600 | ||||||
| chr9:112462600 | A | ATGTG | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(1): Show |
4 | HG01515.hp1 NA18955.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144+3061_1144+306 others(8): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112462600 | ||||||
| chr9:112462600 | ATG | A | 44 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0068 others(41): Show |
45 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.1144+3063_1144+306 others(6): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112462600 | ||||||
| chr9:112462600 | ATGTG | A | 34 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(31): Show |
35 | HG00733.hp2 HG01099.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.1144+3061_1144+306 others(8): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112462600 | ||||||
| chr9:112462600 | ATGTGTG | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(206): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1144+3059_1144+306 others(10): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112462600 | ||||||
| chr9:112462600 | ATGTGTGT others(1): Show |
A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0036 others(12): Show |
17 | HG01081.hp2 HG01261.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1144+3057_1144+306 others(12): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112462600 | ||||||
| chr9:112462600 | ATGTGTGT others(3): Show |
A | 15 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(12): Show |
15 | HG00323.hp1 HG01109.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.1144+3055_1144+306 others(14): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112462600 | ||||||
| chr9:112462773 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1144+3196A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112462773 | |||||||
| chr9:112462808 | C | G | 1 | a0001c0001t0001g0329 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1144+3231C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112462808 | |||||||
| chr9:112463064 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1144+3487G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112463064 | |||||||
| chr9:112463140 | T | C | 1 | a0001c0001t0011g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1144+3563T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112463140 | |||||||
| chr9:112463167 | T | C | 2 | a0001c0001t0006g0006 a0001c0001t0006g0067 |
3 | HG02486.hp2 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1144+3590T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112463167 | |||||||
| chr9:112463259 | CT | C | 307 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(304): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.1144+3698delT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112463259 | ||||||
| chr9:112463259 | CTT | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0113 a0001c0001t0001g0186 others(6): Show |
12 | HG00280.hp1 HG01070.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.1144+3697_1144+369 others(6): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112463259 | ||||||
| chr9:112463376 | G | A | 3 | a0001c0001t0006g0064 a0001c0001t0006g0065 a0001c0001t0006g0066 |
3 | HG02109.hp2 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1144+3799G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112463376 | |||||||
| chr9:112463637 | A | G | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+4060A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112463637 | |||||||
| chr9:112463664 | G | A | 340 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(337): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.1144+4087G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112463664 | |||||||
| chr9:112463697 | C | CTCTG | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+4123_1144+412 others(8): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112463697 | ||||||
| chr9:112463732 | C | T | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+4155C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112463732 | |||||||
| chr9:112463850 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1144+4273G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112463850 | |||||||
| chr9:112463879 | TCA | T | 4 | a0001c0001t0002g0216 a0001c0001t0002g0224 a0001c0001t0002g0225 others(1): Show |
4 | HG01884.hp1 HG02647.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144+4303_1144+430 others(6): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112463879 | |||||||
| chr9:112463951 | G | A | 1 | a0001c0001t0001g0349 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1144+4374G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112463951 | |||||||
| chr9:112463952 | TGCCCAGC others(3): Show |
T | 1 | a0001c0001t0021g0051 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1144+4377_1144+438 others(14): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112463952 | ||||||
| chr9:112464084 | C | G | 1 | a0001c0001t0002g0240 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1144+4507C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112464084 | |||||||
| chr9:112464126 | G | C | 1 | a0001c0001t0002g0178 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1144+4549G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112464126 | |||||||
| chr9:112464213 | GACACACA others(9): Show |
G | 10 | a0001c0001t0001g0084 a0001c0001t0001g0120 a0001c0001t0001g0272 others(7): Show |
10 | HG00323.hp1 HG00639.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1144+4648_1144+466 others(20): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112464213 | ||||||
| chr9:112464213 | GACACACA others(11): Show |
G | 46 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0016 others(43): Show |
49 | HG01099.hp2 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.1144+4648_1144+466 others(22): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112464213 | ||||||
| chr9:112464213 | GACACACA others(13): Show |
G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(261): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.1144+4648_1144+466 others(24): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112464213 | ||||||
| chr9:112464213 | GACACACA others(15): Show |
G | 1 | a0001c0001t0002g0239 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1144+4648_1144+466 others(26): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112464213 | ||||||
| chr9:112464223 | C | G | 1 | a0001c0001t0021g0051 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1144+4646C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112464223 | |||||||
| chr9:112464225 | G | C | 1 | a0001c0001t0021g0051 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1144+4648G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112464225 | |||||||
| chr9:112464225 | G | GAC | 14 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0043 others(11): Show |
14 | HG02155.hp2 NA18943.hp1 NA18955.hp2 others(11): Show |
intron_variant | MODIFIER | c.1144+4680_1144+468 others(6): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112464225 | ||||||
| chr9:112464280 | G | T | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+4703G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112464280 | |||||||
| chr9:112464398 | A | T | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+4821A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112464398 | |||||||
| chr9:112464513 | G | A | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+4936G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112464513 | |||||||
| chr9:112464620 | G | C | 1 | a0001c0001t0001g0298 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1144+5043G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112464620 | |||||||
| chr9:112464820 | C | T | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1144+5243C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112464820 | |||||||
| chr9:112464938 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1144+5361T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112464938 | |||||||
| chr9:112465090 | T | A | 12 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0061 others(9): Show |
12 | HG01081.hp2 HG01261.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1145-5342T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112465090 | |||||||
| chr9:112465159 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1145-5273C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112465159 | |||||||
| chr9:112465161 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0001g0114 |
3 | HG00323.hp2 HG01978.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1145-5271C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112465161 | |||||||
| chr9:112465270 | A | G | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
17 | HG02155.hp2 NA18943.hp1 NA18951.hp2 others(14): Show |
intron_variant | MODIFIER | c.1145-5162A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112465270 | |||||||
| chr9:112465408 | C | T | 1 | a0001c0001t0001g0331 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1145-5024C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112465408 | |||||||
| chr9:112465465 | T | A | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1145-4967T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112465465 | |||||||
| chr9:112465713 | G | A | 3 | a0001c0001t0007g0020 a0001c0001t0007g0026 a0001c0001t0007g0029 |
3 | NA18948.hp1 NA18972.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1145-4719G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112465713 | |||||||
| chr9:112465855 | A | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0117 |
2 | NA19066.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1145-4577A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112465855 | |||||||
| chr9:112465884 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1145-4548T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112465884 | |||||||
| chr9:112465974 | T | C | 1 | a0001c0001t0001g0300 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1145-4458T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112465974 | |||||||
| chr9:112465979 | G | T | 1 | a0001c0001t0006g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1145-4453G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112465979 | |||||||
| chr9:112466000 | A | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1145-4432A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466000 | |||||||
| chr9:112466005 | A | C | 1 | a0001c0001t0001g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1145-4427A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466005 | |||||||
| chr9:112466007 | T | C | 1 | a0001c0001t0002g0179 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1145-4425T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466007 | |||||||
| chr9:112466034 | T | C | 323 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.1145-4398T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466034 | |||||||
| chr9:112466145 | A | G | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG01109.hp2 HG02145.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1145-4287A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466145 | |||||||
| chr9:112466175 | T | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1145-4257T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466175 | |||||||
| chr9:112466319 | G | A | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1145-4113G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466319 | |||||||
| chr9:112466321 | G | A | 7 | a0001c0001t0002g0002 a0001c0001t0002g0190 a0001c0001t0002g0193 others(4): Show |
9 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.1145-4111G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466321 | |||||||
| chr9:112466414 | A | G | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1145-4018A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466414 | |||||||
| chr9:112466459 | A | G | 1 | a0001c0001t0002g0143 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1145-3973A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466459 | |||||||
| chr9:112466466 | T | C | 3 | a0001c0001t0006g0064 a0001c0001t0006g0065 a0001c0001t0006g0066 |
3 | HG02109.hp2 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1145-3966T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466466 | |||||||
| chr9:112466467 | C | T | 1 | a0001c0001t0001g0331 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1145-3965C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466467 | |||||||
| chr9:112466485 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1145-3947G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466485 | |||||||
| chr9:112466562 | AAT | A | 310 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(307): Show |
324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.1145-3869_1145-386 others(6): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466562 | |||||||
| chr9:112466563 | AT | A | 11 | a0001c0001t0001g0072 a0001c0001t0001g0094 a0001c0001t0001g0104 others(8): Show |
11 | HG00738.hp2 HG01256.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1145-3868delT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466563 | |||||||
| chr9:112466713 | G | T | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1145-3719G>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466713 | |||||||
| chr9:112466742 | A | T | 1 | a0001c0001t0021g0051 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1145-3690A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466742 | |||||||
| chr9:112466743 | T | C | 1 | a0001c0001t0021g0051 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1145-3689T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466743 | |||||||
| chr9:112466823 | T | C | 2 | a0001c0001t0001g0270 a0001c0001t0011g0258 |
2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1145-3609T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466823 | |||||||
| chr9:112466906 | A | G | 1 | a0001c0001t0002g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1145-3526A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466906 | |||||||
| chr9:112466918 | T | G | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1145-3514T>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466918 | |||||||
| chr9:112466965 | G | A | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG01109.hp2 HG02145.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1145-3467G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112466965 | |||||||
| chr9:112467167 | T | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1145-3265T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112467167 | |||||||
| chr9:112467206 | G | GT | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1145-3225dupT | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112467206 | ||||||
| chr9:112467408 | G | A | 2 | a0001c0001t0002g0219 a0001c0001t0002g0221 |
2 | NA18956.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1145-3024G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112467408 | |||||||
| chr9:112467413 | G | A | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1145-3019G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112467413 | |||||||
| chr9:112467508 | T | C | 20 | a0001c0002t0002g0037 a0001c0002t0002g0041 a0001c0002t0002g0168 others(17): Show |
20 | HG00621.hp1 HG00673.hp2 HG02129.hp2 others(17): Show |
intron_variant | MODIFIER | c.1145-2924T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112467508 | |||||||
| chr9:112467525 | G | A | 1 | a0001c0001t0004g0090 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1145-2907G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112467525 | |||||||
| chr9:112467715 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1145-2717A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112467715 | |||||||
| chr9:112467778 | G | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1145-2654G>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112467778 | |||||||
| chr9:112467875 | A | C | 3 | a0001c0001t0001g0269 a0001c0001t0001g0318 a0001c0001t0001g0320 |
3 | NA18612.hp2 NA18943.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1145-2557A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112467875 | |||||||
| chr9:112467898 | A | G | 20 | a0001c0002t0002g0037 a0001c0002t0002g0041 a0001c0002t0002g0168 others(17): Show |
20 | HG00621.hp1 HG00673.hp2 HG02129.hp2 others(17): Show |
intron_variant | MODIFIER | c.1145-2534A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112467898 | |||||||
| chr9:112467947 | A | T | 320 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(317): Show |
334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.1145-2485A>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112467947 | |||||||
| chr9:112467981 | G | A | 320 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(317): Show |
334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.1145-2451G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112467981 | |||||||
| chr9:112468047 | ATTGT | A | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1145-2380_1145-237 others(8): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112468047 | ||||||
| chr9:112468186 | C | G | 7 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0185 others(4): Show |
7 | HG02622.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1145-2246C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112468186 | |||||||
| chr9:112468193 | T | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1145-2239T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112468193 | |||||||
| chr9:112468541 | C | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1145-1891C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112468541 | |||||||
| chr9:112468571 | C | T | 1 | a0001c0001t0001g0321 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1145-1861C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112468571 | |||||||
| chr9:112468572 | C | G | 1 | a0001c0001t0001g0186 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1145-1860C>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112468572 | |||||||
| chr9:112468638 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1145-1794C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112468638 | |||||||
| chr9:112468781 | A | G | 2 | a0001c0001t0001g0270 a0001c0001t0011g0258 |
2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1145-1651A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112468781 | |||||||
| chr9:112468925 | A | G | 1 | a0001c0001t0001g0245 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1145-1507A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112468925 | |||||||
| chr9:112468997 | G | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0185 others(4): Show |
7 | HG02622.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1145-1435G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112468997 | |||||||
| chr9:112469237 | A | AAT | 3 | a0001c0001t0001g0269 a0001c0001t0001g0318 a0001c0001t0001g0320 |
3 | NA18612.hp2 NA18943.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1145-1185_1145-118 others(6): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112469237 | ||||||
| chr9:112469368 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1145-1064C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112469368 | |||||||
| chr9:112469391 | G | A | 1 | a0001c0001t0003g0338 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1145-1041G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112469391 | |||||||
| chr9:112469493 | A | C | 1 | a0001c0001t0001g0244 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1145-939A>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112469493 | |||||||
| chr9:112469641 | T | TGG | 56 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0033 others(53): Show |
57 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1145-789_1145-788d others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112469641 | ||||||
| chr9:112469666 | C | CA | 79 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(76): Show |
82 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.1145-743dupA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112469666 | ||||||
| chr9:112469666 | C | CAA | 16 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0001g0101 others(13): Show |
16 | HG01891.hp2 HG01978.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1145-744_1145-743d others(4): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112469666 | ||||||
| chr9:112469666 | CA | C | 13 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0049 others(10): Show |
13 | HG00639.hp1 HG02155.hp2 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.1145-743delA | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112469666 | ||||||
| chr9:112469681 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1145-751A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112469681 | |||||||
| chr9:112469689 | A | G | 1 | a0001c0001t0005g0047 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1145-743A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112469689 | |||||||
| chr9:112469689 | AG | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(55): Show |
60 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1145-741delG | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 112469689 | ||||||
| chr9:112469690 | G | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(31): Show |
35 | HG00735.hp2 HG01123.hp2 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.1145-742G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112469690 | |||||||
| chr9:112469691 | G | A | 2 | a0001c0001t0005g0047 a0001c0001t0021g0051 |
2 | NA18975.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1145-741G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112469691 | |||||||
| chr9:112469767 | T | C | 14 | a0001c0001t0002g0019 a0001c0001t0002g0025 a0001c0001t0002g0028 others(11): Show |
14 | HG00408.hp2 HG02523.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.1145-665T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112469767 | |||||||
| chr9:112469837 | A | G | 2 | a0001c0001t0001g0270 a0001c0001t0011g0258 |
2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1145-595A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112469837 | |||||||
| chr9:112469851 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1145-581A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112469851 | |||||||
| chr9:112470004 | T | A | 1 | a0001c0001t0001g0349 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1145-428T>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112470004 | |||||||
| chr9:112470141 | T | C | 1 | a0001c0001t0002g0260 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1145-291T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112470141 | |||||||
| chr9:112470232 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0120 |
2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1145-200C>T | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112470232 | |||||||
| chr9:112470244 | T | C | 1 | a0001c0001t0005g0053 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1145-188T>C | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112470244 | |||||||
| chr9:112470288 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1145-144G>A | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112470288 | |||||||
| chr9:112470358 | A | G | 1 | a0001c0001t0002g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1145-74A>G | HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 10/10 | chr9 | 112470358 |