Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84064 |
| ensemblid | ENSG00000167220.12 |
| hgncid | 25364 |
| symbol | HDHD2 |
| name | haloacid dehalogenase like hydrolase domain containing 2 |
| refseq_nuc | NM_032124.5 |
| refseq_prot | NP_115500.1 |
| ensembl_nuc | ENST00000300605.11 |
| ensembl_prot | ENSP00000300605.4 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 47107410 |
| end | 47150500 |
| strand | - |
| ver | v1.2 |
| region | chr18:47107410-47150500 |
| region5000 | chr18:47102410-47155500 |
| regionname0 | HDHD2_chr18_47107410_47150500 |
| regionname5000 | HDHD2_chr18_47102410_47155500 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 259 | 359 | 68 | 70 | 174 | 14 | 31 | 126 | HDHD2_chr18_47102410_47155500 | HDHD2 | MAACR others(254): Show |
chr18 | 47102410 | 47155500 |
| a0002 | 0/0 | 259 | 7 | 6 | 0 | 0 | 0 | 1 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | MAACR others(254): Show |
chr18 | 47102410 | 47155500 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 777 | 359 | 68 | 70 | 174 | 14 | 31 | HDHD2_chr18_47102410_47155500 | HDHD2 | ATGGC others(772): Show |
chr18 | 47102410 | 47155500 | ||
| a0002c0002 | 0/0 | 777 | 6 | 6 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | ATGGC others(772): Show |
chr18 | 47102410 | 47155500 | ||
| a0002c0003 | 0/0 | 777 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | ATGGC others(772): Show |
chr18 | 47102410 | 47155500 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2185 | 275 | 46 | 60 | 131 | 10 | 27 | HDHD2_chr18_47102410_47155500 | HDHD2 | AACTT others(2180): Show |
chr18 | 47102410 | 47155500 |
| a0001c0001t0002 | 0/0 | 2185 | 53 | 3 | 7 | 40 | 2 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | AACTT others(2180): Show |
chr18 | 47102410 | 47155500 |
| a0001c0001t0003 | 0/0 | 2185 | 4 | 4 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | AACTT others(2180): Show |
chr18 | 47102410 | 47155500 |
| a0001c0001t0004 | 1/0 | 2185 | 4 | 3 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | AACTT others(2180): Show |
chr18 | 47102410 | 47155500 |
| a0001c0001t0005 | 0/0 | 2185 | 3 | 0 | 1 | 0 | 1 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | AACTT others(2180): Show |
chr18 | 47102410 | 47155500 |
| a0001c0001t0006 | 0/0 | 2185 | 3 | 1 | 1 | 0 | 1 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | AACTT others(2180): Show |
chr18 | 47102410 | 47155500 |
| a0001c0001t0007 | 0/0 | 2185 | 3 | 2 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | AACTT others(2180): Show |
chr18 | 47102410 | 47155500 |
| a0001c0001t0008 | 0/0 | 2185 | 2 | 2 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | AACTT others(2180): Show |
chr18 | 47102410 | 47155500 |
| a0001c0001t0009 | 0/0 | 2185 | 2 | 2 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | AACTT others(2180): Show |
chr18 | 47102410 | 47155500 |
| a0001c0001t0010 | 0/0 | 2185 | 2 | 2 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | AACTT others(2180): Show |
chr18 | 47102410 | 47155500 |
| a0001c0001t0011 | 0/0 | 2185 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | AACTT others(2180): Show |
chr18 | 47102410 | 47155500 |
| a0001c0001t0012 | 0/0 | 2185 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | AACTT others(2180): Show |
chr18 | 47102410 | 47155500 |
| a0001c0001t0013 | 0/0 | 2185 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | AACTT others(2180): Show |
chr18 | 47102410 | 47155500 |
| a0001c0001t0014 | 0/0 | 2185 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | AACTT others(2180): Show |
chr18 | 47102410 | 47155500 |
| a0001c0001t0015 | 0/0 | 2185 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | AACTT others(2180): Show |
chr18 | 47102410 | 47155500 |
| a0001c0001t0016 | 0/0 | 2185 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | AACTT others(2180): Show |
chr18 | 47102410 | 47155500 |
| a0001c0001t0017 | 0/0 | 2185 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | AACTT others(2180): Show |
chr18 | 47102410 | 47155500 |
| a0001c0001t0018 | 0/0 | 2185 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | AACTT others(2180): Show |
chr18 | 47102410 | 47155500 |
| a0002c0002t0001 | 0/0 | 2185 | 6 | 6 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | AACTT others(2180): Show |
chr18 | 47102410 | 47155500 |
| a0002c0003t0001 | 0/0 | 2185 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | AACTT others(2180): Show |
chr18 | 47102410 | 47155500 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 13 | 1 | 3 | 5 | 1 | 3 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0002 | 0/0 | 11 | 0 | 4 | 4 | 3 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 5 | 0 | 1 | 2 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0016 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0003 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0009 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0004g0034 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0005g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0006g0044 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0006g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0007g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0007g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0008g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0009g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0009g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0010g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0010g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0011g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0012g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0013g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0014g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0015g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0016g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0017g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0001c0001t0018g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0002c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0002c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0002c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| a0002c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00099 | hp2 | a0001 | c0001 | t0006 | g0044 | EUR | GBR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | GBR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0047 | EUR | GBR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | FIN | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0019 | EUR | FIN | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0038 | AMR | PUR | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0020 | AMR | CLM | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0020 | EUR | IBS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | ACB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0038 | AFR | ACB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0166 | AFR | ACB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CDX | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0185 | AFR | ACB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | ACB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02258 | hp1 | a0001 | c0001 | t0013 | g0240 | AFR | ACB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | ACB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0082 | AFR | GWD | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | GWD | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0132 | AFR | GWD | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | GWD | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | GWD | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | GWD | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02922 | hp2 | a0001 | c0001 | t0010 | g0080 | AFR | ESN | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0127 | AFR | ESN | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0133 | AFR | MSL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | ESN | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0048 | AFR | ESN | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0078 | AFR | MSL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0144 | AFR | MSL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03490 | hp1 | a0001 | c0001 | t0018 | g0154 | SAS | PJL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | STU | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0054 | SAS | PJL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03831 | hp1 | a0001 | c0001 | t0015 | g0143 | SAS | BEB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0049 | AFR | YRI | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | YRI | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18950 | hp1 | a0001 | c0001 | t0014 | g0246 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18953 | hp1 | a0001 | c0001 | t0016 | g0210 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18993 | hp2 | a0001 | c0001 | t0017 | g0211 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | LWK | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ASW | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ASW | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | TSI | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | TSI | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA20905 | hp1 | a0002 | c0003 | t0001 | g0159 | SAS | GIH | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0234 | AMR | CLM | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0044 | AFR | ACB | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG06807 | hp1 | a0001 | c0001 | t0011 | g0050 | AFR | USA | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | USA | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA20300 | hp1 | a0001 | c0001 | t0012 | g0190 | AFR | USA | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | USA | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | LWK | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| NA21309 | hp2 | a0001 | c0001 | t0010 | g0081 | AFR | LWK | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0196 | REF | REF | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0034 | REF | REF | HDHD2_chr18_47102410_47155500 | HDHD2 | chr18 | 47102410 | 47155500 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:47134552 | C | T | 1 | a0002 | 6 | HG02717.hp1 HG02895.hp2 HG02976.hp2 others(3): Show |
missense_variant | MODERATE | c.254G>A | p.Arg85Gln | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/7 | 387/2185 | 254/780 | 85/259 | chr18 | 47134552 | |||
| chr18:47134553 | G | A | 1 | a0002 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.253C>T | p.Arg85Trp | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/7 | 386/2185 | 253/780 | 85/259 | chr18 | 47134553 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:47107425 | T | G | 1 | a0001c0001t0017 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1257A>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 7/7 | 1257 | chr18 | 47107425 | ||||||
| chr18:47107653 | T | C | 2 | a0001c0001t0009 a0001c0001t0010 |
4 | HG02572.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1029A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 7/7 | 1029 | chr18 | 47107653 | ||||||
| chr18:47107687 | G | T | 1 | a0001c0001t0009 | 2 | HG02572.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*995C>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 7/7 | 995 | chr18 | 47107687 | ||||||
| chr18:47107920 | C | T | 1 | a0001c0001t0006 | 3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*762G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 7/7 | 762 | chr18 | 47107920 | ||||||
| chr18:47107943 | C | T | 1 | a0001c0001t0005 | 3 | HG01361.hp1 HG01515.hp2 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*739G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 7/7 | 739 | chr18 | 47107943 | ||||||
| chr18:47107944 | T | C | 1 | a0001c0001t0007 | 3 | HG01243.hp2 HG01884.hp2 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*738A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 7/7 | 738 | chr18 | 47107944 | ||||||
| chr18:47107962 | A | T | 1 | a0001c0001t0016 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*720T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 7/7 | 720 | chr18 | 47107962 | ||||||
| chr18:47108074 | C | G | 1 | a0001c0001t0013 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*608G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 7/7 | 608 | chr18 | 47108074 | ||||||
| chr18:47108240 | T | C | 1 | a0001c0001t0014 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*442A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 7/7 | 442 | chr18 | 47108240 | ||||||
| chr18:47108306 | C | G | 1 | a0001c0001t0015 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*376G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 7/7 | 376 | chr18 | 47108306 | ||||||
| chr18:47108383 | G | A | 1 | a0001c0001t0018 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*299C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 7/7 | 299 | chr18 | 47108383 | ||||||
| chr18:47108385 | A | G | 6 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(3): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*297T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 7/7 | 297 | chr18 | 47108385 | ||||||
| chr18:47108533 | C | T | 1 | a0001c0001t0005 | 3 | HG01361.hp1 HG01515.hp2 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*149G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 7/7 | 149 | chr18 | 47108533 | ||||||
| chr18:47108576 | G | T | 1 | a0001c0001t0012 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*106C>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 7/7 | 106 | chr18 | 47108576 | ||||||
| chr18:47108669 | T | C | 1 | a0001c0001t0003 | 4 | HG01884.hp1 HG02257.hp2 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*13A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 7/7 | 13 | chr18 | 47108669 | ||||||
| chr18:47108677 | C | T | 19 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(16): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
3_prime_UTR_variant | MODIFIER | c.*5G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 7/7 | 5 | chr18 | 47108677 | ||||||
| chr18:47150435 | C | G | 1 | a0001c0001t0011 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-68G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/7 | 13996 | chr18 | 47150435 | ||||||
| chr18:47150472 | C | T | 1 | a0001c0001t0008 | 2 | HG03139.hp2 NA18522.hp1 |
5_prime_UTR_variant | MODIFIER | c.-105G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/7 | 14033 | chr18 | 47150472 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:47108977 | A | G | 2 | a0001c0001t0008g0048 a0001c0001t0008g0049 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.677-192T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47108977 | |||||||
| chr18:47109134 | T | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0092 |
3 | HG01256.hp2 HG01258.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.677-349A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47109134 | |||||||
| chr18:47109375 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.677-590A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47109375 | |||||||
| chr18:47109800 | T | G | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
53 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.677-1015A>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47109800 | |||||||
| chr18:47109917 | A | C | 2 | a0001c0001t0002g0037 a0001c0001t0002g0181 |
3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.677-1132T>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47109917 | |||||||
| chr18:47110135 | G | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(151): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.677-1350C>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47110135 | |||||||
| chr18:47110338 | GA | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0198 |
3 | HG01517.hp1 HG01993.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.677-1554delT | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47110338 | |||||||
| chr18:47110408 | C | T | 1 | a0001c0001t0012g0190 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.677-1623G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47110408 | |||||||
| chr18:47110412 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.677-1627T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47110412 | |||||||
| chr18:47110539 | G | A | 1 | a0001c0001t0004g0152 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.677-1754C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47110539 | |||||||
| chr18:47110563 | C | A | 2 | a0001c0001t0007g0038 a0001c0001t0007g0185 |
3 | HG01243.hp2 HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.677-1778G>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47110563 | |||||||
| chr18:47110664 | G | A | 20 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0022 others(17): Show |
27 | HG00544.hp2 HG00558.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.677-1879C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47110664 | |||||||
| chr18:47110735 | T | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(73): Show |
117 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.677-1950A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47110735 | |||||||
| chr18:47110901 | A | G | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
53 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.676+2076T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47110901 | |||||||
| chr18:47111195 | C | A | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
53 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.676+1782G>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47111195 | |||||||
| chr18:47111328 | C | T | 1 | a0001c0001t0002g0245 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.676+1649G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47111328 | |||||||
| chr18:47111468 | T | TA | 2 | a0001c0001t0005g0020 a0001c0001t0005g0054 |
3 | HG01361.hp1 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.676+1508dupT | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47111468 | |||||||
| chr18:47111622 | G | A | 5 | a0001c0001t0001g0077 a0001c0001t0009g0078 a0001c0001t0009g0082 others(2): Show |
5 | HG02572.hp2 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+1355C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47111622 | |||||||
| chr18:47111699 | G | A | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG00544.hp1 HG03098.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.676+1278C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47111699 | |||||||
| chr18:47111848 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.676+1129G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47111848 | |||||||
| chr18:47111927 | A | G | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
53 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.676+1050T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47111927 | |||||||
| chr18:47112056 | C | A | 1 | a0001c0001t0001g0077 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676+921G>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47112056 | |||||||
| chr18:47112510 | C | T | 1 | a0001c0001t0013g0240 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.676+467G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47112510 | |||||||
| chr18:47112515 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.676+462T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47112515 | |||||||
| chr18:47112723 | A | T | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG00544.hp1 HG03098.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.676+254T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47112723 | |||||||
| chr18:47112804 | G | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(68): Show |
111 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.676+173C>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47112804 | |||||||
| chr18:47112808 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676+169C>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47112808 | |||||||
| chr18:47112819 | A | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0063 others(6): Show |
13 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.676+158T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47112819 | |||||||
| chr18:47112922 | A | T | 2 | a0001c0001t0005g0020 a0001c0001t0005g0054 |
3 | HG01361.hp1 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.676+55T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 6/6 | chr18 | 47112922 | |||||||
| chr18:47113054 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.613-14T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 5/6 | chr18 | 47113054 | |||||||
| chr18:47113551 | T | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0041 a0001c0001t0001g0183 others(8): Show |
19 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.613-511A>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 5/6 | chr18 | 47113551 | |||||||
| chr18:47113598 | T | A | 1 | a0001c0001t0001g0138 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.613-558A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 5/6 | chr18 | 47113598 | |||||||
| chr18:47113647 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.613-607A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 5/6 | chr18 | 47113647 | |||||||
| chr18:47113690 | A | C | 1 | a0001c0001t0001g0151 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.613-650T>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 5/6 | chr18 | 47113690 | |||||||
| chr18:47113778 | T | C | 2 | a0001c0001t0005g0020 a0001c0001t0005g0054 |
3 | HG01361.hp1 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.613-738A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 5/6 | chr18 | 47113778 | |||||||
| chr18:47113959 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.613-919T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 5/6 | chr18 | 47113959 | |||||||
| chr18:47113993 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.613-953T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 5/6 | chr18 | 47113993 | |||||||
| chr18:47114041 | G | A | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
53 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.613-1001C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 5/6 | chr18 | 47114041 | |||||||
| chr18:47114441 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.612+691C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 5/6 | chr18 | 47114441 | |||||||
| chr18:47114585 | C | T | 1 | a0002c0002t0001g0030 | 2 | HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.612+547G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 5/6 | chr18 | 47114585 | |||||||
| chr18:47114601 | G | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(56): Show |
98 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.612+531C>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 5/6 | chr18 | 47114601 | |||||||
| chr18:47114804 | T | C | 1 | a0001c0001t0002g0239 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.612+328A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 5/6 | chr18 | 47114804 | |||||||
| chr18:47114925 | G | A | 2 | a0001c0001t0005g0020 a0001c0001t0005g0054 |
3 | HG01361.hp1 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.612+207C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 5/6 | chr18 | 47114925 | |||||||
| chr18:47115026 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.612+106G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 5/6 | chr18 | 47115026 | |||||||
| chr18:47115028 | C | T | 2 | a0001c0001t0005g0020 a0001c0001t0005g0054 |
3 | HG01361.hp1 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.612+104G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 5/6 | chr18 | 47115028 | |||||||
| chr18:47115095 | G | C | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
53 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.612+37C>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 5/6 | chr18 | 47115095 | |||||||
| chr18:47115407 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.396-59C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47115407 | |||||||
| chr18:47115505 | C | CAAAGAAC others(312): Show |
1 | a0001c0001t0001g0137 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.396-158_396-157ins others(319): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47115505 | |||||||
| chr18:47115505 | C | CAAAGAAC others(313): Show |
22 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0031 others(19): Show |
31 | HG00597.hp2 HG00673.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.396-158_396-157ins others(320): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47115505 | |||||||
| chr18:47115751 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.396-403T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47115751 | |||||||
| chr18:47115873 | G | T | 1 | a0001c0001t0001g0026 | 2 | HG02074.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.396-525C>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47115873 | |||||||
| chr18:47116076 | G | T | 2 | a0001c0001t0008g0048 a0001c0001t0008g0049 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.396-728C>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47116076 | |||||||
| chr18:47116939 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0079 |
3 | HG02922.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.396-1591A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47116939 | |||||||
| chr18:47117290 | T | C | 4 | a0001c0001t0009g0078 a0001c0001t0009g0082 a0001c0001t0010g0080 others(1): Show |
4 | HG02572.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.396-1942A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47117290 | |||||||
| chr18:47117325 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.396-1977G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47117325 | |||||||
| chr18:47117443 | T | C | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
53 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.396-2095A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47117443 | |||||||
| chr18:47117583 | A | T | 2 | a0001c0001t0002g0037 a0001c0001t0002g0181 |
3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.396-2235T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47117583 | |||||||
| chr18:47117756 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.396-2408G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47117756 | |||||||
| chr18:47118142 | A | G | 2 | a0001c0001t0002g0037 a0001c0001t0002g0181 |
3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.396-2794T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47118142 | |||||||
| chr18:47118159 | G | A | 39 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(36): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.396-2811C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47118159 | |||||||
| chr18:47118170 | G | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0086 a0001c0001t0001g0113 others(2): Show |
6 | HG02056.hp1 HG02129.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.396-2822C>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47118170 | |||||||
| chr18:47118327 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0160 |
3 | HG01070.hp1 HG02698.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.396-2979T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47118327 | |||||||
| chr18:47118505 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.396-3157G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47118505 | |||||||
| chr18:47118658 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.396-3310T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47118658 | |||||||
| chr18:47118704 | C | T | 2 | a0001c0001t0002g0037 a0001c0001t0002g0181 |
3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.396-3356G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47118704 | |||||||
| chr18:47118706 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0079 a0001c0001t0008g0048 others(1): Show |
5 | HG02922.hp1 HG03139.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.396-3358G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47118706 | |||||||
| chr18:47118725 | G | A | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.396-3377C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47118725 | |||||||
| chr18:47118806 | CAGATGAG others(8): Show |
C | 2 | a0001c0001t0007g0038 a0001c0001t0007g0185 |
3 | HG01243.hp2 HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.396-3473_396-3459d others(17): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47118806 | |||||||
| chr18:47118903 | CA | C | 20 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0022 others(17): Show |
27 | HG00544.hp2 HG00558.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.396-3556delT | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47118903 | |||||||
| chr18:47118938 | A | G | 1 | a0001c0001t0010g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.396-3590T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47118938 | |||||||
| chr18:47118943 | A | G | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.396-3595T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47118943 | |||||||
| chr18:47119066 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0079 a0001c0001t0008g0048 others(1): Show |
5 | HG02922.hp1 HG03139.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.396-3718A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47119066 | |||||||
| chr18:47119120 | T | C | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
53 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.396-3772A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47119120 | |||||||
| chr18:47119210 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.396-3862T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47119210 | |||||||
| chr18:47119222 | T | A | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
53 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.396-3874A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47119222 | |||||||
| chr18:47119239 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.396-3891C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47119239 | |||||||
| chr18:47119505 | G | A | 1 | a0001c0001t0018g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.396-4157C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47119505 | |||||||
| chr18:47119516 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0079 a0001c0001t0008g0048 others(1): Show |
5 | HG02922.hp1 HG03139.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.396-4168C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47119516 | |||||||
| chr18:47119524 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.396-4176T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47119524 | |||||||
| chr18:47119548 | T | A | 2 | a0001c0001t0007g0038 a0001c0001t0007g0185 |
3 | HG01243.hp2 HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.396-4200A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47119548 | |||||||
| chr18:47119587 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.396-4239A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47119587 | |||||||
| chr18:47119766 | A | G | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.396-4418T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47119766 | |||||||
| chr18:47119789 | T | C | 32 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(29): Show |
40 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.396-4441A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47119789 | |||||||
| chr18:47119817 | T | C | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG00544.hp1 HG03098.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.396-4469A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47119817 | |||||||
| chr18:47120293 | G | A | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
53 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.396-4945C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47120293 | |||||||
| chr18:47120351 | A | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG00544.hp1 NA18747.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.396-5003T>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47120351 | |||||||
| chr18:47120390 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.396-5042G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47120390 | |||||||
| chr18:47120477 | A | C | 1 | a0001c0001t0001g0209 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.396-5129T>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47120477 | |||||||
| chr18:47120524 | T | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0099 |
2 | HG02015.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.396-5176A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47120524 | |||||||
| chr18:47120641 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.396-5293C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47120641 | |||||||
| chr18:47120647 | C | CCTAGCTT others(342): Show |
1 | a0001c0001t0010g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.396-5648_396-5300d others(351): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47120647 | |||||||
| chr18:47120880 | C | T | 1 | a0001c0001t0002g0250 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.396-5532G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47120880 | |||||||
| chr18:47120920 | G | C | 1 | a0001c0001t0001g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.396-5572C>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47120920 | |||||||
| chr18:47120925 | A | T | 1 | a0001c0001t0001g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.396-5577T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47120925 | |||||||
| chr18:47121065 | G | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0092 |
3 | HG01256.hp2 HG01258.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.396-5717C>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47121065 | |||||||
| chr18:47121133 | G | A | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
53 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.396-5785C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47121133 | |||||||
| chr18:47121149 | C | T | 1 | a0001c0001t0006g0234 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.396-5801G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47121149 | |||||||
| chr18:47121259 | C | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0194 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.396-5911G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47121259 | |||||||
| chr18:47121329 | A | C | 1 | a0001c0001t0001g0055 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.396-5981T>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47121329 | |||||||
| chr18:47121459 | A | C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.396-6111T>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47121459 | |||||||
| chr18:47121694 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.396-6346T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47121694 | |||||||
| chr18:47121926 | G | T | 2 | a0001c0001t0002g0037 a0001c0001t0002g0181 |
3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.396-6578C>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47121926 | |||||||
| chr18:47121949 | A | C | 1 | a0001c0001t0001g0208 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.396-6601T>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47121949 | |||||||
| chr18:47122124 | A | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0194 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.396-6776T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47122124 | |||||||
| chr18:47122707 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.396-7359G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47122707 | |||||||
| chr18:47122819 | T | A | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.395+7425A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47122819 | |||||||
| chr18:47122874 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.395+7370C>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47122874 | |||||||
| chr18:47122889 | T | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0153 |
2 | HG01081.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.395+7355A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47122889 | |||||||
| chr18:47122987 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.395+7257G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47122987 | |||||||
| chr18:47123008 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.395+7236T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47123008 | |||||||
| chr18:47123237 | T | A | 1 | a0001c0001t0001g0021 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.395+7007A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47123237 | |||||||
| chr18:47123354 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.395+6890C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47123354 | |||||||
| chr18:47123390 | C | A | 1 | a0001c0001t0002g0037 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.395+6854G>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47123390 | |||||||
| chr18:47123501 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.395+6743G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47123501 | |||||||
| chr18:47123573 | G | A | 2 | a0001c0001t0005g0020 a0001c0001t0005g0054 |
3 | HG01361.hp1 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.395+6671C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47123573 | |||||||
| chr18:47123579 | T | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.395+6665A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47123579 | |||||||
| chr18:47123765 | A | G | 4 | a0001c0001t0003g0230 a0001c0001t0003g0231 a0001c0001t0003g0232 others(1): Show |
4 | HG01884.hp1 HG02257.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.395+6479T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47123765 | |||||||
| chr18:47123855 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.395+6389G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47123855 | |||||||
| chr18:47123908 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
128 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.395+6336T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47123908 | |||||||
| chr18:47124116 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0123 |
2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.395+6128T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47124116 | |||||||
| chr18:47124236 | C | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.395+6008G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47124236 | |||||||
| chr18:47124249 | G | A | 1 | a0002c0002t0001g0030 | 2 | HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.395+5995C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47124249 | |||||||
| chr18:47124301 | C | T | 1 | a0001c0001t0008g0049 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.395+5943G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47124301 | |||||||
| chr18:47124341 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.395+5903C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47124341 | |||||||
| chr18:47124475 | G | A | 1 | a0001c0001t0002g0243 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.395+5769C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47124475 | |||||||
| chr18:47124706 | C | CA | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
120 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.395+5537dupT | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47124706 | |||||||
| chr18:47124706 | C | CAA | 46 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0052 others(43): Show |
68 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.395+5536_395+5537d others(4): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47124706 | |||||||
| chr18:47124706 | C | CAAA | 11 | a0001c0001t0001g0184 a0001c0001t0002g0037 a0001c0001t0002g0066 others(8): Show |
13 | HG00099.hp2 HG01123.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.395+5535_395+5537d others(5): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47124706 | |||||||
| chr18:47124728 | A | AC | 4 | a0001c0001t0001g0021 a0001c0001t0001g0079 a0001c0001t0008g0048 others(1): Show |
5 | HG02922.hp1 HG03139.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.395+5515dupG | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47124728 | |||||||
| chr18:47124753 | A | C | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.395+5491T>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47124753 | |||||||
| chr18:47124858 | T | C | 2 | a0002c0002t0001g0030 a0002c0002t0001g0132 |
3 | HG02717.hp1 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.395+5386A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47124858 | |||||||
| chr18:47125154 | C | G | 4 | a0001c0001t0009g0078 a0001c0001t0009g0082 a0001c0001t0010g0080 others(1): Show |
4 | HG02572.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.395+5090G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47125154 | |||||||
| chr18:47125187 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.395+5057G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47125187 | |||||||
| chr18:47125192 | T | C | 1 | a0001c0001t0010g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.395+5052A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47125192 | |||||||
| chr18:47125233 | T | A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | NA18944.hp2 NA18984.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.395+5011A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47125233 | |||||||
| chr18:47125292 | T | C | 1 | a0001c0001t0002g0247 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.395+4952A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47125292 | |||||||
| chr18:47125309 | T | A | 1 | a0001c0001t0001g0057 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.395+4935A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47125309 | |||||||
| chr18:47125412 | CACATGTC others(15): Show |
C | 5 | a0001c0001t0002g0236 a0001c0001t0002g0237 a0001c0001t0002g0238 others(2): Show |
5 | NA18968.hp2 NA18969.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.395+4810_395+4831d others(24): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47125412 | |||||||
| chr18:47125713 | G | A | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.395+4531C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47125713 | |||||||
| chr18:47125759 | A | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.395+4485T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47125759 | |||||||
| chr18:47125918 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.395+4326C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47125918 | |||||||
| chr18:47125930 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.395+4314T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47125930 | |||||||
| chr18:47126084 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.395+4160T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47126084 | |||||||
| chr18:47126200 | T | C | 4 | a0001c0001t0003g0230 a0001c0001t0003g0231 a0001c0001t0003g0232 others(1): Show |
4 | HG01884.hp1 HG02257.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.395+4044A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47126200 | |||||||
| chr18:47126203 | A | T | 2 | a0001c0001t0009g0078 a0001c0001t0009g0082 |
2 | HG02572.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.395+4041T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47126203 | |||||||
| chr18:47126285 | G | T | 1 | a0001c0001t0001g0146 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.395+3959C>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47126285 | |||||||
| chr18:47126293 | C | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0225 |
2 | HG02602.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.395+3951G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47126293 | |||||||
| chr18:47126527 | A | C | 1 | a0001c0001t0003g0230 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.395+3717T>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47126527 | |||||||
| chr18:47126583 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG00544.hp1 NA18747.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.395+3661T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47126583 | |||||||
| chr18:47126657 | T | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.395+3587A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47126657 | |||||||
| chr18:47126669 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.395+3575G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47126669 | |||||||
| chr18:47126922 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.395+3322A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47126922 | |||||||
| chr18:47127053 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(152): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.395+3191A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47127053 | |||||||
| chr18:47127116 | G | C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0112 |
2 | HG01891.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.395+3128C>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47127116 | |||||||
| chr18:47127239 | T | C | 16 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0032 others(13): Show |
24 | HG00673.hp1 HG01257.hp1 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.395+3005A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47127239 | |||||||
| chr18:47127489 | G | A | 2 | a0001c0001t0002g0037 a0001c0001t0002g0181 |
3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.395+2755C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47127489 | |||||||
| chr18:47127698 | G | A | 4 | a0001c0001t0002g0037 a0001c0001t0002g0181 a0001c0001t0006g0044 others(1): Show |
6 | HG00099.hp2 HG01123.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.395+2546C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47127698 | |||||||
| chr18:47127710 | C | CA | 13 | a0001c0001t0001g0021 a0001c0001t0001g0079 a0001c0001t0001g0121 others(10): Show |
15 | HG02717.hp1 HG02895.hp2 HG02922.hp1 others(12): Show |
intron_variant | MODIFIER | c.395+2533dupT | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47127710 | |||||||
| chr18:47127710 | CA | C | 6 | a0001c0001t0001g0059 a0001c0001t0001g0149 a0001c0001t0001g0160 others(3): Show |
6 | HG01069.hp1 HG01070.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.395+2533delT | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47127710 | |||||||
| chr18:47127961 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG00140.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.395+2283C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47127961 | |||||||
| chr18:47128032 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0114 others(2): Show |
8 | HG00673.hp2 HG01978.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.395+2212G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47128032 | |||||||
| chr18:47128055 | A | AAG | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.395+2188_395+2189i others(4): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47128055 | |||||||
| chr18:47128119 | T | C | 2 | a0001c0001t0002g0037 a0001c0001t0002g0181 |
3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.395+2125A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47128119 | |||||||
| chr18:47128154 | G | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0219 a0001c0001t0001g0220 others(3): Show |
9 | HG01257.hp2 HG01258.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.395+2090C>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47128154 | |||||||
| chr18:47128312 | A | T | 1 | a0002c0002t0001g0132 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.395+1932T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47128312 | |||||||
| chr18:47128475 | T | C | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
53 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.395+1769A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47128475 | |||||||
| chr18:47128495 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.395+1749T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47128495 | |||||||
| chr18:47128710 | T | C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0216 |
4 | HG00280.hp2 HG01099.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.395+1534A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47128710 | |||||||
| chr18:47128870 | T | C | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
53 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.395+1374A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47128870 | |||||||
| chr18:47128950 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.395+1294T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47128950 | |||||||
| chr18:47128995 | G | T | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.395+1249C>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47128995 | |||||||
| chr18:47129012 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.395+1232A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47129012 | |||||||
| chr18:47129216 | A | T | 1 | a0001c0001t0001g0114 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.395+1028T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47129216 | |||||||
| chr18:47129472 | A | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.395+772T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47129472 | |||||||
| chr18:47129567 | C | A | 1 | a0001c0001t0001g0105 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.395+677G>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47129567 | |||||||
| chr18:47129743 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.395+501G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47129743 | |||||||
| chr18:47129748 | T | A | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.395+496A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47129748 | |||||||
| chr18:47129767 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0079 a0001c0001t0008g0048 others(1): Show |
5 | HG02922.hp1 HG03139.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.395+477C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47129767 | |||||||
| chr18:47129824 | G | C | 1 | a0001c0001t0001g0204 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.395+420C>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47129824 | |||||||
| chr18:47129931 | T | C | 2 | a0001c0001t0002g0037 a0001c0001t0002g0181 |
3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.395+313A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47129931 | |||||||
| chr18:47129987 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.395+257C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47129987 | |||||||
| chr18:47130061 | T | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0178 |
2 | HG02630.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.395+183A>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47130061 | |||||||
| chr18:47130104 | G | A | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.395+140C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47130104 | |||||||
| chr18:47130105 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.395+139G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47130105 | |||||||
| chr18:47130163 | T | G | 1 | a0001c0001t0001g0214 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.395+81A>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 4/6 | chr18 | 47130163 | |||||||
| chr18:47130388 | A | T | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
53 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.311-60T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47130388 | |||||||
| chr18:47130402 | A | G | 1 | a0001c0001t0001g0025 | 2 | HG00408.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.311-74T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47130402 | |||||||
| chr18:47130425 | C | A | 4 | a0001c0001t0009g0078 a0001c0001t0009g0082 a0001c0001t0010g0080 others(1): Show |
4 | HG02572.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.311-97G>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47130425 | |||||||
| chr18:47130481 | TAA | T | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
53 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.311-155_311-154del others(2): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47130481 | |||||||
| chr18:47130503 | G | A | 2 | a0001c0001t0005g0020 a0001c0001t0005g0054 |
3 | HG01361.hp1 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.311-175C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47130503 | |||||||
| chr18:47130676 | A | T | 1 | a0001c0001t0003g0230 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.311-348T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47130676 | |||||||
| chr18:47130718 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.311-390G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47130718 | |||||||
| chr18:47130874 | A | T | 2 | a0001c0001t0008g0048 a0001c0001t0008g0049 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.311-546T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47130874 | |||||||
| chr18:47130968 | C | CTTTA | 4 | a0001c0001t0009g0078 a0001c0001t0009g0082 a0001c0001t0010g0080 others(1): Show |
4 | HG02572.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.311-644_311-641dup others(4): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47130968 | |||||||
| chr18:47131139 | G | A | 2 | a0001c0001t0002g0037 a0001c0001t0002g0181 |
3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.311-811C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47131139 | |||||||
| chr18:47131462 | T | C | 1 | a0001c0001t0010g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.311-1134A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47131462 | |||||||
| chr18:47131465 | C | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG00544.hp1 NA18747.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.311-1137G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47131465 | |||||||
| chr18:47131490 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.311-1162G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47131490 | |||||||
| chr18:47131497 | C | G | 4 | a0001c0001t0002g0037 a0001c0001t0002g0181 a0001c0001t0006g0044 others(1): Show |
6 | HG00099.hp2 HG01123.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.311-1169G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47131497 | |||||||
| chr18:47131556 | G | A | 1 | a0001c0001t0005g0054 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.311-1228C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47131556 | |||||||
| chr18:47131663 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0086 a0001c0001t0001g0113 others(2): Show |
6 | HG02056.hp1 HG02129.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.311-1335G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47131663 | |||||||
| chr18:47131677 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.311-1349A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47131677 | |||||||
| chr18:47131731 | T | C | 31 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0031 others(28): Show |
41 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.311-1403A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47131731 | |||||||
| chr18:47131775 | A | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(60): Show |
103 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.311-1447T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47131775 | |||||||
| chr18:47131839 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.311-1511G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47131839 | |||||||
| chr18:47132075 | C | G | 1 | a0001c0001t0001g0197 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.311-1747G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47132075 | |||||||
| chr18:47132250 | T | C | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
53 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.311-1922A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47132250 | |||||||
| chr18:47132315 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.311-1987T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47132315 | |||||||
| chr18:47132370 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0172 |
2 | NA18954.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.311-2042T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47132370 | |||||||
| chr18:47132420 | T | C | 2 | a0001c0001t0002g0047 a0001c0001t0011g0050 |
3 | HG00140.hp2 HG01993.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.310+2076A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47132420 | |||||||
| chr18:47132630 | T | C | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
53 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.310+1866A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47132630 | |||||||
| chr18:47132678 | A | C | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0002c0003t0001g0159 |
3 | HG01123.hp1 HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.310+1818T>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47132678 | |||||||
| chr18:47132778 | C | G | 35 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(32): Show |
56 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.310+1718G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47132778 | |||||||
| chr18:47132795 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
118 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.310+1701C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47132795 | |||||||
| chr18:47132911 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0172 |
2 | NA18954.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.310+1585T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47132911 | |||||||
| chr18:47132973 | G | C | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.310+1523C>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47132973 | |||||||
| chr18:47133053 | T | G | 1 | a0001c0001t0001g0086 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.310+1443A>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47133053 | |||||||
| chr18:47133107 | T | C | 1 | a0001c0001t0001g0042 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.310+1389A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47133107 | |||||||
| chr18:47133130 | C | T | 1 | a0001c0001t0001g0042 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.310+1366G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47133130 | |||||||
| chr18:47133137 | C | A | 1 | a0001c0001t0001g0042 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.310+1359G>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47133137 | |||||||
| chr18:47133152 | C | T | 1 | a0001c0001t0001g0042 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.310+1344G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47133152 | |||||||
| chr18:47133165 | G | T | 1 | a0001c0001t0001g0042 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.310+1331C>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47133165 | |||||||
| chr18:47133169 | C | T | 1 | a0001c0001t0001g0042 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.310+1327G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47133169 | |||||||
| chr18:47133170 | A | G | 1 | a0001c0001t0001g0042 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.310+1326T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47133170 | |||||||
| chr18:47133172 | T | A | 1 | a0001c0001t0001g0042 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.310+1324A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47133172 | |||||||
| chr18:47133191 | T | C | 1 | a0001c0001t0001g0042 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.310+1305A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47133191 | |||||||
| chr18:47133199 | T | C | 2 | a0001c0001t0009g0078 a0001c0001t0009g0082 |
2 | HG02572.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.310+1297A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47133199 | |||||||
| chr18:47133286 | G | C | 1 | a0001c0001t0001g0205 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.310+1210C>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47133286 | |||||||
| chr18:47133395 | T | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | NA18944.hp2 NA18984.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.310+1101A>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47133395 | |||||||
| chr18:47133478 | C | G | 2 | a0001c0001t0008g0048 a0001c0001t0008g0049 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.310+1018G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47133478 | |||||||
| chr18:47133497 | T | TTGGGTAT others(8): Show |
117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.310+998_310+999ins others(15): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47133497 | |||||||
| chr18:47133842 | ATTTG | A | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
53 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.310+650_310+653del others(4): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47133842 | |||||||
| chr18:47133874 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.310+622A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47133874 | |||||||
| chr18:47133897 | T | C | 2 | a0001c0001t0008g0048 a0001c0001t0008g0049 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.310+599A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47133897 | |||||||
| chr18:47133939 | T | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0228 |
2 | NA18987.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.310+557A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47133939 | |||||||
| chr18:47134080 | G | C | 1 | a0001c0001t0001g0130 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.310+416C>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47134080 | |||||||
| chr18:47134147 | A | G | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.310+349T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 3/6 | chr18 | 47134147 | |||||||
| chr18:47134785 | G | C | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.102-81C>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 2/6 | chr18 | 47134785 | |||||||
| chr18:47134923 | A | G | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.102-219T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 2/6 | chr18 | 47134923 | |||||||
| chr18:47135258 | CT | C | 14 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(11): Show |
15 | HG00544.hp1 HG01070.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.102-555delA | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 2/6 | chr18 | 47135258 | |||||||
| chr18:47135258 | CTTT | C | 31 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(28): Show |
51 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.102-557_102-555del others(3): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 2/6 | chr18 | 47135258 | |||||||
| chr18:47135258 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0235 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.102-564_102-555del others(10): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 2/6 | chr18 | 47135258 | |||||||
| chr18:47135262 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.102-558A>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 2/6 | chr18 | 47135262 | |||||||
| chr18:47135264 | T | C | 2 | a0001c0001t0005g0020 a0001c0001t0005g0054 |
3 | HG01361.hp1 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.102-560A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 2/6 | chr18 | 47135264 | |||||||
| chr18:47135481 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.102-777C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 2/6 | chr18 | 47135481 | |||||||
| chr18:47135488 | C | T | 1 | a0001c0001t0009g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.102-784G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 2/6 | chr18 | 47135488 | |||||||
| chr18:47135562 | A | G | 2 | a0001c0001t0007g0038 a0001c0001t0007g0185 |
3 | HG01243.hp2 HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.101+777T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 2/6 | chr18 | 47135562 | |||||||
| chr18:47135589 | C | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG03098.hp2 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.101+750G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 2/6 | chr18 | 47135589 | |||||||
| chr18:47135611 | T | C | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.101+728A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 2/6 | chr18 | 47135611 | |||||||
| chr18:47135648 | T | C | 1 | a0001c0001t0002g0071 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.101+691A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 2/6 | chr18 | 47135648 | |||||||
| chr18:47135939 | G | A | 35 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(32): Show |
56 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.101+400C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 2/6 | chr18 | 47135939 | |||||||
| chr18:47136038 | A | G | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
53 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.101+301T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 2/6 | chr18 | 47136038 | |||||||
| chr18:47136597 | A | C | 1 | a0001c0001t0001g0024 | 2 | HG00609.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-10-148T>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47136597 | |||||||
| chr18:47136650 | T | A | 3 | a0001c0001t0001g0195 a0001c0001t0001g0207 a0001c0001t0002g0245 |
3 | HG00735.hp1 HG02165.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.-10-201A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47136650 | |||||||
| chr18:47136650 | T | TA | 6 | a0001c0001t0001g0021 a0001c0001t0001g0055 a0001c0001t0001g0056 others(3): Show |
8 | HG02040.hp2 HG02258.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10-202_-10-201ins others(1): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47136650 | |||||||
| chr18:47136650 | T | TAA | 30 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(27): Show |
49 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.-10-202_-10-201ins others(2): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47136650 | |||||||
| chr18:47136651 | T | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.-10-202A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47136651 | |||||||
| chr18:47136651 | T | TA | 7 | a0001c0001t0001g0057 a0001c0001t0001g0129 a0001c0001t0001g0130 others(4): Show |
8 | HG00099.hp2 HG01123.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-203dupT | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47136651 | |||||||
| chr18:47136652 | A | T | 5 | a0001c0001t0001g0148 a0001c0001t0001g0163 a0001c0001t0009g0078 others(2): Show |
5 | HG02572.hp2 HG02922.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-203T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47136652 | |||||||
| chr18:47136836 | T | G | 1 | a0001c0001t0006g0234 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-10-387A>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47136836 | |||||||
| chr18:47136886 | G | A | 1 | a0001c0001t0010g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-10-437C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47136886 | |||||||
| chr18:47136924 | G | A | 4 | a0001c0001t0009g0078 a0001c0001t0009g0082 a0001c0001t0010g0080 others(1): Show |
4 | HG02572.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-475C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47136924 | |||||||
| chr18:47136970 | T | C | 2 | a0001c0001t0005g0020 a0001c0001t0005g0054 |
3 | HG01361.hp1 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-10-521A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47136970 | |||||||
| chr18:47137207 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-10-758C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47137207 | |||||||
| chr18:47137221 | T | C | 1 | a0001c0001t0008g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-10-772A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47137221 | |||||||
| chr18:47137316 | C | T | 31 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(28): Show |
49 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-10-867G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47137316 | |||||||
| chr18:47137437 | C | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG03098.hp2 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-10-988G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47137437 | |||||||
| chr18:47137630 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-10-1181A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47137630 | |||||||
| chr18:47137644 | A | T | 31 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(28): Show |
49 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-10-1195T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47137644 | |||||||
| chr18:47137724 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-10-1275T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47137724 | |||||||
| chr18:47137760 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(62): Show |
107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-10-1311C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47137760 | |||||||
| chr18:47137876 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-10-1427T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47137876 | |||||||
| chr18:47137907 | A | C | 1 | a0001c0001t0001g0147 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-10-1458T>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47137907 | |||||||
| chr18:47137933 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(61): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-10-1484C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47137933 | |||||||
| chr18:47137974 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-10-1525C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47137974 | |||||||
| chr18:47137987 | G | A | 2 | a0001c0001t0005g0020 a0001c0001t0005g0054 |
3 | HG01361.hp1 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-10-1538C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47137987 | |||||||
| chr18:47138025 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-10-1576C>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47138025 | |||||||
| chr18:47138048 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0170 others(1): Show |
7 | HG02451.hp2 HG02886.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-1599G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47138048 | |||||||
| chr18:47138171 | C | CA | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(22): Show |
30 | HG00621.hp1 HG01928.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.-10-1723dupT | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47138171 | |||||||
| chr18:47138171 | CA | C | 51 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(48): Show |
66 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.-10-1723delT | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47138171 | |||||||
| chr18:47138171 | CAA | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(20): Show |
31 | HG00408.hp1 HG00438.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.-10-1724_-10-1723d others(4): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47138171 | |||||||
| chr18:47138171 | CAAA | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-10-1725_-10-1723d others(5): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47138171 | |||||||
| chr18:47138171 | CAAAAAAA others(2): Show |
C | 26 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(23): Show |
43 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.-10-1731_-10-1723d others(11): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47138171 | |||||||
| chr18:47138171 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0002g0009 a0001c0001t0002g0242 |
2 | NA19012.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-10-1732_-10-1723d others(12): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47138171 | |||||||
| chr18:47138171 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0042 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-10-1736_-10-1723d others(16): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47138171 | |||||||
| chr18:47138587 | ATAAGT | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0161 a0001c0001t0001g0184 others(1): Show |
5 | HG02132.hp1 HG02135.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-2143_-10-2139d others(7): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47138587 | |||||||
| chr18:47138681 | T | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.-10-2232A>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47138681 | |||||||
| chr18:47138710 | A | T | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-10-2261T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47138710 | |||||||
| chr18:47138712 | C | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(62): Show |
107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-10-2263G>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47138712 | |||||||
| chr18:47138716 | T | C | 31 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(28): Show |
49 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-10-2267A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47138716 | |||||||
| chr18:47138887 | C | G | 1 | a0001c0001t0001g0021 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-10-2438G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47138887 | |||||||
| chr18:47138998 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-10-2549C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47138998 | |||||||
| chr18:47139110 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-10-2661G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47139110 | |||||||
| chr18:47139247 | A | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(72): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.-10-2798T>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47139247 | |||||||
| chr18:47139247 | A | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0197 a0001c0001t0001g0198 |
4 | HG01070.hp2 HG01517.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-2798T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47139247 | |||||||
| chr18:47139286 | A | G | 31 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(28): Show |
49 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-10-2837T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47139286 | |||||||
| chr18:47139303 | C | CA | 34 | a0001c0001t0001g0162 a0001c0001t0001g0178 a0001c0001t0002g0003 others(31): Show |
52 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.-10-2855dupT | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47139303 | |||||||
| chr18:47139303 | CA | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-10-2855delT | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47139303 | |||||||
| chr18:47139464 | C | CA | 28 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0022 others(25): Show |
41 | HG00099.hp2 HG00423.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.-10-3016dupT | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47139464 | |||||||
| chr18:47139464 | C | CAA | 6 | a0001c0001t0001g0121 a0001c0001t0001g0145 a0001c0001t0001g0171 others(3): Show |
7 | HG01891.hp2 HG02056.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-3017_-10-3016d others(4): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47139464 | |||||||
| chr18:47139464 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0013g0240 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-10-3028_-10-3016d others(15): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47139464 | |||||||
| chr18:47139464 | CA | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(69): Show |
111 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.-10-3016delT | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47139464 | |||||||
| chr18:47139464 | CAA | C | 38 | a0001c0001t0001g0007 a0001c0001t0001g0042 a0001c0001t0001g0051 others(35): Show |
59 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.-10-3017_-10-3016d others(4): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47139464 | |||||||
| chr18:47139464 | CAAA | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0079 a0001c0001t0001g0191 others(3): Show |
7 | HG01884.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-3018_-10-3016d others(5): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47139464 | |||||||
| chr18:47139592 | T | C | 2 | a0001c0001t0005g0020 a0001c0001t0005g0054 |
3 | HG01361.hp1 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-10-3143A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47139592 | |||||||
| chr18:47139641 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-10-3192A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47139641 | |||||||
| chr18:47139643 | G | T | 1 | a0001c0001t0001g0077 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-10-3194C>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47139643 | |||||||
| chr18:47139758 | G | A | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-10-3309C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47139758 | |||||||
| chr18:47139806 | T | G | 4 | a0001c0001t0009g0078 a0001c0001t0009g0082 a0001c0001t0010g0080 others(1): Show |
4 | HG02572.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-3357A>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47139806 | |||||||
| chr18:47139870 | C | G | 1 | a0001c0001t0001g0042 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-10-3421G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47139870 | |||||||
| chr18:47139950 | A | T | 2 | a0001c0001t0002g0037 a0001c0001t0002g0181 |
3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-10-3501T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47139950 | |||||||
| chr18:47139954 | A | C | 1 | a0001c0001t0001g0219 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-10-3505T>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47139954 | |||||||
| chr18:47140026 | A | G | 3 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG03098.hp2 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-10-3577T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47140026 | |||||||
| chr18:47140044 | T | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(59): Show |
103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-10-3595A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47140044 | |||||||
| chr18:47140145 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-10-3696C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47140145 | |||||||
| chr18:47140254 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-10-3805A>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47140254 | |||||||
| chr18:47140315 | C | T | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG00544.hp1 HG03098.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-3866G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47140315 | |||||||
| chr18:47140462 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0106 a0001c0001t0001g0107 |
4 | HG01358.hp1 HG01928.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-4013C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47140462 | |||||||
| chr18:47140527 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0079 |
3 | HG02922.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-10-4078G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47140527 | |||||||
| chr18:47140553 | C | G | 31 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(28): Show |
49 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-10-4104G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47140553 | |||||||
| chr18:47140762 | C | T | 1 | a0001c0001t0012g0190 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-10-4313G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47140762 | |||||||
| chr18:47140842 | G | GA | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.-10-4394dupT | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47140842 | |||||||
| chr18:47141091 | A | G | 31 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(28): Show |
49 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-10-4642T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47141091 | |||||||
| chr18:47141174 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-10-4725G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47141174 | |||||||
| chr18:47141221 | C | T | 2 | a0001c0001t0008g0048 a0001c0001t0008g0049 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-10-4772G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47141221 | |||||||
| chr18:47141457 | C | T | 2 | a0001c0001t0002g0045 a0001c0001t0002g0046 |
4 | HG02040.hp2 NA18982.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-5008G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47141457 | |||||||
| chr18:47141500 | C | G | 3 | a0001c0001t0001g0088 a0001c0001t0001g0115 a0001c0001t0001g0174 |
3 | HG00642.hp1 HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.-10-5051G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47141500 | |||||||
| chr18:47141500 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(153): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.-10-5051G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47141500 | |||||||
| chr18:47141581 | T | C | 2 | a0001c0001t0002g0037 a0001c0001t0002g0181 |
3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-10-5132A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47141581 | |||||||
| chr18:47141656 | GC | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(72): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.-10-5208delG | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47141656 | |||||||
| chr18:47142046 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-10-5597A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47142046 | |||||||
| chr18:47142138 | T | C | 1 | a0001c0001t0001g0217 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-10-5689A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47142138 | |||||||
| chr18:47142278 | T | TA | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(80): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.-10-5830dupT | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47142278 | |||||||
| chr18:47142278 | T | TAA | 36 | a0001c0001t0001g0093 a0001c0001t0002g0003 a0001c0001t0002g0009 others(33): Show |
56 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.-10-5831_-10-5830d others(4): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47142278 | |||||||
| chr18:47142293 | T | G | 1 | a0001c0001t0001g0042 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-10-5844A>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47142293 | |||||||
| chr18:47142342 | C | T | 4 | a0001c0001t0009g0078 a0001c0001t0009g0082 a0001c0001t0010g0080 others(1): Show |
4 | HG02572.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-5893G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47142342 | |||||||
| chr18:47142419 | G | A | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-10-5970C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47142419 | |||||||
| chr18:47142457 | C | A | 1 | a0001c0001t0001g0218 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-10-6008G>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47142457 | |||||||
| chr18:47142457 | C | G | 5 | a0001c0001t0002g0236 a0001c0001t0002g0237 a0001c0001t0002g0238 others(2): Show |
5 | NA18968.hp2 NA18969.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-6008G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47142457 | |||||||
| chr18:47142557 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-10-6108G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47142557 | |||||||
| chr18:47142625 | G | A | 2 | a0001c0001t0005g0020 a0001c0001t0005g0054 |
3 | HG01361.hp1 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-10-6176C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47142625 | |||||||
| chr18:47142748 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0112 |
2 | HG01891.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-10-6299G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47142748 | |||||||
| chr18:47142757 | C | G | 2 | a0001c0001t0005g0020 a0001c0001t0005g0054 |
3 | HG01361.hp1 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-10-6308G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47142757 | |||||||
| chr18:47142762 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-10-6313G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47142762 | |||||||
| chr18:47142786 | A | T | 31 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(28): Show |
49 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-10-6337T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47142786 | |||||||
| chr18:47142802 | A | G | 20 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0022 others(17): Show |
27 | HG00544.hp2 HG00558.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.-10-6353T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47142802 | |||||||
| chr18:47142929 | C | A | 1 | a0001c0001t0001g0168 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-10-6480G>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47142929 | |||||||
| chr18:47142968 | C | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG00544.hp1 NA18747.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.-10-6519G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47142968 | |||||||
| chr18:47143128 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.-10-6679G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47143128 | |||||||
| chr18:47143140 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-10-6691C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47143140 | |||||||
| chr18:47143258 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-10-6809G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47143258 | |||||||
| chr18:47143282 | A | G | 31 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(28): Show |
49 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-10-6833T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47143282 | |||||||
| chr18:47143345 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-10-6896T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47143345 | |||||||
| chr18:47143481 | C | T | 31 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(28): Show |
49 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-11+6897G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47143481 | |||||||
| chr18:47143504 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0170 others(1): Show |
7 | HG02451.hp2 HG02886.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+6874C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47143504 | |||||||
| chr18:47143892 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(72): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.-11+6486C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47143892 | |||||||
| chr18:47143937 | T | C | 2 | a0001c0001t0005g0020 a0001c0001t0005g0054 |
3 | HG01361.hp1 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-11+6441A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47143937 | |||||||
| chr18:47144047 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0112 |
2 | HG01891.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-11+6331G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47144047 | |||||||
| chr18:47144052 | T | C | 2 | a0001c0001t0002g0037 a0001c0001t0002g0181 |
3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-11+6326A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47144052 | |||||||
| chr18:47144059 | T | A | 3 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | HG02083.hp2 NA18966.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-11+6319A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47144059 | |||||||
| chr18:47144099 | G | A | 6 | a0001c0001t0001g0014 a0001c0001t0001g0219 a0001c0001t0001g0220 others(3): Show |
9 | HG01257.hp2 HG01258.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+6279C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47144099 | |||||||
| chr18:47144103 | G | A | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-11+6275C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47144103 | |||||||
| chr18:47144458 | G | C | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-11+5920C>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47144458 | |||||||
| chr18:47144617 | C | A | 1 | a0001c0001t0001g0077 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-11+5761G>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47144617 | |||||||
| chr18:47144618 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-11+5760T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47144618 | |||||||
| chr18:47144732 | C | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-11+5646G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47144732 | |||||||
| chr18:47144756 | C | T | 32 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(29): Show |
40 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.-11+5622G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47144756 | |||||||
| chr18:47144799 | C | CA | 11 | a0001c0001t0001g0036 a0001c0001t0001g0085 a0001c0001t0001g0091 others(8): Show |
12 | HG00741.hp2 HG01256.hp1 HG03492.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+5578dupT | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47144799 | |||||||
| chr18:47144799 | C | CAA | 29 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(26): Show |
47 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-11+5577_-11+5578d others(4): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47144799 | |||||||
| chr18:47144799 | CA | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0079 a0001c0001t0001g0092 others(3): Show |
7 | HG01256.hp2 HG02922.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+5578delT | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47144799 | |||||||
| chr18:47144833 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-11+5545C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47144833 | |||||||
| chr18:47145016 | C | G | 1 | a0001c0001t0001g0023 | 2 | NA18969.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-11+5362G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47145016 | |||||||
| chr18:47145304 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-11+5074G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47145304 | |||||||
| chr18:47145349 | T | C | 2 | a0001c0001t0005g0020 a0001c0001t0005g0054 |
3 | HG01361.hp1 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-11+5029A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47145349 | |||||||
| chr18:47145463 | G | A | 31 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(28): Show |
49 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-11+4915C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47145463 | |||||||
| chr18:47145532 | T | A | 1 | a0001c0001t0001g0021 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-11+4846A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47145532 | |||||||
| chr18:47145687 | C | T | 31 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(28): Show |
49 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-11+4691G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47145687 | |||||||
| chr18:47145928 | G | T | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
52 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.-11+4450C>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47145928 | |||||||
| chr18:47145955 | G | A | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-11+4423C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47145955 | |||||||
| chr18:47146034 | C | A | 30 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(27): Show |
48 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-11+4344G>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47146034 | |||||||
| chr18:47146058 | C | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0092 |
3 | HG01256.hp2 HG01258.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.-11+4320G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47146058 | |||||||
| chr18:47146208 | C | T | 2 | a0001c0001t0002g0037 a0001c0001t0002g0181 |
3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-11+4170G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47146208 | |||||||
| chr18:47146217 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-11+4161T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47146217 | |||||||
| chr18:47146229 | C | CA | 44 | a0001c0001t0001g0043 a0001c0001t0001g0059 a0001c0001t0001g0060 others(41): Show |
66 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11+4148dupT | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47146229 | |||||||
| chr18:47146229 | CA | C | 10 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(7): Show |
10 | HG00408.hp1 HG01168.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11+4148delT | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47146229 | |||||||
| chr18:47146292 | T | C | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-11+4086A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47146292 | |||||||
| chr18:47146550 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-11+3828T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47146550 | |||||||
| chr18:47146582 | G | A | 1 | a0001c0001t0009g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-11+3796C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47146582 | |||||||
| chr18:47146628 | T | G | 2 | a0001c0001t0005g0020 a0001c0001t0005g0054 |
3 | HG01361.hp1 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-11+3750A>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47146628 | |||||||
| chr18:47146678 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.-11+3700G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47146678 | |||||||
| chr18:47146843 | G | A | 2 | a0001c0001t0007g0038 a0001c0001t0007g0185 |
3 | HG01243.hp2 HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-11+3535C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47146843 | |||||||
| chr18:47146896 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-11+3482G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47146896 | |||||||
| chr18:47146897 | G | A | 33 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(30): Show |
52 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.-11+3481C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47146897 | |||||||
| chr18:47146898 | C | T | 4 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
4 | HG03098.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+3480G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47146898 | |||||||
| chr18:47146946 | A | C | 9 | a0001c0001t0002g0010 a0001c0001t0002g0064 a0001c0001t0002g0065 others(6): Show |
12 | HG02040.hp1 HG02056.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+3432T>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47146946 | |||||||
| chr18:47146969 | T | C | 31 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(28): Show |
49 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-11+3409A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47146969 | |||||||
| chr18:47147096 | A | G | 1 | a0001c0001t0009g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-11+3282T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47147096 | |||||||
| chr18:47147372 | G | A | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-11+3006C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47147372 | |||||||
| chr18:47147458 | T | C | 2 | a0001c0001t0007g0038 a0001c0001t0007g0185 |
3 | HG01243.hp2 HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-11+2920A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47147458 | |||||||
| chr18:47147524 | T | A | 1 | a0001c0001t0001g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-11+2854A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47147524 | |||||||
| chr18:47147585 | T | A | 2 | a0001c0001t0008g0048 a0001c0001t0008g0049 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-11+2793A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47147585 | |||||||
| chr18:47147598 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-11+2780C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47147598 | |||||||
| chr18:47147723 | C | T | 30 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(27): Show |
48 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-11+2655G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47147723 | |||||||
| chr18:47147796 | T | C | 31 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(28): Show |
49 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-11+2582A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47147796 | |||||||
| chr18:47147986 | CTTTCTTT others(5): Show |
C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG00140.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-11+2380_-11+2391d others(14): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47147986 | |||||||
| chr18:47147990 | C | CT | 75 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(72): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-11+2387dupA | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47147990 | |||||||
| chr18:47147990 | C | CTT | 10 | a0001c0001t0001g0077 a0001c0001t0001g0182 a0001c0001t0001g0183 others(7): Show |
11 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11+2386_-11+2387d others(4): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47147990 | |||||||
| chr18:47147990 | C | CTTT | 28 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(25): Show |
46 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-11+2385_-11+2387d others(5): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47147990 | |||||||
| chr18:47148092 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-11+2286C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47148092 | |||||||
| chr18:47148146 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-11+2232T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47148146 | |||||||
| chr18:47148216 | G | A | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-11+2162C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47148216 | |||||||
| chr18:47148231 | T | A | 1 | a0001c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-11+2147A>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47148231 | |||||||
| chr18:47148365 | A | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-11+2013T>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47148365 | |||||||
| chr18:47148381 | T | C | 2 | a0001c0001t0002g0037 a0001c0001t0002g0181 |
3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-11+1997A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47148381 | |||||||
| chr18:47148443 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG00280.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-11+1935G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47148443 | |||||||
| chr18:47148577 | G | C | 2 | a0001c0001t0005g0020 a0001c0001t0005g0054 |
3 | HG01361.hp1 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-11+1801C>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47148577 | |||||||
| chr18:47148867 | G | A | 1 | a0001c0001t0002g0250 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-11+1511C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47148867 | |||||||
| chr18:47149091 | G | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(65): Show |
110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-11+1287C>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47149091 | |||||||
| chr18:47149108 | G | A | 1 | a0001c0001t0002g0251 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-11+1270C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47149108 | |||||||
| chr18:47149309 | T | C | 4 | a0001c0001t0003g0230 a0001c0001t0003g0231 a0001c0001t0003g0232 others(1): Show |
4 | HG01884.hp1 HG02257.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+1069A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47149309 | |||||||
| chr18:47149375 | T | C | 2 | a0001c0001t0006g0044 a0001c0001t0006g0234 |
3 | HG00099.hp2 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-11+1003A>G | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47149375 | |||||||
| chr18:47149450 | C | T | 31 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(28): Show |
49 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-11+928G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47149450 | |||||||
| chr18:47149578 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-11+800C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47149578 | |||||||
| chr18:47149640 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-11+738G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47149640 | |||||||
| chr18:47149650 | C | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | NA18944.hp2 NA18984.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+728G>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47149650 | |||||||
| chr18:47149766 | G | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG03098.hp2 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-11+612C>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47149766 | |||||||
| chr18:47150018 | C | T | 2 | a0001c0001t0005g0020 a0001c0001t0005g0054 |
3 | HG01361.hp1 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-11+360G>A | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47150018 | |||||||
| chr18:47150135 | T | TCCGCC | 22 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0045 others(19): Show |
37 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-11+238_-11+242dup others(5): Show |
HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47150135 | |||||||
| chr18:47150268 | G | A | 22 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0045 others(19): Show |
37 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-11+110C>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47150268 | |||||||
| chr18:47150356 | C | A | 22 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0045 others(19): Show |
37 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-11+22G>T | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47150356 | |||||||
| chr18:47150363 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG00544.hp1 NA18747.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.-11+15T>C | HDHD2 | ENSG00000167220.12 | transcript | ENST00000300605.11 | protein_coding | 1/6 | chr18 | 47150363 |