Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8520 |
| ensemblid | ENSG00000128708.13 |
| hgncid | 4821 |
| symbol | HAT1 |
| name | histone acetyltransferase 1 |
| refseq_nuc | NM_003642.4 |
| refseq_prot | NP_003633.2 |
| ensembl_nuc | ENST00000264108.5 |
| ensembl_prot | ENSP00000264108.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 171922461 |
| end | 171983686 |
| strand | + |
| ver | v1.2 |
| region | chr2:171922461-171983686 |
| region5000 | chr2:171917461-171988686 |
| regionname0 | HAT1_chr2_171922461_171983686 |
| regionname5000 | HAT1_chr2_171917461_171988686 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 419 | 317 | 68 | 58 | 140 | 8 | 42 | 110 | HAT1_chr2_171917461_171988686 | HAT1 | MAGFG others(414): Show |
chr2 | 171917461 | 171988686 |
| a0002 | 1/0 | 419 | 9 | 8 | 0 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | MAGFG others(414): Show |
chr2 | 171917461 | 171988686 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1257 | 317 | 68 | 58 | 140 | 8 | 42 | HAT1_chr2_171917461_171988686 | HAT1 | ATGGC others(1252): Show |
chr2 | 171917461 | 171988686 | ||
| a0002c0002 | 1/0 | 1257 | 9 | 8 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | ATGGC others(1252): Show |
chr2 | 171917461 | 171988686 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1634 | 317 | 68 | 58 | 140 | 8 | 42 | HAT1_chr2_171917461_171988686 | HAT1 | GATTC others(1629): Show |
chr2 | 171917461 | 171988686 |
| a0002c0002t0001 | 1/0 | 1634 | 9 | 8 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | GATTC others(1629): Show |
chr2 | 171917461 | 171988686 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0241 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0002c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0002c0002t0001g0246 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0002c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0002c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0002c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0002c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0002c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| a0002c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | GBR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | GBR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0288 | EUR | GBR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | FIN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0300 | EUR | FIN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | IBS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | IBS | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CDX | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0245 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0257 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | ESN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0255 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ESN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0258 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0247 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | BEB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | BEB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | STU | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | STU | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | STU | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | STU | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | STU | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | YRI | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0248 | AFR | YRI | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | YRI | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | YRI | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | LWK | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | LWK | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | YRI | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | YRI | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0256 | AFR | ASW | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0249 | AFR | ASW | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | GIH | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | GIH | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | MSL | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | USA | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | USA | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | USA | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | USA | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | LWK | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | LWK | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0241 | REF | REF | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0246 | REF | REF | HAT1_chr2_171917461_171988686 | HAT1 | chr2 | 171917461 | 171988686 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:171976274 | T | C | 1 | a0001 | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
missense_variant | MODERATE | c.941T>C | p.Val314Ala | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/11 | 981/1634 | 941/1260 | 314/419 | chr2 | 171976274 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:171922612 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0261 a0001c0001t0001g0262 others(63): Show |
67 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.7+105C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171922612 | |||||||
| chr2:171922681 | C | T | 3 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 |
3 | HG02040.hp2 NA19080.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.7+174C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171922681 | |||||||
| chr2:171923159 | G | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0261 a0001c0001t0001g0262 others(52): Show |
56 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.7+652G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171923159 | |||||||
| chr2:171923182 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.7+675A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171923182 | |||||||
| chr2:171923187 | G | A | 6 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(3): Show |
6 | HG02572.hp2 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.7+680G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171923187 | |||||||
| chr2:171923367 | C | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(67): Show |
70 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.7+860C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171923367 | |||||||
| chr2:171923576 | T | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0070 others(65): Show |
69 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.7+1069T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171923576 | |||||||
| chr2:171923622 | T | C | 73 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(70): Show |
73 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.7+1115T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171923622 | |||||||
| chr2:171923880 | T | G | 1 | a0001c0001t0001g0074 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.7+1373T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171923880 | |||||||
| chr2:171924048 | G | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
5 | NA18946.hp1 NA18986.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-1489G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171924048 | |||||||
| chr2:171924210 | A | AT | 9 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0146 others(6): Show |
9 | HG01123.hp2 HG01167.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.8-1313dupT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 171924210 | ||||||
| chr2:171924235 | T | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(2): Show |
5 | HG00099.hp2 HG00738.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-1302T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171924235 | |||||||
| chr2:171924239 | G | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.8-1298G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171924239 | |||||||
| chr2:171924350 | C | G | 1 | a0001c0001t0001g0322 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.8-1187C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171924350 | |||||||
| chr2:171924362 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.8-1175A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171924362 | |||||||
| chr2:171924944 | C | G | 1 | a0001c0001t0001g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.8-593C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171924944 | |||||||
| chr2:171924970 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.8-567C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171924970 | |||||||
| chr2:171924992 | C | A | 4 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(1): Show |
4 | HG01175.hp2 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-545C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171924992 | |||||||
| chr2:171925069 | CT | C | 265 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(262): Show |
265 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.8-447delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 171925069 | ||||||
| chr2:171925069 | CTT | C | 13 | a0001c0001t0001g0007 a0001c0001t0001g0069 a0001c0001t0001g0079 others(10): Show |
13 | HG00099.hp2 HG01256.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.8-448_8-447delTT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 171925069 | ||||||
| chr2:171925180 | C | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0070 others(63): Show |
67 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.8-357C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171925180 | |||||||
| chr2:171925233 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.8-304C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171925233 | |||||||
| chr2:171925291 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0143 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.8-246C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171925291 | |||||||
| chr2:171925360 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.8-177G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 1/10 | chr2 | 171925360 | |||||||
| chr2:171925971 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.112+330G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171925971 | |||||||
| chr2:171926008 | G | A | 1 | a0002c0002t0001g0255 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.112+367G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171926008 | |||||||
| chr2:171926120 | T | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0070 others(65): Show |
69 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.112+479T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171926120 | |||||||
| chr2:171926688 | C | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
4 | HG01109.hp2 HG01168.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+1047C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171926688 | |||||||
| chr2:171926726 | T | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.112+1085T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171926726 | |||||||
| chr2:171926838 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.112+1197A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171926838 | |||||||
| chr2:171927131 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.112+1490C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171927131 | |||||||
| chr2:171927132 | G | A | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG02647.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.112+1491G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171927132 | |||||||
| chr2:171927242 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.112+1601T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171927242 | |||||||
| chr2:171927340 | T | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0261 others(61): Show |
65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.112+1699T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171927340 | |||||||
| chr2:171927424 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0070 others(63): Show |
67 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.112+1783G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171927424 | |||||||
| chr2:171927794 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.112+2153T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171927794 | |||||||
| chr2:171927950 | G | T | 1 | a0001c0001t0001g0243 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.112+2309G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171927950 | |||||||
| chr2:171928034 | C | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.112+2393C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171928034 | |||||||
| chr2:171928066 | T | C | 1 | a0001c0001t0001g0012 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.112+2425T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171928066 | |||||||
| chr2:171928182 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.112+2541G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171928182 | |||||||
| chr2:171928495 | T | A | 77 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(74): Show |
77 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.112+2854T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171928495 | |||||||
| chr2:171928497 | C | T | 77 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(74): Show |
77 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.112+2856C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171928497 | |||||||
| chr2:171928653 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
100 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.112+3012C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171928653 | |||||||
| chr2:171928697 | G | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.112+3056G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171928697 | |||||||
| chr2:171929078 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.112+3437A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171929078 | |||||||
| chr2:171929080 | A | T | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG01070.hp1 HG01071.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.112+3439A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171929080 | |||||||
| chr2:171929204 | T | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0070 others(65): Show |
69 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.112+3563T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171929204 | |||||||
| chr2:171929466 | T | C | 69 | a0001c0001t0001g0067 a0001c0001t0001g0147 a0001c0001t0001g0148 others(66): Show |
69 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.112+3825T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171929466 | |||||||
| chr2:171929555 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.112+3914A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171929555 | |||||||
| chr2:171930033 | T | G | 1 | a0001c0001t0001g0269 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.112+4392T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171930033 | |||||||
| chr2:171930051 | A | T | 1 | a0001c0001t0001g0006 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.112+4410A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171930051 | |||||||
| chr2:171930185 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.112+4544G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171930185 | |||||||
| chr2:171930399 | G | T | 73 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(70): Show |
73 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.112+4758G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171930399 | |||||||
| chr2:171930641 | G | T | 1 | a0001c0001t0001g0311 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.112+5000G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171930641 | |||||||
| chr2:171930835 | G | C | 1 | a0001c0001t0001g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.112+5194G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171930835 | |||||||
| chr2:171931179 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.112+5538C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171931179 | |||||||
| chr2:171931229 | A | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0261 others(61): Show |
65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.112+5588A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171931229 | |||||||
| chr2:171931417 | T | C | 31 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(28): Show |
31 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.112+5776T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171931417 | |||||||
| chr2:171931428 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.112+5787G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171931428 | |||||||
| chr2:171931441 | G | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(2): Show |
5 | HG02083.hp1 NA18998.hp2 NA19070.hp2 others(2): Show |
intron_variant | MODIFIER | c.112+5800G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171931441 | |||||||
| chr2:171931595 | G | C | 1 | a0001c0001t0001g0215 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.112+5954G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171931595 | |||||||
| chr2:171931645 | G | C | 1 | a0001c0001t0001g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.112+6004G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171931645 | |||||||
| chr2:171931702 | T | C | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.112+6061T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171931702 | |||||||
| chr2:171932116 | T | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.112+6475T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171932116 | |||||||
| chr2:171932400 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.112+6759G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171932400 | |||||||
| chr2:171932849 | A | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0070 others(63): Show |
67 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.112+7208A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171932849 | |||||||
| chr2:171933006 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.112+7365T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171933006 | |||||||
| chr2:171933401 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.112+7760T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171933401 | |||||||
| chr2:171933475 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.112+7834C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171933475 | |||||||
| chr2:171933842 | T | G | 1 | a0001c0001t0001g0267 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.112+8201T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171933842 | |||||||
| chr2:171933909 | A | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.112+8268A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171933909 | |||||||
| chr2:171933982 | C | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0260 |
2 | HG00597.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.112+8341C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171933982 | |||||||
| chr2:171934005 | A | G | 3 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 |
3 | NA18986.hp2 NA19010.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.112+8364A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171934005 | |||||||
| chr2:171934048 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.112+8407G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171934048 | |||||||
| chr2:171934754 | G | GT | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
137 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.112+9131dupT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171934754 | ||||||
| chr2:171934754 | G | GTT | 75 | a0001c0001t0001g0005 a0001c0001t0001g0060 a0001c0001t0001g0061 others(72): Show |
75 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.112+9130_112+9131d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171934754 | ||||||
| chr2:171934754 | G | GTTT | 8 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG02027.hp2 NA18966.hp2 NA18971.hp2 others(5): Show |
intron_variant | MODIFIER | c.112+9129_112+9131d others(5): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171934754 | ||||||
| chr2:171934754 | GT | G | 30 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0212 others(27): Show |
31 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.112+9131delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171934754 | ||||||
| chr2:171934899 | G | T | 1 | a0001c0001t0001g0199 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.112+9258G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171934899 | |||||||
| chr2:171935014 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.112+9373C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171935014 | |||||||
| chr2:171935019 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.112+9378G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171935019 | |||||||
| chr2:171935076 | G | A | 69 | a0001c0001t0001g0067 a0001c0001t0001g0147 a0001c0001t0001g0148 others(66): Show |
69 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.112+9435G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171935076 | |||||||
| chr2:171935312 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.112+9671C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171935312 | |||||||
| chr2:171935515 | C | CA | 23 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0086 others(20): Show |
23 | HG00438.hp1 HG00438.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.112+9897dupA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171935515 | ||||||
| chr2:171935515 | C | CAA | 53 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0261 others(50): Show |
54 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.112+9896_112+9897d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171935515 | ||||||
| chr2:171935515 | CA | C | 66 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(63): Show |
66 | HG00140.hp1 HG00609.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.112+9897delA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171935515 | ||||||
| chr2:171935536 | A | AG | 61 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(58): Show |
61 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.112+9895_112+9896i others(3): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171935536 | |||||||
| chr2:171935536 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0058 others(1): Show |
4 | HG01069.hp1 HG01168.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+9895A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171935536 | |||||||
| chr2:171935552 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.112+9911T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171935552 | |||||||
| chr2:171935647 | C | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0270 others(29): Show |
33 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.112+10006C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171935647 | |||||||
| chr2:171935805 | G | T | 4 | a0002c0002t0001g0255 a0002c0002t0001g0256 a0002c0002t0001g0257 others(1): Show |
4 | HG02615.hp2 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+10164G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171935805 | |||||||
| chr2:171935833 | T | C | 1 | a0001c0001t0001g0319 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.112+10192T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171935833 | |||||||
| chr2:171936046 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.112+10405G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171936046 | |||||||
| chr2:171936087 | G | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0070 others(65): Show |
69 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.112+10446G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171936087 | |||||||
| chr2:171936106 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.112+10465T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171936106 | |||||||
| chr2:171936204 | G | T | 4 | a0002c0002t0001g0255 a0002c0002t0001g0256 a0002c0002t0001g0257 others(1): Show |
4 | HG02615.hp2 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-10504G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171936204 | |||||||
| chr2:171936227 | A | G | 4 | a0002c0002t0001g0255 a0002c0002t0001g0256 a0002c0002t0001g0257 others(1): Show |
4 | HG02615.hp2 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-10481A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171936227 | |||||||
| chr2:171936257 | G | C | 1 | a0001c0001t0001g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.113-10451G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171936257 | |||||||
| chr2:171936929 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.113-9779A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171936929 | |||||||
| chr2:171937026 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.113-9682C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171937026 | |||||||
| chr2:171937077 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.113-9631C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171937077 | |||||||
| chr2:171937112 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.113-9596G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171937112 | |||||||
| chr2:171937135 | T | C | 1 | a0001c0001t0001g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.113-9573T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171937135 | |||||||
| chr2:171937170 | G | C | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0320 |
3 | HG01074.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.113-9538G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171937170 | |||||||
| chr2:171937541 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.113-9167C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171937541 | |||||||
| chr2:171937660 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.113-9048T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171937660 | |||||||
| chr2:171937717 | A | C | 1 | a0001c0001t0001g0198 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.113-8991A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171937717 | |||||||
| chr2:171938024 | T | TTC | 27 | a0001c0001t0001g0030 a0001c0001t0001g0062 a0001c0001t0001g0071 others(24): Show |
27 | HG00323.hp2 HG01099.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.113-8634_113-8633d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | ||||||
| chr2:171938024 | T | TTCTC | 27 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0082 others(24): Show |
27 | HG00323.hp1 HG00408.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.113-8636_113-8633d others(6): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | ||||||
| chr2:171938024 | T | TTCTCTC | 30 | a0001c0001t0001g0036 a0001c0001t0001g0070 a0001c0001t0001g0092 others(27): Show |
30 | HG00408.hp2 HG00597.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.113-8638_113-8633d others(8): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | ||||||
| chr2:171938024 | T | TTCTCTCT others(1): Show |
25 | a0001c0001t0001g0067 a0001c0001t0001g0091 a0001c0001t0001g0097 others(22): Show |
25 | HG00558.hp1 HG01361.hp1 HG01981.hp1 others(22): Show |
intron_variant | MODIFIER | c.113-8640_113-8633d others(10): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | ||||||
| chr2:171938024 | T | TTCTCTCT others(3): Show |
17 | a0001c0001t0001g0075 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
17 | HG00438.hp1 HG01071.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.113-8642_113-8633d others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | ||||||
| chr2:171938024 | T | TTCTCTCT others(5): Show |
15 | a0001c0001t0001g0079 a0001c0001t0001g0103 a0001c0001t0001g0141 others(12): Show |
15 | HG00621.hp1 HG00733.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.113-8644_113-8633d others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | ||||||
| chr2:171938024 | T | TTCTCTCT others(7): Show |
9 | a0001c0001t0001g0074 a0001c0001t0001g0100 a0001c0001t0001g0114 others(6): Show |
9 | HG00140.hp1 HG01496.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.113-8646_113-8633d others(16): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | ||||||
| chr2:171938024 | T | TTCTCTCT others(9): Show |
5 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0001g0176 others(2): Show |
5 | HG00597.hp1 HG02300.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-8648_113-8633d others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | ||||||
| chr2:171938024 | T | TTCTCTCT others(13): Show |
2 | a0001c0001t0001g0087 a0001c0001t0001g0101 |
2 | HG01975.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.113-8652_113-8633d others(22): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | ||||||
| chr2:171938024 | T | TTCTCTCT others(15): Show |
2 | a0001c0001t0001g0108 a0001c0001t0001g0128 |
2 | NA18985.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.113-8654_113-8633d others(24): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | ||||||
| chr2:171938024 | TTC | T | 14 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0066 others(11): Show |
14 | HG01168.hp1 HG02165.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.113-8634_113-8633d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | ||||||
| chr2:171938024 | TTCTC | T | 11 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0078 others(8): Show |
11 | HG01175.hp2 HG02027.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.113-8636_113-8633d others(6): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | ||||||
| chr2:171938024 | TTCTCTC | T | 17 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0033 others(14): Show |
17 | HG00733.hp1 HG01074.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.113-8638_113-8633d others(8): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | ||||||
| chr2:171938024 | TTCTCTCT others(1): Show |
T | 8 | a0001c0001t0001g0034 a0001c0001t0001g0064 a0001c0001t0001g0243 others(5): Show |
8 | HG01109.hp2 HG01496.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.113-8640_113-8633d others(10): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | ||||||
| chr2:171938024 | TTCTCTCT others(3): Show |
T | 4 | a0001c0001t0001g0056 a0002c0002t0001g0256 a0002c0002t0001g0257 others(1): Show |
4 | HG02615.hp2 HG03225.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-8642_113-8633d others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | ||||||
| chr2:171938024 | TTCTCTCT others(5): Show |
T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0048 a0001c0001t0001g0063 others(1): Show |
4 | HG01123.hp1 HG01517.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-8644_113-8633d others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | ||||||
| chr2:171938024 | TTCTCTCT others(7): Show |
T | 41 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(38): Show |
41 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.113-8646_113-8633d others(16): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | ||||||
| chr2:171938024 | TTCTCTCT others(9): Show |
T | 2 | a0001c0001t0001g0250 a0001c0001t0001g0319 |
2 | HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.113-8648_113-8633d others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | ||||||
| chr2:171938024 | TTCTCTCT others(11): Show |
T | 1 | a0001c0001t0001g0286 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.113-8650_113-8633d others(20): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | ||||||
| chr2:171938024 | TTCTCTCT others(13): Show |
T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0218 a0001c0001t0001g0226 others(4): Show |
8 | HG00099.hp1 HG01109.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.113-8652_113-8633d others(22): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938024 | ||||||
| chr2:171938039 | T | TCTCTCTC others(5): Show |
1 | a0001c0001t0001g0152 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.113-8658_113-8657i others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938039 | ||||||
| chr2:171938060 | CTCTCTCT others(9): Show |
C | 1 | a0001c0001t0001g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.113-8646_113-8631d others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938060 | ||||||
| chr2:171938064 | CTCTCTCT others(5): Show |
C | 1 | a0001c0001t0001g0212 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.113-8642_113-8631d others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171938064 | ||||||
| chr2:171938075 | T | TC | 3 | a0001c0001t0001g0043 a0001c0001t0001g0183 a0001c0001t0001g0278 |
3 | HG02083.hp2 HG03130.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.113-8633_113-8632i others(3): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938075 | |||||||
| chr2:171938075 | T | TCTC | 3 | a0001c0001t0001g0086 a0001c0001t0001g0113 a0001c0001t0001g0138 |
3 | HG00438.hp2 HG02559.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.113-8633_113-8632i others(5): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938075 | |||||||
| chr2:171938075 | T | TCTCTC | 7 | a0001c0001t0001g0083 a0001c0001t0001g0105 a0001c0001t0001g0137 others(4): Show |
7 | HG00621.hp2 HG00735.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-8633_113-8632i others(7): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938075 | |||||||
| chr2:171938075 | T | TCTCTCTC | 3 | a0001c0001t0001g0185 a0001c0001t0001g0271 a0001c0001t0001g0306 |
3 | HG01934.hp1 HG03490.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.113-8633_113-8632i others(9): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938075 | |||||||
| chr2:171938075 | T | TCTCTCTC others(2): Show |
3 | a0001c0001t0001g0175 a0001c0001t0001g0194 a0001c0001t0001g0260 |
3 | NA18747.hp1 NA18960.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.113-8633_113-8632i others(11): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938075 | |||||||
| chr2:171938075 | T | TCTCTCTC others(4): Show |
2 | a0001c0001t0001g0145 a0001c0001t0001g0195 |
2 | HG01361.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.113-8633_113-8632i others(13): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938075 | |||||||
| chr2:171938075 | T | TCTCTCTC others(8): Show |
1 | a0001c0001t0001g0174 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.113-8633_113-8632i others(17): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938075 | |||||||
| chr2:171938075 | T | TCTCTCTC others(20): Show |
1 | a0001c0001t0001g0132 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.113-8633_113-8632i others(29): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938075 | |||||||
| chr2:171938076 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.113-8632T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938076 | |||||||
| chr2:171938249 | A | G | 31 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(28): Show |
31 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.113-8459A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938249 | |||||||
| chr2:171938382 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.113-8326G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938382 | |||||||
| chr2:171938647 | G | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | NA18963.hp2 NA19057.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.113-8061G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938647 | |||||||
| chr2:171938777 | A | G | 2 | a0001c0001t0001g0211 a0002c0002t0001g0249 |
2 | NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.113-7931A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938777 | |||||||
| chr2:171938977 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.113-7731G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938977 | |||||||
| chr2:171938989 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.113-7719C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171938989 | |||||||
| chr2:171939037 | G | A | 3 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0219 |
3 | HG01123.hp2 HG04199.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.113-7671G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171939037 | |||||||
| chr2:171939040 | T | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0261 others(61): Show |
65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.113-7668T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171939040 | |||||||
| chr2:171939044 | A | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0261 others(61): Show |
65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.113-7664A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171939044 | |||||||
| chr2:171939048 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.113-7660C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171939048 | |||||||
| chr2:171939141 | C | T | 4 | a0002c0002t0001g0255 a0002c0002t0001g0256 a0002c0002t0001g0257 others(1): Show |
4 | HG02615.hp2 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-7567C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171939141 | |||||||
| chr2:171939249 | A | C | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0196 |
3 | HG01934.hp2 HG01943.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.113-7459A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171939249 | |||||||
| chr2:171939426 | G | T | 1 | a0001c0001t0001g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.113-7282G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171939426 | |||||||
| chr2:171939523 | A | T | 1 | a0001c0001t0001g0286 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.113-7185A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171939523 | |||||||
| chr2:171939796 | CT | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0083 others(4): Show |
7 | HG01070.hp2 HG01256.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-6898delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171939796 | ||||||
| chr2:171939981 | G | C | 1 | a0001c0001t0001g0021 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.113-6727G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171939981 | |||||||
| chr2:171940061 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0261 others(61): Show |
65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.113-6647C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171940061 | |||||||
| chr2:171940254 | A | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0214 others(63): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.113-6454A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171940254 | |||||||
| chr2:171940270 | A | C | 1 | a0001c0001t0001g0204 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.113-6438A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171940270 | |||||||
| chr2:171940584 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0261 others(61): Show |
65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.113-6124C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171940584 | |||||||
| chr2:171940761 | C | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0070 others(65): Show |
69 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.113-5947C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171940761 | |||||||
| chr2:171941003 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.113-5705A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171941003 | |||||||
| chr2:171941277 | A | C | 1 | a0001c0001t0001g0056 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.113-5431A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171941277 | |||||||
| chr2:171941369 | C | T | 6 | a0001c0001t0001g0153 a0001c0001t0001g0158 a0001c0001t0001g0192 others(3): Show |
6 | HG00438.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-5339C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171941369 | |||||||
| chr2:171941742 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.113-4966C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171941742 | |||||||
| chr2:171942048 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | NA19067.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.113-4660G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942048 | |||||||
| chr2:171942135 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.113-4573C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942135 | |||||||
| chr2:171942211 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.113-4497T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942211 | |||||||
| chr2:171942255 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0261 others(61): Show |
65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.113-4453G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942255 | |||||||
| chr2:171942259 | A | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0261 others(60): Show |
64 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.113-4449A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942259 | |||||||
| chr2:171942284 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0261 others(61): Show |
65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.113-4424C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942284 | |||||||
| chr2:171942445 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0138 |
2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.113-4263C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942445 | |||||||
| chr2:171942454 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.113-4254C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942454 | |||||||
| chr2:171942681 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.113-4027A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942681 | |||||||
| chr2:171942715 | A | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0059 |
2 | HG01070.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.113-3993A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942715 | |||||||
| chr2:171942743 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.113-3965C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942743 | |||||||
| chr2:171942754 | A | C | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0142 |
3 | HG02895.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.113-3954A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942754 | |||||||
| chr2:171942824 | CAG | C | 3 | a0001c0001t0001g0130 a0001c0001t0001g0137 a0001c0001t0001g0146 |
3 | HG00735.hp2 HG00738.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.113-3883_113-3882d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942824 | |||||||
| chr2:171942953 | AT | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0160 a0001c0001t0001g0161 |
3 | NA18941.hp2 NA18994.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.113-3754delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171942953 | |||||||
| chr2:171943055 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0144 |
2 | HG01168.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.113-3653G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943055 | |||||||
| chr2:171943072 | AG | A | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.113-3635delG | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943072 | |||||||
| chr2:171943072 | AGT | A | 34 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(31): Show |
34 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.113-3635_113-3634d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943072 | |||||||
| chr2:171943074 | T | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.113-3634T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943074 | |||||||
| chr2:171943075 | T | C | 34 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(31): Show |
34 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.113-3633T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943075 | |||||||
| chr2:171943076 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.113-3632T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943076 | |||||||
| chr2:171943262 | C | T | 1 | a0002c0002t0001g0248 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.113-3446C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943262 | |||||||
| chr2:171943275 | G | A | 31 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(28): Show |
31 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.113-3433G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943275 | |||||||
| chr2:171943410 | C | CA | 10 | a0001c0001t0001g0073 a0001c0001t0001g0151 a0001c0001t0001g0250 others(7): Show |
10 | HG02615.hp2 HG02647.hp1 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.113-3273dupA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943410 | ||||||
| chr2:171943410 | C | CAA | 167 | a0001c0001t0001g0001 a0001c0001t0001g0067 a0001c0001t0001g0072 others(164): Show |
168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.113-3274_113-3273d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943410 | ||||||
| chr2:171943410 | C | CAAA | 68 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0071 others(65): Show |
68 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.113-3275_113-3273d others(5): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943410 | ||||||
| chr2:171943410 | C | CAAAA | 7 | a0001c0001t0001g0070 a0001c0001t0001g0075 a0001c0001t0001g0076 others(4): Show |
7 | HG01099.hp2 HG01943.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.113-3276_113-3273d others(6): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943410 | ||||||
| chr2:171943410 | CAAA | C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0024 others(4): Show |
7 | HG00735.hp1 HG01175.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.113-3275_113-3273d others(5): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943410 | ||||||
| chr2:171943410 | CAAAA | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(54): Show |
57 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.113-3276_113-3273d others(6): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943410 | ||||||
| chr2:171943456 | G | T | 1 | a0001c0001t0001g0279 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.113-3252G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943456 | |||||||
| chr2:171943726 | C | CAT | 34 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(31): Show |
34 | HG01257.hp1 HG02165.hp2 HG02451.hp1 others(31): Show |
intron_variant | MODIFIER | c.113-2959_113-2958d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943726 | ||||||
| chr2:171943726 | C | CATAT | 52 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0074 others(49): Show |
52 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.113-2961_113-2958d others(6): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943726 | ||||||
| chr2:171943726 | C | CATATAT | 13 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0001g0089 others(10): Show |
13 | HG00140.hp1 HG00621.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.113-2963_113-2958d others(8): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943726 | ||||||
| chr2:171943726 | C | CATATATA others(5): Show |
1 | a0001c0001t0001g0099 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.113-2969_113-2958d others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943726 | ||||||
| chr2:171943726 | CAT | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.113-2959_113-2958d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943726 | ||||||
| chr2:171943726 | CATATATA others(5): Show |
C | 1 | a0001c0001t0001g0240 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.113-2969_113-2958d others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171943726 | ||||||
| chr2:171943808 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.113-2900C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943808 | |||||||
| chr2:171943857 | A | C | 1 | a0001c0001t0001g0027 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.113-2851A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171943857 | |||||||
| chr2:171944143 | CA | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
105 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.113-2550delA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171944143 | ||||||
| chr2:171944159 | T | A | 69 | a0001c0001t0001g0067 a0001c0001t0001g0147 a0001c0001t0001g0148 others(66): Show |
69 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.113-2549T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171944159 | |||||||
| chr2:171944441 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.113-2267G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171944441 | |||||||
| chr2:171944489 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.113-2219C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171944489 | |||||||
| chr2:171944908 | A | G | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.113-1800A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171944908 | |||||||
| chr2:171944924 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.113-1784C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171944924 | |||||||
| chr2:171945161 | G | A | 69 | a0001c0001t0001g0067 a0001c0001t0001g0147 a0001c0001t0001g0148 others(66): Show |
69 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.113-1547G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171945161 | |||||||
| chr2:171945492 | T | G | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(5): Show |
8 | HG02083.hp1 NA18963.hp2 NA18998.hp2 others(5): Show |
intron_variant | MODIFIER | c.113-1216T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171945492 | |||||||
| chr2:171945498 | A | AT | 64 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0071 others(61): Show |
65 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.113-1191dupT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171945498 | ||||||
| chr2:171945498 | AT | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
97 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.113-1191delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 171945498 | ||||||
| chr2:171945602 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.113-1106T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171945602 | |||||||
| chr2:171945607 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.113-1101C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171945607 | |||||||
| chr2:171945754 | C | T | 4 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0191 others(1): Show |
4 | NA18964.hp2 NA18995.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-954C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171945754 | |||||||
| chr2:171945755 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.113-953G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171945755 | |||||||
| chr2:171945830 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.113-878C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171945830 | |||||||
| chr2:171945831 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.113-877G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171945831 | |||||||
| chr2:171946203 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.113-505A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171946203 | |||||||
| chr2:171946254 | G | C | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0320 |
3 | HG01074.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.113-454G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171946254 | |||||||
| chr2:171946563 | A | G | 3 | a0001c0001t0001g0220 a0001c0001t0001g0222 a0001c0001t0001g0224 |
3 | HG02004.hp1 HG06807.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.113-145A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 2/10 | chr2 | 171946563 | |||||||
| chr2:171946807 | G | C | 1 | a0001c0001t0001g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.188+24G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171946807 | |||||||
| chr2:171946879 | T | G | 1 | a0001c0001t0001g0232 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.188+96T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171946879 | |||||||
| chr2:171947304 | G | T | 1 | a0001c0001t0001g0198 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.188+521G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171947304 | |||||||
| chr2:171947349 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.188+566G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171947349 | |||||||
| chr2:171947358 | A | G | 3 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 |
3 | HG02258.hp2 HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.188+575A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171947358 | |||||||
| chr2:171947430 | A | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0114 |
2 | HG00140.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.188+647A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171947430 | |||||||
| chr2:171947452 | C | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0022 |
2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.188+669C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171947452 | |||||||
| chr2:171947575 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.188+792G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171947575 | |||||||
| chr2:171948430 | G | C | 1 | a0001c0001t0001g0115 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.188+1647G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171948430 | |||||||
| chr2:171948845 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.188+2062A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171948845 | |||||||
| chr2:171948862 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.188+2079G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171948862 | |||||||
| chr2:171949001 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.188+2218G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171949001 | |||||||
| chr2:171949192 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.188+2409A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171949192 | |||||||
| chr2:171949358 | G | T | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.188+2575G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171949358 | |||||||
| chr2:171949673 | C | CA | 8 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0056 others(5): Show |
8 | HG00323.hp1 HG00738.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+2906dupA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 171949673 | ||||||
| chr2:171949673 | CA | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0071 others(61): Show |
65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.188+2906delA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 171949673 | ||||||
| chr2:171949689 | A | T | 5 | a0001c0001t0001g0254 a0002c0002t0001g0255 a0002c0002t0001g0256 others(2): Show |
5 | HG02615.hp2 HG03098.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.188+2906A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171949689 | |||||||
| chr2:171949817 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG02602.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.188+3034A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171949817 | |||||||
| chr2:171949859 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0223 |
2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.189-3022G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171949859 | |||||||
| chr2:171950023 | C | G | 1 | a0001c0001t0001g0021 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.189-2858C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171950023 | |||||||
| chr2:171950396 | G | C | 1 | a0001c0001t0001g0218 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.189-2485G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171950396 | |||||||
| chr2:171950438 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.189-2443C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171950438 | |||||||
| chr2:171950460 | C | T | 65 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(62): Show |
65 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.189-2421C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171950460 | |||||||
| chr2:171950711 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.189-2170C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171950711 | |||||||
| chr2:171950939 | C | T | 1 | a0001c0001t0001g0012 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.189-1942C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171950939 | |||||||
| chr2:171951071 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0069 others(64): Show |
68 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.189-1810G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951071 | |||||||
| chr2:171951101 | G | A | 1 | a0001c0001t0001g0299 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.189-1780G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951101 | |||||||
| chr2:171951112 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.189-1769T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951112 | |||||||
| chr2:171951230 | T | C | 1 | a0001c0001t0001g0321 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.189-1651T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951230 | |||||||
| chr2:171951363 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.189-1518C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951363 | |||||||
| chr2:171951442 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.189-1439C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951442 | |||||||
| chr2:171951585 | A | AT | 44 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0036 others(41): Show |
44 | HG00140.hp1 HG00597.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.189-1277dupT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 171951585 | ||||||
| chr2:171951585 | A | ATT | 7 | a0001c0001t0001g0099 a0001c0001t0001g0195 a0001c0001t0001g0220 others(4): Show |
7 | HG01168.hp2 HG01433.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.189-1278_189-1277d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 171951585 | ||||||
| chr2:171951585 | A | T | 1 | a0001c0001t0001g0242 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.189-1296A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951585 | |||||||
| chr2:171951585 | AT | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0113 others(4): Show |
7 | HG02895.hp2 HG02976.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-1277delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 171951585 | ||||||
| chr2:171951604 | T | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0261 others(60): Show |
64 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.189-1277T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951604 | |||||||
| chr2:171951672 | TC | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0070 others(65): Show |
69 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.189-1201delC | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 171951672 | ||||||
| chr2:171951680 | C | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.189-1201C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951680 | |||||||
| chr2:171951723 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.189-1158C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951723 | |||||||
| chr2:171951724 | G | A | 1 | a0001c0001t0001g0286 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.189-1157G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951724 | |||||||
| chr2:171951773 | C | G | 1 | a0001c0001t0001g0043 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.189-1108C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951773 | |||||||
| chr2:171951773 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.189-1108C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951773 | |||||||
| chr2:171951813 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.189-1068C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951813 | |||||||
| chr2:171951859 | G | A | 3 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 |
3 | HG02723.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.189-1022G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171951859 | |||||||
| chr2:171952068 | A | T | 1 | a0001c0001t0001g0205 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.189-813A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171952068 | |||||||
| chr2:171952211 | C | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0121 |
2 | HG00140.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.189-670C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171952211 | |||||||
| chr2:171952262 | T | C | 3 | a0001c0001t0001g0154 a0001c0001t0001g0160 a0001c0001t0001g0161 |
3 | NA18941.hp2 NA18994.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.189-619T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171952262 | |||||||
| chr2:171952535 | T | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | NA18995.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.189-346T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171952535 | |||||||
| chr2:171952844 | A | G | 1 | a0001c0001t0001g0259 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.189-37A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 3/10 | chr2 | 171952844 | |||||||
| chr2:171953188 | C | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.309+187C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171953188 | |||||||
| chr2:171953207 | G | T | 5 | a0001c0001t0001g0087 a0001c0001t0001g0095 a0001c0001t0001g0119 others(2): Show |
5 | HG01975.hp2 NA18959.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+206G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171953207 | |||||||
| chr2:171953446 | T | C | 2 | a0001c0001t0001g0139 a0001c0001t0001g0141 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.309+445T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171953446 | |||||||
| chr2:171953597 | C | G | 1 | a0001c0001t0001g0319 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.309+596C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171953597 | |||||||
| chr2:171953626 | T | TAAAA | 41 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(38): Show |
41 | HG00558.hp2 HG00609.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.309+651_309+654dup others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | T | TAAAAA | 20 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(17): Show |
20 | HG00735.hp1 HG00738.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.309+650_309+654dup others(5): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | T | TAAAAAAA others(1): Show |
8 | a0001c0001t0001g0018 a0001c0001t0001g0147 a0001c0001t0001g0154 others(5): Show |
8 | HG02818.hp2 NA18941.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.309+647_309+654dup others(8): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | T | TAAAAAAA others(2): Show |
31 | a0001c0001t0001g0001 a0001c0001t0001g0148 a0001c0001t0001g0149 others(28): Show |
32 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.309+646_309+654dup others(9): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | T | TAAAAAAA others(3): Show |
48 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0072 others(45): Show |
48 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.309+645_309+654dup others(10): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | T | TAAAAAAA others(4): Show |
18 | a0001c0001t0001g0073 a0001c0001t0001g0150 a0001c0001t0001g0164 others(15): Show |
18 | HG00323.hp2 HG00621.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.309+644_309+654dup others(11): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | T | TAAAAAAA others(5): Show |
5 | a0001c0001t0001g0176 a0001c0001t0001g0201 a0001c0001t0001g0274 others(2): Show |
5 | HG01943.hp1 HG02300.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.309+643_309+654dup others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | T | TAAAAAAA others(6): Show |
2 | a0001c0001t0001g0244 a0001c0001t0001g0286 |
2 | HG02027.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.309+642_309+654dup others(13): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | T | TAAAAAAA others(7): Show |
3 | a0001c0001t0001g0162 a0001c0001t0001g0171 a0001c0001t0001g0317 |
3 | HG02451.hp1 NA19009.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.309+641_309+654dup others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | T | TAAAAAAA others(8): Show |
7 | a0001c0001t0001g0175 a0001c0001t0001g0203 a0001c0001t0001g0267 others(4): Show |
7 | HG01261.hp2 HG02647.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+640_309+654dup others(15): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | T | TAAAAAAA others(9): Show |
4 | a0001c0001t0001g0280 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+639_309+654dup others(16): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | T | TAAAAAAA others(10): Show |
3 | a0001c0001t0001g0151 a0001c0001t0001g0174 a0001c0001t0001g0281 |
3 | HG06807.hp1 NA18962.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.309+638_309+654dup others(17): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | T | TAAAAAAA others(12): Show |
1 | a0001c0001t0001g0173 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.309+636_309+654dup others(19): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | T | TAAAAAAA others(13): Show |
1 | a0001c0001t0001g0316 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.309+635_309+654dup others(20): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | T | TAAAAAAA others(15): Show |
1 | a0001c0001t0001g0265 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.309+633_309+654dup others(22): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | T | TAAAAAAA others(19): Show |
1 | a0001c0001t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.309+629_309+654dup others(26): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | T | TAAAAAAA others(20): Show |
1 | a0001c0001t0001g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.309+628_309+654dup others(27): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | T | TAAAAAAA others(22): Show |
1 | a0001c0001t0001g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.309+626_309+654dup others(29): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | TAAAAAAA | T | 6 | a0001c0001t0001g0074 a0001c0001t0001g0091 a0001c0001t0001g0104 others(3): Show |
6 | HG00735.hp2 HG00738.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+648_309+654del others(7): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | TAAAAAAA others(1): Show |
T | 62 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0078 others(59): Show |
62 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.309+647_309+654del others(8): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | TAAAAAAA others(2): Show |
T | 6 | a0001c0001t0001g0076 a0001c0001t0001g0087 a0001c0001t0001g0107 others(3): Show |
6 | HG01070.hp1 HG01975.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.309+646_309+654del others(9): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | TAAAAAAA others(3): Show |
T | 29 | a0001c0001t0001g0157 a0001c0001t0001g0214 a0001c0001t0001g0216 others(26): Show |
29 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.309+645_309+654del others(10): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953626 | TAAAAAAA others(4): Show |
T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0263 |
2 | HG01256.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.309+644_309+654del others(11): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171953626 | ||||||
| chr2:171953666 | A | T | 1 | a0001c0001t0001g0151 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.309+665A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171953666 | |||||||
| chr2:171953686 | C | T | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.309+685C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171953686 | |||||||
| chr2:171953839 | A | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.309+838A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171953839 | |||||||
| chr2:171954507 | A | G | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.309+1506A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171954507 | |||||||
| chr2:171954515 | G | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | HG02615.hp1 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.309+1514G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171954515 | |||||||
| chr2:171954529 | T | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0132 |
2 | HG00609.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.309+1528T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171954529 | |||||||
| chr2:171954627 | A | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0227 others(63): Show |
67 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.309+1626A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171954627 | |||||||
| chr2:171954642 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0227 others(63): Show |
67 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.309+1641C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171954642 | |||||||
| chr2:171954704 | G | C | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0142 |
3 | HG02895.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.309+1703G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171954704 | |||||||
| chr2:171954808 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.309+1807G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171954808 | |||||||
| chr2:171954829 | G | A | 1 | a0001c0001t0001g0321 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.309+1828G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171954829 | |||||||
| chr2:171954861 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.309+1860A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171954861 | |||||||
| chr2:171955088 | C | T | 3 | a0001c0001t0001g0291 a0001c0001t0001g0301 a0001c0001t0001g0306 |
3 | HG01361.hp1 HG01934.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.309+2087C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955088 | |||||||
| chr2:171955089 | G | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(61): Show |
64 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.309+2088G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955089 | |||||||
| chr2:171955180 | G | A | 1 | a0001c0001t0001g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.309+2179G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955180 | |||||||
| chr2:171955518 | G | C | 1 | a0001c0001t0001g0269 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.309+2517G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955518 | |||||||
| chr2:171955758 | A | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.309+2757A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955758 | |||||||
| chr2:171955765 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.309+2764C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955765 | |||||||
| chr2:171955772 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.309+2771C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955772 | |||||||
| chr2:171955813 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.309+2812A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955813 | |||||||
| chr2:171955818 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.309+2817A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955818 | |||||||
| chr2:171955937 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.309+2936C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955937 | |||||||
| chr2:171955962 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.309+2961C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955962 | |||||||
| chr2:171955994 | G | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.309+2993G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171955994 | |||||||
| chr2:171956000 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.309+2999G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956000 | |||||||
| chr2:171956001 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.309+3000C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956001 | |||||||
| chr2:171956023 | C | A | 29 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(26): Show |
29 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.309+3022C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956023 | |||||||
| chr2:171956066 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.309+3065C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956066 | |||||||
| chr2:171956178 | T | TA | 84 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0027 others(81): Show |
85 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.309+3200dupA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171956178 | ||||||
| chr2:171956178 | TA | T | 8 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0117 others(5): Show |
8 | HG01070.hp2 HG01256.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.309+3200delA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171956178 | ||||||
| chr2:171956284 | G | T | 1 | a0001c0001t0001g0212 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.309+3283G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956284 | |||||||
| chr2:171956311 | CA | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0227 others(30): Show |
34 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.309+3311delA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956311 | |||||||
| chr2:171956515 | A | AAAAC | 66 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0227 others(63): Show |
67 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.309+3530_309+3533d others(6): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171956515 | ||||||
| chr2:171956520 | A | G | 6 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0089 others(3): Show |
6 | HG00408.hp1 HG00438.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+3519A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956520 | |||||||
| chr2:171956539 | C | G | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.309+3538C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956539 | |||||||
| chr2:171956552 | G | T | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0320 |
3 | HG01074.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.309+3551G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956552 | |||||||
| chr2:171956692 | G | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(95): Show |
98 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.309+3691G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956692 | |||||||
| chr2:171956693 | G | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(95): Show |
98 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.309+3692G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956693 | |||||||
| chr2:171956715 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.309+3714C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956715 | |||||||
| chr2:171956719 | G | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0070 others(67): Show |
71 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.309+3718G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171956719 | |||||||
| chr2:171957380 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.309+4379C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171957380 | |||||||
| chr2:171957583 | G | T | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0320 |
3 | HG01074.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.309+4582G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171957583 | |||||||
| chr2:171957729 | T | C | 69 | a0001c0001t0001g0067 a0001c0001t0001g0147 a0001c0001t0001g0148 others(66): Show |
69 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.309+4728T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171957729 | |||||||
| chr2:171957792 | A | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.309+4791A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171957792 | |||||||
| chr2:171957922 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.309+4921A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171957922 | |||||||
| chr2:171957941 | C | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0227 others(60): Show |
64 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.309+4940C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171957941 | |||||||
| chr2:171957946 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.309+4945C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171957946 | |||||||
| chr2:171958023 | C | G | 1 | a0001c0001t0001g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.309+5022C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171958023 | |||||||
| chr2:171958171 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.309+5170A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171958171 | |||||||
| chr2:171958476 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.309+5475C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171958476 | |||||||
| chr2:171958514 | C | G | 1 | a0001c0001t0001g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.309+5513C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171958514 | |||||||
| chr2:171958680 | A | G | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG02056.hp1 HG03927.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.309+5679A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171958680 | |||||||
| chr2:171958860 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.309+5859G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171958860 | |||||||
| chr2:171958881 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.309+5880A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171958881 | |||||||
| chr2:171958984 | G | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0070 others(68): Show |
72 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.309+5983G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171958984 | |||||||
| chr2:171959486 | T | A | 1 | a0001c0001t0001g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.310-5852T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171959486 | |||||||
| chr2:171959703 | A | G | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.310-5635A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171959703 | |||||||
| chr2:171959727 | A | C | 69 | a0001c0001t0001g0067 a0001c0001t0001g0147 a0001c0001t0001g0148 others(66): Show |
69 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.310-5611A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171959727 | |||||||
| chr2:171960338 | T | C | 1 | a0001c0001t0001g0259 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.310-5000T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171960338 | |||||||
| chr2:171960348 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.310-4990G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171960348 | |||||||
| chr2:171960375 | A | G | 1 | a0001c0001t0001g0305 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.310-4963A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171960375 | |||||||
| chr2:171960390 | C | A | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.310-4948C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171960390 | |||||||
| chr2:171960401 | T | A | 1 | a0001c0001t0001g0242 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.310-4937T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171960401 | |||||||
| chr2:171960482 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.310-4856T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171960482 | |||||||
| chr2:171960534 | T | G | 1 | a0001c0001t0001g0295 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.310-4804T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171960534 | |||||||
| chr2:171960535 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.310-4803C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171960535 | |||||||
| chr2:171960711 | G | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.310-4627G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171960711 | |||||||
| chr2:171960761 | C | T | 70 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(67): Show |
70 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.310-4577C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171960761 | |||||||
| chr2:171960913 | G | GGACAGGT others(11): Show |
1 | a0001c0001t0001g0115 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.310-4424_310-4407d others(20): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171960913 | ||||||
| chr2:171961132 | ACT | A | 6 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(3): Show |
6 | HG00621.hp2 HG02132.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.310-4203_310-4202d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171961132 | ||||||
| chr2:171961268 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.310-4070A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171961268 | |||||||
| chr2:171961409 | GA | G | 5 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0298 others(2): Show |
5 | NA18959.hp1 NA18964.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.310-3925delA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171961409 | ||||||
| chr2:171961576 | ATACT | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0261 others(61): Show |
65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.310-3760_310-3757d others(6): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171961576 | ||||||
| chr2:171961731 | C | G | 1 | a0001c0001t0001g0196 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.310-3607C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171961731 | |||||||
| chr2:171961825 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.310-3513A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171961825 | |||||||
| chr2:171961891 | G | GT | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
84 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.310-3433dupT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171961891 | ||||||
| chr2:171961891 | G | GTT | 7 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(4): Show |
7 | HG01978.hp2 HG02083.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.310-3434_310-3433d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171961891 | ||||||
| chr2:171961891 | GT | G | 38 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0172 others(35): Show |
38 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.310-3433delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171961891 | ||||||
| chr2:171961945 | T | G | 25 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0217 others(22): Show |
25 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.310-3393T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171961945 | |||||||
| chr2:171962004 | T | G | 1 | a0001c0001t0001g0197 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.310-3334T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171962004 | |||||||
| chr2:171962145 | G | A | 4 | a0002c0002t0001g0255 a0002c0002t0001g0256 a0002c0002t0001g0257 others(1): Show |
4 | HG02615.hp2 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-3193G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171962145 | |||||||
| chr2:171962487 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.310-2851C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171962487 | |||||||
| chr2:171962639 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0070 others(63): Show |
67 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.310-2699G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171962639 | |||||||
| chr2:171963176 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.310-2162G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171963176 | |||||||
| chr2:171963192 | C | CATATTTA others(23): Show |
1 | a0001c0001t0001g0322 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.310-2134_310-2105d others(32): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171963192 | ||||||
| chr2:171963605 | T | A | 1 | a0001c0001t0001g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.310-1733T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171963605 | |||||||
| chr2:171963728 | C | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0261 others(54): Show |
58 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.310-1610C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171963728 | |||||||
| chr2:171963738 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.310-1600G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171963738 | |||||||
| chr2:171963793 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.310-1545T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171963793 | |||||||
| chr2:171964701 | G | A | 23 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0219 others(20): Show |
23 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.310-637G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171964701 | |||||||
| chr2:171964706 | T | C | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.310-632T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171964706 | |||||||
| chr2:171964836 | AT | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0261 others(61): Show |
65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.310-497delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 171964836 | ||||||
| chr2:171965218 | T | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0261 others(61): Show |
65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.310-120T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 4/10 | chr2 | 171965218 | |||||||
| chr2:171966124 | G | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(2): Show |
5 | HG00099.hp2 HG00738.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.611+216G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 6/10 | chr2 | 171966124 | |||||||
| chr2:171966171 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.612-238C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 6/10 | chr2 | 171966171 | |||||||
| chr2:171966208 | A | C | 1 | a0001c0001t0001g0050 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.612-201A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 6/10 | chr2 | 171966208 | |||||||
| chr2:171966663 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.716+150T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 7/10 | chr2 | 171966663 | |||||||
| chr2:171966963 | G | GA | 8 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(5): Show |
8 | HG00609.hp1 NA18941.hp1 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+15dupA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171966963 | ||||||
| chr2:171966967 | T | G | 8 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(5): Show |
8 | HG00609.hp1 NA18941.hp1 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+18T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171966967 | |||||||
| chr2:171967073 | C | G | 1 | a0001c0001t0001g0054 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.823+124C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171967073 | |||||||
| chr2:171967535 | C | G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(43): Show |
46 | HG00099.hp2 HG00609.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.823+586C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171967535 | |||||||
| chr2:171967884 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.823+935C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171967884 | |||||||
| chr2:171968797 | T | C | 6 | a0001c0001t0001g0215 a0001c0001t0001g0220 a0001c0001t0001g0221 others(3): Show |
6 | HG01256.hp2 HG02004.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+1848T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171968797 | |||||||
| chr2:171968822 | G | A | 70 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(67): Show |
70 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.823+1873G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171968822 | |||||||
| chr2:171969206 | A | G | 5 | a0001c0001t0001g0039 a0001c0001t0001g0045 a0001c0001t0001g0047 others(2): Show |
5 | HG00609.hp2 NA18949.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.823+2257A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171969206 | |||||||
| chr2:171969645 | A | C | 1 | a0001c0001t0001g0298 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.823+2696A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171969645 | |||||||
| chr2:171969679 | G | A | 7 | a0001c0001t0001g0109 a0001c0001t0001g0130 a0001c0001t0001g0137 others(4): Show |
7 | HG00735.hp2 HG00738.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.823+2730G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171969679 | |||||||
| chr2:171970095 | G | C | 1 | a0001c0001t0001g0193 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.823+3146G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970095 | |||||||
| chr2:171970147 | G | A | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
104 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.823+3198G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970147 | |||||||
| chr2:171970337 | C | G | 1 | a0001c0001t0001g0201 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.823+3388C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970337 | |||||||
| chr2:171970434 | CACACACA others(5): Show |
C | 1 | a0001c0001t0001g0285 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.823+3493_823+3504d others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970434 | ||||||
| chr2:171970496 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0313 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.823+3574_823+3588d others(17): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | ||||||
| chr2:171970496 | C | CTTTTTTT others(12): Show |
2 | a0002c0002t0001g0247 a0002c0002t0001g0249 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.823+3570_823+3588d others(21): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | ||||||
| chr2:171970496 | CT | C | 16 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0001g0080 others(13): Show |
16 | HG00408.hp1 HG00609.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.823+3588delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | ||||||
| chr2:171970496 | CTT | C | 20 | a0001c0001t0001g0079 a0001c0001t0001g0086 a0001c0001t0001g0088 others(17): Show |
20 | HG00438.hp2 HG01069.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.823+3587_823+3588d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | ||||||
| chr2:171970496 | CTTT | C | 13 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0082 others(10): Show |
13 | HG00735.hp2 HG00738.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.823+3586_823+3588d others(5): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | ||||||
| chr2:171970496 | CTTTTTTT others(3): Show |
C | 11 | a0001c0001t0001g0277 a0001c0001t0001g0287 a0001c0001t0001g0290 others(8): Show |
11 | HG01074.hp1 HG01361.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.823+3579_823+3588d others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | ||||||
| chr2:171970496 | CTTTTTTT others(4): Show |
C | 42 | a0001c0001t0001g0071 a0001c0001t0001g0261 a0001c0001t0001g0262 others(39): Show |
42 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.823+3578_823+3588d others(13): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | ||||||
| chr2:171970496 | CTTTTTTT others(5): Show |
C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0134 a0001c0001t0001g0264 others(5): Show |
9 | HG02809.hp1 HG02976.hp1 HG03834.hp2 others(6): Show |
intron_variant | MODIFIER | c.823+3577_823+3588d others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | ||||||
| chr2:171970496 | CTTTTTTT others(6): Show |
C | 10 | a0001c0001t0001g0110 a0001c0001t0001g0147 a0001c0001t0001g0148 others(7): Show |
10 | HG00408.hp2 HG02027.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+3576_823+3588d others(15): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | ||||||
| chr2:171970496 | CTTTTTTT others(7): Show |
C | 57 | a0001c0001t0001g0069 a0001c0001t0001g0150 a0001c0001t0001g0151 others(54): Show |
57 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.823+3575_823+3588d others(16): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | ||||||
| chr2:171970496 | CTTTTTTT others(8): Show |
C | 6 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01123.hp2 HG01943.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+3574_823+3588d others(17): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | ||||||
| chr2:171970496 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0172 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.823+3573_823+3588d others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | ||||||
| chr2:171970496 | CTTTTTTT others(12): Show |
C | 7 | a0001c0001t0001g0083 a0001c0001t0001g0143 a0001c0001t0001g0145 others(4): Show |
7 | HG01256.hp1 HG01258.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.823+3570_823+3588d others(21): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | ||||||
| chr2:171970496 | CTTTTTTT others(13): Show |
C | 34 | a0001c0001t0001g0099 a0001c0001t0001g0114 a0001c0001t0001g0121 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.823+3569_823+3588d others(22): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | ||||||
| chr2:171970496 | CTTTTTTT others(14): Show |
C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0225 |
2 | HG01099.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.823+3568_823+3588d others(23): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | ||||||
| chr2:171970496 | CTTTTTTT others(15): Show |
C | 6 | a0001c0001t0001g0035 a0001c0001t0001g0063 a0001c0001t0001g0064 others(3): Show |
6 | HG01109.hp2 HG01168.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+3567_823+3588d others(24): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | ||||||
| chr2:171970496 | CTTTTTTT others(16): Show |
C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(61): Show |
64 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.823+3566_823+3588d others(25): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | ||||||
| chr2:171970496 | CTTTTTTT others(17): Show |
C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0030 |
2 | HG03491.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.823+3565_823+3588d others(26): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171970496 | ||||||
| chr2:171970580 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0070 others(64): Show |
68 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.823+3631T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970580 | |||||||
| chr2:171970612 | C | T | 4 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0320 others(1): Show |
4 | HG01074.hp1 HG03139.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+3663C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970612 | |||||||
| chr2:171970662 | G | T | 1 | a0001c0001t0001g0043 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.823+3713G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970662 | |||||||
| chr2:171970784 | C | T | 68 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(65): Show |
68 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.823+3835C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970784 | |||||||
| chr2:171970800 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0082 |
2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.823+3851G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970800 | |||||||
| chr2:171970869 | A | G | 1 | a0002c0002t0001g0257 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.823+3920A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970869 | |||||||
| chr2:171970939 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0052 |
3 | HG01261.hp1 HG01433.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.823+3990G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970939 | |||||||
| chr2:171970966 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0011 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.823+4017C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171970966 | |||||||
| chr2:171971199 | C | A | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.823+4250C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171971199 | |||||||
| chr2:171971286 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0134 |
2 | NA18963.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.823+4337G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171971286 | |||||||
| chr2:171971461 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.823+4512T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171971461 | |||||||
| chr2:171971546 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.823+4597C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171971546 | |||||||
| chr2:171971624 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.824-4533G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171971624 | |||||||
| chr2:171971821 | T | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0070 others(65): Show |
69 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.824-4336T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171971821 | |||||||
| chr2:171972007 | T | G | 2 | a0001c0001t0001g0284 a0001c0001t0001g0287 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.824-4150T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171972007 | |||||||
| chr2:171972214 | GT | G | 204 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(201): Show |
204 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.824-3931delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171972214 | ||||||
| chr2:171972223 | T | G | 2 | a0001c0001t0001g0194 a0001c0001t0001g0263 |
2 | HG02572.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.824-3934T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171972223 | |||||||
| chr2:171972253 | T | G | 1 | a0001c0001t0001g0196 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.824-3904T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171972253 | |||||||
| chr2:171972289 | A | G | 31 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(28): Show |
31 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.824-3868A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171972289 | |||||||
| chr2:171972632 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.824-3525A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171972632 | |||||||
| chr2:171972756 | G | T | 1 | a0001c0001t0001g0270 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.824-3401G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171972756 | |||||||
| chr2:171972764 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.824-3393A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171972764 | |||||||
| chr2:171972970 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0244 |
2 | HG02027.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.824-3187G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171972970 | |||||||
| chr2:171973127 | C | A | 1 | a0001c0001t0001g0200 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.824-3030C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171973127 | |||||||
| chr2:171973172 | C | A | 23 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0219 others(20): Show |
23 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.824-2985C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171973172 | |||||||
| chr2:171973400 | C | CA | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(218): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.824-2740dupA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171973400 | ||||||
| chr2:171973400 | C | CAA | 81 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0045 others(78): Show |
82 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.824-2741_824-2740d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171973400 | ||||||
| chr2:171973453 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.824-2704T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171973453 | |||||||
| chr2:171973653 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.824-2504A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171973653 | |||||||
| chr2:171973720 | C | A | 1 | a0001c0001t0001g0215 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.824-2437C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171973720 | |||||||
| chr2:171973787 | C | G | 1 | a0001c0001t0001g0242 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.824-2370C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171973787 | |||||||
| chr2:171973914 | T | C | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.824-2243T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171973914 | |||||||
| chr2:171973946 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0070 others(64): Show |
68 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.824-2211A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171973946 | |||||||
| chr2:171973980 | G | A | 3 | a0001c0001t0001g0282 a0001c0001t0001g0284 a0001c0001t0001g0287 |
3 | HG01261.hp2 HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.824-2177G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171973980 | |||||||
| chr2:171974055 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.824-2102C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974055 | |||||||
| chr2:171974125 | G | C | 1 | a0001c0001t0001g0319 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.824-2032G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974125 | |||||||
| chr2:171974173 | C | CA | 35 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0088 others(32): Show |
35 | HG00408.hp1 HG00621.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.824-1965dupA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171974173 | ||||||
| chr2:171974173 | C | CAA | 58 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0147 others(55): Show |
58 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.824-1966_824-1965d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171974173 | ||||||
| chr2:171974173 | C | CAAA | 14 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(11): Show |
14 | HG00408.hp2 HG00597.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.824-1967_824-1965d others(5): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171974173 | ||||||
| chr2:171974189 | AAAAGAAA others(25): Show |
A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0059 |
2 | HG01070.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.824-1964_824-1933d others(34): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171974189 | ||||||
| chr2:171974190 | AAAGAAAA others(24): Show |
A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(54): Show |
57 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.824-1964_824-1934d others(33): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171974190 | ||||||
| chr2:171974191 | AAGAAAAA others(3): Show |
A | 2 | a0001c0001t0001g0297 a0001c0001t0001g0307 |
2 | HG01943.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.824-1964_824-1955d others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171974191 | ||||||
| chr2:171974191 | AAGAAAAA others(23): Show |
A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0040 others(4): Show |
7 | HG01175.hp1 HG01517.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-1964_824-1935d others(32): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171974191 | ||||||
| chr2:171974192 | AG | A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0222 a0001c0001t0001g0290 others(11): Show |
15 | HG01074.hp1 HG01361.hp1 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.824-1964delG | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974192 | |||||||
| chr2:171974192 | AGAAAAAA others(26): Show |
A | 1 | a0001c0001t0001g0020 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.824-1964_824-1932d others(35): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974192 | |||||||
| chr2:171974193 | G | A | 230 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(227): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.824-1964G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974193 | |||||||
| chr2:171974199 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.824-1958A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974199 | |||||||
| chr2:171974201 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0070 others(66): Show |
70 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.824-1956G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974201 | |||||||
| chr2:171974203 | A | G | 7 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0072 others(4): Show |
7 | HG01123.hp2 HG01934.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.824-1954A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974203 | |||||||
| chr2:171974204 | A | AG | 24 | a0001c0001t0001g0263 a0001c0001t0001g0267 a0001c0001t0001g0270 others(21): Show |
24 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.824-1953_824-1952i others(3): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974204 | |||||||
| chr2:171974204 | A | G | 22 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0264 others(19): Show |
22 | HG01261.hp2 HG01884.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.824-1953A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974204 | |||||||
| chr2:171974207 | G | A | 53 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0072 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.824-1950G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974207 | |||||||
| chr2:171974209 | A | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0072 others(1): Show |
4 | HG01123.hp2 HG01934.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-1948A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974209 | |||||||
| chr2:171974210 | A | AAAG | 15 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0271 others(12): Show |
16 | HG01074.hp1 HG01361.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.824-1945_824-1944i others(5): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171974210 | ||||||
| chr2:171974210 | A | G | 46 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(43): Show |
46 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.824-1947A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974210 | |||||||
| chr2:171974225 | T | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0045 others(3): Show |
6 | HG00609.hp2 HG03710.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-1932T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974225 | |||||||
| chr2:171974280 | T | C | 4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0129 others(1): Show |
4 | HG02559.hp2 HG02572.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-1877T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974280 | |||||||
| chr2:171974442 | T | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.824-1715T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974442 | |||||||
| chr2:171974578 | G | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0022 |
2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.824-1579G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974578 | |||||||
| chr2:171974736 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.824-1421A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974736 | |||||||
| chr2:171974808 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.824-1349G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171974808 | |||||||
| chr2:171975102 | C | CT | 16 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0057 others(13): Show |
16 | HG01074.hp1 HG01934.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.824-1039dupT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171975102 | ||||||
| chr2:171975512 | G | T | 31 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(28): Show |
31 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.824-645G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171975512 | |||||||
| chr2:171976018 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.824-139A>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171976018 | |||||||
| chr2:171976041 | G | A | 4 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0320 others(1): Show |
4 | HG01074.hp1 HG03139.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-116G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | chr2 | 171976041 | |||||||
| chr2:171976066 | C | CAGCTGGG others(8420): Show |
1 | a0001c0001t0001g0260 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8425): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8419): Show |
1 | a0001c0001t0001g0208 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8424): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8423): Show |
1 | a0001c0001t0001g0266 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8428): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8421): Show |
3 | a0001c0001t0001g0292 a0001c0001t0001g0301 a0001c0001t0001g0305 |
3 | HG01361.hp1 HG02818.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8421): Show |
1 | a0001c0001t0001g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8422): Show |
1 | a0001c0001t0001g0265 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8427): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8423): Show |
1 | a0001c0001t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8428): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8419): Show |
2 | a0001c0001t0001g0300 a0001c0001t0001g0307 |
2 | HG00323.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8424): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8419): Show |
1 | a0001c0001t0001g0286 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8424): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8420): Show |
1 | a0001c0001t0001g0289 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8425): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8419): Show |
1 | a0001c0001t0001g0270 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8424): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8420): Show |
13 | a0001c0001t0001g0071 a0001c0001t0001g0272 a0001c0001t0001g0288 others(10): Show |
13 | HG00140.hp2 HG00733.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8425): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8419): Show |
1 | a0001c0001t0001g0278 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8424): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8420): Show |
17 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0267 others(14): Show |
17 | HG01261.hp2 HG01884.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8425): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8421): Show |
1 | a0001c0001t0001g0263 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8420): Show |
7 | a0001c0001t0001g0001 a0001c0001t0001g0273 a0001c0001t0001g0299 others(4): Show |
8 | HG02040.hp2 NA18960.hp1 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8425): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8421): Show |
1 | a0001c0001t0001g0309 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8421): Show |
1 | a0001c0001t0001g0275 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8421): Show |
1 | a0001c0001t0001g0290 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8421): Show |
2 | a0001c0001t0001g0317 a0001c0001t0001g0318 |
2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8422): Show |
2 | a0001c0001t0001g0271 a0001c0001t0001g0296 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8427): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8420): Show |
1 | a0001c0001t0001g0298 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8425): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8431): Show |
1 | a0001c0001t0001g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8436): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8430): Show |
1 | a0001c0001t0001g0070 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8435): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8423): Show |
1 | a0001c0001t0001g0067 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8428): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8412): Show |
1 | a0001c0001t0001g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8417): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8413): Show |
1 | a0001c0001t0001g0072 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8418): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8422): Show |
1 | a0001c0001t0001g0315 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8427): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8421): Show |
3 | a0001c0001t0001g0316 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG03139.hp1 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8419): Show |
1 | a0001c0001t0001g0319 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8424): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8457): Show |
1 | a0001c0001t0001g0253 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8462): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8454): Show |
1 | a0001c0001t0001g0184 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8459): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8448): Show |
1 | a0001c0001t0001g0180 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8453): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8446): Show |
2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | NA19010.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8451): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8446): Show |
1 | a0001c0001t0001g0210 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8451): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8444): Show |
1 | a0001c0001t0001g0185 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8449): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8444): Show |
1 | a0001c0001t0001g0177 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8449): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8443): Show |
1 | a0001c0001t0001g0195 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8448): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8444): Show |
1 | a0001c0001t0001g0170 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8449): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8442): Show |
1 | a0001c0001t0001g0197 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8447): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8441): Show |
1 | a0001c0001t0001g0178 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8446): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8441): Show |
1 | a0001c0001t0001g0154 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8446): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8440): Show |
1 | a0001c0001t0001g0244 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8445): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8439): Show |
2 | a0001c0001t0001g0160 a0001c0001t0001g0175 |
2 | NA18941.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8444): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8436): Show |
1 | a0001c0001t0001g0153 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8441): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8437): Show |
2 | a0001c0001t0001g0192 a0001c0001t0001g0194 |
2 | HG01258.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8442): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8435): Show |
3 | a0001c0001t0001g0157 a0001c0001t0001g0174 a0001c0001t0001g0179 |
3 | HG00621.hp1 HG02523.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8440): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8434): Show |
3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0191 |
3 | NA18942.hp1 NA18964.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8439): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8434): Show |
1 | a0001c0001t0001g0156 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8439): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8432): Show |
3 | a0001c0001t0001g0117 a0001c0001t0001g0151 a0001c0001t0001g0199 |
3 | NA18962.hp2 NA18982.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8437): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8434): Show |
2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8439): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8431): Show |
1 | a0001c0001t0001g0165 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8436): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8430): Show |
1 | a0001c0001t0001g0155 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8435): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8429): Show |
1 | a0001c0001t0001g0168 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8434): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8430): Show |
1 | a0001c0001t0001g0110 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8435): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8430): Show |
3 | a0001c0001t0001g0131 a0001c0001t0001g0152 a0001c0001t0001g0202 |
3 | HG04228.hp1 NA19000.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8435): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8429): Show |
4 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0142 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8434): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8429): Show |
1 | a0001c0001t0001g0123 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8434): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8430): Show |
1 | a0001c0001t0001g0136 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8435): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8430): Show |
1 | a0001c0001t0001g0099 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8435): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8429): Show |
1 | a0001c0001t0001g0201 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8434): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8428): Show |
4 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0001g0204 others(1): Show |
4 | HG00558.hp1 HG02132.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8433): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8429): Show |
2 | a0001c0001t0001g0096 a0001c0001t0001g0161 |
2 | NA19067.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8434): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8428): Show |
1 | a0001c0001t0001g0078 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8433): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8426): Show |
1 | a0001c0001t0001g0190 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8431): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8428): Show |
1 | a0001c0001t0001g0074 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8433): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8427): Show |
1 | a0001c0001t0001g0125 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8432): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8427): Show |
3 | a0001c0001t0001g0124 a0001c0001t0001g0129 a0001c0001t0001g0138 |
3 | HG02559.hp2 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8432): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8428): Show |
6 | a0001c0001t0001g0087 a0001c0001t0001g0105 a0001c0001t0001g0113 others(3): Show |
6 | HG00621.hp2 HG01975.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8433): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8428): Show |
2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | NA18941.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8433): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8429): Show |
1 | a0001c0001t0001g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8434): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8427): Show |
1 | a0001c0001t0001g0090 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8432): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8427): Show |
1 | a0001c0001t0001g0103 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8432): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8427): Show |
1 | a0001c0001t0001g0097 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8432): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8426): Show |
1 | a0001c0001t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8431): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8426): Show |
1 | a0001c0001t0001g0091 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8431): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8427): Show |
9 | a0001c0001t0001g0075 a0001c0001t0001g0089 a0001c0001t0001g0093 others(6): Show |
9 | HG00408.hp1 HG00735.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8432): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8418): Show |
1 | a0001c0001t0001g0198 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8423): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8427): Show |
1 | a0001c0001t0001g0076 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8432): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8427): Show |
2 | a0001c0001t0001g0108 a0001c0001t0001g0132 |
2 | HG00609.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8432): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8428): Show |
1 | a0001c0001t0001g0100 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8433): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8428): Show |
1 | a0001c0001t0001g0104 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8433): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8426): Show |
4 | a0001c0001t0001g0092 a0001c0001t0001g0118 a0001c0001t0001g0182 others(1): Show |
4 | NA18943.hp1 NA18943.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8431): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8426): Show |
1 | a0001c0001t0001g0106 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8431): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8427): Show |
1 | a0001c0001t0001g0115 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8432): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8429): Show |
1 | a0001c0001t0001g0128 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8434): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8426): Show |
9 | a0001c0001t0001g0098 a0001c0001t0001g0111 a0001c0001t0001g0114 others(6): Show |
9 | HG00140.hp1 HG00738.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8431): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8424): Show |
1 | a0001c0001t0001g0088 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8429): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8426): Show |
1 | a0001c0001t0001g0077 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8431): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8426): Show |
1 | a0001c0001t0001g0133 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8431): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8425): Show |
1 | a0001c0001t0001g0120 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8425): Show |
2 | a0001c0001t0001g0086 a0001c0001t0001g0094 |
2 | HG00438.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8425): Show |
1 | a0001c0001t0001g0109 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8427): Show |
1 | a0001c0001t0001g0250 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8432): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8425): Show |
1 | a0001c0001t0001g0150 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8422): Show |
1 | a0001c0001t0001g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8427): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8421): Show |
3 | a0001c0001t0001g0162 a0001c0001t0001g0171 a0001c0001t0001g0203 |
3 | NA19009.hp1 NA19066.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8420): Show |
3 | a0001c0001t0001g0163 a0001c0001t0001g0173 a0001c0001t0001g0183 |
3 | HG02083.hp2 NA18946.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8425): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8421): Show |
1 | a0001c0001t0001g0159 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8418): Show |
1 | a0001c0001t0001g0134 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8423): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8418): Show |
1 | a0001c0001t0001g0149 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8423): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8419): Show |
1 | a0001c0001t0001g0148 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8424): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8420): Show |
1 | a0001c0001t0001g0259 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8425): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8418): Show |
1 | a0001c0001t0001g0147 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8423): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8417): Show |
2 | a0001c0001t0001g0164 a0001c0001t0001g0196 |
2 | NA18953.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8422): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8418): Show |
1 | a0001c0001t0001g0181 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8423): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8416): Show |
1 | a0001c0001t0001g0193 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8421): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8415): Show |
1 | a0001c0001t0001g0158 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8420): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8415): Show |
1 | a0001c0001t0001g0200 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8420): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8415): Show |
2 | a0001c0001t0001g0079 a0001c0001t0001g0082 |
2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8420): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8414): Show |
1 | a0001c0001t0001g0172 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8419): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8412): Show |
1 | a0001c0001t0001g0176 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8417): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8412): Show |
1 | a0001c0001t0001g0207 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8417): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8416): Show |
1 | a0002c0002t0001g0257 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8421): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8415): Show |
1 | a0002c0002t0001g0255 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8420): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8414): Show |
2 | a0002c0002t0001g0256 a0002c0002t0001g0258 |
2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8419): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8406): Show |
1 | a0001c0001t0001g0187 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8411): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8426): Show |
2 | a0001c0001t0001g0143 a0001c0001t0001g0145 |
2 | HG01258.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8431): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8424): Show |
1 | a0001c0001t0001g0083 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8429): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8450): Show |
1 | a0001c0001t0001g0231 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8455): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8440): Show |
2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8445): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8439): Show |
1 | a0001c0001t0001g0219 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8444): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8435): Show |
6 | a0001c0001t0001g0227 a0001c0001t0001g0230 a0001c0001t0001g0235 others(3): Show |
6 | HG02698.hp2 HG03491.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8440): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8435): Show |
2 | a0001c0001t0001g0234 a0001c0001t0001g0236 |
2 | HG01192.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8440): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8434): Show |
1 | a0001c0001t0001g0225 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8439): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8434): Show |
5 | a0001c0001t0001g0228 a0001c0001t0001g0233 a0001c0001t0001g0238 others(2): Show |
5 | HG00733.hp1 HG01496.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8439): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8433): Show |
1 | a0001c0001t0001g0242 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8438): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8431): Show |
1 | a0001c0001t0001g0214 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8436): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8433): Show |
1 | a0001c0001t0001g0212 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8438): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8431): Show |
1 | a0001c0001t0001g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8436): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8425): Show |
1 | a0001c0001t0001g0218 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8425): Show |
1 | a0001c0001t0001g0232 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8425): Show |
3 | a0001c0001t0001g0024 a0001c0001t0001g0046 a0001c0001t0001g0068 |
3 | HG01167.hp2 HG01192.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8425): Show |
1 | a0001c0001t0001g0031 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8426): Show |
1 | a0001c0001t0001g0062 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8431): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8423): Show |
1 | a0001c0001t0001g0032 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8428): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8424): Show |
2 | a0001c0001t0001g0018 a0001c0001t0001g0022 |
2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8429): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8425): Show |
2 | a0001c0001t0001g0040 a0001c0001t0001g0051 |
2 | HG02027.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8424): Show |
1 | a0001c0001t0001g0060 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8429): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8424): Show |
1 | a0001c0001t0001g0026 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8429): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8424): Show |
15 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0014 others(12): Show |
15 | HG00609.hp2 HG00738.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8429): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8424): Show |
1 | a0001c0001t0001g0061 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8429): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8425): Show |
1 | a0001c0001t0001g0050 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8424): Show |
2 | a0001c0001t0001g0030 a0001c0001t0001g0036 |
2 | NA18968.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8429): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8425): Show |
1 | a0001c0001t0001g0064 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8430): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8422): Show |
1 | a0001c0001t0001g0226 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8427): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8414): Show |
1 | a0001c0001t0001g0065 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8419): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8422): Show |
4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0048 others(1): Show |
4 | HG01070.hp2 HG02735.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8427): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8424): Show |
2 | a0001c0001t0001g0038 a0001c0001t0001g0058 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8429): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8423): Show |
24 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(21): Show |
24 | HG00099.hp2 HG00558.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8428): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8424): Show |
1 | a0001c0001t0001g0029 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8429): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8422): Show |
1 | a0001c0001t0001g0063 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8427): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8423): Show |
2 | a0001c0001t0001g0008 a0001c0001t0001g0011 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8428): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8414): Show |
1 | a0001c0001t0001g0028 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8419): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8421): Show |
1 | a0001c0001t0001g0006 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8426): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8417): Show |
1 | a0001c0001t0001g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8422): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8418): Show |
1 | a0001c0001t0001g0229 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8423): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8416): Show |
1 | a0001c0001t0001g0224 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8421): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8415): Show |
1 | a0001c0001t0001g0222 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8420): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8415): Show |
1 | a0001c0001t0001g0215 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8420): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8415): Show |
2 | a0001c0001t0001g0221 a0001c0001t0001g0223 |
2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.824-88_824-87insTG others(8420): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8416): Show |
1 | a0001c0001t0001g0220 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8421): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976066 | C | CAGCTGGG others(8444): Show |
1 | a0001c0001t0001g0240 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.824-88_824-87insTG others(8449): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 171976066 | ||||||
| chr2:171976322 | G | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.975+14G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171976322 | |||||||
| chr2:171976496 | G | C | 6 | a0001c0001t0001g0215 a0001c0001t0001g0220 a0001c0001t0001g0221 others(3): Show |
6 | HG01256.hp2 HG02004.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.975+188G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171976496 | |||||||
| chr2:171976529 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.975+221C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171976529 | |||||||
| chr2:171976678 | C | T | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.975+370C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171976678 | |||||||
| chr2:171976692 | T | C | 2 | a0001c0001t0001g0317 a0001c0001t0001g0318 |
2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.975+384T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171976692 | |||||||
| chr2:171976991 | T | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0261 others(54): Show |
58 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.975+683T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171976991 | |||||||
| chr2:171977065 | G | A | 5 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0280 others(2): Show |
5 | HG02622.hp2 HG02647.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.975+757G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977065 | |||||||
| chr2:171977160 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.975+852G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977160 | |||||||
| chr2:171977401 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0261 others(61): Show |
65 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.975+1093G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977401 | |||||||
| chr2:171977439 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.975+1131G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977439 | |||||||
| chr2:171977461 | T | TA | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(67): Show |
70 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.975+1167dupA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977461 | ||||||
| chr2:171977467 | A | G | 5 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0280 others(2): Show |
5 | HG02622.hp2 HG02647.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.975+1159A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977467 | |||||||
| chr2:171977524 | A | AAAATATA others(9): Show |
1 | a0001c0001t0001g0238 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.975+1217_975+1218i others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | ||||||
| chr2:171977524 | A | AAAATATA others(13): Show |
1 | a0001c0001t0001g0237 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.975+1217_975+1218i others(22): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | ||||||
| chr2:171977524 | A | AAAATATA others(23): Show |
1 | a0001c0001t0001g0235 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.975+1217_975+1218i others(32): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | ||||||
| chr2:171977524 | A | AAT | 8 | a0001c0001t0001g0077 a0001c0001t0001g0105 a0001c0001t0001g0106 others(5): Show |
8 | HG00621.hp2 HG02132.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.975+1249_975+1250d others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | ||||||
| chr2:171977524 | A | AATAT | 3 | a0001c0001t0001g0091 a0001c0001t0001g0104 a0001c0001t0001g0219 |
3 | HG04199.hp2 NA18949.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.975+1247_975+1250d others(6): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | ||||||
| chr2:171977524 | A | AATATAT | 5 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0220 others(2): Show |
5 | HG02004.hp1 HG02922.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.975+1245_975+1250d others(8): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | ||||||
| chr2:171977524 | A | AATATATA others(3): Show |
2 | a0001c0001t0001g0225 a0001c0001t0001g0233 |
2 | HG01099.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.975+1241_975+1250d others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | ||||||
| chr2:171977524 | A | AATATATA others(5): Show |
2 | a0001c0001t0001g0165 a0001c0001t0001g0218 |
2 | HG00099.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.975+1239_975+1250d others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | ||||||
| chr2:171977524 | A | AATATATA others(7): Show |
3 | a0001c0001t0001g0224 a0001c0001t0001g0240 a0001c0001t0001g0252 |
3 | HG01981.hp2 HG02738.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.975+1237_975+1250d others(16): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | ||||||
| chr2:171977524 | A | AATATATA others(9): Show |
1 | a0001c0001t0001g0243 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.975+1235_975+1250d others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | ||||||
| chr2:171977524 | A | AATATATA others(11): Show |
1 | a0001c0001t0001g0226 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.975+1233_975+1250d others(20): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977524 | ||||||
| chr2:171977525 | ATATATAT others(35): Show |
A | 1 | a0001c0001t0001g0228 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.975+1219_975+1260d others(44): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977525 | ||||||
| chr2:171977526 | T | A | 1 | a0001c0001t0001g0251 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.975+1218T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977526 | |||||||
| chr2:171977535 | ATATATAT others(29): Show |
A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.975+1229_975+1264d others(38): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977535 | ||||||
| chr2:171977539 | ATATATAT others(23): Show |
A | 14 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 others(11): Show |
14 | HG02486.hp2 HG02572.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.975+1233_975+1262d others(32): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977539 | ||||||
| chr2:171977539 | ATATATAT others(24): Show |
A | 2 | a0001c0001t0001g0283 a0001c0001t0001g0319 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.975+1233_975+1263d others(33): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977539 | ||||||
| chr2:171977541 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0229 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.975+1235_975+1258d others(26): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977541 | ||||||
| chr2:171977541 | ATATATAT others(23): Show |
A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0261 others(45): Show |
49 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.975+1235_975+1264d others(32): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977541 | ||||||
| chr2:171977542 | TATATATA others(4): Show |
T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0191 |
2 | NA18964.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.975+1235_975+1245d others(13): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977542 | |||||||
| chr2:171977544 | TATATATA others(4): Show |
T | 1 | a0001c0001t0001g0168 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.975+1237_975+1247d others(13): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977544 | |||||||
| chr2:171977551 | ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0234 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.975+1245_975+1256d others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977551 | ||||||
| chr2:171977553 | A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0008 a0001c0001t0001g0011 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.975+1246_975+1247i others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977553 | ||||||
| chr2:171977553 | A | T | 1 | a0001c0001t0001g0197 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.975+1245A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977553 | |||||||
| chr2:171977553 | ATATATTT others(3): Show |
A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0236 |
2 | HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.975+1247_975+1256d others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977553 | ||||||
| chr2:171977555 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0061 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.975+1248_975+1249i others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977555 | ||||||
| chr2:171977555 | A | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0014 others(7): Show |
10 | HG01192.hp1 HG02056.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.975+1247A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977555 | |||||||
| chr2:171977555 | ATATTTTT others(5): Show |
A | 1 | a0001c0001t0001g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.975+1249_975+1260d others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977555 | ||||||
| chr2:171977557 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0206 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(31): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(15): Show |
3 | a0001c0001t0001g0134 a0001c0001t0001g0166 a0001c0001t0001g0207 |
3 | NA18963.hp1 NA18986.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(24): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(26): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0190 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(30): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0231 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(22): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0200 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(26): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0180 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(28): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0175 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(26): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0174 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0153 a0001c0001t0001g0192 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(23): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0195 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(24): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0148 a0001c0001t0001g0156 |
2 | HG02056.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(19): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0183 a0001c0001t0001g0313 |
2 | HG02083.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(20): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(12): Show |
3 | a0001c0001t0001g0157 a0001c0001t0001g0160 a0001c0001t0001g0172 |
3 | HG00323.hp1 HG02523.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(21): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0196 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(22): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0092 a0001c0001t0001g0189 |
2 | NA18943.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(24): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0177 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(25): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0151 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(26): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0186 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(17): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0152 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(11): Show |
3 | a0001c0001t0001g0185 a0001c0001t0001g0198 a0001c0001t0001g0244 |
3 | HG00408.hp2 HG02027.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(20): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0194 a0001c0001t0001g0199 |
2 | NA18747.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(21): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0158 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(23): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0150 a0001c0001t0001g0178 |
2 | NA18990.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(24): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0171 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(26): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0176 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0154 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(16): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0161 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(17): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0179 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0202 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(20): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG00597.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(21): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0159 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(22): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0173 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(23): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0120 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0021 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(13): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0188 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(16): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0022 a0001c0001t0001g0259 a0001c0001t0001g0260 |
3 | HG03209.hp2 NA19063.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(17): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0147 a0001c0001t0001g0182 a0001c0001t0001g0184 |
3 | NA18968.hp1 NA18983.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0170 a0001c0001t0001g0201 |
2 | NA18966.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(19): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0208 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(20): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0162 a0001c0001t0001g0203 |
2 | NA19009.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(22): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(3): Show |
2 | a0001c0001t0001g0036 a0001c0001t0001g0253 |
2 | NA18981.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(4): Show |
2 | a0002c0002t0001g0257 a0002c0002t0001g0258 |
2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(13): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(5): Show |
4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0312 others(1): Show |
4 | HG01109.hp2 HG01517.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+1250_975+1251i others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0167 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(16): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0193 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(17): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0164 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(18): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATTT others(2): Show |
6 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0030 others(3): Show |
6 | HG01975.hp1 HG02735.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.975+1250_975+1251i others(11): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATTT others(3): Show |
3 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG02027.hp1 HG03942.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATTT others(4): Show |
5 | a0001c0001t0001g0023 a0001c0001t0001g0038 a0001c0001t0001g0057 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.975+1250_975+1251i others(13): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATTT others(5): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0066 |
2 | HG01168.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATATTT others(7): Show |
1 | a0001c0001t0001g0155 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(16): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATTTTT others(3): Show |
3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0047 |
3 | HG00609.hp2 NA18952.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATTTTT others(4): Show |
2 | a0001c0001t0001g0018 a0001c0001t0001g0060 |
2 | HG01074.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(13): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATATTTTT others(5): Show |
1 | a0001c0001t0001g0204 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(14): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATTTTTTT others(1): Show |
8 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0029 others(5): Show |
8 | HG00738.hp2 HG01070.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.975+1264_975+1271d others(10): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | ATTTTTTT others(3): Show |
4 | a0001c0001t0001g0026 a0001c0001t0001g0045 a0001c0001t0001g0048 others(1): Show |
4 | HG00735.hp1 NA18949.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.975+1262_975+1271d others(12): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | A | T | 26 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
26 | HG01192.hp1 HG01978.hp2 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.975+1249A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977557 | |||||||
| chr2:171977557 | AT | A | 14 | a0001c0001t0001g0074 a0001c0001t0001g0094 a0001c0001t0001g0095 others(11): Show |
14 | HG00140.hp1 HG00609.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.975+1271delT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977557 | ATTT | A | 6 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0124 others(3): Show |
6 | HG01361.hp2 HG02300.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.975+1269_975+1271d others(5): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171977557 | ||||||
| chr2:171977558 | T | TA | 14 | a0001c0001t0001g0078 a0001c0001t0001g0086 a0001c0001t0001g0088 others(11): Show |
14 | HG00408.hp1 HG00438.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.975+1250_975+1251i others(3): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977558 | |||||||
| chr2:171977558 | T | TATATATA | 3 | a0001c0001t0001g0099 a0001c0001t0001g0108 a0001c0001t0001g0133 |
3 | HG01168.hp2 NA19007.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(9): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977558 | |||||||
| chr2:171977558 | T | TATATATA others(6): Show |
1 | a0001c0001t0001g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(15): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977558 | |||||||
| chr2:171977558 | T | TATATATA others(8): Show |
1 | a0001c0001t0001g0232 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.975+1250_975+1251i others(17): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977558 | |||||||
| chr2:171977558 | T | TATATATA others(12): Show |
2 | a0001c0001t0001g0187 a0001c0001t0001g0251 |
2 | HG03654.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.975+1250_975+1251i others(21): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977558 | |||||||
| chr2:171977558 | T | TATATATA others(16): Show |
1 | a0001c0001t0001g0214 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.975+1250_975+1251i others(25): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977558 | |||||||
| chr2:171977559 | T | A | 34 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0091 others(31): Show |
34 | HG00099.hp1 HG00621.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.975+1251T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977559 | |||||||
| chr2:171977560 | T | A | 25 | a0001c0001t0001g0086 a0001c0001t0001g0099 a0001c0001t0001g0100 others(22): Show |
25 | HG00438.hp2 HG00609.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.975+1252T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977560 | |||||||
| chr2:171977561 | T | A | 25 | a0001c0001t0001g0075 a0001c0001t0001g0091 a0001c0001t0001g0103 others(22): Show |
25 | HG00099.hp1 HG01099.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.975+1253T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977561 | |||||||
| chr2:171977562 | T | A | 18 | a0001c0001t0001g0076 a0001c0001t0001g0100 a0001c0001t0001g0101 others(15): Show |
18 | HG00609.hp1 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.975+1254T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977562 | |||||||
| chr2:171977563 | T | A | 17 | a0001c0001t0001g0091 a0001c0001t0001g0149 a0001c0001t0001g0212 others(14): Show |
17 | HG00099.hp1 HG01099.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.975+1255T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977563 | |||||||
| chr2:171977564 | T | A | 5 | a0001c0001t0001g0130 a0001c0001t0001g0140 a0001c0001t0001g0211 others(2): Show |
5 | HG00738.hp1 HG02300.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.975+1256T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977564 | |||||||
| chr2:171977565 | T | A | 7 | a0001c0001t0001g0149 a0001c0001t0001g0215 a0001c0001t0001g0220 others(4): Show |
7 | HG01256.hp2 HG02622.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.975+1257T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977565 | |||||||
| chr2:171977566 | T | A | 4 | a0001c0001t0001g0070 a0001c0001t0001g0211 a0001c0001t0001g0221 others(1): Show |
4 | HG01943.hp2 HG03017.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+1258T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977566 | |||||||
| chr2:171977567 | T | A | 3 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0242 |
3 | HG02622.hp1 HG03453.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.975+1259T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977567 | |||||||
| chr2:171977568 | T | A | 4 | a0001c0001t0001g0070 a0001c0001t0001g0211 a0001c0001t0001g0221 others(1): Show |
4 | HG01943.hp2 HG03017.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+1260T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977568 | |||||||
| chr2:171977569 | T | A | 2 | a0001c0001t0001g0224 a0001c0001t0001g0242 |
2 | HG02622.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.975+1261T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977569 | |||||||
| chr2:171977572 | T | C | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.975+1264T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977572 | |||||||
| chr2:171977670 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.975+1362C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977670 | |||||||
| chr2:171977710 | C | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.975+1402C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977710 | |||||||
| chr2:171977894 | T | C | 3 | a0001c0001t0001g0134 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | NA18963.hp1 NA19057.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.976-1353T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977894 | |||||||
| chr2:171977957 | T | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | HG02615.hp1 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.976-1290T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171977957 | |||||||
| chr2:171978059 | C | CT | 69 | a0001c0001t0001g0047 a0001c0001t0001g0074 a0001c0001t0001g0075 others(66): Show |
69 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.976-1173dupT | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171978059 | ||||||
| chr2:171978128 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.976-1119G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171978128 | |||||||
| chr2:171978172 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | NA18986.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.976-1075C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171978172 | |||||||
| chr2:171978213 | C | T | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(68): Show |
71 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.976-1034C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171978213 | |||||||
| chr2:171978369 | T | G | 31 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(28): Show |
31 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.976-878T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171978369 | |||||||
| chr2:171978438 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.976-809C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171978438 | |||||||
| chr2:171978562 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.976-685C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171978562 | |||||||
| chr2:171978579 | C | CTGAG | 68 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0070 others(65): Show |
69 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.976-667_976-666ins others(4): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171978579 | ||||||
| chr2:171978671 | G | C | 3 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 |
3 | HG02723.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.976-576G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171978671 | |||||||
| chr2:171978695 | T | G | 13 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0001t0001g0160 others(10): Show |
13 | HG02056.hp2 NA18941.hp2 NA18946.hp2 others(10): Show |
intron_variant | MODIFIER | c.976-552T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171978695 | |||||||
| chr2:171978922 | C | CA | 33 | a0001c0001t0001g0027 a0001c0001t0001g0124 a0001c0001t0001g0125 others(30): Show |
33 | HG00558.hp1 HG00733.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.976-304dupA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 171978922 | ||||||
| chr2:171979046 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0270 others(28): Show |
32 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.976-201G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171979046 | |||||||
| chr2:171979090 | C | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.976-157C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171979090 | |||||||
| chr2:171979240 | A | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0058 |
2 | HG01069.hp1 HG01071.hp1 |
splice_region_variant&intron_variant | LOW | c.976-7A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 9/10 | chr2 | 171979240 | |||||||
| chr2:171979450 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1092+87T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171979450 | |||||||
| chr2:171979516 | T | G | 1 | a0001c0001t0001g0242 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1092+153T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171979516 | |||||||
| chr2:171979559 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1092+196G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171979559 | |||||||
| chr2:171979678 | G | A | 5 | a0001c0001t0001g0039 a0001c0001t0001g0045 a0001c0001t0001g0047 others(2): Show |
5 | HG00609.hp2 NA18949.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1092+315G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171979678 | |||||||
| chr2:171979754 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1092+391C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171979754 | |||||||
| chr2:171979806 | T | TGAAAA | 3 | a0001c0001t0001g0079 a0001c0001t0001g0082 a0001c0001t0001g0182 |
3 | HG02809.hp2 HG02970.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1092+464_1092+468d others(7): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr2 | 171979806 | ||||||
| chr2:171979999 | C | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0065 |
2 | HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1092+636C>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171979999 | |||||||
| chr2:171980111 | T | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1092+748T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980111 | |||||||
| chr2:171980419 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1092+1056A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980419 | |||||||
| chr2:171980622 | G | A | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0320 |
3 | HG01074.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1092+1259G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980622 | |||||||
| chr2:171980681 | C | A | 1 | a0001c0001t0001g0015 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1092+1318C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980681 | |||||||
| chr2:171980855 | C | CA | 6 | a0001c0001t0001g0156 a0001c0001t0001g0165 a0001c0001t0001g0205 others(3): Show |
6 | HG02056.hp2 HG02074.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1092+1508dupA | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr2 | 171980855 | ||||||
| chr2:171980871 | A | T | 1 | a0001c0001t0001g0279 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1092+1508A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980871 | |||||||
| chr2:171980873 | T | A | 1 | a0001c0001t0001g0279 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1092+1510T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980873 | |||||||
| chr2:171980873 | T | TA | 59 | a0001c0001t0001g0001 a0001c0001t0001g0261 a0001c0001t0001g0262 others(56): Show |
60 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.1092+1510_1092+151 others(5): Show |
HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980873 | |||||||
| chr2:171980874 | T | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0070 others(65): Show |
69 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.1092+1511T>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980874 | |||||||
| chr2:171980875 | A | T | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0231 |
3 | HG03942.hp2 NA18986.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1092+1512A>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980875 | |||||||
| chr2:171980941 | G | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(66): Show |
69 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.1092+1578G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980941 | |||||||
| chr2:171980976 | C | T | 68 | a0001c0001t0001g0134 a0001c0001t0001g0147 a0001c0001t0001g0148 others(65): Show |
68 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1092+1613C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171980976 | |||||||
| chr2:171981112 | G | T | 1 | a0001c0001t0001g0275 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1092+1749G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171981112 | |||||||
| chr2:171981332 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1093-1853T>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171981332 | |||||||
| chr2:171981343 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0070 others(65): Show |
69 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.1093-1842G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171981343 | |||||||
| chr2:171982039 | G | C | 1 | a0001c0001t0001g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1093-1146G>C | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171982039 | |||||||
| chr2:171982203 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1093-982A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171982203 | |||||||
| chr2:171982589 | C | T | 3 | a0001c0001t0001g0220 a0001c0001t0001g0222 a0001c0001t0001g0224 |
3 | HG02004.hp1 HG06807.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1093-596C>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171982589 | |||||||
| chr2:171982912 | T | G | 1 | a0001c0001t0001g0096 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1093-273T>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171982912 | |||||||
| chr2:171982914 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1093-271G>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171982914 | |||||||
| chr2:171982915 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1093-270A>G | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171982915 | |||||||
| chr2:171983049 | C | A | 1 | a0001c0001t0001g0148 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1093-136C>A | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171983049 | |||||||
| chr2:171983081 | G | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0270 others(29): Show |
33 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.1093-104G>T | HAT1 | ENSG00000128708.13 | transcript | ENST00000264108.5 | protein_coding | 10/10 | chr2 | 171983081 |