Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64427 |
| ensemblid | ENSG00000115282.21 |
| hgncid | 25759 |
| symbol | TTC31 |
| name | tetratricopeptide repeat domain 31 |
| refseq_nuc | NM_022492.6 |
| refseq_prot | NP_071937.4 |
| ensembl_nuc | ENST00000233623.11 |
| ensembl_prot | ENSP00000233623.6 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 74483081 |
| end | 74494559 |
| strand | + |
| ver | v1.2 |
| region | chr2:74483081-74494559 |
| region5000 | chr2:74478081-74499559 |
| regionname0 | TTC31_chr2_74483081_74494559 |
| regionname5000 | TTC31_chr2_74478081_74499559 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 519 | 192 | 75 | 29 | 75 | 2 | 10 | 58 | TTC31_chr2_74478081_74499559 | TTC31 | MAPIP others(514): Show |
chr2 | 74478081 | 74499559 |
| a0002 | 1/0 | 519 | 121 | 15 | 38 | 36 | 12 | 19 | 30 | TTC31_chr2_74478081_74499559 | TTC31 | MAPIP others(514): Show |
chr2 | 74478081 | 74499559 |
| a0003 | 0/0 | 519 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | MAPIP others(514): Show |
chr2 | 74478081 | 74499559 |
| a0004 | 0/0 | 519 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | MAPIP others(514): Show |
chr2 | 74478081 | 74499559 |
| a0005 | 0/0 | 519 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | MAPIP others(514): Show |
chr2 | 74478081 | 74499559 |
| a0006 | 0/0 | 519 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | MAPIP others(514): Show |
chr2 | 74478081 | 74499559 |
| a0007 | 0/0 | 519 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | MAPIP others(514): Show |
chr2 | 74478081 | 74499559 |
| a0008 | 0/0 | 519 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | MAPIP others(514): Show |
chr2 | 74478081 | 74499559 |
| a0009 | 0/0 | 486 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | MAPIP others(481): Show |
chr2 | 74478081 | 74499559 |
| a0010 | 0/0 | 519 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | MAPIP others(514): Show |
chr2 | 74478081 | 74499559 |
| a0011 | 0/0 | 519 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | MAPIP others(514): Show |
chr2 | 74478081 | 74499559 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1557 | 191 | 74 | 29 | 75 | 2 | 10 | TTC31_chr2_74478081_74499559 | TTC31 | ATGGC others(1552): Show |
chr2 | 74478081 | 74499559 | ||
| a0001c0010 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | ATGGC others(1552): Show |
chr2 | 74478081 | 74499559 | ||
| a0002c0002 | 1/0 | 1557 | 121 | 15 | 38 | 36 | 12 | 19 | TTC31_chr2_74478081_74499559 | TTC31 | ATGGC others(1552): Show |
chr2 | 74478081 | 74499559 | ||
| a0003c0003 | 0/0 | 1557 | 5 | 5 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | ATGGC others(1552): Show |
chr2 | 74478081 | 74499559 | ||
| a0004c0004 | 0/0 | 1557 | 3 | 2 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | ATGGC others(1552): Show |
chr2 | 74478081 | 74499559 | ||
| a0005c0008 | 0/0 | 1557 | 2 | 1 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | ATGGC others(1552): Show |
chr2 | 74478081 | 74499559 | ||
| a0006c0007 | 0/0 | 1557 | 2 | 0 | 0 | 0 | 0 | 2 | TTC31_chr2_74478081_74499559 | TTC31 | ATGGC others(1552): Show |
chr2 | 74478081 | 74499559 | ||
| a0007c0005 | 0/0 | 1557 | 2 | 0 | 0 | 0 | 0 | 2 | TTC31_chr2_74478081_74499559 | TTC31 | ATGGC others(1552): Show |
chr2 | 74478081 | 74499559 | ||
| a0008c0006 | 0/0 | 1557 | 2 | 0 | 0 | 0 | 0 | 2 | TTC31_chr2_74478081_74499559 | TTC31 | ATGGC others(1552): Show |
chr2 | 74478081 | 74499559 | ||
| a0009c0009 | 0/0 | 1458 | 1 | 0 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | ATGGC others(1453): Show |
chr2 | 74478081 | 74499559 | ||
| a0010c0012 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | ATGGC others(1552): Show |
chr2 | 74478081 | 74499559 | ||
| a0011c0011 | 0/0 | 1557 | 1 | 0 | 0 | 0 | 0 | 1 | TTC31_chr2_74478081_74499559 | TTC31 | ATGGC others(1552): Show |
chr2 | 74478081 | 74499559 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2916 | 180 | 67 | 27 | 73 | 2 | 10 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2911): Show |
chr2 | 74478081 | 74499559 |
| a0001c0001t0003 | 0/0 | 2916 | 4 | 3 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2911): Show |
chr2 | 74478081 | 74499559 |
| a0001c0001t0004 | 0/0 | 2916 | 2 | 1 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2911): Show |
chr2 | 74478081 | 74499559 |
| a0001c0001t0005 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2911): Show |
chr2 | 74478081 | 74499559 |
| a0001c0001t0007 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2911): Show |
chr2 | 74478081 | 74499559 |
| a0001c0001t0008 | 0/0 | 2916 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2911): Show |
chr2 | 74478081 | 74499559 |
| a0001c0001t0009 | 0/0 | 2916 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2911): Show |
chr2 | 74478081 | 74499559 |
| a0001c0001t0010 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2911): Show |
chr2 | 74478081 | 74499559 |
| a0001c0010t0001 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2911): Show |
chr2 | 74478081 | 74499559 |
| a0002c0002t0002 | 1/0 | 2916 | 119 | 15 | 37 | 35 | 12 | 19 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2911): Show |
chr2 | 74478081 | 74499559 |
| a0002c0002t0006 | 0/0 | 2916 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2911): Show |
chr2 | 74478081 | 74499559 |
| a0002c0002t0011 | 0/0 | 2916 | 1 | 0 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2911): Show |
chr2 | 74478081 | 74499559 |
| a0003c0003t0001 | 0/0 | 2916 | 5 | 5 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2911): Show |
chr2 | 74478081 | 74499559 |
| a0004c0004t0001 | 0/0 | 2916 | 3 | 2 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2911): Show |
chr2 | 74478081 | 74499559 |
| a0005c0008t0002 | 0/0 | 2916 | 2 | 1 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2911): Show |
chr2 | 74478081 | 74499559 |
| a0006c0007t0002 | 0/0 | 2916 | 2 | 0 | 0 | 0 | 0 | 2 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2911): Show |
chr2 | 74478081 | 74499559 |
| a0007c0005t0002 | 0/0 | 2916 | 2 | 0 | 0 | 0 | 0 | 2 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2911): Show |
chr2 | 74478081 | 74499559 |
| a0008c0006t0002 | 0/0 | 2916 | 2 | 0 | 0 | 0 | 0 | 2 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2911): Show |
chr2 | 74478081 | 74499559 |
| a0009c0009t0002 | 0/0 | 2817 | 1 | 0 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2812): Show |
chr2 | 74478081 | 74499559 |
| a0010c0012t0001 | 0/0 | 2916 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2911): Show |
chr2 | 74478081 | 74499559 |
| a0011c0011t0001 | 0/0 | 2916 | 1 | 0 | 0 | 0 | 0 | 1 | TTC31_chr2_74478081_74499559 | TTC31 | GTCAC others(2911): Show |
chr2 | 74478081 | 74499559 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 89 | 1 | 17 | 60 | 1 | 9 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0003 | 0/0 | 16 | 15 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0005 | 0/0 | 8 | 6 | 2 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0003g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0009g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0001t0010g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0001c0010t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0002 | 0/0 | 77 | 12 | 21 | 28 | 8 | 8 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0004 | 0/0 | 8 | 1 | 1 | 0 | 0 | 6 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0006 | 0/0 | 7 | 0 | 4 | 1 | 2 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0008 | 0/0 | 7 | 0 | 5 | 0 | 1 | 1 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0019 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0050 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0006g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0002c0002t0011g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0003c0003t0001g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0003c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0004c0004t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0004c0004t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0005c0008t0002g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0006c0007t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0006c0007t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0007c0005t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0008c0006t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0009c0009t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0010c0012t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| a0011c0011t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | GBR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | GBR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | FIN | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | FIN | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | FIN | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | FIN | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0022 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0049 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0070 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0042 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01081 | hp2 | a0002 | c0002 | t0011 | g0002 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01167 | hp1 | a0005 | c0008 | t0002 | g0004 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01243 | hp2 | a0004 | c0004 | t0001 | g0071 | AMR | PUR | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0043 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01496 | hp2 | a0009 | c0009 | t0002 | g0037 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0022 | EUR | IBS | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | IBS | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | IBS | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0008 | EUR | IBS | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PEL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | PEL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02080 | hp2 | a0010 | c0012 | t0001 | g0001 | EAS | KHV | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02083 | hp2 | a0002 | c0002 | t0006 | g0002 | EAS | KHV | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CDX | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0019 | SAS | PJL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02630 | hp1 | a0003 | c0003 | t0001 | g0001 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02738 | hp1 | a0006 | c0007 | t0002 | g0006 | SAS | PJL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02738 | hp2 | a0006 | c0007 | t0002 | g0064 | SAS | PJL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02895 | hp2 | a0003 | c0003 | t0001 | g0001 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0001 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0044 | AFR | ESN | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | ESN | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | ESN | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03098 | hp2 | a0004 | c0004 | t0001 | g0021 | AFR | MSL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0004 | AFR | ESN | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0054 | AFR | MSL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03453 | hp2 | a0003 | c0003 | t0001 | g0048 | AFR | MSL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03486 | hp2 | a0004 | c0004 | t0001 | g0021 | AFR | MSL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03491 | hp1 | a0007 | c0005 | t0002 | g0015 | SAS | PJL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0008 | SAS | PJL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0015 | SAS | PJL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03492 | hp2 | a0007 | c0005 | t0002 | g0015 | SAS | PJL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0045 | SAS | PJL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03669 | hp1 | a0011 | c0011 | t0001 | g0067 | SAS | PJL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0004 | SAS | PJL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0004 | SAS | PJL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0004 | SAS | BEB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | BEB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0046 | SAS | BEB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0004 | SAS | STU | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0004 | SAS | STU | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | BEB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0004 | SAS | STU | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG04199 | hp2 | a0008 | c0006 | t0002 | g0002 | SAS | STU | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | STU | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG04204 | hp2 | a0008 | c0006 | t0002 | g0002 | SAS | STU | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18964 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19001 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | LWK | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19043 | hp2 | a0003 | c0003 | t0001 | g0001 | AFR | LWK | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19055 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | ASW | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0006 | EUR | TSI | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0006 | EUR | TSI | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | TSI | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | GIH | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0039 | AMR | CLM | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02559 | hp1 | a0001 | c0010 | t0001 | g0001 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | MSL | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | USA | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA21309 | hp1 | a0005 | c0008 | t0002 | g0004 | AFR | LWK | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0047 | AFR | LWK | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0050 | REF | REF | TTC31_chr2_74478081_74499559 | TTC31 | chr2 | 74478081 | 74499559 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:74483364 | C | T | 5 | a0001 a0003 a0004 others(2): Show |
201 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(198): Show |
missense_variant | MODERATE | c.83C>T | p.Ala28Val | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/13 | 98/2916 | 83/1560 | 28/519 | chr2 | 74483364 | |||
| chr2:74490079 | C | T | 1 | a0010 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.184C>T | p.Arg62Trp | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 3/13 | 199/2916 | 184/1560 | 62/519 | chr2 | 74490079 | |||
| chr2:74491141 | G | A | 1 | a0007 | 2 | HG03491.hp1 HG03492.hp2 |
missense_variant | MODERATE | c.560G>A | p.Arg187Gln | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 6/13 | 575/2916 | 560/1560 | 187/519 | chr2 | 74491141 | |||
| chr2:74491314 | G | A | 1 | a0008 | 2 | HG04199.hp2 HG04204.hp2 |
missense_variant | MODERATE | c.623G>A | p.Gly208Glu | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 7/13 | 638/2916 | 623/1560 | 208/519 | chr2 | 74491314 | |||
| chr2:74491553 | C | T | 1 | a0003 | 5 | HG02630.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
missense_variant | MODERATE | c.757C>T | p.Arg253Cys | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 8/13 | 772/2916 | 757/1560 | 253/519 | chr2 | 74491553 | |||
| chr2:74492141 | T | G | 1 | a0009 | 1 | HG01496.hp2 | missense_variant&splice_region_variant | MODERATE | c.931T>G | p.Leu311Val | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 10/13 | 946/2916 | 931/1560 | 311/519 | chr2 | 74492141 | |||
| chr2:74492143 | GGGTACCA others(49): Show |
G | 1 | a0009 | 1 | HG01496.hp2 | frameshift_variant | HIGH | c.936_991delTACCAGCT others(48): Show |
p.Thr313fs | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 10/13 | 951/2916 | 936/1560 | 312/519 | INFO_REALIGN_3_PRIME | chr2 | 74492143 | ||
| chr2:74492201 | G | T | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.991G>T | p.Ala331Ser | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 10/13 | 1006/2916 | 991/1560 | 331/519 | chr2 | 74492201 | |||
| chr2:74492295 | CTTTATCA others(44): Show |
C | 1 | a0009 | 1 | HG01496.hp2 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.1020-8_1062delTTTA others(47): Show |
p.Leu341fs | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1020/1560 | 340/519 | chr2 | 74492295 | ||||
| chr2:74492365 | G | C | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1081G>C | p.Asp361His | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1096/2916 | 1081/1560 | 361/519 | chr2 | 74492365 | |||
| chr2:74492366 | A | C | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1082A>C | p.Asp361Ala | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1097/2916 | 1082/1560 | 361/519 | chr2 | 74492366 | |||
| chr2:74492368 | G | C | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1084G>C | p.Ala362Pro | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1099/2916 | 1084/1560 | 362/519 | chr2 | 74492368 | |||
| chr2:74492372 | A | C | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1088A>C | p.Gln363Pro | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1103/2916 | 1088/1560 | 363/519 | chr2 | 74492372 | |||
| chr2:74492373 | G | C | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1089G>C | p.Gln363His | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1104/2916 | 1089/1560 | 363/519 | chr2 | 74492373 | |||
| chr2:74492374 | G | C | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1090G>C | p.Val364Leu | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1105/2916 | 1090/1560 | 364/519 | chr2 | 74492374 | |||
| chr2:74492375 | T | C | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1091T>C | p.Val364Ala | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1106/2916 | 1091/1560 | 364/519 | chr2 | 74492375 | |||
| chr2:74492377 | G | C | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1093G>C | p.Ala365Pro | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1108/2916 | 1093/1560 | 365/519 | chr2 | 74492377 | |||
| chr2:74492381 | T | C | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1097T>C | p.Leu366Pro | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1112/2916 | 1097/1560 | 366/519 | chr2 | 74492381 | |||
| chr2:74492383 | A | C | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1099A>C | p.Thr367Pro | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1114/2916 | 1099/1560 | 367/519 | chr2 | 74492383 | |||
| chr2:74492387 | T | C | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1103T>C | p.Leu368Pro | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1118/2916 | 1103/1560 | 368/519 | chr2 | 74492387 | |||
| chr2:74492390 | G | C | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1106G>C | p.Arg369Pro | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1121/2916 | 1106/1560 | 369/519 | chr2 | 74492390 | |||
| chr2:74492395 | G | C | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1111G>C | p.Gly371Arg | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1126/2916 | 1111/1560 | 371/519 | chr2 | 74492395 | |||
| chr2:74492396 | G | C | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1112G>C | p.Gly371Ala | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1127/2916 | 1112/1560 | 371/519 | chr2 | 74492396 | |||
| chr2:74492398 | T | C | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1114T>C | p.Trp372Arg | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1129/2916 | 1114/1560 | 372/519 | chr2 | 74492398 | |||
| chr2:74492399 | G | C | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1115G>C | p.Trp372Ser | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1130/2916 | 1115/1560 | 372/519 | chr2 | 74492399 | |||
| chr2:74492400 | G | C | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1116G>C | p.Trp372Cys | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1131/2916 | 1116/1560 | 372/519 | chr2 | 74492400 | |||
| chr2:74492407 | G | C | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1123G>C | p.Gly375Arg | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1138/2916 | 1123/1560 | 375/519 | chr2 | 74492407 | |||
| chr2:74492408 | G | C | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1124G>C | p.Gly375Ala | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1139/2916 | 1124/1560 | 375/519 | chr2 | 74492408 | |||
| chr2:74492411 | T | A | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1127T>A | p.Leu376His | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1142/2916 | 1127/1560 | 376/519 | chr2 | 74492411 | |||
| chr2:74492413 | T | G | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1129T>G | p.Phe377Val | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1144/2916 | 1129/1560 | 377/519 | chr2 | 74492413 | |||
| chr2:74492414 | T | G | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1130T>G | p.Phe377Cys | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1145/2916 | 1130/1560 | 377/519 | chr2 | 74492414 | |||
| chr2:74492689 | G | A | 1 | a0004 | 3 | HG01243.hp2 HG03098.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.1205G>A | p.Gly402Asp | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 12/13 | 1220/2916 | 1205/1560 | 402/519 | chr2 | 74492689 | |||
| chr2:74492952 | C | T | 1 | a0004 | 3 | HG01243.hp2 HG03098.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.1294C>T | p.Pro432Ser | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1309/2916 | 1294/1560 | 432/519 | chr2 | 74492952 | |||
| chr2:74492971 | T | A | 1 | a0004 | 3 | HG01243.hp2 HG03098.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.1313T>A | p.Leu438His | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1328/2916 | 1313/1560 | 438/519 | chr2 | 74492971 | |||
| chr2:74493013 | C | G | 1 | a0005 | 2 | HG01167.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.1355C>G | p.Pro452Arg | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1370/2916 | 1355/1560 | 452/519 | chr2 | 74493013 | |||
| chr2:74493183 | G | A | 1 | a0006 | 2 | HG02738.hp1 HG02738.hp2 |
missense_variant | MODERATE | c.1525G>A | p.Gly509Arg | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1540/2916 | 1525/1560 | 509/519 | chr2 | 74493183 | |||
| chr2:74493201 | C | G | 1 | a0011 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.1543C>G | p.Leu515Val | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1558/2916 | 1543/1560 | 515/519 | chr2 | 74493201 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:74490682 | G | A | 1 | a0001c0010 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.489G>A | p.Leu163Leu | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 5/13 | 504/2916 | 489/1560 | 163/519 | chr2 | 74490682 | |||
| chr2:74492027 | T | C | 1 | a0004c0004 | 3 | HG01243.hp2 HG03098.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.900T>C | p.Ala300Ala | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 9/13 | 915/2916 | 900/1560 | 300/519 | chr2 | 74492027 | |||
| chr2:74492367 | T | C | 1 | a0009c0009 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.1083T>C | p.Asp361Asp | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1098/2916 | 1083/1560 | 361/519 | chr2 | 74492367 | |||
| chr2:74492376 | G | C | 1 | a0009c0009 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.1092G>C | p.Val364Val | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1107/2916 | 1092/1560 | 364/519 | chr2 | 74492376 | |||
| chr2:74492382 | T | C | 1 | a0009c0009 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.1098T>C | p.Leu366Leu | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1113/2916 | 1098/1560 | 366/519 | chr2 | 74492382 | |||
| chr2:74492388 | A | C | 1 | a0009c0009 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.1104A>C | p.Leu368Leu | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1119/2916 | 1104/1560 | 368/519 | chr2 | 74492388 | |||
| chr2:74492391 | G | C | 1 | a0009c0009 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.1107G>C | p.Arg369Arg | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1122/2916 | 1107/1560 | 369/519 | chr2 | 74492391 | |||
| chr2:74492394 | T | C | 1 | a0009c0009 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.1110T>C | p.Pro370Pro | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/13 | 1125/2916 | 1110/1560 | 370/519 | chr2 | 74492394 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:74493460 | C | T | 1 | a0001c0001t0003 | 4 | HG01123.hp1 HG02055.hp1 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*242C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 242 | chr2 | 74493460 | ||||||
| chr2:74493588 | T | C | 1 | a0001c0001t0005 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*370T>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 370 | chr2 | 74493588 | ||||||
| chr2:74493630 | C | G | 1 | a0002c0002t0011 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*412C>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 412 | chr2 | 74493630 | ||||||
| chr2:74493632 | T | C | 1 | a0001c0001t0004 | 2 | HG01109.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*414T>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 414 | chr2 | 74493632 | ||||||
| chr2:74493928 | A | G | 12 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(9): Show |
199 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*710A>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 710 | chr2 | 74493928 | ||||||
| chr2:74494106 | G | C | 1 | a0001c0001t0007 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*888G>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 888 | chr2 | 74494106 | ||||||
| chr2:74494307 | T | C | 1 | a0001c0001t0008 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1089T>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1089 | chr2 | 74494307 | ||||||
| chr2:74494432 | C | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1214C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1214 | chr2 | 74494432 | ||||||
| chr2:74494433 | C | G | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1215C>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1215 | chr2 | 74494433 | ||||||
| chr2:74494435 | G | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1217G>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1217 | chr2 | 74494435 | ||||||
| chr2:74494437 | A | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1219A>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1219 | chr2 | 74494437 | ||||||
| chr2:74494438 | A | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1220A>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1220 | chr2 | 74494438 | ||||||
| chr2:74494439 | A | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1221A>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1221 | chr2 | 74494439 | ||||||
| chr2:74494440 | A | G | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1222A>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1222 | chr2 | 74494440 | ||||||
| chr2:74494441 | A | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1223A>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1223 | chr2 | 74494441 | ||||||
| chr2:74494443 | G | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1225G>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1225 | chr2 | 74494443 | ||||||
| chr2:74494444 | A | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1226A>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1226 | chr2 | 74494444 | ||||||
| chr2:74494445 | G | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1227G>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1227 | chr2 | 74494445 | ||||||
| chr2:74494446 | G | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1228G>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1228 | chr2 | 74494446 | ||||||
| chr2:74494449 | A | G | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1231A>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1231 | chr2 | 74494449 | ||||||
| chr2:74494450 | G | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1232G>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1232 | chr2 | 74494450 | ||||||
| chr2:74494454 | C | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1236C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1236 | chr2 | 74494454 | ||||||
| chr2:74494457 | C | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1239C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1239 | chr2 | 74494457 | ||||||
| chr2:74494458 | C | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1240C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1240 | chr2 | 74494458 | ||||||
| chr2:74494459 | T | G | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1241T>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1241 | chr2 | 74494459 | ||||||
| chr2:74494460 | C | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1242C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1242 | chr2 | 74494460 | ||||||
| chr2:74494461 | A | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1243A>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1243 | chr2 | 74494461 | ||||||
| chr2:74494463 | A | G | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1245A>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1245 | chr2 | 74494463 | ||||||
| chr2:74494464 | A | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1246A>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1246 | chr2 | 74494464 | ||||||
| chr2:74494465 | G | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1247G>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1247 | chr2 | 74494465 | ||||||
| chr2:74494466 | G | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1248G>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1248 | chr2 | 74494466 | ||||||
| chr2:74494468 | A | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1250A>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1250 | chr2 | 74494468 | ||||||
| chr2:74494470 | A | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1252A>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1252 | chr2 | 74494470 | ||||||
| chr2:74494474 | T | A | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1256T>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1256 | chr2 | 74494474 | ||||||
| chr2:74494477 | G | C | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1259G>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1259 | chr2 | 74494477 | ||||||
| chr2:74494479 | A | C | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1261A>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1261 | chr2 | 74494479 | ||||||
| chr2:74494480 | T | A | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1262T>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1262 | chr2 | 74494480 | ||||||
| chr2:74494482 | G | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1264G>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1264 | chr2 | 74494482 | ||||||
| chr2:74494483 | A | C | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1265A>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1265 | chr2 | 74494483 | ||||||
| chr2:74494484 | A | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1266A>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1266 | chr2 | 74494484 | ||||||
| chr2:74494485 | A | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1267A>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1267 | chr2 | 74494485 | ||||||
| chr2:74494487 | C | T | 1 | a0001c0001t0009 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1269C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1269 | chr2 | 74494487 | ||||||
| chr2:74494488 | G | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1270G>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1270 | chr2 | 74494488 | ||||||
| chr2:74494489 | A | C | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1271A>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1271 | chr2 | 74494489 | ||||||
| chr2:74494490 | A | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1272A>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1272 | chr2 | 74494490 | ||||||
| chr2:74494491 | A | G | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1273A>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1273 | chr2 | 74494491 | ||||||
| chr2:74494492 | G | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1274G>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1274 | chr2 | 74494492 | ||||||
| chr2:74494493 | T | C | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1275T>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1275 | chr2 | 74494493 | ||||||
| chr2:74494495 | T | C | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1277T>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1277 | chr2 | 74494495 | ||||||
| chr2:74494496 | G | C | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1278G>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1278 | chr2 | 74494496 | ||||||
| chr2:74494497 | A | C | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1279A>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1279 | chr2 | 74494497 | ||||||
| chr2:74494498 | G | C | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1280G>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1280 | chr2 | 74494498 | ||||||
| chr2:74494519 | G | C | 1 | a0002c0002t0006 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1301G>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 13/13 | 1301 | chr2 | 74494519 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:74483269 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.41-53C>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 1/12 | chr2 | 74483269 | |||||||
| chr2:74483698 | C | T | 1 | a0004c0004t0001g0071 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.129+288C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74483698 | |||||||
| chr2:74483724 | C | T | 1 | a0001c0001t0003g0013 | 4 | HG01123.hp1 HG02055.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+314C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74483724 | |||||||
| chr2:74484003 | A | AG | 3 | a0001c0001t0001g0018 a0002c0002t0002g0008 a0002c0002t0002g0070 |
11 | HG00639.hp2 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.129+599dupG | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 74484003 | ||||||
| chr2:74484005 | G | C | 1 | a0001c0001t0001g0025 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.129+595G>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74484005 | |||||||
| chr2:74484108 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.129+698G>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74484108 | |||||||
| chr2:74484246 | A | T | 1 | a0002c0002t0002g0069 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.129+836A>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74484246 | |||||||
| chr2:74484247 | T | G | 1 | a0002c0002t0002g0069 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.129+837T>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74484247 | |||||||
| chr2:74484248 | G | A | 1 | a0002c0002t0002g0069 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.129+838G>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74484248 | |||||||
| chr2:74484362 | G | A | 1 | a0001c0001t0004g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.129+952G>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74484362 | |||||||
| chr2:74484441 | T | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0011 others(8): Show |
29 | HG01167.hp2 HG01169.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.129+1031T>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74484441 | |||||||
| chr2:74484497 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0068 |
11 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.129+1087C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74484497 | |||||||
| chr2:74484532 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.129+1122C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74484532 | |||||||
| chr2:74484603 | C | A | 1 | a0001c0001t0001g0032 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.129+1193C>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74484603 | |||||||
| chr2:74484988 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.129+1578T>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74484988 | |||||||
| chr2:74485024 | C | CT | 10 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
19 | HG01109.hp2 HG01167.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.129+1634dupT | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 74485024 | ||||||
| chr2:74485024 | CT | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0035 others(2): Show |
11 | HG02109.hp1 HG02280.hp2 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.129+1634delT | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 74485024 | ||||||
| chr2:74485137 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.129+1727C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74485137 | |||||||
| chr2:74485435 | C | T | 1 | a0011c0011t0001g0067 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.129+2025C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74485435 | |||||||
| chr2:74485469 | CT | C | 32 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0036 others(29): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.129+2077delT | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 74485469 | ||||||
| chr2:74485506 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.129+2096C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74485506 | |||||||
| chr2:74485516 | G | T | 1 | a0003c0003t0001g0048 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.129+2106G>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74485516 | |||||||
| chr2:74485563 | C | A | 1 | a0002c0002t0002g0049 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.129+2153C>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74485563 | |||||||
| chr2:74485564 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0018 others(2): Show |
17 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.129+2154G>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74485564 | |||||||
| chr2:74485607 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.129+2197A>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74485607 | |||||||
| chr2:74485691 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.129+2281C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74485691 | |||||||
| chr2:74485706 | G | T | 1 | a0002c0002t0002g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.129+2296G>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74485706 | |||||||
| chr2:74485712 | C | T | 1 | a0002c0002t0002g0046 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.129+2302C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74485712 | |||||||
| chr2:74485858 | C | A | 1 | a0002c0002t0002g0069 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.129+2448C>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74485858 | |||||||
| chr2:74485859 | T | C | 1 | a0002c0002t0002g0069 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.129+2449T>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74485859 | |||||||
| chr2:74485861 | C | T | 1 | a0002c0002t0002g0069 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.129+2451C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74485861 | |||||||
| chr2:74485904 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0068 |
8 | HG02109.hp1 HG02280.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.129+2494G>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74485904 | |||||||
| chr2:74486295 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.129+2885C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74486295 | |||||||
| chr2:74486550 | G | T | 1 | a0001c0001t0001g0060 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.129+3140G>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74486550 | |||||||
| chr2:74486555 | A | T | 1 | a0001c0001t0001g0060 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.129+3145A>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74486555 | |||||||
| chr2:74486674 | C | T | 1 | a0002c0002t0002g0045 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.129+3264C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74486674 | |||||||
| chr2:74486825 | G | A | 2 | a0002c0002t0002g0015 a0007c0005t0002g0015 |
3 | HG03491.hp1 HG03492.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.130-3200G>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74486825 | |||||||
| chr2:74486893 | C | CA | 5 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0029 others(2): Show |
11 | HG01243.hp1 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.130-3117dupA | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 74486893 | ||||||
| chr2:74487477 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
193 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.130-2548C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74487477 | |||||||
| chr2:74487486 | G | GGGATTAC others(46): Show |
1 | a0009c0009t0002g0037 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.130-2538_130-2486d others(55): Show |
TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 74487486 | ||||||
| chr2:74487530 | A | T | 1 | a0001c0001t0001g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.130-2495A>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74487530 | |||||||
| chr2:74487682 | A | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0023 others(3): Show |
24 | HG00735.hp2 HG01891.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.130-2343A>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74487682 | |||||||
| chr2:74487686 | T | A | 1 | a0001c0001t0001g0011 | 4 | HG01884.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-2339T>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74487686 | |||||||
| chr2:74487687 | A | G | 1 | a0002c0002t0002g0043 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.130-2338A>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74487687 | |||||||
| chr2:74487825 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.130-2200A>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74487825 | |||||||
| chr2:74487879 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.130-2146C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74487879 | |||||||
| chr2:74487973 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0011 others(7): Show |
28 | HG01167.hp2 HG01169.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.130-2052C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74487973 | |||||||
| chr2:74488007 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.130-2018C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74488007 | |||||||
| chr2:74488120 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.130-1905G>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74488120 | |||||||
| chr2:74488311 | T | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0038 |
3 | HG02615.hp1 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.130-1714T>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74488311 | |||||||
| chr2:74488313 | G | A | 1 | a0006c0007t0002g0064 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.130-1712G>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74488313 | |||||||
| chr2:74488465 | A | C | 1 | a0001c0001t0001g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.130-1560A>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74488465 | |||||||
| chr2:74488591 | A | G | 2 | a0002c0002t0002g0022 a0002c0002t0002g0042 |
3 | HG00738.hp2 HG01081.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.130-1434A>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74488591 | |||||||
| chr2:74488699 | A | G | 1 | a0001c0001t0001g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.130-1326A>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74488699 | |||||||
| chr2:74488890 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0068 |
8 | HG02109.hp1 HG02280.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.130-1135C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74488890 | |||||||
| chr2:74488980 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.130-1045C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74488980 | |||||||
| chr2:74489013 | A | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(51): Show |
199 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.130-1012A>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74489013 | |||||||
| chr2:74489025 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0023 |
5 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.130-1000C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74489025 | |||||||
| chr2:74489194 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.130-831G>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74489194 | |||||||
| chr2:74489264 | T | C | 1 | a0002c0002t0002g0039 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.130-761T>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74489264 | |||||||
| chr2:74489585 | A | G | 1 | a0002c0002t0002g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.130-440A>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74489585 | |||||||
| chr2:74489607 | T | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0052 |
2 | NA19000.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.130-418T>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74489607 | |||||||
| chr2:74489765 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0031 |
4 | HG01192.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-260A>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74489765 | |||||||
| chr2:74489868 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.130-157C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 2/12 | chr2 | 74489868 | |||||||
| chr2:74490525 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.462+52T>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 4/12 | chr2 | 74490525 | |||||||
| chr2:74490640 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.463-16G>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 4/12 | chr2 | 74490640 | |||||||
| chr2:74490906 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.546+167G>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 5/12 | chr2 | 74490906 | |||||||
| chr2:74490985 | CTT | C | 2 | a0004c0004t0001g0021 a0004c0004t0001g0071 |
3 | HG01243.hp2 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.547-142_547-141del others(2): Show |
TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 5/12 | chr2 | 74490985 | |||||||
| chr2:74491011 | G | T | 1 | a0001c0001t0001g0016 | 3 | HG02257.hp2 HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.547-117G>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 5/12 | chr2 | 74491011 | |||||||
| chr2:74491072 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.547-56G>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 5/12 | chr2 | 74491072 | |||||||
| chr2:74491092 | G | T | 3 | a0002c0002t0002g0020 a0002c0002t0002g0051 a0002c0002t0002g0069 |
4 | NA18995.hp1 NA19007.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.547-36G>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 5/12 | chr2 | 74491092 | |||||||
| chr2:74491268 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0023 |
5 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.604-27C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 6/12 | chr2 | 74491268 | |||||||
| chr2:74491282 | A | G | 1 | a0002c0002t0002g0041 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.604-13A>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 6/12 | chr2 | 74491282 | |||||||
| chr2:74491383 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG03540.hp1 | splice_region_variant&intron_variant | LOW | c.684+8C>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 7/12 | chr2 | 74491383 | |||||||
| chr2:74491395 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0060 |
2 | HG02148.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.684+20C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 7/12 | chr2 | 74491395 | |||||||
| chr2:74492123 | C | A | 1 | a0009c0009t0002g0037 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.929-16C>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 9/12 | chr2 | 74492123 | |||||||
| chr2:74492245 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0060 |
2 | HG02148.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1019+16G>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 10/12 | chr2 | 74492245 | |||||||
| chr2:74492272 | T | C | 1 | a0009c0009t0002g0037 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1020-32T>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 10/12 | chr2 | 74492272 | |||||||
| chr2:74492275 | G | C | 1 | a0009c0009t0002g0037 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1020-29G>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 10/12 | chr2 | 74492275 | |||||||
| chr2:74492279 | T | C | 1 | a0009c0009t0002g0037 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1020-25T>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 10/12 | chr2 | 74492279 | |||||||
| chr2:74492283 | G | C | 1 | a0009c0009t0002g0037 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1020-21G>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 10/12 | chr2 | 74492283 | |||||||
| chr2:74492288 | C | CCCCCCCC others(38): Show |
1 | a0009c0009t0002g0037 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1020-16_1020-15ins others(45): Show |
TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 10/12 | chr2 | 74492288 | |||||||
| chr2:74492290 | T | C | 1 | a0009c0009t0002g0037 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1020-14T>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 10/12 | chr2 | 74492290 | |||||||
| chr2:74492292 | T | C | 1 | a0009c0009t0002g0037 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1020-12T>C | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 10/12 | chr2 | 74492292 | |||||||
| chr2:74492293 | G | A | 1 | a0009c0009t0002g0037 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1020-11G>A | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 10/12 | chr2 | 74492293 | |||||||
| chr2:74492642 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA19081.hp2 | splice_region_variant&intron_variant | LOW | c.1162-4A>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 11/12 | chr2 | 74492642 | |||||||
| chr2:74492783 | G | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0024 others(23): Show |
123 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1263+36G>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 12/12 | chr2 | 74492783 | |||||||
| chr2:74492841 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0005g0054 others(1): Show |
4 | HG01243.hp2 HG01256.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-81C>T | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 12/12 | chr2 | 74492841 | |||||||
| chr2:74492875 | C | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(80): Show |
328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.1264-47C>G | TTC31 | ENSG00000115282.21 | transcript | ENST00000233623.11 | protein_coding | 12/12 | chr2 | 74492875 |