Search by Gene
| Item | Value |
|---|---|
| geneid | 445347 |
| ensemblid | ENSG00000289746.1 |
| hgncid | |
| symbol | TARP |
| name | TCR gamma alternate reading frame protein |
| refseq_nuc | NM_001003799.2 |
| refseq_prot | NP_001003799.1 |
| ensembl_nuc | ENST00000698248.1 |
| ensembl_prot | ENSP00000513628.1 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 38259643 |
| end | 38273636 |
| strand | - |
| ver | v1.2 |
| region | chr7:38259643-38273636 |
| region5000 | chr7:38254643-38278636 |
| regionname0 | TARP_chr7_38259643_38273636 |
| regionname5000 | TARP_chr7_38254643_38278636 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 58 | 443 | 89 | 76 | 216 | 16 | 46 | TARP_chr7_38254643_38278636 | TARP | MQMFP others(53): Show |
chr7 | 38254643 | 38278636 |
| a0002 | 0/0 | 58 | 5 | 4 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | MQMFP others(53): Show |
chr7 | 38254643 | 38278636 |
| a0003 | 0/0 | 58 | 5 | 5 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | MQMFP others(53): Show |
chr7 | 38254643 | 38278636 |
| a0004 | 0/0 | 58 | 2 | 0 | 0 | 0 | 0 | 2 | TARP_chr7_38254643_38278636 | TARP | MQMFP others(53): Show |
chr7 | 38254643 | 38278636 |
| a0005 | 0/0 | 58 | 1 | 0 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | MQMFP others(53): Show |
chr7 | 38254643 | 38278636 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 174 | 355 | 74 | 66 | 169 | 12 | 34 | TARP_chr7_38254643_38278636 | TARP | ATGCA others(169): Show |
chr7 | 38254643 | 38278636 | ||
| a0001c0002 | 0/0 | 174 | 88 | 15 | 10 | 47 | 4 | 12 | TARP_chr7_38254643_38278636 | TARP | ATGCA others(169): Show |
chr7 | 38254643 | 38278636 | ||
| a0002c0004 | 0/0 | 174 | 5 | 4 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | ATGCA others(169): Show |
chr7 | 38254643 | 38278636 | ||
| a0003c0003 | 0/0 | 174 | 5 | 5 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | ATGCA others(169): Show |
chr7 | 38254643 | 38278636 | ||
| a0004c0005 | 0/0 | 174 | 2 | 0 | 0 | 0 | 0 | 2 | TARP_chr7_38254643_38278636 | TARP | ATGCA others(169): Show |
chr7 | 38254643 | 38278636 | ||
| a0005c0006 | 0/0 | 174 | 1 | 0 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | ATGCA others(169): Show |
chr7 | 38254643 | 38278636 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1016 | 231 | 28 | 61 | 107 | 9 | 26 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0001t0003 | 0/0 | 1016 | 46 | 17 | 2 | 26 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0001t0004 | 0/0 | 1016 | 30 | 0 | 1 | 21 | 3 | 5 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0001t0005 | 0/0 | 1016 | 21 | 21 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0001t0007 | 0/0 | 1016 | 9 | 2 | 0 | 6 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0001t0009 | 0/0 | 1016 | 5 | 1 | 0 | 3 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0001t0010 | 0/0 | 1016 | 4 | 0 | 2 | 2 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0001t0011 | 0/0 | 1016 | 3 | 0 | 0 | 3 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0001t0013 | 0/0 | 1016 | 2 | 2 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0001t0014 | 0/0 | 1016 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0001t0016 | 0/0 | 1016 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0001t0017 | 0/0 | 1016 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0001t0018 | 0/0 | 1016 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0002t0001 | 0/0 | 1016 | 1 | 0 | 0 | 0 | 1 | 0 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0002t0002 | 0/0 | 1016 | 62 | 5 | 8 | 38 | 3 | 8 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0002t0003 | 0/0 | 1016 | 10 | 0 | 0 | 8 | 0 | 2 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0002t0006 | 0/0 | 1016 | 9 | 7 | 2 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0002t0012 | 0/0 | 1016 | 2 | 2 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0002t0015 | 0/0 | 1016 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0002t0019 | 0/0 | 1016 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0002t0020 | 0/0 | 1016 | 1 | 0 | 0 | 0 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0001c0002t0021 | 0/0 | 1016 | 1 | 0 | 0 | 0 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0002c0004t0008 | 0/0 | 1016 | 5 | 4 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0003c0003t0003 | 0/0 | 1016 | 4 | 4 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0003c0003t0006 | 0/0 | 1016 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0004c0005t0002 | 0/0 | 1016 | 2 | 0 | 0 | 0 | 0 | 2 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| a0005c0006t0002 | 0/0 | 1016 | 1 | 0 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | GGGCA others(1011): Show |
chr7 | 38254643 | 38278636 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 54 | 3 | 22 | 20 | 2 | 7 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0002 | 0/0 | 43 | 3 | 2 | 34 | 0 | 4 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0003 | 0/0 | 22 | 0 | 0 | 21 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0008 | 0/0 | 15 | 1 | 7 | 7 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0010 | 0/0 | 8 | 2 | 5 | 0 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0015 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0020 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0028 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0003g0007 | 0/0 | 18 | 0 | 0 | 18 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0003g0014 | 0/0 | 6 | 1 | 2 | 3 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0003g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0003g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0003g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0003g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0004g0004 | 0/0 | 21 | 0 | 1 | 16 | 3 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0004g0022 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0004g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0005g0006 | 0/0 | 18 | 18 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0007g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0007g0026 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0007g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0007g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0009g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0009g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0010g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0010g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0010g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0011g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0011g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0013g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0014g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0016g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0017g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0001t0018g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0002g0005 | 0/0 | 21 | 0 | 2 | 14 | 2 | 3 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0002g0009 | 0/0 | 12 | 0 | 3 | 5 | 1 | 3 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0002g0012 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0002g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0002g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0002g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0003g0011 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0006g0013 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0006g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0012g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0012g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0015g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0019g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0020g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0001c0002t0021g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0002c0004t0008g0019 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0002c0004t0008g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0003c0003t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0003c0003t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0003c0003t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0003c0003t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0004c0005t0002g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| a0005c0006t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0009 | EUR | GBR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | GBR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | GBR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0004 | EUR | FIN | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | FIN | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | FIN | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | CHS | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | CHS | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CHS | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | CHS | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00597 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | CHS | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00597 | hp2 | a0001 | c0001 | t0011 | g0073 | EAS | CHS | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00639 | hp1 | a0001 | c0002 | t0006 | g0013 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | CHS | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | CHS | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0045 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0119 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01192 | hp1 | a0001 | c0001 | t0010 | g0049 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01243 | hp1 | a0002 | c0004 | t0008 | g0019 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01257 | hp1 | a0005 | c0006 | t0002 | g0110 | AMR | CLM | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01358 | hp2 | a0001 | c0002 | t0006 | g0152 | AMR | CLM | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01361 | hp1 | a0001 | c0001 | t0010 | g0049 | AMR | CLM | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | CLM | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0005 | EUR | IBS | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0004 | EUR | IBS | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0004 | EUR | IBS | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0005 | EUR | IBS | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01884 | hp1 | a0003 | c0003 | t0003 | g0038 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0045 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | KHV | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | KHV | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | KHV | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | KHV | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0096 | EAS | KHV | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0097 | EAS | KHV | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0115 | EAS | KHV | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | KHV | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02135 | hp1 | a0001 | c0001 | t0007 | g0098 | EAS | KHV | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | KHV | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | CDX | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | CDX | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | CDX | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0114 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02280 | hp1 | a0003 | c0003 | t0003 | g0089 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | KHV | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02572 | hp1 | a0001 | c0002 | t0006 | g0151 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02572 | hp2 | a0001 | c0002 | t0006 | g0013 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02647 | hp2 | a0001 | c0001 | t0016 | g0080 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02683 | hp2 | a0001 | c0002 | t0003 | g0011 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0009 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0054 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02896 | hp1 | a0001 | c0001 | t0013 | g0032 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02897 | hp1 | a0001 | c0001 | t0013 | g0032 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0044 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | ESN | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02922 | hp2 | a0002 | c0004 | t0008 | g0019 | AFR | ESN | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02965 | hp1 | a0001 | c0002 | t0012 | g0078 | AFR | ESN | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02965 | hp2 | a0001 | c0002 | t0006 | g0013 | AFR | ESN | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02970 | hp1 | a0001 | c0001 | t0009 | g0058 | AFR | ESN | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | ESN | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0103 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0042 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0042 | AFR | MSL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | ESN | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03139 | hp1 | a0002 | c0004 | t0008 | g0019 | AFR | ESN | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03139 | hp2 | a0001 | c0002 | t0006 | g0013 | AFR | ESN | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03195 | hp1 | a0001 | c0002 | t0015 | g0153 | AFR | ESN | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | ESN | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | MSL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | MSL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03225 | hp1 | a0001 | c0002 | t0006 | g0013 | AFR | MSL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0051 | AFR | MSL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0108 | AFR | MSL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0052 | AFR | MSL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0022 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0095 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03491 | hp1 | a0004 | c0005 | t0002 | g0046 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03492 | hp1 | a0004 | c0005 | t0002 | g0046 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0022 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0050 | AFR | ESN | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03516 | hp2 | a0002 | c0004 | t0008 | g0019 | AFR | ESN | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03540 | hp1 | a0003 | c0003 | t0003 | g0085 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03579 | hp1 | a0001 | c0002 | t0012 | g0120 | AFR | MSL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03654 | hp1 | a0001 | c0002 | t0021 | g0113 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03654 | hp2 | a0001 | c0002 | t0003 | g0011 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | STU | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0022 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03710 | hp1 | a0001 | c0001 | t0007 | g0026 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0009 | SAS | PJL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03834 | hp1 | a0001 | c0001 | t0009 | g0068 | SAS | BEB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | BEB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0012 | SAS | BEB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0009 | SAS | BEB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0109 | SAS | STU | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG04204 | hp1 | a0001 | c0002 | t0020 | g0111 | SAS | STU | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | STU | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18522 | hp1 | a0002 | c0004 | t0008 | g0148 | AFR | YRI | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | YRI | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | CHB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | YRI | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18946 | hp1 | a0001 | c0001 | t0009 | g0023 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18952 | hp1 | a0001 | c0001 | t0007 | g0025 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18957 | hp1 | a0001 | c0001 | t0010 | g0132 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18963 | hp1 | a0001 | c0001 | t0011 | g0035 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18965 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18967 | hp1 | a0001 | c0001 | t0007 | g0026 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18968 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18970 | hp2 | a0001 | c0001 | t0009 | g0023 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18989 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18995 | hp2 | a0001 | c0002 | t0003 | g0093 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19002 | hp1 | a0001 | c0001 | t0014 | g0139 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19006 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19007 | hp1 | a0001 | c0001 | t0007 | g0025 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19012 | hp1 | a0001 | c0001 | t0007 | g0026 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | LWK | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19030 | hp2 | a0003 | c0003 | t0006 | g0086 | AFR | LWK | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | LWK | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19057 | hp2 | a0001 | c0001 | t0009 | g0023 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19059 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19065 | hp2 | a0001 | c0002 | t0003 | g0090 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19075 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19075 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19077 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19085 | hp2 | a0001 | c0002 | t0019 | g0116 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19088 | hp1 | a0001 | c0001 | t0011 | g0035 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19090 | hp1 | a0001 | c0001 | t0010 | g0063 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19090 | hp2 | a0001 | c0002 | t0003 | g0092 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19091 | hp1 | a0001 | c0001 | t0007 | g0025 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | YRI | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0044 | AFR | ASW | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA20129 | hp2 | a0001 | c0002 | t0006 | g0013 | AFR | ASW | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | TSI | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | TSI | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0091 | EUR | TSI | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02559 | hp1 | a0001 | c0001 | t0017 | g0122 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | ACB | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03471 | hp1 | a0003 | c0003 | t0003 | g0038 | AFR | MSL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0094 | AFR | MSL | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG06807 | hp1 | a0001 | c0002 | t0006 | g0013 | AFR | USA | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | USA | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | USA | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA20300 | hp2 | a0001 | c0001 | t0018 | g0079 | AFR | USA | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | LWK | TARP_chr7_38254643_38278636 | TARP | chr7 | 38254643 | 38278636 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:38265559 | C | T | 1 | a0002 | 5 | HG01243.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
missense_variant | MODERATE | c.108G>A | p.Met36Ile | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/4 | 170/1016 | 108/177 | 36/58 | chr7 | 38265559 | |||
| chr7:38265563 | A | T | 1 | a0002 | 5 | HG01243.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
missense_variant | MODERATE | c.104T>A | p.Leu35Gln | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/4 | 166/1016 | 104/177 | 35/58 | chr7 | 38265563 | |||
| chr7:38265572 | T | A | 1 | a0004 | 2 | HG03491.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.95A>T | p.Asn32Ile | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/4 | 157/1016 | 95/177 | 32/58 | chr7 | 38265572 | |||
| chr7:38265611 | C | T | 2 | a0002a0005 | 6 | HG01243.hp1 HG01257.hp1 HG02922.hp2 others(3): Show |
missense_variant | MODERATE | c.56G>A | p.Ser19Asn | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/4 | 118/1016 | 56/177 | 19/58 | chr7 | 38265611 | |||
| chr7:38265618 | T | G | 1 | a0003 | 5 | HG01884.hp1 HG02280.hp1 HG03471.hp1 others(2): Show |
missense_variant | MODERATE | c.49A>C | p.Lys17Gln | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/4 | 111/1016 | 49/177 | 17/58 | chr7 | 38265618 | |||
| chr7:38265626 | T | C | 1 | a0002 | 5 | HG01243.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
missense_variant | MODERATE | c.41A>G | p.Gln14Arg | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/4 | 103/1016 | 41/177 | 14/58 | chr7 | 38265626 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:38265541 | G | C | 3 | a0001c0002a0004c0005a0005c0006 | 91 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(88): Show |
synonymous_variant | LOW | c.126C>G | p.Gly42Gly | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/4 | 188/1016 | 126/177 | 42/58 | chr7 | 38265541 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:38259671 | C | T | 1 | a0001c0001t0011 | 3 | HG00597.hp2 NA18963.hp1 NA19088.hp1 |
3_prime_UTR_variant | MODIFIER | c.*749G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 4/4 | 5819 | chr7 | 38259671 | ||||||
| chr7:38259803 | A | C | 6 | a0001c0001t0010a0001c0001t0013a0001c0002t0006others(3): Show | 18 | HG00639.hp1 HG01192.hp1 HG01358.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*617T>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 4/4 | 5687 | chr7 | 38259803 | ||||||
| chr7:38259884 | G | A | 3 | a0001c0001t0004a0001c0001t0013a0001c0001t0017 | 33 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*536C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 4/4 | 5606 | chr7 | 38259884 | ||||||
| chr7:38259946 | G | A | 3 | a0001c0001t0013a0001c0002t0015a0001c0002t0021 | 4 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*474C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 4/4 | 5544 | chr7 | 38259946 | ||||||
| chr7:38259949 | A | G | 1 | a0001c0002t0020 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*471T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 4/4 | 5541 | chr7 | 38259949 | ||||||
| chr7:38259978 | G | A | 7 | a0001c0002t0002a0001c0002t0012a0001c0002t0019others(4): Show | 70 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*442C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 4/4 | 5512 | chr7 | 38259978 | ||||||
| chr7:38260011 | C | G | 1 | a0001c0001t0007 | 9 | HG02135.hp1 HG03041.hp1 HG03098.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*409G>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 4/4 | 5479 | chr7 | 38260011 | ||||||
| chr7:38260040 | G | A | 2 | a0001c0001t0016a0001c0001t0018 | 2 | HG02647.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*380C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 4/4 | 5450 | chr7 | 38260040 | ||||||
| chr7:38260149 | G | T | 1 | a0001c0002t0012 | 2 | HG02965.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*271C>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 4/4 | 5341 | chr7 | 38260149 | ||||||
| chr7:38260188 | A | G | 18 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(15): Show | 203 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*232T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 4/4 | 5302 | chr7 | 38260188 | ||||||
| chr7:38265385 | C | T | 2 | a0001c0001t0014a0002c0004t0008 | 6 | HG01243.hp1 HG02922.hp2 HG03139.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*105G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/4 | 105 | chr7 | 38265385 | ||||||
| chr7:38265388 | C | T | 1 | a0001c0002t0019 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*102G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/4 | 102 | chr7 | 38265388 | ||||||
| chr7:38265442 | T | C | 3 | a0001c0001t0004a0001c0001t0009a0002c0004t0008 | 40 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*48A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/4 | 48 | chr7 | 38265442 | ||||||
| chr7:38265481 | C | A | 1 | a0001c0001t0018 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9G>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/4 | 9 | chr7 | 38265481 | ||||||
| chr7:38265482 | G | A | 6 | a0001c0002t0002a0001c0002t0019a0001c0002t0020others(3): Show | 68 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*8C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/4 | 8 | chr7 | 38265482 | ||||||
| chr7:38273594 | G | T | 1 | a0001c0001t0005 | 21 | HG02257.hp2 HG02258.hp2 HG02559.hp2 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-20C>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/4 | 7928 | chr7 | 38273594 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:38260271 | C | T | 88 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(85): Show | 237 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(234): Show |
intron_variant | MODIFIER | c.*190-41G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38260271 | |||||||
| chr7:38260299 | T | G | 4 | a0001c0002t0006g0013a0001c0002t0006g0151a0001c0002t0006g0152others(1): Show | 10 | HG00639.hp1 HG01358.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.*190-69A>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38260299 | |||||||
| chr7:38260316 | C | T | 1 | a0001c0001t0003g0029 | 3 | HG02630.hp2 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.*190-86G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38260316 | |||||||
| chr7:38260317 | G | A | 1 | a0001c0001t0001g0016 | 5 | HG02145.hp2 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.*190-87C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38260317 | |||||||
| chr7:38260354 | T | C | 5 | a0001c0001t0004g0004a0001c0001t0004g0022a0001c0001t0004g0024others(2): Show | 29 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.*190-124A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38260354 | |||||||
| chr7:38260595 | G | A | 3 | a0001c0001t0007g0025a0001c0001t0007g0026a0001c0001t0007g0098 | 7 | HG02135.hp1 HG03710.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.*190-365C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38260595 | |||||||
| chr7:38260726 | T | C | 1 | a0001c0001t0003g0103 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.*190-496A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38260726 | |||||||
| chr7:38260923 | C | A | 1 | a0001c0001t0007g0098 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.*190-693G>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38260923 | |||||||
| chr7:38260950 | T | A | 14 | a0001c0001t0001g0101a0001c0001t0003g0007a0001c0001t0003g0014others(11): Show | 41 | HG00408.hp2 HG00558.hp1 HG01346.hp2 others(38): Show |
intron_variant | MODIFIER | c.*190-720A>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38260950 | |||||||
| chr7:38261076 | T | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0128a0001c0001t0001g0142others(2): Show | 19 | HG01074.hp2 HG01261.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.*190-846A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38261076 | |||||||
| chr7:38261318 | G | T | 4 | a0001c0002t0006g0013a0001c0002t0006g0151a0001c0002t0006g0152others(1): Show | 10 | HG00639.hp1 HG01358.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.*189+853C>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38261318 | |||||||
| chr7:38261529 | A | G | 11 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(8): Show | 31 | HG00738.hp2 HG00741.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.*189+642T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38261529 | |||||||
| chr7:38261588 | C | G | 1 | a0001c0001t0001g0020 | 3 | HG00642.hp2 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.*189+583G>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38261588 | |||||||
| chr7:38261597 | G | A | 1 | a0001c0001t0009g0058 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.*189+574C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38261597 | |||||||
| chr7:38261673 | G | A | 87 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(84): Show | 236 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(233): Show |
intron_variant | MODIFIER | c.*189+498C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38261673 | |||||||
| chr7:38261729 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.*189+442C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38261729 | |||||||
| chr7:38261762 | C | T | 1 | a0001c0001t0013g0032 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.*189+409G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38261762 | |||||||
| chr7:38261804 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.*189+367C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38261804 | |||||||
| chr7:38261834 | C | T | 4 | a0001c0002t0006g0013a0001c0002t0006g0151a0001c0002t0006g0152others(1): Show | 10 | HG00639.hp1 HG01358.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.*189+337G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38261834 | |||||||
| chr7:38261835 | G | A | 6 | a0001c0001t0004g0004a0001c0001t0004g0022a0001c0001t0004g0024others(3): Show | 30 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.*189+336C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38261835 | |||||||
| chr7:38261870 | C | CA | 13 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0129others(10): Show | 20 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.*189+300dupT | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38261870 | |||||||
| chr7:38261882 | A | AG | 14 | a0001c0001t0001g0101a0001c0001t0003g0007a0001c0001t0003g0014others(11): Show | 41 | HG00408.hp2 HG00558.hp1 HG01346.hp2 others(38): Show |
intron_variant | MODIFIER | c.*189+288_*189+289i others(3): Show |
TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38261882 | |||||||
| chr7:38261887 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.*189+284C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38261887 | |||||||
| chr7:38261951 | A | G | 17 | a0001c0001t0003g0029a0001c0001t0003g0039a0001c0001t0003g0040others(14): Show | 40 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(37): Show |
intron_variant | MODIFIER | c.*189+220T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38261951 | |||||||
| chr7:38261958 | T | A | 9 | a0001c0001t0003g0041a0001c0001t0003g0083a0001c0001t0003g0084others(6): Show | 11 | HG01884.hp1 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.*189+213A>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38261958 | |||||||
| chr7:38261958 | T | G | 1 | a0001c0001t0003g0087 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.*189+213A>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38261958 | |||||||
| chr7:38262020 | A | G | 2 | a0001c0002t0012g0078a0001c0002t0012g0120 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.*189+151T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38262020 | |||||||
| chr7:38262046 | T | A | 1 | a0001c0001t0003g0040 | 2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.*189+125A>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38262046 | |||||||
| chr7:38262140 | T | A | 76 | a0001c0001t0001g0101a0001c0001t0003g0007a0001c0001t0003g0014others(73): Show | 205 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.*189+31A>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 3/3 | chr7 | 38262140 | |||||||
| chr7:38262231 | G | A | 1 | a0001c0002t0021g0113 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.*142-13C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38262231 | |||||||
| chr7:38262248 | T | C | 1 | a0001c0001t0001g0021 | 3 | HG01106.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.*142-30A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38262248 | |||||||
| chr7:38262296 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.*142-78C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38262296 | |||||||
| chr7:38262529 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.*142-311T>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38262529 | |||||||
| chr7:38262647 | T | C | 1 | a0001c0001t0004g0095 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.*142-429A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38262647 | |||||||
| chr7:38262729 | C | T | 1 | a0001c0001t0001g0048 | 2 | HG00741.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.*142-511G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38262729 | |||||||
| chr7:38262847 | C | A | 1 | a0001c0002t0002g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.*142-629G>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38262847 | |||||||
| chr7:38262865 | C | G | 36 | a0001c0002t0001g0091a0001c0002t0002g0005a0001c0002t0002g0009others(33): Show | 91 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.*142-647G>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38262865 | |||||||
| chr7:38262874 | G | A | 1 | a0001c0002t0002g0112 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.*142-656C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38262874 | |||||||
| chr7:38262967 | T | C | 53 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0041others(50): Show | 129 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.*142-749A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38262967 | |||||||
| chr7:38263001 | A | G | 1 | a0001c0002t0002g0117 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.*142-783T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38263001 | |||||||
| chr7:38263079 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.*142-861G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38263079 | |||||||
| chr7:38263291 | A | C | 1 | a0001c0001t0003g0029 | 3 | HG02630.hp2 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.*142-1073T>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38263291 | |||||||
| chr7:38263356 | A | G | 1 | a0001c0001t0003g0103 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.*142-1138T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38263356 | |||||||
| chr7:38263448 | G | A | 2 | a0001c0001t0016g0080a0001c0001t0018g0079 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.*142-1230C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38263448 | |||||||
| chr7:38263519 | T | C | 76 | a0001c0001t0001g0101a0001c0001t0003g0007a0001c0001t0003g0014others(73): Show | 205 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.*142-1301A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38263519 | |||||||
| chr7:38263579 | G | A | 6 | a0001c0001t0004g0004a0001c0001t0004g0022a0001c0001t0004g0024others(3): Show | 30 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.*142-1361C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38263579 | |||||||
| chr7:38263632 | A | T | 2 | a0001c0001t0001g0140a0001c0001t0014g0139 | 2 | HG00423.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.*142-1414T>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38263632 | |||||||
| chr7:38263690 | T | A | 4 | a0001c0002t0006g0013a0001c0002t0006g0151a0001c0002t0006g0152others(1): Show | 10 | HG00639.hp1 HG01358.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.*142-1472A>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38263690 | |||||||
| chr7:38263782 | G | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0055others(3): Show | 12 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.*142-1564C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38263782 | |||||||
| chr7:38263810 | A | G | 7 | a0001c0001t0003g0041a0001c0001t0003g0087a0001c0001t0003g0088others(4): Show | 9 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.*141+1539T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38263810 | |||||||
| chr7:38263830 | T | A | 2 | a0001c0002t0002g0108a0001c0002t0002g0114 | 2 | HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.*141+1519A>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38263830 | |||||||
| chr7:38263884 | C | A | 25 | a0001c0002t0002g0005a0001c0002t0002g0009a0001c0002t0002g0012others(22): Show | 67 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.*141+1465G>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38263884 | |||||||
| chr7:38263935 | T | C | 27 | a0001c0002t0002g0005a0001c0002t0002g0009a0001c0002t0002g0012others(24): Show | 70 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.*141+1414A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38263935 | |||||||
| chr7:38264027 | A | G | 1 | a0003c0003t0003g0085 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.*141+1322T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38264027 | |||||||
| chr7:38264039 | G | A | 1 | a0001c0002t0002g0115 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.*141+1310C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38264039 | |||||||
| chr7:38264052 | A | T | 4 | a0001c0002t0006g0013a0001c0002t0006g0151a0001c0002t0006g0152others(1): Show | 10 | HG00639.hp1 HG01358.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.*141+1297T>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38264052 | |||||||
| chr7:38264058 | T | C | 3 | a0003c0003t0003g0038a0003c0003t0003g0085a0003c0003t0006g0086 | 4 | HG01884.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.*141+1291A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38264058 | |||||||
| chr7:38264155 | TATA | T | 1 | a0001c0001t0007g0025 | 3 | NA18952.hp1 NA19007.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.*141+1191_*141+119 others(7): Show |
TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38264155 | |||||||
| chr7:38264159 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.*141+1190T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38264159 | |||||||
| chr7:38264215 | A | C | 1 | a0001c0002t0002g0112 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.*141+1134T>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38264215 | |||||||
| chr7:38264230 | T | C | 1 | a0001c0001t0017g0122 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.*141+1119A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38264230 | |||||||
| chr7:38264269 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.*141+1080G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38264269 | |||||||
| chr7:38264422 | C | T | 6 | a0001c0001t0004g0004a0001c0001t0004g0022a0001c0001t0004g0024others(3): Show | 30 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.*141+927G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38264422 | |||||||
| chr7:38264473 | C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0069others(7): Show | 45 | HG01074.hp2 HG01261.hp1 HG01934.hp1 others(42): Show |
intron_variant | MODIFIER | c.*141+876G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38264473 | |||||||
| chr7:38264495 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.*141+854C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38264495 | |||||||
| chr7:38264546 | A | C | 18 | a0001c0001t0003g0029a0001c0001t0003g0039a0001c0001t0003g0040others(15): Show | 41 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.*141+803T>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38264546 | |||||||
| chr7:38264589 | C | CA | 20 | a0001c0001t0001g0036a0001c0001t0001g0101a0001c0001t0003g0007others(17): Show | 72 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.*141+759dupT | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38264589 | |||||||
| chr7:38264666 | G | A | 10 | a0001c0001t0003g0007a0001c0001t0003g0053a0001c0001t0003g0102others(7): Show | 32 | HG00408.hp2 HG00558.hp1 HG02135.hp1 others(29): Show |
intron_variant | MODIFIER | c.*141+683C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38264666 | |||||||
| chr7:38264849 | C | T | 1 | a0001c0002t0006g0152 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.*141+500G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38264849 | |||||||
| chr7:38264934 | T | C | 2 | a0001c0002t0012g0078a0001c0002t0012g0120 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.*141+415A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38264934 | |||||||
| chr7:38264941 | T | G | 7 | a0001c0001t0004g0004a0001c0001t0004g0022a0001c0001t0004g0024others(4): Show | 33 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.*141+408A>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38264941 | |||||||
| chr7:38264963 | C | T | 1 | a0001c0002t0020g0111 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.*141+386G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38264963 | |||||||
| chr7:38264987 | A | C | 1 | a0001c0001t0001g0060 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.*141+362T>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38264987 | |||||||
| chr7:38265152 | T | C | 2 | a0002c0004t0008g0019a0002c0004t0008g0148 | 5 | HG01243.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.*141+197A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38265152 | |||||||
| chr7:38265200 | A | G | 1 | a0001c0001t0003g0099 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.*141+149T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38265200 | |||||||
| chr7:38265223 | T | C | 2 | a0002c0004t0008g0019a0002c0004t0008g0148 | 5 | HG01243.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.*141+126A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38265223 | |||||||
| chr7:38265245 | A | T | 2 | a0002c0004t0008g0019a0002c0004t0008g0148 | 5 | HG01243.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.*141+104T>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38265245 | |||||||
| chr7:38265260 | ATGTT | A | 2 | a0002c0004t0008g0019a0002c0004t0008g0148 | 5 | HG01243.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.*141+85_*141+88del others(4): Show |
TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38265260 | |||||||
| chr7:38265316 | G | T | 1 | a0001c0002t0019g0116 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.*141+33C>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38265316 | |||||||
| chr7:38265325 | C | T | 78 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0003g0007others(75): Show | 209 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.*141+24G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38265325 | |||||||
| chr7:38265336 | C | T | 2 | a0001c0001t0001g0055a0001c0001t0014g0139 | 2 | HG01496.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.*141+13G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 2/3 | chr7 | 38265336 | |||||||
| chr7:38265738 | C | T | 2 | a0001c0002t0002g0012a0001c0002t0002g0115 | 8 | HG00438.hp2 HG00673.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-60G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38265738 | |||||||
| chr7:38265739 | A | G | 80 | a0001c0001t0001g0059a0001c0001t0001g0100a0001c0001t0001g0101others(77): Show | 211 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.-12-61T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38265739 | |||||||
| chr7:38265800 | T | C | 7 | a0001c0001t0001g0034a0001c0001t0009g0023a0001c0001t0017g0122others(4): Show | 16 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.-12-122A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38265800 | |||||||
| chr7:38265803 | G | A | 27 | a0001c0002t0002g0005a0001c0002t0002g0009a0001c0002t0002g0012others(24): Show | 70 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.-12-125C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38265803 | |||||||
| chr7:38265912 | A | G | 2 | a0001c0001t0001g0143a0001c0002t0006g0151 | 2 | HG02572.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.-12-234T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38265912 | |||||||
| chr7:38265982 | T | G | 18 | a0001c0001t0001g0081a0001c0001t0003g0029a0001c0001t0003g0039others(15): Show | 41 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(38): Show |
intron_variant | MODIFIER | c.-12-304A>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38265982 | |||||||
| chr7:38266002 | A | G | 10 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(7): Show | 30 | HG00738.hp2 HG00741.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.-12-324T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266002 | |||||||
| chr7:38266052 | T | C | 53 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0003g0007others(50): Show | 135 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.-12-374A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266052 | |||||||
| chr7:38266136 | T | C | 1 | a0001c0002t0002g0045 | 2 | HG00733.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.-12-458A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266136 | |||||||
| chr7:38266177 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-12-499A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266177 | |||||||
| chr7:38266296 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-12-618C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266296 | |||||||
| chr7:38266313 | T | TTTG | 6 | a0001c0001t0003g0094a0001c0002t0001g0091a0001c0002t0003g0011others(3): Show | 12 | HG00597.hp1 HG02683.hp2 HG03471.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12-638_-12-636dup others(3): Show |
TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266313 | |||||||
| chr7:38266330 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-12-652A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266330 | |||||||
| chr7:38266461 | C | A | 1 | a0001c0001t0001g0136 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-12-783G>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266461 | |||||||
| chr7:38266464 | G | A | 2 | a0001c0001t0016g0080a0001c0001t0018g0079 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-12-786C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266464 | |||||||
| chr7:38266494 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-12-816C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266494 | |||||||
| chr7:38266498 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG00140.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.-12-820G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266498 | |||||||
| chr7:38266502 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-12-824T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266502 | |||||||
| chr7:38266612 | T | G | 17 | a0001c0001t0001g0081a0001c0001t0003g0039a0001c0001t0003g0040others(14): Show | 38 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.-12-934A>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266612 | |||||||
| chr7:38266686 | G | C | 9 | a0001c0001t0003g0041a0001c0001t0003g0083a0001c0001t0003g0084others(6): Show | 11 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-12-1008C>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266686 | |||||||
| chr7:38266690 | A | G | 11 | a0001c0001t0003g0094a0001c0001t0003g0105a0001c0001t0004g0022others(8): Show | 18 | HG02135.hp1 HG02622.hp1 HG02647.hp2 others(15): Show |
intron_variant | MODIFIER | c.-12-1012T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266690 | |||||||
| chr7:38266739 | A | G | 2 | a0001c0001t0016g0080a0001c0001t0018g0079 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-12-1061T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266739 | |||||||
| chr7:38266800 | T | A | 1 | a0001c0001t0001g0069 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-12-1122A>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266800 | |||||||
| chr7:38266829 | C | A | 1 | a0001c0001t0001g0144 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-12-1151G>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266829 | |||||||
| chr7:38266830 | T | G | 6 | a0001c0001t0003g0094a0001c0002t0001g0091a0001c0002t0003g0011others(3): Show | 12 | HG00597.hp1 HG02683.hp2 HG03471.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12-1152A>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266830 | |||||||
| chr7:38266845 | C | A | 2 | a0001c0001t0016g0080a0001c0001t0018g0079 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-12-1167G>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266845 | |||||||
| chr7:38266859 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-12-1181A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266859 | |||||||
| chr7:38266921 | T | G | 4 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0055others(1): Show | 10 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-1243A>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266921 | |||||||
| chr7:38266956 | C | T | 90 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(87): Show | 241 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.-12-1278G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266956 | |||||||
| chr7:38266993 | T | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(7): Show | 30 | HG00738.hp2 HG00741.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.-12-1315A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38266993 | |||||||
| chr7:38267077 | G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(7): Show | 30 | HG00738.hp2 HG00741.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.-12-1399C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38267077 | |||||||
| chr7:38267114 | C | G | 1 | a0001c0001t0001g0033 | 2 | HG01261.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-12-1436G>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38267114 | |||||||
| chr7:38267181 | T | C | 1 | a0001c0001t0001g0031 | 2 | HG01884.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-12-1503A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38267181 | |||||||
| chr7:38267211 | G | T | 2 | a0001c0001t0016g0080a0001c0001t0018g0079 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-12-1533C>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38267211 | |||||||
| chr7:38267402 | A | C | 1 | a0001c0001t0001g0126 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-12-1724T>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38267402 | |||||||
| chr7:38267405 | T | A | 1 | a0001c0001t0003g0104 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-12-1727A>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38267405 | |||||||
| chr7:38267505 | G | A | 89 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(86): Show | 240 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.-12-1827C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38267505 | |||||||
| chr7:38267519 | T | C | 15 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0003g0007others(12): Show | 42 | HG00408.hp2 HG00558.hp1 HG01346.hp2 others(39): Show |
intron_variant | MODIFIER | c.-12-1841A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38267519 | |||||||
| chr7:38267667 | T | G | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-12-1989A>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38267667 | |||||||
| chr7:38267781 | G | T | 5 | a0001c0001t0004g0022a0001c0001t0005g0006a0001c0001t0005g0050others(2): Show | 24 | HG02257.hp2 HG02258.hp2 HG02559.hp2 others(21): Show |
intron_variant | MODIFIER | c.-12-2103C>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38267781 | |||||||
| chr7:38267930 | G | T | 1 | a0001c0002t0002g0108 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-12-2252C>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38267930 | |||||||
| chr7:38267936 | T | C | 1 | a0001c0001t0003g0105 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-12-2258A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38267936 | |||||||
| chr7:38268005 | A | T | 1 | a0001c0001t0005g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-12-2327T>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38268005 | |||||||
| chr7:38268009 | T | G | 1 | a0001c0001t0001g0071 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-12-2331A>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38268009 | |||||||
| chr7:38268021 | G | A | 89 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(86): Show | 240 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.-12-2343C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38268021 | |||||||
| chr7:38268029 | C | G | 1 | a0001c0001t0003g0087 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12-2351G>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38268029 | |||||||
| chr7:38268184 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-12-2506T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38268184 | |||||||
| chr7:38268242 | T | C | 1 | a0001c0001t0001g0031 | 2 | HG01884.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-12-2564A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38268242 | |||||||
| chr7:38268266 | A | G | 1 | a0002c0004t0008g0148 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-12-2588T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38268266 | |||||||
| chr7:38268289 | G | C | 4 | a0001c0002t0006g0013a0001c0002t0006g0151a0001c0002t0006g0152others(1): Show | 10 | HG00639.hp1 HG01358.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-2611C>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38268289 | |||||||
| chr7:38268389 | A | G | 27 | a0001c0002t0002g0005a0001c0002t0002g0009a0001c0002t0002g0012others(24): Show | 70 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.-12-2711T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38268389 | |||||||
| chr7:38268390 | T | C | 4 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0140others(1): Show | 6 | HG00423.hp1 HG00741.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-2712A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38268390 | |||||||
| chr7:38268461 | A | C | 3 | a0001c0001t0003g0083a0001c0001t0003g0084a0001c0001t0003g0094 | 3 | HG02622.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-12-2783T>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38268461 | |||||||
| chr7:38268505 | T | C | 1 | a0001c0001t0003g0029 | 3 | HG02630.hp2 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-12-2827A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38268505 | |||||||
| chr7:38268517 | C | T | 27 | a0001c0002t0002g0005a0001c0002t0002g0009a0001c0002t0002g0012others(24): Show | 70 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.-12-2839G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38268517 | |||||||
| chr7:38268620 | T | C | 1 | a0001c0001t0005g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-2942A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38268620 | |||||||
| chr7:38268648 | G | A | 12 | a0001c0002t0002g0005a0001c0002t0002g0012a0001c0002t0002g0027others(9): Show | 42 | HG00438.hp2 HG00673.hp1 HG01515.hp1 others(39): Show |
intron_variant | MODIFIER | c.-12-2970C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38268648 | |||||||
| chr7:38268716 | C | T | 1 | a0001c0001t0003g0039 | 2 | HG02055.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-12-3038G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38268716 | |||||||
| chr7:38268770 | T | TAA | 1 | a0001c0001t0001g0030 | 3 | HG02258.hp1 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-12-3093_-12-3092i others(4): Show |
TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38268770 | |||||||
| chr7:38268849 | G | C | 5 | a0001c0001t0003g0088a0003c0003t0003g0038a0003c0003t0003g0085others(2): Show | 6 | HG01884.hp1 HG02280.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-3171C>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38268849 | |||||||
| chr7:38268939 | C | A | 1 | a0001c0001t0001g0072 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-12-3261G>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38268939 | |||||||
| chr7:38268961 | T | C | 2 | a0001c0001t0016g0080a0001c0001t0018g0079 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-12-3283A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38268961 | |||||||
| chr7:38269074 | C | G | 2 | a0001c0001t0016g0080a0001c0001t0018g0079 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-12-3396G>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38269074 | |||||||
| chr7:38269085 | G | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(7): Show | 30 | HG00738.hp2 HG00741.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.-12-3407C>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38269085 | |||||||
| chr7:38269137 | T | G | 2 | a0001c0001t0016g0080a0001c0001t0018g0079 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-12-3459A>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38269137 | |||||||
| chr7:38269238 | A | G | 6 | a0001c0001t0003g0039a0001c0001t0003g0082a0001c0001t0005g0006others(3): Show | 24 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.-12-3560T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38269238 | |||||||
| chr7:38269252 | A | G | 1 | a0001c0002t0003g0090 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-12-3574T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38269252 | |||||||
| chr7:38269257 | A | G | 2 | a0001c0002t0012g0078a0001c0002t0012g0120 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-12-3579T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38269257 | |||||||
| chr7:38269345 | G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(7): Show | 30 | HG00738.hp2 HG00741.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.-12-3667C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38269345 | |||||||
| chr7:38269385 | C | G | 1 | a0001c0001t0013g0032 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-12-3707G>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38269385 | |||||||
| chr7:38269501 | A | C | 69 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(66): Show | 197 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.-12-3823T>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38269501 | |||||||
| chr7:38269748 | C | T | 15 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0003g0007others(12): Show | 42 | HG00408.hp2 HG00558.hp1 HG01346.hp2 others(39): Show |
intron_variant | MODIFIER | c.-13+3839G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38269748 | |||||||
| chr7:38269842 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-13+3745T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38269842 | |||||||
| chr7:38269847 | T | C | 1 | a0001c0001t0011g0073 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-13+3740A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38269847 | |||||||
| chr7:38270050 | A | T | 90 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(87): Show | 241 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.-13+3537T>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270050 | |||||||
| chr7:38270060 | C | G | 1 | a0001c0001t0009g0058 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-13+3527G>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270060 | |||||||
| chr7:38270065 | G | A | 1 | a0001c0002t0003g0093 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-13+3522C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270065 | |||||||
| chr7:38270109 | A | C | 5 | a0001c0001t0018g0079a0001c0002t0002g0106a0003c0003t0003g0038others(2): Show | 6 | HG01884.hp1 HG03471.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+3478T>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270109 | |||||||
| chr7:38270116 | T | C | 1 | a0001c0002t0002g0107 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-13+3471A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270116 | |||||||
| chr7:38270218 | C | T | 18 | a0001c0001t0001g0081a0001c0001t0003g0029a0001c0001t0003g0039others(15): Show | 41 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(38): Show |
intron_variant | MODIFIER | c.-13+3369G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270218 | |||||||
| chr7:38270249 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-13+3338T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270249 | |||||||
| chr7:38270289 | G | A | 7 | a0001c0001t0004g0004a0001c0001t0004g0022a0001c0001t0004g0024others(4): Show | 33 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.-13+3298C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270289 | |||||||
| chr7:38270330 | C | G | 79 | a0001c0001t0001g0081a0001c0001t0001g0100a0001c0001t0001g0101others(76): Show | 210 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.-13+3257G>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270330 | |||||||
| chr7:38270374 | G | C | 1 | a0001c0001t0003g0105 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-13+3213C>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270374 | |||||||
| chr7:38270378 | T | C | 1 | a0001c0001t0003g0105 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-13+3209A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270378 | |||||||
| chr7:38270384 | G | A | 1 | a0001c0001t0003g0105 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-13+3203C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270384 | |||||||
| chr7:38270419 | A | G | 1 | a0001c0001t0003g0105 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-13+3168T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270419 | |||||||
| chr7:38270433 | G | A | 1 | a0001c0001t0003g0105 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-13+3154C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270433 | |||||||
| chr7:38270440 | G | A | 4 | a0001c0002t0006g0013a0001c0002t0006g0151a0001c0002t0006g0152others(1): Show | 10 | HG00639.hp1 HG01358.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13+3147C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270440 | |||||||
| chr7:38270444 | C | T | 1 | a0001c0001t0003g0105 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-13+3143G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270444 | |||||||
| chr7:38270481 | G | A | 1 | a0001c0001t0003g0105 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-13+3106C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270481 | |||||||
| chr7:38270576 | G | C | 79 | a0001c0001t0001g0081a0001c0001t0001g0100a0001c0001t0001g0101others(76): Show | 210 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.-13+3011C>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270576 | |||||||
| chr7:38270586 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-13+3001A>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270586 | |||||||
| chr7:38270629 | T | G | 1 | a0001c0001t0004g0024 | 3 | NA18964.hp2 NA19058.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-13+2958A>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270629 | |||||||
| chr7:38270651 | A | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(7): Show | 30 | HG00738.hp2 HG00741.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.-13+2936T>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270651 | |||||||
| chr7:38270659 | G | A | 80 | a0001c0001t0001g0037a0001c0001t0001g0081a0001c0001t0001g0100others(77): Show | 212 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.-13+2928C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270659 | |||||||
| chr7:38270711 | A | G | 7 | a0001c0001t0004g0004a0001c0001t0004g0022a0001c0001t0004g0024others(4): Show | 33 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.-13+2876T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270711 | |||||||
| chr7:38270728 | C | T | 1 | a0001c0002t0002g0043 | 2 | NA18941.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.-13+2859G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270728 | |||||||
| chr7:38270905 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-13+2682G>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270905 | |||||||
| chr7:38270911 | C | T | 2 | a0001c0001t0003g0083a0001c0001t0003g0084 | 2 | HG02622.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-13+2676G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270911 | |||||||
| chr7:38270916 | C | T | 3 | a0001c0002t0002g0027a0001c0002t0002g0106a0001c0002t0002g0107 | 5 | HG02040.hp2 HG02056.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+2671G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270916 | |||||||
| chr7:38270925 | GA | G | 3 | a0001c0002t0002g0027a0001c0002t0002g0106a0001c0002t0002g0107 | 5 | HG02040.hp2 HG02056.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+2661delT | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38270925 | |||||||
| chr7:38271005 | C | G | 1 | a0001c0001t0003g0082 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-13+2582G>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38271005 | |||||||
| chr7:38271008 | T | G | 1 | a0001c0001t0016g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-13+2579A>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38271008 | |||||||
| chr7:38271088 | A | G | 27 | a0001c0002t0002g0005a0001c0002t0002g0009a0001c0002t0002g0012others(24): Show | 70 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.-13+2499T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38271088 | |||||||
| chr7:38271207 | T | A | 1 | a0001c0001t0001g0074 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-13+2380A>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38271207 | |||||||
| chr7:38271215 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-13+2372G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38271215 | |||||||
| chr7:38271220 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-13+2367G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38271220 | |||||||
| chr7:38271308 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-13+2279C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38271308 | |||||||
| chr7:38271363 | T | C | 1 | a0001c0002t0002g0119 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-13+2224A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38271363 | |||||||
| chr7:38271429 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-13+2158A>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38271429 | |||||||
| chr7:38271497 | G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(7): Show | 30 | HG00738.hp2 HG00741.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.-13+2090C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38271497 | |||||||
| chr7:38271520 | C | G | 4 | a0001c0001t0005g0006a0001c0001t0005g0050a0001c0001t0005g0051others(1): Show | 21 | HG02257.hp2 HG02258.hp2 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.-13+2067G>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38271520 | |||||||
| chr7:38271548 | GA | G | 25 | a0001c0002t0002g0005a0001c0002t0002g0009a0001c0002t0002g0012others(22): Show | 68 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.-13+2038delT | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38271548 | |||||||
| chr7:38271576 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-13+2011C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38271576 | |||||||
| chr7:38271599 | G | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(7): Show | 30 | HG00738.hp2 HG00741.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.-13+1988C>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38271599 | |||||||
| chr7:38271628 | A | G | 27 | a0001c0002t0002g0005a0001c0002t0002g0009a0001c0002t0002g0012others(24): Show | 70 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.-13+1959T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38271628 | |||||||
| chr7:38271646 | T | A | 27 | a0001c0002t0002g0005a0001c0002t0002g0009a0001c0002t0002g0012others(24): Show | 70 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.-13+1941A>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38271646 | |||||||
| chr7:38271770 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-13+1817T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38271770 | |||||||
| chr7:38271847 | G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 18 | HG01074.hp2 HG01261.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-13+1740C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38271847 | |||||||
| chr7:38271961 | A | G | 4 | a0001c0002t0006g0013a0001c0002t0006g0151a0001c0002t0006g0152others(1): Show | 10 | HG00639.hp1 HG01358.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13+1626T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38271961 | |||||||
| chr7:38272026 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-13+1561A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38272026 | |||||||
| chr7:38272104 | C | G | 1 | a0001c0001t0001g0123 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-13+1483G>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38272104 | |||||||
| chr7:38272189 | C | T | 91 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(88): Show | 243 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(240): Show |
intron_variant | MODIFIER | c.-13+1398G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38272189 | |||||||
| chr7:38272208 | C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0055 | 6 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+1379G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38272208 | |||||||
| chr7:38272217 | A | G | 1 | a0001c0001t0003g0094 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-13+1370T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38272217 | |||||||
| chr7:38272230 | G | A | 1 | a0001c0002t0002g0121 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-13+1357C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38272230 | |||||||
| chr7:38272230 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-13+1357C>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38272230 | |||||||
| chr7:38272270 | C | T | 5 | a0001c0002t0001g0091a0001c0002t0003g0011a0001c0002t0003g0090others(2): Show | 11 | HG00597.hp1 HG02683.hp2 HG03654.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+1317G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38272270 | |||||||
| chr7:38272351 | A | G | 79 | a0001c0001t0001g0081a0001c0001t0001g0100a0001c0001t0001g0101others(76): Show | 210 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.-13+1236T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38272351 | |||||||
| chr7:38272635 | T | A | 1 | a0001c0002t0002g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-13+952A>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38272635 | |||||||
| chr7:38272661 | T | C | 1 | a0001c0001t0001g0048 | 2 | HG00741.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.-13+926A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38272661 | |||||||
| chr7:38272720 | C | T | 1 | a0001c0001t0005g0050 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-13+867G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38272720 | |||||||
| chr7:38272743 | A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0030 | 7 | HG02109.hp1 HG02258.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+844T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38272743 | |||||||
| chr7:38272766 | G | A | 1 | a0001c0001t0003g0146 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-13+821C>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38272766 | |||||||
| chr7:38272982 | C | T | 17 | a0001c0001t0001g0081a0001c0001t0003g0039a0001c0001t0003g0040others(14): Show | 38 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.-13+605G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38272982 | |||||||
| chr7:38272999 | C | T | 2 | a0001c0001t0016g0080a0001c0001t0018g0079 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-13+588G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38272999 | |||||||
| chr7:38273024 | A | G | 10 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(7): Show | 30 | HG00738.hp2 HG00741.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.-13+563T>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38273024 | |||||||
| chr7:38273150 | C | T | 1 | a0001c0002t0012g0078 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-13+437G>A | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38273150 | |||||||
| chr7:38273195 | T | C | 1 | a0001c0001t0003g0029 | 3 | HG02630.hp2 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-13+392A>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38273195 | |||||||
| chr7:38273246 | CT | C | 117 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(114): Show | 349 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(346): Show |
intron_variant | MODIFIER | c.-13+340delA | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38273246 | |||||||
| chr7:38273268 | C | G | 1 | a0001c0001t0003g0053 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-13+319G>C | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38273268 | |||||||
| chr7:38273478 | G | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(7): Show | 30 | HG00738.hp2 HG00741.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.-13+109C>G | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38273478 | |||||||
| chr7:38273548 | C | A | 4 | a0001c0002t0006g0013a0001c0002t0006g0151a0001c0002t0006g0152others(1): Show | 10 | HG00639.hp1 HG01358.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13+39G>T | TARP | ENSG00000289746.1 | transcript | ENST00000698248.1 | protein_coding | 1/3 | chr7 | 38273548 |