Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1743 |
| ensemblid | ENSG00000119689.15 |
| hgncid | 2911 |
| symbol | DLST |
| name | dihydrolipoamide S-succinyltransferase |
| refseq_nuc | NM_001933.5 |
| refseq_prot | NP_001924.2 |
| ensembl_nuc | ENST00000334220.9 |
| ensembl_prot | ENSP00000335304.4 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 74881916 |
| end | 74903743 |
| strand | + |
| ver | v1.2 |
| region | chr14:74881916-74903743 |
| region5000 | chr14:74876916-74908743 |
| regionname0 | DLST_chr14_74881916_74903743 |
| regionname5000 | DLST_chr14_74876916_74908743 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 453 | 384 | 87 | 72 | 172 | 10 | 41 | 137 | DLST_chr14_74876916_74908743 | DLST | MLSRS others(448): Show |
chr14 | 74876916 | 74908743 |
| a0002 | 0/0 | 453 | 3 | 1 | 0 | 1 | 0 | 1 | 0 | DLST_chr14_74876916_74908743 | DLST | MLSRS others(448): Show |
chr14 | 74876916 | 74908743 |
| a0003 | 0/0 | 453 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | MLSRS others(448): Show |
chr14 | 74876916 | 74908743 |
| a0004 | 0/0 | 453 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | MLSRS others(448): Show |
chr14 | 74876916 | 74908743 |
| a0005 | 0/0 | 453 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | MLSRS others(448): Show |
chr14 | 74876916 | 74908743 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1359 | 172 | 66 | 30 | 50 | 2 | 24 | DLST_chr14_74876916_74908743 | DLST | ATGCT others(1354): Show |
chr14 | 74876916 | 74908743 | ||
| a0001c0002 | 1/1 | 1359 | 122 | 2 | 23 | 78 | 5 | 12 | DLST_chr14_74876916_74908743 | DLST | ATGCT others(1354): Show |
chr14 | 74876916 | 74908743 | ||
| a0001c0003 | 0/0 | 1359 | 89 | 19 | 18 | 44 | 3 | 5 | DLST_chr14_74876916_74908743 | DLST | ATGCT others(1354): Show |
chr14 | 74876916 | 74908743 | ||
| a0001c0006 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATGCT others(1354): Show |
chr14 | 74876916 | 74908743 | ||
| a0002c0005 | 0/0 | 1359 | 3 | 1 | 0 | 1 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | ATGCT others(1354): Show |
chr14 | 74876916 | 74908743 | ||
| a0003c0004 | 0/0 | 1359 | 3 | 3 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATGCT others(1354): Show |
chr14 | 74876916 | 74908743 | ||
| a0004c0007 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATGCT others(1354): Show |
chr14 | 74876916 | 74908743 | ||
| a0005c0008 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATGCT others(1354): Show |
chr14 | 74876916 | 74908743 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2813 | 119 | 28 | 25 | 46 | 2 | 18 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0001c0001t0002 | 0/0 | 2813 | 5 | 5 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0001c0001t0004 | 0/0 | 2813 | 30 | 23 | 4 | 0 | 0 | 3 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0001c0001t0005 | 0/0 | 2813 | 6 | 5 | 0 | 0 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0001c0001t0007 | 0/0 | 2813 | 5 | 0 | 0 | 3 | 0 | 2 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0001c0001t0010 | 0/0 | 2813 | 3 | 2 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0001c0001t0011 | 0/0 | 2813 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0001c0001t0012 | 0/0 | 2813 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0001c0001t0013 | 0/0 | 2813 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0001c0001t0014 | 0/0 | 2813 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0001c0002t0001 | 0/0 | 2813 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0001c0002t0002 | 1/0 | 2813 | 105 | 2 | 20 | 67 | 4 | 11 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0001c0002t0003 | 0/0 | 2813 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0001c0002t0006 | 0/0 | 2813 | 5 | 0 | 0 | 5 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0001c0002t0008 | 0/1 | 2813 | 5 | 0 | 2 | 0 | 1 | 1 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0001c0002t0009 | 0/0 | 2813 | 5 | 0 | 0 | 5 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0001c0003t0003 | 0/0 | 2813 | 86 | 16 | 18 | 44 | 3 | 5 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0001c0003t0015 | 0/0 | 2813 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0001c0003t0016 | 0/0 | 2813 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0001c0003t0017 | 0/0 | 2813 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0001c0006t0003 | 0/0 | 2813 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0002c0005t0003 | 0/0 | 2813 | 3 | 1 | 0 | 1 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0003c0004t0003 | 0/0 | 2813 | 3 | 3 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0004c0007t0010 | 0/0 | 2813 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| a0005c0008t0002 | 0/0 | 2813 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | ATATC others(2808): Show |
chr14 | 74876916 | 74908743 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 30 | 0 | 9 | 12 | 0 | 9 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0005 | 0/0 | 11 | 0 | 8 | 3 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0007 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0009 | 0/0 | 6 | 1 | 2 | 0 | 1 | 2 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0004g0006 | 0/0 | 10 | 5 | 2 | 0 | 0 | 3 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0004g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0004g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0005g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0007g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0007g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0007g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0007g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0007g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0010g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0010g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0010g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0011g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0012g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0013g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0001t0014g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0001 | 1/0 | 35 | 1 | 11 | 17 | 1 | 4 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0004 | 0/0 | 16 | 0 | 1 | 15 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0012 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0016 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0022 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0006g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0006g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0008g0001 | 0/1 | 3 | 0 | 1 | 0 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0008g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0008g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0009g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0002t0009g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0003 | 0/0 | 25 | 2 | 4 | 16 | 2 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0008 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0018 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0036 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0015g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0016g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0003t0017g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0001c0006t0003g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0002c0005t0003g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0002c0005t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0003c0004t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0003c0004t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0004c0007t0010g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| a0005c0008t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0003 | t0003 | g0128 | EUR | GBR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0102 | EUR | GBR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00280 | hp1 | a0001 | c0003 | t0003 | g0003 | EUR | FIN | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0097 | EUR | FIN | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00408 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | CHS | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0104 | EAS | CHS | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | CHS | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00621 | hp1 | a0001 | c0001 | t0013 | g0015 | EAS | CHS | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00621 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | CHS | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00642 | hp1 | a0001 | c0003 | t0003 | g0029 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0174 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00673 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | CHS | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00673 | hp2 | a0001 | c0001 | t0007 | g0053 | EAS | CHS | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00733 | hp1 | a0001 | c0003 | t0003 | g0124 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00735 | hp2 | a0001 | c0003 | t0003 | g0029 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0109 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00738 | hp2 | a0001 | c0003 | t0003 | g0127 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG00741 | hp2 | a0001 | c0002 | t0008 | g0001 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0022 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01081 | hp2 | a0001 | c0001 | t0010 | g0044 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01106 | hp1 | a0001 | c0003 | t0003 | g0133 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01167 | hp1 | a0001 | c0006 | t0003 | g0003 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01167 | hp2 | a0001 | c0003 | t0003 | g0018 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01168 | hp2 | a0001 | c0003 | t0003 | g0018 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01175 | hp1 | a0001 | c0003 | t0003 | g0079 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01175 | hp2 | a0001 | c0002 | t0008 | g0033 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01192 | hp1 | a0001 | c0003 | t0003 | g0081 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01243 | hp2 | a0001 | c0003 | t0003 | g0003 | AMR | PUR | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01256 | hp2 | a0001 | c0003 | t0003 | g0136 | AMR | CLM | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | CLM | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01257 | hp2 | a0001 | c0003 | t0003 | g0035 | AMR | CLM | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01261 | hp2 | a0001 | c0003 | t0003 | g0134 | AMR | CLM | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0026 | AMR | CLM | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0112 | AMR | CLM | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01358 | hp2 | a0001 | c0003 | t0003 | g0003 | AMR | CLM | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01361 | hp1 | a0001 | c0003 | t0003 | g0018 | AMR | CLM | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | CLM | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01433 | hp2 | a0001 | c0003 | t0003 | g0003 | AMR | CLM | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0026 | AMR | CLM | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0016 | EUR | IBS | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01884 | hp1 | a0001 | c0003 | t0003 | g0121 | AFR | ACB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01891 | hp2 | a0001 | c0003 | t0003 | g0036 | AFR | ACB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01943 | hp2 | a0001 | c0003 | t0003 | g0018 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0077 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01981 | hp1 | a0001 | c0002 | t0003 | g0080 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02015 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | KHV | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02055 | hp1 | a0001 | c0003 | t0003 | g0028 | AFR | ACB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02055 | hp2 | a0002 | c0005 | t0003 | g0132 | AFR | ACB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02071 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | KHV | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | KHV | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02129 | hp2 | a0002 | c0005 | t0003 | g0003 | EAS | KHV | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0059 | AFR | ACB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02148 | hp2 | a0001 | c0003 | t0003 | g0003 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CDX | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0106 | EAS | CDX | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | CDX | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | CDX | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02257 | hp1 | a0001 | c0003 | t0003 | g0119 | AFR | ACB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ACB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02451 | hp1 | a0004 | c0007 | t0010 | g0047 | AFR | ACB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0107 | EAS | KHV | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0051 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02615 | hp1 | a0001 | c0003 | t0003 | g0117 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02615 | hp2 | a0001 | c0003 | t0003 | g0126 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0066 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0070 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0057 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02647 | hp1 | a0001 | c0001 | t0010 | g0045 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0069 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02698 | hp1 | a0001 | c0002 | t0008 | g0001 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0022 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02717 | hp1 | a0001 | c0003 | t0003 | g0130 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02723 | hp1 | a0003 | c0004 | t0003 | g0043 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0022 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02735 | hp2 | a0002 | c0005 | t0003 | g0003 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02738 | hp1 | a0001 | c0001 | t0007 | g0048 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0063 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02895 | hp1 | a0001 | c0001 | t0014 | g0024 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02897 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0046 | AFR | ESN | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | ESN | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02970 | hp2 | a0003 | c0004 | t0003 | g0173 | AFR | ESN | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02976 | hp1 | a0003 | c0004 | t0003 | g0043 | AFR | ESN | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02976 | hp2 | a0001 | c0003 | t0003 | g0023 | AFR | ESN | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03017 | hp2 | a0001 | c0003 | t0003 | g0129 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0071 | AFR | MSL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03130 | hp2 | a0001 | c0001 | t0012 | g0064 | AFR | ESN | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03139 | hp2 | a0001 | c0001 | t0011 | g0093 | AFR | ESN | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | ESN | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0062 | AFR | ESN | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03225 | hp2 | a0001 | c0003 | t0003 | g0023 | AFR | MSL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03239 | hp1 | a0001 | c0003 | t0003 | g0135 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | MSL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03490 | hp2 | a0001 | c0003 | t0003 | g0003 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03491 | hp2 | a0001 | c0003 | t0003 | g0037 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03579 | hp1 | a0001 | c0003 | t0003 | g0003 | AFR | MSL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0016 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | STU | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0100 | SAS | BEB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG04115 | hp1 | a0001 | c0003 | t0003 | g0036 | SAS | STU | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0082 | SAS | BEB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0094 | SAS | STU | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | STU | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG04228 | hp1 | a0001 | c0001 | t0007 | g0055 | SAS | STU | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | YRI | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18747 | hp1 | a0001 | c0003 | t0003 | g0008 | EAS | CHB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18747 | hp2 | a0001 | c0003 | t0003 | g0087 | EAS | CHB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18906 | hp1 | a0001 | c0003 | t0015 | g0125 | AFR | YRI | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18906 | hp2 | a0001 | c0003 | t0003 | g0123 | AFR | YRI | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18940 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18944 | hp1 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18945 | hp2 | a0001 | c0002 | t0006 | g0021 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18950 | hp2 | a0001 | c0002 | t0009 | g0001 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18951 | hp1 | a0001 | c0002 | t0009 | g0001 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18951 | hp2 | a0001 | c0003 | t0003 | g0008 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18952 | hp1 | a0001 | c0003 | t0003 | g0131 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18953 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18954 | hp1 | a0001 | c0001 | t0007 | g0054 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18954 | hp2 | a0001 | c0003 | t0003 | g0172 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18959 | hp1 | a0001 | c0003 | t0003 | g0120 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18959 | hp2 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18960 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18963 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18964 | hp1 | a0001 | c0001 | t0007 | g0056 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18964 | hp2 | a0001 | c0002 | t0006 | g0021 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18965 | hp2 | a0001 | c0003 | t0003 | g0037 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18967 | hp1 | a0001 | c0003 | t0003 | g0083 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18972 | hp2 | a0001 | c0003 | t0003 | g0090 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18977 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18978 | hp2 | a0001 | c0003 | t0003 | g0008 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18980 | hp2 | a0001 | c0003 | t0003 | g0118 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18983 | hp2 | a0001 | c0003 | t0003 | g0008 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18986 | hp1 | a0001 | c0002 | t0006 | g0021 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18987 | hp1 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18993 | hp2 | a0001 | c0003 | t0003 | g0089 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18995 | hp2 | a0001 | c0003 | t0003 | g0008 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18997 | hp1 | a0001 | c0003 | t0003 | g0086 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18997 | hp2 | a0001 | c0002 | t0002 | g0114 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18998 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19003 | hp1 | a0001 | c0003 | t0003 | g0085 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19005 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19006 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19009 | hp1 | a0001 | c0002 | t0006 | g0091 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | LWK | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0065 | AFR | LWK | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19043 | hp2 | a0001 | c0003 | t0003 | g0035 | AFR | LWK | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19054 | hp2 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19056 | hp2 | a0001 | c0002 | t0006 | g0030 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19058 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19060 | hp1 | a0001 | c0003 | t0003 | g0008 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19066 | hp1 | a0001 | c0002 | t0009 | g0001 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19068 | hp1 | a0001 | c0002 | t0009 | g0001 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19075 | hp1 | a0001 | c0003 | t0003 | g0088 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19075 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19077 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19078 | hp1 | a0001 | c0003 | t0003 | g0122 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19078 | hp2 | a0001 | c0003 | t0003 | g0139 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0113 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19079 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19080 | hp1 | a0001 | c0003 | t0003 | g0084 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19084 | hp1 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19088 | hp2 | a0001 | c0003 | t0003 | g0008 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19090 | hp2 | a0001 | c0003 | t0003 | g0008 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19091 | hp1 | a0001 | c0002 | t0009 | g0074 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19091 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | YRI | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0115 | AFR | ASW | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA20129 | hp2 | a0001 | c0003 | t0003 | g0028 | AFR | ASW | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | TSI | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA20805 | hp1 | a0001 | c0002 | t0008 | g0076 | EUR | TSI | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA20805 | hp2 | a0001 | c0003 | t0003 | g0003 | EUR | TSI | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | GIH | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0052 | SAS | GIH | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0067 | AFR | ACB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02486 | hp2 | a0001 | c0003 | t0003 | g0116 | AFR | ACB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | ACB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG02559 | hp2 | a0001 | c0003 | t0003 | g0023 | AFR | ACB | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0050 | AFR | MSL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | USA | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0049 | AFR | USA | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18955 | hp1 | a0005 | c0008 | t0002 | g0175 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA18955 | hp2 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA20300 | hp1 | a0001 | c0003 | t0017 | g0078 | AFR | USA | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | USA | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0068 | AFR | LWK | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| NA21309 | hp2 | a0001 | c0003 | t0016 | g0073 | AFR | LWK | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0008 | g0001 | REF | REF | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0001 | REF | REF | DLST_chr14_74876916_74908743 | DLST | chr14 | 74876916 | 74908743 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74889278 | A | G | 1 | a0005 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.203A>G | p.Asp68Gly | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 5/15 | 241/2813 | 203/1362 | 68/453 | chr14 | 74889278 | |||
| chr14:74891138 | C | T | 1 | a0004 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.413C>T | p.Thr138Ile | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/15 | 451/2813 | 413/1362 | 138/453 | chr14 | 74891138 | |||
| chr14:74893363 | C | T | 1 | a0002 | 3 | HG02055.hp2 HG02129.hp2 HG02735.hp2 |
missense_variant | MODERATE | c.611C>T | p.Pro204Leu | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 9/15 | 649/2813 | 611/1362 | 204/453 | chr14 | 74893363 | |||
| chr14:74894391 | T | A | 1 | a0003 | 3 | HG02723.hp1 HG02970.hp2 HG02976.hp1 |
missense_variant | MODERATE | c.752T>A | p.Phe251Tyr | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/15 | 790/2813 | 752/1362 | 251/453 | chr14 | 74894391 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74892967 | G | A | 6 | a0001c0001 a0001c0003 a0001c0006 others(3): Show |
269 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(266): Show |
synonymous_variant | LOW | c.576G>A | p.Gln192Gln | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 8/15 | 614/2813 | 576/1362 | 192/453 | chr14 | 74892967 | |||
| chr14:74898381 | G | A | 1 | a0001c0006 | 1 | HG01167.hp1 | synonymous_variant | LOW | c.783G>A | p.Glu261Glu | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 11/15 | 821/2813 | 783/1362 | 261/453 | chr14 | 74898381 | |||
| chr14:74901104 | C | T | 4 | a0001c0003 a0001c0006 a0002c0005 others(1): Show |
96 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
synonymous_variant | LOW | c.1098C>T | p.Gly366Gly | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 14/15 | 1136/2813 | 1098/1362 | 366/453 | chr14 | 74901104 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74881947 | C | A | 1 | a0001c0002t0006 | 5 | NA18945.hp2 NA18964.hp2 NA18986.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-7C>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 1/15 | 7 | chr14 | 74881947 | ||||||
| chr14:74902432 | C | A | 1 | a0001c0001t0011 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*102C>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 15/15 | 102 | chr14 | 74902432 | ||||||
| chr14:74902643 | T | C | 10 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(7): Show |
168 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*313T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 15/15 | 313 | chr14 | 74902643 | ||||||
| chr14:74902676 | T | C | 9 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(6): Show |
167 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*346T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 15/15 | 346 | chr14 | 74902676 | ||||||
| chr14:74902682 | C | T | 8 | a0001c0002t0003 a0001c0003t0003 a0001c0003t0015 others(5): Show |
97 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*352C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 15/15 | 352 | chr14 | 74902682 | ||||||
| chr14:74902724 | A | G | 1 | a0001c0002t0009 | 5 | NA18950.hp2 NA18951.hp1 NA19066.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*394A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 15/15 | 394 | chr14 | 74902724 | ||||||
| chr14:74902784 | C | T | 2 | a0001c0001t0010 a0004c0007t0010 |
4 | HG01081.hp2 HG02451.hp1 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*454C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 15/15 | 454 | chr14 | 74902784 | ||||||
| chr14:74902895 | C | G | 1 | a0001c0002t0009 | 5 | NA18950.hp2 NA18951.hp1 NA19066.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*565C>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 15/15 | 565 | chr14 | 74902895 | ||||||
| chr14:74903019 | G | A | 1 | a0001c0001t0012 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*689G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 15/15 | 689 | chr14 | 74903019 | ||||||
| chr14:74903088 | A | G | 1 | a0001c0001t0005 | 6 | HG02922.hp2 HG03195.hp1 HG03453.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*758A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 15/15 | 758 | chr14 | 74903088 | ||||||
| chr14:74903152 | C | T | 1 | a0001c0003t0017 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*822C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 15/15 | 822 | chr14 | 74903152 | ||||||
| chr14:74903187 | C | G | 1 | a0001c0003t0016 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*857C>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 15/15 | 857 | chr14 | 74903187 | ||||||
| chr14:74903245 | C | T | 1 | a0001c0002t0008 | 4 | HG00741.hp2 HG01175.hp2 HG02698.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*915C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 15/15 | 915 | chr14 | 74903245 | ||||||
| chr14:74903420 | C | T | 10 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(7): Show |
168 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*1090C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 15/15 | 1090 | chr14 | 74903420 | ||||||
| chr14:74903430 | C | A | 5 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(2): Show |
43 | HG00673.hp2 HG00741.hp1 HG01168.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1100C>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 15/15 | 1100 | chr14 | 74903430 | ||||||
| chr14:74903459 | G | C | 1 | a0001c0001t0013 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1129G>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 15/15 | 1129 | chr14 | 74903459 | ||||||
| chr14:74903606 | G | T | 1 | a0001c0001t0007 | 5 | HG00673.hp2 HG02738.hp1 HG04228.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1276G>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 15/15 | 1276 | chr14 | 74903606 | ||||||
| chr14:74903687 | C | G | 2 | a0001c0003t0015 a0001c0003t0017 |
2 | NA18906.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1357C>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 15/15 | 1357 | chr14 | 74903687 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74882256 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.63+240C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 1/14 | chr14 | 74882256 | |||||||
| chr14:74882352 | C | G | 1 | a0005c0008t0002g0175 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.64-239C>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 1/14 | chr14 | 74882352 | |||||||
| chr14:74882398 | T | C | 35 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0004g0006 others(32): Show |
49 | HG00673.hp2 HG00741.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.64-193T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 1/14 | chr14 | 74882398 | |||||||
| chr14:74882426 | C | T | 1 | a0001c0001t0004g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.64-165C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 1/14 | chr14 | 74882426 | |||||||
| chr14:74882429 | CGTGTTGA others(19): Show |
C | 1 | a0001c0002t0002g0174 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.64-155_64-130delAT others(24): Show |
DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 74882429 | ||||||
| chr14:74882543 | T | G | 1 | a0001c0002t0002g0072 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.64-48T>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 1/14 | chr14 | 74882543 | |||||||
| chr14:74882729 | T | C | 35 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0004g0006 others(32): Show |
49 | HG00673.hp2 HG00741.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.97+105T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74882729 | |||||||
| chr14:74882730 | G | A | 1 | a0001c0003t0016g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.97+106G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74882730 | |||||||
| chr14:74882773 | A | G | 2 | a0003c0004t0003g0043 a0003c0004t0003g0173 |
3 | HG02723.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.97+149A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74882773 | |||||||
| chr14:74882954 | G | A | 4 | a0001c0001t0010g0044 a0001c0001t0010g0045 a0001c0001t0010g0046 others(1): Show |
4 | HG01081.hp2 HG02451.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+330G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74882954 | |||||||
| chr14:74883020 | C | T | 16 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(13): Show |
28 | HG00741.hp1 HG01168.hp1 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.97+396C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74883020 | |||||||
| chr14:74883060 | T | C | 1 | a0001c0002t0009g0074 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.97+436T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74883060 | |||||||
| chr14:74883066 | G | A | 29 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(26): Show |
43 | HG00673.hp2 HG00741.hp1 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.97+442G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74883066 | |||||||
| chr14:74883131 | A | T | 1 | a0001c0003t0003g0172 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.97+507A>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74883131 | |||||||
| chr14:74883137 | TACAAAAA others(28): Show |
T | 1 | a0001c0003t0003g0172 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.97+514_97+548delAC others(33): Show |
DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74883137 | |||||||
| chr14:74883152 | G | C | 1 | a0001c0002t0002g0004 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.97+528G>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74883152 | |||||||
| chr14:74883179 | C | A | 1 | a0001c0003t0003g0172 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.97+555C>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74883179 | |||||||
| chr14:74883183 | T | G | 1 | a0001c0003t0003g0172 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.97+559T>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74883183 | |||||||
| chr14:74883185 | C | T | 1 | a0001c0003t0003g0172 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.97+561C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74883185 | |||||||
| chr14:74883186 | T | G | 1 | a0001c0003t0003g0172 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.97+562T>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74883186 | |||||||
| chr14:74883202 | C | G | 83 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(80): Show |
169 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(166): Show |
intron_variant | MODIFIER | c.97+578C>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74883202 | |||||||
| chr14:74883294 | C | CA | 31 | a0001c0001t0001g0140 a0001c0001t0004g0006 a0001c0001t0004g0024 others(28): Show |
43 | HG00673.hp2 HG00741.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.97+690dupA | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 74883294 | ||||||
| chr14:74883294 | C | CAA | 9 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0071 others(6): Show |
11 | HG02602.hp2 HG02738.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.97+689_97+690dupAA | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 74883294 | ||||||
| chr14:74883294 | CA | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0169 a0001c0001t0001g0170 others(1): Show |
7 | HG02109.hp1 HG02145.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.97+690delA | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 74883294 | ||||||
| chr14:74883395 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.97+771A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74883395 | |||||||
| chr14:74883426 | A | G | 11 | a0001c0001t0004g0006 a0001c0001t0004g0025 a0001c0001t0004g0026 others(8): Show |
23 | HG00741.hp1 HG01168.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.97+802A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74883426 | |||||||
| chr14:74883504 | A | T | 1 | a0001c0001t0005g0052 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.97+880A>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74883504 | |||||||
| chr14:74883507 | T | TTAGATTT others(17): Show |
2 | a0001c0001t0005g0052 a0001c0002t0002g0051 |
2 | HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.97+884_97+907dupTA others(22): Show |
DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 74883507 | ||||||
| chr14:74883549 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.97+925A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74883549 | |||||||
| chr14:74883571 | C | A | 1 | a0001c0003t0003g0028 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97+947C>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74883571 | |||||||
| chr14:74883663 | T | G | 3 | a0001c0002t0003g0080 a0001c0003t0003g0029 a0001c0003t0003g0081 |
4 | HG00642.hp1 HG00735.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+1039T>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74883663 | |||||||
| chr14:74883961 | C | T | 1 | a0001c0002t0002g0138 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.97+1337C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74883961 | |||||||
| chr14:74883978 | T | C | 1 | a0001c0002t0002g0082 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.97+1354T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74883978 | |||||||
| chr14:74884278 | T | C | 1 | a0001c0002t0002g0016 | 4 | HG01106.hp2 HG01433.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-1308T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74884278 | |||||||
| chr14:74884278 | T | G | 9 | a0001c0003t0003g0010 a0001c0003t0003g0083 a0001c0003t0003g0084 others(6): Show |
13 | NA18747.hp2 NA18944.hp1 NA18955.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-1308T>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74884278 | |||||||
| chr14:74884292 | C | T | 5 | a0001c0001t0004g0024 a0001c0001t0004g0062 a0001c0001t0004g0063 others(2): Show |
5 | HG02818.hp1 HG02895.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-1294C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74884292 | |||||||
| chr14:74884372 | A | G | 4 | a0001c0001t0004g0027 a0001c0001t0004g0068 a0001c0001t0004g0069 others(1): Show |
5 | HG02630.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-1214A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74884372 | |||||||
| chr14:74884403 | A | G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(81): Show |
170 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.98-1183A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74884403 | |||||||
| chr14:74884603 | A | C | 16 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(13): Show |
28 | HG00741.hp1 HG01168.hp1 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.98-983A>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74884603 | |||||||
| chr14:74884684 | A | G | 1 | a0001c0003t0003g0136 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.98-902A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74884684 | |||||||
| chr14:74884784 | A | G | 48 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(45): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.98-802A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74884784 | |||||||
| chr14:74884944 | G | A | 48 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(45): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.98-642G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74884944 | |||||||
| chr14:74885180 | T | C | 5 | a0001c0002t0002g0011 a0001c0002t0002g0030 a0001c0002t0006g0021 others(2): Show |
11 | NA18939.hp1 NA18940.hp1 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.98-406T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74885180 | |||||||
| chr14:74885253 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.98-333A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 2/14 | chr14 | 74885253 | |||||||
| chr14:74885791 | C | G | 4 | a0001c0001t0010g0044 a0001c0001t0010g0045 a0001c0001t0010g0046 others(1): Show |
4 | HG01081.hp2 HG02451.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.146+157C>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74885791 | |||||||
| chr14:74885849 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.146+215C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74885849 | |||||||
| chr14:74885852 | T | C | 49 | a0001c0002t0003g0080 a0001c0003t0003g0003 a0001c0003t0003g0008 others(46): Show |
96 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.146+218T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74885852 | |||||||
| chr14:74885923 | C | T | 1 | a0001c0003t0003g0018 | 4 | HG01167.hp2 HG01168.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.146+289C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74885923 | |||||||
| chr14:74886001 | C | G | 4 | a0001c0001t0010g0044 a0001c0001t0010g0045 a0001c0001t0010g0046 others(1): Show |
4 | HG01081.hp2 HG02451.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.146+367C>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74886001 | |||||||
| chr14:74886011 | G | GTTACTCA others(331): Show |
1 | a0001c0003t0003g0089 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.146+389_146+390ins others(338): Show |
DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr14 | 74886011 | ||||||
| chr14:74886011 | G | GTTACTCA others(333): Show |
1 | a0001c0003t0003g0090 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.146+389_146+390ins others(340): Show |
DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr14 | 74886011 | ||||||
| chr14:74886597 | G | A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(29): Show |
81 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.146+963G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74886597 | |||||||
| chr14:74886612 | G | A | 1 | a0001c0001t0001g0013 | 5 | NA18966.hp2 NA18971.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.146+978G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74886612 | |||||||
| chr14:74886653 | A | G | 2 | a0001c0001t0004g0058 a0001c0001t0004g0059 |
2 | HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.146+1019A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74886653 | |||||||
| chr14:74886673 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.146+1039A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74886673 | |||||||
| chr14:74886684 | C | T | 1 | a0001c0002t0002g0115 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.146+1050C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74886684 | |||||||
| chr14:74886947 | C | T | 3 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0071 |
3 | HG02818.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.146+1313C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74886947 | |||||||
| chr14:74886987 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0160 a0001c0001t0001g0161 others(4): Show |
17 | HG00423.hp1 HG01934.hp1 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.146+1353C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74886987 | |||||||
| chr14:74887097 | G | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.146+1463G>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74887097 | |||||||
| chr14:74887150 | C | T | 1 | a0001c0003t0003g0135 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.146+1516C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74887150 | |||||||
| chr14:74887152 | T | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(129): Show |
265 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(262): Show |
intron_variant | MODIFIER | c.146+1518T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74887152 | |||||||
| chr14:74887200 | G | GTTCACAT others(1): Show |
30 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0004g0006 others(27): Show |
44 | HG00673.hp2 HG00741.hp1 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.146+1572_146+1573i others(10): Show |
DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr14 | 74887200 | ||||||
| chr14:74887324 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.146+1690T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74887324 | |||||||
| chr14:74887565 | T | G | 1 | a0001c0001t0001g0141 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.147-1530T>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74887565 | |||||||
| chr14:74887597 | TAAAAATT others(1): Show |
T | 2 | a0001c0003t0003g0028 a0001c0003t0003g0116 |
3 | HG02055.hp1 HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.147-1492_147-1485d others(10): Show |
DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr14 | 74887597 | ||||||
| chr14:74887601 | A | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.147-1494A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74887601 | |||||||
| chr14:74887695 | C | G | 11 | a0001c0001t0004g0006 a0001c0001t0004g0025 a0001c0001t0004g0026 others(8): Show |
23 | HG00741.hp1 HG01168.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.147-1400C>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74887695 | |||||||
| chr14:74887795 | G | A | 2 | a0001c0003t0003g0089 a0001c0003t0003g0090 |
2 | NA18972.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.147-1300G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74887795 | |||||||
| chr14:74887897 | A | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(128): Show |
264 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(261): Show |
intron_variant | MODIFIER | c.147-1198A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74887897 | |||||||
| chr14:74888173 | C | T | 1 | a0001c0003t0003g0134 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.147-922C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74888173 | |||||||
| chr14:74888189 | A | G | 2 | a0001c0001t0004g0058 a0001c0001t0004g0059 |
2 | HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.147-906A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74888189 | |||||||
| chr14:74888230 | A | G | 1 | a0001c0002t0002g0114 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.147-865A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74888230 | |||||||
| chr14:74888274 | G | GT | 14 | a0001c0001t0001g0007 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
25 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.147-803dupT | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr14 | 74888274 | ||||||
| chr14:74888274 | GT | G | 46 | a0001c0001t0007g0048 a0001c0001t0007g0053 a0001c0001t0007g0054 others(43): Show |
93 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.147-803delT | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr14 | 74888274 | ||||||
| chr14:74888276 | T | G | 1 | a0001c0003t0003g0117 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.147-819T>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74888276 | |||||||
| chr14:74888317 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.147-778G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74888317 | |||||||
| chr14:74888500 | T | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(133): Show |
271 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(268): Show |
intron_variant | MODIFIER | c.147-595T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74888500 | |||||||
| chr14:74888580 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.147-515G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74888580 | |||||||
| chr14:74888599 | C | T | 1 | a0001c0003t0003g0129 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.147-496C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74888599 | |||||||
| chr14:74888766 | G | A | 1 | a0001c0003t0003g0023 | 3 | HG02559.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.147-329G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74888766 | |||||||
| chr14:74888785 | A | T | 1 | a0001c0001t0007g0056 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.147-310A>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74888785 | |||||||
| chr14:74888801 | T | G | 3 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0071 |
3 | HG02818.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.147-294T>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | chr14 | 74888801 | |||||||
| chr14:74889064 | TA | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(133): Show |
271 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(268): Show |
intron_variant | MODIFIER | c.147-27delA | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr14 | 74889064 | ||||||
| chr14:74889228 | A | G | 2 | a0001c0002t0002g0034 a0001c0002t0002g0110 |
3 | NA18969.hp1 NA19058.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.200-47A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 4/14 | chr14 | 74889228 | |||||||
| chr14:74889367 | A | AT | 97 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(94): Show |
216 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.274+38dupT | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr14 | 74889367 | ||||||
| chr14:74889367 | A | ATT | 17 | a0001c0001t0001g0019 a0001c0001t0001g0154 a0001c0001t0001g0155 others(14): Show |
20 | HG00673.hp2 HG01106.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.274+37_274+38dupTT | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr14 | 74889367 | ||||||
| chr14:74889367 | A | T | 1 | a0001c0003t0003g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.274+18A>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 5/14 | chr14 | 74889367 | |||||||
| chr14:74889400 | T | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(129): Show |
265 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(262): Show |
intron_variant | MODIFIER | c.274+51T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 5/14 | chr14 | 74889400 | |||||||
| chr14:74889409 | C | T | 1 | a0001c0003t0003g0087 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.274+60C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 5/14 | chr14 | 74889409 | |||||||
| chr14:74889526 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.274+177G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 5/14 | chr14 | 74889526 | |||||||
| chr14:74889676 | C | T | 11 | a0001c0001t0004g0006 a0001c0001t0004g0025 a0001c0001t0004g0026 others(8): Show |
23 | HG00741.hp1 HG01168.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.275-221C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 5/14 | chr14 | 74889676 | |||||||
| chr14:74889791 | G | A | 3 | a0001c0001t0004g0057 a0001c0001t0004g0058 a0001c0001t0004g0059 |
3 | HG02145.hp2 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.275-106G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 5/14 | chr14 | 74889791 | |||||||
| chr14:74889812 | A | T | 1 | a0001c0003t0003g0023 | 3 | HG02559.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.275-85A>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 5/14 | chr14 | 74889812 | |||||||
| chr14:74889857 | C | T | 2 | a0001c0001t0004g0025 a0001c0001t0004g0066 |
3 | HG02257.hp2 HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.275-40C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 5/14 | chr14 | 74889857 | |||||||
| chr14:74889971 | C | T | 5 | a0001c0001t0007g0048 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
5 | HG00673.hp2 HG02738.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.330+19C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 6/14 | chr14 | 74889971 | |||||||
| chr14:74890096 | T | TA | 54 | a0001c0001t0004g0068 a0001c0001t0010g0044 a0001c0001t0010g0045 others(51): Show |
100 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.330+154dupA | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr14 | 74890096 | ||||||
| chr14:74890124 | C | CT | 8 | a0001c0001t0004g0070 a0001c0001t0007g0048 a0001c0001t0010g0045 others(5): Show |
8 | HG00438.hp2 HG02165.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+195dupT | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr14 | 74890124 | ||||||
| chr14:74890124 | CT | C | 87 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0019 others(84): Show |
169 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.330+195delT | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr14 | 74890124 | ||||||
| chr14:74890124 | CTTT | C | 5 | a0001c0001t0001g0038 a0001c0001t0001g0142 a0001c0001t0001g0143 others(2): Show |
8 | HG02602.hp1 HG02922.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+193_330+195del others(3): Show |
DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr14 | 74890124 | ||||||
| chr14:74890146 | T | G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(30): Show |
81 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.330+194T>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 6/14 | chr14 | 74890146 | |||||||
| chr14:74890147 | T | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(30): Show |
81 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.330+195T>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 6/14 | chr14 | 74890147 | |||||||
| chr14:74890150 | G | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(30): Show |
81 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.330+198G>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 6/14 | chr14 | 74890150 | |||||||
| chr14:74890152 | C | CAG | 103 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0019 others(100): Show |
190 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.330+202_330+203dup others(2): Show |
DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr14 | 74890152 | ||||||
| chr14:74890152 | C | G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(30): Show |
81 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.330+200C>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 6/14 | chr14 | 74890152 | |||||||
| chr14:74890184 | A | G | 1 | a0005c0008t0002g0175 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.330+232A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 6/14 | chr14 | 74890184 | |||||||
| chr14:74890468 | G | A | 1 | a0001c0003t0003g0133 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.330+516G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 6/14 | chr14 | 74890468 | |||||||
| chr14:74890738 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.331-318C>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 6/14 | chr14 | 74890738 | |||||||
| chr14:74890872 | T | A | 10 | a0001c0002t0001g0137 a0001c0002t0002g0004 a0001c0002t0002g0075 others(7): Show |
25 | HG00408.hp1 HG01358.hp1 HG01928.hp1 others(22): Show |
intron_variant | MODIFIER | c.331-184T>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 6/14 | chr14 | 74890872 | |||||||
| chr14:74891008 | A | G | 2 | a0001c0001t0004g0025 a0001c0001t0004g0066 |
3 | HG02257.hp2 HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.331-48A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 6/14 | chr14 | 74891008 | |||||||
| chr14:74891246 | C | T | 3 | a0001c0001t0005g0020 a0001c0001t0005g0050 a0001c0001t0005g0052 |
5 | HG02922.hp2 HG03195.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.442+79C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | chr14 | 74891246 | |||||||
| chr14:74891359 | TA | T | 3 | a0001c0003t0003g0086 a0001c0003t0003g0127 a0001c0003t0003g0128 |
3 | HG00140.hp1 HG00738.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.442+198delA | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr14 | 74891359 | ||||||
| chr14:74891489 | A | G | 11 | a0001c0001t0004g0006 a0001c0001t0004g0025 a0001c0001t0004g0026 others(8): Show |
23 | HG00741.hp1 HG01168.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.442+322A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | chr14 | 74891489 | |||||||
| chr14:74891657 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.442+490A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | chr14 | 74891657 | |||||||
| chr14:74891762 | A | G | 1 | a0001c0002t0002g0075 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.442+595A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | chr14 | 74891762 | |||||||
| chr14:74891778 | A | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.442+611A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | chr14 | 74891778 | |||||||
| chr14:74891853 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.442+686A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | chr14 | 74891853 | |||||||
| chr14:74891880 | A | T | 1 | a0001c0002t0001g0137 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.442+713A>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | chr14 | 74891880 | |||||||
| chr14:74891916 | C | T | 5 | a0001c0001t0007g0048 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
5 | HG00673.hp2 HG02738.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.442+749C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | chr14 | 74891916 | |||||||
| chr14:74891964 | A | G | 1 | a0001c0003t0003g0126 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.442+797A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | chr14 | 74891964 | |||||||
| chr14:74892114 | C | G | 46 | a0001c0002t0003g0080 a0001c0003t0003g0003 a0001c0003t0003g0008 others(43): Show |
92 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.443-720C>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | chr14 | 74892114 | |||||||
| chr14:74892158 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0169 a0001c0001t0001g0170 others(1): Show |
7 | HG02109.hp1 HG02145.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.443-676C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | chr14 | 74892158 | |||||||
| chr14:74892173 | C | T | 5 | a0001c0002t0002g0022 a0001c0002t0002g0094 a0001c0002t0002g0097 others(2): Show |
7 | HG00140.hp2 HG00280.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.443-661C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | chr14 | 74892173 | |||||||
| chr14:74892340 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.443-494C>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | chr14 | 74892340 | |||||||
| chr14:74892383 | G | A | 1 | a0001c0003t0003g0083 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.443-451G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | chr14 | 74892383 | |||||||
| chr14:74892501 | A | T | 47 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(44): Show |
119 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.443-333A>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | chr14 | 74892501 | |||||||
| chr14:74892512 | GT | G | 56 | a0001c0001t0001g0014 a0001c0001t0001g0041 a0001c0001t0001g0145 others(53): Show |
108 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.443-311delT | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr14 | 74892512 | ||||||
| chr14:74892523 | T | C | 12 | a0001c0001t0001g0142 a0001c0001t0004g0006 a0001c0001t0004g0025 others(9): Show |
24 | HG00741.hp1 HG01168.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.443-311T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | chr14 | 74892523 | |||||||
| chr14:74892526 | T | C | 48 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(45): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.443-308T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | chr14 | 74892526 | |||||||
| chr14:74892679 | T | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0157 a0001c0001t0001g0160 others(5): Show |
18 | HG00423.hp1 HG01934.hp1 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.443-155T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | chr14 | 74892679 | |||||||
| chr14:74892738 | T | C | 48 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(45): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.443-96T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 7/14 | chr14 | 74892738 | |||||||
| chr14:74893027 | C | T | 47 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(44): Show |
119 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.595+41C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 8/14 | chr14 | 74893027 | |||||||
| chr14:74893054 | ACT | A | 35 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0004g0006 others(32): Show |
49 | HG00673.hp2 HG00741.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.595+71_595+72delCT | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr14 | 74893054 | ||||||
| chr14:74893114 | G | A | 3 | a0001c0001t0004g0024 a0001c0001t0004g0144 a0001c0001t0014g0024 |
3 | HG02559.hp1 HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.595+128G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 8/14 | chr14 | 74893114 | |||||||
| chr14:74893221 | G | C | 1 | a0001c0001t0004g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.596-127G>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 8/14 | chr14 | 74893221 | |||||||
| chr14:74893254 | A | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0157 a0001c0001t0001g0160 others(5): Show |
18 | HG00423.hp1 HG01934.hp1 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.596-94A>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 8/14 | chr14 | 74893254 | |||||||
| chr14:74893557 | A | T | 1 | a0001c0001t0001g0042 | 2 | HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.672+133A>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 9/14 | chr14 | 74893557 | |||||||
| chr14:74893682 | A | G | 3 | a0001c0001t0005g0020 a0001c0001t0005g0050 a0001c0001t0005g0052 |
5 | HG02922.hp2 HG03195.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.672+258A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 9/14 | chr14 | 74893682 | |||||||
| chr14:74893716 | G | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(131): Show |
269 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(266): Show |
intron_variant | MODIFIER | c.672+292G>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 9/14 | chr14 | 74893716 | |||||||
| chr14:74893725 | C | T | 1 | a0001c0003t0003g0083 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.672+301C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 9/14 | chr14 | 74893725 | |||||||
| chr14:74893819 | T | C | 2 | a0001c0003t0003g0089 a0001c0003t0003g0090 |
2 | NA18972.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.672+395T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 9/14 | chr14 | 74893819 | |||||||
| chr14:74893895 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.673-417A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 9/14 | chr14 | 74893895 | |||||||
| chr14:74893984 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.673-328C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 9/14 | chr14 | 74893984 | |||||||
| chr14:74894005 | T | C | 1 | a0001c0001t0012g0064 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.673-307T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 9/14 | chr14 | 74894005 | |||||||
| chr14:74894188 | G | T | 4 | a0001c0001t0010g0044 a0001c0001t0010g0045 a0001c0001t0010g0046 others(1): Show |
4 | HG01081.hp2 HG02451.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.673-124G>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 9/14 | chr14 | 74894188 | |||||||
| chr14:74894203 | G | A | 95 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(92): Show |
214 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.673-109G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 9/14 | chr14 | 74894203 | |||||||
| chr14:74894243 | C | T | 1 | a0001c0002t0002g0075 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.673-69C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 9/14 | chr14 | 74894243 | |||||||
| chr14:74894275 | A | G | 1 | a0001c0002t0002g0096 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.673-37A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 9/14 | chr14 | 74894275 | |||||||
| chr14:74894474 | C | G | 132 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(129): Show |
265 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(262): Show |
intron_variant | MODIFIER | c.770+65C>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74894474 | |||||||
| chr14:74894490 | G | A | 5 | a0001c0001t0007g0048 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
5 | HG00673.hp2 HG02738.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+81G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74894490 | |||||||
| chr14:74894665 | C | T | 2 | a0001c0001t0004g0058 a0001c0001t0004g0059 |
2 | HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.770+256C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74894665 | |||||||
| chr14:74895062 | A | C | 4 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0092 others(1): Show |
6 | HG02723.hp2 HG02886.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.770+653A>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74895062 | |||||||
| chr14:74895407 | T | C | 5 | a0001c0001t0007g0048 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
5 | HG00673.hp2 HG02738.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+998T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74895407 | |||||||
| chr14:74895415 | C | T | 1 | a0001c0003t0003g0117 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.770+1006C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74895415 | |||||||
| chr14:74895688 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.770+1279C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74895688 | |||||||
| chr14:74895751 | T | C | 1 | a0001c0001t0004g0057 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.770+1342T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74895751 | |||||||
| chr14:74895768 | C | T | 47 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(44): Show |
119 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.770+1359C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74895768 | |||||||
| chr14:74895849 | T | C | 60 | a0001c0001t0004g0057 a0001c0001t0004g0058 a0001c0001t0004g0059 others(57): Show |
109 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.770+1440T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74895849 | |||||||
| chr14:74895852 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.770+1443C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74895852 | |||||||
| chr14:74895878 | A | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0167 |
2 | HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.770+1469A>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74895878 | |||||||
| chr14:74895907 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0013g0015 |
5 | HG00609.hp1 HG00621.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+1498T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74895907 | |||||||
| chr14:74896129 | C | T | 1 | a0001c0001t0005g0049 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.770+1720C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74896129 | |||||||
| chr14:74896237 | C | A | 3 | a0001c0002t0002g0017 a0001c0002t0002g0103 a0001c0002t0002g0107 |
6 | HG00544.hp2 HG02523.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.770+1828C>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74896237 | |||||||
| chr14:74896373 | G | T | 1 | a0001c0001t0007g0055 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.770+1964G>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74896373 | |||||||
| chr14:74896470 | A | G | 2 | a0001c0003t0015g0125 a0001c0003t0017g0078 |
2 | NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.771-1899A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74896470 | |||||||
| chr14:74896548 | C | T | 1 | a0001c0003t0003g0124 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.771-1821C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74896548 | |||||||
| chr14:74896666 | G | A | 48 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(45): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.771-1703G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74896666 | |||||||
| chr14:74896747 | G | A | 1 | a0003c0004t0003g0173 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.771-1622G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74896747 | |||||||
| chr14:74896902 | G | A | 1 | a0001c0003t0003g0084 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.771-1467G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74896902 | |||||||
| chr14:74896938 | C | T | 48 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(45): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.771-1431C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74896938 | |||||||
| chr14:74897102 | A | G | 1 | a0001c0002t0002g0109 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.771-1267A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74897102 | |||||||
| chr14:74897319 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.771-1050C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74897319 | |||||||
| chr14:74897379 | A | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(48): Show |
123 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.771-990A>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74897379 | |||||||
| chr14:74897477 | A | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0042 others(8): Show |
31 | HG00423.hp1 HG01243.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.771-892A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74897477 | |||||||
| chr14:74897521 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.771-848T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74897521 | |||||||
| chr14:74897693 | C | T | 1 | a0001c0001t0004g0069 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.771-676C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74897693 | |||||||
| chr14:74897748 | C | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(127): Show |
263 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(260): Show |
intron_variant | MODIFIER | c.771-621C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74897748 | |||||||
| chr14:74897856 | A | G | 3 | a0001c0001t0010g0044 a0001c0001t0010g0046 a0004c0007t0010g0047 |
3 | HG01081.hp2 HG02451.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.771-513A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74897856 | |||||||
| chr14:74897913 | G | A | 1 | a0001c0001t0002g0031 | 2 | HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.771-456G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74897913 | |||||||
| chr14:74897938 | G | GT | 36 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0140 others(33): Show |
49 | HG00140.hp2 HG00673.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.771-415dupT | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 74897938 | ||||||
| chr14:74897938 | G | T | 4 | a0001c0001t0001g0009 a0001c0001t0002g0032 a0001c0001t0005g0052 others(1): Show |
10 | HG00733.hp2 HG01261.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.771-431G>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74897938 | |||||||
| chr14:74897938 | GT | G | 6 | a0001c0001t0001g0146 a0001c0001t0010g0044 a0001c0001t0010g0045 others(3): Show |
6 | HG01081.hp2 HG01978.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.771-415delT | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr14 | 74897938 | ||||||
| chr14:74897958 | T | G | 1 | a0001c0001t0001g0147 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.771-411T>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74897958 | |||||||
| chr14:74898185 | G | A | 2 | a0001c0002t0006g0021 a0001c0002t0006g0091 |
4 | NA18945.hp2 NA18964.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.771-184G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74898185 | |||||||
| chr14:74898268 | G | A | 1 | a0001c0002t0002g0104 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.771-101G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74898268 | |||||||
| chr14:74898356 | A | G | 1 | a0001c0001t0004g0069 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.771-13A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74898356 | |||||||
| chr14:74898359 | A | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(132): Show |
270 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(267): Show |
intron_variant | MODIFIER | c.771-10A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 10/14 | chr14 | 74898359 | |||||||
| chr14:74898534 | GGGAGGTA others(13): Show |
G | 1 | a0001c0002t0002g0101 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.901+36_901+55delGG others(18): Show |
DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 11/14 | chr14 | 74898534 | |||||||
| chr14:74898595 | T | G | 1 | a0001c0001t0001g0019 | 4 | HG02109.hp1 HG02145.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.901+96T>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 11/14 | chr14 | 74898595 | |||||||
| chr14:74898684 | C | T | 29 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(26): Show |
43 | HG00673.hp2 HG00741.hp1 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.901+185C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 11/14 | chr14 | 74898684 | |||||||
| chr14:74898842 | T | TA | 11 | a0001c0001t0004g0006 a0001c0001t0004g0025 a0001c0001t0004g0026 others(8): Show |
23 | HG00741.hp1 HG01168.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.901+344dupA | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr14 | 74898842 | ||||||
| chr14:74899018 | G | A | 1 | a0001c0001t0001g0039 | 2 | HG01109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.901+519G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 11/14 | chr14 | 74899018 | |||||||
| chr14:74899026 | A | G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(81): Show |
170 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.901+527A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 11/14 | chr14 | 74899026 | |||||||
| chr14:74899621 | A | G | 5 | a0001c0001t0007g0048 a0001c0001t0007g0053 a0001c0001t0007g0054 others(2): Show |
5 | HG00673.hp2 HG02738.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.902-302A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 11/14 | chr14 | 74899621 | |||||||
| chr14:74899744 | C | T | 49 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(46): Show |
96 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.902-179C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 11/14 | chr14 | 74899744 | |||||||
| chr14:74900091 | G | A | 1 | a0001c0001t0004g0065 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.975+95G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 12/14 | chr14 | 74900091 | |||||||
| chr14:74900103 | G | C | 1 | a0001c0003t0003g0119 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.975+107G>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 12/14 | chr14 | 74900103 | |||||||
| chr14:74900615 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1059+243T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 13/14 | chr14 | 74900615 | |||||||
| chr14:74900646 | T | C | 50 | a0001c0002t0003g0080 a0001c0003t0003g0003 a0001c0003t0003g0008 others(47): Show |
97 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1059+274T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 13/14 | chr14 | 74900646 | |||||||
| chr14:74900659 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1059+287C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 13/14 | chr14 | 74900659 | |||||||
| chr14:74900707 | C | A | 1 | a0001c0001t0007g0053 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1059+335C>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 13/14 | chr14 | 74900707 | |||||||
| chr14:74900759 | G | C | 1 | a0001c0003t0003g0120 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1060-307G>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 13/14 | chr14 | 74900759 | |||||||
| chr14:74900778 | A | G | 4 | a0001c0003t0003g0008 a0001c0003t0003g0120 a0001c0003t0003g0122 others(1): Show |
11 | NA18747.hp1 NA18951.hp2 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.1060-288A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 13/14 | chr14 | 74900778 | |||||||
| chr14:74900834 | C | T | 1 | a0001c0003t0016g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1060-232C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 13/14 | chr14 | 74900834 | |||||||
| chr14:74900835 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1060-231C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 13/14 | chr14 | 74900835 | |||||||
| chr14:74900891 | ATTC | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(21): Show |
72 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1060-172_1060-170d others(5): Show |
DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr14 | 74900891 | ||||||
| chr14:74900926 | A | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1060-140A>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 13/14 | chr14 | 74900926 | |||||||
| chr14:74900951 | C | T | 1 | a0001c0002t0002g0101 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1060-115C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 13/14 | chr14 | 74900951 | |||||||
| chr14:74900956 | C | T | 1 | a0001c0002t0002g0101 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1060-110C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 13/14 | chr14 | 74900956 | |||||||
| chr14:74900967 | C | A | 1 | a0001c0002t0002g0101 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1060-99C>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 13/14 | chr14 | 74900967 | |||||||
| chr14:74900973 | G | GGCTCAGG others(6): Show |
1 | a0001c0002t0002g0101 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1060-93_1060-92ins others(13): Show |
DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 13/14 | chr14 | 74900973 | |||||||
| chr14:74900974 | C | G | 1 | a0001c0002t0002g0101 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1060-92C>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 13/14 | chr14 | 74900974 | |||||||
| chr14:74901037 | G | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(132): Show |
270 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(267): Show |
intron_variant | MODIFIER | c.1060-29G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 13/14 | chr14 | 74901037 | |||||||
| chr14:74901560 | C | T | 1 | a0001c0001t0004g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1227+327C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 14/14 | chr14 | 74901560 | |||||||
| chr14:74901739 | T | C | 2 | a0001c0001t0002g0032 a0001c0001t0002g0092 |
3 | HG02723.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1228-457T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 14/14 | chr14 | 74901739 | |||||||
| chr14:74901805 | G | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(133): Show |
271 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(268): Show |
intron_variant | MODIFIER | c.1228-391G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 14/14 | chr14 | 74901805 | |||||||
| chr14:74901844 | AT | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(95): Show |
221 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.1228-335delT | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr14 | 74901844 | ||||||
| chr14:74901844 | ATT | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0145 a0001c0001t0001g0160 others(12): Show |
17 | HG00673.hp2 HG01257.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.1228-336_1228-335d others(4): Show |
DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr14 | 74901844 | ||||||
| chr14:74901861 | T | A | 1 | a0001c0001t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1228-335T>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 14/14 | chr14 | 74901861 | |||||||
| chr14:74901862 | A | T | 1 | a0001c0001t0005g0049 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1228-334A>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 14/14 | chr14 | 74901862 | |||||||
| chr14:74901907 | A | G | 2 | a0001c0001t0004g0058 a0001c0001t0004g0059 |
2 | HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1228-289A>G | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 14/14 | chr14 | 74901907 | |||||||
| chr14:74901923 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1228-273G>A | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 14/14 | chr14 | 74901923 | |||||||
| chr14:74901988 | C | T | 12 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0042 others(9): Show |
32 | HG00423.hp1 HG01243.hp1 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.1228-208C>T | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 14/14 | chr14 | 74901988 | |||||||
| chr14:74902067 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1228-129T>C | DLST | ENSG00000119689.15 | transcript | ENST00000334220.9 | protein_coding | 14/14 | chr14 | 74902067 |