Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5966 |
| ensemblid | ENSG00000162924.16 |
| hgncid | 9954 |
| symbol | REL |
| name | REL proto-oncogene, NF-kB subunit |
| refseq_nuc | NM_001291746.2 |
| refseq_prot | NP_001278675.1 |
| ensembl_nuc | ENST00000394479.4 |
| ensembl_prot | ENSP00000377989.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 60881574 |
| end | 60931612 |
| strand | + |
| ver | v1.2 |
| region | chr2:60881574-60931612 |
| region5000 | chr2:60876574-60936612 |
| regionname0 | REL_chr2_60881574_60931612 |
| regionname5000 | REL_chr2_60876574_60936612 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 587 | 271 | 71 | 68 | 88 | 16 | 26 | 68 | REL_chr2_60876574_60936612 | REL | MASGA others(582): Show |
chr2 | 60876574 | 60936612 |
| a0002 | 0/0 | 587 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | MASGA others(582): Show |
chr2 | 60876574 | 60936612 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1761 | 263 | 65 | 67 | 88 | 16 | 25 | REL_chr2_60876574_60936612 | REL | ATGGC others(1756): Show |
chr2 | 60876574 | 60936612 | ||
| a0001c0002 | 0/0 | 1761 | 6 | 5 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ATGGC others(1756): Show |
chr2 | 60876574 | 60936612 | ||
| a0001c0004 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ATGGC others(1756): Show |
chr2 | 60876574 | 60936612 | ||
| a0001c0005 | 0/0 | 1761 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | ATGGC others(1756): Show |
chr2 | 60876574 | 60936612 | ||
| a0002c0003 | 0/0 | 1761 | 5 | 5 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ATGGC others(1756): Show |
chr2 | 60876574 | 60936612 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 11108 | 77 | 8 | 22 | 34 | 3 | 10 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0002 | 0/0 | 11105 | 25 | 2 | 14 | 1 | 3 | 5 | REL_chr2_60876574_60936612 | REL | ACTCG others(11100): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0003 | 0/0 | 11104 | 20 | 0 | 1 | 18 | 1 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11099): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0004 | 0/0 | 11106 | 14 | 1 | 8 | 0 | 3 | 2 | REL_chr2_60876574_60936612 | REL | ACTCG others(11101): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0005 | 0/0 | 11103 | 12 | 1 | 2 | 4 | 3 | 2 | REL_chr2_60876574_60936612 | REL | ACTCG others(11098): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0006 | 0/0 | 11108 | 12 | 12 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0007 | 0/0 | 11108 | 11 | 0 | 0 | 11 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0008 | 0/0 | 11103 | 6 | 0 | 3 | 0 | 1 | 2 | REL_chr2_60876574_60936612 | REL | ACTCG others(11098): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0009 | 0/0 | 11107 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11102): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0010 | 0/0 | 11105 | 5 | 5 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11100): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0012 | 0/0 | 11103 | 4 | 1 | 3 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11098): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0013 | 0/0 | 11103 | 4 | 0 | 2 | 0 | 1 | 1 | REL_chr2_60876574_60936612 | REL | ACTCG others(11098): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0014 | 1/0 | 11108 | 4 | 0 | 2 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0015 | 0/0 | 11108 | 4 | 4 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0016 | 0/0 | 11107 | 3 | 3 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11102): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0017 | 0/0 | 11109 | 3 | 3 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11104): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0018 | 0/0 | 11106 | 3 | 3 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11101): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0019 | 0/0 | 11104 | 2 | 1 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11099): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0020 | 0/0 | 11108 | 2 | 0 | 0 | 2 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0021 | 0/0 | 11107 | 2 | 2 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11102): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0022 | 0/0 | 11107 | 2 | 2 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11102): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0023 | 0/0 | 11107 | 2 | 2 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11102): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0024 | 0/0 | 11108 | 2 | 2 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0025 | 0/0 | 11109 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11104): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0026 | 0/0 | 11108 | 2 | 0 | 0 | 2 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0027 | 0/0 | 11108 | 2 | 0 | 1 | 0 | 1 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0028 | 0/0 | 11108 | 2 | 0 | 0 | 2 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0029 | 0/0 | 11106 | 2 | 2 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11101): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0030 | 0/0 | 11104 | 2 | 0 | 0 | 2 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11099): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0031 | 0/0 | 11106 | 2 | 2 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11101): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0032 | 0/0 | 11103 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11098): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0033 | 0/0 | 11106 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11101): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0034 | 0/1 | 11103 | 1 | 0 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11098): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0035 | 0/0 | 11103 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11098): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0036 | 0/0 | 11108 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0037 | 0/0 | 11107 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11102): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0038 | 0/0 | 11108 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0039 | 0/0 | 11107 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11102): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0042 | 0/0 | 11108 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0043 | 0/0 | 11109 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | ACTCG others(11104): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0044 | 0/0 | 11108 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0045 | 0/0 | 11108 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0046 | 0/0 | 11108 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0047 | 0/0 | 11108 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0048 | 0/0 | 11107 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11102): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0049 | 0/0 | 11108 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0050 | 0/0 | 11108 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0051 | 0/0 | 11107 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | ACTCG others(11102): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0052 | 0/0 | 11108 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0053 | 0/0 | 11107 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11102): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0054 | 0/0 | 11104 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11099): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0055 | 0/0 | 11105 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11100): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0056 | 0/0 | 11104 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11099): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0057 | 0/0 | 11104 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11099): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0058 | 0/0 | 11104 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11099): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0059 | 0/0 | 11104 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11099): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0060 | 0/0 | 11108 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11103): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0061 | 0/0 | 11106 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11101): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0062 | 0/0 | 11103 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11098): Show |
chr2 | 60876574 | 60936612 |
| a0001c0001t0063 | 0/0 | 11107 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | GCTCG others(11102): Show |
chr2 | 60876574 | 60936612 |
| a0001c0002t0011 | 0/0 | 11103 | 5 | 5 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11098): Show |
chr2 | 60876574 | 60936612 |
| a0001c0002t0041 | 0/0 | 11103 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11098): Show |
chr2 | 60876574 | 60936612 |
| a0001c0004t0040 | 0/0 | 11107 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11102): Show |
chr2 | 60876574 | 60936612 |
| a0001c0005t0025 | 0/0 | 11109 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | ACTCG others(11104): Show |
chr2 | 60876574 | 60936612 |
| a0002c0003t0009 | 0/0 | 11107 | 5 | 5 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | ACTCG others(11102): Show |
chr2 | 60876574 | 60936612 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0002g0006 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0002g0012 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0003g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0004g0009 | 0/0 | 4 | 0 | 1 | 0 | 3 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0004g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0005g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0006g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0006g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0007g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0007g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0007g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0007g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0007g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0007g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0007g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0008g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0008g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0008g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0008g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0008g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0008g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0010g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0010g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0010g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0010g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0012g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0012g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0012g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0012g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0013g0002 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0014g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0014g0004 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0014g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0015g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0015g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0015g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0015g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0016g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0016g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0017g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0017g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0017g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0018g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0018g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0018g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0019g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0019g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0020g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0020g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0021g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0021g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0022g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0022g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0023g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0023g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0024g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0024g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0025g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0026g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0026g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0027g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0027g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0028g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0028g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0029g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0029g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0030g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0030g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0031g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0032g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0033g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0034g0143 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0035g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0036g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0037g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0038g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0039g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0042g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0043g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0044g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0045g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0046g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0047g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0048g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0049g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0050g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0051g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0052g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0053g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0054g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0055g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0056g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0057g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0058g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0059g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0060g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0061g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0062g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0001t0063g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0002t0011g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0002t0011g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0002t0011g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0002t0011g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0002t0041g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0004t0040g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0001c0005t0025g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0002c0003t0009g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0002c0003t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0002c0003t0009g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0002c0003t0009g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| a0002c0003t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0120 | EUR | GBR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00140 | hp2 | a0001 | c0001 | t0027 | g0051 | EUR | GBR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0124 | EUR | FIN | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00280 | hp2 | a0001 | c0001 | t0013 | g0002 | EUR | FIN | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0121 | EUR | FIN | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0187 | EUR | FIN | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00408 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | CHS | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00639 | hp2 | a0001 | c0001 | t0060 | g0003 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0206 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00735 | hp1 | a0001 | c0001 | t0052 | g0110 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0195 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0026 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01069 | hp2 | a0001 | c0001 | t0013 | g0002 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0196 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01099 | hp1 | a0001 | c0001 | t0042 | g0074 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01109 | hp1 | a0001 | c0002 | t0041 | g0010 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01109 | hp2 | a0001 | c0001 | t0033 | g0157 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01168 | hp2 | a0001 | c0001 | t0008 | g0136 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0135 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0026 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01175 | hp2 | a0001 | c0001 | t0014 | g0004 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01192 | hp2 | a0001 | c0001 | t0008 | g0138 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01243 | hp2 | a0001 | c0001 | t0062 | g0118 | AMR | PUR | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0034 | AMR | CLM | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | CLM | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0204 | AMR | CLM | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0205 | AMR | CLM | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | CLM | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01358 | hp1 | a0001 | c0001 | t0050 | g0004 | AMR | CLM | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01358 | hp2 | a0001 | c0001 | t0035 | g0002 | AMR | CLM | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | CLM | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01361 | hp2 | a0001 | c0001 | t0027 | g0075 | AMR | CLM | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01496 | hp1 | a0001 | c0001 | t0013 | g0002 | AMR | CLM | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0009 | EUR | IBS | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0144 | EUR | IBS | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0154 | EUR | IBS | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | IBS | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0148 | EUR | IBS | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0009 | EUR | IBS | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01884 | hp2 | a0001 | c0002 | t0011 | g0010 | AFR | ACB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01891 | hp1 | a0001 | c0002 | t0011 | g0010 | AFR | ACB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01891 | hp2 | a0001 | c0004 | t0040 | g0176 | AFR | ACB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01952 | hp2 | a0001 | c0001 | t0032 | g0141 | AMR | PEL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01978 | hp1 | a0001 | c0001 | t0014 | g0001 | AMR | PEL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02004 | hp2 | a0001 | c0001 | t0012 | g0153 | AMR | PEL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02027 | hp1 | a0001 | c0001 | t0026 | g0167 | EAS | KHV | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02040 | hp1 | a0001 | c0001 | t0036 | g0056 | EAS | KHV | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02040 | hp2 | a0001 | c0001 | t0053 | g0095 | EAS | KHV | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02055 | hp1 | a0001 | c0001 | t0018 | g0212 | AFR | ACB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | ACB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | KHV | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02071 | hp2 | a0001 | c0001 | t0026 | g0166 | EAS | KHV | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02148 | hp2 | a0001 | c0001 | t0012 | g0149 | AMR | PEL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02257 | hp1 | a0001 | c0001 | t0010 | g0126 | AFR | ACB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02257 | hp2 | a0001 | c0001 | t0019 | g0139 | AFR | ACB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02280 | hp1 | a0001 | c0001 | t0063 | g0102 | AFR | ACB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02280 | hp2 | a0001 | c0001 | t0023 | g0128 | AFR | ACB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02451 | hp1 | a0001 | c0001 | t0047 | g0070 | AFR | ACB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02451 | hp2 | a0001 | c0001 | t0022 | g0178 | AFR | ACB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0131 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02602 | hp1 | a0001 | c0001 | t0008 | g0137 | SAS | PJL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02615 | hp1 | a0001 | c0001 | t0049 | g0112 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02615 | hp2 | a0001 | c0001 | t0046 | g0019 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02622 | hp2 | a0001 | c0002 | t0011 | g0114 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02630 | hp1 | a0001 | c0001 | t0031 | g0024 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0077 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02723 | hp1 | a0002 | c0003 | t0009 | g0161 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02723 | hp2 | a0001 | c0001 | t0045 | g0109 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0145 | SAS | PJL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02809 | hp1 | a0001 | c0001 | t0021 | g0104 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02809 | hp2 | a0001 | c0001 | t0016 | g0016 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0152 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02818 | hp2 | a0001 | c0001 | t0017 | g0076 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02886 | hp1 | a0002 | c0003 | t0009 | g0163 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02886 | hp2 | a0001 | c0001 | t0017 | g0018 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02897 | hp2 | a0001 | c0001 | t0024 | g0093 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ESN | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02922 | hp2 | a0001 | c0001 | t0021 | g0103 | AFR | ESN | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02965 | hp1 | a0002 | c0003 | t0009 | g0165 | AFR | ESN | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | ESN | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ESN | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0023 | AFR | ESN | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02976 | hp1 | a0001 | c0001 | t0031 | g0024 | AFR | ESN | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02976 | hp2 | a0001 | c0001 | t0017 | g0030 | AFR | ESN | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0194 | SAS | PJL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03041 | hp1 | a0001 | c0001 | t0015 | g0067 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03098 | hp1 | a0002 | c0003 | t0009 | g0164 | AFR | MSL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03098 | hp2 | a0001 | c0001 | t0016 | g0160 | AFR | MSL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03130 | hp1 | a0001 | c0001 | t0018 | g0211 | AFR | ESN | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03130 | hp2 | a0001 | c0001 | t0015 | g0018 | AFR | ESN | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03139 | hp1 | a0001 | c0001 | t0024 | g0027 | AFR | ESN | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03225 | hp1 | a0001 | c0001 | t0037 | g0168 | AFR | MSL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03239 | hp1 | a0001 | c0001 | t0008 | g0134 | SAS | PJL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03239 | hp2 | a0001 | c0001 | t0014 | g0064 | SAS | PJL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0071 | AFR | MSL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03486 | hp2 | a0001 | c0001 | t0023 | g0172 | AFR | MSL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0208 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03540 | hp2 | a0001 | c0002 | t0011 | g0115 | AFR | GWD | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | MSL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03579 | hp2 | a0001 | c0001 | t0016 | g0016 | AFR | MSL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0185 | SAS | PJL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03710 | hp2 | a0001 | c0001 | t0051 | g0028 | SAS | PJL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | BEB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03831 | hp2 | a0001 | c0005 | t0025 | g0042 | SAS | BEB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03927 | hp1 | a0001 | c0001 | t0013 | g0002 | SAS | BEB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | STU | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG04184 | hp2 | a0001 | c0001 | t0043 | g0087 | SAS | BEB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0146 | SAS | STU | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18522 | hp1 | a0001 | c0001 | t0018 | g0210 | AFR | YRI | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18522 | hp2 | a0001 | c0001 | t0029 | g0209 | AFR | YRI | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18906 | hp1 | a0001 | c0001 | t0061 | g0173 | AFR | YRI | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | YRI | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18939 | hp2 | a0001 | c0001 | t0020 | g0158 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18940 | hp2 | a0001 | c0001 | t0057 | g0215 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0156 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18946 | hp1 | a0001 | c0001 | t0028 | g0072 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18946 | hp2 | a0001 | c0001 | t0048 | g0083 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18952 | hp2 | a0001 | c0001 | t0007 | g0090 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18957 | hp2 | a0001 | c0001 | t0007 | g0101 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0147 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18961 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18963 | hp1 | a0001 | c0001 | t0007 | g0094 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18963 | hp2 | a0001 | c0001 | t0030 | g0188 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18965 | hp2 | a0001 | c0001 | t0007 | g0099 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18967 | hp2 | a0001 | c0001 | t0054 | g0193 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18968 | hp2 | a0001 | c0001 | t0007 | g0088 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18983 | hp2 | a0001 | c0001 | t0059 | g0014 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18991 | hp1 | a0001 | c0001 | t0028 | g0073 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18992 | hp2 | a0001 | c0001 | t0020 | g0159 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18995 | hp1 | a0001 | c0001 | t0056 | g0214 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19030 | hp1 | a0001 | c0001 | t0009 | g0031 | AFR | LWK | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19030 | hp2 | a0001 | c0002 | t0011 | g0113 | AFR | LWK | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19043 | hp2 | a0001 | c0001 | t0022 | g0179 | AFR | LWK | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19070 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19074 | hp1 | a0001 | c0001 | t0007 | g0091 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19074 | hp2 | a0001 | c0001 | t0030 | g0189 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19075 | hp1 | a0001 | c0001 | t0005 | g0155 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19079 | hp1 | a0001 | c0001 | t0038 | g0045 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19079 | hp2 | a0001 | c0001 | t0007 | g0092 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19081 | hp1 | a0001 | c0001 | t0055 | g0190 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19081 | hp2 | a0001 | c0001 | t0044 | g0032 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19087 | hp1 | a0001 | c0001 | t0058 | g0197 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19087 | hp2 | a0001 | c0001 | t0025 | g0063 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA19091 | hp2 | a0001 | c0001 | t0007 | g0098 | EAS | JPT | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA20129 | hp1 | a0001 | c0001 | t0039 | g0133 | AFR | ASW | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | ASW | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0009 | EUR | TSI | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | TSI | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA20805 | hp1 | a0001 | c0001 | t0008 | g0140 | EUR | TSI | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | TSI | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01123 | hp1 | a0001 | c0001 | t0012 | g0150 | AMR | CLM | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG01123 | hp2 | a0001 | c0001 | t0019 | g0142 | AMR | CLM | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02109 | hp1 | a0001 | c0001 | t0015 | g0065 | AFR | ACB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02109 | hp2 | a0001 | c0001 | t0010 | g0023 | AFR | ACB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0169 | AFR | ACB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0170 | AFR | ACB | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | MSL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG03471 | hp2 | a0002 | c0003 | t0009 | g0162 | AFR | MSL | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG06807 | hp1 | a0001 | c0001 | t0015 | g0019 | AFR | USA | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| HG06807 | hp2 | a0001 | c0001 | t0012 | g0151 | AFR | USA | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA21309 | hp1 | a0001 | c0001 | t0010 | g0127 | AFR | LWK | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| NA21309 | hp2 | a0001 | c0001 | t0029 | g0207 | AFR | LWK | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0034 | g0143 | REF | REF | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0014 | g0004 | REF | REF | REL_chr2_60876574_60936612 | REL | chr2 | 60876574 | 60936612 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:60921853 | C | G | 1 | a0002 | 5 | HG02723.hp1 HG02886.hp1 HG02965.hp1 others(2): Show |
missense_variant | MODERATE | c.1082C>G | p.Pro361Arg | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 1349/11108 | 1082/1764 | 361/587 | chr2 | 60921853 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:60894414 | A | G | 1 | a0001c0005 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.171A>G | p.Gly57Gly | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/10 | 438/11108 | 171/1764 | 57/587 | chr2 | 60894414 | |||
| chr2:60894435 | A | G | 1 | a0001c0002 | 6 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
synonymous_variant | LOW | c.192A>G | p.Thr64Thr | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/10 | 459/11108 | 192/1764 | 64/587 | chr2 | 60894435 | |||
| chr2:60922076 | T | C | 1 | a0001c0004 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.1305T>C | p.Asp435Asp | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 1572/11108 | 1305/1764 | 435/587 | chr2 | 60922076 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:60881574 | A | G | 1 | a0001c0001t0063 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-267A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/10 | 267 | chr2 | 60881574 | ||||||
| chr2:60881582 | C | T | 1 | a0001c0001t0062 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-259C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/10 | 259 | chr2 | 60881582 | ||||||
| chr2:60881603 | C | G | 2 | a0001c0001t0031 a0001c0001t0061 |
3 | HG02630.hp1 HG02976.hp1 NA18906.hp1 |
5_prime_UTR_variant | MODIFIER | c.-238C>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/10 | 238 | chr2 | 60881603 | ||||||
| chr2:60881694 | G | A | 9 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0012 others(6): Show |
33 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(30): Show |
5_prime_UTR_variant | MODIFIER | c.-147G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/10 | 147 | chr2 | 60881694 | ||||||
| chr2:60881791 | C | G | 1 | a0001c0001t0060 | 1 | HG00639.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-50C>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/10 | chr2 | 60881791 | |||||||
| chr2:60923562 | T | G | 1 | a0001c0001t0036 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1027T>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 1027 | chr2 | 60923562 | ||||||
| chr2:60923801 | T | C | 2 | a0001c0001t0021 a0001c0001t0037 |
3 | HG02809.hp1 HG02922.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1266T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 1266 | chr2 | 60923801 | ||||||
| chr2:60924198 | C | T | 4 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0013 others(1): Show |
21 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1663C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 1663 | chr2 | 60924198 | ||||||
| chr2:60924393 | A | G | 2 | a0001c0001t0031 a0001c0001t0061 |
3 | HG02630.hp1 HG02976.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1858A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 1858 | chr2 | 60924393 | ||||||
| chr2:60924526 | A | T | 13 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0018 others(10): Show |
49 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1991A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 1991 | chr2 | 60924526 | ||||||
| chr2:60924662 | C | T | 1 | a0001c0001t0059 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2127C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 2127 | chr2 | 60924662 | ||||||
| chr2:60924698 | A | G | 1 | a0001c0001t0052 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2163A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 2163 | chr2 | 60924698 | ||||||
| chr2:60924743 | G | T | 1 | a0001c0001t0051 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2208G>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 2208 | chr2 | 60924743 | ||||||
| chr2:60924832 | A | G | 1 | a0001c0001t0063 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2297A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 2297 | chr2 | 60924832 | ||||||
| chr2:60924848 | TCA | T | 8 | a0001c0001t0003 a0001c0001t0030 a0001c0001t0054 others(5): Show |
28 | HG00323.hp2 HG00597.hp1 HG01261.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2314_*2315delCA | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 2314 | chr2 | 60924848 | ||||||
| chr2:60925295 | G | A | 1 | a0001c0001t0022 | 2 | HG02451.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2760G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 2760 | chr2 | 60925295 | ||||||
| chr2:60925606 | G | C | 1 | a0001c0001t0038 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3071G>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 3071 | chr2 | 60925606 | ||||||
| chr2:60925696 | AT | A | 38 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(35): Show |
139 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*3175delT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 3175 | INFO_REALIGN_3_PRIME | chr2 | 60925696 | |||||
| chr2:60925712 | A | G | 1 | a0001c0001t0050 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3177A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 3177 | chr2 | 60925712 | ||||||
| chr2:60925947 | G | T | 61 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(58): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
3_prime_UTR_variant | MODIFIER | c.*3412G>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 3412 | chr2 | 60925947 | ||||||
| chr2:60925948 | T | G | 1 | a0001c0001t0024 | 2 | HG02897.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3413T>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 3413 | chr2 | 60925948 | ||||||
| chr2:60926096 | T | C | 2 | a0001c0001t0023 a0001c0001t0039 |
3 | HG02280.hp2 HG03486.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3561T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 3561 | chr2 | 60926096 | ||||||
| chr2:60926430 | T | C | 1 | a0001c0001t0024 | 2 | HG02897.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3895T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 3895 | chr2 | 60926430 | ||||||
| chr2:60926637 | A | G | 2 | a0001c0001t0023 a0001c0001t0039 |
3 | HG02280.hp2 HG03486.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4102A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 4102 | chr2 | 60926637 | ||||||
| chr2:60926668 | G | A | 7 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0012 others(4): Show |
30 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*4133G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 4133 | chr2 | 60926668 | ||||||
| chr2:60926970 | T | G | 1 | a0001c0001t0030 | 2 | NA18963.hp2 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4435T>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 4435 | chr2 | 60926970 | ||||||
| chr2:60927107 | G | A | 1 | a0001c0001t0052 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4572G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 4572 | chr2 | 60927107 | ||||||
| chr2:60927190 | T | C | 34 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(31): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*4655T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 4655 | chr2 | 60927190 | ||||||
| chr2:60927191 | G | A | 1 | a0001c0004t0040 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4656G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 4656 | chr2 | 60927191 | ||||||
| chr2:60927375 | T | C | 1 | a0001c0001t0008 | 6 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4840T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 4840 | chr2 | 60927375 | ||||||
| chr2:60927388 | C | G | 1 | a0001c0001t0049 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4853C>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 4853 | chr2 | 60927388 | ||||||
| chr2:60927591 | C | T | 1 | a0001c0001t0028 | 2 | NA18946.hp1 NA18991.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5056C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 5056 | chr2 | 60927591 | ||||||
| chr2:60927819 | T | C | 1 | a0001c0001t0054 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5284T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 5284 | chr2 | 60927819 | ||||||
| chr2:60927877 | C | G | 1 | a0001c0001t0013 | 4 | HG00280.hp2 HG01069.hp2 HG01496.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5342C>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 5342 | chr2 | 60927877 | ||||||
| chr2:60927996 | A | G | 1 | a0001c0001t0018 | 3 | HG02055.hp1 HG03130.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5461A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 5461 | chr2 | 60927996 | ||||||
| chr2:60928013 | A | G | 1 | a0001c0001t0051 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5478A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 5478 | chr2 | 60928013 | ||||||
| chr2:60928154 | C | CA | 7 | a0001c0001t0017 a0001c0001t0019 a0001c0001t0025 others(4): Show |
11 | HG01123.hp2 HG02257.hp2 HG02630.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5636dupA | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 5637 | INFO_REALIGN_3_PRIME | chr2 | 60928154 | |||||
| chr2:60928154 | CA | C | 12 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0018 others(9): Show |
48 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*5636delA | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 5636 | INFO_REALIGN_3_PRIME | chr2 | 60928154 | |||||
| chr2:60928273 | C | G | 1 | a0001c0001t0047 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5738C>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 5738 | chr2 | 60928273 | ||||||
| chr2:60928295 | C | A | 1 | a0001c0001t0051 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5760C>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 5760 | chr2 | 60928295 | ||||||
| chr2:60928361 | G | A | 1 | a0001c0001t0010 | 5 | HG02109.hp2 HG02257.hp1 HG02572.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5826G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 5826 | chr2 | 60928361 | ||||||
| chr2:60928516 | G | A | 1 | a0001c0001t0061 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5981G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 5981 | chr2 | 60928516 | ||||||
| chr2:60928555 | G | C | 1 | a0001c0001t0029 | 2 | NA18522.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6020G>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 6020 | chr2 | 60928555 | ||||||
| chr2:60928779 | C | A | 1 | a0001c0001t0039 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6244C>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 6244 | chr2 | 60928779 | ||||||
| chr2:60928831 | A | C | 2 | a0001c0001t0012 a0001c0001t0027 |
6 | HG00140.hp2 HG01123.hp1 HG01361.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6296A>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 6296 | chr2 | 60928831 | ||||||
| chr2:60928908 | T | A | 1 | a0001c0001t0056 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6373T>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 6373 | chr2 | 60928908 | ||||||
| chr2:60928923 | T | C | 5 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0013 others(2): Show |
23 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*6388T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 6388 | chr2 | 60928923 | ||||||
| chr2:60928939 | A | G | 1 | a0001c0001t0046 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6404A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 6404 | chr2 | 60928939 | ||||||
| chr2:60929007 | G | A | 9 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0020 others(6): Show |
43 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*6472G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 6472 | chr2 | 60929007 | ||||||
| chr2:60929041 | A | G | 4 | a0001c0001t0015 a0001c0001t0017 a0001c0001t0046 others(1): Show |
9 | HG02109.hp1 HG02451.hp1 HG02615.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6506A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 6506 | chr2 | 60929041 | ||||||
| chr2:60929078 | C | G | 1 | a0001c0001t0058 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6543C>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 6543 | chr2 | 60929078 | ||||||
| chr2:60929091 | CAG | C | 7 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0031 others(4): Show |
40 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*6560_*6561delGA | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 6560 | INFO_REALIGN_3_PRIME | chr2 | 60929091 | |||||
| chr2:60929099 | T | A | 2 | a0001c0001t0007 a0001c0001t0043 |
12 | HG00408.hp1 HG04184.hp2 NA18952.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6564T>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 6564 | chr2 | 60929099 | ||||||
| chr2:60929278 | G | C | 5 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0017 others(2): Show |
21 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*6743G>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 6743 | chr2 | 60929278 | ||||||
| chr2:60929295 | G | A | 38 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(35): Show |
140 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*6760G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 6760 | chr2 | 60929295 | ||||||
| chr2:60929505 | A | G | 1 | a0001c0001t0045 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6970A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 6970 | chr2 | 60929505 | ||||||
| chr2:60929562 | A | G | 1 | a0001c0001t0022 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7027A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 7027 | chr2 | 60929562 | ||||||
| chr2:60929603 | T | C | 1 | a0001c0001t0044 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7068T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 7068 | chr2 | 60929603 | ||||||
| chr2:60929726 | G | T | 1 | a0001c0001t0024 | 2 | HG02897.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7191G>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 7191 | chr2 | 60929726 | ||||||
| chr2:60929826 | T | A | 1 | a0001c0002t0041 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7291T>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 7291 | chr2 | 60929826 | ||||||
| chr2:60930106 | A | T | 1 | a0001c0001t0042 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7571A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 7571 | chr2 | 60930106 | ||||||
| chr2:60930585 | G | A | 1 | a0001c0001t0060 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8050G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 8050 | chr2 | 60930585 | ||||||
| chr2:60930668 | TAAAC | T | 7 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0012 others(4): Show |
30 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*8137_*8140delCAAA | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 8137 | INFO_REALIGN_3_PRIME | chr2 | 60930668 | |||||
| chr2:60930671 | A | C | 1 | a0001c0001t0016 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8136A>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 8136 | chr2 | 60930671 | ||||||
| chr2:60930839 | T | C | 1 | a0001c0001t0063 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8304T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 8304 | chr2 | 60930839 | ||||||
| chr2:60930995 | C | T | 1 | a0001c0001t0049 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8460C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 8460 | chr2 | 60930995 | ||||||
| chr2:60931003 | T | C | 1 | a0001c0001t0026 | 2 | HG02027.hp1 HG02071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8468T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 8468 | chr2 | 60931003 | ||||||
| chr2:60931179 | CTG | C | 3 | a0001c0001t0062 a0001c0002t0011 a0001c0002t0041 |
7 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*8646_*8647delGT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 8646 | INFO_REALIGN_3_PRIME | chr2 | 60931179 | |||||
| chr2:60931243 | C | T | 1 | a0001c0001t0049 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8708C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 8708 | chr2 | 60931243 | ||||||
| chr2:60931246 | C | T | 1 | a0001c0001t0016 | 3 | HG02809.hp2 HG03098.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8711C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 8711 | chr2 | 60931246 | ||||||
| chr2:60931284 | T | C | 1 | a0001c0001t0037 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8749T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 8749 | chr2 | 60931284 | ||||||
| chr2:60931545 | A | G | 1 | a0001c0001t0046 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9010A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 10/10 | 9010 | chr2 | 60931545 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:60881861 | A | T | 38 | a0001c0001t0003g0008 a0001c0001t0003g0014 a0001c0001t0003g0025 others(35): Show |
47 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.10+11A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60881861 | |||||||
| chr2:60882012 | A | G | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
4 | HG00642.hp2 HG01256.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.10+162A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60882012 | |||||||
| chr2:60882125 | C | T | 2 | a0001c0001t0022g0178 a0001c0001t0022g0179 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.10+275C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60882125 | |||||||
| chr2:60882159 | A | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.10+309A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60882159 | |||||||
| chr2:60882219 | G | A | 1 | a0001c0001t0003g0184 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.10+369G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60882219 | |||||||
| chr2:60883037 | A | C | 5 | a0001c0001t0003g0014 a0001c0001t0003g0213 a0001c0001t0056g0214 others(2): Show |
6 | NA18940.hp2 NA18952.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.10+1187A>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60883037 | |||||||
| chr2:60883122 | CTAAATGC others(4): Show |
C | 1 | a0001c0004t0040g0176 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.10+1280_10+1290del others(11): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 60883122 | ||||||
| chr2:60883405 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.10+1555C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60883405 | |||||||
| chr2:60883427 | G | A | 1 | a0001c0001t0024g0027 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.10+1577G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60883427 | |||||||
| chr2:60883552 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.10+1702A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60883552 | |||||||
| chr2:60883607 | T | C | 1 | a0001c0004t0040g0176 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.10+1757T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60883607 | |||||||
| chr2:60883744 | A | G | 2 | a0001c0001t0031g0024 a0001c0001t0061g0173 |
3 | HG02630.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.10+1894A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60883744 | |||||||
| chr2:60883844 | C | CT | 45 | a0001c0001t0001g0171 a0001c0001t0005g0002 a0001c0001t0005g0144 others(42): Show |
52 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.10+2012dupT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 60883844 | ||||||
| chr2:60883844 | CT | C | 8 | a0001c0001t0001g0029 a0001c0001t0001g0177 a0001c0001t0001g0180 others(5): Show |
8 | HG00733.hp1 HG01256.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.10+2012delT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 60883844 | ||||||
| chr2:60883959 | T | TA | 32 | a0001c0001t0002g0033 a0001c0001t0005g0002 a0001c0001t0005g0034 others(29): Show |
36 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.10+2122dupA | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 60883959 | ||||||
| chr2:60884354 | A | G | 20 | a0001c0001t0005g0002 a0001c0001t0005g0034 a0001c0001t0005g0144 others(17): Show |
24 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.10+2504A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60884354 | |||||||
| chr2:60884364 | TATG | T | 1 | a0001c0001t0001g0013 | 3 | NA18966.hp2 NA18988.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.10+2517_10+2519del others(3): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 60884364 | ||||||
| chr2:60884788 | A | G | 2 | a0001c0001t0019g0142 a0001c0001t0032g0141 |
2 | HG01123.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.10+2938A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60884788 | |||||||
| chr2:60885099 | G | A | 10 | a0001c0001t0003g0008 a0001c0001t0003g0025 a0001c0001t0003g0186 others(7): Show |
14 | HG00323.hp2 HG00597.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.10+3249G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60885099 | |||||||
| chr2:60885130 | A | G | 2 | a0001c0001t0023g0172 a0001c0001t0039g0133 |
2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.10+3280A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60885130 | |||||||
| chr2:60885221 | G | C | 2 | a0001c0001t0005g0144 a0001c0001t0005g0145 |
2 | HG01515.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.10+3371G>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60885221 | |||||||
| chr2:60885296 | T | C | 1 | a0001c0001t0005g0146 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.10+3446T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60885296 | |||||||
| chr2:60885417 | G | T | 31 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0012 others(28): Show |
42 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.10+3567G>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60885417 | |||||||
| chr2:60885449 | C | A | 2 | a0001c0001t0022g0178 a0001c0001t0022g0179 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.10+3599C>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60885449 | |||||||
| chr2:60885668 | A | G | 1 | a0001c0001t0018g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10+3818A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60885668 | |||||||
| chr2:60886496 | C | T | 1 | a0001c0001t0010g0023 | 2 | HG02109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.10+4646C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60886496 | |||||||
| chr2:60886525 | G | T | 1 | a0001c0004t0040g0176 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.10+4675G>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60886525 | |||||||
| chr2:60886566 | G | A | 5 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0001t0008g0136 others(2): Show |
5 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.10+4716G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60886566 | |||||||
| chr2:60886656 | A | G | 2 | a0001c0001t0031g0024 a0001c0001t0061g0173 |
3 | HG02630.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.10+4806A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60886656 | |||||||
| chr2:60887191 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0035 |
3 | HG01168.hp1 HG01261.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.11-4492T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60887191 | |||||||
| chr2:60887350 | A | G | 9 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0106 others(6): Show |
11 | HG00735.hp1 HG01884.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.11-4333A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60887350 | |||||||
| chr2:60887804 | A | G | 38 | a0001c0001t0003g0008 a0001c0001t0003g0014 a0001c0001t0003g0025 others(35): Show |
47 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.11-3879A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60887804 | |||||||
| chr2:60887904 | T | G | 30 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0012 others(27): Show |
40 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.11-3779T>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60887904 | |||||||
| chr2:60888001 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.11-3682C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60888001 | |||||||
| chr2:60888461 | A | G | 2 | a0001c0001t0021g0103 a0001c0001t0021g0104 |
2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.11-3222A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60888461 | |||||||
| chr2:60888553 | A | T | 1 | a0001c0001t0002g0132 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.11-3130A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60888553 | |||||||
| chr2:60888557 | G | A | 1 | a0001c0001t0004g0194 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.11-3126G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60888557 | |||||||
| chr2:60888873 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.11-2810T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60888873 | |||||||
| chr2:60889106 | C | G | 33 | a0001c0001t0001g0183 a0001c0001t0002g0006 a0001c0001t0002g0011 others(30): Show |
44 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.11-2577C>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60889106 | |||||||
| chr2:60889120 | GAA | G | 41 | a0001c0001t0003g0008 a0001c0001t0003g0014 a0001c0001t0003g0025 others(38): Show |
50 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.11-2561_11-2560del others(2): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 60889120 | ||||||
| chr2:60889346 | A | G | 40 | a0001c0001t0003g0008 a0001c0001t0003g0014 a0001c0001t0003g0025 others(37): Show |
49 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.11-2337A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60889346 | |||||||
| chr2:60889455 | A | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0035 others(28): Show |
41 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.11-2228A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60889455 | |||||||
| chr2:60889464 | T | C | 18 | a0001c0001t0005g0002 a0001c0001t0005g0034 a0001c0001t0005g0144 others(15): Show |
22 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.11-2219T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60889464 | |||||||
| chr2:60889465 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.11-2218A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60889465 | |||||||
| chr2:60889694 | C | T | 2 | a0001c0001t0006g0005 a0001c0001t0006g0077 |
5 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.11-1989C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60889694 | |||||||
| chr2:60889783 | C | T | 1 | a0001c0001t0017g0076 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.11-1900C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60889783 | |||||||
| chr2:60889898 | G | A | 1 | a0001c0001t0016g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.11-1785G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60889898 | |||||||
| chr2:60890154 | G | A | 2 | a0001c0001t0004g0195 a0001c0001t0004g0196 |
2 | HG00738.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.11-1529G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60890154 | |||||||
| chr2:60890281 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0105 |
2 | HG00597.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.11-1402T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60890281 | |||||||
| chr2:60890311 | G | A | 1 | a0001c0001t0051g0028 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.11-1372G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60890311 | |||||||
| chr2:60890342 | C | T | 1 | a0001c0001t0027g0075 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.11-1341C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60890342 | |||||||
| chr2:60890387 | G | C | 1 | a0001c0001t0008g0134 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.11-1296G>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60890387 | |||||||
| chr2:60890680 | C | T | 1 | a0001c0001t0010g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.11-1003C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60890680 | |||||||
| chr2:60890978 | A | C | 32 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0012 others(29): Show |
43 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.11-705A>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60890978 | |||||||
| chr2:60891071 | G | C | 5 | a0001c0002t0011g0010 a0001c0002t0011g0113 a0001c0002t0011g0114 others(2): Show |
6 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.11-612G>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60891071 | |||||||
| chr2:60891174 | C | T | 18 | a0001c0001t0005g0002 a0001c0001t0005g0034 a0001c0001t0005g0144 others(15): Show |
22 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.11-509C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60891174 | |||||||
| chr2:60891255 | C | T | 2 | a0001c0001t0002g0129 a0001c0001t0002g0130 |
2 | HG00741.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.11-428C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60891255 | |||||||
| chr2:60891309 | G | A | 2 | a0002c0003t0009g0161 a0002c0003t0009g0162 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.11-374G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60891309 | |||||||
| chr2:60891352 | G | A | 1 | a0001c0001t0063g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.11-331G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60891352 | |||||||
| chr2:60891604 | A | G | 34 | a0001c0001t0001g0183 a0001c0001t0002g0006 a0001c0001t0002g0011 others(31): Show |
45 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.11-79A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60891604 | |||||||
| chr2:60891634 | A | G | 1 | a0001c0001t0051g0028 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.11-49A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 1/9 | chr2 | 60891634 | |||||||
| chr2:60891870 | A | T | 1 | a0001c0001t0042g0074 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.153+45A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60891870 | |||||||
| chr2:60891951 | T | G | 1 | a0001c0001t0010g0023 | 2 | HG02109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.153+126T>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60891951 | |||||||
| chr2:60891965 | G | T | 1 | a0001c0001t0002g0033 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.153+140G>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60891965 | |||||||
| chr2:60892111 | T | C | 1 | a0001c0001t0058g0197 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.153+286T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60892111 | |||||||
| chr2:60892336 | G | A | 111 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0012 others(108): Show |
136 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.153+511G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60892336 | |||||||
| chr2:60892424 | A | T | 1 | a0001c0004t0040g0176 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.153+599A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60892424 | |||||||
| chr2:60892664 | A | T | 2 | a0001c0001t0028g0072 a0001c0001t0028g0073 |
2 | NA18946.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.153+839A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60892664 | |||||||
| chr2:60892754 | T | A | 44 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(41): Show |
53 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.153+929T>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60892754 | |||||||
| chr2:60892778 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.153+953G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60892778 | |||||||
| chr2:60892815 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.153+990C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60892815 | |||||||
| chr2:60892997 | A | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0020 others(175): Show |
221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.153+1172A>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60892997 | |||||||
| chr2:60893316 | A | G | 2 | a0001c0001t0002g0129 a0001c0001t0002g0130 |
2 | HG00741.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.154-1081A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60893316 | |||||||
| chr2:60893325 | G | T | 2 | a0001c0001t0002g0129 a0001c0001t0002g0130 |
2 | HG00741.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.154-1072G>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60893325 | |||||||
| chr2:60893607 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.154-790T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60893607 | |||||||
| chr2:60893861 | T | A | 1 | a0001c0001t0063g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.154-536T>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60893861 | |||||||
| chr2:60894001 | A | G | 1 | a0001c0001t0063g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.154-396A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60894001 | |||||||
| chr2:60894015 | G | A | 1 | a0001c0001t0015g0065 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.154-382G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60894015 | |||||||
| chr2:60894107 | A | G | 1 | a0001c0001t0033g0157 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.154-290A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60894107 | |||||||
| chr2:60894144 | A | C | 1 | a0002c0003t0009g0165 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.154-253A>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60894144 | |||||||
| chr2:60894154 | G | A | 1 | a0001c0001t0022g0178 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.154-243G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60894154 | |||||||
| chr2:60894357 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(217): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.154-40G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 2/9 | chr2 | 60894357 | |||||||
| chr2:60894795 | A | G | 3 | a0001c0001t0018g0210 a0001c0001t0018g0211 a0001c0001t0018g0212 |
3 | HG02055.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.302+250A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60894795 | |||||||
| chr2:60894851 | C | CT | 8 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0081 others(5): Show |
8 | HG00673.hp2 HG01192.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.302+328dupT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 60894851 | ||||||
| chr2:60894851 | CT | C | 11 | a0001c0001t0001g0079 a0001c0001t0002g0117 a0001c0001t0003g0186 others(8): Show |
11 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.302+328delT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 60894851 | ||||||
| chr2:60895021 | T | G | 1 | a0001c0001t0026g0167 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.302+476T>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60895021 | |||||||
| chr2:60895180 | A | G | 1 | a0001c0001t0018g0211 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.302+635A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60895180 | |||||||
| chr2:60895182 | C | T | 9 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0001t0008g0136 others(6): Show |
9 | HG01123.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.302+637C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60895182 | |||||||
| chr2:60895398 | C | A | 32 | a0001c0001t0003g0008 a0001c0001t0003g0014 a0001c0001t0003g0025 others(29): Show |
41 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.302+853C>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60895398 | |||||||
| chr2:60895493 | A | G | 2 | a0001c0001t0004g0194 a0001c0001t0004g0206 |
2 | HG00733.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.302+948A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60895493 | |||||||
| chr2:60895750 | C | G | 1 | a0001c0001t0001g0171 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.302+1205C>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60895750 | |||||||
| chr2:60895838 | G | A | 28 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0012 others(25): Show |
39 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.302+1293G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60895838 | |||||||
| chr2:60896058 | A | G | 4 | a0001c0001t0005g0155 a0001c0001t0005g0156 a0001c0001t0020g0158 others(1): Show |
4 | NA18939.hp2 NA18941.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.302+1513A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60896058 | |||||||
| chr2:60896103 | A | C | 1 | a0001c0001t0001g0060 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.302+1558A>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60896103 | |||||||
| chr2:60896243 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.302+1698A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60896243 | |||||||
| chr2:60896257 | C | T | 2 | a0001c0001t0005g0148 a0001c0001t0005g0154 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.302+1712C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60896257 | |||||||
| chr2:60896870 | A | T | 4 | a0001c0001t0010g0023 a0001c0001t0010g0126 a0001c0001t0010g0127 others(1): Show |
5 | HG02109.hp2 HG02257.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+2325A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60896870 | |||||||
| chr2:60897098 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.302+2553G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60897098 | |||||||
| chr2:60897253 | T | C | 5 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(2): Show |
5 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+2708T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60897253 | |||||||
| chr2:60897303 | C | CT | 34 | a0001c0001t0001g0183 a0001c0001t0002g0006 a0001c0001t0002g0011 others(31): Show |
45 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.302+2769dupT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 60897303 | ||||||
| chr2:60897331 | A | G | 33 | a0001c0001t0001g0183 a0001c0001t0002g0006 a0001c0001t0002g0011 others(30): Show |
44 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.302+2786A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60897331 | |||||||
| chr2:60897597 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.302+3052C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60897597 | |||||||
| chr2:60897715 | T | C | 32 | a0001c0001t0005g0002 a0001c0001t0005g0034 a0001c0001t0005g0144 others(29): Show |
36 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.302+3170T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60897715 | |||||||
| chr2:60897863 | TA | T | 100 | a0001c0001t0001g0100 a0001c0001t0001g0106 a0001c0001t0002g0006 others(97): Show |
125 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.303-3111delA | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 60897863 | ||||||
| chr2:60897878 | A | G | 1 | a0001c0004t0040g0176 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.303-3114A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60897878 | |||||||
| chr2:60897908 | C | T | 1 | a0001c0001t0012g0153 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.303-3084C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60897908 | |||||||
| chr2:60898196 | C | T | 1 | a0001c0004t0040g0176 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.303-2796C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60898196 | |||||||
| chr2:60898300 | G | A | 1 | a0001c0004t0040g0176 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.303-2692G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60898300 | |||||||
| chr2:60898415 | G | C | 1 | a0001c0001t0010g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.303-2577G>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60898415 | |||||||
| chr2:60898503 | G | A | 3 | a0001c0001t0021g0103 a0001c0001t0021g0104 a0001c0001t0037g0168 |
3 | HG02809.hp1 HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.303-2489G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60898503 | |||||||
| chr2:60898890 | C | T | 1 | a0001c0001t0003g0192 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.303-2102C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60898890 | |||||||
| chr2:60898931 | A | G | 6 | a0001c0001t0062g0118 a0001c0002t0011g0010 a0001c0002t0011g0113 others(3): Show |
7 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.303-2061A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60898931 | |||||||
| chr2:60898951 | T | A | 1 | a0001c0001t0001g0038 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.303-2041T>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60898951 | |||||||
| chr2:60898963 | A | G | 1 | a0001c0001t0017g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.303-2029A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60898963 | |||||||
| chr2:60899094 | C | G | 2 | a0001c0001t0016g0016 a0001c0001t0016g0160 |
3 | HG02809.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.303-1898C>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60899094 | |||||||
| chr2:60899212 | A | G | 1 | a0001c0001t0042g0074 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.303-1780A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60899212 | |||||||
| chr2:60899490 | A | T | 34 | a0001c0001t0003g0008 a0001c0001t0003g0014 a0001c0001t0003g0025 others(31): Show |
43 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.303-1502A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60899490 | |||||||
| chr2:60899529 | A | G | 26 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0012 others(23): Show |
36 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.303-1463A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60899529 | |||||||
| chr2:60899722 | G | A | 1 | a0001c0001t0032g0141 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.303-1270G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60899722 | |||||||
| chr2:60900527 | C | CT | 5 | a0001c0001t0002g0125 a0001c0001t0028g0072 a0001c0001t0028g0073 others(2): Show |
5 | HG02738.hp2 HG03710.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-452dupT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 60900527 | ||||||
| chr2:60900539 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.303-453T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60900539 | |||||||
| chr2:60900600 | C | T | 1 | a0001c0001t0051g0028 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.303-392C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60900600 | |||||||
| chr2:60900682 | C | T | 3 | a0001c0001t0015g0019 a0001c0001t0015g0065 a0001c0001t0046g0019 |
3 | HG02109.hp1 HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.303-310C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60900682 | |||||||
| chr2:60900844 | C | T | 1 | a0001c0001t0063g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.303-148C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 3/9 | chr2 | 60900844 | |||||||
| chr2:60901133 | G | A | 29 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0012 others(26): Show |
40 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.394+50G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60901133 | |||||||
| chr2:60901148 | CT | C | 55 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0117 others(52): Show |
70 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.394+66delT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60901148 | |||||||
| chr2:60901149 | T | C | 56 | a0001c0001t0002g0012 a0001c0001t0002g0022 a0001c0001t0002g0116 others(53): Show |
66 | HG00280.hp1 HG00280.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.394+66T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60901149 | |||||||
| chr2:60901150 | CT | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(97): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.394+90delT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60901150 | ||||||
| chr2:60901150 | CTT | C | 19 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0100 others(16): Show |
23 | HG00280.hp1 HG00558.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.394+89_394+90delTT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60901150 | ||||||
| chr2:60901150 | CTTT | C | 10 | a0001c0001t0010g0023 a0001c0001t0010g0126 a0001c0001t0010g0127 others(7): Show |
12 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.394+88_394+90delTT others(1): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60901150 | ||||||
| chr2:60901151 | T | C | 55 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0117 others(52): Show |
70 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.394+68T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60901151 | |||||||
| chr2:60901236 | A | G | 1 | a0001c0001t0042g0074 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.394+153A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60901236 | |||||||
| chr2:60901480 | T | G | 1 | a0001c0004t0040g0176 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.394+397T>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60901480 | |||||||
| chr2:60902526 | C | T | 1 | a0001c0001t0005g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.394+1443C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60902526 | |||||||
| chr2:60902533 | G | GT | 112 | a0001c0001t0001g0183 a0001c0001t0002g0006 a0001c0001t0002g0011 others(109): Show |
137 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.394+1461dupT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60902533 | ||||||
| chr2:60902595 | C | CT | 12 | a0001c0001t0001g0062 a0001c0001t0001g0105 a0001c0001t0002g0122 others(9): Show |
12 | HG00597.hp2 HG01361.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.394+1530dupT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60902595 | ||||||
| chr2:60902625 | G | A | 1 | a0001c0001t0043g0087 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.394+1542G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60902625 | |||||||
| chr2:60902672 | C | T | 1 | a0001c0001t0063g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.394+1589C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60902672 | |||||||
| chr2:60902724 | G | T | 2 | a0001c0001t0006g0005 a0001c0001t0006g0077 |
5 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+1641G>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60902724 | |||||||
| chr2:60903171 | C | T | 1 | a0001c0004t0040g0176 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.394+2088C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60903171 | |||||||
| chr2:60903214 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.394+2131A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60903214 | |||||||
| chr2:60903497 | C | T | 36 | a0001c0001t0003g0008 a0001c0001t0003g0014 a0001c0001t0003g0025 others(33): Show |
45 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.394+2414C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60903497 | |||||||
| chr2:60903535 | A | T | 2 | a0001c0001t0016g0016 a0001c0001t0016g0160 |
3 | HG02809.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.394+2452A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60903535 | |||||||
| chr2:60903748 | G | C | 33 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0012 others(30): Show |
44 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.394+2665G>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60903748 | |||||||
| chr2:60903971 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.394+2888C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60903971 | |||||||
| chr2:60904037 | A | T | 2 | a0001c0001t0022g0178 a0001c0001t0022g0179 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.394+2954A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60904037 | |||||||
| chr2:60904087 | T | C | 2 | a0001c0001t0003g0198 a0001c0001t0003g0199 |
2 | NA18965.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.394+3004T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60904087 | |||||||
| chr2:60904272 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.394+3189C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60904272 | |||||||
| chr2:60904370 | C | G | 2 | a0001c0001t0007g0098 a0001c0001t0007g0101 |
2 | NA18957.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.394+3287C>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60904370 | |||||||
| chr2:60904405 | TA | T | 23 | a0001c0001t0001g0100 a0001c0001t0002g0006 a0001c0001t0002g0011 others(20): Show |
32 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.394+3338delA | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60904405 | ||||||
| chr2:60904430 | G | A | 1 | a0001c0001t0016g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.394+3347G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60904430 | |||||||
| chr2:60904579 | AT | A | 5 | a0001c0001t0062g0118 a0001c0002t0011g0010 a0001c0002t0011g0114 others(2): Show |
6 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.394+3497delT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60904579 | |||||||
| chr2:60904580 | T | A | 1 | a0001c0002t0011g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.394+3497T>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60904580 | |||||||
| chr2:60904580 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.394+3497T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60904580 | |||||||
| chr2:60904582 | A | T | 1 | a0001c0002t0011g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.394+3499A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60904582 | |||||||
| chr2:60904584 | T | A | 1 | a0001c0002t0011g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.394+3501T>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60904584 | |||||||
| chr2:60904584 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.394+3501T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60904584 | |||||||
| chr2:60904811 | G | A | 1 | a0001c0001t0007g0088 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.394+3728G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60904811 | |||||||
| chr2:60904894 | T | A | 32 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0012 others(29): Show |
43 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.394+3811T>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60904894 | |||||||
| chr2:60904979 | A | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0107 |
5 | HG02622.hp1 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+3896A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60904979 | |||||||
| chr2:60905000 | C | T | 1 | a0001c0001t0023g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.394+3917C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60905000 | |||||||
| chr2:60905169 | A | T | 1 | a0001c0001t0027g0075 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.394+4086A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60905169 | |||||||
| chr2:60905188 | G | A | 1 | a0001c0001t0051g0028 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.394+4105G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60905188 | |||||||
| chr2:60905244 | G | A | 3 | a0001c0001t0012g0149 a0001c0001t0012g0150 a0001c0001t0012g0153 |
3 | HG01123.hp1 HG02004.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.394+4161G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60905244 | |||||||
| chr2:60905558 | T | A | 1 | a0001c0001t0001g0062 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.394+4475T>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60905558 | |||||||
| chr2:60905747 | C | T | 2 | a0001c0001t0022g0178 a0001c0001t0022g0179 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.394+4664C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60905747 | |||||||
| chr2:60905886 | A | G | 1 | a0001c0001t0002g0124 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.394+4803A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60905886 | |||||||
| chr2:60906096 | G | C | 2 | a0001c0001t0001g0108 a0001c0001t0045g0109 |
2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.394+5013G>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60906096 | |||||||
| chr2:60906164 | A | G | 1 | a0001c0001t0002g0006 | 4 | HG01256.hp1 HG01258.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.394+5081A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60906164 | |||||||
| chr2:60906658 | A | G | 29 | a0001c0001t0001g0183 a0001c0001t0002g0006 a0001c0001t0002g0011 others(26): Show |
40 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.394+5575A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60906658 | |||||||
| chr2:60906845 | GTGTGTGT others(5): Show |
G | 2 | a0001c0001t0006g0169 a0001c0001t0006g0170 |
2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.394+5770_394+5781d others(14): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60906845 | ||||||
| chr2:60906857 | A | G | 1 | a0001c0001t0023g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.394+5774A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60906857 | |||||||
| chr2:60906857 | ATGTG | A | 28 | a0001c0001t0005g0002 a0001c0001t0005g0034 a0001c0001t0005g0144 others(25): Show |
32 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.394+5785_394+5788d others(6): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60906857 | ||||||
| chr2:60906870 | T | C | 2 | a0001c0001t0018g0210 a0001c0001t0018g0211 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.394+5787T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60906870 | |||||||
| chr2:60906893 | G | A | 3 | a0001c0001t0023g0128 a0001c0001t0023g0172 a0001c0001t0039g0133 |
3 | HG02280.hp2 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.394+5810G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60906893 | |||||||
| chr2:60906893 | G | GTA | 10 | a0001c0001t0001g0017 a0001c0001t0001g0039 a0001c0001t0001g0047 others(7): Show |
11 | HG00597.hp2 HG01496.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.394+5830_394+5831d others(4): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60906893 | ||||||
| chr2:60906893 | G | GTGTATAT others(3): Show |
1 | a0001c0001t0004g0206 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.394+5811_394+5812i others(12): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60906893 | ||||||
| chr2:60906895 | A | G | 4 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0022g0179 others(1): Show |
4 | HG01516.hp2 HG01928.hp2 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.394+5812A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60906895 | |||||||
| chr2:60906909 | A | AT | 6 | a0001c0001t0002g0012 a0001c0001t0002g0022 a0001c0001t0002g0124 others(3): Show |
9 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.394+5827dupT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60906909 | ||||||
| chr2:60906911 | A | AT | 21 | a0001c0001t0001g0183 a0001c0001t0002g0006 a0001c0001t0002g0011 others(18): Show |
26 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.394+5829dupT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60906911 | ||||||
| chr2:60906911 | A | T | 12 | a0001c0001t0002g0012 a0001c0001t0002g0022 a0001c0001t0002g0124 others(9): Show |
17 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.394+5828A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60906911 | |||||||
| chr2:60906913 | A | AT | 17 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0082 others(14): Show |
19 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.394+5846dupT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60906913 | ||||||
| chr2:60906913 | A | ATATATAT | 6 | a0001c0001t0003g0014 a0001c0001t0003g0184 a0001c0001t0003g0202 others(3): Show |
8 | HG01515.hp1 HG01517.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.394+5831_394+5832i others(9): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60906913 | ||||||
| chr2:60906913 | A | ATATATAT others(2): Show |
5 | a0001c0001t0003g0187 a0001c0001t0004g0204 a0001c0001t0004g0205 others(2): Show |
5 | HG00323.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+5831_394+5832i others(11): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60906913 | ||||||
| chr2:60906913 | A | ATATATAT others(4): Show |
2 | a0001c0001t0023g0172 a0001c0001t0039g0133 |
2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.394+5831_394+5832i others(13): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60906913 | ||||||
| chr2:60906913 | A | ATT | 8 | a0001c0001t0006g0077 a0001c0001t0031g0024 a0001c0001t0061g0173 others(5): Show |
9 | HG02630.hp1 HG02630.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.394+5845_394+5846d others(4): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60906913 | ||||||
| chr2:60906913 | A | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0069 others(61): Show |
80 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.394+5830A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60906913 | |||||||
| chr2:60906914 | T | TA | 18 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(15): Show |
20 | HG00673.hp2 HG00735.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.394+5831_394+5832i others(3): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60906914 | |||||||
| chr2:60906914 | T | TATA | 4 | a0001c0001t0016g0016 a0001c0001t0018g0210 a0001c0001t0018g0212 others(1): Show |
5 | HG01891.hp2 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+5831_394+5832i others(5): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60906914 | |||||||
| chr2:60906914 | T | TATATATA | 15 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0025 others(12): Show |
19 | HG00597.hp1 HG00738.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.394+5831_394+5832i others(9): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60906914 | |||||||
| chr2:60906915 | T | A | 12 | a0001c0001t0001g0041 a0001c0001t0001g0060 a0001c0001t0001g0089 others(9): Show |
12 | HG01070.hp1 HG02257.hp1 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.394+5832T>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60906915 | |||||||
| chr2:60906916 | T | A | 4 | a0001c0001t0020g0158 a0001c0001t0020g0159 a0001c0001t0030g0188 others(1): Show |
4 | NA18939.hp2 NA18963.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.394+5833T>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60906916 | |||||||
| chr2:60906917 | T | A | 1 | a0001c0001t0004g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.394+5834T>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60906917 | |||||||
| chr2:60906948 | T | C | 3 | a0001c0001t0007g0090 a0001c0001t0007g0091 a0001c0001t0007g0099 |
3 | NA18952.hp2 NA18965.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.394+5865T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60906948 | |||||||
| chr2:60907068 | C | T | 1 | a0001c0001t0009g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.394+5985C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60907068 | |||||||
| chr2:60907225 | C | T | 4 | a0001c0001t0012g0149 a0001c0001t0012g0150 a0001c0001t0012g0151 others(1): Show |
4 | HG01123.hp1 HG02004.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.394+6142C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60907225 | |||||||
| chr2:60907410 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.394+6327G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60907410 | |||||||
| chr2:60907451 | C | G | 1 | a0001c0001t0004g0026 | 2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.394+6368C>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60907451 | |||||||
| chr2:60907629 | A | C | 34 | a0001c0001t0001g0055 a0001c0001t0001g0183 a0001c0001t0002g0006 others(31): Show |
45 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.394+6546A>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60907629 | |||||||
| chr2:60907839 | C | T | 1 | a0001c0001t0014g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.394+6756C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60907839 | |||||||
| chr2:60907928 | G | C | 1 | a0001c0001t0051g0028 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.394+6845G>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60907928 | |||||||
| chr2:60908120 | A | G | 1 | a0001c0001t0015g0065 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.394+7037A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60908120 | |||||||
| chr2:60908222 | G | C | 1 | a0001c0001t0001g0081 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.394+7139G>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60908222 | |||||||
| chr2:60908358 | CT | C | 5 | a0001c0001t0001g0048 a0001c0001t0001g0082 a0001c0001t0001g0084 others(2): Show |
5 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.394+7278delT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60908358 | ||||||
| chr2:60908411 | C | T | 1 | a0001c0001t0008g0138 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.394+7328C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60908411 | |||||||
| chr2:60908878 | G | A | 9 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0001t0008g0136 others(6): Show |
9 | HG01123.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.394+7795G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60908878 | |||||||
| chr2:60908994 | G | T | 29 | a0001c0001t0005g0002 a0001c0001t0005g0034 a0001c0001t0005g0144 others(26): Show |
33 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.395-7883G>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60908994 | |||||||
| chr2:60909363 | A | C | 37 | a0001c0001t0003g0008 a0001c0001t0003g0014 a0001c0001t0003g0025 others(34): Show |
46 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.395-7514A>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60909363 | |||||||
| chr2:60909417 | A | C | 1 | a0001c0001t0012g0150 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.395-7460A>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60909417 | |||||||
| chr2:60909489 | C | T | 1 | a0001c0001t0016g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.395-7388C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60909489 | |||||||
| chr2:60909628 | C | T | 1 | a0001c0001t0049g0112 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.395-7249C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60909628 | |||||||
| chr2:60909697 | T | C | 7 | a0001c0001t0016g0016 a0001c0001t0016g0160 a0002c0003t0009g0161 others(4): Show |
8 | HG02723.hp1 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.395-7180T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60909697 | |||||||
| chr2:60909950 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.395-6927A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60909950 | |||||||
| chr2:60910092 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.395-6785T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60910092 | |||||||
| chr2:60910193 | C | T | 1 | a0001c0004t0040g0176 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.395-6684C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60910193 | |||||||
| chr2:60910371 | G | A | 9 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0001t0008g0136 others(6): Show |
9 | HG01123.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.395-6506G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60910371 | |||||||
| chr2:60910389 | C | T | 1 | a0001c0001t0061g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.395-6488C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60910389 | |||||||
| chr2:60910482 | CA | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
231 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.395-6381delA | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60910482 | ||||||
| chr2:60910482 | CAA | C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0012 others(26): Show |
39 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.395-6382_395-6381d others(4): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60910482 | ||||||
| chr2:60910486 | A | C | 1 | a0001c0001t0016g0016 | 2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.395-6391A>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60910486 | |||||||
| chr2:60910487 | A | C | 1 | a0001c0001t0004g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.395-6390A>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60910487 | |||||||
| chr2:60910490 | A | C | 1 | a0001c0001t0008g0140 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.395-6387A>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60910490 | |||||||
| chr2:60910543 | G | C | 1 | a0001c0001t0051g0028 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.395-6334G>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60910543 | |||||||
| chr2:60910669 | C | A | 1 | a0001c0001t0055g0190 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.395-6208C>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60910669 | |||||||
| chr2:60910855 | C | A | 1 | a0001c0001t0001g0040 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.395-6022C>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60910855 | |||||||
| chr2:60910887 | A | G | 37 | a0001c0001t0003g0008 a0001c0001t0003g0014 a0001c0001t0003g0025 others(34): Show |
46 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.395-5990A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60910887 | |||||||
| chr2:60911008 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.395-5869T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60911008 | |||||||
| chr2:60911627 | A | T | 1 | a0001c0001t0001g0054 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.395-5250A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60911627 | |||||||
| chr2:60911677 | C | T | 7 | a0001c0001t0016g0016 a0001c0001t0016g0160 a0002c0003t0009g0161 others(4): Show |
8 | HG02723.hp1 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.395-5200C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60911677 | |||||||
| chr2:60911722 | C | T | 1 | a0001c0001t0051g0028 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.395-5155C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60911722 | |||||||
| chr2:60911735 | T | C | 2 | a0001c0001t0002g0129 a0001c0001t0002g0130 |
2 | HG00741.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.395-5142T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60911735 | |||||||
| chr2:60911766 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.395-5111C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60911766 | |||||||
| chr2:60911776 | G | A | 29 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0012 others(26): Show |
39 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.395-5101G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60911776 | |||||||
| chr2:60911994 | C | CA | 22 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0001g0044 others(19): Show |
24 | HG00673.hp1 HG01109.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.395-4858dupA | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60911994 | ||||||
| chr2:60911994 | CA | C | 16 | a0001c0001t0002g0121 a0001c0001t0002g0124 a0001c0001t0003g0201 others(13): Show |
16 | HG00280.hp1 HG00323.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.395-4858delA | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60911994 | ||||||
| chr2:60911994 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0023g0128 a0001c0001t0023g0172 a0001c0001t0039g0133 |
3 | HG02280.hp2 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.395-4867_395-4858d others(12): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60911994 | ||||||
| chr2:60912638 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.395-4239C>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60912638 | |||||||
| chr2:60912893 | T | C | 1 | a0001c0001t0001g0050 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.395-3984T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60912893 | |||||||
| chr2:60912978 | T | G | 5 | a0002c0003t0009g0161 a0002c0003t0009g0162 a0002c0003t0009g0163 others(2): Show |
5 | HG02723.hp1 HG02886.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-3899T>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60912978 | |||||||
| chr2:60913047 | G | C | 1 | a0001c0001t0002g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.395-3830G>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60913047 | |||||||
| chr2:60913281 | A | T | 1 | a0001c0001t0031g0024 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.395-3596A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60913281 | |||||||
| chr2:60913282 | T | A | 3 | a0001c0001t0007g0098 a0001c0001t0007g0101 a0002c0003t0009g0163 |
3 | HG02886.hp1 NA18957.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.395-3595T>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60913282 | |||||||
| chr2:60913363 | G | A | 1 | a0001c0001t0003g0201 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.395-3514G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60913363 | |||||||
| chr2:60913536 | C | G | 2 | a0001c0001t0010g0126 a0001c0001t0010g0131 |
2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.395-3341C>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60913536 | |||||||
| chr2:60913595 | C | G | 2 | a0001c0001t0008g0135 a0001c0001t0008g0136 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.395-3282C>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60913595 | |||||||
| chr2:60914226 | C | T | 1 | a0001c0001t0063g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.395-2651C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60914226 | |||||||
| chr2:60914480 | G | C | 28 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0012 others(25): Show |
39 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.395-2397G>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60914480 | |||||||
| chr2:60914497 | GTTTA | G | 7 | a0001c0001t0016g0016 a0001c0001t0016g0160 a0002c0003t0009g0161 others(4): Show |
8 | HG02723.hp1 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.395-2376_395-2373d others(6): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60914497 | ||||||
| chr2:60914736 | A | T | 1 | a0001c0001t0019g0142 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.395-2141A>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60914736 | |||||||
| chr2:60914835 | G | GT | 75 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0061 others(72): Show |
94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.395-2026dupT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 60914835 | ||||||
| chr2:60914839 | T | TG | 2 | a0001c0001t0031g0024 a0001c0001t0061g0173 |
3 | HG02630.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.395-2038_395-2037i others(3): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60914839 | |||||||
| chr2:60914842 | T | G | 1 | a0001c0001t0063g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.395-2035T>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60914842 | |||||||
| chr2:60914900 | T | G | 6 | a0001c0001t0062g0118 a0001c0002t0011g0010 a0001c0002t0011g0113 others(3): Show |
7 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.395-1977T>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60914900 | |||||||
| chr2:60914980 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.395-1897C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60914980 | |||||||
| chr2:60915068 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.395-1809T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60915068 | |||||||
| chr2:60915083 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.395-1794G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60915083 | |||||||
| chr2:60915182 | C | T | 3 | a0001c0001t0018g0210 a0001c0001t0018g0211 a0001c0001t0018g0212 |
3 | HG02055.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.395-1695C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60915182 | |||||||
| chr2:60915570 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.395-1307A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60915570 | |||||||
| chr2:60915592 | T | C | 2 | a0001c0001t0022g0178 a0001c0001t0022g0179 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.395-1285T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60915592 | |||||||
| chr2:60915724 | T | C | 1 | a0001c0001t0051g0028 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.395-1153T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60915724 | |||||||
| chr2:60916023 | T | G | 1 | a0001c0001t0031g0024 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.395-854T>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60916023 | |||||||
| chr2:60916077 | C | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0061 |
3 | HG00408.hp2 NA18967.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.395-800C>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60916077 | |||||||
| chr2:60916077 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.395-800C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60916077 | |||||||
| chr2:60916531 | C | T | 1 | a0001c0001t0004g0195 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.395-346C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60916531 | |||||||
| chr2:60916556 | A | G | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.395-321A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 4/9 | chr2 | 60916556 | |||||||
| chr2:60917073 | A | C | 2 | a0001c0001t0026g0166 a0001c0001t0026g0167 |
2 | HG02027.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.535+56A>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 5/9 | chr2 | 60917073 | |||||||
| chr2:60917148 | T | C | 1 | a0001c0001t0063g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.535+131T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 5/9 | chr2 | 60917148 | |||||||
| chr2:60917471 | T | G | 3 | a0001c0001t0004g0208 a0001c0001t0029g0207 a0001c0001t0029g0209 |
3 | HG03540.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.535+454T>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 5/9 | chr2 | 60917471 | |||||||
| chr2:60917530 | G | GT | 60 | a0001c0001t0001g0111 a0001c0001t0001g0182 a0001c0001t0002g0006 others(57): Show |
74 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.535+529dupT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 60917530 | ||||||
| chr2:60917530 | G | GTT | 7 | a0001c0001t0002g0120 a0001c0001t0002g0125 a0001c0001t0005g0145 others(4): Show |
8 | HG00140.hp1 HG02630.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.535+528_535+529dup others(2): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 60917530 | ||||||
| chr2:60917583 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.535+566G>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 5/9 | chr2 | 60917583 | |||||||
| chr2:60917680 | C | CTG | 20 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0046 others(17): Show |
20 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.536-477_536-476dup others(2): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 60917680 | ||||||
| chr2:60917680 | C | CTGTG | 36 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0054 others(33): Show |
45 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.536-479_536-476dup others(4): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 60917680 | ||||||
| chr2:60917680 | C | CTGTGTG | 7 | a0001c0001t0001g0108 a0001c0001t0003g0025 a0001c0001t0003g0202 others(4): Show |
8 | HG01257.hp2 HG01261.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.536-481_536-476dup others(6): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 60917680 | ||||||
| chr2:60917680 | C | CTGTGTGT others(1): Show |
8 | a0001c0001t0001g0111 a0001c0001t0003g0014 a0001c0001t0003g0213 others(5): Show |
9 | HG02040.hp2 HG02572.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.536-483_536-476dup others(8): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 60917680 | ||||||
| chr2:60917680 | C | CTGTGTGT others(3): Show |
1 | a0001c0001t0029g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.536-485_536-476dup others(10): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 60917680 | ||||||
| chr2:60917680 | CTG | C | 28 | a0001c0001t0001g0017 a0001c0001t0001g0039 a0001c0001t0001g0048 others(25): Show |
37 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.536-477_536-476del others(2): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 60917680 | ||||||
| chr2:60917680 | CTGTG | C | 22 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0177 others(19): Show |
26 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.536-479_536-476del others(4): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 60917680 | ||||||
| chr2:60917680 | CTGTGTGT others(13): Show |
C | 1 | a0001c0001t0010g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.536-495_536-476del others(20): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 60917680 | ||||||
| chr2:60917717 | C | T | 111 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0012 others(108): Show |
135 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.536-474C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 5/9 | chr2 | 60917717 | |||||||
| chr2:60918345 | C | T | 3 | a0001c0001t0018g0210 a0001c0001t0018g0211 a0001c0001t0018g0212 |
3 | HG02055.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.641-49C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 6/9 | chr2 | 60918345 | |||||||
| chr2:60918363 | A | AT | 10 | a0001c0001t0001g0021 a0001c0001t0001g0106 a0001c0001t0001g0107 others(7): Show |
11 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.641-18dupT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 60918363 | ||||||
| chr2:60918363 | AT | A | 2 | a0001c0001t0006g0005 a0001c0001t0006g0077 |
5 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.641-18delT | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 60918363 | ||||||
| chr2:60918944 | C | A | 1 | a0001c0001t0002g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.853+338C>A | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 7/9 | chr2 | 60918944 | |||||||
| chr2:60919066 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0105 |
2 | HG00597.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.853+460T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 7/9 | chr2 | 60919066 | |||||||
| chr2:60919204 | A | G | 33 | a0001c0001t0003g0008 a0001c0001t0003g0014 a0001c0001t0003g0025 others(30): Show |
42 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.853+598A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 7/9 | chr2 | 60919204 | |||||||
| chr2:60919254 | A | G | 1 | a0001c0004t0040g0176 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.853+648A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 7/9 | chr2 | 60919254 | |||||||
| chr2:60919411 | GGTTTTTT others(1): Show |
G | 3 | a0001c0001t0021g0103 a0001c0001t0021g0104 a0001c0001t0037g0168 |
3 | HG02809.hp1 HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.854-607_854-600del others(8): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 60919411 | ||||||
| chr2:60919475 | G | C | 6 | a0001c0001t0003g0014 a0001c0001t0003g0213 a0001c0001t0056g0214 others(3): Show |
7 | NA18940.hp2 NA18952.hp1 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.854-566G>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 7/9 | chr2 | 60919475 | |||||||
| chr2:60919667 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.854-374C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 7/9 | chr2 | 60919667 | |||||||
| chr2:60919671 | C | T | 1 | a0001c0005t0025g0042 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.854-370C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 7/9 | chr2 | 60919671 | |||||||
| chr2:60920242 | C | T | 1 | a0002c0003t0009g0163 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.922+133C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 8/9 | chr2 | 60920242 | |||||||
| chr2:60920346 | A | C | 2 | a0001c0001t0027g0051 a0001c0001t0027g0075 |
2 | HG00140.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.923-228A>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 8/9 | chr2 | 60920346 | |||||||
| chr2:60920462 | A | G | 1 | a0001c0001t0057g0215 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.923-112A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 8/9 | chr2 | 60920462 | |||||||
| chr2:60920924 | A | C | 1 | a0001c0001t0002g0033 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.991+282A>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 9/9 | chr2 | 60920924 | |||||||
| chr2:60921148 | TAGA | T | 57 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0012 others(54): Show |
71 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.991+512_991+514del others(3): Show |
REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 60921148 | ||||||
| chr2:60921433 | C | G | 6 | a0001c0001t0062g0118 a0001c0002t0011g0010 a0001c0002t0011g0113 others(3): Show |
7 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.992-330C>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 9/9 | chr2 | 60921433 | |||||||
| chr2:60921536 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.992-227A>G | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 9/9 | chr2 | 60921536 | |||||||
| chr2:60921572 | C | T | 1 | a0001c0001t0063g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.992-191C>T | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 9/9 | chr2 | 60921572 | |||||||
| chr2:60921650 | T | C | 7 | a0001c0001t0007g0088 a0001c0001t0007g0090 a0001c0001t0007g0091 others(4): Show |
7 | NA18952.hp2 NA18957.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.992-113T>C | REL | ENSG00000162924.16 | transcript | ENST00000394479.4 | protein_coding | 9/9 | chr2 | 60921650 |