Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 27249 |
| ensemblid | ENSG00000168288.13 |
| hgncid | 25221 |
| symbol | MMADHC |
| name | metabolism of cobalamin associated D |
| refseq_nuc | NM_015702.3 |
| refseq_prot | NP_056517.1 |
| ensembl_nuc | ENST00000303319.10 |
| ensembl_prot | ENSP00000301920.5 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 149569637 |
| end | 149587775 |
| strand | - |
| ver | v1.2 |
| region | chr2:149569637-149587775 |
| region5000 | chr2:149564637-149592775 |
| regionname0 | MMADHC_chr2_149569637_149587775 |
| regionname5000 | MMADHC_chr2_149564637_149592775 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 296 | 324 | 85 | 70 | 111 | 14 | 42 | 73 | MMADHC_chr2_149564637_149592775 | MMADHC | MANVL others(291): Show |
chr2 | 149564637 | 149592775 |
| a0002 | 0/0 | 296 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | MANVL others(291): Show |
chr2 | 149564637 | 149592775 |
| a0003 | 0/0 | 296 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | MANVL others(291): Show |
chr2 | 149564637 | 149592775 |
| a0004 | 0/0 | 296 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | MANVL others(291): Show |
chr2 | 149564637 | 149592775 |
| a0005 | 0/0 | 296 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MMADHC_chr2_149564637_149592775 | MMADHC | MANVL others(291): Show |
chr2 | 149564637 | 149592775 |
| a0006 | 0/0 | 296 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | MANVL others(291): Show |
chr2 | 149564637 | 149592775 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 888 | 233 | 40 | 61 | 85 | 13 | 34 | MMADHC_chr2_149564637_149592775 | MMADHC | ATGGC others(883): Show |
chr2 | 149564637 | 149592775 | ||
| a0001c0002 | 1/1 | 888 | 90 | 44 | 9 | 26 | 1 | 8 | MMADHC_chr2_149564637_149592775 | MMADHC | ATGGC others(883): Show |
chr2 | 149564637 | 149592775 | ||
| a0001c0007 | 0/0 | 888 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | ATGGC others(883): Show |
chr2 | 149564637 | 149592775 | ||
| a0002c0003 | 0/0 | 888 | 5 | 5 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | ATGGC others(883): Show |
chr2 | 149564637 | 149592775 | ||
| a0003c0004 | 0/0 | 888 | 2 | 0 | 2 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | ATGGC others(883): Show |
chr2 | 149564637 | 149592775 | ||
| a0004c0006 | 0/0 | 888 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | ATGGC others(883): Show |
chr2 | 149564637 | 149592775 | ||
| a0005c0005 | 0/0 | 888 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | ATGGC others(883): Show |
chr2 | 149564637 | 149592775 | ||
| a0006c0008 | 0/0 | 888 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | ATGGC others(883): Show |
chr2 | 149564637 | 149592775 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1392 | 159 | 18 | 26 | 83 | 9 | 23 | MMADHC_chr2_149564637_149592775 | MMADHC | CCTTT others(1387): Show |
chr2 | 149564637 | 149592775 |
| a0001c0001t0002 | 0/0 | 1392 | 53 | 12 | 27 | 1 | 4 | 9 | MMADHC_chr2_149564637_149592775 | MMADHC | CCTTT others(1387): Show |
chr2 | 149564637 | 149592775 |
| a0001c0001t0003 | 0/0 | 1392 | 8 | 8 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | CCTTT others(1387): Show |
chr2 | 149564637 | 149592775 |
| a0001c0001t0004 | 0/0 | 1392 | 7 | 0 | 7 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | CCTTT others(1387): Show |
chr2 | 149564637 | 149592775 |
| a0001c0001t0005 | 0/0 | 1392 | 5 | 2 | 1 | 0 | 0 | 2 | MMADHC_chr2_149564637_149592775 | MMADHC | CCTTT others(1387): Show |
chr2 | 149564637 | 149592775 |
| a0001c0001t0007 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | CCTTT others(1387): Show |
chr2 | 149564637 | 149592775 |
| a0001c0002t0002 | 0/1 | 1392 | 87 | 42 | 9 | 26 | 1 | 8 | MMADHC_chr2_149564637_149592775 | MMADHC | CCTTT others(1387): Show |
chr2 | 149564637 | 149592775 |
| a0001c0002t0006 | 1/0 | 1392 | 2 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | CCTTT others(1387): Show |
chr2 | 149564637 | 149592775 |
| a0001c0002t0008 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | CCTTT others(1387): Show |
chr2 | 149564637 | 149592775 |
| a0001c0007t0002 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | CCTTT others(1387): Show |
chr2 | 149564637 | 149592775 |
| a0002c0003t0002 | 0/0 | 1392 | 5 | 5 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | CCTTT others(1387): Show |
chr2 | 149564637 | 149592775 |
| a0003c0004t0002 | 0/0 | 1392 | 2 | 0 | 2 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | CCTTT others(1387): Show |
chr2 | 149564637 | 149592775 |
| a0004c0006t0002 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | CCTTT others(1387): Show |
chr2 | 149564637 | 149592775 |
| a0005c0005t0001 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | CCTTT others(1387): Show |
chr2 | 149564637 | 149592775 |
| a0006c0008t0002 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | CCTTT others(1387): Show |
chr2 | 149564637 | 149592775 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 66 | 5 | 12 | 34 | 3 | 12 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0004 | 0/0 | 10 | 0 | 5 | 5 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0012 | 0/0 | 5 | 2 | 2 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0003 | 0/0 | 14 | 0 | 11 | 0 | 0 | 3 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0005 | 0/0 | 8 | 0 | 3 | 1 | 2 | 2 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0014 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0003g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0004g0009 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0005g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0001t0007g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0002 | 0/1 | 42 | 10 | 7 | 17 | 1 | 6 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0010 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0013 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0023 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0006g0035 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0002t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0001c0007t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0002c0003t0002g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0002c0003t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0002c0003t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0003c0004t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0003c0004t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0004c0006t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0005c0005t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| a0006c0008t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | GBR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | GBR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | FIN | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | CHS | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | CHS | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0119 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0088 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG00741 | hp2 | a0003 | c0004 | t0002 | g0111 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01168 | hp2 | a0003 | c0004 | t0002 | g0112 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0096 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | CLM | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | IBS | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0026 | EUR | IBS | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0026 | EUR | IBS | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ACB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | KHV | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0081 | AFR | ACB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | CDX | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CDX | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0013 | AFR | ACB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PEL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02451 | hp1 | a0002 | c0003 | t0002 | g0024 | AFR | ACB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02572 | hp1 | a0001 | c0007 | t0002 | g0099 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0082 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02622 | hp1 | a0002 | c0003 | t0002 | g0108 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0034 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0037 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0034 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0115 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0098 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0118 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0104 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0013 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02886 | hp2 | a0002 | c0003 | t0002 | g0024 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | ESN | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | ESN | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0103 | AFR | ESN | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | ESN | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02970 | hp2 | a0002 | c0003 | t0002 | g0024 | AFR | ESN | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0100 | AFR | ESN | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | MSL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ESN | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ESN | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03209 | hp1 | a0002 | c0003 | t0002 | g0084 | AFR | MSL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0022 | AFR | MSL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0094 | AFR | MSL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | MSL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0109 | AFR | MSL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | MSL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0023 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0025 | AFR | ESN | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0110 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0025 | AFR | GWD | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03579 | hp1 | a0001 | c0002 | t0006 | g0035 | AFR | MSL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | MSL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | STU | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | STU | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0117 | SAS | STU | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18522 | hp1 | a0004 | c0006 | t0002 | g0102 | AFR | YRI | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0037 | AFR | YRI | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0101 | EAS | CHB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18967 | hp2 | a0001 | c0001 | t0007 | g0040 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19001 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | LWK | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0025 | AFR | LWK | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | LWK | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | LWK | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0113 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19085 | hp1 | a0005 | c0005 | t0001 | g0063 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | YRI | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | YRI | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0039 | AFR | ASW | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ASW | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | TSI | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | TSI | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | GIH | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02109 | hp2 | a0001 | c0002 | t0008 | g0095 | AFR | ACB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | ACB | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0013 | AFR | USA | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | USA | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0116 | AFR | USA | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | USA | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA21309 | hp1 | a0006 | c0008 | t0002 | g0089 | AFR | LWK | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0106 | AFR | LWK | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0002 | REF | REF | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0006 | g0035 | REF | REF | MMADHC_chr2_149564637_149592775 | MMADHC | chr2 | 149564637 | 149592775 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:149575805 | T | G | 1 | a0005 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.515A>C | p.Lys172Thr | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/8 | 679/1392 | 515/891 | 172/296 | chr2 | 149575805 | |||
| chr2:149576442 | C | T | 1 | a0004 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.473G>A | p.Arg158Gln | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 5/8 | 637/1392 | 473/891 | 158/296 | chr2 | 149576442 | |||
| chr2:149576487 | C | A | 1 | a0002 | 5 | HG02451.hp1 HG02622.hp1 HG02886.hp2 others(2): Show |
missense_variant | MODERATE | c.428G>T | p.Ser143Ile | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 5/8 | 592/1392 | 428/891 | 143/296 | chr2 | 149576487 | |||
| chr2:149576501 | T | G | 1 | a0006 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.414A>C | p.Glu138Asp | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 5/8 | 578/1392 | 414/891 | 138/296 | chr2 | 149576501 | |||
| chr2:149576503 | C | T | 1 | a0002 | 5 | HG02451.hp1 HG02622.hp1 HG02886.hp2 others(2): Show |
missense_variant | MODERATE | c.412G>A | p.Glu138Lys | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 5/8 | 576/1392 | 412/891 | 138/296 | chr2 | 149576503 | |||
| chr2:149582194 | T | G | 1 | a0003 | 2 | HG00741.hp2 HG01168.hp2 |
missense_variant | MODERATE | c.87A>C | p.Lys29Asn | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/8 | 251/1392 | 87/891 | 29/296 | chr2 | 149582194 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:149570157 | T | C | 1 | a0001c0007 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.708A>G | p.Pro236Pro | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 8/8 | 872/1392 | 708/891 | 236/296 | chr2 | 149570157 | |||
| chr2:149576462 | C | T | 3 | a0001c0001 a0005c0005 a0006c0008 |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
synonymous_variant | LOW | c.453G>A | p.Gln151Gln | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 5/8 | 617/1392 | 453/891 | 151/296 | chr2 | 149576462 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:149569757 | C | T | 1 | a0001c0002t0008 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*217G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 8/8 | 217 | chr2 | 149569757 | ||||||
| chr2:149569810 | T | C | 1 | a0001c0001t0004 | 7 | HG00741.hp1 HG01069.hp2 HG01070.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*164A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 8/8 | 164 | chr2 | 149569810 | ||||||
| chr2:149569848 | T | C | 3 | a0001c0001t0001 a0001c0001t0007 a0005c0005t0001 |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*126A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 8/8 | 126 | chr2 | 149569848 | ||||||
| chr2:149569885 | A | G | 14 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(11): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
3_prime_UTR_variant | MODIFIER | c.*89T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 8/8 | 89 | chr2 | 149569885 | ||||||
| chr2:149587115 | G | T | 1 | a0001c0001t0007 | 1 | NA18967.hp2 | 5_prime_UTR_variant | MODIFIER | c.-18C>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/8 | 18 | chr2 | 149587115 | ||||||
| chr2:149587146 | A | G | 1 | a0001c0001t0003 | 8 | HG02055.hp2 HG02895.hp1 HG02922.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-49T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/8 | 49 | chr2 | 149587146 | ||||||
| chr2:149587756 | T | C | 1 | a0001c0001t0005 | 5 | HG00639.hp1 HG02559.hp2 HG02738.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-145A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 1/8 | 659 | chr2 | 149587756 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:149570369 | A | G | 1 | a0001c0001t0002g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.697-201T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 7/7 | chr2 | 149570369 | |||||||
| chr2:149570623 | C | T | 1 | a0001c0002t0002g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.697-455G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 7/7 | chr2 | 149570623 | |||||||
| chr2:149570666 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.696+419T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 7/7 | chr2 | 149570666 | |||||||
| chr2:149570678 | C | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(54): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.696+407G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 7/7 | chr2 | 149570678 | |||||||
| chr2:149570682 | A | T | 9 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0026 others(6): Show |
26 | HG00140.hp2 HG00738.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.696+403T>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 7/7 | chr2 | 149570682 | |||||||
| chr2:149570912 | G | A | 2 | a0001c0001t0002g0092 a0001c0001t0002g0093 |
2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.696+173C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 7/7 | chr2 | 149570912 | |||||||
| chr2:149571002 | C | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(54): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.696+83G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 7/7 | chr2 | 149571002 | |||||||
| chr2:149571266 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.610-95T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149571266 | |||||||
| chr2:149571363 | A | C | 1 | a0001c0002t0002g0037 | 2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.610-192T>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149571363 | |||||||
| chr2:149571392 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.610-221G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149571392 | |||||||
| chr2:149571454 | C | T | 1 | a0001c0002t0002g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.610-283G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149571454 | |||||||
| chr2:149571673 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.610-502C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149571673 | |||||||
| chr2:149571680 | T | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(54): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.610-509A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149571680 | |||||||
| chr2:149571681 | G | A | 6 | a0001c0001t0002g0085 a0001c0001t0002g0090 a0001c0001t0002g0091 others(3): Show |
6 | HG02615.hp2 HG02723.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.610-510C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149571681 | |||||||
| chr2:149571683 | G | C | 1 | a0001c0001t0002g0047 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.610-512C>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149571683 | |||||||
| chr2:149571697 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.610-526C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149571697 | |||||||
| chr2:149571790 | G | GA | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(55): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.610-620dupT | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149571790 | |||||||
| chr2:149572040 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.610-869T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149572040 | |||||||
| chr2:149572311 | C | T | 1 | a0001c0001t0005g0119 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.610-1140G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149572311 | |||||||
| chr2:149572322 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0087 |
6 | HG02145.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.610-1151C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149572322 | |||||||
| chr2:149572335 | C | CAAAAAAA others(3): Show |
51 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(48): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.610-1174_610-1165d others(12): Show |
MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149572335 | |||||||
| chr2:149572335 | C | CAAAAAAA others(4): Show |
4 | a0001c0001t0001g0031 a0001c0001t0001g0065 a0001c0001t0001g0071 others(1): Show |
5 | HG01978.hp2 HG02074.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.610-1175_610-1165d others(13): Show |
MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149572335 | |||||||
| chr2:149572335 | C | CAAAAAAA others(5): Show |
4 | a0001c0001t0001g0066 a0001c0001t0005g0038 a0001c0001t0005g0117 others(1): Show |
5 | HG02559.hp2 HG02738.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.610-1176_610-1165d others(14): Show |
MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149572335 | |||||||
| chr2:149572335 | C | CAAAAAAA others(6): Show |
19 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0026 others(16): Show |
44 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.610-1165_610-1164i others(15): Show |
MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149572335 | |||||||
| chr2:149572335 | C | CAAAAAAA others(7): Show |
7 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0093 others(4): Show |
7 | HG00639.hp1 HG01106.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.610-1165_610-1164i others(16): Show |
MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149572335 | |||||||
| chr2:149572335 | C | CAAAAAAA others(8): Show |
3 | a0001c0002t0002g0082 a0001c0002t0002g0094 a0001c0002t0008g0095 |
3 | HG02109.hp2 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.610-1165_610-1164i others(17): Show |
MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149572335 | |||||||
| chr2:149572335 | C | CAAAAAAA others(9): Show |
3 | a0001c0001t0002g0086 a0001c0002t0002g0039 a0001c0002t0002g0081 |
3 | HG02145.hp2 HG02895.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.610-1165_610-1164i others(18): Show |
MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149572335 | |||||||
| chr2:149572335 | C | CAAAAAAA others(10): Show |
2 | a0001c0001t0002g0018 a0001c0001t0004g0009 |
10 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.610-1165_610-1164i others(19): Show |
MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149572335 | |||||||
| chr2:149572335 | C | CAAAAAAA others(11): Show |
2 | a0001c0001t0002g0087 a0001c0001t0004g0088 |
2 | HG00741.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.610-1165_610-1164i others(20): Show |
MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149572335 | |||||||
| chr2:149572348 | T | C | 1 | a0001c0001t0002g0043 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.610-1177A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149572348 | |||||||
| chr2:149572416 | A | T | 1 | a0001c0002t0002g0105 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.610-1245T>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149572416 | |||||||
| chr2:149572522 | C | T | 4 | a0001c0002t0002g0013 a0001c0002t0002g0098 a0001c0002t0002g0116 others(1): Show |
8 | HG00735.hp2 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.610-1351G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149572522 | |||||||
| chr2:149572559 | C | T | 4 | a0001c0001t0005g0038 a0001c0001t0005g0117 a0001c0001t0005g0118 others(1): Show |
5 | HG00639.hp1 HG02559.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.610-1388G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149572559 | |||||||
| chr2:149572683 | T | C | 10 | a0001c0002t0002g0013 a0001c0002t0002g0025 a0001c0002t0002g0098 others(7): Show |
18 | HG00735.hp2 HG02257.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.610-1512A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149572683 | |||||||
| chr2:149572905 | G | T | 3 | a0001c0001t0002g0014 a0001c0001t0002g0041 a0001c0001t0002g0042 |
6 | HG01256.hp2 HG01258.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.610-1734C>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149572905 | |||||||
| chr2:149572912 | T | C | 1 | a0001c0001t0002g0091 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.610-1741A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149572912 | |||||||
| chr2:149572937 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.610-1766G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149572937 | |||||||
| chr2:149573008 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.610-1837G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149573008 | |||||||
| chr2:149573042 | G | A | 2 | a0001c0001t0002g0092 a0001c0001t0002g0093 |
2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.610-1871C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149573042 | |||||||
| chr2:149573051 | T | G | 1 | a0001c0001t0001g0028 | 2 | NA18967.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.610-1880A>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149573051 | |||||||
| chr2:149573170 | T | C | 6 | a0001c0001t0002g0085 a0001c0001t0002g0090 a0001c0001t0002g0091 others(3): Show |
6 | HG02615.hp2 HG02723.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.610-1999A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149573170 | |||||||
| chr2:149573244 | T | TCAAA | 4 | a0001c0001t0005g0038 a0001c0001t0005g0117 a0001c0001t0005g0118 others(1): Show |
5 | HG02145.hp2 HG02559.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.610-2077_610-2074d others(6): Show |
MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149573244 | |||||||
| chr2:149573244 | TCAAA | T | 6 | a0001c0001t0002g0085 a0001c0001t0002g0090 a0001c0001t0002g0091 others(3): Show |
6 | HG02615.hp2 HG02723.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.610-2077_610-2074d others(6): Show |
MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149573244 | |||||||
| chr2:149573268 | C | A | 1 | a0001c0001t0005g0119 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.610-2097G>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149573268 | |||||||
| chr2:149573363 | A | G | 4 | a0001c0001t0005g0038 a0001c0001t0005g0117 a0001c0001t0005g0118 others(1): Show |
5 | HG00639.hp1 HG02559.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.610-2192T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149573363 | |||||||
| chr2:149573401 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.610-2230T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149573401 | |||||||
| chr2:149573523 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(58): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.609+2188A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149573523 | |||||||
| chr2:149573606 | T | A | 1 | a0001c0001t0001g0020 | 3 | NA18947.hp2 NA19007.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.609+2105A>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149573606 | |||||||
| chr2:149573853 | C | A | 2 | a0001c0002t0002g0010 a0001c0002t0002g0104 |
7 | HG01884.hp2 HG02809.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.609+1858G>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149573853 | |||||||
| chr2:149573871 | A | C | 1 | a0001c0002t0002g0104 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.609+1840T>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149573871 | |||||||
| chr2:149573875 | C | CA | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(79): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.609+1835dupT | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149573875 | |||||||
| chr2:149573888 | T | C | 7 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0026 others(4): Show |
18 | HG00140.hp2 HG00738.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.609+1823A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149573888 | |||||||
| chr2:149574002 | C | A | 1 | a0001c0001t0002g0053 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.609+1709G>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149574002 | |||||||
| chr2:149574126 | A | G | 7 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0026 others(4): Show |
18 | HG00140.hp2 HG00738.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.609+1585T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149574126 | |||||||
| chr2:149574160 | A | G | 2 | a0001c0002t0002g0010 a0001c0002t0002g0104 |
7 | HG01884.hp2 HG02809.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.609+1551T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149574160 | |||||||
| chr2:149574409 | A | G | 6 | a0001c0002t0002g0025 a0001c0002t0002g0106 a0001c0002t0002g0109 others(3): Show |
10 | HG02451.hp1 HG02622.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.609+1302T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149574409 | |||||||
| chr2:149574559 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.609+1152C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149574559 | |||||||
| chr2:149574582 | A | AG | 4 | a0001c0001t0005g0038 a0001c0001t0005g0117 a0001c0001t0005g0118 others(1): Show |
5 | HG00639.hp1 HG02559.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+1128dupC | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149574582 | |||||||
| chr2:149574606 | T | C | 4 | a0001c0002t0002g0013 a0001c0002t0002g0098 a0001c0002t0002g0116 others(1): Show |
8 | HG00735.hp2 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.609+1105A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149574606 | |||||||
| chr2:149574824 | T | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(62): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.609+887A>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149574824 | |||||||
| chr2:149574840 | G | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(54): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.609+871C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149574840 | |||||||
| chr2:149574861 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.609+850G>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149574861 | |||||||
| chr2:149574909 | G | A | 9 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0026 others(6): Show |
26 | HG00140.hp2 HG00738.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.609+802C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149574909 | |||||||
| chr2:149574914 | C | A | 1 | a0001c0001t0001g0061 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.609+797G>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149574914 | |||||||
| chr2:149574999 | G | A | 2 | a0001c0002t0002g0094 a0001c0002t0008g0095 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.609+712C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149574999 | |||||||
| chr2:149575191 | G | A | 1 | a0004c0006t0002g0102 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.609+520C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149575191 | |||||||
| chr2:149575212 | T | G | 1 | a0001c0001t0001g0049 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.609+499A>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149575212 | |||||||
| chr2:149575377 | TGGGGAGA others(5): Show |
T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(55): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.609+322_609+333del others(12): Show |
MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149575377 | |||||||
| chr2:149575392 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.609+319C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149575392 | |||||||
| chr2:149575398 | G | A | 2 | a0001c0002t0002g0094 a0001c0002t0008g0095 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.609+313C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149575398 | |||||||
| chr2:149575544 | A | C | 1 | a0001c0002t0002g0103 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.609+167T>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149575544 | |||||||
| chr2:149575595 | T | C | 2 | a0003c0004t0002g0111 a0003c0004t0002g0112 |
2 | HG00741.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.609+116A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149575595 | |||||||
| chr2:149575597 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.609+114G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149575597 | |||||||
| chr2:149575610 | TGAATAAA others(86): Show |
T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG02572.hp2 HG03041.hp1 |
splice_region_variant&intron_variant | LOW | c.609+8_609+100delTT others(91): Show |
MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 6/7 | chr2 | 149575610 | |||||||
| chr2:149575863 | C | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(54): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.479-22G>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 5/7 | chr2 | 149575863 | |||||||
| chr2:149575955 | G | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(58): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.479-114C>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 5/7 | chr2 | 149575955 | |||||||
| chr2:149576072 | AG | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0087 |
6 | HG02145.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.479-232delC | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 5/7 | chr2 | 149576072 | |||||||
| chr2:149576169 | ACT | A | 6 | a0001c0001t0002g0085 a0001c0001t0002g0090 a0001c0001t0002g0091 others(3): Show |
6 | HG02615.hp2 HG02723.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.478+266_478+267del others(2): Show |
MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 5/7 | chr2 | 149576169 | |||||||
| chr2:149576176 | T | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(58): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.478+261A>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 5/7 | chr2 | 149576176 | |||||||
| chr2:149576274 | C | T | 1 | a0001c0001t0001g0030 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.478+163G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 5/7 | chr2 | 149576274 | |||||||
| chr2:149576303 | C | T | 6 | a0001c0001t0002g0085 a0001c0001t0002g0090 a0001c0001t0002g0091 others(3): Show |
6 | HG02615.hp2 HG02723.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.478+134G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 5/7 | chr2 | 149576303 | |||||||
| chr2:149576357 | G | C | 1 | a0001c0002t0002g0096 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.478+80C>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 5/7 | chr2 | 149576357 | |||||||
| chr2:149576410 | T | A | 3 | a0002c0003t0002g0024 a0002c0003t0002g0084 a0002c0003t0002g0108 |
5 | HG02451.hp1 HG02622.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.478+27A>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 5/7 | chr2 | 149576410 | |||||||
| chr2:149576431 | A | C | 6 | a0001c0001t0002g0085 a0001c0001t0002g0090 a0001c0001t0002g0091 others(3): Show |
6 | HG02615.hp2 HG02723.hp1 HG02965.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.478+6T>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 5/7 | chr2 | 149576431 | |||||||
| chr2:149576614 | C | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(58): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.373-72G>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149576614 | |||||||
| chr2:149576633 | T | G | 1 | a0001c0001t0005g0119 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.373-91A>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149576633 | |||||||
| chr2:149576673 | G | T | 1 | a0001c0002t0002g0107 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.373-131C>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149576673 | |||||||
| chr2:149576870 | G | A | 1 | a0001c0001t0002g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.373-328C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149576870 | |||||||
| chr2:149576900 | C | T | 1 | a0001c0002t0002g0094 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.373-358G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149576900 | |||||||
| chr2:149576932 | A | G | 1 | a0001c0001t0002g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.373-390T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149576932 | |||||||
| chr2:149577103 | A | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0087 |
6 | HG02145.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.373-561T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149577103 | |||||||
| chr2:149577221 | T | C | 1 | a0001c0002t0002g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.373-679A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149577221 | |||||||
| chr2:149577445 | C | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(61): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.373-903G>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149577445 | |||||||
| chr2:149577472 | C | G | 5 | a0001c0002t0002g0025 a0001c0002t0002g0109 a0002c0003t0002g0024 others(2): Show |
9 | HG02451.hp1 HG02622.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.373-930G>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149577472 | |||||||
| chr2:149577589 | C | T | 2 | a0001c0002t0002g0081 a0001c0002t0002g0082 |
2 | HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.373-1047G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149577589 | |||||||
| chr2:149577891 | G | A | 1 | a0001c0001t0002g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.373-1349C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149577891 | |||||||
| chr2:149577923 | C | A | 1 | a0001c0001t0005g0119 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.373-1381G>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149577923 | |||||||
| chr2:149577972 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG00621.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.373-1430G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149577972 | |||||||
| chr2:149578031 | A | AAAC | 2 | a0001c0001t0004g0009 a0001c0001t0004g0088 |
7 | HG00741.hp1 HG01069.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.372+1397_372+1399d others(5): Show |
MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149578031 | |||||||
| chr2:149578031 | AAAC | A | 4 | a0001c0001t0005g0038 a0001c0001t0005g0117 a0001c0001t0005g0118 others(1): Show |
5 | HG00639.hp1 HG02559.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+1397_372+1399d others(5): Show |
MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149578031 | |||||||
| chr2:149578179 | A | C | 1 | a0001c0001t0001g0011 | 5 | HG02135.hp1 NA18950.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.372+1252T>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149578179 | |||||||
| chr2:149578183 | AG | A | 4 | a0001c0002t0002g0013 a0001c0002t0002g0098 a0001c0002t0002g0116 others(1): Show |
8 | HG00735.hp2 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.372+1247delC | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149578183 | |||||||
| chr2:149578543 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.372+888A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149578543 | |||||||
| chr2:149578562 | A | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0087 |
6 | HG02145.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.372+869T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149578562 | |||||||
| chr2:149578919 | G | GA | 7 | a0001c0001t0001g0012 a0001c0001t0001g0065 a0001c0001t0001g0066 others(4): Show |
16 | HG00741.hp1 HG01069.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.372+511dupT | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149578919 | |||||||
| chr2:149578931 | C | A | 1 | a0001c0001t0002g0044 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.372+500G>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149578931 | |||||||
| chr2:149578983 | T | C | 5 | a0001c0002t0002g0023 a0001c0002t0002g0100 a0001c0002t0002g0107 others(2): Show |
7 | HG00408.hp1 HG00741.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.372+448A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149578983 | |||||||
| chr2:149578986 | C | CT | 10 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0045 others(7): Show |
19 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.372+444dupA | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149578986 | |||||||
| chr2:149579025 | T | C | 6 | a0001c0001t0002g0085 a0001c0001t0002g0090 a0001c0001t0002g0091 others(3): Show |
6 | HG02615.hp2 HG02723.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.372+406A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149579025 | |||||||
| chr2:149579188 | T | G | 5 | a0001c0002t0002g0025 a0001c0002t0002g0109 a0002c0003t0002g0024 others(2): Show |
9 | HG02451.hp1 HG02622.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.372+243A>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149579188 | |||||||
| chr2:149579312 | T | C | 1 | a0001c0001t0002g0067 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.372+119A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149579312 | |||||||
| chr2:149579316 | T | C | 2 | a0001c0001t0004g0009 a0001c0001t0004g0088 |
7 | HG00741.hp1 HG01069.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.372+115A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149579316 | |||||||
| chr2:149579326 | T | C | 1 | a0001c0002t0002g0110 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.372+105A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149579326 | |||||||
| chr2:149579353 | A | G | 1 | a0001c0001t0002g0041 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.372+78T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149579353 | |||||||
| chr2:149579375 | C | CAA | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(62): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.372+54_372+55dupTT | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 4/7 | chr2 | 149579375 | |||||||
| chr2:149579686 | T | C | 3 | a0001c0001t0002g0018 a0001c0001t0002g0086 a0001c0001t0002g0087 |
6 | HG02145.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.155-38A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149579686 | |||||||
| chr2:149579799 | T | A | 1 | a0001c0001t0002g0032 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.155-151A>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149579799 | |||||||
| chr2:149580010 | A | G | 1 | a0001c0001t0002g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.155-362T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149580010 | |||||||
| chr2:149580085 | C | T | 1 | a0001c0002t0002g0100 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.155-437G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149580085 | |||||||
| chr2:149580327 | C | T | 17 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0026 others(14): Show |
39 | HG00140.hp2 HG00738.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.155-679G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149580327 | |||||||
| chr2:149580437 | G | T | 2 | a0001c0002t0002g0081 a0001c0002t0002g0082 |
2 | HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.155-789C>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149580437 | |||||||
| chr2:149580539 | A | G | 1 | a0001c0001t0005g0118 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.155-891T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149580539 | |||||||
| chr2:149580560 | C | T | 1 | a0006c0008t0002g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.155-912G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149580560 | |||||||
| chr2:149580746 | A | G | 2 | a0001c0002t0002g0022 a0001c0002t0002g0034 |
5 | HG02622.hp2 HG02647.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-1098T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149580746 | |||||||
| chr2:149580860 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0068 |
4 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-1212A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149580860 | |||||||
| chr2:149580914 | T | C | 9 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0026 others(6): Show |
26 | HG00140.hp2 HG00738.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.154+1213A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149580914 | |||||||
| chr2:149580942 | C | G | 1 | a0001c0001t0001g0052 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.154+1185G>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149580942 | |||||||
| chr2:149580944 | G | C | 1 | a0001c0001t0002g0033 | 2 | HG00642.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.154+1183C>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149580944 | |||||||
| chr2:149581023 | C | G | 3 | a0001c0001t0005g0038 a0001c0001t0005g0117 a0001c0001t0005g0118 |
4 | HG02559.hp2 HG02738.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+1104G>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149581023 | |||||||
| chr2:149581111 | G | A | 2 | a0001c0001t0004g0009 a0001c0001t0004g0088 |
7 | HG00741.hp1 HG01069.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+1016C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149581111 | |||||||
| chr2:149581112 | G | A | 2 | a0001c0001t0004g0009 a0001c0001t0004g0088 |
7 | HG00741.hp1 HG01069.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+1015C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149581112 | |||||||
| chr2:149581234 | A | T | 1 | a0001c0001t0002g0051 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.154+893T>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149581234 | |||||||
| chr2:149581314 | G | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0028 |
6 | NA18967.hp1 NA18968.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.154+813C>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149581314 | |||||||
| chr2:149581377 | C | T | 1 | a0001c0001t0001g0004 | 10 | HG01123.hp2 HG01496.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.154+750G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149581377 | |||||||
| chr2:149581520 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(62): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.154+607C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149581520 | |||||||
| chr2:149581583 | A | C | 1 | a0001c0001t0001g0008 | 6 | HG02040.hp1 HG02083.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.154+544T>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149581583 | |||||||
| chr2:149581685 | T | C | 4 | a0001c0002t0002g0013 a0001c0002t0002g0098 a0001c0002t0002g0116 others(1): Show |
8 | HG00735.hp2 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+442A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149581685 | |||||||
| chr2:149581940 | C | T | 3 | a0001c0001t0005g0038 a0001c0001t0005g0117 a0001c0001t0005g0118 |
4 | HG02559.hp2 HG02738.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+187G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149581940 | |||||||
| chr2:149581944 | C | T | 1 | a0001c0001t0003g0083 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.154+183G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149581944 | |||||||
| chr2:149581953 | C | CCTTTTT | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(61): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.154+173_154+174ins others(6): Show |
MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149581953 | |||||||
| chr2:149581953 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.154+174G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 3/7 | chr2 | 149581953 | |||||||
| chr2:149582301 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.10-30C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149582301 | |||||||
| chr2:149582450 | A | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0002t0002g0081 others(2): Show |
9 | HG02145.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.10-179T>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149582450 | |||||||
| chr2:149582523 | A | G | 1 | a0001c0002t0002g0097 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.10-252T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149582523 | |||||||
| chr2:149582539 | G | C | 2 | a0001c0002t0002g0081 a0001c0002t0002g0082 |
2 | HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.10-268C>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149582539 | |||||||
| chr2:149582614 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.10-343G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149582614 | |||||||
| chr2:149582800 | A | G | 1 | a0001c0002t0002g0096 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.10-529T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149582800 | |||||||
| chr2:149582855 | TATCTTTC others(19): Show |
T | 1 | a0001c0001t0003g0006 | 2 | NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.10-610_10-585delTG others(24): Show |
MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149582855 | |||||||
| chr2:149582885 | T | C | 1 | a0001c0001t0002g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.10-614A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149582885 | |||||||
| chr2:149582950 | G | A | 1 | a0003c0004t0002g0112 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.10-679C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149582950 | |||||||
| chr2:149583109 | C | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0049 |
4 | NA18951.hp2 NA18971.hp1 NA19059.hp1 others(1): Show |
intron_variant | MODIFIER | c.10-838G>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149583109 | |||||||
| chr2:149583110 | C | T | 1 | a0001c0001t0001g0015 | 4 | HG03491.hp2 HG03492.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-839G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149583110 | |||||||
| chr2:149583129 | C | T | 2 | a0001c0002t0002g0094 a0001c0002t0008g0095 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.10-858G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149583129 | |||||||
| chr2:149583217 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.10-946C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149583217 | |||||||
| chr2:149583227 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.10-956T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149583227 | |||||||
| chr2:149583294 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.10-1023C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149583294 | |||||||
| chr2:149583496 | G | A | 1 | a0001c0002t0002g0082 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.10-1225C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149583496 | |||||||
| chr2:149583584 | C | T | 1 | a0001c0002t0002g0034 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.10-1313G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149583584 | |||||||
| chr2:149583660 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.10-1389G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149583660 | |||||||
| chr2:149584290 | A | G | 4 | a0001c0001t0005g0038 a0001c0001t0005g0117 a0001c0001t0005g0118 others(1): Show |
5 | HG00639.hp1 HG02559.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.10-2019T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149584290 | |||||||
| chr2:149584314 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.10-2043A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149584314 | |||||||
| chr2:149584434 | C | A | 2 | a0001c0002t0002g0036 a0001c0002t0002g0113 |
3 | HG00423.hp1 HG02165.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.10-2163G>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149584434 | |||||||
| chr2:149584471 | A | G | 2 | a0001c0002t0002g0094 a0001c0002t0008g0095 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.10-2200T>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149584471 | |||||||
| chr2:149584554 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.10-2283A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149584554 | |||||||
| chr2:149584701 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(58): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.9+2388C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149584701 | |||||||
| chr2:149584722 | T | A | 1 | a0001c0001t0001g0074 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.9+2367A>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149584722 | |||||||
| chr2:149584811 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.9+2278C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149584811 | |||||||
| chr2:149584977 | G | A | 1 | a0001c0001t0002g0026 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.9+2112C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149584977 | |||||||
| chr2:149585012 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.9+2077C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149585012 | |||||||
| chr2:149585037 | C | T | 6 | a0001c0001t0002g0085 a0001c0001t0002g0090 a0001c0001t0002g0091 others(3): Show |
6 | HG02615.hp2 HG02723.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.9+2052G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149585037 | |||||||
| chr2:149585042 | C | CA | 9 | a0001c0001t0001g0078 a0001c0001t0002g0114 a0001c0001t0004g0009 others(6): Show |
15 | HG00423.hp2 HG00639.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.9+2046dupT | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149585042 | |||||||
| chr2:149585098 | A | C | 1 | a0006c0008t0002g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.9+1991T>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149585098 | |||||||
| chr2:149585325 | G | A | 5 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0092 others(2): Show |
5 | HG02615.hp2 HG02723.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.9+1764C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149585325 | |||||||
| chr2:149585664 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(79): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.9+1425G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149585664 | |||||||
| chr2:149585867 | A | C | 1 | a0001c0001t0001g0046 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.9+1222T>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149585867 | |||||||
| chr2:149586051 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.9+1038A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149586051 | |||||||
| chr2:149586105 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0045 a0001c0001t0001g0080 |
8 | HG01261.hp1 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.9+984G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149586105 | |||||||
| chr2:149586669 | G | C | 1 | a0001c0001t0001g0080 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.9+420C>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149586669 | |||||||
| chr2:149586792 | G | T | 1 | a0002c0003t0002g0084 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.9+297C>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149586792 | |||||||
| chr2:149586833 | TA | T | 7 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0026 others(4): Show |
18 | HG00140.hp2 HG00738.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.9+255delT | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149586833 | |||||||
| chr2:149586962 | T | C | 1 | a0001c0001t0005g0119 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.9+127A>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149586962 | |||||||
| chr2:149587075 | G | A | 1 | a0001c0001t0002g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.9+14C>T | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149587075 | |||||||
| chr2:149587077 | T | G | 1 | a0001c0002t0002g0115 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.9+12A>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 2/7 | chr2 | 149587077 | |||||||
| chr2:149587175 | C | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(65): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.-52-26G>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 1/7 | chr2 | 149587175 | |||||||
| chr2:149587228 | G | T | 2 | a0001c0002t0002g0081 a0001c0002t0002g0082 |
2 | HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-52-79C>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 1/7 | chr2 | 149587228 | |||||||
| chr2:149587299 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(61): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.-52-150G>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 1/7 | chr2 | 149587299 | |||||||
| chr2:149587408 | G | C | 1 | a0001c0002t0002g0037 | 2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-53+256C>G | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 1/7 | chr2 | 149587408 | |||||||
| chr2:149587437 | G | T | 1 | a0001c0002t0002g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-53+227C>A | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 1/7 | chr2 | 149587437 | |||||||
| chr2:149587630 | T | G | 1 | a0001c0002t0002g0116 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-53+34A>C | MMADHC | ENSG00000168288.13 | transcript | ENST00000303319.10 | protein_coding | 1/7 | chr2 | 149587630 |