Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 100287284 |
| ensemblid | ENSG00000205693.4 |
| hgncid | 40023 |
| symbol | MANSC4 |
| name | MANSC domain containing 4 |
| refseq_nuc | NM_001146221.5 |
| refseq_prot | NP_001139693.1 |
| ensembl_nuc | ENST00000381273.4 |
| ensembl_prot | ENSP00000370673.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 27762427 |
| end | 27780236 |
| strand | - |
| ver | v1.2 |
| region | chr12:27762427-27780236 |
| region5000 | chr12:27757427-27785236 |
| regionname0 | MANSC4_chr12_27762427_27780236 |
| regionname5000 | MANSC4_chr12_27757427_27785236 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 340 | 174 | 39 | 39 | 71 | 6 | 19 | 57 | MANSC4_chr12_27757427_27785236 | MANSC4 | MHVAE others(335): Show |
chr12 | 27757427 | 27785236 |
| a0002 | 1/1 | 340 | 165 | 46 | 26 | 70 | 7 | 14 | 55 | MANSC4_chr12_27757427_27785236 | MANSC4 | MHVAE others(335): Show |
chr12 | 27757427 | 27785236 |
| a0003 | 0/0 | 340 | 65 | 1 | 9 | 46 | 3 | 6 | 31 | MANSC4_chr12_27757427_27785236 | MANSC4 | MHVAE others(335): Show |
chr12 | 27757427 | 27785236 |
| a0004 | 0/0 | 207 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | MHVAE others(202): Show |
chr12 | 27757427 | 27785236 |
| a0005 | 0/0 | 340 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | MHVAE others(335): Show |
chr12 | 27757427 | 27785236 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1020 | 173 | 39 | 38 | 71 | 6 | 19 | MANSC4_chr12_27757427_27785236 | MANSC4 | ATGCA others(1015): Show |
chr12 | 27757427 | 27785236 | ||
| a0001c0004 | 0/0 | 1020 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | ATGCA others(1015): Show |
chr12 | 27757427 | 27785236 | ||
| a0002c0002 | 1/1 | 1020 | 164 | 46 | 26 | 69 | 7 | 14 | MANSC4_chr12_27757427_27785236 | MANSC4 | ATGCA others(1015): Show |
chr12 | 27757427 | 27785236 | ||
| a0002c0007 | 0/0 | 1020 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | ATGCA others(1015): Show |
chr12 | 27757427 | 27785236 | ||
| a0003c0003 | 0/0 | 1020 | 65 | 1 | 9 | 46 | 3 | 6 | MANSC4_chr12_27757427_27785236 | MANSC4 | ATGCA others(1015): Show |
chr12 | 27757427 | 27785236 | ||
| a0004c0006 | 0/0 | 1020 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | ATGCA others(1015): Show |
chr12 | 27757427 | 27785236 | ||
| a0005c0005 | 0/0 | 1020 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | ATGCA others(1015): Show |
chr12 | 27757427 | 27785236 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1667 | 168 | 35 | 38 | 70 | 6 | 19 | MANSC4_chr12_27757427_27785236 | MANSC4 | GGATG others(1662): Show |
chr12 | 27757427 | 27785236 |
| a0001c0001t0003 | 0/0 | 1667 | 4 | 4 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | GGATG others(1662): Show |
chr12 | 27757427 | 27785236 |
| a0001c0001t0007 | 0/0 | 1667 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | GGATG others(1662): Show |
chr12 | 27757427 | 27785236 |
| a0001c0004t0001 | 0/0 | 1667 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | GGATG others(1662): Show |
chr12 | 27757427 | 27785236 |
| a0002c0002t0001 | 1/1 | 1667 | 156 | 39 | 26 | 69 | 7 | 13 | MANSC4_chr12_27757427_27785236 | MANSC4 | GGATG others(1662): Show |
chr12 | 27757427 | 27785236 |
| a0002c0002t0004 | 0/0 | 1667 | 3 | 3 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | GGATG others(1662): Show |
chr12 | 27757427 | 27785236 |
| a0002c0002t0005 | 0/0 | 1667 | 3 | 3 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | GGATG others(1662): Show |
chr12 | 27757427 | 27785236 |
| a0002c0002t0006 | 0/0 | 1667 | 2 | 1 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | GGATG others(1662): Show |
chr12 | 27757427 | 27785236 |
| a0002c0007t0001 | 0/0 | 1667 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | GGATG others(1662): Show |
chr12 | 27757427 | 27785236 |
| a0003c0003t0001 | 0/0 | 1667 | 4 | 0 | 2 | 0 | 2 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | GGATG others(1662): Show |
chr12 | 27757427 | 27785236 |
| a0003c0003t0002 | 0/0 | 1670 | 61 | 1 | 7 | 46 | 1 | 6 | MANSC4_chr12_27757427_27785236 | MANSC4 | GGATG others(1665): Show |
chr12 | 27757427 | 27785236 |
| a0004c0006t0001 | 0/0 | 1667 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | GGATG others(1662): Show |
chr12 | 27757427 | 27785236 |
| a0005c0005t0001 | 0/0 | 1667 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | GGATG others(1662): Show |
chr12 | 27757427 | 27785236 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 50 | 12 | 8 | 23 | 2 | 5 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0003 | 0/0 | 17 | 0 | 2 | 15 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0009 | 0/0 | 9 | 1 | 2 | 5 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0011 | 0/0 | 6 | 2 | 0 | 4 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0030 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0031 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0032 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0033 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0052 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0003g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0001t0007g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0001c0004t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0002 | 0/0 | 18 | 2 | 4 | 10 | 1 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0004 | 0/0 | 16 | 0 | 0 | 16 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0006 | 0/0 | 11 | 8 | 3 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0007 | 0/0 | 11 | 1 | 1 | 4 | 0 | 5 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0010 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0015 | 1/0 | 5 | 2 | 0 | 1 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0018 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0026 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0027 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0029 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0041 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0004g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0005g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0002t0006g0047 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0002c0007t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0001g0016 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0005 | 0/0 | 13 | 0 | 3 | 10 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0008 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0012 | 0/0 | 6 | 0 | 0 | 3 | 1 | 2 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0020 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0034 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0003c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0004c0006t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| a0005c0005t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0003 | c0003 | t0002 | g0012 | EUR | GBR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0041 | EUR | FIN | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0102 | EUR | FIN | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | CHS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | CHS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | CHS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00558 | hp2 | a0003 | c0003 | t0002 | g0008 | EAS | CHS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00597 | hp1 | a0003 | c0003 | t0002 | g0039 | EAS | CHS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00597 | hp2 | a0002 | c0007 | t0001 | g0065 | EAS | CHS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00609 | hp1 | a0003 | c0003 | t0002 | g0034 | EAS | CHS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00609 | hp2 | a0003 | c0003 | t0002 | g0012 | EAS | CHS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00642 | hp1 | a0003 | c0003 | t0002 | g0159 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0119 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | CHS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00673 | hp2 | a0003 | c0003 | t0002 | g0008 | EAS | CHS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00735 | hp2 | a0003 | c0003 | t0002 | g0020 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0163 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0070 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0108 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0116 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01192 | hp1 | a0003 | c0003 | t0001 | g0016 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01255 | hp1 | a0003 | c0003 | t0001 | g0016 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0041 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01256 | hp1 | a0003 | c0003 | t0002 | g0005 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01258 | hp2 | a0003 | c0003 | t0002 | g0005 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0103 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0117 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0026 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0026 | EUR | IBS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0010 | EUR | IBS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0026 | EUR | IBS | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0086 | AFR | ACB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0114 | AFR | ACB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0062 | AFR | ACB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01934 | hp1 | a0003 | c0003 | t0002 | g0020 | AMR | PEL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01934 | hp2 | a0003 | c0003 | t0002 | g0156 | AMR | PEL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01978 | hp2 | a0003 | c0003 | t0002 | g0005 | AMR | PEL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02015 | hp2 | a0003 | c0003 | t0002 | g0043 | EAS | KHV | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | KHV | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02027 | hp2 | a0003 | c0003 | t0002 | g0008 | EAS | KHV | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02040 | hp2 | a0003 | c0003 | t0002 | g0020 | EAS | KHV | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | ACB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | KHV | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02056 | hp2 | a0003 | c0003 | t0002 | g0034 | EAS | KHV | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02074 | hp2 | a0003 | c0003 | t0002 | g0043 | EAS | KHV | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | KHV | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02129 | hp2 | a0003 | c0003 | t0002 | g0008 | EAS | KHV | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02132 | hp2 | a0003 | c0003 | t0002 | g0008 | EAS | KHV | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | KHV | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | ACB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | CDX | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02165 | hp1 | a0003 | c0003 | t0002 | g0012 | EAS | CDX | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02165 | hp2 | a0001 | c0001 | t0007 | g0169 | EAS | CDX | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0083 | AFR | ACB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02273 | hp1 | a0001 | c0004 | t0001 | g0093 | AMR | PEL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | ACB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | ACB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0067 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02622 | hp1 | a0002 | c0002 | t0004 | g0044 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0081 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0088 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02723 | hp1 | a0002 | c0002 | t0005 | g0040 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0027 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0084 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0113 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0072 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | ESN | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0170 | AFR | ESN | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03017 | hp1 | a0003 | c0003 | t0002 | g0161 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0061 | AFR | MSL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03130 | hp2 | a0002 | c0002 | t0004 | g0044 | AFR | ESN | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03139 | hp1 | a0003 | c0003 | t0002 | g0060 | AFR | ESN | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | ESN | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0082 | AFR | ESN | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0109 | AFR | ESN | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03225 | hp2 | a0002 | c0002 | t0005 | g0040 | AFR | MSL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03239 | hp1 | a0004 | c0006 | t0001 | g0133 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | MSL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0140 | AFR | MSL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03486 | hp2 | a0002 | c0002 | t0004 | g0118 | AFR | MSL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03491 | hp1 | a0003 | c0003 | t0002 | g0012 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | MSL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03669 | hp1 | a0002 | c0002 | t0006 | g0047 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03669 | hp2 | a0003 | c0003 | t0002 | g0012 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | STU | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0015 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03710 | hp1 | a0003 | c0003 | t0002 | g0056 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0027 | SAS | PJL | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03834 | hp2 | a0003 | c0003 | t0002 | g0160 | SAS | BEB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03927 | hp1 | a0003 | c0003 | t0002 | g0020 | SAS | BEB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | STU | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | STU | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0096 | SAS | STU | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0100 | SAS | STU | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0007 | SAS | STU | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | STU | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | STU | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | YRI | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18612 | hp1 | a0003 | c0003 | t0002 | g0055 | EAS | CHB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18612 | hp2 | a0003 | c0003 | t0002 | g0158 | EAS | CHB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18942 | hp2 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18944 | hp2 | a0003 | c0003 | t0002 | g0008 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18947 | hp2 | a0003 | c0003 | t0002 | g0012 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18950 | hp2 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18957 | hp1 | a0003 | c0003 | t0002 | g0008 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18959 | hp1 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18961 | hp2 | a0003 | c0003 | t0002 | g0034 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18962 | hp1 | a0003 | c0003 | t0002 | g0168 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18962 | hp2 | a0003 | c0003 | t0002 | g0021 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18971 | hp2 | a0003 | c0003 | t0002 | g0154 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18973 | hp2 | a0003 | c0003 | t0002 | g0078 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18981 | hp2 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18990 | hp2 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18992 | hp1 | a0003 | c0003 | t0002 | g0077 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18994 | hp1 | a0003 | c0003 | t0002 | g0155 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18994 | hp2 | a0003 | c0003 | t0002 | g0157 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18995 | hp1 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18997 | hp2 | a0003 | c0003 | t0002 | g0008 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19000 | hp1 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19005 | hp1 | a0003 | c0003 | t0002 | g0058 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19007 | hp2 | a0003 | c0003 | t0002 | g0021 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19010 | hp2 | a0003 | c0003 | t0002 | g0162 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19011 | hp2 | a0003 | c0003 | t0002 | g0008 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19012 | hp1 | a0003 | c0003 | t0002 | g0153 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | LWK | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19054 | hp2 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19058 | hp2 | a0003 | c0003 | t0002 | g0079 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19066 | hp1 | a0003 | c0003 | t0002 | g0021 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19077 | hp2 | a0003 | c0003 | t0002 | g0152 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19079 | hp1 | a0003 | c0003 | t0002 | g0039 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19082 | hp2 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19084 | hp2 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA19088 | hp2 | a0005 | c0005 | t0001 | g0139 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | ASW | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ASW | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA20752 | hp1 | a0003 | c0003 | t0001 | g0016 | EUR | TSI | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0029 | EUR | TSI | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA20805 | hp1 | a0003 | c0003 | t0001 | g0016 | EUR | TSI | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0166 | SAS | GIH | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0007 | SAS | GIH | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0037 | AFR | ACB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0064 | AFR | ACB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02559 | hp1 | a0002 | c0002 | t0005 | g0087 | AFR | ACB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0037 | AFR | USA | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | USA | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA20300 | hp1 | a0002 | c0002 | t0006 | g0047 | AFR | USA | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | USA | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0106 | REF | REF | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0015 | REF | REF | MANSC4_chr12_27757427_27785236 | MANSC4 | chr12 | 27757427 | 27785236 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27762785 | A | T | 3 | a0001 a0004 a0005 |
176 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(173): Show |
missense_variant | MODERATE | c.976T>A | p.Ser326Thr | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 4/4 | 1309/1667 | 976/1023 | 326/340 | chr12 | 27762785 | |||
| chr12:27763139 | C | A | 1 | a0004 | 1 | HG03239.hp1 | stop_gained | HIGH | c.622G>T | p.Glu208* | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 4/4 | 955/1667 | 622/1023 | 208/340 | chr12 | 27763139 | |||
| chr12:27763273 | G | A | 1 | a0003 | 65 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(62): Show |
missense_variant | MODERATE | c.488C>T | p.Thr163Met | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 4/4 | 821/1667 | 488/1023 | 163/340 | chr12 | 27763273 | |||
| chr12:27763273 | G | T | 1 | a0005 | 1 | NA19088.hp2 | missense_variant | MODERATE | c.488C>A | p.Thr163Lys | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 4/4 | 821/1667 | 488/1023 | 163/340 | chr12 | 27763273 | |||
| chr12:27763291 | A | G | 1 | a0003 | 65 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(62): Show |
missense_variant | MODERATE | c.470T>C | p.Leu157Ser | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 4/4 | 803/1667 | 470/1023 | 157/340 | chr12 | 27763291 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27763011 | A | G | 1 | a0003c0003 | 65 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(62): Show |
synonymous_variant | LOW | c.750T>C | p.Pro250Pro | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 4/4 | 1083/1667 | 750/1023 | 250/340 | chr12 | 27763011 | |||
| chr12:27763359 | G | C | 1 | a0002c0007 | 1 | HG00597.hp2 | synonymous_variant | LOW | c.402C>G | p.Pro134Pro | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 4/4 | 735/1667 | 402/1023 | 134/340 | chr12 | 27763359 | |||
| chr12:27771148 | G | T | 1 | a0001c0004 | 1 | HG02273.hp1 | synonymous_variant | LOW | c.129C>A | p.Ile43Ile | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/4 | 462/1667 | 129/1023 | 43/340 | chr12 | 27771148 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27762471 | A | G | 1 | a0002c0002t0004 | 3 | HG02622.hp1 HG03130.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*267T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 4/4 | 267 | chr12 | 27762471 | ||||||
| chr12:27762652 | A | ATTT | 1 | a0003c0003t0002 | 61 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*83_*85dupAAA | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 4/4 | 85 | chr12 | 27762652 | ||||||
| chr12:27762674 | G | A | 1 | a0002c0002t0005 | 3 | HG02559.hp1 HG02723.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*64C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 4/4 | 64 | chr12 | 27762674 | ||||||
| chr12:27771552 | G | A | 1 | a0002c0002t0006 | 2 | HG03669.hp1 NA20300.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-276C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/4 | chr12 | 27771552 | |||||||
| chr12:27780213 | G | A | 1 | a0001c0001t0007 | 1 | HG02165.hp2 | 5_prime_UTR_variant | MODIFIER | c.-310C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/4 | 8937 | chr12 | 27780213 | ||||||
| chr12:27780230 | G | A | 1 | a0001c0001t0003 | 4 | HG02055.hp1 HG02280.hp1 HG02970.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-327C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/4 | 8954 | chr12 | 27780230 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27763538 | T | C | 1 | a0002c0002t0001g0150 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.365-142A>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27763538 | |||||||
| chr12:27763695 | A | G | 2 | a0002c0002t0001g0119 a0002c0002t0001g0140 |
2 | HG00642.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.365-299T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27763695 | |||||||
| chr12:27763743 | T | G | 1 | a0002c0002t0001g0062 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.365-347A>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27763743 | |||||||
| chr12:27763811 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(81): Show |
201 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.365-415C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27763811 | |||||||
| chr12:27763848 | A | G | 1 | a0001c0001t0001g0042 | 2 | HG01106.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.365-452T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27763848 | |||||||
| chr12:27763905 | A | AT | 6 | a0002c0002t0001g0013 a0002c0002t0001g0024 a0002c0002t0001g0061 others(3): Show |
12 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.365-510dupA | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27763905 | |||||||
| chr12:27764114 | C | T | 7 | a0002c0002t0001g0006 a0002c0002t0001g0062 a0002c0002t0001g0081 others(4): Show |
17 | HG00738.hp1 HG00741.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.365-718G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27764114 | |||||||
| chr12:27764321 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0076 |
5 | HG01074.hp2 HG01978.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.365-925C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27764321 | |||||||
| chr12:27764417 | C | T | 2 | a0002c0002t0005g0040 a0002c0002t0005g0087 |
3 | HG02559.hp1 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.365-1021G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27764417 | |||||||
| chr12:27764581 | CT | C | 2 | a0002c0002t0005g0040 a0002c0002t0005g0087 |
3 | HG02559.hp1 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.365-1186delA | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27764581 | |||||||
| chr12:27764602 | A | G | 5 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0090 others(2): Show |
9 | HG00733.hp1 HG01099.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.365-1206T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27764602 | |||||||
| chr12:27764620 | G | T | 28 | a0003c0003t0001g0016 a0003c0003t0002g0005 a0003c0003t0002g0008 others(25): Show |
65 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.365-1224C>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27764620 | |||||||
| chr12:27764853 | A | AT | 10 | a0002c0002t0001g0004 a0002c0002t0001g0023 a0002c0002t0001g0036 others(7): Show |
28 | HG00544.hp2 HG00597.hp2 HG02056.hp1 others(25): Show |
intron_variant | MODIFIER | c.365-1458dupA | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27764853 | |||||||
| chr12:27764915 | G | A | 28 | a0003c0003t0001g0016 a0003c0003t0002g0005 a0003c0003t0002g0008 others(25): Show |
65 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.365-1519C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27764915 | |||||||
| chr12:27765020 | G | A | 28 | a0003c0003t0001g0016 a0003c0003t0002g0005 a0003c0003t0002g0008 others(25): Show |
65 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.365-1624C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27765020 | |||||||
| chr12:27765026 | G | T | 1 | a0002c0002t0001g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.365-1630C>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27765026 | |||||||
| chr12:27765027 | G | C | 5 | a0001c0001t0001g0030 a0001c0001t0001g0048 a0001c0001t0001g0111 others(2): Show |
8 | HG01074.hp1 HG01192.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.365-1631C>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27765027 | |||||||
| chr12:27765120 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0073 a0001c0001t0001g0124 |
5 | HG01109.hp2 HG01943.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.364+1545T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27765120 | |||||||
| chr12:27765494 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.364+1171T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27765494 | |||||||
| chr12:27765511 | C | G | 28 | a0003c0003t0001g0016 a0003c0003t0002g0005 a0003c0003t0002g0008 others(25): Show |
65 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.364+1154G>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27765511 | |||||||
| chr12:27765580 | C | T | 1 | a0002c0002t0001g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.364+1085G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27765580 | |||||||
| chr12:27765599 | C | A | 1 | a0002c0002t0001g0097 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.364+1066G>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27765599 | |||||||
| chr12:27765964 | T | C | 1 | a0002c0002t0001g0088 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.364+701A>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27765964 | |||||||
| chr12:27766024 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.364+641G>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27766024 | |||||||
| chr12:27766041 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.364+624T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27766041 | |||||||
| chr12:27766052 | G | T | 3 | a0002c0002t0001g0017 a0002c0002t0001g0112 a0002c0002t0001g0115 |
6 | NA18940.hp1 NA18969.hp2 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.364+613C>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27766052 | |||||||
| chr12:27766073 | C | CTTT | 27 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(24): Show |
65 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.364+589_364+591dup others(3): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27766073 | |||||||
| chr12:27766124 | G | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0128 |
5 | NA18949.hp2 NA18956.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.364+541C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27766124 | |||||||
| chr12:27766212 | T | C | 31 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(28): Show |
69 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.364+453A>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27766212 | |||||||
| chr12:27766285 | C | G | 5 | a0002c0002t0001g0006 a0002c0002t0001g0062 a0002c0002t0001g0081 others(2): Show |
15 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.364+380G>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27766285 | |||||||
| chr12:27766317 | T | C | 2 | a0002c0002t0004g0044 a0002c0002t0004g0118 |
3 | HG02622.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.364+348A>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27766317 | |||||||
| chr12:27766558 | T | G | 30 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(27): Show |
68 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.364+107A>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 3/3 | chr12 | 27766558 | |||||||
| chr12:27766816 | C | T | 1 | a0002c0007t0001g0065 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.230-17G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27766816 | |||||||
| chr12:27766982 | C | CT | 4 | a0002c0002t0001g0037 a0002c0002t0001g0038 a0002c0002t0004g0044 others(1): Show |
7 | HG02486.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.230-184dupA | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27766982 | |||||||
| chr12:27766983 | T | C | 30 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(27): Show |
68 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.230-184A>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27766983 | |||||||
| chr12:27767068 | C | T | 30 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(27): Show |
68 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.230-269G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27767068 | |||||||
| chr12:27767154 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.230-355T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27767154 | |||||||
| chr12:27767353 | C | T | 1 | a0005c0005t0001g0139 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.230-554G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27767353 | |||||||
| chr12:27767533 | G | A | 1 | a0002c0002t0001g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.230-734C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27767533 | |||||||
| chr12:27767646 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(107): Show |
268 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.230-847T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27767646 | |||||||
| chr12:27767696 | T | TCAA | 3 | a0001c0001t0003g0054 a0002c0002t0001g0119 a0002c0002t0001g0140 |
4 | HG00642.hp2 HG02280.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.230-900_230-898dup others(3): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27767696 | |||||||
| chr12:27767850 | G | A | 2 | a0002c0002t0004g0044 a0002c0002t0004g0118 |
3 | HG02622.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.230-1051C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27767850 | |||||||
| chr12:27768030 | G | A | 2 | a0002c0002t0001g0101 a0002c0002t0001g0104 |
2 | HG00558.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.230-1231C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768030 | |||||||
| chr12:27768083 | T | C | 2 | a0001c0001t0003g0170 a0001c0001t0003g0171 |
2 | HG02055.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.230-1284A>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768083 | |||||||
| chr12:27768147 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.230-1348G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768147 | |||||||
| chr12:27768168 | G | A | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.230-1369C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768168 | |||||||
| chr12:27768213 | CA | C | 1 | a0002c0002t0001g0027 | 3 | HG01358.hp2 HG02735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.230-1415delT | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768213 | |||||||
| chr12:27768235 | T | TAA | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.230-1438_230-1437d others(4): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768235 | |||||||
| chr12:27768402 | C | CA | 50 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0066 others(47): Show |
119 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.230-1604dupT | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768402 | |||||||
| chr12:27768402 | C | CAA | 6 | a0002c0002t0001g0098 a0002c0002t0001g0103 a0002c0002t0001g0105 others(3): Show |
6 | HG00673.hp1 HG01346.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.230-1605_230-1604d others(4): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768402 | |||||||
| chr12:27768402 | CA | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(61): Show |
174 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.230-1604delT | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768402 | |||||||
| chr12:27768415 | AAAAAAAA others(7): Show |
A | 25 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0003c0003t0001g0016 others(22): Show |
60 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.230-1630_230-1617d others(16): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768415 | |||||||
| chr12:27768416 | AAAAAAAG others(6): Show |
A | 4 | a0001c0001t0001g0057 a0003c0003t0002g0020 a0003c0003t0002g0077 others(1): Show |
7 | HG00735.hp2 HG01358.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.230-1630_230-1618d others(15): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768416 | |||||||
| chr12:27768417 | A | G | 1 | a0003c0003t0002g0060 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.230-1618T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768417 | |||||||
| chr12:27768417 | AAAAAAG | A | 7 | a0002c0002t0001g0013 a0002c0002t0001g0024 a0002c0002t0001g0061 others(4): Show |
13 | HG00738.hp1 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.230-1624_230-1619d others(8): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768417 | |||||||
| chr12:27768418 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(55): Show |
158 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.230-1619T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768418 | |||||||
| chr12:27768424 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.230-1625T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768424 | |||||||
| chr12:27768537 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.230-1738T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768537 | |||||||
| chr12:27768597 | G | C | 1 | a0001c0001t0001g0129 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.230-1798C>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768597 | |||||||
| chr12:27768637 | C | T | 3 | a0002c0002t0001g0037 a0002c0002t0004g0044 a0002c0002t0004g0118 |
5 | HG02486.hp1 HG02622.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.230-1838G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768637 | |||||||
| chr12:27768640 | CTTTTT | C | 28 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(25): Show |
66 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.230-1846_230-1842d others(7): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768640 | |||||||
| chr12:27768688 | A | G | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.230-1889T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768688 | |||||||
| chr12:27768744 | A | G | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.230-1945T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768744 | |||||||
| chr12:27768885 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.230-2086G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768885 | |||||||
| chr12:27768893 | G | A | 1 | a0002c0002t0001g0163 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.230-2094C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27768893 | |||||||
| chr12:27769035 | G | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(106): Show |
267 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.229+2013C>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27769035 | |||||||
| chr12:27769141 | T | C | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.229+1907A>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27769141 | |||||||
| chr12:27769486 | G | A | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.229+1562C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27769486 | |||||||
| chr12:27769574 | A | G | 7 | a0002c0002t0001g0013 a0002c0002t0001g0024 a0002c0002t0001g0061 others(4): Show |
13 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.229+1474T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27769574 | |||||||
| chr12:27769576 | C | G | 3 | a0002c0002t0001g0072 a0002c0002t0001g0113 a0002c0002t0001g0114 |
3 | HG01891.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.229+1472G>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27769576 | |||||||
| chr12:27769787 | C | A | 1 | a0003c0003t0002g0155 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.229+1261G>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27769787 | |||||||
| chr12:27769963 | G | T | 1 | a0003c0003t0002g0156 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.229+1085C>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27769963 | |||||||
| chr12:27769992 | A | G | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.229+1056T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27769992 | |||||||
| chr12:27770005 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.229+1043T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770005 | |||||||
| chr12:27770021 | A | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(54): Show |
156 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.229+1027T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770021 | |||||||
| chr12:27770057 | G | A | 6 | a0002c0002t0001g0006 a0002c0002t0001g0062 a0002c0002t0001g0086 others(3): Show |
17 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.229+991C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770057 | |||||||
| chr12:27770086 | T | C | 1 | a0002c0002t0001g0038 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.229+962A>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770086 | |||||||
| chr12:27770186 | A | T | 31 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(28): Show |
69 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.229+862T>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770186 | |||||||
| chr12:27770202 | AGT | A | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.229+844_229+845del others(2): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770202 | |||||||
| chr12:27770229 | T | G | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.229+819A>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770229 | |||||||
| chr12:27770243 | C | T | 1 | a0002c0002t0001g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.229+805G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770243 | |||||||
| chr12:27770250 | G | A | 1 | a0002c0002t0001g0147 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.229+798C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770250 | |||||||
| chr12:27770308 | G | A | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.229+740C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770308 | |||||||
| chr12:27770329 | T | C | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.229+719A>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770329 | |||||||
| chr12:27770383 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.229+665C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770383 | |||||||
| chr12:27770392 | G | T | 3 | a0002c0002t0001g0037 a0002c0002t0004g0044 a0002c0002t0004g0118 |
5 | HG02486.hp1 HG02622.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.229+656C>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770392 | |||||||
| chr12:27770415 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(55): Show |
157 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.229+633C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770415 | |||||||
| chr12:27770436 | C | CT | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.229+611dupA | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770436 | |||||||
| chr12:27770463 | T | A | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.229+585A>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770463 | |||||||
| chr12:27770465 | G | A | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.229+583C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770465 | |||||||
| chr12:27770518 | A | AC | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.229+529dupG | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770518 | |||||||
| chr12:27770595 | T | C | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.229+453A>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770595 | |||||||
| chr12:27770885 | A | T | 1 | a0002c0002t0001g0110 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.229+163T>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770885 | |||||||
| chr12:27770923 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.229+125G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 2/3 | chr12 | 27770923 | |||||||
| chr12:27771725 | A | G | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-306-143T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27771725 | |||||||
| chr12:27771864 | T | G | 3 | a0003c0003t0002g0157 a0003c0003t0002g0158 a0003c0003t0002g0159 |
3 | HG00642.hp1 NA18612.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-306-282A>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27771864 | |||||||
| chr12:27771931 | C | T | 6 | a0002c0002t0001g0006 a0002c0002t0001g0062 a0002c0002t0001g0086 others(3): Show |
17 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-306-349G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27771931 | |||||||
| chr12:27772045 | A | C | 1 | a0002c0002t0005g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-306-463T>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27772045 | |||||||
| chr12:27772055 | CCAAA | C | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-306-477_-306-474d others(6): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27772055 | |||||||
| chr12:27772104 | T | A | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-306-522A>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27772104 | |||||||
| chr12:27772175 | CTG | C | 5 | a0002c0002t0001g0013 a0002c0002t0001g0024 a0002c0002t0001g0061 others(2): Show |
11 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-306-595_-306-594d others(4): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27772175 | |||||||
| chr12:27772244 | T | C | 3 | a0002c0002t0001g0010 a0002c0002t0001g0069 a0002c0002t0001g0108 |
8 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-306-662A>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27772244 | |||||||
| chr12:27772378 | T | C | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-306-796A>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27772378 | |||||||
| chr12:27772510 | A | G | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-306-928T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27772510 | |||||||
| chr12:27772744 | G | C | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-306-1162C>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27772744 | |||||||
| chr12:27772797 | C | T | 1 | a0002c0002t0001g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-306-1215G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27772797 | |||||||
| chr12:27772965 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-306-1383C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27772965 | |||||||
| chr12:27773090 | C | G | 7 | a0002c0002t0001g0013 a0002c0002t0001g0024 a0002c0002t0001g0061 others(4): Show |
13 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-306-1508G>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27773090 | |||||||
| chr12:27773381 | GGTAGAGG others(27): Show |
G | 1 | a0001c0001t0001g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-306-1833_-306-180 others(38): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27773381 | |||||||
| chr12:27773495 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-306-1913T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27773495 | |||||||
| chr12:27773520 | T | C | 5 | a0002c0002t0001g0018 a0002c0002t0001g0070 a0002c0002t0001g0092 others(2): Show |
8 | HG00741.hp1 HG01433.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.-306-1938A>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27773520 | |||||||
| chr12:27773656 | A | G | 1 | a0002c0002t0001g0163 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-306-2074T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27773656 | |||||||
| chr12:27773741 | C | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(103): Show |
263 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.-306-2159G>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27773741 | |||||||
| chr12:27773851 | T | G | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-306-2269A>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27773851 | |||||||
| chr12:27773965 | T | C | 1 | a0002c0002t0001g0164 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-306-2383A>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27773965 | |||||||
| chr12:27774022 | G | T | 2 | a0002c0002t0001g0026 a0002c0002t0001g0103 |
4 | HG01346.hp2 HG01496.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.-306-2440C>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27774022 | |||||||
| chr12:27774070 | C | T | 1 | a0003c0003t0002g0155 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-306-2488G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27774070 | |||||||
| chr12:27774167 | A | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(68): Show |
187 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.-306-2585T>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27774167 | |||||||
| chr12:27774168 | C | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(98): Show |
255 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.-306-2586G>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27774168 | |||||||
| chr12:27774170 | A | C | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-306-2588T>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27774170 | |||||||
| chr12:27774171 | A | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(60): Show |
168 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.-306-2589T>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27774171 | |||||||
| chr12:27774173 | A | C | 1 | a0002c0002t0001g0102 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-306-2591T>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27774173 | |||||||
| chr12:27774179 | C | A | 1 | a0002c0002t0001g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-306-2597G>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27774179 | |||||||
| chr12:27774211 | G | T | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-306-2629C>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27774211 | |||||||
| chr12:27774412 | GT | G | 7 | a0002c0002t0001g0013 a0002c0002t0001g0024 a0002c0002t0001g0061 others(4): Show |
13 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-306-2831delA | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27774412 | |||||||
| chr12:27774450 | A | G | 23 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(20): Show |
50 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.-306-2868T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27774450 | |||||||
| chr12:27774495 | AAG | A | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-306-2915_-306-291 others(6): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27774495 | |||||||
| chr12:27774697 | A | T | 1 | a0003c0003t0002g0078 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-306-3115T>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27774697 | |||||||
| chr12:27774902 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0142 |
2 | HG02257.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-306-3320A>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27774902 | |||||||
| chr12:27774948 | T | C | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-306-3366A>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27774948 | |||||||
| chr12:27774979 | G | A | 1 | a0001c0001t0001g0033 | 3 | HG01081.hp2 HG01346.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-306-3397C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27774979 | |||||||
| chr12:27775002 | C | T | 1 | a0001c0001t0001g0048 | 2 | HG02258.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-306-3420G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775002 | |||||||
| chr12:27775007 | G | C | 7 | a0002c0002t0001g0013 a0002c0002t0001g0024 a0002c0002t0001g0061 others(4): Show |
13 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-306-3425C>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775007 | |||||||
| chr12:27775023 | CAAAA | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0030 others(31): Show |
98 | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.-306-3445_-306-344 others(8): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775023 | |||||||
| chr12:27775023 | CAAAATAA others(1): Show |
C | 20 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0031 others(17): Show |
50 | HG00408.hp1 HG00544.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-306-3449_-306-344 others(12): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775023 | |||||||
| chr12:27775023 | CAAAATAA others(5): Show |
C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0145 |
2 | HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-306-3453_-306-344 others(16): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775023 | |||||||
| chr12:27775024 | A | AAAAT | 22 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0090 others(19): Show |
46 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-306-3446_-306-344 others(8): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775024 | |||||||
| chr12:27775024 | A | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0005c0005t0001g0139 |
8 | HG03486.hp1 HG03831.hp1 HG06807.hp2 others(5): Show |
intron_variant | MODIFIER | c.-306-3442T>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775024 | |||||||
| chr12:27775024 | AAAAT | A | 51 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0057 others(48): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.-306-3446_-306-344 others(8): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775024 | |||||||
| chr12:27775024 | AAAATAAA others(1): Show |
A | 22 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0002c0002t0001g0002 others(19): Show |
42 | HG00323.hp1 HG00621.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-306-3450_-306-344 others(12): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775024 | |||||||
| chr12:27775024 | AAAATAAA others(5): Show |
A | 1 | a0003c0003t0002g0060 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-306-3454_-306-344 others(16): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775024 | |||||||
| chr12:27775024 | AAAATAAA others(17): Show |
A | 7 | a0002c0002t0001g0013 a0002c0002t0001g0024 a0002c0002t0001g0061 others(4): Show |
13 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-306-3466_-306-344 others(28): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775024 | |||||||
| chr12:27775066 | A | C | 1 | a0002c0002t0001g0101 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-306-3484T>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775066 | |||||||
| chr12:27775093 | A | G | 7 | a0002c0002t0001g0013 a0002c0002t0001g0024 a0002c0002t0001g0061 others(4): Show |
13 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-306-3511T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775093 | |||||||
| chr12:27775095 | A | G | 1 | a0002c0002t0001g0100 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-306-3513T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775095 | |||||||
| chr12:27775436 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-306-3854C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775436 | |||||||
| chr12:27775528 | A | G | 7 | a0002c0002t0001g0013 a0002c0002t0001g0024 a0002c0002t0001g0061 others(4): Show |
13 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-306-3946T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775528 | |||||||
| chr12:27775545 | C | A | 5 | a0002c0002t0001g0037 a0002c0002t0001g0038 a0002c0002t0001g0119 others(2): Show |
8 | HG00642.hp2 HG02486.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-306-3963G>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775545 | |||||||
| chr12:27775610 | C | T | 24 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0063 others(21): Show |
58 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.-306-4028G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775610 | |||||||
| chr12:27775724 | A | G | 7 | a0002c0002t0001g0013 a0002c0002t0001g0024 a0002c0002t0001g0061 others(4): Show |
13 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-306-4142T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775724 | |||||||
| chr12:27775769 | GT | G | 25 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(22): Show |
52 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.-306-4188delA | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775769 | |||||||
| chr12:27775799 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(55): Show |
157 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.-306-4217T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775799 | |||||||
| chr12:27775865 | G | A | 8 | a0002c0002t0001g0013 a0002c0002t0001g0024 a0002c0002t0001g0061 others(5): Show |
14 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-306-4283C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775865 | |||||||
| chr12:27775934 | AC | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(56): Show |
158 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.-307+4275delG | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775934 | |||||||
| chr12:27775941 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-307+4269A>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775941 | |||||||
| chr12:27775979 | A | T | 2 | a0001c0001t0001g0051 a0002c0002t0004g0118 |
3 | HG02922.hp2 HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-307+4231T>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27775979 | |||||||
| chr12:27776083 | T | C | 1 | a0002c0002t0001g0109 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-307+4127A>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27776083 | |||||||
| chr12:27776088 | C | CA | 11 | a0001c0001t0001g0050 a0001c0001t0001g0142 a0001c0001t0001g0143 others(8): Show |
14 | HG02055.hp1 HG02129.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-307+4121dupT | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27776088 | |||||||
| chr12:27776088 | C | CAAAA | 24 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0003c0003t0001g0016 others(21): Show |
61 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-307+4118_-307+412 others(8): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27776088 | |||||||
| chr12:27776088 | CA | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
43 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.-307+4121delT | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27776088 | |||||||
| chr12:27776363 | A | G | 4 | a0002c0002t0001g0013 a0002c0002t0001g0061 a0002c0002t0001g0081 others(1): Show |
8 | HG02615.hp1 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-307+3847T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27776363 | |||||||
| chr12:27776424 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(104): Show |
264 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.-307+3786C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27776424 | |||||||
| chr12:27776558 | C | T | 1 | a0002c0002t0001g0150 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-307+3652G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27776558 | |||||||
| chr12:27776568 | G | A | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-307+3642C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27776568 | |||||||
| chr12:27776690 | G | A | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-307+3520C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27776690 | |||||||
| chr12:27776810 | T | C | 1 | a0002c0002t0001g0163 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-307+3400A>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27776810 | |||||||
| chr12:27776841 | A | G | 29 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(26): Show |
67 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-307+3369T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27776841 | |||||||
| chr12:27777214 | G | A | 1 | a0003c0003t0002g0079 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-307+2996C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27777214 | |||||||
| chr12:27777308 | C | G | 4 | a0003c0003t0002g0055 a0003c0003t0002g0152 a0003c0003t0002g0153 others(1): Show |
4 | NA18612.hp1 NA18971.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.-307+2902G>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27777308 | |||||||
| chr12:27777842 | T | A | 1 | a0001c0001t0001g0144 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-307+2368A>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27777842 | |||||||
| chr12:27777922 | A | G | 1 | a0003c0003t0002g0162 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-307+2288T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27777922 | |||||||
| chr12:27777935 | A | AT | 6 | a0001c0001t0001g0121 a0001c0001t0001g0149 a0002c0002t0001g0089 others(3): Show |
6 | HG01099.hp1 HG02155.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-307+2274dupA | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27777935 | |||||||
| chr12:27777961 | C | T | 6 | a0002c0002t0001g0006 a0002c0002t0001g0062 a0002c0002t0001g0086 others(3): Show |
17 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-307+2249G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27777961 | |||||||
| chr12:27777998 | G | T | 1 | a0001c0001t0001g0053 | 2 | HG00408.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-307+2212C>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27777998 | |||||||
| chr12:27778028 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-307+2182G>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778028 | |||||||
| chr12:27778221 | G | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(54): Show |
156 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.-307+1989C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778221 | |||||||
| chr12:27778225 | C | CA | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(61): Show |
162 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.-307+1984dupT | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778225 | |||||||
| chr12:27778225 | C | CAA | 5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0145 others(2): Show |
7 | HG02647.hp2 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-307+1983_-307+198 others(6): Show |
MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778225 | |||||||
| chr12:27778225 | CA | C | 35 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(32): Show |
84 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.-307+1984delT | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778225 | |||||||
| chr12:27778241 | T | A | 1 | a0001c0001t0001g0148 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-307+1969A>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778241 | |||||||
| chr12:27778244 | A | AT | 8 | a0001c0001t0001g0085 a0002c0002t0001g0013 a0002c0002t0001g0024 others(5): Show |
14 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-307+1965dupA | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778244 | |||||||
| chr12:27778269 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-307+1941T>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778269 | |||||||
| chr12:27778321 | A | C | 6 | a0003c0003t0002g0008 a0003c0003t0002g0034 a0003c0003t0002g0039 others(3): Show |
17 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.-307+1889T>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778321 | |||||||
| chr12:27778483 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-307+1727G>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778483 | |||||||
| chr12:27778533 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-307+1677A>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778533 | |||||||
| chr12:27778565 | T | A | 2 | a0003c0003t0002g0160 a0003c0003t0002g0161 |
2 | HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-307+1645A>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778565 | |||||||
| chr12:27778565 | T | C | 1 | a0002c0002t0001g0150 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-307+1645A>G | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778565 | |||||||
| chr12:27778565 | T | TA | 8 | a0001c0001t0001g0059 a0002c0002t0001g0151 a0003c0003t0002g0034 others(5): Show |
10 | HG00609.hp1 HG00642.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-307+1644dupT | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778565 | |||||||
| chr12:27778568 | A | T | 2 | a0002c0002t0001g0038 a0003c0003t0002g0060 |
3 | HG02896.hp2 HG02897.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-307+1642T>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778568 | |||||||
| chr12:27778576 | AC | A | 3 | a0003c0003t0002g0005 a0003c0003t0002g0077 a0003c0003t0002g0162 |
15 | HG01256.hp1 HG01258.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.-307+1633delG | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778576 | |||||||
| chr12:27778577 | C | A | 26 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(23): Show |
52 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.-307+1633G>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778577 | |||||||
| chr12:27778578 | C | A | 23 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(20): Show |
50 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.-307+1632G>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778578 | |||||||
| chr12:27778619 | G | A | 1 | a0002c0002t0001g0163 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-307+1591C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778619 | |||||||
| chr12:27778720 | C | T | 1 | a0002c0002t0001g0037 | 2 | HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-307+1490G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778720 | |||||||
| chr12:27778759 | C | A | 1 | a0002c0002t0001g0164 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-307+1451G>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778759 | |||||||
| chr12:27778823 | G | A | 2 | a0001c0001t0001g0165 a0002c0002t0001g0166 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-307+1387C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778823 | |||||||
| chr12:27778900 | G | T | 1 | a0002c0002t0001g0036 | 2 | NA18954.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-307+1310C>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778900 | |||||||
| chr12:27778907 | C | A | 1 | a0001c0001t0001g0167 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-307+1303G>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27778907 | |||||||
| chr12:27779177 | T | G | 1 | a0003c0003t0002g0060 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-307+1033A>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27779177 | |||||||
| chr12:27779228 | A | AG | 19 | a0001c0001t0001g0035 a0001c0001t0001g0063 a0001c0001t0001g0066 others(16): Show |
22 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.-307+981dupC | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27779228 | |||||||
| chr12:27779352 | C | G | 1 | a0003c0003t0002g0060 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-307+858G>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27779352 | |||||||
| chr12:27779469 | G | A | 1 | a0003c0003t0002g0168 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-307+741C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27779469 | |||||||
| chr12:27779567 | G | A | 1 | a0001c0001t0001g0053 | 2 | HG00408.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-307+643C>T | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27779567 | |||||||
| chr12:27779629 | C | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0059 others(3): Show |
13 | HG00323.hp2 HG01175.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.-307+581G>C | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27779629 | |||||||
| chr12:27779980 | C | T | 1 | a0003c0003t0002g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-307+230G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27779980 | |||||||
| chr12:27780200 | C | T | 1 | a0003c0003t0002g0055 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-307+10G>A | MANSC4 | ENSG00000205693.4 | transcript | ENST00000381273.4 | protein_coding | 1/3 | chr12 | 27780200 |