Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4171 |
| ensemblid | ENSG00000073111.14 |
| hgncid | 6944 |
| symbol | MCM2 |
| name | minichromosome maintenance complex component 2 |
| refseq_nuc | NM_004526.4 |
| refseq_prot | NP_004517.2 |
| ensembl_nuc | ENST00000265056.12 |
| ensembl_prot | ENSP00000265056.7 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 127598411 |
| end | 127622436 |
| strand | + |
| ver | v1.2 |
| region | chr3:127598411-127622436 |
| region5000 | chr3:127593411-127627436 |
| regionname0 | MCM2_chr3_127598411_127622436 |
| regionname5000 | MCM2_chr3_127593411_127627436 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 904 | 396 | 87 | 74 | 172 | 16 | 45 | 124 | MCM2_chr3_127593411_127627436 | MCM2 | MAESS others(899): Show |
chr3 | 127593411 | 127627436 |
| a0002 | 0/0 | 904 | 11 | 7 | 4 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | MAESS others(899): Show |
chr3 | 127593411 | 127627436 |
| a0003 | 0/0 | 904 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | MCM2_chr3_127593411_127627436 | MCM2 | MAESS others(899): Show |
chr3 | 127593411 | 127627436 |
| a0004 | 0/0 | 904 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | MCM2_chr3_127593411_127627436 | MCM2 | MAESS others(899): Show |
chr3 | 127593411 | 127627436 |
| a0005 | 0/0 | 904 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | MAESS others(899): Show |
chr3 | 127593411 | 127627436 |
| a0006 | 0/0 | 904 | 3 | 0 | 0 | 2 | 0 | 1 | 2 | MCM2_chr3_127593411_127627436 | MCM2 | MAESS others(899): Show |
chr3 | 127593411 | 127627436 |
| a0007 | 0/0 | 904 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | MAESS others(899): Show |
chr3 | 127593411 | 127627436 |
| a0008 | 0/0 | 904 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | MAESS others(899): Show |
chr3 | 127593411 | 127627436 |
| a0009 | 0/0 | 904 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | MAESS others(899): Show |
chr3 | 127593411 | 127627436 |
| a0010 | 0/0 | 904 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | MAESS others(899): Show |
chr3 | 127593411 | 127627436 |
| a0011 | 0/0 | 904 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | MAESS others(899): Show |
chr3 | 127593411 | 127627436 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2712 | 173 | 42 | 41 | 56 | 10 | 23 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0001c0002 | 1/0 | 2712 | 144 | 17 | 28 | 72 | 6 | 20 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0001c0003 | 0/0 | 2712 | 43 | 1 | 1 | 41 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0001c0004 | 0/0 | 2712 | 21 | 19 | 2 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0001c0006 | 0/0 | 2712 | 7 | 6 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0001c0011 | 0/0 | 2712 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0001c0014 | 0/0 | 2712 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0001c0015 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0001c0017 | 0/0 | 2712 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0001c0019 | 0/0 | 2712 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0001c0020 | 0/0 | 2712 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0001c0021 | 0/0 | 2712 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0001c0023 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0002c0005 | 0/0 | 2712 | 11 | 7 | 4 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0003c0008 | 0/0 | 2712 | 4 | 0 | 0 | 4 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0004c0007 | 0/0 | 2712 | 4 | 0 | 0 | 4 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0005c0010 | 0/0 | 2712 | 3 | 3 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0006c0009 | 0/0 | 2712 | 3 | 0 | 0 | 2 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0007c0018 | 0/0 | 2712 | 1 | 0 | 0 | 0 | 1 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0008c0016 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0009c0012 | 0/0 | 2712 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0010c0013 | 0/0 | 2712 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 | ||
| a0011c0022 | 0/0 | 2712 | 1 | 0 | 0 | 0 | 1 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | ATGGC others(2707): Show |
chr3 | 127593411 | 127627436 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3434 | 172 | 42 | 41 | 55 | 10 | 23 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0001c0001t0005 | 0/0 | 3447 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3442): Show |
chr3 | 127593411 | 127627436 |
| a0001c0002t0001 | 1/0 | 3434 | 142 | 17 | 28 | 70 | 6 | 20 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0001c0002t0002 | 0/0 | 3434 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0001c0002t0003 | 0/0 | 3434 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0001c0003t0001 | 0/0 | 3434 | 43 | 1 | 1 | 41 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0001c0004t0001 | 0/0 | 3434 | 20 | 18 | 2 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0001c0004t0004 | 0/0 | 3434 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0001c0006t0001 | 0/0 | 3434 | 7 | 6 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0001c0011t0001 | 0/0 | 3434 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0001c0014t0001 | 0/0 | 3434 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0001c0015t0001 | 0/0 | 3434 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0001c0017t0001 | 0/0 | 3434 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0001c0019t0001 | 0/0 | 3434 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0001c0020t0001 | 0/0 | 3434 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0001c0021t0001 | 0/0 | 3434 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0001c0023t0001 | 0/0 | 3434 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0002c0005t0001 | 0/0 | 3434 | 11 | 7 | 4 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0003c0008t0001 | 0/0 | 3434 | 4 | 0 | 0 | 4 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0004c0007t0001 | 0/0 | 3434 | 4 | 0 | 0 | 4 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0005c0010t0001 | 0/0 | 3434 | 3 | 3 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0006c0009t0001 | 0/0 | 3434 | 3 | 0 | 0 | 2 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0007c0018t0001 | 0/0 | 3434 | 1 | 0 | 0 | 0 | 1 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0008c0016t0001 | 0/0 | 3434 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0009c0012t0001 | 0/0 | 3434 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0010c0013t0001 | 0/0 | 3434 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| a0011c0022t0001 | 0/0 | 3434 | 1 | 0 | 0 | 0 | 1 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | CTTTT others(3429): Show |
chr3 | 127593411 | 127627436 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 19 | 4 | 7 | 6 | 2 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0003 | 0/0 | 13 | 1 | 2 | 9 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 5 | 0 | 0 | 4 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0007 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0010 | 0/0 | 7 | 1 | 0 | 6 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0012 | 0/0 | 6 | 2 | 2 | 0 | 1 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0018 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0020 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0001t0005g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0001 | 1/0 | 23 | 0 | 4 | 14 | 0 | 4 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0009 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0011 | 0/0 | 7 | 0 | 3 | 0 | 2 | 2 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0016 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0028 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0002t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0006 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0013 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0004t0001g0004 | 0/0 | 10 | 8 | 2 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0004t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0004t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0004t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0004t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0004t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0004t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0004t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0004t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0006t0001g0052 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0006t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0006t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0006t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0006t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0006t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0011t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0014t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0015t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0017t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0019t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0020t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0021t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0001c0023t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0002c0005t0001g0054 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0002c0005t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0002c0005t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0002c0005t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0002c0005t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0002c0005t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0002c0005t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0002c0005t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0002c0005t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0003c0008t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0004c0007t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0004c0007t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0005c0010t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0006c0009t0001g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0007c0018t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0008c0016t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0009c0012t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0010c0013t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| a0011c0022t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0011 | EUR | GBR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | GBR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0046 | EUR | GBR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | FIN | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00280 | hp2 | a0007 | c0018 | t0001 | g0178 | EUR | FIN | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | FIN | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0064 | EUR | FIN | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | CHS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00438 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | CHS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | CHS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00544 | hp1 | a0003 | c0008 | t0001 | g0006 | EAS | CHS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | CHS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | CHS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00597 | hp1 | a0001 | c0003 | t0001 | g0040 | EAS | CHS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00609 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | CHS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | CHS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0173 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | CHS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0188 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00735 | hp1 | a0001 | c0006 | t0001 | g0052 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00738 | hp1 | a0002 | c0005 | t0001 | g0054 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0095 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01074 | hp2 | a0002 | c0005 | t0001 | g0212 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01109 | hp2 | a0001 | c0004 | t0001 | g0004 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01167 | hp2 | a0002 | c0005 | t0001 | g0207 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01169 | hp1 | a0002 | c0005 | t0001 | g0203 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0145 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01255 | hp1 | a0001 | c0021 | t0001 | g0004 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0048 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0063 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0170 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0208 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0166 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0189 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0187 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0174 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0011 | EUR | IBS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0199 | EUR | IBS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0171 | EUR | IBS | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01891 | hp2 | a0001 | c0004 | t0004 | g0021 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0176 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0047 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0179 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0163 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0107 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02040 | hp2 | a0001 | c0003 | t0001 | g0136 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02055 | hp1 | a0001 | c0004 | t0001 | g0043 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0032 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02071 | hp2 | a0001 | c0017 | t0001 | g0008 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02074 | hp2 | a0003 | c0008 | t0001 | g0006 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02135 | hp1 | a0001 | c0019 | t0001 | g0001 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02135 | hp2 | a0001 | c0003 | t0001 | g0017 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02155 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | CDX | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02165 | hp1 | a0001 | c0003 | t0001 | g0147 | EAS | CDX | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CDX | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02257 | hp1 | a0001 | c0006 | t0001 | g0108 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0202 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0169 | AMR | PEL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0004 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02615 | hp1 | a0001 | c0006 | t0001 | g0194 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02622 | hp2 | a0001 | c0004 | t0001 | g0044 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02630 | hp1 | a0001 | c0006 | t0001 | g0193 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02630 | hp2 | a0001 | c0004 | t0001 | g0150 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02647 | hp1 | a0001 | c0004 | t0001 | g0004 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0177 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02717 | hp1 | a0001 | c0004 | t0001 | g0004 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0219 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0075 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0165 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0050 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02809 | hp1 | a0002 | c0005 | t0001 | g0055 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02809 | hp2 | a0005 | c0010 | t0001 | g0003 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02818 | hp1 | a0001 | c0004 | t0001 | g0004 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02886 | hp1 | a0005 | c0010 | t0001 | g0003 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02895 | hp1 | a0001 | c0015 | t0001 | g0021 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02922 | hp1 | a0005 | c0010 | t0001 | g0003 | AFR | ESN | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02965 | hp1 | a0001 | c0004 | t0001 | g0021 | AFR | ESN | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02970 | hp1 | a0001 | c0004 | t0001 | g0004 | AFR | ESN | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0218 | AFR | ESN | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0056 | AFR | ESN | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03041 | hp1 | a0001 | c0004 | t0001 | g0149 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0205 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03098 | hp1 | a0001 | c0004 | t0001 | g0043 | AFR | MSL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | MSL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03195 | hp2 | a0001 | c0004 | t0001 | g0004 | AFR | ESN | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03225 | hp1 | a0001 | c0006 | t0001 | g0052 | AFR | MSL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0112 | AFR | MSL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0006 | AFR | MSL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03486 | hp2 | a0008 | c0016 | t0001 | g0216 | AFR | MSL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0164 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03516 | hp1 | a0001 | c0004 | t0001 | g0159 | AFR | ESN | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03516 | hp2 | a0002 | c0005 | t0001 | g0214 | AFR | ESN | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03540 | hp1 | a0002 | c0005 | t0001 | g0055 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | GWD | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0058 | AFR | MSL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03579 | hp2 | a0002 | c0005 | t0001 | g0215 | AFR | MSL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0211 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0033 | SAS | STU | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | STU | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0213 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0050 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03710 | hp2 | a0006 | c0009 | t0001 | g0014 | SAS | PJL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0049 | SAS | BEB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03942 | hp2 | a0001 | c0020 | t0001 | g0033 | SAS | BEB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0168 | SAS | STU | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0172 | SAS | STU | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0175 | SAS | STU | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | YRI | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18522 | hp2 | a0001 | c0004 | t0001 | g0004 | AFR | YRI | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0086 | EAS | CHB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | CHB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18906 | hp1 | a0002 | c0005 | t0001 | g0054 | AFR | YRI | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0056 | AFR | YRI | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18939 | hp2 | a0004 | c0007 | t0001 | g0015 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18941 | hp1 | a0001 | c0003 | t0001 | g0070 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18942 | hp2 | a0006 | c0009 | t0001 | g0014 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18946 | hp1 | a0009 | c0012 | t0001 | g0006 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18949 | hp1 | a0001 | c0003 | t0001 | g0151 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18952 | hp1 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18953 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18953 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18962 | hp1 | a0001 | c0003 | t0001 | g0111 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18963 | hp2 | a0001 | c0003 | t0001 | g0069 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18965 | hp2 | a0003 | c0008 | t0001 | g0006 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18968 | hp1 | a0010 | c0013 | t0001 | g0006 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18970 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18975 | hp1 | a0004 | c0007 | t0001 | g0015 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18975 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18984 | hp1 | a0001 | c0003 | t0001 | g0061 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18985 | hp1 | a0004 | c0007 | t0001 | g0015 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18993 | hp2 | a0001 | c0003 | t0001 | g0143 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0077 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18995 | hp1 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18998 | hp2 | a0001 | c0003 | t0001 | g0115 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19005 | hp2 | a0004 | c0007 | t0001 | g0140 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19010 | hp1 | a0001 | c0003 | t0001 | g0076 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0158 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0044 | AFR | LWK | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19030 | hp2 | a0002 | c0005 | t0001 | g0201 | AFR | LWK | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | LWK | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | LWK | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19056 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19057 | hp1 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19060 | hp2 | a0001 | c0003 | t0001 | g0121 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19063 | hp2 | a0001 | c0003 | t0001 | g0057 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19064 | hp2 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19065 | hp2 | a0001 | c0003 | t0001 | g0103 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19066 | hp1 | a0006 | c0009 | t0001 | g0014 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19068 | hp2 | a0003 | c0008 | t0001 | g0006 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19070 | hp2 | a0001 | c0003 | t0001 | g0118 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19077 | hp2 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19079 | hp1 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19082 | hp1 | a0001 | c0003 | t0001 | g0079 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19085 | hp1 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19091 | hp1 | a0001 | c0014 | t0001 | g0073 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA19240 | hp2 | a0002 | c0005 | t0001 | g0206 | AFR | YRI | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ASW | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ASW | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | TSI | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA20805 | hp1 | a0011 | c0022 | t0001 | g0002 | EUR | TSI | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | TSI | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA20905 | hp1 | a0001 | c0011 | t0001 | g0106 | SAS | GIH | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0049 | SAS | GIH | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01123 | hp1 | a0001 | c0004 | t0001 | g0004 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02109 | hp1 | a0001 | c0004 | t0001 | g0021 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0220 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02486 | hp1 | a0001 | c0023 | t0001 | g0120 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0078 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0004 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG03471 | hp2 | a0001 | c0006 | t0001 | g0195 | AFR | MSL | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | USA | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| HG06807 | hp2 | a0001 | c0006 | t0001 | g0192 | AFR | USA | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18955 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | USA | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | USA | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0098 | REF | REF | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0001 | REF | REF | MCM2_chr3_127593411_127627436 | MCM2 | chr3 | 127593411 | 127627436 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:127599364 | G | C | 1 | a0004 | 4 | NA18939.hp2 NA18975.hp1 NA18985.hp1 others(1): Show |
missense_variant | MODERATE | c.53G>C | p.Arg18Pro | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/16 | 109/3434 | 53/2715 | 18/904 | chr3 | 127599364 | |||
| chr3:127599409 | G | A | 1 | a0006 | 3 | HG03710.hp2 NA18942.hp2 NA19066.hp1 |
missense_variant | MODERATE | c.98G>A | p.Arg33Gln | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/16 | 154/3434 | 98/2715 | 33/904 | chr3 | 127599409 | |||
| chr3:127599515 | T | G | 1 | a0002 | 11 | HG00738.hp1 HG01074.hp2 HG01167.hp2 others(8): Show |
missense_variant | MODERATE | c.204T>G | p.Asp68Glu | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/16 | 260/3434 | 204/2715 | 68/904 | chr3 | 127599515 | |||
| chr3:127606271 | G | A | 1 | a0009 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.827G>A | p.Arg276His | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 5/16 | 883/3434 | 827/2715 | 276/904 | chr3 | 127606271 | |||
| chr3:127617393 | G | A | 2 | a0009 a0010 |
2 | NA18946.hp1 NA18968.hp1 |
missense_variant | MODERATE | c.1888G>A | p.Ala630Thr | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 11/16 | 1944/3434 | 1888/2715 | 630/904 | chr3 | 127617393 | |||
| chr3:127618067 | G | A | 3 | a0003 a0009 a0010 |
6 | HG00544.hp1 HG02074.hp2 NA18946.hp1 others(3): Show |
missense_variant | MODERATE | c.1999G>A | p.Val667Met | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 12/16 | 2055/3434 | 1999/2715 | 667/904 | chr3 | 127618067 | |||
| chr3:127619192 | G | A | 1 | a0008 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.2179G>A | p.Ala727Thr | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 13/16 | 2235/3434 | 2179/2715 | 727/904 | chr3 | 127619192 | |||
| chr3:127621082 | C | T | 1 | a0007 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.2458C>T | p.Arg820Cys | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 15/16 | 2514/3434 | 2458/2715 | 820/904 | chr3 | 127621082 | |||
| chr3:127621194 | C | T | 1 | a0011 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.2570C>T | p.Thr857Ile | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 15/16 | 2626/3434 | 2570/2715 | 857/904 | chr3 | 127621194 | |||
| chr3:127621197 | T | C | 1 | a0005 | 3 | HG02809.hp2 HG02886.hp1 HG02922.hp1 |
missense_variant | MODERATE | c.2573T>C | p.Ile858Thr | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 15/16 | 2629/3434 | 2573/2715 | 858/904 | chr3 | 127621197 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:127599437 | T | C | 1 | a0001c0011 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.126T>C | p.Pro42Pro | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/16 | 182/3434 | 126/2715 | 42/904 | chr3 | 127599437 | |||
| chr3:127604749 | G | A | 4 | a0001c0003 a0003c0008 a0009c0012 others(1): Show |
49 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(46): Show |
synonymous_variant | LOW | c.378G>A | p.Arg126Arg | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 3/16 | 434/3434 | 378/2715 | 126/904 | chr3 | 127604749 | |||
| chr3:127604963 | C | T | 1 | a0001c0006 | 7 | HG00735.hp1 HG02257.hp1 HG02615.hp1 others(4): Show |
synonymous_variant | LOW | c.480C>T | p.Asp160Asp | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 4/16 | 536/3434 | 480/2715 | 160/904 | chr3 | 127604963 | |||
| chr3:127604987 | C | T | 10 | a0001c0001 a0001c0003 a0001c0023 others(7): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
synonymous_variant | LOW | c.504C>T | p.Ile168Ile | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 4/16 | 560/3434 | 504/2715 | 168/904 | chr3 | 127604987 | |||
| chr3:127608477 | C | T | 1 | a0001c0021 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.1197C>T | p.Leu399Leu | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 7/16 | 1253/3434 | 1197/2715 | 399/904 | chr3 | 127608477 | |||
| chr3:127608999 | C | G | 1 | a0001c0023 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.1404C>G | p.Ser468Ser | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/16 | 1460/3434 | 1404/2715 | 468/904 | chr3 | 127608999 | |||
| chr3:127616998 | G | A | 1 | a0001c0014 | 1 | NA19091.hp1 | synonymous_variant | LOW | c.1653G>A | p.Ala551Ala | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 10/16 | 1709/3434 | 1653/2715 | 551/904 | chr3 | 127616998 | |||
| chr3:127618054 | G | A | 1 | a0001c0015 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.1986G>A | p.Val662Val | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 12/16 | 2042/3434 | 1986/2715 | 662/904 | chr3 | 127618054 | |||
| chr3:127620793 | C | T | 1 | a0001c0020 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.2361C>T | p.Ile787Ile | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 14/16 | 2417/3434 | 2361/2715 | 787/904 | chr3 | 127620793 | |||
| chr3:127620859 | C | T | 1 | a0001c0019 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.2427C>T | p.Ser809Ser | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 14/16 | 2483/3434 | 2427/2715 | 809/904 | chr3 | 127620859 | |||
| chr3:127621180 | G | A | 1 | a0001c0017 | 1 | HG02071.hp2 | synonymous_variant | LOW | c.2556G>A | p.Gly852Gly | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 15/16 | 2612/3434 | 2556/2715 | 852/904 | chr3 | 127621180 | |||
| chr3:127621740 | C | T | 3 | a0001c0004 a0001c0015 a0001c0021 |
23 | HG01109.hp2 HG01123.hp1 HG01255.hp1 others(20): Show |
synonymous_variant | LOW | c.2682C>T | p.Asp894Asp | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 2738/3434 | 2682/2715 | 894/904 | chr3 | 127621740 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:127621789 | A | T | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16A>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 16 | chr3 | 127621789 | ||||||
| chr3:127621792 | A | T | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*19A>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 19 | chr3 | 127621792 | ||||||
| chr3:127621797 | T | G | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*24T>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 24 | chr3 | 127621797 | ||||||
| chr3:127621799 | C | A | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*26C>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 26 | chr3 | 127621799 | ||||||
| chr3:127621801 | T | A | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*28T>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 28 | chr3 | 127621801 | ||||||
| chr3:127621805 | A | C | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*32A>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 32 | chr3 | 127621805 | ||||||
| chr3:127621806 | T | C | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*33T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 33 | chr3 | 127621806 | ||||||
| chr3:127621809 | T | A | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*36T>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 36 | chr3 | 127621809 | ||||||
| chr3:127621811 | G | A | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*38G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 38 | chr3 | 127621811 | ||||||
| chr3:127621812 | T | A | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*39T>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 39 | chr3 | 127621812 | ||||||
| chr3:127621813 | T | C | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*40T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 40 | chr3 | 127621813 | ||||||
| chr3:127621816 | G | C | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*43G>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 43 | chr3 | 127621816 | ||||||
| chr3:127621817 | G | T | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*44G>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 44 | chr3 | 127621817 | ||||||
| chr3:127621818 | G | GCAGGATC others(6): Show |
1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*45_*46insCAGGATCA others(5): Show |
MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 46 | chr3 | 127621818 | ||||||
| chr3:127621820 | G | T | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*47G>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 47 | chr3 | 127621820 | ||||||
| chr3:127621821 | G | T | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*48G>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 48 | chr3 | 127621821 | ||||||
| chr3:127621852 | A | T | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*79A>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 79 | chr3 | 127621852 | ||||||
| chr3:127621855 | A | T | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*82A>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 82 | chr3 | 127621855 | ||||||
| chr3:127621858 | G | T | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*85G>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 85 | chr3 | 127621858 | ||||||
| chr3:127621861 | C | T | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*88C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 88 | chr3 | 127621861 | ||||||
| chr3:127621862 | T | C | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*89T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 89 | chr3 | 127621862 | ||||||
| chr3:127621866 | T | A | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*93T>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 93 | chr3 | 127621866 | ||||||
| chr3:127621869 | A | G | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*96A>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 96 | chr3 | 127621869 | ||||||
| chr3:127621890 | G | T | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*117G>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 117 | chr3 | 127621890 | ||||||
| chr3:127621892 | T | A | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*119T>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 119 | chr3 | 127621892 | ||||||
| chr3:127621893 | T | A | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*120T>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 120 | chr3 | 127621893 | ||||||
| chr3:127621903 | T | G | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*130T>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 130 | chr3 | 127621903 | ||||||
| chr3:127621909 | G | C | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*136G>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 136 | chr3 | 127621909 | ||||||
| chr3:127621910 | C | T | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 137 | chr3 | 127621910 | ||||||
| chr3:127621911 | T | G | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*138T>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 138 | chr3 | 127621911 | ||||||
| chr3:127621921 | A | C | 1 | a0001c0004t0004 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*148A>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 148 | chr3 | 127621921 | ||||||
| chr3:127621936 | T | G | 1 | a0001c0001t0005 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*163T>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 163 | chr3 | 127621936 | ||||||
| chr3:127622089 | G | T | 1 | a0001c0002t0003 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*316G>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 316 | chr3 | 127622089 | ||||||
| chr3:127622289 | G | A | 1 | a0001c0002t0002 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*516G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 16/16 | 516 | chr3 | 127622289 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:127598536 | C | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0221 a0001c0001t0001g0222 others(1): Show |
8 | HG01496.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.6+64C>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 1/15 | chr3 | 127598536 | |||||||
| chr3:127598793 | CT | C | 9 | a0001c0001t0001g0030 a0001c0001t0001g0059 a0001c0001t0001g0060 others(6): Show |
10 | HG00323.hp1 HG00323.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.6+334delT | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 127598793 | ||||||
| chr3:127598854 | A | T | 3 | a0001c0002t0001g0218 a0001c0002t0001g0219 a0001c0002t0001g0220 |
3 | HG02109.hp2 HG02717.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.6+382A>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 1/15 | chr3 | 127598854 | |||||||
| chr3:127599637 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.236+90G>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127599637 | |||||||
| chr3:127599677 | C | G | 1 | a0001c0001t0001g0217 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.236+130C>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127599677 | |||||||
| chr3:127599778 | C | G | 22 | a0001c0002t0001g0009 a0001c0002t0001g0028 a0001c0002t0001g0029 others(19): Show |
36 | HG00738.hp1 HG01074.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.236+231C>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127599778 | |||||||
| chr3:127599873 | A | C | 2 | a0001c0002t0001g0219 a0001c0002t0001g0220 |
2 | HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.236+326A>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127599873 | |||||||
| chr3:127599949 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.236+402T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127599949 | |||||||
| chr3:127600055 | G | A | 1 | a0001c0002t0001g0067 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.236+508G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127600055 | |||||||
| chr3:127600464 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.236+917T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127600464 | |||||||
| chr3:127600482 | A | G | 1 | a0008c0016t0001g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.236+935A>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127600482 | |||||||
| chr3:127600514 | G | A | 2 | a0001c0002t0001g0219 a0001c0002t0001g0220 |
2 | HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.236+967G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127600514 | |||||||
| chr3:127600613 | T | C | 1 | a0001c0003t0001g0069 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.236+1066T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127600613 | |||||||
| chr3:127600657 | C | G | 1 | a0001c0001t0001g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.236+1110C>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127600657 | |||||||
| chr3:127600679 | G | C | 2 | a0001c0003t0001g0057 a0001c0003t0001g0070 |
2 | NA18941.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.236+1132G>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127600679 | |||||||
| chr3:127600709 | T | A | 3 | a0001c0002t0001g0071 a0001c0002t0001g0072 a0001c0014t0001g0073 |
3 | NA18955.hp2 NA18979.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.236+1162T>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127600709 | |||||||
| chr3:127600876 | C | CA | 14 | a0001c0001t0001g0221 a0001c0002t0001g0031 a0001c0002t0001g0058 others(11): Show |
15 | HG01934.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.236+1346dupA | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 127600876 | ||||||
| chr3:127600876 | CA | C | 7 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0002t0001g0053 others(4): Show |
8 | HG00099.hp2 HG01516.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+1346delA | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 127600876 | ||||||
| chr3:127600982 | C | G | 1 | a0001c0014t0001g0073 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.236+1435C>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127600982 | |||||||
| chr3:127601012 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.236+1465C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127601012 | |||||||
| chr3:127601056 | C | T | 1 | a0001c0002t0001g0213 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.236+1509C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127601056 | |||||||
| chr3:127601059 | T | G | 1 | a0001c0002t0001g0083 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.236+1512T>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127601059 | |||||||
| chr3:127601267 | C | T | 5 | a0001c0006t0001g0052 a0001c0006t0001g0192 a0001c0006t0001g0193 others(2): Show |
6 | HG00735.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.236+1720C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127601267 | |||||||
| chr3:127601353 | G | A | 4 | a0001c0002t0001g0031 a0001c0002t0001g0058 a0001c0002t0001g0074 others(1): Show |
5 | HG02723.hp1 HG03098.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.236+1806G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127601353 | |||||||
| chr3:127601520 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.236+1973C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127601520 | |||||||
| chr3:127601550 | C | A | 2 | a0001c0006t0001g0192 a0001c0006t0001g0193 |
2 | HG02630.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.236+2003C>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127601550 | |||||||
| chr3:127601611 | G | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0197 |
8 | HG00741.hp2 HG01167.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+2064G>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127601611 | |||||||
| chr3:127601686 | C | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(185): Show |
334 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.236+2139C>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127601686 | |||||||
| chr3:127601944 | T | G | 1 | a0001c0003t0001g0032 | 2 | HG02056.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.236+2397T>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127601944 | |||||||
| chr3:127602045 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG03239.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.236+2498C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127602045 | |||||||
| chr3:127602100 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.237-2508C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127602100 | |||||||
| chr3:127602162 | C | CT | 17 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0152 others(14): Show |
22 | HG00733.hp1 HG01361.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.237-2426dupT | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 127602162 | ||||||
| chr3:127602162 | CT | C | 6 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0002t0001g0058 others(3): Show |
6 | HG01069.hp1 HG01975.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-2426delT | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 127602162 | ||||||
| chr3:127602294 | T | G | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | HG02818.hp2 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.237-2314T>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127602294 | |||||||
| chr3:127602477 | G | A | 1 | a0001c0002t0001g0074 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.237-2131G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127602477 | |||||||
| chr3:127602493 | A | G | 2 | a0001c0003t0001g0079 a0001c0003t0001g0151 |
2 | NA18949.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.237-2115A>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127602493 | |||||||
| chr3:127602849 | G | A | 1 | a0001c0002t0001g0163 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.237-1759G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127602849 | |||||||
| chr3:127602860 | C | T | 1 | a0001c0002t0001g0218 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.237-1748C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127602860 | |||||||
| chr3:127602984 | G | A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(38): Show |
87 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.237-1624G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127602984 | |||||||
| chr3:127603020 | G | GT | 6 | a0001c0001t0001g0066 a0001c0002t0001g0031 a0001c0002t0001g0058 others(3): Show |
7 | HG01433.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-1578dupT | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 127603020 | ||||||
| chr3:127603106 | T | G | 3 | a0001c0002t0001g0046 a0001c0002t0001g0219 a0001c0002t0001g0220 |
4 | HG00140.hp2 HG01256.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-1502T>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127603106 | |||||||
| chr3:127603145 | C | T | 5 | a0001c0006t0001g0052 a0001c0006t0001g0192 a0001c0006t0001g0193 others(2): Show |
6 | HG00735.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.237-1463C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127603145 | |||||||
| chr3:127603157 | C | T | 2 | a0001c0002t0001g0185 a0001c0002t0001g0186 |
2 | NA18973.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.237-1451C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127603157 | |||||||
| chr3:127603247 | C | T | 1 | a0001c0002t0001g0031 | 2 | HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.237-1361C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127603247 | |||||||
| chr3:127603250 | C | T | 1 | a0001c0002t0001g0184 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.237-1358C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127603250 | |||||||
| chr3:127603318 | T | G | 22 | a0001c0002t0001g0009 a0001c0002t0001g0028 a0001c0002t0001g0029 others(19): Show |
36 | HG00738.hp1 HG01074.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.237-1290T>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127603318 | |||||||
| chr3:127603680 | G | C | 1 | a0001c0011t0001g0106 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.237-928G>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127603680 | |||||||
| chr3:127603755 | G | A | 1 | a0001c0003t0001g0107 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.237-853G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127603755 | |||||||
| chr3:127603786 | C | T | 3 | a0001c0002t0001g0181 a0001c0002t0001g0182 a0001c0002t0001g0183 |
3 | NA19003.hp1 NA19057.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.237-822C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127603786 | |||||||
| chr3:127603913 | G | A | 6 | a0001c0006t0001g0052 a0001c0006t0001g0108 a0001c0006t0001g0192 others(3): Show |
7 | HG00735.hp1 HG02257.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-695G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127603913 | |||||||
| chr3:127603979 | A | C | 1 | a0001c0002t0001g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.237-629A>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127603979 | |||||||
| chr3:127604059 | A | G | 13 | a0001c0002t0001g0031 a0001c0002t0001g0058 a0001c0002t0001g0075 others(10): Show |
15 | HG00735.hp1 HG02109.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-549A>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127604059 | |||||||
| chr3:127604170 | C | G | 11 | a0001c0004t0001g0004 a0001c0004t0001g0021 a0001c0004t0001g0043 others(8): Show |
23 | HG01109.hp2 HG01123.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.237-438C>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127604170 | |||||||
| chr3:127604281 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.237-327G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 2/15 | chr3 | 127604281 | |||||||
| chr3:127605172 | G | A | 5 | a0001c0002t0001g0031 a0001c0002t0001g0058 a0001c0002t0001g0075 others(2): Show |
6 | HG02723.hp1 HG03098.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.673+16G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 4/15 | chr3 | 127605172 | |||||||
| chr3:127605306 | G | A | 1 | a0001c0002t0001g0074 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.673+150G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 4/15 | chr3 | 127605306 | |||||||
| chr3:127605353 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.673+197G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 4/15 | chr3 | 127605353 | |||||||
| chr3:127605434 | C | CT | 40 | a0001c0001t0001g0104 a0001c0001t0001g0146 a0001c0002t0001g0008 others(37): Show |
67 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.673+301dupT | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 127605434 | ||||||
| chr3:127605434 | CT | C | 32 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0059 others(29): Show |
38 | HG00735.hp1 HG01069.hp1 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.673+301delT | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 127605434 | ||||||
| chr3:127605463 | G | A | 1 | a0001c0002t0001g0166 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.673+307G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 4/15 | chr3 | 127605463 | |||||||
| chr3:127605712 | T | A | 1 | a0001c0002t0001g0167 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.674-406T>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 4/15 | chr3 | 127605712 | |||||||
| chr3:127605720 | G | A | 1 | a0001c0004t0001g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.674-398G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 4/15 | chr3 | 127605720 | |||||||
| chr3:127605842 | G | A | 8 | a0001c0002t0001g0218 a0001c0002t0001g0220 a0001c0006t0001g0052 others(5): Show |
9 | HG00735.hp1 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.674-276G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 4/15 | chr3 | 127605842 | |||||||
| chr3:127605894 | C | T | 3 | a0002c0005t0001g0212 a0002c0005t0001g0214 a0002c0005t0001g0215 |
3 | HG01074.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.674-224C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 4/15 | chr3 | 127605894 | |||||||
| chr3:127605908 | A | G | 1 | a0001c0001t0001g0036 | 2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.674-210A>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 4/15 | chr3 | 127605908 | |||||||
| chr3:127606110 | C | G | 1 | a0001c0002t0001g0218 | 1 | HG02970.hp2 | splice_region_variant&intron_variant | LOW | c.674-8C>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 4/15 | chr3 | 127606110 | |||||||
| chr3:127606112 | T | C | 16 | a0001c0002t0001g0031 a0001c0002t0001g0058 a0001c0002t0001g0075 others(13): Show |
18 | HG00735.hp1 HG02109.hp2 HG02257.hp1 others(15): Show |
splice_region_variant&intron_variant | LOW | c.674-6T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 4/15 | chr3 | 127606112 | |||||||
| chr3:127606407 | G | A | 1 | a0001c0002t0001g0220 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.893+70G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 5/15 | chr3 | 127606407 | |||||||
| chr3:127606455 | C | T | 1 | a0001c0004t0001g0150 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.893+118C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 5/15 | chr3 | 127606455 | |||||||
| chr3:127606481 | G | C | 1 | a0001c0002t0001g0219 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.894-129G>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 5/15 | chr3 | 127606481 | |||||||
| chr3:127606942 | T | G | 1 | a0001c0002t0001g0169 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1101+125T>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 6/15 | chr3 | 127606942 | |||||||
| chr3:127607042 | G | A | 1 | a0001c0002t0001g0180 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1101+225G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 6/15 | chr3 | 127607042 | |||||||
| chr3:127607147 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1101+330C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 6/15 | chr3 | 127607147 | |||||||
| chr3:127607283 | G | A | 1 | a0001c0002t0001g0102 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1101+466G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 6/15 | chr3 | 127607283 | |||||||
| chr3:127607363 | C | T | 1 | a0001c0002t0001g0219 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1101+546C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 6/15 | chr3 | 127607363 | |||||||
| chr3:127607436 | G | A | 1 | a0001c0002t0001g0188 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1101+619G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 6/15 | chr3 | 127607436 | |||||||
| chr3:127607477 | C | T | 3 | a0001c0003t0001g0042 a0001c0003t0001g0143 a0001c0003t0001g0158 |
4 | NA18993.hp2 NA19011.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101+660C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 6/15 | chr3 | 127607477 | |||||||
| chr3:127607500 | G | T | 1 | a0001c0002t0001g0142 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1101+683G>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 6/15 | chr3 | 127607500 | |||||||
| chr3:127607546 | C | T | 1 | a0001c0002t0001g0074 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1101+729C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 6/15 | chr3 | 127607546 | |||||||
| chr3:127607568 | G | A | 2 | a0001c0003t0001g0017 a0001c0003t0001g0144 |
6 | HG00558.hp1 HG02135.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101+751G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 6/15 | chr3 | 127607568 | |||||||
| chr3:127607581 | C | G | 1 | a0001c0001t0001g0141 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1101+764C>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 6/15 | chr3 | 127607581 | |||||||
| chr3:127607862 | G | A | 1 | a0001c0002t0001g0213 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1102-520G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 6/15 | chr3 | 127607862 | |||||||
| chr3:127608100 | C | G | 1 | a0001c0002t0001g0211 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1102-282C>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 6/15 | chr3 | 127608100 | |||||||
| chr3:127608672 | T | C | 5 | a0001c0002t0001g0047 a0001c0002t0001g0080 a0001c0002t0001g0163 others(2): Show |
6 | HG01346.hp2 HG01361.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1236+156T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 7/15 | chr3 | 127608672 | |||||||
| chr3:127608742 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1237-90C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 7/15 | chr3 | 127608742 | |||||||
| chr3:127609189 | A | G | 1 | a0001c0002t0001g0210 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1428+166A>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127609189 | |||||||
| chr3:127609286 | G | A | 6 | a0001c0002t0001g0031 a0001c0002t0001g0075 a0001c0002t0001g0213 others(3): Show |
7 | HG02109.hp2 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1428+263G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127609286 | |||||||
| chr3:127609424 | G | A | 2 | a0001c0003t0001g0061 a0001c0003t0001g0118 |
2 | NA18984.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1428+401G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127609424 | |||||||
| chr3:127609480 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1428+457T>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127609480 | |||||||
| chr3:127609512 | C | T | 21 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0028 others(18): Show |
40 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.1428+489C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127609512 | |||||||
| chr3:127609560 | G | A | 1 | a0001c0023t0001g0120 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1428+537G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127609560 | |||||||
| chr3:127609683 | G | A | 3 | a0001c0001t0001g0093 a0001c0002t0001g0033 a0001c0020t0001g0033 |
3 | HG03688.hp1 HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1428+660G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127609683 | |||||||
| chr3:127609703 | T | C | 1 | a0001c0002t0001g0170 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1428+680T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127609703 | |||||||
| chr3:127609837 | C | CT | 18 | a0001c0001t0001g0090 a0001c0001t0001g0093 a0001c0001t0001g0137 others(15): Show |
21 | HG00741.hp1 HG01346.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.1428+841dupT | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 127609837 | ||||||
| chr3:127609837 | CT | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1428+841delT | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 127609837 | ||||||
| chr3:127609837 | CTT | C | 19 | a0001c0001t0001g0038 a0001c0001t0001g0062 a0001c0001t0001g0197 others(16): Show |
29 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.1428+840_1428+841d others(4): Show |
MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 127609837 | ||||||
| chr3:127609837 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0094 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1428+828_1428+841d others(16): Show |
MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 127609837 | ||||||
| chr3:127610059 | G | A | 1 | a0001c0002t0001g0176 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1428+1036G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127610059 | |||||||
| chr3:127610123 | T | A | 1 | a0001c0004t0001g0043 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1428+1100T>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127610123 | |||||||
| chr3:127610123 | T | C | 2 | a0001c0002t0001g0218 a0002c0005t0001g0206 |
2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1428+1100T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127610123 | |||||||
| chr3:127610191 | G | A | 2 | a0001c0002t0001g0218 a0002c0005t0001g0206 |
2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1428+1168G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127610191 | |||||||
| chr3:127610243 | T | C | 1 | a0001c0002t0001g0172 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1428+1220T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127610243 | |||||||
| chr3:127610349 | A | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0117 a0001c0001t0001g0119 others(2): Show |
9 | HG02165.hp2 HG02683.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1428+1326A>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127610349 | |||||||
| chr3:127610359 | G | T | 11 | a0001c0004t0001g0004 a0001c0004t0001g0021 a0001c0004t0001g0043 others(8): Show |
23 | HG01109.hp2 HG01123.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.1428+1336G>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127610359 | |||||||
| chr3:127610402 | T | A | 1 | a0001c0002t0001g0031 | 2 | HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1428+1379T>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127610402 | |||||||
| chr3:127610412 | AGGTTAGC others(11): Show |
A | 1 | a0001c0003t0001g0144 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1428+1394_1428+141 others(22): Show |
MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 127610412 | ||||||
| chr3:127610530 | C | T | 2 | a0001c0002t0001g0218 a0002c0005t0001g0206 |
2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1428+1507C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127610530 | |||||||
| chr3:127610674 | C | T | 1 | a0001c0002t0001g0183 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1428+1651C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127610674 | |||||||
| chr3:127610707 | A | T | 1 | a0001c0002t0001g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1428+1684A>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127610707 | |||||||
| chr3:127610940 | T | C | 1 | a0001c0002t0001g0177 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1428+1917T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127610940 | |||||||
| chr3:127610942 | G | C | 16 | a0001c0002t0001g0031 a0001c0002t0001g0058 a0001c0002t0001g0075 others(13): Show |
18 | HG00735.hp1 HG02109.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1428+1919G>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127610942 | |||||||
| chr3:127610980 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1428+1957A>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127610980 | |||||||
| chr3:127611012 | C | T | 1 | a0001c0003t0001g0121 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1428+1989C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127611012 | |||||||
| chr3:127611022 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1428+1999C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127611022 | |||||||
| chr3:127611086 | G | A | 11 | a0001c0002t0001g0011 a0001c0002t0001g0048 a0001c0002t0001g0063 others(8): Show |
18 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1428+2063G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127611086 | |||||||
| chr3:127611121 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1428+2098C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127611121 | |||||||
| chr3:127611292 | A | C | 2 | a0001c0002t0001g0218 a0002c0005t0001g0206 |
2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1428+2269A>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127611292 | |||||||
| chr3:127611402 | T | C | 31 | a0001c0003t0001g0006 a0001c0003t0001g0013 a0001c0003t0001g0017 others(28): Show |
49 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1428+2379T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127611402 | |||||||
| chr3:127611434 | C | T | 1 | a0001c0002t0001g0213 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1428+2411C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127611434 | |||||||
| chr3:127611674 | GCAGCTGA others(319): Show |
G | 14 | a0001c0002t0001g0031 a0001c0002t0001g0075 a0001c0002t0001g0213 others(11): Show |
16 | HG00735.hp1 HG02109.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1428+2665_1428+299 others(4): Show |
MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 127611674 | ||||||
| chr3:127611682 | C | CT | 21 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0009 others(18): Show |
30 | HG00408.hp2 HG00558.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.1428+2693dupT | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 127611682 | ||||||
| chr3:127611682 | C | CTT | 23 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0009 others(20): Show |
44 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1428+2692_1428+269 others(6): Show |
MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 127611682 | ||||||
| chr3:127611682 | C | CTTT | 19 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0016 others(16): Show |
26 | HG00280.hp2 HG01261.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.1428+2691_1428+269 others(7): Show |
MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 127611682 | ||||||
| chr3:127611682 | C | CTTTT | 8 | a0001c0002t0001g0029 a0001c0002t0001g0047 a0001c0002t0001g0051 others(5): Show |
10 | HG00323.hp2 HG01361.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1428+2690_1428+269 others(8): Show |
MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 127611682 | ||||||
| chr3:127611682 | CT | C | 15 | a0001c0001t0001g0045 a0001c0002t0001g0001 a0001c0002t0001g0011 others(12): Show |
20 | HG00099.hp1 HG00738.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.1428+2693delT | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 127611682 | ||||||
| chr3:127611682 | CTT | C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0023 others(15): Show |
25 | HG00544.hp2 HG00639.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1428+2692_1428+269 others(6): Show |
MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 127611682 | ||||||
| chr3:127611682 | CTTT | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
71 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.1428+2691_1428+269 others(7): Show |
MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 127611682 | ||||||
| chr3:127611682 | CTTTT | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(90): Show |
157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.1428+2690_1428+269 others(8): Show |
MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 127611682 | ||||||
| chr3:127611682 | CTTTTT | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0019 others(3): Show |
6 | HG02258.hp2 HG02896.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1428+2689_1428+269 others(9): Show |
MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 127611682 | ||||||
| chr3:127611682 | CTTTTTTT others(8): Show |
C | 2 | a0002c0005t0001g0212 a0002c0005t0001g0215 |
2 | HG01074.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1428+2679_1428+269 others(19): Show |
MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 127611682 | ||||||
| chr3:127611682 | CTTTTTTT others(14): Show |
C | 1 | a0001c0021t0001g0004 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1428+2673_1428+269 others(25): Show |
MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 127611682 | ||||||
| chr3:127611721 | C | T | 4 | a0001c0002t0001g0029 a0001c0002t0001g0205 a0001c0002t0001g0208 others(1): Show |
6 | HG01346.hp1 HG01884.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1428+2698C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127611721 | |||||||
| chr3:127611844 | G | A | 8 | a0002c0005t0001g0054 a0002c0005t0001g0055 a0002c0005t0001g0201 others(5): Show |
10 | HG00738.hp1 HG01074.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1428+2821G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127611844 | |||||||
| chr3:127611910 | G | A | 1 | a0001c0002t0001g0112 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1428+2887G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127611910 | |||||||
| chr3:127611921 | G | T | 3 | a0001c0004t0001g0004 a0001c0004t0001g0021 a0001c0015t0001g0021 |
3 | HG01109.hp2 HG02895.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1428+2898G>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127611921 | |||||||
| chr3:127612021 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1428+2998T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127612021 | |||||||
| chr3:127612068 | C | T | 22 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0019 others(19): Show |
50 | HG00099.hp2 HG00597.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1428+3045C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127612068 | |||||||
| chr3:127612138 | G | A | 1 | a0001c0002t0001g0220 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1428+3115G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127612138 | |||||||
| chr3:127612156 | T | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG00423.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1428+3133T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127612156 | |||||||
| chr3:127612199 | G | A | 1 | a0001c0002t0001g0219 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1428+3176G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127612199 | |||||||
| chr3:127612221 | T | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0110 a0001c0001t0001g0130 |
5 | HG00639.hp2 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1428+3198T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127612221 | |||||||
| chr3:127612304 | T | A | 1 | a0001c0001t0001g0122 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1428+3281T>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127612304 | |||||||
| chr3:127612405 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0135 |
5 | HG00140.hp1 HG01175.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1428+3382A>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127612405 | |||||||
| chr3:127612698 | CGTTTGCT others(43): Show |
C | 1 | a0001c0002t0001g0182 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1429-3151_1429-310 others(54): Show |
MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 127612698 | ||||||
| chr3:127612723 | C | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0126 |
3 | HG02615.hp2 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1429-3139C>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127612723 | |||||||
| chr3:127613168 | A | G | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(114): Show |
213 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.1429-2694A>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127613168 | |||||||
| chr3:127613264 | G | T | 6 | a0001c0002t0001g0031 a0001c0002t0001g0075 a0001c0002t0001g0213 others(3): Show |
7 | HG02109.hp2 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1429-2598G>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127613264 | |||||||
| chr3:127613307 | C | G | 1 | a0001c0002t0001g0218 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1429-2555C>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127613307 | |||||||
| chr3:127613349 | TC | T | 2 | a0001c0002t0001g0029 a0001c0002t0001g0209 |
4 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1429-2512delC | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127613349 | |||||||
| chr3:127613353 | C | G | 2 | a0001c0002t0001g0029 a0001c0002t0001g0209 |
4 | HG01884.hp2 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1429-2509C>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127613353 | |||||||
| chr3:127613395 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1429-2467A>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127613395 | |||||||
| chr3:127614033 | A | G | 1 | a0001c0002t0001g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1429-1829A>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127614033 | |||||||
| chr3:127614060 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1429-1802G>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127614060 | |||||||
| chr3:127614115 | T | G | 1 | a0001c0002t0001g0173 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1429-1747T>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127614115 | |||||||
| chr3:127614231 | C | T | 1 | a0001c0002t0001g0209 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1429-1631C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127614231 | |||||||
| chr3:127614261 | ACT | A | 6 | a0001c0002t0001g0029 a0001c0002t0001g0056 a0001c0002t0001g0202 others(3): Show |
9 | HG01346.hp1 HG01884.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1429-1596_1429-159 others(6): Show |
MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 127614261 | ||||||
| chr3:127614340 | CTGT | C | 39 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0014 others(36): Show |
74 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1429-1514_1429-151 others(7): Show |
MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 127614340 | ||||||
| chr3:127614730 | C | T | 6 | a0001c0006t0001g0052 a0001c0006t0001g0108 a0001c0006t0001g0192 others(3): Show |
7 | HG00735.hp1 HG02257.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1429-1132C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127614730 | |||||||
| chr3:127614792 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1429-1070T>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127614792 | |||||||
| chr3:127614832 | T | C | 6 | a0001c0006t0001g0052 a0001c0006t0001g0108 a0001c0006t0001g0192 others(3): Show |
7 | HG00735.hp1 HG02257.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1429-1030T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127614832 | |||||||
| chr3:127614898 | T | C | 1 | a0002c0005t0001g0206 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1429-964T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127614898 | |||||||
| chr3:127614903 | C | G | 1 | a0001c0002t0001g0112 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1429-959C>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127614903 | |||||||
| chr3:127614949 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1429-913C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127614949 | |||||||
| chr3:127614989 | A | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(108): Show |
207 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1429-873A>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127614989 | |||||||
| chr3:127615007 | G | A | 1 | a0002c0005t0001g0206 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1429-855G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127615007 | |||||||
| chr3:127615026 | G | GCACCCCA others(28): Show |
1 | a0001c0003t0001g0144 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1429-836_1429-835i others(37): Show |
MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127615026 | |||||||
| chr3:127615027 | G | C | 1 | a0001c0003t0001g0144 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1429-835G>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127615027 | |||||||
| chr3:127615030 | G | C | 1 | a0001c0003t0001g0144 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1429-832G>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127615030 | |||||||
| chr3:127615031 | G | A | 1 | a0001c0003t0001g0144 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1429-831G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127615031 | |||||||
| chr3:127615067 | T | C | 1 | a0001c0003t0001g0144 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1429-795T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127615067 | |||||||
| chr3:127615069 | C | A | 1 | a0001c0003t0001g0144 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1429-793C>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127615069 | |||||||
| chr3:127615073 | T | C | 1 | a0001c0003t0001g0144 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1429-789T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127615073 | |||||||
| chr3:127615074 | T | A | 1 | a0001c0003t0001g0144 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1429-788T>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127615074 | |||||||
| chr3:127615076 | A | C | 1 | a0001c0003t0001g0144 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1429-786A>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127615076 | |||||||
| chr3:127615077 | G | A | 1 | a0001c0003t0001g0144 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1429-785G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127615077 | |||||||
| chr3:127615169 | G | A | 2 | a0001c0001t0001g0092 a0001c0002t0001g0095 |
2 | HG01069.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1429-693G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127615169 | |||||||
| chr3:127615221 | C | G | 16 | a0001c0002t0001g0031 a0001c0002t0001g0075 a0001c0002t0001g0213 others(13): Show |
18 | HG00735.hp1 HG02109.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1429-641C>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127615221 | |||||||
| chr3:127615261 | A | G | 2 | a0001c0001t0001g0014 a0006c0009t0001g0014 |
6 | HG03710.hp2 NA18942.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.1429-601A>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127615261 | |||||||
| chr3:127615575 | T | C | 3 | a0002c0005t0001g0054 a0002c0005t0001g0203 a0002c0005t0001g0207 |
4 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1429-287T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127615575 | |||||||
| chr3:127615703 | C | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0154 |
2 | HG04115.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1429-159C>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127615703 | |||||||
| chr3:127615733 | A | C | 1 | a0001c0001t0001g0126 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1429-129A>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127615733 | |||||||
| chr3:127615755 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0030 others(7): Show |
23 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1429-107G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 8/15 | chr3 | 127615755 | |||||||
| chr3:127616056 | G | A | 1 | a0001c0002t0001g0218 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1522+101G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 9/15 | chr3 | 127616056 | |||||||
| chr3:127616083 | G | A | 1 | a0001c0002t0001g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1522+128G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 9/15 | chr3 | 127616083 | |||||||
| chr3:127616399 | C | A | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(179): Show |
328 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.1522+444C>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 9/15 | chr3 | 127616399 | |||||||
| chr3:127616439 | G | A | 1 | a0001c0002t0001g0028 | 3 | HG01255.hp2 NA18961.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1523-429G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 9/15 | chr3 | 127616439 | |||||||
| chr3:127616471 | C | G | 1 | a0001c0002t0001g0175 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1523-397C>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 9/15 | chr3 | 127616471 | |||||||
| chr3:127616555 | C | T | 1 | a0002c0005t0001g0206 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1523-313C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 9/15 | chr3 | 127616555 | |||||||
| chr3:127616643 | C | T | 1 | a0001c0002t0001g0179 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1523-225C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 9/15 | chr3 | 127616643 | |||||||
| chr3:127617130 | G | A | 2 | a0001c0002t0001g0056 a0001c0002t0001g0202 |
3 | HG02257.hp2 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1773+12G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 10/15 | chr3 | 127617130 | |||||||
| chr3:127617497 | G | A | 1 | a0001c0001t0001g0045 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1900+92G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 11/15 | chr3 | 127617497 | |||||||
| chr3:127617707 | G | A | 1 | a0002c0005t0001g0206 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1901-262G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 11/15 | chr3 | 127617707 | |||||||
| chr3:127617770 | T | C | 5 | a0002c0005t0001g0054 a0002c0005t0001g0055 a0002c0005t0001g0201 others(2): Show |
7 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1901-199T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 11/15 | chr3 | 127617770 | |||||||
| chr3:127617943 | G | C | 1 | a0001c0002t0001g0049 | 2 | HG03834.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1901-26G>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 11/15 | chr3 | 127617943 | |||||||
| chr3:127618091 | A | G | 183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(180): Show |
329 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.2013+10A>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 12/15 | chr3 | 127618091 | |||||||
| chr3:127618100 | C | T | 1 | a0001c0006t0001g0195 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2013+19C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 12/15 | chr3 | 127618100 | |||||||
| chr3:127618241 | G | A | 1 | a0001c0002t0001g0218 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2013+160G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 12/15 | chr3 | 127618241 | |||||||
| chr3:127618577 | TTCTC | T | 6 | a0001c0006t0001g0052 a0001c0006t0001g0108 a0001c0006t0001g0192 others(3): Show |
7 | HG00735.hp1 HG02257.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2014-445_2014-442d others(6): Show |
MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr3 | 127618577 | ||||||
| chr3:127618649 | T | TC | 6 | a0001c0006t0001g0052 a0001c0006t0001g0108 a0001c0006t0001g0192 others(3): Show |
7 | HG00735.hp1 HG02257.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2014-377dupC | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr3 | 127618649 | ||||||
| chr3:127618899 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0030 others(7): Show |
23 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.2014-128G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 12/15 | chr3 | 127618899 | |||||||
| chr3:127619437 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0084 a0001c0001t0001g0099 others(1): Show |
7 | HG01975.hp2 HG02273.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.2265+159G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 13/15 | chr3 | 127619437 | |||||||
| chr3:127619446 | C | G | 1 | a0001c0001t0001g0217 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2265+168C>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 13/15 | chr3 | 127619446 | |||||||
| chr3:127619513 | A | G | 2 | a0001c0002t0001g0064 a0007c0018t0001g0178 |
2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.2265+235A>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 13/15 | chr3 | 127619513 | |||||||
| chr3:127619674 | A | G | 22 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0019 others(19): Show |
50 | HG00099.hp2 HG00597.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.2265+396A>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 13/15 | chr3 | 127619674 | |||||||
| chr3:127619797 | T | C | 2 | a0001c0002t0001g0058 a0008c0016t0001g0216 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2265+519T>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 13/15 | chr3 | 127619797 | |||||||
| chr3:127619935 | G | A | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | HG02818.hp2 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2265+657G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 13/15 | chr3 | 127619935 | |||||||
| chr3:127619965 | C | T | 1 | a0002c0005t0001g0206 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2265+687C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 13/15 | chr3 | 127619965 | |||||||
| chr3:127619977 | C | T | 21 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0028 others(18): Show |
40 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.2265+699C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 13/15 | chr3 | 127619977 | |||||||
| chr3:127620169 | C | T | 1 | a0001c0003t0001g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2266-529C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 13/15 | chr3 | 127620169 | |||||||
| chr3:127620228 | G | A | 1 | a0001c0002t0001g0074 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2266-470G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 13/15 | chr3 | 127620228 | |||||||
| chr3:127620308 | G | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0116 a0001c0001t0001g0134 others(2): Show |
6 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.2266-390G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 13/15 | chr3 | 127620308 | |||||||
| chr3:127620330 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2266-368A>G | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 13/15 | chr3 | 127620330 | |||||||
| chr3:127620339 | G | A | 1 | a0001c0006t0001g0194 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2266-359G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 13/15 | chr3 | 127620339 | |||||||
| chr3:127620361 | G | A | 4 | a0001c0002t0001g0139 a0001c0002t0001g0142 a0001c0002t0001g0148 others(1): Show |
4 | NA18961.hp2 NA18965.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.2266-337G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 13/15 | chr3 | 127620361 | |||||||
| chr3:127620894 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0125 |
2 | HG03017.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2448+14G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 14/15 | chr3 | 127620894 | |||||||
| chr3:127621031 | C | T | 1 | a0001c0002t0001g0174 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2449-42C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 14/15 | chr3 | 127621031 | |||||||
| chr3:127621273 | G | A | 1 | a0001c0002t0001g0048 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2604+45G>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 15/15 | chr3 | 127621273 | |||||||
| chr3:127621311 | G | C | 2 | a0001c0002t0001g0058 a0008c0016t0001g0216 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2604+83G>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 15/15 | chr3 | 127621311 | |||||||
| chr3:127621436 | T | A | 1 | a0001c0002t0001g0063 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2604+208T>A | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 15/15 | chr3 | 127621436 | |||||||
| chr3:127621490 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0036 |
4 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2605-173C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 15/15 | chr3 | 127621490 | |||||||
| chr3:127621528 | C | T | 1 | a0001c0003t0001g0039 | 2 | NA18952.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2605-135C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 15/15 | chr3 | 127621528 | |||||||
| chr3:127621539 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2605-124C>T | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 15/15 | chr3 | 127621539 | |||||||
| chr3:127621568 | G | C | 1 | a0008c0016t0001g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2605-95G>C | MCM2 | ENSG00000073111.14 | transcript | ENST00000265056.12 | protein_coding | 15/15 | chr3 | 127621568 |