Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 149175 |
| ensemblid | ENSG00000185090.15 |
| hgncid | 26452 |
| symbol | MANEAL |
| name | mannosidase endo-alpha like |
| refseq_nuc | NM_001113482.2 |
| refseq_prot | NP_001106954.1 |
| ensembl_nuc | ENST00000373045.11 |
| ensembl_prot | ENSP00000362136.6 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 37793847 |
| end | 37801133 |
| strand | + |
| ver | v1.2 |
| region | chr1:37793847-37801133 |
| region5000 | chr1:37788847-37806133 |
| regionname0 | MANEAL_chr1_37793847_37801133 |
| regionname5000 | MANEAL_chr1_37788847_37806133 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 457 | 425 | 87 | 69 | 209 | 14 | 44 | 163 | MANEAL_chr1_37788847_37806133 | MANEAL | MARRR others(452): Show |
chr1 | 37788847 | 37806133 |
| a0002 | 0/0 | 458 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | MANEAL_chr1_37788847_37806133 | MANEAL | MARRR others(453): Show |
chr1 | 37788847 | 37806133 |
| a0003 | 0/0 | 457 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | MARRR others(452): Show |
chr1 | 37788847 | 37806133 |
| a0004 | 0/0 | 457 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MANEAL_chr1_37788847_37806133 | MANEAL | MARRR others(452): Show |
chr1 | 37788847 | 37806133 |
| a0005 | 0/0 | 457 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | MARRR others(452): Show |
chr1 | 37788847 | 37806133 |
| a0006 | 0/0 | 457 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | MARRR others(452): Show |
chr1 | 37788847 | 37806133 |
| a0007 | 0/0 | 272 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | MARRR others(267): Show |
chr1 | 37788847 | 37806133 |
| a0008 | 0/0 | 457 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | MARRR others(452): Show |
chr1 | 37788847 | 37806133 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1371 | 416 | 82 | 67 | 208 | 13 | 44 | MANEAL_chr1_37788847_37806133 | MANEAL | ATGGC others(1366): Show |
chr1 | 37788847 | 37806133 | ||
| a0001c0002 | 0/0 | 1371 | 6 | 5 | 1 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | ATGGC others(1366): Show |
chr1 | 37788847 | 37806133 | ||
| a0001c0004 | 0/0 | 1371 | 2 | 0 | 1 | 0 | 1 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | ATGGC others(1366): Show |
chr1 | 37788847 | 37806133 | ||
| a0001c0007 | 0/0 | 1371 | 1 | 0 | 0 | 1 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | ATGGC others(1366): Show |
chr1 | 37788847 | 37806133 | ||
| a0002c0003 | 0/0 | 1374 | 5 | 0 | 0 | 5 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | ATGGC others(1369): Show |
chr1 | 37788847 | 37806133 | ||
| a0003c0006 | 0/0 | 1371 | 2 | 2 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | ATGGC others(1366): Show |
chr1 | 37788847 | 37806133 | ||
| a0004c0005 | 0/0 | 1371 | 2 | 0 | 0 | 2 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | ATGGC others(1366): Show |
chr1 | 37788847 | 37806133 | ||
| a0005c0009 | 0/0 | 1371 | 1 | 0 | 1 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | ATGGC others(1366): Show |
chr1 | 37788847 | 37806133 | ||
| a0006c0010 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | ATGGC others(1366): Show |
chr1 | 37788847 | 37806133 | ||
| a0007c0008 | 0/0 | 1309 | 1 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | ATGGC others(1304): Show |
chr1 | 37788847 | 37806133 | ||
| a0008c0011 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | ATGGC others(1366): Show |
chr1 | 37788847 | 37806133 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2640 | 294 | 62 | 44 | 140 | 11 | 35 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2635): Show |
chr1 | 37788847 | 37806133 |
| a0001c0001t0002 | 0/0 | 2636 | 94 | 4 | 22 | 59 | 2 | 7 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2631): Show |
chr1 | 37788847 | 37806133 |
| a0001c0001t0003 | 0/0 | 2640 | 7 | 6 | 1 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2635): Show |
chr1 | 37788847 | 37806133 |
| a0001c0001t0004 | 0/0 | 2640 | 5 | 5 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2635): Show |
chr1 | 37788847 | 37806133 |
| a0001c0001t0005 | 0/0 | 2640 | 6 | 0 | 0 | 6 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2635): Show |
chr1 | 37788847 | 37806133 |
| a0001c0001t0006 | 0/0 | 2640 | 3 | 3 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2635): Show |
chr1 | 37788847 | 37806133 |
| a0001c0001t0007 | 0/0 | 2640 | 2 | 0 | 0 | 2 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2635): Show |
chr1 | 37788847 | 37806133 |
| a0001c0001t0008 | 0/0 | 2640 | 2 | 2 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2635): Show |
chr1 | 37788847 | 37806133 |
| a0001c0001t0009 | 0/0 | 2640 | 1 | 0 | 0 | 0 | 0 | 1 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2635): Show |
chr1 | 37788847 | 37806133 |
| a0001c0001t0010 | 0/0 | 2640 | 1 | 0 | 0 | 1 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2635): Show |
chr1 | 37788847 | 37806133 |
| a0001c0001t0011 | 0/0 | 2640 | 1 | 0 | 0 | 0 | 0 | 1 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2635): Show |
chr1 | 37788847 | 37806133 |
| a0001c0002t0001 | 0/0 | 2640 | 6 | 5 | 1 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2635): Show |
chr1 | 37788847 | 37806133 |
| a0001c0004t0002 | 0/0 | 2636 | 2 | 0 | 1 | 0 | 1 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2631): Show |
chr1 | 37788847 | 37806133 |
| a0001c0007t0001 | 0/0 | 2640 | 1 | 0 | 0 | 1 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2635): Show |
chr1 | 37788847 | 37806133 |
| a0002c0003t0001 | 0/0 | 2643 | 5 | 0 | 0 | 5 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2638): Show |
chr1 | 37788847 | 37806133 |
| a0003c0006t0001 | 0/0 | 2640 | 2 | 2 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2635): Show |
chr1 | 37788847 | 37806133 |
| a0004c0005t0001 | 0/0 | 2640 | 2 | 0 | 0 | 2 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2635): Show |
chr1 | 37788847 | 37806133 |
| a0005c0009t0001 | 0/0 | 2640 | 1 | 0 | 1 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2635): Show |
chr1 | 37788847 | 37806133 |
| a0006c0010t0004 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2635): Show |
chr1 | 37788847 | 37806133 |
| a0007c0008t0001 | 0/0 | 2578 | 1 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2573): Show |
chr1 | 37788847 | 37806133 |
| a0008c0011t0001 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | AGGCG others(2635): Show |
chr1 | 37788847 | 37806133 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 159 | 33 | 25 | 75 | 5 | 20 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0002 | 0/0 | 88 | 0 | 15 | 56 | 6 | 11 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0004 | 1/0 | 15 | 14 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0010 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0002g0003 | 0/0 | 84 | 1 | 20 | 54 | 2 | 7 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0002g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0003g0007 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0004g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0005g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0006g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0007g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0008g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0009g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0001t0011g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0002t0001g0001 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0004t0002g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0001c0007t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0002c0003t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0003c0006t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0004c0005t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0005c0009t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0006c0010t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0007c0008t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| a0008c0011t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00280 | hp1 | a0001 | c0004 | t0002 | g0003 | EUR | FIN | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01433 | hp2 | a0005 | c0009 | t0001 | g0001 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01943 | hp2 | a0001 | c0004 | t0002 | g0003 | AMR | PEL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | ACB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0001 | AFR | ACB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | ACB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02615 | hp1 | a0006 | c0010 | t0004 | g0006 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02723 | hp2 | a0003 | c0006 | t0001 | g0014 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02735 | hp1 | a0001 | c0001 | t0009 | g0004 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02922 | hp2 | a0003 | c0006 | t0001 | g0014 | AFR | ESN | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0032 | AFR | ESN | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03209 | hp2 | a0007 | c0008 | t0001 | g0034 | AFR | MSL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | MSL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | MSL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | ESN | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | STU | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG04115 | hp2 | a0001 | c0001 | t0011 | g0002 | SAS | STU | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | STU | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18945 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18963 | hp2 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18966 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18970 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18971 | hp2 | a0004 | c0005 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18973 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18989 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18991 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19001 | hp2 | a0001 | c0007 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19003 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19011 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | LWK | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | LWK | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19065 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19066 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19076 | hp2 | a0004 | c0005 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ASW | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | USA | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | USA | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18955 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | USA | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA21309 | hp1 | a0008 | c0011 | t0001 | g0001 | AFR | LWK | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | MANEAL_chr1_37788847_37806133 | MANEAL | chr1 | 37788847 | 37806133 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:37794210 | A | G | 1 | a0008 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.28A>G | p.Ile10Val | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 1/4 | 364/2640 | 28/1374 | 10/457 | chr1 | 37794210 | |||
| chr1:37794300 | C | T | 1 | a0003 | 2 | HG02723.hp2 HG02922.hp2 |
missense_variant | MODERATE | c.118C>T | p.Pro40Ser | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 1/4 | 454/2640 | 118/1374 | 40/457 | chr1 | 37794300 | |||
| chr1:37794389 | C | CCCG | 1 | a0002 | 5 | NA18955.hp1 NA18966.hp1 NA18989.hp2 others(2): Show |
disruptive_inframe_insertion | MODERATE | c.222_224dupGCC | p.Pro75dup | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 1/4 | 561/2640 | 225/1374 | 75/457 | INFO_REALIGN_3_PRIME | chr1 | 37794389 | ||
| chr1:37794586 | C | T | 1 | a0004 | 2 | NA18971.hp2 NA19076.hp2 |
missense_variant | MODERATE | c.404C>T | p.Pro135Leu | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 1/4 | 740/2640 | 404/1374 | 135/457 | chr1 | 37794586 | |||
| chr1:37799587 | T | A | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.758T>A | p.Phe253Tyr | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1094/2640 | 758/1374 | 253/457 | chr1 | 37799587 | |||
| chr1:37799592 | C | G | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.763C>G | p.Arg255Gly | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1099/2640 | 763/1374 | 255/457 | chr1 | 37799592 | |||
| chr1:37799593 | G | T | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.764G>T | p.Arg255Leu | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1100/2640 | 764/1374 | 255/457 | chr1 | 37799593 | |||
| chr1:37799599 | A | C | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.770A>C | p.Lys257Thr | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1106/2640 | 770/1374 | 257/457 | chr1 | 37799599 | |||
| chr1:37799603 | C | G | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.774C>G | p.Asn258Lys | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1110/2640 | 774/1374 | 258/457 | chr1 | 37799603 | |||
| chr1:37799623 | C | A | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.794C>A | p.Pro265Gln | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1130/2640 | 794/1374 | 265/457 | chr1 | 37799623 | |||
| chr1:37799631 | T | A | 1 | a0005 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.802T>A | p.Tyr268Asn | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1138/2640 | 802/1374 | 268/457 | chr1 | 37799631 | |||
| chr1:37799640 | G | C | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.811G>C | p.Asp271His | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1147/2640 | 811/1374 | 271/457 | chr1 | 37799640 | |||
| chr1:37799641 | A | G | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.812A>G | p.Asp271Gly | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1148/2640 | 812/1374 | 271/457 | chr1 | 37799641 | |||
| chr1:37799642 | C | A | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.813C>A | p.Asp271Glu | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1149/2640 | 813/1374 | 271/457 | chr1 | 37799642 | |||
| chr1:37799648 | C | A | 1 | a0007 | 1 | HG03209.hp2 | stop_gained | HIGH | c.819C>A | p.Tyr273* | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1155/2640 | 819/1374 | 273/457 | chr1 | 37799648 | |||
| chr1:37799658 | C | A | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.829C>A | p.Pro277Thr | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1165/2640 | 829/1374 | 277/457 | chr1 | 37799658 | |||
| chr1:37799671 | C | G | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.842C>G | p.Ala281Gly | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1178/2640 | 842/1374 | 281/457 | chr1 | 37799671 | |||
| chr1:37799706 | C | A | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.877C>A | p.Arg293Ser | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1213/2640 | 877/1374 | 293/457 | chr1 | 37799706 | |||
| chr1:37799709 | A | C | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.880A>C | p.Asn294His | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1216/2640 | 880/1374 | 294/457 | chr1 | 37799709 | |||
| chr1:37799712 | A | C | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.883A>C | p.Thr295Pro | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1219/2640 | 883/1374 | 295/457 | chr1 | 37799712 | |||
| chr1:37799713 | C | T | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.884C>T | p.Thr295Met | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1220/2640 | 884/1374 | 295/457 | chr1 | 37799713 | |||
| chr1:37799720 | C | G | 1 | a0007 | 1 | HG03209.hp2 | stop_gained | HIGH | c.891C>G | p.Tyr297* | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1227/2640 | 891/1374 | 297/457 | chr1 | 37799720 | |||
| chr1:37799721 | G | C | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.892G>C | p.Asp298His | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1228/2640 | 892/1374 | 298/457 | chr1 | 37799721 | |||
| chr1:37799724 | G | C | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.895G>C | p.Gly299Arg | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1231/2640 | 895/1374 | 299/457 | chr1 | 37799724 | |||
| chr1:37799727 | G | T | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.898G>T | p.Val300Phe | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1234/2640 | 898/1374 | 300/457 | chr1 | 37799727 | |||
| chr1:37799766 | G | A | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.937G>A | p.Asp313Asn | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1273/2640 | 937/1374 | 313/457 | chr1 | 37799766 | |||
| chr1:37799767 | A | G | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.938A>G | p.Asp313Gly | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1274/2640 | 938/1374 | 313/457 | chr1 | 37799767 | |||
| chr1:37799779 | C | A | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.950C>A | p.Ala317Asp | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1286/2640 | 950/1374 | 317/457 | chr1 | 37799779 | |||
| chr1:37799789 | C | A | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.960C>A | p.Asp320Glu | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1296/2640 | 960/1374 | 320/457 | chr1 | 37799789 | |||
| chr1:37799844 | A | T | 1 | a0005 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.1015A>T | p.Asn339Tyr | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1351/2640 | 1015/1374 | 339/457 | chr1 | 37799844 | |||
| chr1:37799856 | G | C | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1027G>C | p.Val343Leu | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1363/2640 | 1027/1374 | 343/457 | chr1 | 37799856 | |||
| chr1:37799896 | C | T | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1067C>T | p.Pro356Leu | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1403/2640 | 1067/1374 | 356/457 | chr1 | 37799896 | |||
| chr1:37799922 | A | C | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1093A>C | p.Thr365Pro | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1429/2640 | 1093/1374 | 365/457 | chr1 | 37799922 | |||
| chr1:37799925 | A | T | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1096A>T | p.Ser366Cys | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1432/2640 | 1096/1374 | 366/457 | chr1 | 37799925 | |||
| chr1:37799929 | T | A | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1100T>A | p.Ile367Asn | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1436/2640 | 1100/1374 | 367/457 | chr1 | 37799929 | |||
| chr1:37799942 | C | G | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1113C>G | p.Asn371Lys | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1449/2640 | 1113/1374 | 371/457 | chr1 | 37799942 | |||
| chr1:37799943 | A | G | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1114A>G | p.Asn372Asp | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1450/2640 | 1114/1374 | 372/457 | chr1 | 37799943 | |||
| chr1:37799944 | A | G | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1115A>G | p.Asn372Ser | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1451/2640 | 1115/1374 | 372/457 | chr1 | 37799944 | |||
| chr1:37799946 | C | T | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1117C>T | p.His373Tyr | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1453/2640 | 1117/1374 | 373/457 | chr1 | 37799946 | |||
| chr1:37799947 | A | C | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1118A>C | p.His373Pro | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1454/2640 | 1118/1374 | 373/457 | chr1 | 37799947 | |||
| chr1:37799950 | A | G | 1 | a0006 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.1121A>G | p.Asn374Ser | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1457/2640 | 1121/1374 | 374/457 | chr1 | 37799950 | |||
| chr1:37799952 | ACGCGCAA others(3): Show |
A | 1 | a0007 | 1 | HG03209.hp2 | frameshift_variant | HIGH | c.1124_1133delCGCGCA others(4): Show |
p.Thr375fs | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1460/2640 | 1124/1374 | 375/457 | chr1 | 37799952 | |||
| chr1:37799965 | T | A | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1136T>A | p.Val379Asp | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1472/2640 | 1136/1374 | 379/457 | chr1 | 37799965 | |||
| chr1:37799974 | A | G | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1145A>G | p.Lys382Arg | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1481/2640 | 1145/1374 | 382/457 | chr1 | 37799974 | |||
| chr1:37799975 | G | T | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1146G>T | p.Lys382Asn | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1482/2640 | 1146/1374 | 382/457 | chr1 | 37799975 | |||
| chr1:37799980 | A | C | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1151A>C | p.Tyr384Ser | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1487/2640 | 1151/1374 | 384/457 | chr1 | 37799980 | |||
| chr1:37799989 | C | G | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1160C>G | p.Ala387Gly | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1496/2640 | 1160/1374 | 387/457 | chr1 | 37799989 | |||
| chr1:37799992 | T | A | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1163T>A | p.Leu388Gln | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1499/2640 | 1163/1374 | 388/457 | chr1 | 37799992 | |||
| chr1:37799994 | C | T | 1 | a0007 | 1 | HG03209.hp2 | stop_gained | HIGH | c.1165C>T | p.Gln389* | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1501/2640 | 1165/1374 | 389/457 | chr1 | 37799994 | |||
| chr1:37800025 | T | A | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1196T>A | p.Val399Asp | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1532/2640 | 1196/1374 | 399/457 | chr1 | 37800025 | |||
| chr1:37800030 | A | T | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1201A>T | p.Ile401Phe | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1537/2640 | 1201/1374 | 401/457 | chr1 | 37800030 | |||
| chr1:37800037 | C | G | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1208C>G | p.Ser403Cys | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1544/2640 | 1208/1374 | 403/457 | chr1 | 37800037 | |||
| chr1:37800039 | T | A | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1210T>A | p.Phe404Ile | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1546/2640 | 1210/1374 | 404/457 | chr1 | 37800039 | |||
| chr1:37800040 | T | C | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1211T>C | p.Phe404Ser | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1547/2640 | 1211/1374 | 404/457 | chr1 | 37800040 | |||
| chr1:37800044 | T | A | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1215T>A | p.Asn405Lys | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1551/2640 | 1215/1374 | 405/457 | chr1 | 37800044 | |||
| chr1:37800046 | AGTGGCAC others(45): Show |
A | 1 | a0007 | 1 | HG03209.hp2 | frameshift_variant | HIGH | c.1218_1269delGTGGCA others(46): Show |
p.Glu406fs | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1554/2640 | 1218/1374 | 406/457 | chr1 | 37800046 | |||
| chr1:37800099 | C | T | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1270C>T | p.Arg424Cys | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1606/2640 | 1270/1374 | 424/457 | chr1 | 37800099 | |||
| chr1:37800102 | C | G | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1273C>G | p.Leu425Val | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1609/2640 | 1273/1374 | 425/457 | chr1 | 37800102 | |||
| chr1:37800115 | A | T | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1286A>T | p.Tyr429Phe | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1622/2640 | 1286/1374 | 429/457 | chr1 | 37800115 | |||
| chr1:37800117 | C | A | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1288C>A | p.Leu430Met | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1624/2640 | 1288/1374 | 430/457 | chr1 | 37800117 | |||
| chr1:37800118 | T | A | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1289T>A | p.Leu430Gln | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1625/2640 | 1289/1374 | 430/457 | chr1 | 37800118 | |||
| chr1:37800120 | C | A | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1291C>A | p.Pro431Thr | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1627/2640 | 1291/1374 | 431/457 | chr1 | 37800120 | |||
| chr1:37800121 | C | G | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1292C>G | p.Pro431Arg | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1628/2640 | 1292/1374 | 431/457 | chr1 | 37800121 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:37794200 | C | T | 1 | a0001c0002 | 6 | HG01109.hp2 HG02809.hp1 HG03098.hp1 others(3): Show |
synonymous_variant | LOW | c.18C>T | p.Arg6Arg | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 1/4 | 354/2640 | 18/1374 | 6/457 | chr1 | 37794200 | |||
| chr1:37794530 | G | A | 1 | a0001c0007 | 1 | NA19001.hp2 | synonymous_variant | LOW | c.348G>A | p.Pro116Pro | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 1/4 | 684/2640 | 348/1374 | 116/457 | chr1 | 37794530 | |||
| chr1:37799624 | A | T | 1 | a0007c0008 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.795A>T | p.Pro265Pro | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1131/2640 | 795/1374 | 265/457 | chr1 | 37799624 | |||
| chr1:37799729 | C | G | 1 | a0007c0008 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.900C>G | p.Val300Val | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1236/2640 | 900/1374 | 300/457 | chr1 | 37799729 | |||
| chr1:37799780 | C | T | 1 | a0007c0008 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.951C>T | p.Ala317Ala | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1287/2640 | 951/1374 | 317/457 | chr1 | 37799780 | |||
| chr1:37799831 | T | A | 1 | a0007c0008 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1002T>A | p.Gly334Gly | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1338/2640 | 1002/1374 | 334/457 | chr1 | 37799831 | |||
| chr1:37799894 | C | A | 1 | a0007c0008 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1065C>A | p.Ile355Ile | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1401/2640 | 1065/1374 | 355/457 | chr1 | 37799894 | |||
| chr1:37799903 | G | T | 1 | a0007c0008 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1074G>T | p.Val358Val | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1410/2640 | 1074/1374 | 358/457 | chr1 | 37799903 | |||
| chr1:37799912 | C | A | 1 | a0007c0008 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1083C>A | p.Gly361Gly | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1419/2640 | 1083/1374 | 361/457 | chr1 | 37799912 | |||
| chr1:37799924 | C | A | 1 | a0007c0008 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1095C>A | p.Thr365Thr | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1431/2640 | 1095/1374 | 365/457 | chr1 | 37799924 | |||
| chr1:37799933 | G | A | 1 | a0007c0008 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1104G>A | p.Arg368Arg | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1440/2640 | 1104/1374 | 368/457 | chr1 | 37799933 | |||
| chr1:37799936 | C | A | 1 | a0007c0008 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1107C>A | p.Pro369Pro | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1443/2640 | 1107/1374 | 369/457 | chr1 | 37799936 | |||
| chr1:37799948 | C | T | 1 | a0007c0008 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1119C>T | p.His373His | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1455/2640 | 1119/1374 | 373/457 | chr1 | 37799948 | |||
| chr1:37799981 | T | C | 1 | a0001c0004 | 2 | HG00280.hp1 HG01943.hp2 |
synonymous_variant | LOW | c.1152T>C | p.Tyr384Tyr | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1488/2640 | 1152/1374 | 384/457 | chr1 | 37799981 | |||
| chr1:37799987 | G | A | 1 | a0007c0008 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1158G>A | p.Thr386Thr | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1494/2640 | 1158/1374 | 386/457 | chr1 | 37799987 | |||
| chr1:37800002 | C | A | 1 | a0007c0008 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1173C>A | p.Ala391Ala | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1509/2640 | 1173/1374 | 391/457 | chr1 | 37800002 | |||
| chr1:37800032 | T | C | 1 | a0007c0008 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1203T>C | p.Ile401Ile | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1539/2640 | 1203/1374 | 401/457 | chr1 | 37800032 | |||
| chr1:37800035 | C | A | 1 | a0007c0008 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1206C>A | p.Thr402Thr | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1542/2640 | 1206/1374 | 402/457 | chr1 | 37800035 | |||
| chr1:37800041 | C | T | 1 | a0007c0008 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1212C>T | p.Phe404Phe | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1548/2640 | 1212/1374 | 404/457 | chr1 | 37800041 | |||
| chr1:37800104 | G | T | 1 | a0007c0008 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1275G>T | p.Leu425Leu | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1611/2640 | 1275/1374 | 425/457 | chr1 | 37800104 | |||
| chr1:37800122 | T | G | 1 | a0007c0008 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1293T>G | p.Pro431Pro | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 1629/2640 | 1293/1374 | 431/457 | chr1 | 37800122 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:37793863 | C | G | 1 | a0001c0001t0005 | 6 | NA18945.hp1 NA18972.hp2 NA18973.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-320C>G | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 1/4 | 320 | chr1 | 37793863 | ||||||
| chr1:37793959 | G | C | 1 | a0001c0001t0009 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-224G>C | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 1/4 | 224 | chr1 | 37793959 | ||||||
| chr1:37794055 | G | A | 1 | a0001c0001t0010 | 1 | NA18970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-128G>A | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 1/4 | 128 | chr1 | 37794055 | ||||||
| chr1:37794128 | C | T | 1 | a0001c0001t0008 | 2 | HG02451.hp1 HG03225.hp2 |
5_prime_UTR_variant | MODIFIER | c.-55C>T | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 1/4 | 55 | chr1 | 37794128 | ||||||
| chr1:37800316 | C | T | 2 | a0001c0001t0004 a0006c0010t0004 |
6 | HG02615.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*113C>T | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 113 | chr1 | 37800316 | ||||||
| chr1:37800339 | C | T | 1 | a0001c0001t0007 | 2 | NA18963.hp2 NA18991.hp1 |
3_prime_UTR_variant | MODIFIER | c.*136C>T | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 136 | chr1 | 37800339 | ||||||
| chr1:37800558 | T | A | 1 | a0001c0001t0003 | 7 | HG01069.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*355T>A | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 355 | chr1 | 37800558 | ||||||
| chr1:37800920 | T | C | 1 | a0001c0001t0006 | 3 | HG02145.hp2 HG02451.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*717T>C | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 717 | chr1 | 37800920 | ||||||
| chr1:37801053 | AACTG | A | 2 | a0001c0001t0002 a0001c0004t0002 |
96 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*856_*859delCTGA | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 856 | INFO_REALIGN_3_PRIME | chr1 | 37801053 | |||||
| chr1:37801117 | T | G | 1 | a0001c0001t0011 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*914T>G | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 4/4 | 914 | chr1 | 37801117 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:37794761 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.550+29G>A | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 1/3 | chr1 | 37794761 | |||||||
| chr1:37794765 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.550+33C>T | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 1/3 | chr1 | 37794765 | |||||||
| chr1:37794831 | C | T | 13 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0002g0003 others(10): Show |
108 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.550+99C>T | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 1/3 | chr1 | 37794831 | |||||||
| chr1:37794908 | C | T | 1 | a0001c0001t0001g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.550+176C>T | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 1/3 | chr1 | 37794908 | |||||||
| chr1:37795061 | C | T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0029 others(4): Show |
100 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.550+329C>T | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 1/3 | chr1 | 37795061 | |||||||
| chr1:37795324 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.551-413G>A | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 1/3 | chr1 | 37795324 | |||||||
| chr1:37795377 | A | G | 2 | a0001c0001t0003g0007 a0001c0001t0003g0027 |
5 | HG01069.hp2 HG02109.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.551-360A>G | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 1/3 | chr1 | 37795377 | |||||||
| chr1:37795426 | G | C | 3 | a0001c0001t0006g0015 a0001c0001t0006g0032 a0003c0006t0001g0014 |
5 | HG02145.hp2 HG02451.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.551-311G>C | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 1/3 | chr1 | 37795426 | |||||||
| chr1:37795462 | C | A | 1 | a0001c0001t0001g0018 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.551-275C>A | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 1/3 | chr1 | 37795462 | |||||||
| chr1:37795638 | T | G | 1 | a0001c0001t0001g0005 | 7 | HG00558.hp2 HG02129.hp1 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.551-99T>G | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 1/3 | chr1 | 37795638 | |||||||
| chr1:37795955 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.660+109G>A | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 2/3 | chr1 | 37795955 | |||||||
| chr1:37795985 | G | A | 1 | a0001c0001t0002g0011 | 3 | HG02647.hp2 HG02717.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.660+139G>A | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 2/3 | chr1 | 37795985 | |||||||
| chr1:37796625 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.661-119A>G | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 2/3 | chr1 | 37796625 | |||||||
| chr1:37796841 | G | C | 1 | a0001c0001t0001g0018 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.737+21G>C | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37796841 | |||||||
| chr1:37797133 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.737+313C>T | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37797133 | |||||||
| chr1:37797216 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.737+396C>T | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37797216 | |||||||
| chr1:37797360 | C | T | 1 | a0001c0001t0002g0012 | 3 | HG02027.hp1 NA18982.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.737+540C>T | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37797360 | |||||||
| chr1:37797464 | CT | C | 39 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(36): Show |
401 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(398): Show |
intron_variant | MODIFIER | c.737+660delT | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 37797464 | ||||||
| chr1:37797464 | CTT | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0003c0006t0001g0014 others(1): Show |
8 | HG01884.hp1 HG02723.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.737+659_737+660del others(2): Show |
MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 37797464 | ||||||
| chr1:37797554 | TCTGCCTC others(19): Show |
T | 1 | a0001c0001t0001g0001 | 4 | HG02615.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+742_737+767del others(26): Show |
MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 37797554 | ||||||
| chr1:37797645 | A | G | 1 | a0001c0001t0003g0027 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.737+825A>G | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37797645 | |||||||
| chr1:37797689 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.737+869C>T | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37797689 | |||||||
| chr1:37797890 | C | G | 1 | a0001c0001t0001g0010 | 3 | HG01167.hp2 HG01169.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.737+1070C>G | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37797890 | |||||||
| chr1:37797967 | T | C | 1 | a0001c0001t0006g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.737+1147T>C | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37797967 | |||||||
| chr1:37798076 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.737+1256A>G | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37798076 | |||||||
| chr1:37798150 | TA | T | 3 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0006c0010t0004g0006 |
6 | HG02615.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.737+1337delA | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 37798150 | ||||||
| chr1:37798158 | C | CA | 2 | a0001c0001t0001g0033 a0001c0001t0002g0011 |
4 | HG02647.hp2 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+1341dupA | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 37798158 | ||||||
| chr1:37798162 | C | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0002g0003 others(9): Show |
104 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.737+1342C>A | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37798162 | |||||||
| chr1:37798338 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.738-1229G>A | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37798338 | |||||||
| chr1:37798679 | G | C | 1 | a0001c0001t0001g0013 | 2 | HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.738-888G>C | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37798679 | |||||||
| chr1:37798907 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.738-660C>T | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37798907 | |||||||
| chr1:37798995 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.738-572G>A | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37798995 | |||||||
| chr1:37799066 | A | G | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-501A>G | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799066 | |||||||
| chr1:37799074 | A | C | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-493A>C | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799074 | |||||||
| chr1:37799086 | C | A | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.738-481C>A | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799086 | |||||||
| chr1:37799147 | T | G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(20): Show |
223 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.738-420T>G | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799147 | |||||||
| chr1:37799148 | C | G | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-419C>G | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799148 | |||||||
| chr1:37799186 | C | A | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-381C>A | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799186 | |||||||
| chr1:37799187 | G | A | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-380G>A | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799187 | |||||||
| chr1:37799206 | G | T | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-361G>T | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799206 | |||||||
| chr1:37799213 | T | G | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-354T>G | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799213 | |||||||
| chr1:37799230 | G | A | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-337G>A | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799230 | |||||||
| chr1:37799254 | C | G | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-313C>G | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799254 | |||||||
| chr1:37799266 | A | G | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-301A>G | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799266 | |||||||
| chr1:37799273 | A | G | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-294A>G | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799273 | |||||||
| chr1:37799319 | G | T | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-248G>T | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799319 | |||||||
| chr1:37799328 | T | A | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-239T>A | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799328 | |||||||
| chr1:37799347 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.738-220G>A | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799347 | |||||||
| chr1:37799364 | G | T | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-203G>T | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799364 | |||||||
| chr1:37799376 | G | T | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-191G>T | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799376 | |||||||
| chr1:37799377 | A | G | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-190A>G | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799377 | |||||||
| chr1:37799378 | G | A | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-189G>A | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799378 | |||||||
| chr1:37799380 | C | A | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-187C>A | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799380 | |||||||
| chr1:37799433 | G | T | 1 | a0001c0001t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.738-134G>T | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799433 | |||||||
| chr1:37799468 | C | G | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-99C>G | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799468 | |||||||
| chr1:37799471 | A | T | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-96A>T | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799471 | |||||||
| chr1:37799487 | A | G | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-80A>G | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799487 | |||||||
| chr1:37799540 | G | C | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-27G>C | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799540 | |||||||
| chr1:37799541 | C | G | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.738-26C>G | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799541 | |||||||
| chr1:37799559 | C | A | 1 | a0007c0008t0001g0034 | 1 | HG03209.hp2 | splice_region_variant&intron_variant | LOW | c.738-8C>A | MANEAL | ENSG00000185090.15 | transcript | ENST00000373045.11 | protein_coding | 3/3 | chr1 | 37799559 |