Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11184 |
| ensemblid | ENSG00000104814.13 |
| hgncid | 6863 |
| symbol | MAP4K1 |
| name | mitogen-activated protein kinase kinase kinase kinase 1 |
| refseq_nuc | NM_001042600.3 |
| refseq_prot | NP_001036065.1 |
| ensembl_nuc | ENST00000396857.7 |
| ensembl_prot | ENSP00000380066.1 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 38587641 |
| end | 38617953 |
| strand | - |
| ver | v1.2 |
| region | chr19:38587641-38617953 |
| region5000 | chr19:38582641-38622953 |
| regionname0 | MAP4K1_chr19_38587641_38617953 |
| regionname5000 | MAP4K1_chr19_38582641_38622953 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 821 | 334 | 80 | 66 | 139 | 8 | 39 | 101 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | MDVVD others(816): Show |
chr19 | 38582641 | 38622953 |
| a0002 | 0/0 | 821 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | MDVVD others(816): Show |
chr19 | 38582641 | 38622953 |
| a0003 | 0/0 | 821 | 3 | 0 | 0 | 1 | 0 | 2 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | MDVVD others(816): Show |
chr19 | 38582641 | 38622953 |
| a0004 | 0/0 | 821 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | MDVVD others(816): Show |
chr19 | 38582641 | 38622953 |
| a0005 | 0/0 | 821 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | MDVVD others(816): Show |
chr19 | 38582641 | 38622953 |
| a0006 | 0/0 | 821 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | MDVVD others(816): Show |
chr19 | 38582641 | 38622953 |
| a0007 | 0/0 | 821 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | MDVVD others(816): Show |
chr19 | 38582641 | 38622953 |
| a0008 | 0/0 | 821 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | MDVVD others(816): Show |
chr19 | 38582641 | 38622953 |
| a0009 | 0/0 | 821 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | MDVVD others(816): Show |
chr19 | 38582641 | 38622953 |
| a0010 | 0/0 | 821 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | MDVVD others(816): Show |
chr19 | 38582641 | 38622953 |
| a0011 | 0/0 | 821 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | MDVVD others(816): Show |
chr19 | 38582641 | 38622953 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2463 | 243 | 66 | 53 | 86 | 8 | 28 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0001c0002 | 0/0 | 2463 | 56 | 4 | 4 | 38 | 0 | 10 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0001c0003 | 0/0 | 2463 | 11 | 0 | 1 | 10 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0001c0004 | 0/0 | 2463 | 9 | 5 | 3 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0001c0005 | 0/0 | 2463 | 4 | 4 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0001c0007 | 0/0 | 2463 | 3 | 0 | 3 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0001c0009 | 0/0 | 2463 | 3 | 0 | 0 | 3 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0001c0014 | 0/0 | 2463 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0001c0015 | 0/0 | 2463 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0001c0018 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0001c0019 | 0/0 | 2463 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0001c0020 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0002c0008 | 0/0 | 2463 | 3 | 0 | 0 | 3 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0003c0006 | 0/0 | 2463 | 3 | 0 | 0 | 1 | 0 | 2 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0004c0016 | 0/0 | 2463 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0005c0012 | 0/0 | 2463 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0006c0013 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0007c0017 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0008c0022 | 0/0 | 2463 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0009c0021 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0010c0010 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 | ||
| a0011c0011 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | ATGGA others(2458): Show |
chr19 | 38582641 | 38622953 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2631 | 241 | 66 | 53 | 86 | 8 | 26 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0001c0001t0002 | 0/0 | 2631 | 2 | 0 | 0 | 0 | 0 | 2 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0001c0002t0001 | 0/0 | 2631 | 56 | 4 | 4 | 38 | 0 | 10 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0001c0003t0001 | 0/0 | 2631 | 11 | 0 | 1 | 10 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0001c0004t0001 | 0/0 | 2631 | 9 | 5 | 3 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0001c0005t0001 | 0/0 | 2631 | 4 | 4 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0001c0007t0001 | 0/0 | 2631 | 3 | 0 | 3 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0001c0009t0001 | 0/0 | 2631 | 3 | 0 | 0 | 3 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0001c0014t0001 | 0/0 | 2631 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0001c0015t0001 | 0/0 | 2631 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0001c0018t0001 | 0/0 | 2631 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0001c0019t0001 | 0/0 | 2631 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0001c0020t0001 | 0/0 | 2631 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0002c0008t0001 | 0/0 | 2631 | 3 | 0 | 0 | 3 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0003c0006t0001 | 0/0 | 2631 | 3 | 0 | 0 | 1 | 0 | 2 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0004c0016t0001 | 0/0 | 2631 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0005c0012t0001 | 0/0 | 2631 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0006c0013t0001 | 0/0 | 2631 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0007c0017t0001 | 0/0 | 2631 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0008c0022t0001 | 0/0 | 2631 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0009c0021t0001 | 0/0 | 2631 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0010c0010t0001 | 0/0 | 2631 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| a0011c0011t0001 | 0/0 | 2631 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | AGTTG others(2626): Show |
chr19 | 38582641 | 38622953 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0004 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0004t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0004t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0004t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0004t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0004t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0004t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0004t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0005t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0005t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0005t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0005t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0007t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0007t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0007t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0009t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0009t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0009t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0014t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0015t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0018t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0019t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0001c0020t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0002c0008t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0002c0008t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0002c0008t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0003c0006t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0003c0006t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0004c0016t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0005c0012t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0006c0013t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0007c0017t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0008c0022t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0009c0021t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0010c0010t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| a0011c0011t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | GBR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | GBR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | FIN | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0211 | EUR | FIN | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00423 | hp1 | a0001 | c0020 | t0001 | g0239 | EAS | CHS | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00438 | hp2 | a0001 | c0003 | t0001 | g0307 | EAS | CHS | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00544 | hp1 | a0002 | c0008 | t0001 | g0171 | EAS | CHS | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | CHS | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | CHS | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | CHS | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG00741 | hp2 | a0001 | c0007 | t0001 | g0141 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0227 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0269 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01106 | hp1 | a0004 | c0016 | t0001 | g0152 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01168 | hp2 | a0001 | c0004 | t0001 | g0210 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01169 | hp1 | a0001 | c0004 | t0001 | g0213 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01256 | hp1 | a0001 | c0007 | t0001 | g0142 | AMR | CLM | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01256 | hp2 | a0001 | c0004 | t0001 | g0208 | AMR | CLM | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01258 | hp1 | a0001 | c0007 | t0001 | g0140 | AMR | CLM | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | IBS | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | IBS | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0265 | AFR | ACB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01891 | hp2 | a0001 | c0005 | t0001 | g0218 | AFR | ACB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0267 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01952 | hp1 | a0001 | c0019 | t0001 | g0243 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01978 | hp2 | a0001 | c0014 | t0001 | g0154 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0311 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02040 | hp1 | a0001 | c0009 | t0001 | g0253 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02071 | hp2 | a0001 | c0009 | t0001 | g0315 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02074 | hp2 | a0002 | c0008 | t0001 | g0220 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02132 | hp2 | a0001 | c0009 | t0001 | g0272 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0240 | AFR | ACB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0242 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CDX | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CDX | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02257 | hp1 | a0001 | c0005 | t0001 | g0216 | AFR | ACB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02300 | hp2 | a0005 | c0012 | t0001 | g0189 | AMR | PEL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02451 | hp2 | a0006 | c0013 | t0001 | g0219 | AFR | ACB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0273 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0249 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0312 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02896 | hp2 | a0007 | c0017 | t0001 | g0016 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0013 | AFR | ESN | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02970 | hp1 | a0001 | c0004 | t0001 | g0334 | AFR | ESN | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | ESN | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0022 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | ESN | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03139 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | ESN | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03453 | hp1 | a0001 | c0005 | t0001 | g0217 | AFR | MSL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | MSL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0266 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | MSL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0261 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0238 | SAS | PJL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0241 | SAS | BEB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03834 | hp1 | a0003 | c0006 | t0001 | g0007 | SAS | BEB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03927 | hp2 | a0008 | c0022 | t0001 | g0335 | SAS | BEB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03942 | hp1 | a0001 | c0015 | t0001 | g0068 | SAS | BEB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0306 | SAS | BEB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG04115 | hp1 | a0003 | c0006 | t0001 | g0007 | SAS | STU | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | STU | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0245 | SAS | BEB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | STU | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0260 | SAS | STU | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | STU | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18522 | hp2 | a0001 | c0018 | t0001 | g0190 | AFR | YRI | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | CHB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | CHB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | CHB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18941 | hp1 | a0001 | c0003 | t0001 | g0248 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0257 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0319 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18951 | hp2 | a0002 | c0008 | t0001 | g0172 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18959 | hp1 | a0009 | c0021 | t0001 | g0143 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18964 | hp2 | a0010 | c0010 | t0001 | g0286 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0316 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18974 | hp2 | a0003 | c0006 | t0001 | g0074 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18984 | hp2 | a0011 | c0011 | t0001 | g0176 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18990 | hp1 | a0001 | c0003 | t0001 | g0246 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18991 | hp2 | a0001 | c0003 | t0001 | g0310 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0264 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | LWK | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | LWK | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0317 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19057 | hp2 | a0001 | c0004 | t0001 | g0059 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19063 | hp1 | a0001 | c0003 | t0001 | g0277 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19074 | hp1 | a0001 | c0003 | t0001 | g0262 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19083 | hp1 | a0001 | c0003 | t0001 | g0247 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19088 | hp1 | a0001 | c0003 | t0001 | g0270 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA19240 | hp2 | a0001 | c0005 | t0001 | g0215 | AFR | YRI | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ASW | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ASW | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0309 | SAS | GIH | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0258 | AMR | CLM | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ACB | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | USA | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | USA | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | USA | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA20300 | hp2 | a0001 | c0004 | t0001 | g0014 | AFR | USA | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| NA21309 | hp2 | a0001 | c0004 | t0001 | g0012 | AFR | LWK | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0092 | REF | REF | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0102 | REF | REF | MAP4K1_chr19_38582641_38622953 | MAP4K1 | chr19 | 38582641 | 38622953 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:38596425 | G | C | 1 | a0004 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.2003C>G | p.Ser668Cys | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 26/31 | 2061/2631 | 2003/2466 | 668/821 | chr19 | 38596425 | |||
| chr19:38605619 | G | A | 1 | a0007 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.1312C>T | p.Arg438Cys | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 18/31 | 1370/2631 | 1312/2466 | 438/821 | chr19 | 38605619 | |||
| chr19:38605690 | A | G | 1 | a0006 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.1241T>C | p.Met414Thr | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 18/31 | 1299/2631 | 1241/2466 | 414/821 | chr19 | 38605690 | |||
| chr19:38605696 | C | T | 1 | a0005 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.1235G>A | p.Gly412Glu | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 18/31 | 1293/2631 | 1235/2466 | 412/821 | chr19 | 38605696 | |||
| chr19:38608126 | G | A | 1 | a0002 | 3 | HG00544.hp1 HG02074.hp2 NA18951.hp2 |
missense_variant | MODERATE | c.1051C>T | p.Pro351Ser | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 14/31 | 1109/2631 | 1051/2466 | 351/821 | chr19 | 38608126 | |||
| chr19:38609932 | C | G | 1 | a0011 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.904G>C | p.Asp302His | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 12/31 | 962/2631 | 904/2466 | 302/821 | chr19 | 38609932 | |||
| chr19:38609937 | A | G | 1 | a0003 | 3 | HG03834.hp1 HG04115.hp1 NA18974.hp2 |
missense_variant | MODERATE | c.899T>C | p.Ile300Thr | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 12/31 | 957/2631 | 899/2466 | 300/821 | chr19 | 38609937 | |||
| chr19:38609994 | C | T | 1 | a0010 | 1 | NA18964.hp2 | missense_variant | MODERATE | c.842G>A | p.Arg281Gln | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 12/31 | 900/2631 | 842/2466 | 281/821 | chr19 | 38609994 | |||
| chr19:38612665 | G | A | 1 | a0009 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.611C>T | p.Thr204Met | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 9/31 | 669/2631 | 611/2466 | 204/821 | chr19 | 38612665 | |||
| chr19:38617394 | G | A | 1 | a0008 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.208C>T | p.Arg70Trp | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 3/31 | 266/2631 | 208/2466 | 70/821 | chr19 | 38617394 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:38595940 | A | G | 2 | a0001c0003 a0002c0008 |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
splice_region_variant&synonymous_variant | LOW | c.2178T>C | p.Asp726Asp | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 27/31 | 2236/2631 | 2178/2466 | 726/821 | chr19 | 38595940 | |||
| chr19:38595964 | T | C | 7 | a0001c0002 a0001c0003 a0001c0004 others(4): Show |
82 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(79): Show |
synonymous_variant | LOW | c.2154A>G | p.Glu718Glu | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 27/31 | 2212/2631 | 2154/2466 | 718/821 | chr19 | 38595964 | |||
| chr19:38597339 | C | T | 1 | a0001c0015 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.1824G>A | p.Arg608Arg | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 24/31 | 1882/2631 | 1824/2466 | 608/821 | chr19 | 38597339 | |||
| chr19:38601502 | C | T | 1 | a0001c0014 | 1 | HG01978.hp2 | synonymous_variant | LOW | c.1470G>A | p.Leu490Leu | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 20/31 | 1528/2631 | 1470/2466 | 490/821 | chr19 | 38601502 | |||
| chr19:38605590 | G | A | 1 | a0001c0020 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.1341C>T | p.Ser447Ser | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 18/31 | 1399/2631 | 1341/2466 | 447/821 | chr19 | 38605590 | |||
| chr19:38605665 | C | G | 1 | a0001c0019 | 1 | HG01952.hp1 | synonymous_variant | LOW | c.1266G>C | p.Pro422Pro | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 18/31 | 1324/2631 | 1266/2466 | 422/821 | chr19 | 38605665 | |||
| chr19:38607872 | G | A | 1 | a0001c0018 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.1149C>T | p.Asp383Asp | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 16/31 | 1207/2631 | 1149/2466 | 383/821 | chr19 | 38607872 | |||
| chr19:38609657 | A | C | 1 | a0001c0007 | 3 | HG00741.hp2 HG01256.hp1 HG01258.hp1 |
synonymous_variant | LOW | c.945T>G | p.Pro315Pro | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/31 | 1003/2631 | 945/2466 | 315/821 | chr19 | 38609657 | |||
| chr19:38609954 | G | A | 5 | a0001c0002 a0001c0003 a0001c0009 others(2): Show |
72 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(69): Show |
synonymous_variant | LOW | c.882C>T | p.Pro294Pro | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 12/31 | 940/2631 | 882/2466 | 294/821 | chr19 | 38609954 | |||
| chr19:38611077 | G | T | 1 | a0001c0005 | 4 | HG01891.hp2 HG02257.hp1 HG03453.hp1 others(1): Show |
synonymous_variant | LOW | c.784C>A | p.Arg262Arg | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/31 | 842/2631 | 784/2466 | 262/821 | chr19 | 38611077 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:38587707 | G | C | 1 | a0001c0001t0002 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*41C>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 31/31 | 41 | chr19 | 38587707 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:38587844 | C | T | 3 | a0001c0001t0001g0151 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG03490.hp1 HG03492.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2397-27G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38587844 | |||||||
| chr19:38587934 | T | C | 105 | a0001c0001t0001g0101 a0001c0001t0001g0113 a0001c0001t0001g0147 others(102): Show |
105 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.2397-117A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38587934 | |||||||
| chr19:38587978 | AAGG | A | 4 | a0001c0005t0001g0215 a0001c0005t0001g0216 a0001c0005t0001g0217 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2397-164_2397-162d others(5): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38587978 | |||||||
| chr19:38588030 | GTCTGGCA others(10): Show |
G | 1 | a0001c0001t0001g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2397-230_2397-214d others(19): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38588030 | |||||||
| chr19:38588211 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2397-394G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38588211 | |||||||
| chr19:38588222 | G | A | 1 | a0001c0002t0001g0256 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2397-405C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38588222 | |||||||
| chr19:38588275 | A | G | 1 | a0001c0005t0001g0218 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2397-458T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38588275 | |||||||
| chr19:38588428 | T | C | 4 | a0001c0002t0001g0234 a0001c0002t0001g0237 a0001c0002t0001g0323 others(1): Show |
4 | HG01952.hp1 NA19000.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.2397-611A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38588428 | |||||||
| chr19:38588431 | T | C | 4 | a0001c0002t0001g0234 a0001c0002t0001g0237 a0001c0002t0001g0323 others(1): Show |
4 | HG01952.hp1 NA19000.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.2397-614A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38588431 | |||||||
| chr19:38588506 | T | C | 1 | a0004c0016t0001g0152 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2397-689A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38588506 | |||||||
| chr19:38588584 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG00642.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2397-767T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38588584 | |||||||
| chr19:38588612 | G | T | 2 | a0001c0002t0001g0268 a0001c0002t0001g0276 |
2 | HG02056.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.2397-795C>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38588612 | |||||||
| chr19:38588626 | A | AC | 173 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0020 others(170): Show |
174 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.2397-810dupG | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38588626 | |||||||
| chr19:38588632 | G | A | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0197 |
3 | NA18949.hp2 NA18998.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2397-815C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38588632 | |||||||
| chr19:38588700 | C | T | 87 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(84): Show |
87 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.2397-883G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38588700 | |||||||
| chr19:38588724 | C | T | 2 | a0001c0001t0001g0282 a0001c0001t0001g0291 |
2 | HG02083.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.2397-907G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38588724 | |||||||
| chr19:38588730 | C | T | 2 | a0001c0001t0002g0166 a0001c0001t0002g0167 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2397-913G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38588730 | |||||||
| chr19:38588751 | C | CA | 9 | a0001c0001t0001g0151 a0001c0001t0001g0201 a0001c0001t0001g0202 others(6): Show |
9 | HG00741.hp2 HG02738.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.2397-935dupT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38588751 | |||||||
| chr19:38588751 | CA | C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0099 others(6): Show |
9 | HG01069.hp1 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2397-935delT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38588751 | |||||||
| chr19:38588768 | A | T | 1 | a0001c0001t0001g0044 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2397-951T>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38588768 | |||||||
| chr19:38588950 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0125 |
2 | NA18942.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.2397-1133C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38588950 | |||||||
| chr19:38589107 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1290T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589107 | |||||||
| chr19:38589108 | C | G | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1291G>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589108 | |||||||
| chr19:38589109 | A | T | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1292T>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589109 | |||||||
| chr19:38589110 | A | T | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1293T>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589110 | |||||||
| chr19:38589113 | A | T | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1296T>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589113 | |||||||
| chr19:38589120 | C | A | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1303G>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589120 | |||||||
| chr19:38589121 | A | T | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1304T>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589121 | |||||||
| chr19:38589131 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1314G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589131 | |||||||
| chr19:38589132 | A | T | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1315T>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589132 | |||||||
| chr19:38589133 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1316T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589133 | |||||||
| chr19:38589138 | T | G | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1321A>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589138 | |||||||
| chr19:38589140 | C | A | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1323G>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589140 | |||||||
| chr19:38589141 | T | G | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1324A>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589141 | |||||||
| chr19:38589145 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1328T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589145 | |||||||
| chr19:38589146 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1329G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589146 | |||||||
| chr19:38589149 | G | T | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1332C>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589149 | |||||||
| chr19:38589152 | G | T | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1335C>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589152 | |||||||
| chr19:38589165 | C | A | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1348G>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589165 | |||||||
| chr19:38589166 | G | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0163 |
2 | HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2397-1349C>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589166 | |||||||
| chr19:38589166 | G | T | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1349C>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589166 | |||||||
| chr19:38589168 | T | C | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1351A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589168 | |||||||
| chr19:38589171 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1354G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589171 | |||||||
| chr19:38589177 | C | A | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1360G>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589177 | |||||||
| chr19:38589183 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1366T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589183 | |||||||
| chr19:38589184 | T | G | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1367A>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589184 | |||||||
| chr19:38589186 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2397-1369G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589186 | |||||||
| chr19:38589258 | G | T | 1 | a0001c0001t0001g0329 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2397-1441C>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589258 | |||||||
| chr19:38589432 | T | A | 1 | a0001c0001t0001g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2397-1615A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589432 | |||||||
| chr19:38589478 | C | T | 1 | a0007c0017t0001g0016 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2397-1661G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589478 | |||||||
| chr19:38589519 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0147 a0001c0001t0001g0163 |
3 | HG02300.hp1 HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2397-1702C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589519 | |||||||
| chr19:38589540 | C | T | 14 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0248 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2397-1723G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589540 | |||||||
| chr19:38589541 | G | A | 1 | a0007c0017t0001g0016 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2397-1724C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589541 | |||||||
| chr19:38589641 | C | G | 1 | a0001c0001t0001g0211 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2397-1824G>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589641 | |||||||
| chr19:38589668 | G | A | 5 | a0001c0005t0001g0215 a0001c0005t0001g0216 a0001c0005t0001g0217 others(2): Show |
5 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2397-1851C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589668 | |||||||
| chr19:38589761 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2397-1944C>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589761 | |||||||
| chr19:38589778 | C | G | 1 | a0001c0001t0001g0147 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2397-1961G>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589778 | |||||||
| chr19:38589814 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2397-1997C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589814 | |||||||
| chr19:38589879 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2397-2062T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38589879 | |||||||
| chr19:38590021 | A | C | 1 | a0001c0001t0001g0333 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2397-2204T>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590021 | |||||||
| chr19:38590088 | C | G | 23 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0063 others(20): Show |
24 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.2397-2271G>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590088 | |||||||
| chr19:38590171 | A | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0039 |
2 | HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2397-2354T>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590171 | |||||||
| chr19:38590177 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2397-2360T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590177 | |||||||
| chr19:38590304 | T | C | 334 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(331): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.2397-2487A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590304 | |||||||
| chr19:38590305 | T | C | 1 | a0001c0002t0001g0251 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2397-2488A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590305 | |||||||
| chr19:38590306 | T | A | 334 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(331): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.2397-2489A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590306 | |||||||
| chr19:38590309 | T | A | 1 | a0001c0002t0001g0251 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2397-2492A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590309 | |||||||
| chr19:38590310 | T | A | 334 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(331): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.2397-2493A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590310 | |||||||
| chr19:38590312 | T | A | 1 | a0001c0002t0001g0251 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2397-2495A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590312 | |||||||
| chr19:38590314 | T | G | 334 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(331): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.2397-2497A>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590314 | |||||||
| chr19:38590315 | T | G | 1 | a0001c0002t0001g0251 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2397-2498A>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590315 | |||||||
| chr19:38590317 | T | C | 334 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(331): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.2397-2500A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590317 | |||||||
| chr19:38590373 | G | GAAA | 7 | a0001c0002t0001g0227 a0001c0002t0001g0254 a0001c0002t0001g0268 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.2397-2559_2397-255 others(7): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590373 | |||||||
| chr19:38590373 | G | GAAAA | 6 | a0001c0002t0001g0232 a0001c0002t0001g0242 a0001c0002t0001g0244 others(3): Show |
6 | HG00609.hp1 HG02015.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.2397-2560_2397-255 others(8): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590373 | |||||||
| chr19:38590373 | G | GAAAAAAA others(3): Show |
3 | a0001c0002t0001g0245 a0001c0002t0001g0318 a0001c0002t0001g0320 |
3 | HG04184.hp2 NA18943.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.2397-2566_2397-255 others(14): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590373 | |||||||
| chr19:38590373 | G | GAAAAAAA others(4): Show |
2 | a0001c0002t0001g0018 a0001c0002t0001g0259 |
2 | NA19003.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2397-2567_2397-255 others(15): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590373 | |||||||
| chr19:38590373 | G | GAAAAAAA others(5): Show |
2 | a0001c0002t0001g0312 a0001c0002t0001g0316 |
2 | HG02738.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.2397-2568_2397-255 others(16): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590373 | |||||||
| chr19:38590373 | G | GAAAAAAA others(12): Show |
1 | a0001c0002t0001g0321 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2397-2575_2397-255 others(23): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590373 | |||||||
| chr19:38590373 | GA | G | 10 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0031 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.2397-2557delT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590373 | |||||||
| chr19:38590373 | GAA | G | 9 | a0001c0001t0001g0076 a0001c0001t0001g0093 a0001c0001t0001g0117 others(6): Show |
9 | HG01517.hp1 HG02027.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.2397-2558_2397-255 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590373 | |||||||
| chr19:38590373 | GAAA | G | 8 | a0001c0001t0001g0035 a0001c0001t0001g0058 a0001c0001t0001g0060 others(5): Show |
9 | HG00738.hp2 HG01169.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.2397-2559_2397-255 others(7): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590373 | |||||||
| chr19:38590373 | GAAAA | G | 11 | a0001c0001t0001g0036 a0001c0001t0001g0062 a0001c0001t0001g0080 others(8): Show |
11 | HG01109.hp1 HG01168.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.2397-2560_2397-255 others(8): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590373 | |||||||
| chr19:38590373 | GAAAAA | G | 11 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0044 others(8): Show |
11 | HG00733.hp2 HG02083.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2397-2561_2397-255 others(9): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590373 | |||||||
| chr19:38590373 | GAAAAAA | G | 20 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0045 others(17): Show |
21 | HG00609.hp2 HG00738.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.2397-2562_2397-255 others(10): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590373 | |||||||
| chr19:38590373 | GAAAAAAA others(3): Show |
G | 1 | a0001c0001t0001g0081 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2397-2566_2397-255 others(14): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590373 | |||||||
| chr19:38590373 | GAAAAAAA others(8): Show |
G | 1 | a0001c0001t0001g0103 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2397-2571_2397-255 others(19): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590373 | |||||||
| chr19:38590383 | AAAAAAAA others(20): Show |
A | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2397-2593_2397-256 others(31): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590383 | |||||||
| chr19:38590384 | AAAAAAAA others(17): Show |
A | 1 | a0001c0001t0001g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2397-2591_2397-256 others(28): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590384 | |||||||
| chr19:38590384 | AAAAAAAA others(21): Show |
A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
6 | HG00642.hp2 HG02622.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2397-2595_2397-256 others(32): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590384 | |||||||
| chr19:38590385 | AAAAAAAA others(18): Show |
A | 1 | a0001c0001t0001g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2397-2593_2397-256 others(29): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590385 | |||||||
| chr19:38590386 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0302 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2397-2570_2397-256 others(14): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590386 | |||||||
| chr19:38590386 | A | ATATATAT others(6): Show |
1 | a0010c0010t0001g0286 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2397-2570_2397-256 others(17): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590386 | |||||||
| chr19:38590386 | A | T | 2 | a0001c0001t0001g0079 a0001c0007t0001g0141 |
2 | HG00741.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.2397-2569T>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590386 | |||||||
| chr19:38590386 | AAAAAAAA others(3): Show |
A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0146 |
3 | HG03225.hp1 HG03225.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2397-2579_2397-257 others(14): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590386 | |||||||
| chr19:38590386 | AAAAAAAA others(15): Show |
A | 1 | a0001c0001t0001g0067 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2397-2591_2397-257 others(26): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590386 | |||||||
| chr19:38590386 | AAAAAAAA others(17): Show |
A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0001c0001t0001g0148 |
3 | HG00735.hp2 HG02698.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2397-2593_2397-257 others(28): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590386 | |||||||
| chr19:38590386 | AAAAAAAA others(23): Show |
A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0173 |
2 | HG00733.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.2397-2599_2397-257 others(34): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590386 | |||||||
| chr19:38590387 | AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0001g0329 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2397-2587_2397-257 others(21): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590387 | |||||||
| chr19:38590387 | AAAAAAAA others(16): Show |
A | 6 | a0001c0001t0001g0065 a0001c0001t0001g0170 a0001c0001t0001g0180 others(3): Show |
6 | HG01070.hp2 HG01106.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.2397-2593_2397-257 others(27): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590387 | |||||||
| chr19:38590387 | AAAAAAAA others(22): Show |
A | 1 | a0001c0001t0001g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2397-2599_2397-257 others(33): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590387 | |||||||
| chr19:38590388 | A | AATATATA others(5): Show |
2 | a0001c0001t0001g0136 a0001c0001t0001g0283 |
2 | HG03041.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.2397-2572_2397-257 others(16): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590388 | |||||||
| chr19:38590388 | A | AATATATA others(7): Show |
1 | a0001c0001t0001g0084 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2397-2572_2397-257 others(18): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590388 | |||||||
| chr19:38590388 | A | AATATATA others(9): Show |
1 | a0001c0001t0001g0197 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2397-2572_2397-257 others(20): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590388 | |||||||
| chr19:38590388 | A | AT | 3 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0008c0022t0001g0335 |
3 | HG01943.hp2 HG01975.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2397-2572_2397-257 others(5): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590388 | |||||||
| chr19:38590388 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0002 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2397-2572_2397-257 others(15): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590388 | |||||||
| chr19:38590388 | A | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0043 others(14): Show |
17 | HG00642.hp1 HG00741.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.2397-2571T>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590388 | |||||||
| chr19:38590388 | AAAAAAAA others(7): Show |
A | 3 | a0001c0001t0001g0137 a0002c0008t0001g0171 a0002c0008t0001g0220 |
3 | HG00544.hp1 HG02074.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2397-2585_2397-257 others(18): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590388 | |||||||
| chr19:38590388 | AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0298 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2397-2587_2397-257 others(20): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590388 | |||||||
| chr19:38590388 | AAAAAAAA others(17): Show |
A | 1 | a0001c0001t0001g0019 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2397-2595_2397-257 others(28): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590388 | |||||||
| chr19:38590388 | AAAAAAAA others(19): Show |
A | 1 | a0001c0001t0001g0150 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2397-2597_2397-257 others(30): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590388 | |||||||
| chr19:38590388 | AAAAAAAA others(21): Show |
A | 1 | a0001c0001t0001g0191 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2397-2599_2397-257 others(32): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590388 | |||||||
| chr19:38590388 | AAAAAAAA others(23): Show |
A | 25 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(22): Show |
25 | HG00621.hp2 HG01123.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.2397-2601_2397-257 others(34): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590388 | |||||||
| chr19:38590388 | AAAAAAAA others(25): Show |
A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0155 a0001c0001t0001g0297 |
3 | HG02071.hp1 HG02080.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.2397-2603_2397-257 others(36): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590388 | |||||||
| chr19:38590389 | AAAAAAAT others(8): Show |
A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0331 |
2 | HG02647.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2397-2587_2397-257 others(19): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590389 | |||||||
| chr19:38590389 | AAAAAAAT others(10): Show |
A | 1 | a0006c0013t0001g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2397-2589_2397-257 others(21): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590389 | |||||||
| chr19:38590389 | AAAAAAAT others(12): Show |
A | 4 | a0001c0001t0001g0049 a0001c0001t0001g0326 a0001c0001t0001g0327 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2397-2591_2397-257 others(23): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590389 | |||||||
| chr19:38590390 | A | AATATATA others(3): Show |
2 | a0001c0001t0001g0100 a0001c0001t0001g0145 |
2 | HG00438.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2397-2574_2397-257 others(14): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590390 | |||||||
| chr19:38590390 | A | AATATATA others(7): Show |
1 | a0001c0001t0001g0005 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2397-2574_2397-257 others(18): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590390 | |||||||
| chr19:38590390 | A | AT | 3 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0001g0183 |
3 | HG02897.hp2 HG03209.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.2397-2574_2397-257 others(5): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590390 | |||||||
| chr19:38590390 | A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0206 a0001c0001t0001g0209 |
2 | HG00140.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.2397-2574_2397-257 others(15): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590390 | |||||||
| chr19:38590390 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0153 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2397-2574_2397-257 others(17): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590390 | |||||||
| chr19:38590390 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0077 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2397-2574_2397-257 others(19): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590390 | |||||||
| chr19:38590390 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0072 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2397-2574_2397-257 others(23): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590390 | |||||||
| chr19:38590390 | A | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(50): Show |
55 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.2397-2573T>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590390 | |||||||
| chr19:38590390 | AAAAAATA others(5): Show |
A | 1 | a0001c0003t0001g0246 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2397-2585_2397-257 others(16): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590390 | |||||||
| chr19:38590390 | AAAAAATA others(7): Show |
A | 5 | a0001c0003t0001g0257 a0001c0003t0001g0258 a0001c0003t0001g0262 others(2): Show |
5 | HG01123.hp1 NA18945.hp1 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.2397-2587_2397-257 others(18): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590390 | |||||||
| chr19:38590390 | AAAAAATA others(23): Show |
A | 1 | a0001c0001t0001g0161 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2397-2603_2397-257 others(34): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590390 | |||||||
| chr19:38590390 | AAAAAATA others(25): Show |
A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(4): Show |
8 | HG00423.hp2 HG00558.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.2397-2605_2397-257 others(36): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590390 | |||||||
| chr19:38590391 | AAAAATAT others(8): Show |
A | 1 | a0002c0008t0001g0172 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2397-2589_2397-257 others(19): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590391 | |||||||
| chr19:38590392 | A | AATATATA others(7): Show |
1 | a0001c0001t0001g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2397-2576_2397-257 others(18): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590392 | |||||||
| chr19:38590392 | A | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
86 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.2397-2575T>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590392 | |||||||
| chr19:38590392 | AAAATATA others(7): Show |
A | 2 | a0001c0003t0001g0248 a0001c0003t0001g0307 |
2 | HG00438.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.2397-2589_2397-257 others(18): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590392 | |||||||
| chr19:38590392 | AAAATATA others(15): Show |
A | 1 | a0001c0001t0001g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2397-2597_2397-257 others(26): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590392 | |||||||
| chr19:38590392 | AAAATATA others(17): Show |
A | 1 | a0001c0001t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2397-2599_2397-257 others(28): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590392 | |||||||
| chr19:38590393 | AAATATAT others(10): Show |
A | 1 | a0001c0001t0001g0163 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2397-2593_2397-257 others(21): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590393 | |||||||
| chr19:38590394 | A | AAAAAAAA others(13): Show |
1 | a0001c0002t0001g0221 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2397-2578_2397-257 others(24): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAA others(12): Show |
2 | a0001c0002t0001g0271 a0001c0002t0001g0323 |
2 | NA18612.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2397-2578_2397-257 others(23): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAA others(13): Show |
1 | a0001c0002t0001g0237 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2397-2578_2397-257 others(24): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAA others(19): Show |
1 | a0001c0002t0001g0275 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2397-2578_2397-257 others(30): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAA others(15): Show |
1 | a0001c0002t0001g0223 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2397-2578_2397-257 others(26): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAA others(8): Show |
1 | a0001c0019t0001g0243 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2397-2578_2397-257 others(19): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAA others(12): Show |
1 | a0001c0002t0001g0022 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2397-2578_2397-257 others(23): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAA others(9): Show |
1 | a0001c0002t0001g0234 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2397-2578_2397-257 others(20): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAA others(13): Show |
2 | a0001c0002t0001g0235 a0001c0002t0001g0240 |
2 | HG02145.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.2397-2578_2397-257 others(24): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAA others(25): Show |
1 | a0001c0002t0001g0222 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2397-2578_2397-257 others(36): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAA others(10): Show |
2 | a0001c0002t0001g0228 a0001c0002t0001g0233 |
2 | NA18947.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2397-2578_2397-257 others(21): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAA others(12): Show |
1 | a0001c0002t0001g0276 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2397-2578_2397-257 others(23): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAA others(24): Show |
1 | a0001c0002t0001g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2397-2578_2397-257 others(35): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAA others(13): Show |
1 | a0001c0002t0001g0260 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2397-2578_2397-257 others(24): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAA others(12): Show |
1 | a0001c0002t0001g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2397-2578_2397-257 others(23): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAA others(16): Show |
2 | a0001c0002t0001g0226 a0001c0002t0001g0266 |
2 | HG03540.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.2397-2578_2397-257 others(27): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAA others(3): Show |
1 | a0001c0002t0001g0306 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2397-2578_2397-257 others(14): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAA others(13): Show |
1 | a0001c0002t0001g0252 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2397-2578_2397-257 others(24): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAA others(10): Show |
1 | a0001c0002t0001g0250 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2397-2578_2397-257 others(21): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAA others(12): Show |
1 | a0001c0002t0001g0251 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2397-2578_2397-257 others(23): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAA others(21): Show |
1 | a0001c0002t0001g0309 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2397-2578_2397-257 others(32): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAAAT others(10): Show |
1 | a0001c0002t0001g0261 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2397-2578_2397-257 others(21): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | AAAAAATA others(9): Show |
1 | a0001c0002t0001g0263 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2397-2578_2397-257 others(20): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | A | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.2397-2577T>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | AATATATA others(3): Show |
A | 4 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0328 others(1): Show |
4 | HG03130.hp2 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2397-2587_2397-257 others(14): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590394 | AATATATA others(11): Show |
A | 4 | a0001c0005t0001g0215 a0001c0005t0001g0216 a0001c0005t0001g0217 others(1): Show |
4 | HG00423.hp1 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2397-2595_2397-257 others(22): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590394 | |||||||
| chr19:38590395 | AT | A | 3 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0015 |
3 | HG02965.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2397-2579delA | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590395 | |||||||
| chr19:38590395 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0333 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2397-2589_2397-257 others(15): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590395 | |||||||
| chr19:38590395 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0203 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2397-2595_2397-257 others(21): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590395 | |||||||
| chr19:38590395 | ATATATAT others(12): Show |
A | 1 | a0001c0005t0001g0218 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2397-2597_2397-257 others(23): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590395 | |||||||
| chr19:38590396 | T | A | 33 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0224 others(30): Show |
33 | HG00609.hp1 HG01069.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.2397-2579A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590396 | |||||||
| chr19:38590398 | T | A | 33 | a0001c0002t0001g0017 a0001c0002t0001g0224 a0001c0002t0001g0225 others(30): Show |
33 | HG00609.hp1 HG01069.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.2397-2581A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590398 | |||||||
| chr19:38590400 | T | A | 28 | a0001c0002t0001g0225 a0001c0002t0001g0227 a0001c0002t0001g0232 others(25): Show |
28 | HG00609.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.2397-2583A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590400 | |||||||
| chr19:38590402 | T | A | 20 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0002t0001g0227 others(17): Show |
20 | HG01069.hp1 HG01071.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.2397-2585A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590402 | |||||||
| chr19:38590404 | T | A | 12 | a0001c0001t0001g0337 a0001c0001t0002g0166 a0001c0001t0002g0167 others(9): Show |
12 | HG01069.hp1 HG01071.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.2397-2587A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590404 | |||||||
| chr19:38590406 | T | A | 6 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0328 others(3): Show |
6 | HG02896.hp2 HG02970.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2397-2589A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590406 | |||||||
| chr19:38590408 | T | A | 5 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0328 others(2): Show |
5 | HG01109.hp2 HG02896.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2397-2591A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590408 | |||||||
| chr19:38590410 | T | A | 4 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0333 others(1): Show |
4 | HG01109.hp2 HG02896.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2397-2593A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590410 | |||||||
| chr19:38590412 | T | A | 1 | a0001c0001t0001g0201 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2397-2595A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590412 | |||||||
| chr19:38590414 | T | A | 2 | a0001c0001t0001g0203 a0001c0020t0001g0239 |
2 | HG00423.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2397-2597A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590414 | |||||||
| chr19:38590415 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2397-2598T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590415 | |||||||
| chr19:38590416 | T | A | 2 | a0001c0001t0001g0203 a0001c0020t0001g0239 |
2 | HG00423.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2397-2599A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590416 | |||||||
| chr19:38590418 | T | A | 1 | a0001c0020t0001g0239 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2397-2601A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590418 | |||||||
| chr19:38590420 | T | A | 1 | a0001c0020t0001g0239 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2397-2603A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590420 | |||||||
| chr19:38590422 | T | A | 1 | a0001c0020t0001g0239 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2397-2605A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590422 | |||||||
| chr19:38590436 | T | A | 6 | a0001c0001t0001g0126 a0001c0005t0001g0215 a0001c0005t0001g0216 others(3): Show |
6 | HG01358.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2397-2619A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590436 | |||||||
| chr19:38590472 | T | G | 82 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0022 others(79): Show |
82 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.2397-2655A>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590472 | |||||||
| chr19:38590484 | G | A | 1 | a0001c0001t0001g0336 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2397-2667C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590484 | |||||||
| chr19:38590495 | C | G | 1 | a0001c0001t0001g0300 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2397-2678G>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590495 | |||||||
| chr19:38590621 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2396+2661G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590621 | |||||||
| chr19:38590744 | G | A | 10 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0201 others(7): Show |
10 | HG01109.hp2 HG02615.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.2396+2538C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590744 | |||||||
| chr19:38590755 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2396+2527C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590755 | |||||||
| chr19:38590898 | C | A | 1 | a0001c0001t0001g0181 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2396+2384G>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590898 | |||||||
| chr19:38590901 | T | C | 14 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0248 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2396+2381A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590901 | |||||||
| chr19:38590965 | T | TCA | 21 | a0001c0001t0001g0019 a0001c0001t0001g0038 a0001c0001t0001g0050 others(18): Show |
21 | HG00621.hp2 HG00642.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.2396+2315_2396+231 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590965 | |||||||
| chr19:38590965 | T | TCACA | 5 | a0001c0001t0001g0024 a0001c0001t0001g0097 a0001c0001t0001g0125 others(2): Show |
5 | HG00642.hp2 HG02040.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.2396+2313_2396+231 others(8): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590965 | |||||||
| chr19:38590965 | TCA | T | 54 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0093 others(51): Show |
54 | HG00558.hp1 HG01884.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.2396+2315_2396+231 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590965 | |||||||
| chr19:38590965 | TCACA | T | 27 | a0001c0001t0001g0030 a0001c0001t0001g0329 a0001c0001t0001g0330 others(24): Show |
27 | HG00438.hp2 HG00544.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.2396+2313_2396+231 others(8): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590965 | |||||||
| chr19:38590965 | TCACACA | T | 20 | a0001c0001t0001g0203 a0001c0002t0001g0017 a0001c0002t0001g0225 others(17): Show |
20 | HG00423.hp1 HG00609.hp1 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.2396+2311_2396+231 others(10): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590965 | |||||||
| chr19:38590965 | TCACACAC others(1): Show |
T | 9 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(6): Show |
9 | HG01109.hp2 HG02615.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.2396+2309_2396+231 others(12): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590965 | |||||||
| chr19:38590965 | TCACACAC others(3): Show |
T | 3 | a0001c0001t0001g0080 a0001c0001t0001g0337 a0001c0002t0001g0254 |
3 | HG02083.hp2 HG02155.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2396+2307_2396+231 others(14): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38590965 | |||||||
| chr19:38591002 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2396+2280A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38591002 | |||||||
| chr19:38591091 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2396+2191C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38591091 | |||||||
| chr19:38591198 | G | GAA | 10 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0201 others(7): Show |
10 | HG01109.hp2 HG02615.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.2396+2082_2396+208 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38591198 | |||||||
| chr19:38591209 | G | T | 1 | a0001c0001t0001g0200 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2396+2073C>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38591209 | |||||||
| chr19:38591214 | A | G | 14 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0248 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2396+2068T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38591214 | |||||||
| chr19:38591316 | G | T | 68 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0022 others(65): Show |
68 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.2396+1966C>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38591316 | |||||||
| chr19:38591347 | G | A | 68 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0022 others(65): Show |
68 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.2396+1935C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38591347 | |||||||
| chr19:38591391 | C | T | 14 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0248 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2396+1891G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38591391 | |||||||
| chr19:38591463 | A | G | 28 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0029 others(25): Show |
29 | HG00642.hp1 HG01884.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.2396+1819T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38591463 | |||||||
| chr19:38591526 | C | CA | 7 | a0001c0001t0001g0110 a0001c0001t0001g0128 a0001c0001t0001g0161 others(4): Show |
7 | HG00733.hp2 HG01517.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.2396+1755dupT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38591526 | |||||||
| chr19:38591526 | CA | C | 92 | a0001c0001t0001g0008 a0001c0001t0001g0101 a0001c0001t0001g0118 others(89): Show |
93 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.2396+1755delT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38591526 | |||||||
| chr19:38591526 | CAA | C | 17 | a0001c0001t0001g0326 a0001c0002t0001g0321 a0001c0003t0001g0246 others(14): Show |
17 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.2396+1754_2396+175 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38591526 | |||||||
| chr19:38591878 | G | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0288 |
2 | NA18747.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2396+1404C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38591878 | |||||||
| chr19:38591893 | C | G | 1 | a0001c0001t0001g0182 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2396+1389G>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38591893 | |||||||
| chr19:38591928 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2396+1354C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38591928 | |||||||
| chr19:38591966 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2396+1316C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38591966 | |||||||
| chr19:38591970 | C | CA | 29 | a0001c0001t0001g0075 a0001c0001t0001g0116 a0001c0001t0001g0146 others(26): Show |
29 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.2396+1311dupT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38591970 | |||||||
| chr19:38591970 | C | CAA | 8 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0201 others(5): Show |
8 | HG01109.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.2396+1310_2396+131 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38591970 | |||||||
| chr19:38592053 | C | T | 3 | a0001c0001t0001g0328 a0001c0001t0001g0336 a0001c0001t0001g0337 |
3 | HG02970.hp2 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2396+1229G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38592053 | |||||||
| chr19:38592107 | A | G | 6 | a0001c0001t0001g0326 a0001c0001t0001g0327 a0001c0001t0001g0329 others(3): Show |
6 | HG02559.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2396+1175T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38592107 | |||||||
| chr19:38592127 | AG | A | 5 | a0001c0005t0001g0215 a0001c0005t0001g0216 a0001c0005t0001g0217 others(2): Show |
5 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2396+1154delC | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38592127 | |||||||
| chr19:38592302 | C | T | 1 | a0002c0008t0001g0172 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2396+980G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38592302 | |||||||
| chr19:38592311 | A | C | 1 | a0001c0003t0001g0310 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2396+971T>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38592311 | |||||||
| chr19:38592312 | C | A | 1 | a0001c0003t0001g0310 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2396+970G>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38592312 | |||||||
| chr19:38592451 | T | C | 6 | a0001c0001t0001g0071 a0001c0001t0001g0109 a0001c0001t0001g0110 others(3): Show |
6 | HG00733.hp2 HG00738.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2396+831A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38592451 | |||||||
| chr19:38592587 | T | A | 1 | a0001c0001t0001g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2396+695A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38592587 | |||||||
| chr19:38592684 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0163 |
2 | HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2396+598C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38592684 | |||||||
| chr19:38592715 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2396+567C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38592715 | |||||||
| chr19:38592917 | C | A | 1 | a0001c0001t0001g0203 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2396+365G>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38592917 | |||||||
| chr19:38592917 | C | CAATA | 9 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0002t0001g0018 others(6): Show |
9 | HG01168.hp2 HG01169.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.2396+361_2396+364d others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38592917 | |||||||
| chr19:38592917 | C | CAATAAAT others(1): Show |
4 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0201 others(1): Show |
4 | HG02615.hp2 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2396+357_2396+364d others(10): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38592917 | |||||||
| chr19:38592917 | C | CAATAAAT others(5): Show |
5 | a0001c0001t0001g0163 a0001c0001t0001g0328 a0001c0001t0001g0333 others(2): Show |
5 | HG01109.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2396+353_2396+364d others(14): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38592917 | |||||||
| chr19:38592917 | C | CAATAAAT others(9): Show |
1 | a0001c0001t0001g0147 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2396+349_2396+364d others(18): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38592917 | |||||||
| chr19:38592917 | CAATA | C | 14 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0248 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2396+361_2396+364d others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38592917 | |||||||
| chr19:38592917 | CAATAAAT others(1): Show |
C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0051 |
3 | HG02622.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2396+357_2396+364d others(10): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38592917 | |||||||
| chr19:38592955 | C | G | 1 | a0001c0002t0001g0252 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2396+327G>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38592955 | |||||||
| chr19:38593048 | C | T | 6 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0233 others(3): Show |
6 | HG00558.hp1 NA18747.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.2396+234G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38593048 | |||||||
| chr19:38593061 | T | C | 2 | a0001c0001t0002g0166 a0001c0001t0002g0167 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2396+221A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38593061 | |||||||
| chr19:38593088 | GAAACA | G | 14 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0248 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2396+189_2396+193d others(7): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | 38593088 | |||||||
| chr19:38593427 | G | A | 1 | a0004c0016t0001g0152 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2341-90C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38593427 | |||||||
| chr19:38593431 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2341-94C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38593431 | |||||||
| chr19:38593646 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0146 |
2 | NA19066.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2341-309C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38593646 | |||||||
| chr19:38593669 | G | A | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0328 others(2): Show |
5 | HG02615.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2341-332C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38593669 | |||||||
| chr19:38593670 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2341-333A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38593670 | |||||||
| chr19:38593683 | G | A | 14 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0248 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2341-346C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38593683 | |||||||
| chr19:38593685 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2341-348C>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38593685 | |||||||
| chr19:38593843 | TA | T | 14 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0248 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2341-507delT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38593843 | |||||||
| chr19:38593893 | A | G | 107 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(104): Show |
107 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.2341-556T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38593893 | |||||||
| chr19:38593928 | A | G | 14 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0248 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2341-591T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38593928 | |||||||
| chr19:38594026 | C | T | 14 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0248 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2341-689G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594026 | |||||||
| chr19:38594107 | T | C | 14 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0248 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2341-770A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594107 | |||||||
| chr19:38594115 | C | T | 21 | a0001c0002t0001g0017 a0001c0002t0001g0225 a0001c0002t0001g0227 others(18): Show |
21 | HG00423.hp1 HG00609.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.2341-778G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594115 | |||||||
| chr19:38594176 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2341-839A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594176 | |||||||
| chr19:38594180 | G | T | 1 | a0001c0001t0001g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2341-843C>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594180 | |||||||
| chr19:38594184 | C | G | 14 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0248 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2341-847G>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594184 | |||||||
| chr19:38594328 | G | C | 14 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0248 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2341-991C>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594328 | |||||||
| chr19:38594345 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2341-1008A>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594345 | |||||||
| chr19:38594359 | G | T | 1 | a0001c0002t0001g0316 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2341-1022C>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594359 | |||||||
| chr19:38594455 | C | A | 14 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0248 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2340+1030G>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594455 | |||||||
| chr19:38594469 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2340+1016C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594469 | |||||||
| chr19:38594774 | A | C | 1 | a0001c0003t0001g0310 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2340+711T>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594774 | |||||||
| chr19:38594783 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2340+702T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594783 | |||||||
| chr19:38594806 | C | A | 14 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0248 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2340+679G>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594806 | |||||||
| chr19:38594814 | A | C | 1 | a0006c0013t0001g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2340+671T>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594814 | |||||||
| chr19:38594889 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2340+596G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594889 | |||||||
| chr19:38594957 | T | TTATC | 32 | a0001c0001t0001g0021 a0001c0001t0001g0129 a0001c0001t0001g0147 others(29): Show |
32 | HG00558.hp1 HG01168.hp2 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.2340+524_2340+527d others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594957 | |||||||
| chr19:38594957 | T | TTATCTAT others(1): Show |
34 | a0001c0001t0001g0148 a0001c0001t0001g0196 a0001c0001t0001g0201 others(31): Show |
34 | HG00438.hp2 HG00544.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.2340+520_2340+527d others(10): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594957 | |||||||
| chr19:38594957 | T | TTATCTAT others(5): Show |
3 | a0001c0002t0001g0263 a0001c0002t0001g0321 a0001c0005t0001g0215 |
3 | NA18939.hp1 NA18974.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2340+516_2340+527d others(14): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594957 | |||||||
| chr19:38594957 | TTATC | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.2340+524_2340+527d others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594957 | |||||||
| chr19:38594957 | TTATCTAT others(1): Show |
T | 9 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0328 others(6): Show |
10 | HG00280.hp1 HG01109.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.2340+520_2340+527d others(10): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594957 | |||||||
| chr19:38594957 | TTATCTAT others(5): Show |
T | 1 | a0001c0001t0001g0150 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2340+516_2340+527d others(14): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594957 | |||||||
| chr19:38594975 | A | ATCTATCT others(5): Show |
4 | a0001c0001t0001g0326 a0001c0001t0001g0327 a0001c0001t0001g0330 others(1): Show |
4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2340+509_2340+510i others(14): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38594975 | |||||||
| chr19:38595204 | G | A | 12 | a0001c0001t0001g0071 a0001c0001t0001g0082 a0001c0001t0001g0098 others(9): Show |
12 | HG00733.hp2 HG00741.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.2340+281C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38595204 | |||||||
| chr19:38595206 | G | T | 14 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0248 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2340+279C>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38595206 | |||||||
| chr19:38595243 | C | G | 3 | a0001c0004t0001g0208 a0001c0004t0001g0210 a0001c0004t0001g0213 |
3 | HG01168.hp2 HG01169.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.2340+242G>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38595243 | |||||||
| chr19:38595305 | T | A | 2 | a0001c0001t0002g0166 a0001c0001t0002g0167 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2340+180A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38595305 | |||||||
| chr19:38595473 | G | A | 1 | a0002c0008t0001g0171 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2340+12C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 29/30 | chr19 | 38595473 | |||||||
| chr19:38595600 | T | C | 14 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0248 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2269+40A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 28/30 | chr19 | 38595600 | |||||||
| chr19:38595743 | G | C | 14 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0248 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2180-14C>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 27/30 | chr19 | 38595743 | |||||||
| chr19:38595873 | G | A | 2 | a0001c0003t0001g0247 a0001c0003t0001g0310 |
2 | NA18991.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2179+66C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 27/30 | chr19 | 38595873 | |||||||
| chr19:38596598 | G | C | 1 | a0001c0002t0001g0323 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1942-112C>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 25/30 | chr19 | 38596598 | |||||||
| chr19:38596747 | A | G | 79 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0022 others(76): Show |
79 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1942-261T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 25/30 | chr19 | 38596747 | |||||||
| chr19:38596798 | C | T | 2 | a0001c0002t0001g0232 a0001c0002t0001g0308 |
2 | NA18994.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1941+236G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 25/30 | chr19 | 38596798 | |||||||
| chr19:38596828 | A | G | 1 | a0001c0001t0001g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1941+206T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 25/30 | chr19 | 38596828 | |||||||
| chr19:38596898 | TGGGCGGG others(14): Show |
T | 14 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0248 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1941+115_1941+135d others(23): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 25/30 | chr19 | 38596898 | |||||||
| chr19:38596936 | G | C | 1 | a0001c0001t0001g0193 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1941+98C>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 25/30 | chr19 | 38596936 | |||||||
| chr19:38597010 | C | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0157 |
3 | HG01099.hp2 HG01496.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1941+24G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 25/30 | chr19 | 38597010 | |||||||
| chr19:38597450 | T | C | 3 | a0001c0001t0001g0301 a0001c0001t0001g0303 a0001c0001t0001g0304 |
3 | NA18952.hp1 NA18963.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1778+36A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 23/30 | chr19 | 38597450 | |||||||
| chr19:38597633 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1670-39A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38597633 | |||||||
| chr19:38597660 | T | C | 5 | a0001c0005t0001g0215 a0001c0005t0001g0216 a0001c0005t0001g0217 others(2): Show |
5 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1670-66A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38597660 | |||||||
| chr19:38597759 | T | C | 3 | a0001c0003t0001g0248 a0001c0003t0001g0277 a0001c0003t0001g0307 |
3 | HG00438.hp2 NA18941.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1670-165A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38597759 | |||||||
| chr19:38597812 | T | G | 1 | a0001c0001t0001g0191 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1670-218A>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38597812 | |||||||
| chr19:38597821 | A | T | 117 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(114): Show |
117 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1670-227T>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38597821 | |||||||
| chr19:38597973 | C | T | 3 | a0001c0001t0001g0328 a0001c0001t0001g0336 a0001c0001t0001g0337 |
3 | HG02970.hp2 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1670-379G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38597973 | |||||||
| chr19:38598062 | G | A | 5 | a0001c0005t0001g0215 a0001c0005t0001g0216 a0001c0005t0001g0217 others(2): Show |
5 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1670-468C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38598062 | |||||||
| chr19:38598071 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1670-477G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38598071 | |||||||
| chr19:38598192 | G | A | 32 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(29): Show |
32 | HG00621.hp2 HG00733.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.1670-598C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38598192 | |||||||
| chr19:38598219 | C | T | 31 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(28): Show |
31 | HG00621.hp2 HG00733.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1670-625G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38598219 | |||||||
| chr19:38598236 | G | T | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1670-642C>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38598236 | |||||||
| chr19:38598320 | C | T | 6 | a0001c0001t0001g0326 a0001c0001t0001g0327 a0001c0001t0001g0329 others(3): Show |
6 | HG02559.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1670-726G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38598320 | |||||||
| chr19:38598327 | G | A | 34 | a0001c0002t0001g0018 a0001c0002t0001g0022 a0001c0002t0001g0221 others(31): Show |
34 | HG00558.hp1 HG01952.hp1 HG02015.hp2 others(31): Show |
intron_variant | MODIFIER | c.1670-733C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38598327 | |||||||
| chr19:38598575 | T | C | 7 | a0001c0002t0001g0241 a0001c0002t0001g0245 a0001c0002t0001g0249 others(4): Show |
7 | HG02735.hp1 HG02738.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.1670-981A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38598575 | |||||||
| chr19:38598674 | G | C | 1 | a0001c0001t0001g0205 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1670-1080C>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38598674 | |||||||
| chr19:38598741 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1670-1147G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38598741 | |||||||
| chr19:38598856 | A | C | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1669+1069T>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38598856 | |||||||
| chr19:38598889 | T | C | 34 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(31): Show |
34 | HG00621.hp2 HG00733.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.1669+1036A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38598889 | |||||||
| chr19:38598983 | A | C | 8 | a0001c0003t0001g0246 a0001c0003t0001g0248 a0001c0003t0001g0257 others(5): Show |
8 | HG00438.hp2 HG01123.hp1 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.1669+942T>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38598983 | |||||||
| chr19:38599012 | C | CA | 91 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0027 others(88): Show |
92 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.1669+912dupT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38599012 | |||||||
| chr19:38599012 | C | CAA | 11 | a0001c0001t0001g0010 a0001c0001t0001g0151 a0001c0001t0001g0165 others(8): Show |
11 | HG01099.hp1 HG02027.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.1669+911_1669+912d others(4): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38599012 | |||||||
| chr19:38599012 | CA | C | 9 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0201 others(6): Show |
9 | HG00438.hp1 HG03130.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1669+912delT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38599012 | |||||||
| chr19:38599029 | A | C | 3 | a0001c0002t0001g0275 a0001c0002t0001g0311 a0001c0002t0001g0321 |
3 | HG02015.hp2 NA18941.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1669+896T>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38599029 | |||||||
| chr19:38599057 | G | A | 7 | a0001c0001t0001g0192 a0001c0001t0001g0204 a0001c0001t0001g0205 others(4): Show |
7 | HG00140.hp1 HG00280.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1669+868C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38599057 | |||||||
| chr19:38599188 | TA | T | 10 | a0001c0001t0001g0147 a0001c0001t0001g0163 a0001c0001t0001g0181 others(7): Show |
10 | HG01109.hp2 HG01169.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.1669+736delT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38599188 | |||||||
| chr19:38599284 | G | T | 1 | a0001c0001t0001g0188 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1669+641C>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38599284 | |||||||
| chr19:38599341 | C | A | 14 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0248 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1669+584G>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38599341 | |||||||
| chr19:38599347 | C | CA | 110 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0027 others(107): Show |
111 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1669+577dupT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38599347 | |||||||
| chr19:38599347 | C | CAA | 21 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0149 others(18): Show |
21 | HG00558.hp1 HG01175.hp2 HG02615.hp2 others(18): Show |
intron_variant | MODIFIER | c.1669+576_1669+577d others(4): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38599347 | |||||||
| chr19:38599426 | C | G | 1 | a0001c0001t0001g0186 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1669+499G>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38599426 | |||||||
| chr19:38599457 | T | G | 38 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(35): Show |
38 | HG00621.hp2 HG00733.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.1669+468A>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38599457 | |||||||
| chr19:38599487 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0112 |
2 | HG00140.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1669+438G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38599487 | |||||||
| chr19:38599648 | G | C | 38 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(35): Show |
38 | HG00621.hp2 HG00733.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.1669+277C>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38599648 | |||||||
| chr19:38599669 | G | GA | 81 | a0001c0001t0001g0098 a0001c0001t0001g0111 a0001c0001t0001g0203 others(78): Show |
81 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1669+255dupT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38599669 | |||||||
| chr19:38599850 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1669+75G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38599850 | |||||||
| chr19:38599851 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1669+74C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 22/30 | chr19 | 38599851 | |||||||
| chr19:38600062 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1608+15C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 21/30 | chr19 | 38600062 | |||||||
| chr19:38600389 | G | C | 71 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0022 others(68): Show |
71 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1532-236C>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 20/30 | chr19 | 38600389 | |||||||
| chr19:38600393 | A | G | 149 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(146): Show |
149 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.1532-240T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 20/30 | chr19 | 38600393 | |||||||
| chr19:38600440 | A | C | 2 | a0001c0001t0002g0166 a0001c0001t0002g0167 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1532-287T>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 20/30 | chr19 | 38600440 | |||||||
| chr19:38600559 | T | C | 8 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0201 others(5): Show |
8 | HG01109.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1532-406A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 20/30 | chr19 | 38600559 | |||||||
| chr19:38600580 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1532-427C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 20/30 | chr19 | 38600580 | |||||||
| chr19:38600799 | A | AT | 20 | a0001c0001t0001g0055 a0001c0001t0001g0070 a0001c0001t0001g0072 others(17): Show |
20 | HG00621.hp1 HG01071.hp1 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.1531+641dupA | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 20/30 | chr19 | 38600799 | |||||||
| chr19:38600799 | A | T | 1 | a0001c0001t0001g0289 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1531+642T>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 20/30 | chr19 | 38600799 | |||||||
| chr19:38600799 | ATT | A | 6 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0197 others(3): Show |
6 | HG00544.hp1 HG02074.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.1531+640_1531+641d others(4): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 20/30 | chr19 | 38600799 | |||||||
| chr19:38600799 | ATTT | A | 49 | a0001c0001t0001g0151 a0001c0001t0001g0173 a0001c0001t0001g0191 others(46): Show |
49 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.1531+639_1531+641d others(5): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 20/30 | chr19 | 38600799 | |||||||
| chr19:38600799 | ATTTT | A | 74 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(71): Show |
74 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.1531+638_1531+641d others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 20/30 | chr19 | 38600799 | |||||||
| chr19:38601028 | A | T | 133 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(130): Show |
133 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.1531+413T>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 20/30 | chr19 | 38601028 | |||||||
| chr19:38601222 | T | A | 3 | a0002c0008t0001g0171 a0002c0008t0001g0172 a0002c0008t0001g0220 |
3 | HG00544.hp1 HG02074.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1531+219A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 20/30 | chr19 | 38601222 | |||||||
| chr19:38601541 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1447-16G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38601541 | |||||||
| chr19:38601561 | G | A | 1 | a0001c0005t0001g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1447-36C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38601561 | |||||||
| chr19:38601583 | A | G | 1 | a0001c0005t0001g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1447-58T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38601583 | |||||||
| chr19:38601711 | GTTTTTGT others(3): Show |
G | 1 | a0006c0013t0001g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1447-196_1447-187d others(12): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38601711 | |||||||
| chr19:38601717 | G | GT | 6 | a0001c0001t0001g0075 a0001c0001t0001g0145 a0001c0001t0001g0326 others(3): Show |
6 | HG02145.hp1 HG02738.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1447-193dupA | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38601717 | |||||||
| chr19:38601724 | T | G | 1 | a0001c0002t0001g0276 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1447-199A>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38601724 | |||||||
| chr19:38601765 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1447-240G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38601765 | |||||||
| chr19:38601928 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1447-403G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38601928 | |||||||
| chr19:38601970 | G | C | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0022 others(69): Show |
72 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1447-445C>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38601970 | |||||||
| chr19:38602101 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1447-576T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602101 | |||||||
| chr19:38602123 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1447-598A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602123 | |||||||
| chr19:38602191 | T | A | 1 | a0001c0001t0001g0043 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1447-666A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602191 | |||||||
| chr19:38602237 | G | A | 80 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0022 others(77): Show |
80 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1447-712C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602237 | |||||||
| chr19:38602291 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1447-766A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602291 | |||||||
| chr19:38602360 | C | G | 1 | a0001c0001t0001g0313 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1447-835G>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602360 | |||||||
| chr19:38602377 | C | CAT | 4 | a0001c0001t0001g0151 a0002c0008t0001g0171 a0002c0008t0001g0172 others(1): Show |
4 | HG00544.hp1 HG02074.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.1447-854_1447-853d others(4): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602377 | |||||||
| chr19:38602384 | A | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1447-859T>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602384 | |||||||
| chr19:38602411 | G | GAC | 8 | a0001c0001t0001g0203 a0001c0001t0001g0326 a0001c0001t0001g0327 others(5): Show |
8 | HG01978.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1447-888_1447-887d others(4): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602411 | |||||||
| chr19:38602411 | GAC | G | 34 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(31): Show |
34 | HG00621.hp2 HG00733.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.1447-888_1447-887d others(4): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602411 | |||||||
| chr19:38602411 | GACACAC | G | 78 | a0001c0001t0001g0165 a0001c0002t0001g0017 a0001c0002t0001g0018 others(75): Show |
78 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1447-892_1447-887d others(8): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602411 | |||||||
| chr19:38602429 | CACATATA others(33): Show |
C | 2 | a0001c0001t0001g0083 a0001c0001t0001g0112 |
2 | HG00140.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1447-944_1447-905d others(42): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602429 | |||||||
| chr19:38602441 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1447-916G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602441 | |||||||
| chr19:38602483 | CATATACA others(1): Show |
C | 9 | a0001c0001t0001g0071 a0001c0001t0001g0098 a0001c0001t0001g0109 others(6): Show |
9 | HG00733.hp2 HG00738.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1447-966_1447-959d others(10): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602483 | |||||||
| chr19:38602487 | T | C | 35 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(32): Show |
35 | HG00621.hp2 HG00733.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.1447-962A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602487 | |||||||
| chr19:38602510 | G | GTACATAT others(9): Show |
1 | a0006c0013t0001g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1447-1001_1447-986 others(19): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602510 | |||||||
| chr19:38602539 | C | CATATACA others(21): Show |
1 | a0001c0001t0001g0203 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1447-1042_1447-101 others(32): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602539 | |||||||
| chr19:38602545 | CAT | C | 7 | a0001c0001t0001g0326 a0001c0001t0001g0327 a0001c0001t0001g0329 others(4): Show |
7 | HG01891.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1447-1022_1447-102 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602545 | |||||||
| chr19:38602559 | CAT | C | 34 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(31): Show |
34 | HG00621.hp2 HG00733.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.1447-1036_1447-103 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602559 | |||||||
| chr19:38602561 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1447-1036A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602561 | |||||||
| chr19:38602573 | CAT | C | 6 | a0001c0001t0001g0083 a0001c0001t0001g0091 a0001c0001t0001g0112 others(3): Show |
6 | HG00140.hp2 HG01175.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1447-1050_1447-104 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602573 | |||||||
| chr19:38602639 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1447-1114G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602639 | |||||||
| chr19:38602641 | T | TATACATA others(151): Show |
1 | a0001c0001t0001g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1447-1117_1447-111 others(162): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602641 | |||||||
| chr19:38602653 | C | CAT | 149 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(146): Show |
149 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.1447-1130_1447-112 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602653 | |||||||
| chr19:38602675 | T | C | 1 | a0006c0013t0001g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1447-1150A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602675 | |||||||
| chr19:38602680 | A | ATATACAT others(19): Show |
1 | a0001c0001t0001g0064 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1447-1181_1447-115 others(30): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602680 | |||||||
| chr19:38602680 | ATATACAT others(19): Show |
A | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0145 |
3 | HG02145.hp1 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1447-1181_1447-115 others(30): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602680 | |||||||
| chr19:38602711 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1447-1186G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602711 | |||||||
| chr19:38602732 | GTATACAT others(65): Show |
G | 6 | a0001c0001t0001g0326 a0001c0001t0001g0327 a0001c0001t0001g0329 others(3): Show |
6 | HG02559.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1447-1279_1447-120 others(76): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602732 | |||||||
| chr19:38602733 | T | C | 1 | a0006c0013t0001g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1447-1208A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602733 | |||||||
| chr19:38602756 | A | G | 78 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0022 others(75): Show |
78 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1447-1231T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602756 | |||||||
| chr19:38602762 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1447-1237C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602762 | |||||||
| chr19:38602781 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1447-1256A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602781 | |||||||
| chr19:38602797 | CAT | C | 32 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(29): Show |
32 | HG00621.hp2 HG00733.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.1447-1274_1447-127 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602797 | |||||||
| chr19:38602797 | CATACATA others(1): Show |
C | 84 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0002t0001g0017 others(81): Show |
84 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1447-1280_1447-127 others(12): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602797 | |||||||
| chr19:38602803 | T | C | 2 | a0001c0001t0001g0195 a0005c0012t0001g0189 |
2 | HG01243.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1447-1278A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602803 | |||||||
| chr19:38602825 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1447-1300G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602825 | |||||||
| chr19:38602871 | TAC | T | 3 | a0002c0008t0001g0171 a0002c0008t0001g0172 a0002c0008t0001g0220 |
3 | HG00544.hp1 HG02074.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1447-1348_1447-134 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602871 | |||||||
| chr19:38602873 | C | T | 77 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0022 others(74): Show |
77 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.1447-1348G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602873 | |||||||
| chr19:38602888 | A | G | 2 | a0001c0001t0001g0206 a0001c0001t0001g0209 |
2 | HG00140.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1447-1363T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602888 | |||||||
| chr19:38602947 | TATATACA others(3): Show |
T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0188 |
2 | HG03239.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1447-1432_1447-142 others(14): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602947 | |||||||
| chr19:38602957 | C | CATACAT | 132 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(129): Show |
132 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1447-1433_1447-143 others(10): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602957 | |||||||
| chr19:38602968 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1447-1443C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602968 | |||||||
| chr19:38602968 | GCA | G | 3 | a0002c0008t0001g0171 a0002c0008t0001g0172 a0002c0008t0001g0220 |
3 | HG00544.hp1 HG02074.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1447-1445_1447-144 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602968 | |||||||
| chr19:38602987 | C | CAT | 128 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(125): Show |
128 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.1447-1464_1447-146 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38602987 | |||||||
| chr19:38603002 | A | G | 2 | a0001c0001t0002g0166 a0001c0001t0002g0167 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1447-1477T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603002 | |||||||
| chr19:38603003 | T | C | 10 | a0001c0002t0001g0222 a0001c0002t0001g0223 a0001c0002t0001g0224 others(7): Show |
10 | HG02040.hp1 HG02071.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1447-1478A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603003 | |||||||
| chr19:38603051 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1447-1526G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603051 | |||||||
| chr19:38603052 | GCATATAC others(7): Show |
G | 6 | a0001c0001t0001g0326 a0001c0001t0001g0327 a0001c0001t0001g0329 others(3): Show |
6 | HG02559.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1447-1541_1447-152 others(18): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603052 | |||||||
| chr19:38603056 | ATACATAT others(55): Show |
A | 1 | a0006c0013t0001g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1447-1593_1447-153 others(66): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603056 | |||||||
| chr19:38603059 | C | CAT | 143 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(140): Show |
143 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.1447-1536_1447-153 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603059 | |||||||
| chr19:38603070 | ATACATAT others(9): Show |
A | 19 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0037 others(16): Show |
20 | HG00735.hp1 HG00735.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1447-1561_1447-154 others(20): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603070 | |||||||
| chr19:38603070 | ATACATAT others(25): Show |
A | 1 | a0001c0001t0001g0058 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1447-1577_1447-154 others(36): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603070 | |||||||
| chr19:38603079 | T | TAC | 138 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(135): Show |
138 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.1447-1556_1447-155 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603079 | |||||||
| chr19:38603084 | A | G | 1 | a0001c0001t0001g0295 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1447-1559T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603084 | |||||||
| chr19:38603085 | T | C | 3 | a0001c0003t0001g0257 a0001c0003t0001g0262 a0001c0003t0001g0270 |
3 | NA18945.hp1 NA19074.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1447-1560A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603085 | |||||||
| chr19:38603086 | G | A | 147 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(144): Show |
147 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1447-1561C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603086 | |||||||
| chr19:38603088 | A | G | 1 | a0001c0001t0001g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1447-1563T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603088 | |||||||
| chr19:38603098 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0001g0188 |
3 | HG03239.hp2 HG04115.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1447-1573T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603098 | |||||||
| chr19:38603114 | A | G | 36 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(33): Show |
36 | HG00621.hp2 HG00733.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1447-1589T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603114 | |||||||
| chr19:38603118 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0333 |
2 | HG01109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1447-1593C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603118 | |||||||
| chr19:38603130 | G | A | 1 | a0006c0013t0001g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1447-1605C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603130 | |||||||
| chr19:38603131 | C | CATATACA others(1): Show |
124 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(121): Show |
124 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.1447-1614_1447-160 others(12): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603131 | |||||||
| chr19:38603139 | T | TATATAC | 4 | a0001c0005t0001g0215 a0001c0005t0001g0216 a0001c0005t0001g0217 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-1620_1447-161 others(10): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603139 | |||||||
| chr19:38603145 | C | CATATAT | 3 | a0002c0008t0001g0171 a0002c0008t0001g0172 a0002c0008t0001g0220 |
3 | HG00544.hp1 HG02074.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1447-1621_1447-162 others(10): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603145 | |||||||
| chr19:38603166 | A | G | 4 | a0001c0005t0001g0215 a0001c0005t0001g0216 a0001c0005t0001g0217 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-1641T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603166 | |||||||
| chr19:38603196 | A | G | 1 | a0001c0004t0001g0059 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1447-1671T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603196 | |||||||
| chr19:38603221 | TATACATA others(5): Show |
T | 1 | a0001c0001t0001g0182 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1447-1708_1447-169 others(16): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603221 | |||||||
| chr19:38603222 | A | G | 1 | a0001c0004t0001g0059 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1447-1697T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603222 | |||||||
| chr19:38603233 | CAT | C | 88 | a0001c0001t0001g0024 a0001c0001t0001g0035 a0001c0001t0001g0038 others(85): Show |
88 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.1447-1710_1447-170 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603233 | |||||||
| chr19:38603235 | T | A | 1 | a0001c0001t0001g0043 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1447-1710A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603235 | |||||||
| chr19:38603253 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1447-1728A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603253 | |||||||
| chr19:38603283 | T | A | 1 | a0001c0001t0001g0203 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1447-1758A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603283 | |||||||
| chr19:38603285 | TAC | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0030 others(23): Show |
27 | HG00642.hp1 HG01891.hp1 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.1447-1762_1447-176 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603285 | |||||||
| chr19:38603295 | C | T | 143 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(140): Show |
143 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.1447-1770G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603295 | |||||||
| chr19:38603296 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1447-1771T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603296 | |||||||
| chr19:38603332 | G | A | 16 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0058 others(13): Show |
17 | HG01169.hp2 HG01943.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.1447-1807C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603332 | |||||||
| chr19:38603333 | C | CATATACA others(17): Show |
2 | a0001c0001t0001g0010 a0001c0001t0001g0305 |
2 | HG02738.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1447-1832_1447-180 others(28): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603333 | |||||||
| chr19:38603348 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1447-1823T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603348 | |||||||
| chr19:38603361 | TAC | T | 26 | a0001c0002t0001g0018 a0001c0002t0001g0022 a0001c0002t0001g0221 others(23): Show |
26 | HG01952.hp1 HG02015.hp2 HG02040.hp1 others(23): Show |
intron_variant | MODIFIER | c.1447-1838_1447-183 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603361 | |||||||
| chr19:38603397 | T | C | 134 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(131): Show |
134 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1447-1872A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603397 | |||||||
| chr19:38603410 | ATATACAC others(1): Show |
A | 81 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0022 others(78): Show |
81 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1447-1893_1447-188 others(12): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603410 | |||||||
| chr19:38603435 | CAT | C | 6 | a0001c0004t0001g0012 a0001c0004t0001g0013 a0001c0004t0001g0014 others(3): Show |
6 | HG02896.hp2 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1447-1912_1447-191 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603435 | |||||||
| chr19:38603556 | G | A | 14 | a0001c0001t0001g0192 a0001c0001t0001g0204 a0001c0001t0001g0205 others(11): Show |
14 | HG00140.hp1 HG00280.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.1446+1853C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603556 | |||||||
| chr19:38603608 | G | A | 78 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0022 others(75): Show |
78 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1446+1801C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603608 | |||||||
| chr19:38603695 | C | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0163 |
2 | HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1446+1714G>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603695 | |||||||
| chr19:38603700 | T | G | 1 | a0001c0001t0001g0087 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1446+1709A>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603700 | |||||||
| chr19:38603705 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1446+1704G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603705 | |||||||
| chr19:38603710 | G | T | 1 | a0001c0001t0001g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1446+1699C>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603710 | |||||||
| chr19:38603711 | C | T | 1 | a0007c0017t0001g0016 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1446+1698G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603711 | |||||||
| chr19:38603749 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1446+1660G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603749 | |||||||
| chr19:38603797 | A | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0163 |
2 | HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1446+1612T>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603797 | |||||||
| chr19:38603957 | C | G | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1446+1452G>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603957 | |||||||
| chr19:38603958 | T | C | 1 | a0006c0013t0001g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1446+1451A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603958 | |||||||
| chr19:38603971 | G | A | 35 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(32): Show |
35 | HG00621.hp2 HG00733.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.1446+1438C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603971 | |||||||
| chr19:38603985 | G | GA | 8 | a0001c0001t0001g0087 a0001c0001t0001g0118 a0001c0001t0001g0145 others(5): Show |
8 | HG02145.hp1 HG03490.hp1 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.1446+1423dupT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603985 | |||||||
| chr19:38603985 | GA | G | 80 | a0001c0001t0001g0047 a0001c0001t0001g0088 a0001c0001t0001g0287 others(77): Show |
80 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.1446+1423delT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38603985 | |||||||
| chr19:38604098 | C | A | 1 | a0001c0001t0001g0147 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1446+1311G>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604098 | |||||||
| chr19:38604128 | C | CA | 20 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0043 others(17): Show |
20 | HG00642.hp1 HG01258.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.1446+1280dupT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604128 | |||||||
| chr19:38604128 | C | CAA | 10 | a0001c0001t0001g0149 a0001c0001t0001g0192 a0001c0001t0002g0166 others(7): Show |
10 | HG01168.hp2 HG01169.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.1446+1279_1446+128 others(6): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604128 | |||||||
| chr19:38604128 | C | CAAA | 14 | a0001c0001t0001g0148 a0001c0001t0001g0201 a0001c0001t0001g0202 others(11): Show |
14 | HG00140.hp1 HG00280.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.1446+1278_1446+128 others(7): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604128 | |||||||
| chr19:38604128 | C | CAAAAAA | 23 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(20): Show |
23 | HG00621.hp2 HG00733.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1446+1275_1446+128 others(10): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604128 | |||||||
| chr19:38604128 | C | CAAAAAAA | 9 | a0001c0001t0001g0010 a0001c0001t0001g0178 a0001c0001t0001g0181 others(6): Show |
9 | HG01123.hp2 HG02027.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.1446+1274_1446+128 others(11): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604128 | |||||||
| chr19:38604128 | CA | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0058 a0001c0001t0001g0061 others(5): Show |
9 | HG01515.hp2 HG02965.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.1446+1280delT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604128 | |||||||
| chr19:38604128 | CAAA | C | 6 | a0001c0001t0001g0326 a0001c0001t0001g0327 a0001c0001t0001g0330 others(3): Show |
6 | HG02451.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1446+1278_1446+128 others(7): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604128 | |||||||
| chr19:38604128 | CAAAAAAA others(5): Show |
C | 79 | a0001c0002t0001g0018 a0001c0002t0001g0022 a0001c0002t0001g0221 others(76): Show |
79 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1446+1269_1446+128 others(16): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604128 | |||||||
| chr19:38604128 | CAAAAAAA others(6): Show |
C | 1 | a0001c0002t0001g0017 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1446+1268_1446+128 others(17): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604128 | |||||||
| chr19:38604139 | A | T | 1 | a0001c0002t0001g0224 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1446+1270T>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604139 | |||||||
| chr19:38604140 | A | C | 1 | a0001c0002t0001g0224 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1446+1269T>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604140 | |||||||
| chr19:38604211 | G | C | 1 | a0007c0017t0001g0016 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1446+1198C>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604211 | |||||||
| chr19:38604253 | A | G | 151 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(148): Show |
151 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.1446+1156T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604253 | |||||||
| chr19:38604261 | A | G | 2 | a0001c0001t0001g0132 a0001c0001t0001g0136 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1446+1148T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604261 | |||||||
| chr19:38604364 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1446+1045C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604364 | |||||||
| chr19:38604407 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1446+1002G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604407 | |||||||
| chr19:38604530 | A | ACTGTAAT others(110): Show |
3 | a0001c0002t0001g0017 a0001c0002t0001g0236 a0001c0002t0001g0274 |
3 | NA18977.hp1 NA19064.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1446+878_1446+879i others(119): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604530 | |||||||
| chr19:38604722 | G | A | 1 | a0006c0013t0001g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1446+687C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604722 | |||||||
| chr19:38604747 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1446+662C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604747 | |||||||
| chr19:38604789 | C | A | 1 | a0001c0001t0001g0087 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1446+620G>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604789 | |||||||
| chr19:38604980 | C | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0163 |
2 | HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1446+429G>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604980 | |||||||
| chr19:38604981 | G | A | 10 | a0001c0001t0001g0192 a0001c0001t0001g0204 a0001c0001t0001g0205 others(7): Show |
10 | HG00140.hp1 HG00280.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.1446+428C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38604981 | |||||||
| chr19:38605022 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1446+387C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38605022 | |||||||
| chr19:38605086 | TA | T | 93 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0057 others(90): Show |
93 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1446+322delT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38605086 | |||||||
| chr19:38605086 | TAA | T | 6 | a0001c0002t0001g0022 a0001c0002t0001g0251 a0001c0002t0001g0252 others(3): Show |
6 | HG02040.hp1 HG03017.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.1446+321_1446+322d others(4): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38605086 | |||||||
| chr19:38605337 | C | G | 81 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0022 others(78): Show |
81 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1446+72G>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | 38605337 | |||||||
| chr19:38605494 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19055.hp2 | splice_region_variant&intron_variant | LOW | c.1364-3C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 18/30 | chr19 | 38605494 | |||||||
| chr19:38605516 | G | A | 1 | a0001c0002t0001g0233 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1364-25C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 18/30 | chr19 | 38605516 | |||||||
| chr19:38605889 | T | C | 9 | a0001c0001t0001g0147 a0001c0001t0001g0163 a0001c0001t0001g0326 others(6): Show |
9 | HG02451.hp2 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1201-159A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 17/30 | chr19 | 38605889 | |||||||
| chr19:38606015 | G | T | 1 | a0001c0001t0001g0173 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1200+158C>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 17/30 | chr19 | 38606015 | |||||||
| chr19:38606160 | C | G | 14 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0044 others(11): Show |
14 | HG02258.hp2 HG02451.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1200+13G>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 17/30 | chr19 | 38606160 | |||||||
| chr19:38606299 | C | T | 1 | a0001c0002t0001g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1158-84G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 16/30 | chr19 | 38606299 | |||||||
| chr19:38606396 | A | C | 4 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0015 others(1): Show |
4 | HG02965.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1158-181T>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 16/30 | chr19 | 38606396 | |||||||
| chr19:38606538 | CG | C | 34 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(31): Show |
34 | HG00621.hp2 HG00733.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.1158-324delC | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 16/30 | chr19 | 38606538 | |||||||
| chr19:38606692 | CA | C | 9 | a0001c0001t0001g0147 a0001c0001t0001g0163 a0001c0001t0001g0326 others(6): Show |
9 | HG02451.hp2 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1158-478delT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 16/30 | chr19 | 38606692 | |||||||
| chr19:38606863 | G | A | 9 | a0001c0001t0001g0147 a0001c0001t0001g0163 a0001c0001t0001g0326 others(6): Show |
9 | HG02451.hp2 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1158-648C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 16/30 | chr19 | 38606863 | |||||||
| chr19:38607037 | G | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0022 others(69): Show |
72 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1158-822C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 16/30 | chr19 | 38607037 | |||||||
| chr19:38607131 | G | C | 126 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(123): Show |
126 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.1157+733C>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 16/30 | chr19 | 38607131 | |||||||
| chr19:38607226 | G | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0096 a0001c0001t0001g0097 others(3): Show |
7 | HG00642.hp2 HG02622.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1157+638C>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 16/30 | chr19 | 38607226 | |||||||
| chr19:38607493 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0204 |
2 | HG00735.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1157+371C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 16/30 | chr19 | 38607493 | |||||||
| chr19:38607559 | C | CA | 16 | a0001c0001t0001g0034 a0001c0001t0001g0044 a0001c0001t0001g0045 others(13): Show |
16 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1157+304dupT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 16/30 | chr19 | 38607559 | |||||||
| chr19:38607559 | CA | C | 118 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(115): Show |
118 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.1157+304delT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 16/30 | chr19 | 38607559 | |||||||
| chr19:38607559 | CAA | C | 9 | a0001c0001t0001g0179 a0001c0001t0001g0192 a0001c0001t0001g0193 others(6): Show |
9 | HG00558.hp1 HG01975.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1157+303_1157+304d others(4): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 16/30 | chr19 | 38607559 | |||||||
| chr19:38607559 | CAAAAAAA others(3): Show |
C | 1 | a0009c0021t0001g0143 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1157+295_1157+304d others(12): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 16/30 | chr19 | 38607559 | |||||||
| chr19:38607574 | A | G | 1 | a0006c0013t0001g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1157+290T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 16/30 | chr19 | 38607574 | |||||||
| chr19:38607730 | G | A | 13 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(10): Show |
13 | HG00140.hp1 HG00280.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.1157+134C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 16/30 | chr19 | 38607730 | |||||||
| chr19:38608067 | A | C | 3 | a0002c0008t0001g0171 a0002c0008t0001g0172 a0002c0008t0001g0220 |
3 | HG00544.hp1 HG02074.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1066-34T>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 14/30 | chr19 | 38608067 | |||||||
| chr19:38608094 | G | A | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0157 |
3 | HG01099.hp2 HG01496.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1065+18C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 14/30 | chr19 | 38608094 | |||||||
| chr19:38608257 | C | CG | 11 | a0001c0001t0001g0089 a0001c0001t0001g0148 a0001c0001t0001g0149 others(8): Show |
11 | HG00741.hp1 HG01109.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1007-88dupC | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608257 | |||||||
| chr19:38608257 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1007-87G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608257 | |||||||
| chr19:38608588 | G | A | 1 | a0001c0002t0001g0242 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1007-418C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608588 | |||||||
| chr19:38608715 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1007-545C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608715 | |||||||
| chr19:38608740 | T | C | 150 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(147): Show |
150 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.1007-570A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608740 | |||||||
| chr19:38608763 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1007-593C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608763 | |||||||
| chr19:38608795 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG04199.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1007-625C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608795 | |||||||
| chr19:38608799 | C | CA | 63 | a0001c0001t0001g0035 a0001c0001t0001g0048 a0001c0001t0001g0049 others(60): Show |
63 | HG00438.hp2 HG00609.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1007-630dupT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608799 | |||||||
| chr19:38608799 | C | CAA | 8 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0168 others(5): Show |
8 | HG01496.hp1 HG01517.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1007-631_1007-630d others(4): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608799 | |||||||
| chr19:38608799 | C | CAAAAAAA others(3): Show |
4 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0004t0001g0208 others(1): Show |
4 | HG01069.hp2 HG01243.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-639_1007-630d others(12): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608799 | |||||||
| chr19:38608799 | C | CAAAAAAA others(4): Show |
4 | a0001c0001t0001g0204 a0001c0001t0001g0211 a0001c0004t0001g0210 others(1): Show |
4 | HG00280.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007-640_1007-630d others(13): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608799 | |||||||
| chr19:38608799 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1007-641_1007-630d others(14): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608799 | |||||||
| chr19:38608799 | CA | C | 8 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0061 others(5): Show |
8 | HG02717.hp2 HG03490.hp2 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.1007-630delT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608799 | |||||||
| chr19:38608822 | A | C | 1 | a0004c0016t0001g0152 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1007-652T>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608822 | |||||||
| chr19:38608827 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0205 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1007-658_1007-657i others(14): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608827 | |||||||
| chr19:38608828 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0001g0181 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1007-659_1007-658i others(21): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608828 | |||||||
| chr19:38608828 | A | AAAAAAAA others(6): Show |
4 | a0001c0001t0001g0195 a0001c0001t0001g0198 a0001c0001t0001g0324 others(1): Show |
4 | HG00621.hp2 HG01243.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-659_1007-658i others(15): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608828 | |||||||
| chr19:38608828 | A | AAAAAAAA others(5): Show |
13 | a0001c0001t0001g0027 a0001c0001t0001g0175 a0001c0001t0001g0178 others(10): Show |
13 | HG01943.hp1 HG02027.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1007-659_1007-658i others(14): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608828 | |||||||
| chr19:38608828 | A | AAAAAAAA others(4): Show |
10 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0165 others(7): Show |
10 | HG01975.hp1 HG02004.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1007-659_1007-658i others(13): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608828 | |||||||
| chr19:38608828 | A | ACAAAAAA others(4): Show |
1 | a0011c0011t0001g0176 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1007-659_1007-658i others(13): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608828 | |||||||
| chr19:38608828 | A | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0061 a0001c0001t0001g0173 others(4): Show |
7 | HG00733.hp1 HG01099.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.1007-658T>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608828 | |||||||
| chr19:38608841 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1007-671G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608841 | |||||||
| chr19:38608980 | C | A | 6 | a0001c0001t0001g0326 a0001c0001t0001g0327 a0001c0001t0001g0329 others(3): Show |
6 | HG02559.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1006+616G>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38608980 | |||||||
| chr19:38609440 | G | A | 4 | a0001c0005t0001g0215 a0001c0005t0001g0216 a0001c0005t0001g0217 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006+156C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38609440 | |||||||
| chr19:38609480 | T | A | 2 | a0001c0002t0001g0225 a0001c0002t0001g0320 |
2 | NA18962.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1006+116A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38609480 | |||||||
| chr19:38609520 | C | T | 3 | a0002c0008t0001g0171 a0002c0008t0001g0172 a0002c0008t0001g0220 |
3 | HG00544.hp1 HG02074.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1006+76G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38609520 | |||||||
| chr19:38609588 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp1 | splice_region_variant&intron_variant | LOW | c.1006+8G>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | 38609588 | |||||||
| chr19:38609776 | C | A | 4 | a0001c0005t0001g0215 a0001c0005t0001g0216 a0001c0005t0001g0217 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-102G>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 12/30 | chr19 | 38609776 | |||||||
| chr19:38609791 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.928-117G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 12/30 | chr19 | 38609791 | |||||||
| chr19:38609822 | G | C | 78 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0022 others(75): Show |
78 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.927+87C>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 12/30 | chr19 | 38609822 | |||||||
| chr19:38610048 | G | A | 79 | a0001c0001t0001g0203 a0001c0002t0001g0017 a0001c0002t0001g0018 others(76): Show |
79 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.811-23C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38610048 | |||||||
| chr19:38610097 | A | G | 135 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(132): Show |
135 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.811-72T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38610097 | |||||||
| chr19:38610100 | G | A | 2 | a0001c0001t0001g0174 a0001c0018t0001g0190 |
2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.811-75C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38610100 | |||||||
| chr19:38610168 | C | T | 86 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0163 others(83): Show |
86 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.811-143G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38610168 | |||||||
| chr19:38610169 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02523.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.811-144C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38610169 | |||||||
| chr19:38610262 | G | C | 4 | a0001c0005t0001g0215 a0001c0005t0001g0216 a0001c0005t0001g0217 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-237C>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38610262 | |||||||
| chr19:38610339 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0146 |
2 | NA19066.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.811-314C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38610339 | |||||||
| chr19:38610342 | A | T | 1 | a0001c0001t0001g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.811-317T>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38610342 | |||||||
| chr19:38610353 | G | A | 4 | a0001c0005t0001g0215 a0001c0005t0001g0216 a0001c0005t0001g0217 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-328C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38610353 | |||||||
| chr19:38610372 | A | AT | 68 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0030 others(65): Show |
70 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.811-348dupA | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38610372 | |||||||
| chr19:38610372 | A | ATT | 5 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0001g0073 others(2): Show |
6 | HG02074.hp1 HG02647.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.811-349_811-348dup others(2): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38610372 | |||||||
| chr19:38610372 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0001g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.811-365_811-348dup others(18): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38610372 | |||||||
| chr19:38610372 | A | ATTTTTTT others(13): Show |
1 | a0001c0001t0001g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.811-367_811-348dup others(20): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38610372 | |||||||
| chr19:38610372 | AT | A | 37 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0052 others(34): Show |
39 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.811-348delA | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38610372 | |||||||
| chr19:38610372 | ATT | A | 32 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0214 others(29): Show |
32 | HG00423.hp1 HG00438.hp2 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.811-349_811-348del others(2): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38610372 | |||||||
| chr19:38610372 | ATTT | A | 57 | a0001c0001t0001g0151 a0001c0001t0001g0163 a0001c0001t0001g0203 others(54): Show |
57 | HG00558.hp1 HG00609.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.811-350_811-348del others(3): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38610372 | |||||||
| chr19:38610379 | T | A | 1 | a0001c0001t0001g0136 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.811-354A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38610379 | |||||||
| chr19:38610535 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.811-510C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38610535 | |||||||
| chr19:38610697 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.810+354C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38610697 | |||||||
| chr19:38611028 | G | A | 3 | a0001c0002t0001g0275 a0001c0002t0001g0311 a0001c0002t0001g0321 |
3 | HG02015.hp2 NA18941.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.810+23C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38611028 | |||||||
| chr19:38611029 | A | G | 135 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(132): Show |
135 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.810+22T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 11/30 | chr19 | 38611029 | |||||||
| chr19:38611230 | T | C | 135 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(132): Show |
135 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.728+13A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 10/30 | chr19 | 38611230 | |||||||
| chr19:38611239 | G | A | 85 | a0001c0001t0001g0147 a0001c0001t0001g0163 a0001c0001t0001g0203 others(82): Show |
85 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(82): Show |
splice_region_variant&intron_variant | LOW | c.728+4C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 10/30 | chr19 | 38611239 | |||||||
| chr19:38611513 | T | G | 10 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(7): Show |
10 | HG00140.hp1 HG00280.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.666-208A>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 9/30 | chr19 | 38611513 | |||||||
| chr19:38611705 | C | T | 3 | a0002c0008t0001g0171 a0002c0008t0001g0172 a0002c0008t0001g0220 |
3 | HG00544.hp1 HG02074.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.666-400G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 9/30 | chr19 | 38611705 | |||||||
| chr19:38611710 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.666-405A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 9/30 | chr19 | 38611710 | |||||||
| chr19:38611824 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.666-519G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 9/30 | chr19 | 38611824 | |||||||
| chr19:38611830 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.666-525C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 9/30 | chr19 | 38611830 | |||||||
| chr19:38611899 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.666-594C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 9/30 | chr19 | 38611899 | |||||||
| chr19:38611918 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0146 |
2 | NA19066.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.666-613C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 9/30 | chr19 | 38611918 | |||||||
| chr19:38611972 | C | A | 1 | a0001c0002t0001g0224 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.665+639G>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 9/30 | chr19 | 38611972 | |||||||
| chr19:38612190 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG01257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.665+421A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 9/30 | chr19 | 38612190 | |||||||
| chr19:38612428 | AAAAAT | A | 3 | a0001c0007t0001g0140 a0001c0007t0001g0141 a0001c0007t0001g0142 |
3 | HG00741.hp2 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.665+178_665+182del others(5): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 9/30 | chr19 | 38612428 | |||||||
| chr19:38612465 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.665+146T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 9/30 | chr19 | 38612465 | |||||||
| chr19:38612756 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.534-14G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 8/30 | chr19 | 38612756 | |||||||
| chr19:38612916 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.534-174C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 8/30 | chr19 | 38612916 | |||||||
| chr19:38612950 | G | T | 1 | a0001c0001t0001g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.534-208C>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 8/30 | chr19 | 38612950 | |||||||
| chr19:38613078 | C | T | 4 | a0001c0001t0001g0147 a0001c0001t0001g0163 a0001c0001t0002g0166 others(1): Show |
4 | HG03209.hp1 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-336G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 8/30 | chr19 | 38613078 | |||||||
| chr19:38613124 | A | C | 47 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(44): Show |
47 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.534-382T>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 8/30 | chr19 | 38613124 | |||||||
| chr19:38613164 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.534-422G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 8/30 | chr19 | 38613164 | |||||||
| chr19:38613168 | C | T | 2 | a0001c0001t0001g0328 a0001c0001t0001g0336 |
2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.534-426G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 8/30 | chr19 | 38613168 | |||||||
| chr19:38613331 | G | GA | 48 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(45): Show |
48 | HG00621.hp2 HG00733.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.533+548dupT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 8/30 | chr19 | 38613331 | |||||||
| chr19:38613346 | AC | A | 4 | a0001c0001t0001g0151 a0002c0008t0001g0171 a0002c0008t0001g0172 others(1): Show |
4 | HG00544.hp1 HG02074.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.533+533delG | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 8/30 | chr19 | 38613346 | |||||||
| chr19:38613347 | C | A | 1 | a0001c0001t0001g0333 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.533+533G>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 8/30 | chr19 | 38613347 | |||||||
| chr19:38613484 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.533+396G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 8/30 | chr19 | 38613484 | |||||||
| chr19:38613735 | C | A | 151 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(148): Show |
151 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.533+145G>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 8/30 | chr19 | 38613735 | |||||||
| chr19:38613768 | G | A | 3 | a0002c0008t0001g0171 a0002c0008t0001g0172 a0002c0008t0001g0220 |
3 | HG00544.hp1 HG02074.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.533+112C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 8/30 | chr19 | 38613768 | |||||||
| chr19:38613778 | G | A | 1 | a0001c0003t0001g0277 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.533+102C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 8/30 | chr19 | 38613778 | |||||||
| chr19:38613797 | A | G | 13 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(10): Show |
13 | HG00280.hp1 HG00735.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.533+83T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 8/30 | chr19 | 38613797 | |||||||
| chr19:38613810 | C | T | 84 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(81): Show |
84 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.533+70G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 8/30 | chr19 | 38613810 | |||||||
| chr19:38613860 | G | A | 4 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0015 others(1): Show |
4 | HG02965.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.533+20C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 8/30 | chr19 | 38613860 | |||||||
| chr19:38614094 | G | A | 4 | a0001c0001t0001g0326 a0001c0001t0001g0327 a0001c0001t0001g0330 others(1): Show |
4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.418-9C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 6/30 | chr19 | 38614094 | |||||||
| chr19:38614673 | C | G | 1 | a0001c0001t0001g0029 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.314-228G>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 4/30 | chr19 | 38614673 | |||||||
| chr19:38614787 | T | A | 1 | a0001c0009t0001g0315 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.314-342A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 4/30 | chr19 | 38614787 | |||||||
| chr19:38614921 | C | CA | 33 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0054 others(30): Show |
33 | HG00438.hp2 HG00735.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.314-477dupT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 4/30 | chr19 | 38614921 | |||||||
| chr19:38614921 | CA | C | 23 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0026 others(20): Show |
23 | HG00544.hp1 HG01069.hp1 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.314-477delT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 4/30 | chr19 | 38614921 | |||||||
| chr19:38614921 | CAAAAAAA others(6): Show |
C | 14 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(11): Show |
14 | HG00140.hp1 HG00280.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.314-489_314-477del others(13): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 4/30 | chr19 | 38614921 | |||||||
| chr19:38614986 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.314-541T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 4/30 | chr19 | 38614986 | |||||||
| chr19:38615015 | T | C | 1 | a0001c0001t0001g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.314-570A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 4/30 | chr19 | 38615015 | |||||||
| chr19:38615107 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.314-662C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 4/30 | chr19 | 38615107 | |||||||
| chr19:38615352 | C | T | 28 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0029 others(25): Show |
29 | HG00642.hp1 HG01884.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.313+843G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 4/30 | chr19 | 38615352 | |||||||
| chr19:38615382 | CACA | C | 35 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(32): Show |
35 | HG00621.hp2 HG00733.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.313+810_313+812del others(3): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 4/30 | chr19 | 38615382 | |||||||
| chr19:38615688 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.313+507G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 4/30 | chr19 | 38615688 | |||||||
| chr19:38615754 | A | T | 9 | a0001c0004t0001g0012 a0001c0004t0001g0013 a0001c0004t0001g0014 others(6): Show |
9 | HG00544.hp1 HG02074.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.313+441T>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 4/30 | chr19 | 38615754 | |||||||
| chr19:38615801 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.313+394C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 4/30 | chr19 | 38615801 | |||||||
| chr19:38615819 | G | A | 6 | a0001c0002t0001g0225 a0001c0002t0001g0316 a0001c0002t0001g0317 others(3): Show |
6 | NA18943.hp2 NA18949.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.313+376C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 4/30 | chr19 | 38615819 | |||||||
| chr19:38615848 | G | A | 1 | a0007c0017t0001g0016 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.313+347C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 4/30 | chr19 | 38615848 | |||||||
| chr19:38615927 | G | A | 1 | a0001c0001t0001g0333 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.313+268C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 4/30 | chr19 | 38615927 | |||||||
| chr19:38615971 | T | TA | 9 | a0001c0001t0001g0165 a0001c0001t0001g0168 a0001c0001t0001g0169 others(6): Show |
9 | HG01891.hp2 HG02155.hp1 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+223dupT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 4/30 | chr19 | 38615971 | |||||||
| chr19:38615971 | TA | T | 10 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(7): Show |
10 | HG01517.hp2 HG02735.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+223delT | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 4/30 | chr19 | 38615971 | |||||||
| chr19:38616157 | AG | A | 52 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0174 others(49): Show |
52 | HG00544.hp1 HG00621.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.313+37delC | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 4/30 | chr19 | 38616157 | |||||||
| chr19:38616284 | A | G | 110 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0229 others(107): Show |
111 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.249-25T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 3/30 | chr19 | 38616284 | |||||||
| chr19:38616339 | C | T | 1 | a0002c0008t0001g0220 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.249-80G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 3/30 | chr19 | 38616339 | |||||||
| chr19:38616375 | T | A | 1 | a0006c0013t0001g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.249-116A>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 3/30 | chr19 | 38616375 | |||||||
| chr19:38616382 | A | C | 1 | a0001c0001t0001g0021 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.249-123T>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 3/30 | chr19 | 38616382 | |||||||
| chr19:38616463 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.249-204A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 3/30 | chr19 | 38616463 | |||||||
| chr19:38616516 | T | C | 24 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(21): Show |
24 | HG00140.hp1 HG00280.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.249-257A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 3/30 | chr19 | 38616516 | |||||||
| chr19:38616591 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.249-332G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 3/30 | chr19 | 38616591 | |||||||
| chr19:38616601 | G | C | 118 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0229 others(115): Show |
119 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.249-342C>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 3/30 | chr19 | 38616601 | |||||||
| chr19:38616612 | C | G | 1 | a0001c0001t0001g0019 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.249-353G>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 3/30 | chr19 | 38616612 | |||||||
| chr19:38616730 | C | T | 1 | a0001c0002t0001g0018 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.249-471G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 3/30 | chr19 | 38616730 | |||||||
| chr19:38616737 | A | G | 1 | a0001c0002t0001g0017 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.249-478T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 3/30 | chr19 | 38616737 | |||||||
| chr19:38616776 | A | G | 8 | a0001c0001t0001g0336 a0001c0001t0001g0337 a0001c0004t0001g0012 others(5): Show |
8 | HG02896.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.249-517T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 3/30 | chr19 | 38616776 | |||||||
| chr19:38617014 | G | A | 1 | a0001c0004t0001g0334 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.248+340C>T | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 3/30 | chr19 | 38617014 | |||||||
| chr19:38617050 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.248+304T>C | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 3/30 | chr19 | 38617050 | |||||||
| chr19:38617071 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.248+283G>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 3/30 | chr19 | 38617071 | |||||||
| chr19:38617513 | G | T | 2 | a0001c0001t0001g0336 a0001c0001t0001g0337 |
2 | HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.157+55C>A | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 2/30 | chr19 | 38617513 | |||||||
| chr19:38617514 | T | C | 2 | a0001c0001t0001g0336 a0001c0001t0001g0337 |
2 | HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.157+54A>G | MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 2/30 | chr19 | 38617514 |