Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4225 |
| ensemblid | ENSG00000141434.12 |
| hgncid | 7020 |
| symbol | MEP1B |
| name | meprin A subunit beta |
| refseq_nuc | NM_005925.3 |
| refseq_prot | NP_005916.2 |
| ensembl_nuc | ENST00000269202.11 |
| ensembl_prot | ENSP00000269202.6 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 32190039 |
| end | 32220404 |
| strand | + |
| ver | v1.2 |
| region | chr18:32190039-32220404 |
| region5000 | chr18:32185039-32225404 |
| regionname0 | MEP1B_chr18_32190039_32220404 |
| regionname5000 | MEP1B_chr18_32185039_32225404 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 701 | 182 | 49 | 34 | 77 | 7 | 15 | 59 | MEP1B_chr18_32185039_32225404 | MEP1B | MDLWN others(696): Show |
chr18 | 32185039 | 32225404 |
| a0002 | 0/0 | 701 | 110 | 19 | 16 | 59 | 5 | 11 | 53 | MEP1B_chr18_32185039_32225404 | MEP1B | MDLWN others(696): Show |
chr18 | 32185039 | 32225404 |
| a0003 | 0/1 | 701 | 33 | 13 | 8 | 0 | 4 | 7 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | MDLWN others(696): Show |
chr18 | 32185039 | 32225404 |
| a0004 | 0/0 | 701 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | MDLWN others(696): Show |
chr18 | 32185039 | 32225404 |
| a0005 | 0/0 | 701 | 3 | 0 | 1 | 2 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | MDLWN others(696): Show |
chr18 | 32185039 | 32225404 |
| a0006 | 0/0 | 701 | 3 | 1 | 1 | 0 | 0 | 1 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | MDLWN others(696): Show |
chr18 | 32185039 | 32225404 |
| a0007 | 0/0 | 701 | 3 | 0 | 0 | 0 | 2 | 1 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | MDLWN others(696): Show |
chr18 | 32185039 | 32225404 |
| a0008 | 0/0 | 701 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | MDLWN others(696): Show |
chr18 | 32185039 | 32225404 |
| a0009 | 1/0 | 701 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | MDLWN others(696): Show |
chr18 | 32185039 | 32225404 |
| a0010 | 0/0 | 124 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | MDLWN others(119): Show |
chr18 | 32185039 | 32225404 |
| a0011 | 0/0 | 701 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | MDLWN others(696): Show |
chr18 | 32185039 | 32225404 |
| a0012 | 0/0 | 701 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | MDLWN others(696): Show |
chr18 | 32185039 | 32225404 |
| a0013 | 0/0 | 701 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | MDLWN others(696): Show |
chr18 | 32185039 | 32225404 |
| a0014 | 0/0 | 701 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | MDLWN others(696): Show |
chr18 | 32185039 | 32225404 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2103 | 157 | 30 | 34 | 72 | 7 | 14 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0001c0006 | 0/0 | 2103 | 14 | 14 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0001c0009 | 0/0 | 2103 | 6 | 0 | 0 | 5 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0001c0010 | 0/0 | 2103 | 4 | 4 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0001c0018 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0002c0002 | 0/0 | 2103 | 46 | 8 | 10 | 19 | 2 | 7 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0002c0003 | 0/0 | 2103 | 45 | 7 | 3 | 33 | 0 | 2 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0002c0005 | 0/0 | 2103 | 19 | 4 | 3 | 7 | 3 | 2 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0003c0004 | 0/1 | 2103 | 23 | 7 | 5 | 0 | 3 | 7 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0003c0007 | 0/0 | 2103 | 10 | 6 | 3 | 0 | 1 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0004c0008 | 0/0 | 2103 | 8 | 8 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0005c0014 | 0/0 | 2103 | 2 | 0 | 0 | 2 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0005c0022 | 0/0 | 2103 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0006c0011 | 0/0 | 2103 | 3 | 1 | 1 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0007c0012 | 0/0 | 2103 | 3 | 0 | 0 | 0 | 2 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0008c0013 | 0/0 | 2103 | 2 | 2 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0009c0021 | 1/0 | 2103 | 1 | 0 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0010c0017 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0011c0015 | 0/0 | 2103 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0012c0020 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0013c0019 | 0/0 | 2103 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 | ||
| a0014c0016 | 0/0 | 2103 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATGGA others(2098): Show |
chr18 | 32185039 | 32225404 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2297 | 156 | 30 | 34 | 72 | 7 | 13 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0001c0001t0003 | 0/0 | 2297 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0001c0006t0002 | 0/0 | 2297 | 14 | 14 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0001c0009t0001 | 0/0 | 2297 | 6 | 0 | 0 | 5 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0001c0010t0001 | 0/0 | 2297 | 4 | 4 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0001c0018t0001 | 0/0 | 2297 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0002c0002t0001 | 0/0 | 2297 | 46 | 8 | 10 | 19 | 2 | 7 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0002c0003t0001 | 0/0 | 2297 | 45 | 7 | 3 | 33 | 0 | 2 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0002c0005t0001 | 0/0 | 2297 | 19 | 4 | 3 | 7 | 3 | 2 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0003c0004t0001 | 0/1 | 2297 | 23 | 7 | 5 | 0 | 3 | 7 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0003c0007t0001 | 0/0 | 2297 | 10 | 6 | 3 | 0 | 1 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0004c0008t0001 | 0/0 | 2297 | 8 | 8 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0005c0014t0001 | 0/0 | 2297 | 2 | 0 | 0 | 2 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0005c0022t0001 | 0/0 | 2297 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0006c0011t0001 | 0/0 | 2297 | 3 | 1 | 1 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0007c0012t0001 | 0/0 | 2297 | 3 | 0 | 0 | 0 | 2 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0008c0013t0001 | 0/0 | 2297 | 2 | 2 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0009c0021t0001 | 1/0 | 2297 | 1 | 0 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0010c0017t0001 | 0/0 | 2297 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0011c0015t0001 | 0/0 | 2297 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0012c0020t0001 | 0/0 | 2297 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0013c0019t0001 | 0/0 | 2297 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| a0014c0016t0001 | 0/0 | 2297 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | ATAGT others(2292): Show |
chr18 | 32185039 | 32225404 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 28 | 0 | 10 | 12 | 1 | 5 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0003 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0019 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0006t0002g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0006t0002g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0006t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0006t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0006t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0006t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0006t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0006t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0009t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0009t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0009t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0009t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0009t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0010t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0010t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0001c0018t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0013 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0003t0001g0002 | 0/0 | 15 | 0 | 0 | 15 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0003t0001g0004 | 0/0 | 8 | 5 | 0 | 3 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0003t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0003t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0003t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0003t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0003t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0005t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0005t0001g0010 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0005t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0005t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0005t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0005t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0005t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0005t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0005t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0002c0005t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0032 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0004t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0007t0001g0017 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0007t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0007t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0007t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0007t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0007t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0007t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0003c0007t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0004c0008t0001g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0004c0008t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0004c0008t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0005c0014t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0005c0022t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0006c0011t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0006c0011t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0007c0012t0001g0011 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0008c0013t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0008c0013t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0009c0021t0001g0109 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0010c0017t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0011c0015t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0012c0020t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0013c0019t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| a0014c0016t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | GBR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00099 | hp2 | a0003 | c0004 | t0001 | g0081 | EUR | GBR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00140 | hp1 | a0003 | c0004 | t0001 | g0032 | EUR | GBR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | GBR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | FIN | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0208 | EUR | FIN | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00323 | hp1 | a0002 | c0005 | t0001 | g0160 | EUR | FIN | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | FIN | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00423 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | CHS | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | CHS | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0097 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00733 | hp2 | a0005 | c0022 | t0001 | g0201 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00735 | hp1 | a0003 | c0004 | t0001 | g0110 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00738 | hp1 | a0003 | c0007 | t0001 | g0176 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0044 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0044 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01074 | hp2 | a0003 | c0004 | t0001 | g0080 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01081 | hp1 | a0003 | c0004 | t0001 | g0079 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0188 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01167 | hp1 | a0002 | c0005 | t0001 | g0010 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01169 | hp1 | a0002 | c0005 | t0001 | g0010 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01175 | hp2 | a0006 | c0011 | t0001 | g0038 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01192 | hp1 | a0003 | c0004 | t0001 | g0158 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0207 | AMR | PUR | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01261 | hp2 | a0003 | c0004 | t0001 | g0106 | AMR | CLM | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | CLM | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0096 | AMR | CLM | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01515 | hp2 | a0002 | c0005 | t0001 | g0034 | EUR | IBS | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | IBS | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01516 | hp2 | a0007 | c0012 | t0001 | g0011 | EUR | IBS | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01517 | hp1 | a0002 | c0005 | t0001 | g0034 | EUR | IBS | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01517 | hp2 | a0007 | c0012 | t0001 | g0011 | EUR | IBS | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01884 | hp1 | a0010 | c0017 | t0001 | g0187 | AFR | ACB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01891 | hp1 | a0002 | c0005 | t0001 | g0010 | AFR | ACB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01891 | hp2 | a0001 | c0006 | t0002 | g0016 | AFR | ACB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01934 | hp1 | a0002 | c0003 | t0001 | g0030 | AMR | PEL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01943 | hp1 | a0003 | c0007 | t0001 | g0175 | AMR | PEL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0093 | AMR | PEL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01978 | hp2 | a0002 | c0005 | t0001 | g0111 | AMR | PEL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0112 | AMR | PEL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02027 | hp1 | a0002 | c0005 | t0001 | g0092 | EAS | KHV | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02055 | hp1 | a0001 | c0006 | t0002 | g0016 | AFR | ACB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02056 | hp1 | a0011 | c0015 | t0001 | g0001 | EAS | KHV | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02056 | hp2 | a0005 | c0014 | t0001 | g0001 | EAS | KHV | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02074 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | KHV | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02145 | hp1 | a0002 | c0005 | t0001 | g0010 | AFR | ACB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02148 | hp2 | a0002 | c0003 | t0001 | g0030 | AMR | PEL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CDX | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CDX | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02257 | hp2 | a0001 | c0006 | t0002 | g0063 | AFR | ACB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02258 | hp1 | a0003 | c0007 | t0001 | g0017 | AFR | ACB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02280 | hp2 | a0001 | c0006 | t0002 | g0007 | AFR | ACB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02293 | hp1 | a0002 | c0003 | t0001 | g0184 | AMR | PEL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02451 | hp1 | a0003 | c0004 | t0001 | g0056 | AFR | ACB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02451 | hp2 | a0001 | c0006 | t0002 | g0016 | AFR | ACB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | KHV | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0125 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02615 | hp1 | a0002 | c0003 | t0001 | g0004 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02622 | hp1 | a0004 | c0008 | t0001 | g0005 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02630 | hp1 | a0001 | c0010 | t0001 | g0200 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02647 | hp1 | a0004 | c0008 | t0001 | g0005 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02647 | hp2 | a0003 | c0007 | t0001 | g0193 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02698 | hp1 | a0002 | c0003 | t0001 | g0068 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02698 | hp2 | a0003 | c0004 | t0001 | g0085 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02723 | hp1 | a0001 | c0006 | t0002 | g0060 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02723 | hp2 | a0003 | c0007 | t0001 | g0177 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02735 | hp2 | a0013 | c0019 | t0001 | g0045 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02818 | hp2 | a0001 | c0006 | t0002 | g0189 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02886 | hp1 | a0001 | c0006 | t0002 | g0007 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02886 | hp2 | a0003 | c0007 | t0001 | g0178 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02895 | hp1 | a0001 | c0010 | t0001 | g0025 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02895 | hp2 | a0003 | c0007 | t0001 | g0179 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02896 | hp1 | a0008 | c0013 | t0001 | g0054 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02897 | hp1 | a0001 | c0010 | t0001 | g0025 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02897 | hp2 | a0008 | c0013 | t0001 | g0053 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0051 | AFR | ESN | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02965 | hp2 | a0002 | c0003 | t0001 | g0075 | AFR | ESN | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02970 | hp2 | a0001 | c0006 | t0002 | g0061 | AFR | ESN | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02976 | hp2 | a0003 | c0004 | t0001 | g0113 | AFR | ESN | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03041 | hp1 | a0003 | c0007 | t0001 | g0174 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03041 | hp2 | a0001 | c0006 | t0002 | g0007 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03098 | hp1 | a0001 | c0006 | t0002 | g0183 | AFR | MSL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03098 | hp2 | a0004 | c0008 | t0001 | g0005 | AFR | MSL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03130 | hp1 | a0004 | c0008 | t0001 | g0005 | AFR | ESN | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03130 | hp2 | a0002 | c0003 | t0001 | g0070 | AFR | ESN | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03139 | hp1 | a0001 | c0018 | t0001 | g0170 | AFR | ESN | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03139 | hp2 | a0002 | c0005 | t0001 | g0010 | AFR | ESN | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03209 | hp1 | a0004 | c0008 | t0001 | g0164 | AFR | MSL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03209 | hp2 | a0003 | c0004 | t0001 | g0052 | AFR | MSL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03225 | hp1 | a0002 | c0005 | t0001 | g0055 | AFR | MSL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0041 | AFR | MSL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03239 | hp2 | a0007 | c0012 | t0001 | g0011 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03453 | hp1 | a0003 | c0004 | t0001 | g0104 | AFR | MSL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03486 | hp1 | a0003 | c0004 | t0001 | g0181 | AFR | MSL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0206 | AFR | MSL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0211 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03516 | hp1 | a0001 | c0010 | t0001 | g0025 | AFR | ESN | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03516 | hp2 | a0004 | c0008 | t0001 | g0005 | AFR | ESN | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03540 | hp1 | a0001 | c0006 | t0002 | g0007 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03654 | hp1 | a0002 | c0005 | t0001 | g0159 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03654 | hp2 | a0003 | c0004 | t0001 | g0084 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03669 | hp1 | a0003 | c0004 | t0001 | g0031 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0204 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0212 | SAS | STU | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03688 | hp2 | a0002 | c0003 | t0001 | g0064 | SAS | STU | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03704 | hp1 | a0003 | c0004 | t0001 | g0011 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0013 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0013 | SAS | BEB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03831 | hp2 | a0006 | c0011 | t0001 | g0038 | SAS | BEB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03834 | hp1 | a0003 | c0004 | t0001 | g0082 | SAS | BEB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03942 | hp1 | a0002 | c0005 | t0001 | g0105 | SAS | BEB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0173 | SAS | BEB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG04184 | hp1 | a0003 | c0004 | t0001 | g0083 | SAS | BEB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG04184 | hp2 | a0001 | c0009 | t0001 | g0072 | SAS | BEB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0210 | SAS | STU | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG04199 | hp2 | a0003 | c0004 | t0001 | g0031 | SAS | STU | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | YRI | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18747 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | CHB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0205 | AFR | YRI | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18906 | hp2 | a0001 | c0006 | t0002 | g0062 | AFR | YRI | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18941 | hp1 | a0002 | c0003 | t0001 | g0069 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18942 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18943 | hp1 | a0002 | c0003 | t0001 | g0015 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18944 | hp1 | a0002 | c0005 | t0001 | g0009 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18946 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18949 | hp2 | a0002 | c0003 | t0001 | g0074 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18951 | hp1 | a0002 | c0003 | t0001 | g0008 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18952 | hp2 | a0002 | c0003 | t0001 | g0077 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18954 | hp1 | a0002 | c0003 | t0001 | g0073 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18959 | hp2 | a0002 | c0005 | t0001 | g0009 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18961 | hp1 | a0001 | c0009 | t0001 | g0067 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18961 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18964 | hp2 | a0002 | c0003 | t0001 | g0015 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18966 | hp1 | a0002 | c0005 | t0001 | g0009 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18967 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18968 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18969 | hp1 | a0002 | c0005 | t0001 | g0009 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18972 | hp2 | a0002 | c0003 | t0001 | g0029 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18973 | hp2 | a0002 | c0005 | t0001 | g0144 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18974 | hp2 | a0001 | c0009 | t0001 | g0066 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18977 | hp1 | a0002 | c0003 | t0001 | g0029 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18981 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18982 | hp1 | a0014 | c0016 | t0001 | g0008 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18983 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18983 | hp2 | a0001 | c0009 | t0001 | g0028 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18990 | hp2 | a0001 | c0009 | t0001 | g0028 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18992 | hp2 | a0002 | c0003 | t0001 | g0071 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19001 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19002 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19004 | hp2 | a0002 | c0003 | t0001 | g0008 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19006 | hp1 | a0002 | c0003 | t0001 | g0015 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19007 | hp2 | a0002 | c0005 | t0001 | g0009 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19009 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19012 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19030 | hp1 | a0004 | c0008 | t0001 | g0088 | AFR | LWK | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19043 | hp2 | a0004 | c0008 | t0001 | g0005 | AFR | LWK | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19058 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19060 | hp1 | a0005 | c0014 | t0001 | g0001 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19064 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19065 | hp1 | a0001 | c0009 | t0001 | g0076 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19077 | hp1 | a0002 | c0003 | t0001 | g0008 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19079 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19085 | hp1 | a0002 | c0003 | t0001 | g0065 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19090 | hp2 | a0002 | c0003 | t0001 | g0008 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19091 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19240 | hp1 | a0002 | c0003 | t0001 | g0004 | AFR | YRI | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0041 | AFR | YRI | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0090 | AFR | ASW | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA20129 | hp2 | a0006 | c0011 | t0001 | g0156 | AFR | ASW | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0203 | EUR | TSI | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA20752 | hp2 | a0003 | c0004 | t0001 | g0086 | EUR | TSI | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA20805 | hp1 | a0003 | c0007 | t0001 | g0017 | EUR | TSI | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | TSI | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG01123 | hp2 | a0003 | c0007 | t0001 | g0017 | AMR | CLM | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02109 | hp2 | a0001 | c0006 | t0002 | g0007 | AFR | ACB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG02559 | hp2 | a0012 | c0020 | t0001 | g0182 | AFR | ACB | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03471 | hp1 | a0002 | c0003 | t0001 | g0004 | AFR | MSL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | USA | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | USA | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0172 | AFR | USA | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA20300 | hp2 | a0003 | c0004 | t0001 | g0032 | AFR | USA | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0047 | AFR | LWK | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| NA21309 | hp2 | a0003 | c0004 | t0001 | g0163 | AFR | LWK | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| homoSapiens | chm13v2 | a0003 | c0004 | t0001 | g0078 | REF | REF | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| homoSapiens | grch38p0 | a0009 | c0021 | t0001 | g0109 | REF | REF | MEP1B_chr18_32185039_32225404 | MEP1B | chr18 | 32185039 | 32225404 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:32192678 | G | A | 1 | a0011 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.115G>A | p.Asp39Asn | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 3/15 | 147/2297 | 115/2106 | 39/701 | chr18 | 32192678 | |||
| chr18:32202925 | T | C | 1 | a0008 | 2 | HG02896.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.283T>C | p.Phe95Leu | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 6/15 | 315/2297 | 283/2106 | 95/701 | chr18 | 32202925 | |||
| chr18:32202990 | A | G | 1 | a0007 | 3 | HG01516.hp2 HG01517.hp2 HG03239.hp2 |
missense_variant | MODERATE | c.348A>G | p.Ile116Met | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 6/15 | 380/2297 | 348/2106 | 116/701 | chr18 | 32202990 | |||
| chr18:32204187 | G | A | 1 | a0010 | 1 | HG01884.hp1 | stop_gained | HIGH | c.374G>A | p.Trp125* | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/15 | 406/2297 | 374/2106 | 125/701 | chr18 | 32204187 | |||
| chr18:32204207 | C | G | 1 | a0005 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.394C>G | p.Arg132Gly | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/15 | 426/2297 | 394/2106 | 132/701 | chr18 | 32204207 | |||
| chr18:32204208 | G | A | 1 | a0005 | 2 | HG02056.hp2 NA19060.hp1 |
missense_variant | MODERATE | c.395G>A | p.Arg132Gln | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/15 | 427/2297 | 395/2106 | 132/701 | chr18 | 32204208 | |||
| chr18:32210557 | G | A | 1 | a0004 | 8 | HG02622.hp1 HG02647.hp1 HG03098.hp2 others(5): Show |
missense_variant | MODERATE | c.976G>A | p.Val326Met | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 10/15 | 1008/2297 | 976/2106 | 326/701 | chr18 | 32210557 | |||
| chr18:32213202 | T | A | 1 | a0012 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.1222T>A | p.Ser408Thr | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 11/15 | 1254/2297 | 1222/2106 | 408/701 | chr18 | 32213202 | |||
| chr18:32213218 | G | A | 1 | a0014 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.1238G>A | p.Gly413Asp | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 11/15 | 1270/2297 | 1238/2106 | 413/701 | chr18 | 32213218 | |||
| chr18:32213383 | C | T | 1 | a0006 | 3 | HG01175.hp2 HG03831.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.1403C>T | p.Ala468Val | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 11/15 | 1435/2297 | 1403/2106 | 468/701 | chr18 | 32213383 | |||
| chr18:32215138 | T | C | 10 | a0001 a0002 a0004 others(7): Show |
311 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
missense_variant | MODERATE | c.1636T>C | p.Ser546Pro | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/15 | 1668/2297 | 1636/2106 | 546/701 | chr18 | 32215138 | |||
| chr18:32217096 | G | A | 1 | a0013 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.1865G>A | p.Arg622Gln | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 13/15 | 1897/2297 | 1865/2106 | 622/701 | chr18 | 32217096 | |||
| chr18:32217958 | C | T | 7 | a0002 a0003 a0007 others(4): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): Show |
missense_variant | MODERATE | c.2084C>T | p.Pro695Leu | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/15 | 2116/2297 | 2084/2106 | 695/701 | chr18 | 32217958 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:32192796 | G | A | 3 | a0001c0009 a0002c0003 a0014c0016 |
52 | HG00423.hp2 HG01934.hp1 HG02074.hp2 others(49): Show |
synonymous_variant | LOW | c.150G>A | p.Glu50Glu | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/15 | 182/2297 | 150/2106 | 50/701 | chr18 | 32192796 | |||
| chr18:32208144 | G | A | 8 | a0001c0010 a0001c0018 a0002c0002 others(5): Show |
80 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(77): Show |
synonymous_variant | LOW | c.792G>A | p.Ser264Ser | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/15 | 824/2297 | 792/2106 | 264/701 | chr18 | 32208144 | |||
| chr18:32213147 | T | C | 1 | a0001c0018 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.1167T>C | p.His389His | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 11/15 | 1199/2297 | 1167/2106 | 389/701 | chr18 | 32213147 | |||
| chr18:32213249 | G | A | 2 | a0001c0010 a0004c0008 |
12 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(9): Show |
synonymous_variant | LOW | c.1269G>A | p.Ser423Ser | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 11/15 | 1301/2297 | 1269/2106 | 423/701 | chr18 | 32213249 | |||
| chr18:32215113 | T | C | 13 | a0001c0001 a0001c0009 a0001c0010 others(10): Show |
249 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
synonymous_variant | LOW | c.1611T>C | p.Ser537Ser | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/15 | 1643/2297 | 1611/2106 | 537/701 | chr18 | 32215113 | |||
| chr18:32215197 | C | T | 2 | a0001c0010 a0004c0008 |
12 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(9): Show |
synonymous_variant | LOW | c.1695C>T | p.His565His | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/15 | 1727/2297 | 1695/2106 | 565/701 | chr18 | 32215197 | |||
| chr18:32217827 | C | T | 2 | a0001c0010 a0004c0008 |
12 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(9): Show |
synonymous_variant | LOW | c.1953C>T | p.Asp651Asp | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/15 | 1985/2297 | 1953/2106 | 651/701 | chr18 | 32217827 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:32220292 | T | G | 1 | a0001c0001t0003 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*47T>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 15/15 | 47 | chr18 | 32220292 | ||||||
| chr18:32220361 | A | C | 1 | a0001c0006t0002 | 14 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*116A>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 15/15 | 116 | chr18 | 32220361 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:32190204 | TG | T | 26 | a0001c0001t0001g0043 a0001c0001t0001g0194 a0001c0001t0001g0195 others(23): Show |
36 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.63+72delG | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 1/14 | chr18 | 32190204 | |||||||
| chr18:32190253 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.63+120T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 1/14 | chr18 | 32190253 | |||||||
| chr18:32190271 | G | C | 1 | a0002c0002t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.63+138G>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 1/14 | chr18 | 32190271 | |||||||
| chr18:32190489 | C | T | 1 | a0001c0001t0001g0042 | 2 | HG01123.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.63+356C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 1/14 | chr18 | 32190489 | |||||||
| chr18:32190515 | G | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
5 | HG00609.hp2 NA18972.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+382G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 1/14 | chr18 | 32190515 | |||||||
| chr18:32190788 | T | C | 5 | a0002c0002t0001g0051 a0002c0005t0001g0055 a0003c0004t0001g0052 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+655T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 1/14 | chr18 | 32190788 | |||||||
| chr18:32190917 | C | T | 25 | a0001c0001t0001g0043 a0001c0001t0001g0195 a0001c0001t0001g0199 others(22): Show |
35 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.63+784C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 1/14 | chr18 | 32190917 | |||||||
| chr18:32190963 | A | G | 1 | a0003c0007t0001g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.63+830A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 1/14 | chr18 | 32190963 | |||||||
| chr18:32191175 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
6 | HG02027.hp2 NA18941.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-647C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 1/14 | chr18 | 32191175 | |||||||
| chr18:32191176 | A | G | 1 | a0001c0006t0002g0189 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.64-646A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 1/14 | chr18 | 32191176 | |||||||
| chr18:32191207 | G | GT | 9 | a0001c0001t0001g0040 a0001c0001t0001g0186 a0001c0001t0001g0192 others(6): Show |
11 | HG01109.hp1 HG01884.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-601dupT | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 32191207 | ||||||
| chr18:32191501 | G | A | 90 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0043 others(87): Show |
148 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.64-321G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 1/14 | chr18 | 32191501 | |||||||
| chr18:32192011 | C | G | 43 | a0001c0001t0001g0043 a0001c0001t0001g0091 a0001c0001t0001g0194 others(40): Show |
58 | HG00280.hp2 HG00673.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.82+171C>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 2/14 | chr18 | 32192011 | |||||||
| chr18:32192201 | A | G | 4 | a0001c0006t0002g0016 a0001c0006t0002g0189 a0004c0008t0001g0005 others(1): Show |
11 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.82+361A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 2/14 | chr18 | 32192201 | |||||||
| chr18:32192338 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.83-308C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 2/14 | chr18 | 32192338 | |||||||
| chr18:32192445 | C | T | 12 | a0003c0004t0001g0011 a0003c0004t0001g0031 a0003c0004t0001g0032 others(9): Show |
16 | HG00099.hp2 HG00140.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-201C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 2/14 | chr18 | 32192445 | |||||||
| chr18:32192537 | C | CACTT | 4 | a0001c0006t0002g0016 a0001c0006t0002g0189 a0004c0008t0001g0005 others(1): Show |
11 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.83-107_83-106insTT others(2): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr18 | 32192537 | ||||||
| chr18:32192559 | G | T | 2 | a0008c0013t0001g0053 a0008c0013t0001g0054 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.83-87G>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 2/14 | chr18 | 32192559 | |||||||
| chr18:32192729 | G | A | 1 | a0003c0004t0001g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.127+39G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 3/14 | chr18 | 32192729 | |||||||
| chr18:32193001 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.171+184T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | chr18 | 32193001 | |||||||
| chr18:32193013 | A | C | 48 | a0001c0001t0001g0180 a0001c0009t0001g0028 a0001c0009t0001g0066 others(45): Show |
81 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.171+196A>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | chr18 | 32193013 | |||||||
| chr18:32193044 | A | G | 2 | a0001c0009t0001g0076 a0002c0003t0001g0077 |
2 | NA18952.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.171+227A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | chr18 | 32193044 | |||||||
| chr18:32193208 | A | G | 41 | a0001c0001t0001g0043 a0001c0001t0001g0091 a0001c0001t0001g0194 others(38): Show |
52 | HG00280.hp2 HG00673.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.171+391A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | chr18 | 32193208 | |||||||
| chr18:32193337 | C | T | 4 | a0001c0006t0002g0016 a0001c0006t0002g0189 a0004c0008t0001g0005 others(1): Show |
11 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+520C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | chr18 | 32193337 | |||||||
| chr18:32193644 | T | C | 6 | a0001c0001t0001g0195 a0002c0002t0001g0012 a0002c0002t0001g0089 others(3): Show |
9 | HG02523.hp2 NA18955.hp2 NA18974.hp1 others(6): Show |
intron_variant | MODIFIER | c.171+827T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | chr18 | 32193644 | |||||||
| chr18:32193980 | G | A | 4 | a0001c0006t0002g0016 a0001c0006t0002g0189 a0004c0008t0001g0005 others(1): Show |
11 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+1163G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | chr18 | 32193980 | |||||||
| chr18:32194100 | A | C | 1 | a0001c0001t0001g0050 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.171+1283A>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | chr18 | 32194100 | |||||||
| chr18:32194190 | TAC | T | 47 | a0001c0001t0001g0023 a0001c0001t0001g0043 a0001c0001t0001g0091 others(44): Show |
61 | HG00280.hp1 HG00280.hp2 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.172-1214_172-1213d others(4): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr18 | 32194190 | ||||||
| chr18:32194285 | A | G | 1 | a0001c0001t0001g0022 | 3 | HG02165.hp2 NA18963.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.172-1122A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | chr18 | 32194285 | |||||||
| chr18:32194400 | C | G | 4 | a0001c0006t0002g0016 a0001c0006t0002g0189 a0004c0008t0001g0005 others(1): Show |
11 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-1007C>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | chr18 | 32194400 | |||||||
| chr18:32194436 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.172-971G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | chr18 | 32194436 | |||||||
| chr18:32194539 | C | T | 4 | a0001c0006t0002g0016 a0001c0006t0002g0189 a0004c0008t0001g0005 others(1): Show |
11 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-868C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | chr18 | 32194539 | |||||||
| chr18:32194635 | T | G | 1 | a0001c0001t0001g0171 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.172-772T>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | chr18 | 32194635 | |||||||
| chr18:32194751 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.172-656T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | chr18 | 32194751 | |||||||
| chr18:32195150 | C | T | 2 | a0008c0013t0001g0053 a0008c0013t0001g0054 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.172-257C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | chr18 | 32195150 | |||||||
| chr18:32195253 | AAAGTAGG others(9): Show |
A | 1 | a0001c0018t0001g0170 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.172-152_172-137del others(16): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr18 | 32195253 | ||||||
| chr18:32195263 | T | TAC | 4 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0151 others(1): Show |
4 | HG00609.hp1 HG00741.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-118_172-117dup others(2): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr18 | 32195263 | ||||||
| chr18:32195263 | T | TACACAC | 3 | a0001c0006t0002g0183 a0002c0005t0001g0010 a0002c0005t0001g0055 |
7 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-122_172-117dup others(6): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr18 | 32195263 | ||||||
| chr18:32195263 | TAC | T | 104 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0035 others(101): Show |
164 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.172-118_172-117del others(2): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr18 | 32195263 | ||||||
| chr18:32195263 | TACAC | T | 6 | a0001c0001t0001g0194 a0002c0002t0001g0013 a0002c0002t0001g0204 others(3): Show |
6 | HG02145.hp2 HG03491.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-120_172-117del others(4): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr18 | 32195263 | ||||||
| chr18:32195570 | A | G | 4 | a0001c0006t0002g0016 a0001c0006t0002g0189 a0004c0008t0001g0005 others(1): Show |
11 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.250+85A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32195570 | |||||||
| chr18:32195625 | GA | G | 4 | a0001c0006t0002g0016 a0001c0006t0002g0189 a0004c0008t0001g0005 others(1): Show |
11 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.250+150delA | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32195625 | ||||||
| chr18:32195735 | A | G | 4 | a0001c0006t0002g0016 a0001c0006t0002g0189 a0004c0008t0001g0005 others(1): Show |
11 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.250+250A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32195735 | |||||||
| chr18:32195902 | G | A | 1 | a0003c0007t0001g0174 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.250+417G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32195902 | |||||||
| chr18:32196174 | G | A | 2 | a0001c0001t0001g0199 a0002c0002t0001g0090 |
2 | HG01981.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.250+689G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32196174 | |||||||
| chr18:32196259 | C | T | 1 | a0002c0002t0001g0090 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.250+774C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32196259 | |||||||
| chr18:32196318 | C | T | 2 | a0008c0013t0001g0053 a0008c0013t0001g0054 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.250+833C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32196318 | |||||||
| chr18:32196343 | G | A | 1 | a0003c0004t0001g0104 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.250+858G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32196343 | |||||||
| chr18:32196352 | C | T | 1 | a0001c0001t0001g0039 | 2 | NA18968.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.250+867C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32196352 | |||||||
| chr18:32196499 | G | C | 1 | a0002c0005t0001g0105 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.250+1014G>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32196499 | |||||||
| chr18:32196578 | T | C | 15 | a0003c0004t0001g0011 a0003c0004t0001g0031 a0003c0004t0001g0032 others(12): Show |
19 | HG00099.hp2 HG00140.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.250+1093T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32196578 | |||||||
| chr18:32196648 | C | T | 1 | a0003c0004t0001g0086 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.250+1163C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32196648 | |||||||
| chr18:32196683 | A | G | 55 | a0001c0001t0001g0023 a0001c0001t0001g0043 a0001c0001t0001g0091 others(52): Show |
80 | HG00280.hp1 HG00280.hp2 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.250+1198A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32196683 | |||||||
| chr18:32196719 | A | G | 54 | a0001c0001t0001g0023 a0001c0001t0001g0043 a0001c0001t0001g0091 others(51): Show |
79 | HG00280.hp1 HG00280.hp2 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.250+1234A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32196719 | |||||||
| chr18:32196789 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.250+1304C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32196789 | |||||||
| chr18:32196875 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.250+1390C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32196875 | |||||||
| chr18:32196909 | C | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0022 |
9 | HG00423.hp1 HG02129.hp2 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.250+1424C>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32196909 | |||||||
| chr18:32196937 | C | T | 3 | a0001c0006t0002g0183 a0002c0005t0001g0010 a0002c0005t0001g0055 |
7 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.250+1452C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32196937 | |||||||
| chr18:32197131 | C | G | 1 | a0012c0020t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.250+1646C>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32197131 | |||||||
| chr18:32197153 | C | T | 4 | a0001c0001t0001g0014 a0001c0006t0002g0183 a0002c0005t0001g0010 others(1): Show |
10 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.250+1668C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32197153 | |||||||
| chr18:32197176 | G | A | 1 | a0002c0002t0001g0051 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.250+1691G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32197176 | |||||||
| chr18:32197212 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.250+1727A>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32197212 | |||||||
| chr18:32197308 | C | T | 7 | a0001c0006t0002g0016 a0001c0006t0002g0183 a0001c0006t0002g0189 others(4): Show |
18 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.250+1823C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32197308 | |||||||
| chr18:32197405 | G | GT | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.250+1933dupT | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32197405 | ||||||
| chr18:32197522 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.250+2037C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32197522 | |||||||
| chr18:32197545 | G | A | 7 | a0001c0006t0002g0016 a0001c0006t0002g0183 a0001c0006t0002g0189 others(4): Show |
18 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.250+2060G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32197545 | |||||||
| chr18:32197599 | T | C | 3 | a0001c0006t0002g0183 a0002c0005t0001g0010 a0002c0005t0001g0055 |
7 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.250+2114T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32197599 | |||||||
| chr18:32197624 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.250+2139C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32197624 | |||||||
| chr18:32197783 | T | C | 1 | a0002c0003t0001g0065 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.250+2298T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32197783 | |||||||
| chr18:32197847 | G | T | 1 | a0001c0001t0001g0165 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.250+2362G>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32197847 | |||||||
| chr18:32197916 | T | C | 4 | a0001c0006t0002g0183 a0001c0006t0002g0189 a0002c0005t0001g0010 others(1): Show |
8 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.250+2431T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32197916 | |||||||
| chr18:32197995 | C | G | 5 | a0001c0006t0002g0007 a0001c0006t0002g0060 a0001c0006t0002g0061 others(2): Show |
9 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.250+2510C>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32197995 | |||||||
| chr18:32198086 | G | C | 19 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(16): Show |
31 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.250+2601G>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32198086 | |||||||
| chr18:32198127 | G | T | 19 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(16): Show |
31 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.250+2642G>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32198127 | |||||||
| chr18:32198173 | C | T | 20 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(17): Show |
32 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.250+2688C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32198173 | |||||||
| chr18:32198299 | A | G | 21 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(18): Show |
35 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.250+2814A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32198299 | |||||||
| chr18:32198307 | G | A | 1 | a0001c0018t0001g0170 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.250+2822G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32198307 | |||||||
| chr18:32198353 | A | G | 7 | a0001c0006t0002g0007 a0001c0006t0002g0016 a0001c0006t0002g0060 others(4): Show |
13 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.250+2868A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32198353 | |||||||
| chr18:32198397 | G | A | 4 | a0003c0007t0001g0174 a0003c0007t0001g0177 a0003c0007t0001g0178 others(1): Show |
4 | HG02723.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.250+2912G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32198397 | |||||||
| chr18:32198424 | G | T | 17 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(14): Show |
27 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.250+2939G>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32198424 | |||||||
| chr18:32198454 | T | C | 1 | a0002c0003t0001g0015 | 3 | NA18943.hp1 NA18964.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.250+2969T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32198454 | |||||||
| chr18:32198669 | C | T | 11 | a0002c0002t0001g0033 a0002c0002t0001g0093 a0002c0002t0001g0094 others(8): Show |
12 | HG00673.hp2 HG00733.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.250+3184C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32198669 | |||||||
| chr18:32198698 | G | C | 1 | a0001c0001t0001g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.250+3213G>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32198698 | |||||||
| chr18:32198698 | G | T | 1 | a0001c0001t0001g0027 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.250+3213G>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32198698 | |||||||
| chr18:32198715 | C | T | 1 | a0003c0004t0001g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.250+3230C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32198715 | |||||||
| chr18:32198841 | A | G | 101 | a0001c0001t0001g0014 a0001c0001t0001g0180 a0001c0001t0001g0209 others(98): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.250+3356A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32198841 | |||||||
| chr18:32199040 | C | T | 101 | a0001c0001t0001g0014 a0001c0001t0001g0180 a0001c0001t0001g0209 others(98): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.250+3555C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32199040 | |||||||
| chr18:32199118 | C | T | 3 | a0001c0001t0001g0157 a0006c0011t0001g0038 a0006c0011t0001g0156 |
4 | HG01070.hp2 HG01175.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.250+3633C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32199118 | |||||||
| chr18:32199131 | G | C | 101 | a0001c0001t0001g0014 a0001c0001t0001g0180 a0001c0001t0001g0209 others(98): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.250+3646G>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32199131 | |||||||
| chr18:32199242 | G | A | 101 | a0001c0001t0001g0014 a0001c0001t0001g0180 a0001c0001t0001g0209 others(98): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.251-3651G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32199242 | |||||||
| chr18:32199524 | G | A | 101 | a0001c0001t0001g0014 a0001c0001t0001g0180 a0001c0001t0001g0209 others(98): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.251-3369G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32199524 | |||||||
| chr18:32199591 | GT | G | 101 | a0001c0001t0001g0014 a0001c0001t0001g0180 a0001c0001t0001g0209 others(98): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.251-3295delT | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32199591 | ||||||
| chr18:32199632 | CTTTTG | C | 7 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0118 others(4): Show |
15 | HG00673.hp1 HG01433.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.251-3256_251-3252d others(7): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32199632 | ||||||
| chr18:32199658 | C | CCCTT | 6 | a0003c0004t0001g0031 a0003c0004t0001g0079 a0003c0004t0001g0080 others(3): Show |
7 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.251-3234_251-3233i others(6): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32199658 | ||||||
| chr18:32199658 | C | CCCTTCCT others(5): Show |
1 | a0003c0007t0001g0175 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.251-3234_251-3233i others(14): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32199658 | ||||||
| chr18:32199658 | CCTTT | C | 23 | a0001c0018t0001g0170 a0002c0002t0001g0044 a0002c0002t0001g0047 others(20): Show |
28 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.251-3233_251-3230d others(6): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32199658 | ||||||
| chr18:32199658 | CCTTTCGT others(1): Show |
C | 27 | a0001c0001t0001g0209 a0002c0002t0001g0012 a0002c0002t0001g0013 others(24): Show |
44 | HG00280.hp2 HG00673.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.251-3233_251-3226d others(10): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32199658 | ||||||
| chr18:32199658 | CCTTTCGT others(5): Show |
C | 22 | a0001c0009t0001g0072 a0001c0009t0001g0076 a0002c0002t0001g0099 others(19): Show |
45 | HG00423.hp2 HG01934.hp1 HG02027.hp1 others(42): Show |
intron_variant | MODIFIER | c.251-3233_251-3222d others(14): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32199658 | ||||||
| chr18:32199658 | CCTTTCGT others(9): Show |
C | 6 | a0002c0003t0001g0074 a0002c0003t0001g0184 a0003c0007t0001g0179 others(3): Show |
11 | HG02293.hp1 HG02622.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.251-3233_251-3218d others(18): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32199658 | ||||||
| chr18:32199660 | T | C | 23 | a0001c0001t0001g0014 a0001c0001t0001g0180 a0002c0002t0001g0051 others(20): Show |
26 | HG00099.hp2 HG00738.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.251-3233T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32199660 | |||||||
| chr18:32199660 | T | TTTCG | 3 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0042 |
3 | HG01123.hp1 HG01884.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.251-3225_251-3222d others(6): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32199660 | ||||||
| chr18:32199664 | G | C | 46 | a0001c0001t0001g0014 a0001c0001t0001g0180 a0001c0018t0001g0170 others(43): Show |
54 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.251-3229G>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32199664 | |||||||
| chr18:32199664 | G | GTTCCTTC others(13): Show |
1 | a0001c0006t0002g0007 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.251-3226_251-3225i others(22): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32199664 | ||||||
| chr18:32199668 | G | C | 74 | a0001c0001t0001g0014 a0001c0001t0001g0180 a0001c0001t0001g0209 others(71): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.251-3225G>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32199668 | |||||||
| chr18:32199668 | G | GTTCC | 35 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(32): Show |
48 | HG00280.hp1 HG00621.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.251-3185_251-3182d others(6): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32199668 | ||||||
| chr18:32199668 | G | GTTCCTTC others(1): Show |
24 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0022 others(21): Show |
30 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.251-3189_251-3182d others(10): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32199668 | ||||||
| chr18:32199668 | G | GTTCCTTC others(5): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0147 a0001c0006t0002g0061 |
3 | HG00323.hp2 HG02970.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.251-3193_251-3182d others(14): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32199668 | ||||||
| chr18:32199668 | G | GTTCCTTC others(9): Show |
2 | a0001c0001t0001g0035 a0001c0001t0001g0148 |
2 | HG01167.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.251-3197_251-3182d others(18): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32199668 | ||||||
| chr18:32199668 | G | GTTCCTTC others(17): Show |
1 | a0001c0006t0002g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.251-3205_251-3182d others(26): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32199668 | ||||||
| chr18:32199668 | GTTCC | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0116 others(8): Show |
20 | HG00738.hp2 HG00741.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.251-3185_251-3182d others(6): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32199668 | ||||||
| chr18:32199672 | C | G | 1 | a0001c0001t0001g0155 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.251-3221C>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32199672 | |||||||
| chr18:32199704 | C | CTTCCTTC others(18): Show |
1 | a0001c0001t0001g0103 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.251-3182_251-3181i others(27): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32199704 | ||||||
| chr18:32199797 | T | C | 118 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0035 others(115): Show |
181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.251-3096T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32199797 | |||||||
| chr18:32199844 | T | G | 1 | a0002c0002t0001g0093 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.251-3049T>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32199844 | |||||||
| chr18:32199865 | G | A | 3 | a0003c0007t0001g0177 a0003c0007t0001g0178 a0003c0007t0001g0179 |
3 | HG02723.hp2 HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.251-3028G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32199865 | |||||||
| chr18:32199882 | T | C | 3 | a0004c0008t0001g0005 a0004c0008t0001g0088 a0004c0008t0001g0164 |
8 | HG02622.hp1 HG02647.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.251-3011T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32199882 | |||||||
| chr18:32199899 | C | T | 1 | a0002c0002t0001g0212 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.251-2994C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32199899 | |||||||
| chr18:32199922 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0107 a0003c0007t0001g0193 |
5 | HG01884.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.251-2971G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32199922 | |||||||
| chr18:32199935 | TC | T | 4 | a0003c0007t0001g0174 a0003c0007t0001g0177 a0003c0007t0001g0178 others(1): Show |
4 | HG02723.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-2956delC | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32199935 | ||||||
| chr18:32199955 | T | A | 1 | a0003c0004t0001g0163 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.251-2938T>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32199955 | |||||||
| chr18:32199963 | T | G | 1 | a0012c0020t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.251-2930T>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32199963 | |||||||
| chr18:32200013 | T | C | 7 | a0001c0006t0002g0007 a0001c0006t0002g0016 a0001c0006t0002g0060 others(4): Show |
13 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.251-2880T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32200013 | |||||||
| chr18:32200026 | AT | A | 7 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0171 others(4): Show |
12 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.251-2857delT | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32200026 | ||||||
| chr18:32200059 | T | A | 17 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(14): Show |
27 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.251-2834T>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32200059 | |||||||
| chr18:32200159 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.251-2734C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32200159 | |||||||
| chr18:32200312 | C | T | 20 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(17): Show |
35 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.251-2581C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32200312 | |||||||
| chr18:32200397 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0180 |
4 | HG02258.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-2496T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32200397 | |||||||
| chr18:32200505 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.251-2388C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32200505 | |||||||
| chr18:32200533 | TGACTCA | T | 47 | a0001c0009t0001g0072 a0001c0009t0001g0076 a0002c0003t0001g0002 others(44): Show |
84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.251-2355_251-2350d others(8): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32200533 | ||||||
| chr18:32200585 | A | G | 20 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(17): Show |
35 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.251-2308A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32200585 | |||||||
| chr18:32200739 | C | T | 38 | a0001c0001t0001g0209 a0002c0002t0001g0012 a0002c0002t0001g0013 others(35): Show |
47 | HG00280.hp2 HG00673.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.251-2154C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32200739 | |||||||
| chr18:32200805 | A | G | 3 | a0004c0008t0001g0005 a0004c0008t0001g0088 a0004c0008t0001g0164 |
8 | HG02622.hp1 HG02647.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.251-2088A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32200805 | |||||||
| chr18:32200931 | C | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0102 a0001c0001t0001g0107 others(1): Show |
6 | HG01884.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.251-1962C>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32200931 | |||||||
| chr18:32200977 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.251-1916A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32200977 | |||||||
| chr18:32201250 | A | G | 2 | a0002c0005t0001g0010 a0002c0005t0001g0055 |
6 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-1643A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32201250 | |||||||
| chr18:32201299 | T | TAC | 20 | a0001c0001t0001g0091 a0001c0001t0001g0124 a0001c0001t0001g0126 others(17): Show |
22 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.251-1561_251-1560d others(4): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32201299 | ||||||
| chr18:32201299 | T | TACAC | 40 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(37): Show |
56 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.251-1563_251-1560d others(6): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32201299 | ||||||
| chr18:32201299 | T | TACACAC | 32 | a0001c0001t0001g0209 a0001c0006t0002g0060 a0001c0006t0002g0061 others(29): Show |
46 | HG00280.hp2 HG00673.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.251-1565_251-1560d others(8): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32201299 | ||||||
| chr18:32201299 | T | TACACACA others(1): Show |
9 | a0001c0001t0001g0014 a0001c0001t0001g0120 a0001c0001t0001g0153 others(6): Show |
11 | HG01243.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.251-1567_251-1560d others(10): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32201299 | ||||||
| chr18:32201299 | T | TACACACA others(3): Show |
2 | a0002c0002t0001g0161 a0002c0002t0001g0162 |
2 | NA18952.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.251-1569_251-1560d others(12): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32201299 | ||||||
| chr18:32201299 | TAC | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0119 a0001c0001t0001g0152 others(1): Show |
6 | HG00609.hp1 HG00673.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-1561_251-1560d others(4): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32201299 | ||||||
| chr18:32201299 | TACAC | T | 3 | a0002c0005t0001g0055 a0008c0013t0001g0053 a0008c0013t0001g0054 |
3 | HG02896.hp1 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.251-1563_251-1560d others(6): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32201299 | ||||||
| chr18:32201299 | TACACAC | T | 2 | a0001c0006t0002g0189 a0002c0005t0001g0010 |
6 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-1565_251-1560d others(8): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32201299 | ||||||
| chr18:32201309 | C | CACAA | 27 | a0001c0009t0001g0072 a0001c0009t0001g0076 a0002c0003t0001g0002 others(24): Show |
60 | HG00323.hp1 HG00423.hp2 HG01515.hp2 others(57): Show |
intron_variant | MODIFIER | c.251-1581_251-1580i others(6): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 32201309 | ||||||
| chr18:32201374 | G | A | 20 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(17): Show |
35 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.251-1519G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32201374 | |||||||
| chr18:32201453 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.251-1440T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32201453 | |||||||
| chr18:32201525 | G | C | 20 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(17): Show |
35 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.251-1368G>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32201525 | |||||||
| chr18:32201558 | T | C | 20 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(17): Show |
35 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.251-1335T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32201558 | |||||||
| chr18:32201682 | C | T | 17 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(14): Show |
27 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.251-1211C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32201682 | |||||||
| chr18:32201741 | C | T | 4 | a0001c0006t0002g0061 a0004c0008t0001g0005 a0004c0008t0001g0088 others(1): Show |
9 | HG02622.hp1 HG02647.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.251-1152C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32201741 | |||||||
| chr18:32201742 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.251-1151G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32201742 | |||||||
| chr18:32201912 | A | T | 20 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(17): Show |
35 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.251-981A>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32201912 | |||||||
| chr18:32201938 | C | G | 38 | a0001c0001t0001g0209 a0002c0002t0001g0012 a0002c0002t0001g0013 others(35): Show |
47 | HG00280.hp2 HG00673.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.251-955C>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32201938 | |||||||
| chr18:32202003 | A | G | 20 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(17): Show |
35 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.251-890A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32202003 | |||||||
| chr18:32202282 | A | C | 1 | a0001c0001t0001g0057 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.251-611A>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32202282 | |||||||
| chr18:32202357 | T | C | 1 | a0001c0010t0001g0200 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.251-536T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32202357 | |||||||
| chr18:32202426 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0180 |
4 | HG02258.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-467A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32202426 | |||||||
| chr18:32202441 | C | T | 20 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(17): Show |
35 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.251-452C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32202441 | |||||||
| chr18:32202710 | A | T | 1 | a0003c0004t0001g0104 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.251-183A>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 5/14 | chr18 | 32202710 | |||||||
| chr18:32203102 | T | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0180 |
4 | HG02258.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.368+92T>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 6/14 | chr18 | 32203102 | |||||||
| chr18:32203200 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.368+190C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 6/14 | chr18 | 32203200 | |||||||
| chr18:32203201 | G | A | 22 | a0001c0018t0001g0170 a0003c0004t0001g0011 a0003c0004t0001g0031 others(19): Show |
26 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.368+191G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 6/14 | chr18 | 32203201 | |||||||
| chr18:32203271 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0130 |
2 | NA18951.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.368+261G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 6/14 | chr18 | 32203271 | |||||||
| chr18:32203300 | T | G | 3 | a0002c0003t0001g0008 a0002c0003t0001g0071 a0014c0016t0001g0008 |
6 | NA18951.hp1 NA18982.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.368+290T>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 6/14 | chr18 | 32203300 | |||||||
| chr18:32203303 | A | G | 1 | a0002c0002t0001g0051 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.368+293A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 6/14 | chr18 | 32203303 | |||||||
| chr18:32203334 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.368+324T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 6/14 | chr18 | 32203334 | |||||||
| chr18:32203406 | C | T | 4 | a0002c0002t0001g0012 a0002c0002t0001g0196 a0002c0002t0001g0197 others(1): Show |
7 | NA18974.hp1 NA18980.hp1 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.368+396C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 6/14 | chr18 | 32203406 | |||||||
| chr18:32203409 | G | C | 1 | a0012c0020t0001g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.368+399G>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 6/14 | chr18 | 32203409 | |||||||
| chr18:32203515 | T | G | 97 | a0001c0001t0001g0014 a0001c0001t0001g0180 a0001c0001t0001g0209 others(94): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.368+505T>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 6/14 | chr18 | 32203515 | |||||||
| chr18:32203545 | G | A | 1 | a0005c0022t0001g0201 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.368+535G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 6/14 | chr18 | 32203545 | |||||||
| chr18:32203601 | T | A | 1 | a0001c0001t0001g0168 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.369-581T>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 6/14 | chr18 | 32203601 | |||||||
| chr18:32203611 | C | T | 1 | a0010c0017t0001g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.369-571C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 6/14 | chr18 | 32203611 | |||||||
| chr18:32203701 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.369-481T>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 6/14 | chr18 | 32203701 | |||||||
| chr18:32203922 | T | A | 95 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0035 others(92): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.369-260T>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 6/14 | chr18 | 32203922 | |||||||
| chr18:32204141 | G | T | 4 | a0001c0010t0001g0025 a0001c0010t0001g0200 a0002c0002t0001g0051 others(1): Show |
6 | HG01884.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.369-41G>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 6/14 | chr18 | 32204141 | |||||||
| chr18:32204383 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0186 |
2 | HG00140.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.547+23T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32204383 | |||||||
| chr18:32204407 | C | T | 22 | a0003c0004t0001g0011 a0003c0004t0001g0031 a0003c0004t0001g0032 others(19): Show |
26 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.547+47C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32204407 | |||||||
| chr18:32204459 | C | T | 2 | a0002c0005t0001g0111 a0002c0005t0001g0160 |
2 | HG00323.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.547+99C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32204459 | |||||||
| chr18:32204521 | G | C | 1 | a0003c0004t0001g0106 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.547+161G>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32204521 | |||||||
| chr18:32204622 | C | T | 73 | a0001c0001t0001g0014 a0001c0001t0001g0180 a0001c0010t0001g0025 others(70): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.547+262C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32204622 | |||||||
| chr18:32204736 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.547+376T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32204736 | |||||||
| chr18:32204963 | T | A | 1 | a0003c0004t0001g0079 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.547+603T>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32204963 | |||||||
| chr18:32205289 | G | A | 3 | a0002c0002t0001g0044 a0002c0002t0001g0203 a0002c0002t0001g0208 |
4 | HG00280.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.547+929G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32205289 | |||||||
| chr18:32205342 | A | T | 1 | a0002c0002t0001g0098 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.547+982A>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32205342 | |||||||
| chr18:32205375 | G | C | 1 | a0002c0002t0001g0095 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.547+1015G>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32205375 | |||||||
| chr18:32205476 | C | T | 4 | a0001c0001t0001g0059 a0001c0001t0001g0150 a0001c0001t0001g0168 others(1): Show |
4 | HG02055.hp2 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.547+1116C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32205476 | |||||||
| chr18:32205489 | G | A | 1 | a0001c0018t0001g0170 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.547+1129G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32205489 | |||||||
| chr18:32205509 | C | G | 92 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0035 others(89): Show |
124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.547+1149C>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32205509 | |||||||
| chr18:32205630 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.547+1270T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32205630 | |||||||
| chr18:32205734 | T | A | 3 | a0004c0008t0001g0005 a0004c0008t0001g0088 a0004c0008t0001g0164 |
8 | HG02622.hp1 HG02647.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.547+1374T>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32205734 | |||||||
| chr18:32205743 | T | TATA | 4 | a0001c0010t0001g0025 a0001c0010t0001g0200 a0002c0002t0001g0051 others(1): Show |
6 | HG01884.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+1383_547+1384i others(5): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32205743 | |||||||
| chr18:32205744 | G | T | 4 | a0001c0010t0001g0025 a0001c0010t0001g0200 a0002c0002t0001g0051 others(1): Show |
6 | HG01884.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+1384G>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32205744 | |||||||
| chr18:32206045 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.548-1207G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32206045 | |||||||
| chr18:32206131 | G | C | 18 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(15): Show |
33 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.548-1121G>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32206131 | |||||||
| chr18:32206430 | CT | C | 12 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(9): Show |
16 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.548-805delT | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr18 | 32206430 | ||||||
| chr18:32206449 | A | G | 1 | a0002c0003t0001g0065 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.548-803A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32206449 | |||||||
| chr18:32206607 | A | ATTTAT | 4 | a0003c0007t0001g0174 a0003c0007t0001g0177 a0003c0007t0001g0178 others(1): Show |
4 | HG02723.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.548-627_548-623dup others(5): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr18 | 32206607 | ||||||
| chr18:32206698 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.548-554G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32206698 | |||||||
| chr18:32206713 | C | G | 19 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(16): Show |
34 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.548-539C>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32206713 | |||||||
| chr18:32206986 | C | T | 1 | a0002c0002t0001g0044 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.548-266C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32206986 | |||||||
| chr18:32206989 | G | A | 16 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(13): Show |
26 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.548-263G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32206989 | |||||||
| chr18:32207018 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.548-234C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32207018 | |||||||
| chr18:32207139 | T | C | 16 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(13): Show |
26 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.548-113T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 7/14 | chr18 | 32207139 | |||||||
| chr18:32207532 | G | T | 7 | a0001c0006t0002g0007 a0001c0006t0002g0016 a0001c0006t0002g0060 others(4): Show |
13 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.766+62G>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 8/14 | chr18 | 32207532 | |||||||
| chr18:32207575 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0107 a0003c0007t0001g0193 |
5 | HG01884.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.766+105T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 8/14 | chr18 | 32207575 | |||||||
| chr18:32207744 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.766+274C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 8/14 | chr18 | 32207744 | |||||||
| chr18:32207937 | C | A | 90 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0035 others(87): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.767-182C>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 8/14 | chr18 | 32207937 | |||||||
| chr18:32208084 | T | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0001g0166 |
3 | NA18951.hp2 NA18978.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.767-35T>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 8/14 | chr18 | 32208084 | |||||||
| chr18:32208394 | A | G | 15 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(12): Show |
25 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.919+123A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32208394 | |||||||
| chr18:32208550 | C | G | 12 | a0003c0004t0001g0011 a0003c0004t0001g0031 a0003c0004t0001g0032 others(9): Show |
16 | HG00099.hp2 HG00140.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.919+279C>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32208550 | |||||||
| chr18:32208571 | C | G | 1 | a0002c0002t0001g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.919+300C>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32208571 | |||||||
| chr18:32208608 | A | C | 3 | a0004c0008t0001g0005 a0004c0008t0001g0088 a0004c0008t0001g0164 |
8 | HG02622.hp1 HG02647.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+337A>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32208608 | |||||||
| chr18:32208716 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.919+445T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32208716 | |||||||
| chr18:32208820 | T | A | 19 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(16): Show |
34 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.919+549T>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32208820 | |||||||
| chr18:32209132 | T | G | 5 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0116 others(2): Show |
7 | HG00733.hp2 HG01074.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+861T>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32209132 | |||||||
| chr18:32209202 | T | C | 67 | a0001c0010t0001g0025 a0001c0010t0001g0200 a0001c0018t0001g0170 others(64): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.919+931T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32209202 | |||||||
| chr18:32209249 | G | A | 41 | a0001c0010t0001g0025 a0001c0010t0001g0200 a0002c0002t0001g0012 others(38): Show |
52 | HG00280.hp2 HG00673.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.919+978G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32209249 | |||||||
| chr18:32209310 | A | C | 74 | a0001c0001t0001g0014 a0001c0001t0001g0180 a0001c0006t0002g0189 others(71): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.919+1039A>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32209310 | |||||||
| chr18:32209367 | G | C | 26 | a0001c0018t0001g0170 a0003c0004t0001g0011 a0003c0004t0001g0031 others(23): Show |
30 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.919+1096G>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32209367 | |||||||
| chr18:32209469 | A | G | 5 | a0001c0006t0002g0189 a0003c0007t0001g0174 a0003c0007t0001g0177 others(2): Show |
5 | HG02723.hp2 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.920-1032A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32209469 | |||||||
| chr18:32209470 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0180 |
4 | HG02258.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-1031G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32209470 | |||||||
| chr18:32209486 | C | CA | 46 | a0001c0001t0001g0136 a0001c0006t0002g0189 a0001c0010t0001g0025 others(43): Show |
57 | HG00280.hp2 HG00673.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.920-999dupA | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 32209486 | ||||||
| chr18:32209486 | C | CAA | 6 | a0001c0001t0001g0115 a0001c0006t0002g0062 a0002c0002t0001g0047 others(3): Show |
11 | HG02622.hp1 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.920-1000_920-999du others(3): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 32209486 | ||||||
| chr18:32209486 | C | CAAA | 14 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(11): Show |
24 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.920-1001_920-999du others(4): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 32209486 | ||||||
| chr18:32209486 | CA | C | 9 | a0001c0001t0001g0108 a0001c0001t0001g0123 a0001c0001t0001g0157 others(6): Show |
9 | HG01070.hp2 HG02451.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-999delA | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 32209486 | ||||||
| chr18:32209598 | A | G | 74 | a0001c0001t0001g0014 a0001c0001t0001g0180 a0001c0006t0002g0189 others(71): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.920-903A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32209598 | |||||||
| chr18:32209676 | T | A | 1 | a0001c0018t0001g0170 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.920-825T>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32209676 | |||||||
| chr18:32209710 | TA | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(211): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.920-789delA | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 32209710 | ||||||
| chr18:32209753 | T | C | 16 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(13): Show |
24 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.920-748T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32209753 | |||||||
| chr18:32209818 | A | AG | 125 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0023 others(122): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.920-677dupG | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 32209818 | ||||||
| chr18:32209818 | A | G | 3 | a0001c0001t0001g0131 a0001c0001t0001g0149 a0002c0002t0001g0097 |
3 | HG00733.hp1 HG01071.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.920-683A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32209818 | |||||||
| chr18:32209844 | C | A | 1 | a0002c0002t0001g0173 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.920-657C>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32209844 | |||||||
| chr18:32209848 | G | A | 1 | a0002c0002t0001g0210 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.920-653G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32209848 | |||||||
| chr18:32209918 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.920-583G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32209918 | |||||||
| chr18:32209932 | G | A | 19 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(16): Show |
34 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.920-569G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32209932 | |||||||
| chr18:32209981 | G | A | 5 | a0001c0006t0002g0189 a0003c0007t0001g0174 a0003c0007t0001g0177 others(2): Show |
5 | HG02723.hp2 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.920-520G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32209981 | |||||||
| chr18:32210021 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG00323.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.920-480C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32210021 | |||||||
| chr18:32210059 | A | G | 4 | a0001c0001t0001g0059 a0001c0001t0001g0150 a0001c0001t0001g0168 others(1): Show |
4 | HG02055.hp2 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-442A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32210059 | |||||||
| chr18:32210066 | T | C | 19 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(16): Show |
34 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.920-435T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32210066 | |||||||
| chr18:32210184 | G | A | 7 | a0001c0006t0002g0007 a0001c0006t0002g0016 a0001c0006t0002g0060 others(4): Show |
13 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.920-317G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32210184 | |||||||
| chr18:32210413 | C | T | 19 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(16): Show |
34 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.920-88C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32210413 | |||||||
| chr18:32210415 | C | T | 93 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0035 others(90): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.920-86C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32210415 | |||||||
| chr18:32210461 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0145 |
2 | HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.920-40C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32210461 | |||||||
| chr18:32210495 | T | C | 3 | a0004c0008t0001g0005 a0004c0008t0001g0088 a0004c0008t0001g0164 |
8 | HG02622.hp1 HG02647.hp1 HG03098.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.920-6T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 9/14 | chr18 | 32210495 | |||||||
| chr18:32210777 | T | C | 3 | a0004c0008t0001g0005 a0004c0008t0001g0088 a0004c0008t0001g0164 |
8 | HG02622.hp1 HG02647.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1135+61T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 10/14 | chr18 | 32210777 | |||||||
| chr18:32210805 | A | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0180 |
4 | HG02258.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135+89A>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 10/14 | chr18 | 32210805 | |||||||
| chr18:32210926 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(118): Show |
220 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1135+210G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 10/14 | chr18 | 32210926 | |||||||
| chr18:32211055 | C | T | 1 | a0006c0011t0001g0156 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1135+339C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 10/14 | chr18 | 32211055 | |||||||
| chr18:32211248 | G | A | 1 | a0001c0001t0001g0037 | 2 | HG02523.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1135+532G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 10/14 | chr18 | 32211248 | |||||||
| chr18:32211269 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0191 |
4 | HG00544.hp2 NA18955.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135+553T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 10/14 | chr18 | 32211269 | |||||||
| chr18:32211521 | A | C | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1135+805A>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 10/14 | chr18 | 32211521 | |||||||
| chr18:32211626 | A | G | 1 | a0002c0002t0001g0051 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1135+910A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 10/14 | chr18 | 32211626 | |||||||
| chr18:32211631 | G | C | 2 | a0003c0004t0001g0080 a0003c0004t0001g0085 |
2 | HG01074.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1135+915G>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 10/14 | chr18 | 32211631 | |||||||
| chr18:32211688 | G | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0138 a0001c0001t0001g0195 |
3 | HG00597.hp2 NA18955.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1135+972G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 10/14 | chr18 | 32211688 | |||||||
| chr18:32211735 | G | A | 1 | a0002c0002t0001g0185 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1135+1019G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 10/14 | chr18 | 32211735 | |||||||
| chr18:32212024 | T | C | 5 | a0001c0010t0001g0025 a0001c0010t0001g0200 a0004c0008t0001g0005 others(2): Show |
12 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1136-1092T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 10/14 | chr18 | 32212024 | |||||||
| chr18:32212522 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(136): Show |
251 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.1136-594A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 10/14 | chr18 | 32212522 | |||||||
| chr18:32212567 | T | A | 1 | a0001c0001t0001g0146 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1136-549T>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 10/14 | chr18 | 32212567 | |||||||
| chr18:32212833 | T | C | 5 | a0001c0010t0001g0025 a0001c0010t0001g0200 a0004c0008t0001g0005 others(2): Show |
12 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1136-283T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 10/14 | chr18 | 32212833 | |||||||
| chr18:32212908 | G | A | 1 | a0001c0001t0003g0125 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1136-208G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 10/14 | chr18 | 32212908 | |||||||
| chr18:32212937 | C | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0035 others(8): Show |
17 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1136-179C>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 10/14 | chr18 | 32212937 | |||||||
| chr18:32213563 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(117): Show |
219 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(216): Show |
splice_region_variant&intron_variant | LOW | c.1579+4C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 11/14 | chr18 | 32213563 | |||||||
| chr18:32213718 | C | T | 1 | a0002c0002t0001g0206 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1579+159C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 11/14 | chr18 | 32213718 | |||||||
| chr18:32213745 | C | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(142): Show |
263 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1579+186C>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 11/14 | chr18 | 32213745 | |||||||
| chr18:32213919 | G | A | 2 | a0002c0002t0001g0045 a0013c0019t0001g0045 |
2 | HG02735.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1579+360G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 11/14 | chr18 | 32213919 | |||||||
| chr18:32213961 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1579+402T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 11/14 | chr18 | 32213961 | |||||||
| chr18:32213976 | A | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0152 |
2 | HG00609.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1579+417A>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 11/14 | chr18 | 32213976 | |||||||
| chr18:32214021 | C | T | 5 | a0001c0010t0001g0025 a0001c0010t0001g0200 a0004c0008t0001g0005 others(2): Show |
12 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1579+462C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 11/14 | chr18 | 32214021 | |||||||
| chr18:32214104 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(117): Show |
219 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.1579+545G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 11/14 | chr18 | 32214104 | |||||||
| chr18:32214284 | A | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(134): Show |
249 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1579+725A>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 11/14 | chr18 | 32214284 | |||||||
| chr18:32214353 | C | A | 1 | a0001c0001t0001g0140 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1580-729C>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 11/14 | chr18 | 32214353 | |||||||
| chr18:32214390 | T | C | 39 | a0002c0002t0001g0012 a0002c0002t0001g0013 a0002c0002t0001g0033 others(36): Show |
48 | HG00280.hp2 HG00673.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.1580-692T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 11/14 | chr18 | 32214390 | |||||||
| chr18:32214409 | C | T | 2 | a0002c0003t0001g0030 a0002c0003t0001g0184 |
3 | HG01934.hp1 HG02148.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1580-673C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 11/14 | chr18 | 32214409 | |||||||
| chr18:32214623 | G | A | 1 | a0002c0002t0001g0206 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1580-459G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 11/14 | chr18 | 32214623 | |||||||
| chr18:32214647 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1580-435A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 11/14 | chr18 | 32214647 | |||||||
| chr18:32215301 | T | A | 30 | a0001c0001t0001g0018 a0001c0001t0001g0102 a0001c0001t0001g0107 others(27): Show |
65 | HG00323.hp1 HG00423.hp2 HG01515.hp2 others(62): Show |
intron_variant | MODIFIER | c.1759+40T>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32215301 | |||||||
| chr18:32215304 | G | T | 1 | a0002c0002t0001g0205 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1759+43G>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32215304 | |||||||
| chr18:32215362 | T | G | 1 | a0003c0004t0001g0086 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1759+101T>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32215362 | |||||||
| chr18:32215498 | G | A | 2 | a0002c0003t0001g0068 a0002c0005t0001g0159 |
2 | HG02698.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1759+237G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32215498 | |||||||
| chr18:32215620 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1759+359C>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32215620 | |||||||
| chr18:32215729 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1759+468C>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32215729 | |||||||
| chr18:32215740 | T | C | 5 | a0002c0002t0001g0206 a0003c0004t0001g0113 a0003c0004t0001g0181 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1759+479T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32215740 | |||||||
| chr18:32215755 | C | T | 1 | a0003c0004t0001g0163 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1759+494C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32215755 | |||||||
| chr18:32215756 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1759+495G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32215756 | |||||||
| chr18:32215780 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(142): Show |
262 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.1759+519T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32215780 | |||||||
| chr18:32215812 | A | G | 1 | a0001c0018t0001g0170 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1759+551A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32215812 | |||||||
| chr18:32215953 | CATGCATA others(27): Show |
C | 1 | a0002c0002t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1759+695_1759+728d others(36): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr18 | 32215953 | ||||||
| chr18:32215969 | C | CATAT | 3 | a0002c0005t0001g0009 a0003c0004t0001g0032 a0007c0012t0001g0011 |
3 | HG00140.hp1 HG03239.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.1759+755_1759+758d others(6): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr18 | 32215969 | ||||||
| chr18:32215969 | C | CATATATA others(3): Show |
1 | a0002c0003t0001g0002 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1759+749_1759+758d others(12): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr18 | 32215969 | ||||||
| chr18:32215969 | CAT | C | 8 | a0001c0009t0001g0076 a0002c0003t0001g0002 a0002c0003t0001g0004 others(5): Show |
10 | HG00099.hp2 HG00423.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1759+757_1759+758d others(4): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr18 | 32215969 | ||||||
| chr18:32215969 | CATAT | C | 10 | a0001c0001t0001g0103 a0002c0003t0001g0002 a0003c0004t0001g0082 others(7): Show |
11 | HG00735.hp1 HG01243.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.1759+755_1759+758d others(6): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr18 | 32215969 | ||||||
| chr18:32215969 | CATATAT | C | 10 | a0001c0001t0001g0023 a0002c0003t0001g0002 a0002c0003t0001g0008 others(7): Show |
11 | HG00735.hp2 HG01074.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1759+753_1759+758d others(8): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr18 | 32215969 | ||||||
| chr18:32215969 | CATATATA others(1): Show |
C | 10 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0008 others(7): Show |
15 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.1759+751_1759+758d others(10): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr18 | 32215969 | ||||||
| chr18:32215969 | CATATATA others(3): Show |
C | 10 | a0002c0003t0001g0002 a0002c0003t0001g0008 a0002c0003t0001g0015 others(7): Show |
15 | HG01978.hp2 HG02074.hp2 HG02293.hp1 others(12): Show |
intron_variant | MODIFIER | c.1759+749_1759+758d others(12): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr18 | 32215969 | ||||||
| chr18:32215969 | CATATATA others(5): Show |
C | 2 | a0002c0003t0001g0004 a0002c0003t0001g0064 |
2 | HG03688.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1759+747_1759+758d others(14): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr18 | 32215969 | ||||||
| chr18:32215969 | CATATATA others(7): Show |
C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0180 |
4 | HG02258.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1759+745_1759+758d others(16): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr18 | 32215969 | ||||||
| chr18:32215969 | CATATATA others(9): Show |
C | 9 | a0001c0001t0001g0023 a0001c0001t0001g0114 a0001c0001t0001g0115 others(6): Show |
10 | HG01106.hp2 HG01358.hp2 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1759+743_1759+758d others(18): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr18 | 32215969 | ||||||
| chr18:32215969 | CATATATA others(11): Show |
C | 7 | a0001c0001t0001g0018 a0001c0001t0001g0042 a0001c0001t0001g0107 others(4): Show |
10 | HG00280.hp1 HG01884.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1759+741_1759+758d others(20): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr18 | 32215969 | ||||||
| chr18:32215969 | CATATATA others(13): Show |
C | 5 | a0001c0001t0001g0035 a0001c0001t0001g0042 a0001c0001t0001g0057 others(2): Show |
6 | HG01123.hp1 HG02615.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1759+739_1759+758d others(22): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr18 | 32215969 | ||||||
| chr18:32215969 | CATATATA others(15): Show |
C | 4 | a0002c0002t0001g0093 a0003c0004t0001g0052 a0003c0004t0001g0104 others(1): Show |
4 | HG01884.hp1 HG01975.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1759+737_1759+758d others(24): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr18 | 32215969 | ||||||
| chr18:32215969 | CATATATA others(17): Show |
C | 26 | a0001c0001t0001g0001 a0001c0018t0001g0170 a0002c0002t0001g0013 others(23): Show |
30 | HG00280.hp2 HG00673.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1759+735_1759+758d others(26): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr18 | 32215969 | ||||||
| chr18:32215969 | CATATATA others(19): Show |
C | 27 | a0001c0006t0002g0007 a0001c0006t0002g0060 a0001c0006t0002g0061 others(24): Show |
40 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1759+733_1759+758d others(28): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr18 | 32215969 | ||||||
| chr18:32215969 | CATATATA others(21): Show |
C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0024 others(9): Show |
16 | HG01074.hp1 HG01261.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.1759+731_1759+758d others(30): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr18 | 32215969 | ||||||
| chr18:32215969 | CATATATA others(23): Show |
C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
151 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.1759+729_1759+758d others(32): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr18 | 32215969 | ||||||
| chr18:32215994 | A | G | 1 | a0002c0002t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1759+733A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32215994 | |||||||
| chr18:32215995 | T | C | 1 | a0002c0002t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1759+734T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32215995 | |||||||
| chr18:32216038 | A | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0190 a0001c0001t0001g0192 |
5 | HG02027.hp2 NA18941.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.1759+777A>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32216038 | |||||||
| chr18:32216222 | C | T | 17 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0035 others(14): Show |
30 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1760-769C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32216222 | |||||||
| chr18:32216225 | A | T | 8 | a0001c0006t0002g0007 a0001c0006t0002g0016 a0001c0006t0002g0060 others(5): Show |
14 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1760-766A>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32216225 | |||||||
| chr18:32216364 | T | C | 1 | a0001c0006t0002g0063 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1760-627T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32216364 | |||||||
| chr18:32216367 | C | A | 1 | a0002c0003t0001g0069 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1760-624C>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32216367 | |||||||
| chr18:32216443 | A | C | 6 | a0001c0010t0001g0025 a0001c0010t0001g0200 a0001c0018t0001g0170 others(3): Show |
13 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1760-548A>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32216443 | |||||||
| chr18:32216475 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1760-516G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32216475 | |||||||
| chr18:32216639 | C | T | 5 | a0001c0010t0001g0025 a0001c0010t0001g0200 a0004c0008t0001g0005 others(2): Show |
12 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1760-352C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32216639 | |||||||
| chr18:32216671 | A | C | 1 | a0001c0001t0001g0101 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1760-320A>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32216671 | |||||||
| chr18:32216800 | C | T | 17 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0035 others(14): Show |
30 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1760-191C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32216800 | |||||||
| chr18:32216847 | A | G | 1 | a0001c0018t0001g0170 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1760-144A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 12/14 | chr18 | 32216847 | |||||||
| chr18:32217437 | C | G | 1 | a0002c0002t0001g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1886+320C>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 13/14 | chr18 | 32217437 | |||||||
| chr18:32217515 | C | T | 29 | a0002c0002t0001g0044 a0002c0002t0001g0203 a0002c0002t0001g0208 others(26): Show |
62 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1887-246C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 13/14 | chr18 | 32217515 | |||||||
| chr18:32217585 | T | C | 17 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0035 others(14): Show |
30 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1887-176T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 13/14 | chr18 | 32217585 | |||||||
| chr18:32217701 | G | A | 1 | a0002c0003t0001g0070 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1887-60G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 13/14 | chr18 | 32217701 | |||||||
| chr18:32217995 | T | C | 123 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0035 others(120): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.2091+30T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/14 | chr18 | 32217995 | |||||||
| chr18:32218109 | T | C | 1 | a0003c0004t0001g0080 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2091+144T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/14 | chr18 | 32218109 | |||||||
| chr18:32218229 | T | C | 1 | a0003c0004t0001g0082 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2091+264T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/14 | chr18 | 32218229 | |||||||
| chr18:32218522 | G | A | 1 | a0003c0004t0001g0083 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2091+557G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/14 | chr18 | 32218522 | |||||||
| chr18:32218577 | G | A | 5 | a0001c0010t0001g0025 a0001c0010t0001g0200 a0004c0008t0001g0005 others(2): Show |
12 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.2091+612G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/14 | chr18 | 32218577 | |||||||
| chr18:32218583 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0057 |
3 | HG02615.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2091+618G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/14 | chr18 | 32218583 | |||||||
| chr18:32218648 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2091+683G>A | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/14 | chr18 | 32218648 | |||||||
| chr18:32218715 | A | G | 3 | a0001c0001t0001g0135 a0001c0001t0001g0143 a0001c0001t0001g0167 |
3 | HG01109.hp2 HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2091+750A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/14 | chr18 | 32218715 | |||||||
| chr18:32218927 | A | G | 1 | a0001c0006t0002g0189 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2091+962A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/14 | chr18 | 32218927 | |||||||
| chr18:32218967 | C | T | 2 | a0003c0004t0001g0032 a0003c0004t0001g0081 |
3 | HG00099.hp2 HG00140.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2091+1002C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/14 | chr18 | 32218967 | |||||||
| chr18:32219277 | C | T | 6 | a0001c0010t0001g0025 a0001c0010t0001g0200 a0001c0018t0001g0170 others(3): Show |
13 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.2092-954C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/14 | chr18 | 32219277 | |||||||
| chr18:32219350 | T | C | 17 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0035 others(14): Show |
30 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.2092-881T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/14 | chr18 | 32219350 | |||||||
| chr18:32219416 | C | T | 8 | a0001c0006t0002g0007 a0001c0006t0002g0016 a0001c0006t0002g0060 others(5): Show |
14 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2092-815C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/14 | chr18 | 32219416 | |||||||
| chr18:32219608 | T | C | 28 | a0002c0002t0001g0044 a0002c0002t0001g0203 a0002c0002t0001g0208 others(25): Show |
61 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.2092-623T>C | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/14 | chr18 | 32219608 | |||||||
| chr18:32219810 | G | GCACA | 34 | a0002c0002t0001g0172 a0002c0002t0001g0206 a0002c0003t0001g0073 others(31): Show |
40 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.2092-403_2092-400d others(6): Show |
MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr18 | 32219810 | ||||||
| chr18:32219875 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2092-356A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/14 | chr18 | 32219875 | |||||||
| chr18:32219960 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2092-271A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/14 | chr18 | 32219960 | |||||||
| chr18:32219975 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2092-256C>T | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/14 | chr18 | 32219975 | |||||||
| chr18:32220156 | A | G | 124 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0035 others(121): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.2092-75A>G | MEP1B | ENSG00000141434.12 | transcript | ENST00000269202.11 | protein_coding | 14/14 | chr18 | 32220156 |