Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10691 |
| ensemblid | ENSG00000162419.13 |
| hgncid | 4370 |
| symbol | GMEB1 |
| name | glucocorticoid modulatory element binding protein 1 |
| refseq_nuc | NM_001319674.2 |
| refseq_prot | NP_001306603.1 |
| ensembl_nuc | ENST00000373816.6 |
| ensembl_prot | ENSP00000362922.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 28668784 |
| end | 28719353 |
| strand | + |
| ver | v1.2 |
| region | chr1:28668784-28719353 |
| region5000 | chr1:28663784-28724353 |
| regionname0 | GMEB1_chr1_28668784_28719353 |
| regionname5000 | GMEB1_chr1_28663784_28724353 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 563 | 289 | 90 | 64 | 84 | 17 | 32 | 62 | GMEB1_chr1_28663784_28724353 | GMEB1 | MANAE others(558): Show |
chr1 | 28663784 | 28724353 |
| a0002 | 0/0 | 563 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | MANAE others(558): Show |
chr1 | 28663784 | 28724353 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1689 | 279 | 84 | 61 | 84 | 17 | 31 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGGC others(1684): Show |
chr1 | 28663784 | 28724353 | ||
| a0001c0002 | 0/0 | 1689 | 3 | 2 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGGC others(1684): Show |
chr1 | 28663784 | 28724353 | ||
| a0001c0003 | 0/0 | 1689 | 2 | 2 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGGC others(1684): Show |
chr1 | 28663784 | 28724353 | ||
| a0001c0004 | 0/0 | 1689 | 2 | 0 | 1 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGGC others(1684): Show |
chr1 | 28663784 | 28724353 | ||
| a0001c0005 | 0/0 | 1689 | 2 | 2 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGGC others(1684): Show |
chr1 | 28663784 | 28724353 | ||
| a0001c0006 | 0/0 | 1689 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGGC others(1684): Show |
chr1 | 28663784 | 28724353 | ||
| a0002c0007 | 0/0 | 1689 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGGC others(1684): Show |
chr1 | 28663784 | 28724353 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6357 | 83 | 38 | 21 | 8 | 7 | 9 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6352): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0002 | 0/1 | 6359 | 79 | 8 | 15 | 41 | 5 | 9 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6354): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0003 | 1/0 | 6358 | 43 | 16 | 1 | 21 | 1 | 3 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6353): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0004 | 0/0 | 6358 | 10 | 2 | 4 | 3 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6353): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0005 | 0/0 | 6360 | 3 | 0 | 3 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6355): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0006 | 0/0 | 6358 | 4 | 4 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6353): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0007 | 0/0 | 6358 | 4 | 1 | 0 | 2 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6353): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0008 | 0/0 | 6357 | 3 | 0 | 0 | 0 | 2 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6352): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0009 | 0/0 | 6360 | 3 | 2 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6355): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0010 | 0/0 | 6357 | 3 | 0 | 3 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6352): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0011 | 0/0 | 6359 | 3 | 1 | 0 | 2 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6354): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0012 | 0/0 | 6357 | 3 | 0 | 3 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6352): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0013 | 0/0 | 6356 | 3 | 0 | 1 | 0 | 2 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6351): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0014 | 0/0 | 6354 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6349): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0015 | 0/0 | 6356 | 3 | 0 | 2 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6351): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0017 | 0/0 | 6360 | 2 | 0 | 0 | 2 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6355): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0018 | 0/0 | 6355 | 2 | 2 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6350): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0019 | 0/0 | 6360 | 2 | 1 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6355): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0020 | 0/0 | 6360 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6355): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0021 | 0/0 | 6358 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6353): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0022 | 0/0 | 6357 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6352): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0023 | 0/0 | 6359 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6354): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0024 | 0/0 | 6359 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6354): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0025 | 0/0 | 6359 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6354): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0027 | 0/0 | 6358 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6353): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0028 | 0/0 | 6358 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6353): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0029 | 0/0 | 6359 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6354): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0030 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6352): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0031 | 0/0 | 6357 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6352): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0032 | 0/0 | 6358 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6353): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0033 | 0/0 | 6358 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6353): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0034 | 0/0 | 6345 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6340): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0035 | 0/0 | 6358 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6353): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0036 | 0/0 | 6358 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6353): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0037 | 0/0 | 6360 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6355): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0039 | 0/0 | 6361 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6356): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0041 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6352): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0042 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6352): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0043 | 0/0 | 6357 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6352): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0044 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6352): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0045 | 0/0 | 6358 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6353): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0046 | 0/0 | 6356 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6351): Show |
chr1 | 28663784 | 28724353 |
| a0001c0001t0047 | 0/0 | 6354 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6349): Show |
chr1 | 28663784 | 28724353 |
| a0001c0002t0016 | 0/0 | 6361 | 2 | 1 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6356): Show |
chr1 | 28663784 | 28724353 |
| a0001c0002t0026 | 0/0 | 6360 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6355): Show |
chr1 | 28663784 | 28724353 |
| a0001c0003t0014 | 0/0 | 6354 | 2 | 2 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6349): Show |
chr1 | 28663784 | 28724353 |
| a0001c0004t0003 | 0/0 | 6358 | 2 | 0 | 1 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6353): Show |
chr1 | 28663784 | 28724353 |
| a0001c0005t0038 | 0/0 | 6359 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6354): Show |
chr1 | 28663784 | 28724353 |
| a0001c0005t0040 | 0/0 | 6360 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6355): Show |
chr1 | 28663784 | 28724353 |
| a0001c0006t0005 | 0/0 | 6360 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6355): Show |
chr1 | 28663784 | 28724353 |
| a0002c0007t0002 | 0/0 | 6359 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | ATGCT others(6354): Show |
chr1 | 28663784 | 28724353 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0081 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0005g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0006g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0007g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0007g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0008g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0008g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0008g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0009g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0009g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0009g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0010g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0010g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0010g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0011g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0011g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0011g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0012g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0012g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0012g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0013g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0013g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0013g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0014g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0015g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0015g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0015g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0017g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0017g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0018g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0018g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0019g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0019g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0020g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0021g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0022g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0023g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0024g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0025g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0027g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0028g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0029g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0030g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0031g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0032g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0033g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0034g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0035g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0036g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0037g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0039g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0041g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0042g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0043g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0044g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0045g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0046g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0047g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0002t0016g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0002t0016g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0002t0026g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0003t0014g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0003t0014g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0004t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0004t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0005t0038g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0005t0040g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0006t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0002c0007t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0110 | EUR | GBR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0067 | EUR | GBR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0078 | EUR | GBR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | FIN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | FIN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00323 | hp1 | a0001 | c0001 | t0013 | g0176 | EUR | FIN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00323 | hp2 | a0001 | c0001 | t0013 | g0149 | EUR | FIN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | CHS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00597 | hp1 | a0001 | c0001 | t0011 | g0286 | EAS | CHS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | CHS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00609 | hp1 | a0001 | c0001 | t0015 | g0156 | EAS | CHS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | CHS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00639 | hp2 | a0001 | c0001 | t0022 | g0277 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | CHS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00735 | hp1 | a0001 | c0001 | t0012 | g0169 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0009 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00741 | hp2 | a0001 | c0001 | t0012 | g0211 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01070 | hp2 | a0001 | c0001 | t0019 | g0136 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01074 | hp1 | a0001 | c0001 | t0010 | g0101 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01074 | hp2 | a0001 | c0001 | t0012 | g0168 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01081 | hp1 | a0001 | c0006 | t0005 | g0225 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01099 | hp1 | a0001 | c0001 | t0015 | g0253 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01099 | hp2 | a0001 | c0001 | t0010 | g0239 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0131 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01106 | hp2 | a0001 | c0001 | t0021 | g0174 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0138 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0152 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01192 | hp1 | a0001 | c0001 | t0023 | g0219 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01243 | hp2 | a0001 | c0001 | t0009 | g0082 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01255 | hp1 | a0001 | c0001 | t0029 | g0073 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01255 | hp2 | a0001 | c0002 | t0016 | g0011 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01258 | hp2 | a0001 | c0004 | t0003 | g0088 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01261 | hp2 | a0001 | c0001 | t0010 | g0113 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0153 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0228 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0069 | EUR | IBS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01516 | hp2 | a0001 | c0001 | t0008 | g0179 | EUR | IBS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01517 | hp1 | a0001 | c0001 | t0008 | g0257 | EUR | IBS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0066 | EUR | IBS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0083 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01891 | hp2 | a0001 | c0005 | t0038 | g0086 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01928 | hp2 | a0001 | c0001 | t0013 | g0235 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01952 | hp1 | a0001 | c0001 | t0020 | g0227 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | KHV | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02055 | hp1 | a0001 | c0005 | t0040 | g0199 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0251 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | KHV | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0278 | EAS | KHV | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02145 | hp1 | a0001 | c0001 | t0025 | g0005 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0202 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0098 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CDX | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CDX | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | CDX | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | CDX | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02257 | hp1 | a0001 | c0001 | t0047 | g0197 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02257 | hp2 | a0001 | c0001 | t0042 | g0125 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02258 | hp2 | a0001 | c0001 | t0011 | g0285 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0213 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02293 | hp2 | a0001 | c0001 | t0015 | g0241 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02572 | hp2 | a0001 | c0001 | t0018 | g0217 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0273 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0280 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02615 | hp1 | a0001 | c0001 | t0019 | g0275 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0206 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02723 | hp1 | a0001 | c0001 | t0018 | g0043 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0154 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0111 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02738 | hp1 | a0001 | c0001 | t0028 | g0281 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02738 | hp2 | a0001 | c0001 | t0039 | g0200 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02818 | hp1 | a0001 | c0001 | t0014 | g0041 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02818 | hp2 | a0001 | c0001 | t0034 | g0122 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02970 | hp1 | a0001 | c0001 | t0044 | g0095 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0119 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02976 | hp2 | a0001 | c0001 | t0041 | g0126 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03098 | hp2 | a0001 | c0003 | t0014 | g0196 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03139 | hp1 | a0001 | c0001 | t0030 | g0188 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03225 | hp1 | a0001 | c0002 | t0026 | g0084 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03239 | hp1 | a0001 | c0001 | t0008 | g0092 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03239 | hp2 | a0001 | c0001 | t0045 | g0271 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0104 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0212 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03654 | hp2 | a0001 | c0001 | t0031 | g0272 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | STU | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0091 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | BEB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | BEB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | BEB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG04115 | hp1 | a0001 | c0001 | t0032 | g0256 | SAS | STU | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG04115 | hp2 | a0001 | c0001 | t0007 | g0279 | SAS | STU | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | BEB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG04184 | hp2 | a0001 | c0001 | t0027 | g0284 | SAS | BEB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | STU | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG04199 | hp2 | a0001 | c0004 | t0003 | g0232 | SAS | STU | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | STU | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | YRI | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | YRI | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18906 | hp2 | a0001 | c0003 | t0014 | g0042 | AFR | YRI | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18939 | hp1 | a0001 | c0001 | t0007 | g0268 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18960 | hp2 | a0001 | c0001 | t0007 | g0187 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18968 | hp1 | a0001 | c0001 | t0011 | g0105 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18998 | hp1 | a0001 | c0001 | t0017 | g0039 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18999 | hp1 | a0001 | c0001 | t0046 | g0157 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19012 | hp2 | a0001 | c0001 | t0033 | g0242 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | LWK | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0231 | AFR | LWK | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19067 | hp1 | a0001 | c0001 | t0017 | g0037 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19083 | hp1 | a0001 | c0001 | t0024 | g0283 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19083 | hp2 | a0001 | c0001 | t0037 | g0047 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ASW | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ASW | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA20752 | hp1 | a0002 | c0007 | t0002 | g0226 | EUR | TSI | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | TSI | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0038 | EUR | TSI | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA20905 | hp1 | a0001 | c0001 | t0035 | g0093 | SAS | GIH | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | GIH | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01123 | hp2 | a0001 | c0001 | t0043 | g0148 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02109 | hp1 | a0001 | c0001 | t0036 | g0252 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0162 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0094 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | USA | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0208 | AFR | USA | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | USA | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0099 | AFR | USA | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA21309 | hp2 | a0001 | c0002 | t0016 | g0085 | AFR | LWK | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0081 | REF | REF | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0165 | REF | REF | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:28714522 | A | G | 1 | a0002 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.1441A>G | p.Met481Val | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 1527/6358 | 1441/1692 | 481/563 | chr1 | 28714522 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:28683738 | A | G | 1 | a0001c0005 | 2 | HG01891.hp2 HG02055.hp1 |
splice_region_variant&synonymous_variant | LOW | c.126A>G | p.Gln42Gln | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/10 | 212/6358 | 126/1692 | 42/563 | chr1 | 28683738 | |||
| chr1:28696972 | A | G | 1 | a0001c0002 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.486A>G | p.Lys162Lys | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/10 | 572/6358 | 486/1692 | 162/563 | chr1 | 28696972 | |||
| chr1:28702529 | C | A | 1 | a0001c0006 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.690C>A | p.Ala230Ala | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/10 | 776/6358 | 690/1692 | 230/563 | chr1 | 28702529 | |||
| chr1:28710632 | T | C | 1 | a0001c0003 | 2 | HG03098.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.981T>C | p.Tyr327Tyr | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/10 | 1067/6358 | 981/1692 | 327/563 | chr1 | 28710632 | |||
| chr1:28714287 | A | G | 1 | a0001c0004 | 2 | HG01258.hp2 HG04199.hp2 |
synonymous_variant | LOW | c.1206A>G | p.Pro402Pro | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 1292/6358 | 1206/1692 | 402/563 | chr1 | 28714287 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:28668810 | C | T | 1 | a0001c0001t0047 | 1 | HG02257.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-60C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/10 | chr1 | 28668810 | |||||||
| chr1:28714873 | T | A | 1 | a0001c0001t0020 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*100T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 100 | chr1 | 28714873 | ||||||
| chr1:28714884 | A | C | 1 | a0001c0001t0019 | 2 | HG01070.hp2 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*111A>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 111 | chr1 | 28714884 | ||||||
| chr1:28714980 | T | G | 2 | a0001c0001t0008 a0001c0001t0021 |
4 | HG01106.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*207T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 207 | chr1 | 28714980 | ||||||
| chr1:28715173 | TC | T | 2 | a0001c0001t0015 a0001c0001t0046 |
4 | HG00609.hp1 HG01099.hp1 HG02293.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*401delC | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 401 | chr1 | 28715173 | ||||||
| chr1:28715370 | G | A | 1 | a0001c0001t0022 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*597G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 597 | chr1 | 28715370 | ||||||
| chr1:28715381 | G | A | 1 | a0001c0001t0023 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*608G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 608 | chr1 | 28715381 | ||||||
| chr1:28715450 | AAATT | A | 4 | a0001c0001t0014 a0001c0001t0018 a0001c0001t0047 others(1): Show |
6 | HG02257.hp1 HG02572.hp2 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*679_*682delATTA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 679 | INFO_REALIGN_3_PRIME | chr1 | 28715450 | |||||
| chr1:28715603 | C | CA | 12 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(9): Show |
24 | HG00738.hp2 HG01070.hp2 HG01081.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*850dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 851 | INFO_REALIGN_3_PRIME | chr1 | 28715603 | |||||
| chr1:28715603 | CA | C | 5 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0045 others(2): Show |
8 | HG00323.hp1 HG00323.hp2 HG01928.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*850delA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 850 | INFO_REALIGN_3_PRIME | chr1 | 28715603 | |||||
| chr1:28715840 | C | A | 1 | a0001c0001t0029 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1067C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 1067 | chr1 | 28715840 | ||||||
| chr1:28715913 | G | A | 1 | a0001c0001t0030 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1140G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 1140 | chr1 | 28715913 | ||||||
| chr1:28716093 | G | A | 1 | a0001c0001t0010 | 3 | HG01074.hp1 HG01099.hp2 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1320G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 1320 | chr1 | 28716093 | ||||||
| chr1:28716149 | G | T | 1 | a0001c0001t0028 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1376G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 1376 | chr1 | 28716149 | ||||||
| chr1:28716741 | TG | T | 20 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(17): Show |
127 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*1979delG | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 1979 | INFO_REALIGN_3_PRIME | chr1 | 28716741 | |||||
| chr1:28716750 | G | C | 1 | a0001c0001t0031 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1977G>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 1977 | chr1 | 28716750 | ||||||
| chr1:28716888 | C | T | 2 | a0001c0002t0016 a0001c0002t0026 |
3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2115C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 2115 | chr1 | 28716888 | ||||||
| chr1:28716985 | T | C | 2 | a0001c0002t0016 a0001c0002t0026 |
3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2212T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 2212 | chr1 | 28716985 | ||||||
| chr1:28717185 | G | GT | 18 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(15): Show |
111 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*2428dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 2429 | INFO_REALIGN_3_PRIME | chr1 | 28717185 | |||||
| chr1:28717185 | G | GTT | 5 | a0001c0001t0017 a0001c0001t0020 a0001c0001t0039 others(2): Show |
7 | HG01255.hp2 HG01952.hp1 HG02055.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2427_*2428dupTT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 2429 | INFO_REALIGN_3_PRIME | chr1 | 28717185 | |||||
| chr1:28717402 | C | T | 1 | a0001c0001t0036 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2629C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 2629 | chr1 | 28717402 | ||||||
| chr1:28717427 | C | T | 1 | a0001c0001t0044 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2654C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 2654 | chr1 | 28717427 | ||||||
| chr1:28717451 | A | G | 2 | a0001c0005t0038 a0001c0005t0040 |
2 | HG01891.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2678A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 2678 | chr1 | 28717451 | ||||||
| chr1:28717698 | C | G | 1 | a0001c0001t0043 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2925C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 2925 | chr1 | 28717698 | ||||||
| chr1:28717835 | A | G | 1 | a0001c0001t0035 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3062A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 3062 | chr1 | 28717835 | ||||||
| chr1:28718100 | T | C | 3 | a0001c0001t0012 a0001c0001t0027 a0001c0001t0032 |
5 | HG00735.hp1 HG00741.hp2 HG01074.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3327T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 3327 | chr1 | 28718100 | ||||||
| chr1:28718329 | G | A | 1 | a0001c0001t0041 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3556G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 3556 | chr1 | 28718329 | ||||||
| chr1:28718434 | T | C | 21 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0009 others(18): Show |
107 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*3661T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 3661 | chr1 | 28718434 | ||||||
| chr1:28718469 | C | T | 1 | a0001c0001t0046 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3696C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 3696 | chr1 | 28718469 | ||||||
| chr1:28718611 | A | G | 19 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0009 others(16): Show |
105 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*3838A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 3838 | chr1 | 28718611 | ||||||
| chr1:28718634 | G | GT | 3 | a0001c0001t0011 a0001c0001t0037 a0001c0001t0039 |
5 | HG00597.hp1 HG02258.hp2 HG02738.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3870dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 3871 | INFO_REALIGN_3_PRIME | chr1 | 28718634 | |||||
| chr1:28718682 | AAGAATTG others(6): Show |
A | 1 | a0001c0001t0034 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3912_*3924delAATT others(9): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 3912 | INFO_REALIGN_3_PRIME | chr1 | 28718682 | |||||
| chr1:28718769 | G | A | 1 | a0001c0001t0033 | 1 | NA19012.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3996G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 3996 | chr1 | 28718769 | ||||||
| chr1:28718837 | G | T | 1 | a0001c0001t0020 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4064G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 4064 | chr1 | 28718837 | ||||||
| chr1:28718981 | G | A | 1 | a0001c0001t0009 | 3 | HG01243.hp2 HG01884.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4208G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 4208 | chr1 | 28718981 | ||||||
| chr1:28719051 | C | T | 1 | a0001c0001t0025 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4278C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 4278 | chr1 | 28719051 | ||||||
| chr1:28719107 | G | A | 1 | a0001c0001t0022 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4334G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 4334 | chr1 | 28719107 | ||||||
| chr1:28719224 | G | C | 2 | a0001c0001t0006 a0001c0001t0042 |
5 | HG02145.hp2 HG02257.hp2 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4451G>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 4451 | chr1 | 28719224 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:28668871 | C | CG | 4 | a0001c0001t0002g0004 a0001c0001t0003g0006 a0001c0001t0004g0007 others(1): Show |
4 | HG01261.hp1 HG02145.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+36dupG | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28668871 | ||||||
| chr1:28668887 | C | CG | 89 | a0001c0001t0001g0210 a0001c0001t0001g0233 a0001c0001t0001g0234 others(86): Show |
89 | HG00597.hp2 HG00609.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.-31+55dupG | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28668887 | ||||||
| chr1:28668887 | C | G | 3 | a0001c0001t0001g0287 a0001c0001t0004g0007 a0001c0001t0011g0286 |
3 | HG00597.hp1 HG03688.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.-31+48C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28668887 | |||||||
| chr1:28668901 | C | CG | 5 | a0001c0001t0002g0198 a0001c0001t0003g0006 a0001c0001t0011g0285 others(2): Show |
5 | HG02258.hp2 HG04184.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31+67dupG | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28668901 | ||||||
| chr1:28668904 | G | A | 1 | a0001c0005t0040g0199 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-31+65G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28668904 | |||||||
| chr1:28669034 | C | CG | 21 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0210 others(18): Show |
21 | HG00140.hp1 HG00673.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.-31+202dupG | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28669034 | ||||||
| chr1:28669042 | T | G | 6 | a0001c0001t0002g0004 a0001c0001t0002g0201 a0001c0001t0006g0202 others(3): Show |
6 | HG00597.hp1 HG01261.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31+203T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28669042 | |||||||
| chr1:28669042 | T | TG | 8 | a0001c0001t0001g0282 a0001c0001t0002g0276 a0001c0001t0002g0280 others(5): Show |
8 | HG00639.hp2 HG01192.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.-31+209dupG | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28669042 | ||||||
| chr1:28669062 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+223G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28669062 | |||||||
| chr1:28669106 | C | T | 1 | a0001c0001t0019g0275 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-31+267C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28669106 | |||||||
| chr1:28669158 | T | TG | 13 | a0001c0001t0001g0274 a0001c0001t0001g0282 a0001c0001t0002g0193 others(10): Show |
13 | HG00597.hp1 HG01167.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.-31+326dupG | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28669158 | ||||||
| chr1:28669247 | G | C | 106 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(103): Show |
106 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-31+408G>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28669247 | |||||||
| chr1:28669278 | G | A | 1 | a0001c0001t0024g0283 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-31+439G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28669278 | |||||||
| chr1:28669361 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-31+522C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28669361 | |||||||
| chr1:28669423 | C | G | 1 | a0001c0001t0003g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-31+584C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28669423 | |||||||
| chr1:28669700 | C | T | 1 | a0001c0001t0027g0284 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-31+861C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28669700 | |||||||
| chr1:28670077 | A | G | 1 | a0001c0003t0014g0196 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-31+1238A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670077 | |||||||
| chr1:28670153 | T | TTTTA | 4 | a0001c0001t0009g0082 a0001c0001t0009g0083 a0001c0001t0009g0231 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+1334_-31+1337d others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28670153 | ||||||
| chr1:28670153 | T | TTTTATTT others(5): Show |
51 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0051 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.-31+1326_-31+1337d others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28670153 | ||||||
| chr1:28670153 | T | TTTTATTT others(9): Show |
21 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0044 others(18): Show |
21 | HG00597.hp2 HG00609.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.-31+1322_-31+1337d others(18): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28670153 | ||||||
| chr1:28670153 | T | TTTTATTT others(13): Show |
17 | a0001c0001t0002g0008 a0001c0001t0002g0025 a0001c0001t0002g0026 others(14): Show |
17 | HG00438.hp1 HG00673.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.-31+1318_-31+1337d others(22): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28670153 | ||||||
| chr1:28670153 | T | TTTTATTT others(17): Show |
5 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(2): Show |
5 | HG01433.hp2 HG02148.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+1337_-31+1338i others(26): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28670153 | ||||||
| chr1:28670173 | A | ATTTATTT others(17): Show |
1 | a0001c0001t0002g0024 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-31+1337_-31+1338i others(26): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28670173 | ||||||
| chr1:28670173 | A | G | 1 | a0001c0001t0003g0016 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-31+1334A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670173 | |||||||
| chr1:28670248 | G | C | 3 | a0001c0001t0001g0089 a0001c0004t0003g0088 a0001c0004t0003g0232 |
3 | HG01258.hp2 HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-31+1409G>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670248 | |||||||
| chr1:28670364 | G | A | 1 | a0001c0001t0006g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-31+1525G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670364 | |||||||
| chr1:28670388 | C | T | 1 | a0001c0001t0001g0015 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-31+1549C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670388 | |||||||
| chr1:28670433 | T | C | 1 | a0001c0001t0003g0090 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-31+1594T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670433 | |||||||
| chr1:28670509 | A | G | 106 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(103): Show |
106 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-31+1670A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670509 | |||||||
| chr1:28670619 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-31+1780C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670619 | |||||||
| chr1:28670650 | T | G | 1 | a0001c0001t0003g0091 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-31+1811T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670650 | |||||||
| chr1:28670663 | C | T | 1 | a0001c0001t0002g0087 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-31+1824C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670663 | |||||||
| chr1:28670692 | T | C | 1 | a0001c0001t0008g0092 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-31+1853T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670692 | |||||||
| chr1:28670719 | C | T | 101 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(98): Show |
101 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.-31+1880C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670719 | |||||||
| chr1:28670745 | T | C | 97 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(94): Show |
97 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-31+1906T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670745 | |||||||
| chr1:28670754 | T | G | 1 | a0001c0001t0035g0093 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-31+1915T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670754 | |||||||
| chr1:28670763 | G | A | 1 | a0001c0001t0022g0277 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-31+1924G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670763 | |||||||
| chr1:28671436 | C | T | 1 | a0001c0001t0030g0188 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-31+2597C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28671436 | |||||||
| chr1:28671597 | T | G | 3 | a0001c0002t0016g0011 a0001c0002t0016g0085 a0001c0002t0026g0084 |
3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-31+2758T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28671597 | |||||||
| chr1:28671772 | AAAAT | A | 3 | a0001c0001t0001g0233 a0001c0001t0004g0094 a0001c0001t0044g0095 |
3 | HG02970.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-31+2937_-31+2940d others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28671772 | ||||||
| chr1:28671960 | A | G | 1 | a0001c0001t0035g0093 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-31+3121A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28671960 | |||||||
| chr1:28672034 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-31+3195C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28672034 | |||||||
| chr1:28672112 | C | CA | 8 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0234 others(5): Show |
8 | HG01243.hp2 HG01884.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.-31+3283dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672112 | ||||||
| chr1:28672123 | T | C | 1 | a0001c0001t0003g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-31+3284T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28672123 | |||||||
| chr1:28672125 | A | T | 1 | a0001c0001t0001g0269 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-31+3286A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28672125 | |||||||
| chr1:28672164 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-31+3325G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28672164 | |||||||
| chr1:28672197 | T | TTTTA | 58 | a0001c0001t0001g0017 a0001c0001t0001g0114 a0001c0001t0001g0115 others(55): Show |
59 | HG00639.hp2 HG00733.hp1 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.-31+3394_-31+3397d others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672197 | ||||||
| chr1:28672197 | T | TTTTATTT others(1): Show |
22 | a0001c0001t0001g0112 a0001c0001t0001g0238 a0001c0001t0001g0269 others(19): Show |
23 | HG00099.hp1 HG00673.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.-31+3390_-31+3397d others(10): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672197 | ||||||
| chr1:28672197 | T | TTTTATTT others(5): Show |
3 | a0001c0001t0011g0286 a0001c0005t0038g0086 a0001c0005t0040g0199 |
3 | HG00597.hp1 HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-31+3386_-31+3397d others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672197 | ||||||
| chr1:28672197 | TTTTA | T | 5 | a0001c0001t0002g0215 a0001c0001t0009g0082 a0001c0001t0009g0083 others(2): Show |
5 | HG01243.hp2 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+3394_-31+3397d others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672197 | ||||||
| chr1:28672197 | TTTTATTT others(1): Show |
T | 96 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(93): Show |
96 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-31+3390_-31+3397d others(10): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672197 | ||||||
| chr1:28672197 | TTTTATTT others(9): Show |
T | 1 | a0001c0001t0024g0283 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-31+3382_-31+3397d others(18): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672197 | ||||||
| chr1:28672306 | C | T | 1 | a0001c0001t0002g0050 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-31+3467C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28672306 | |||||||
| chr1:28672384 | A | AT | 6 | a0001c0001t0002g0049 a0001c0001t0002g0203 a0001c0001t0002g0221 others(3): Show |
6 | HG02055.hp1 HG02738.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+3557dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672384 | ||||||
| chr1:28672419 | T | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0247 |
2 | NA18957.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-31+3580T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28672419 | |||||||
| chr1:28672443 | TC | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0114 others(26): Show |
30 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.-31+3606delC | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672443 | ||||||
| chr1:28672487 | T | G | 2 | a0001c0001t0006g0202 a0001c0001t0006g0206 |
2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-31+3648T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28672487 | |||||||
| chr1:28672682 | G | A | 1 | a0001c0001t0003g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-31+3843G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28672682 | |||||||
| chr1:28672736 | C | CT | 106 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(103): Show |
106 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-31+3916dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672736 | ||||||
| chr1:28672736 | CT | C | 6 | a0001c0001t0003g0191 a0001c0001t0010g0239 a0001c0001t0011g0285 others(3): Show |
6 | HG01099.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+3916delT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672736 | ||||||
| chr1:28672741 | T | C | 19 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0090 others(16): Show |
20 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-31+3902T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28672741 | |||||||
| chr1:28673000 | G | A | 106 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(103): Show |
106 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-31+4161G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673000 | |||||||
| chr1:28673076 | G | A | 1 | a0001c0001t0003g0240 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-31+4237G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673076 | |||||||
| chr1:28673136 | C | T | 2 | a0001c0001t0002g0080 a0001c0001t0002g0230 |
2 | HG00733.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-31+4297C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673136 | |||||||
| chr1:28673319 | C | G | 1 | a0001c0001t0002g0079 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-31+4480C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673319 | |||||||
| chr1:28673344 | C | T | 1 | a0001c0001t0003g0016 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-31+4505C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673344 | |||||||
| chr1:28673582 | A | G | 1 | a0001c0001t0002g0195 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-31+4743A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673582 | |||||||
| chr1:28673711 | T | G | 1 | a0001c0001t0002g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-31+4872T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673711 | |||||||
| chr1:28673726 | A | G | 3 | a0001c0001t0003g0140 a0001c0001t0003g0141 a0001c0001t0003g0246 |
3 | NA18943.hp1 NA18947.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-31+4887A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673726 | |||||||
| chr1:28673876 | C | G | 1 | a0001c0001t0001g0249 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-31+5037C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673876 | |||||||
| chr1:28673916 | G | T | 3 | a0001c0001t0002g0076 a0001c0001t0002g0077 a0001c0001t0002g0078 |
3 | HG00140.hp2 HG00735.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.-31+5077G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673916 | |||||||
| chr1:28673919 | G | T | 13 | a0001c0001t0001g0100 a0001c0001t0001g0142 a0001c0001t0001g0184 others(10): Show |
13 | HG02080.hp1 NA18939.hp1 NA18947.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+5080G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673919 | |||||||
| chr1:28674649 | C | T | 1 | a0001c0001t0036g0252 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-31+5810C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28674649 | |||||||
| chr1:28674675 | G | T | 2 | a0001c0001t0002g0080 a0001c0001t0002g0230 |
2 | HG00733.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-31+5836G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28674675 | |||||||
| chr1:28674708 | C | CT | 53 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0089 others(50): Show |
54 | HG00099.hp1 HG00597.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.-31+5897dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28674708 | ||||||
| chr1:28674708 | C | CTT | 25 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0001g0139 others(22): Show |
25 | HG00639.hp2 HG01070.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-31+5896_-31+5897d others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28674708 | ||||||
| chr1:28674708 | CT | C | 94 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(91): Show |
94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.-31+5897delT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28674708 | ||||||
| chr1:28674719 | T | A | 4 | a0001c0001t0015g0156 a0001c0001t0015g0241 a0001c0001t0015g0253 others(1): Show |
4 | HG00609.hp1 HG01099.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31+5880T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28674719 | |||||||
| chr1:28674773 | C | T | 1 | a0001c0001t0002g0220 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-31+5934C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28674773 | |||||||
| chr1:28674875 | C | T | 1 | a0001c0001t0004g0153 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-31+6036C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28674875 | |||||||
| chr1:28674876 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0030g0188 |
2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-31+6037G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28674876 | |||||||
| chr1:28674879 | C | T | 3 | a0001c0001t0001g0129 a0001c0005t0038g0086 a0001c0005t0040g0199 |
3 | HG01891.hp2 HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-31+6040C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28674879 | |||||||
| chr1:28675007 | C | T | 3 | a0001c0001t0001g0233 a0001c0001t0004g0094 a0001c0001t0044g0095 |
3 | HG02970.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-31+6168C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675007 | |||||||
| chr1:28675008 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-31+6169C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675008 | |||||||
| chr1:28675014 | C | T | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-31+6175C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675014 | |||||||
| chr1:28675018 | C | CT | 85 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0015 others(82): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.-31+6196dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28675018 | ||||||
| chr1:28675068 | A | C | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-31+6229A>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675068 | |||||||
| chr1:28675296 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-31+6457C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675296 | |||||||
| chr1:28675306 | C | T | 19 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0090 others(16): Show |
20 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-31+6467C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675306 | |||||||
| chr1:28675309 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0269 |
2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-31+6470G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675309 | |||||||
| chr1:28675381 | T | C | 97 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(94): Show |
97 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-31+6542T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675381 | |||||||
| chr1:28675399 | TCG | T | 3 | a0001c0001t0002g0076 a0001c0001t0002g0077 a0001c0001t0002g0078 |
3 | HG00140.hp2 HG00735.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.-31+6561_-31+6562d others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675399 | |||||||
| chr1:28675401 | G | A | 1 | a0001c0001t0002g0049 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-31+6562G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675401 | |||||||
| chr1:28675573 | G | A | 2 | a0001c0001t0003g0016 a0001c0001t0033g0242 |
2 | NA18965.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-31+6734G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675573 | |||||||
| chr1:28675679 | C | CA | 7 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0150 others(4): Show |
8 | HG00323.hp2 HG01109.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.-31+6856dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28675679 | ||||||
| chr1:28675679 | CA | C | 100 | a0001c0001t0001g0142 a0001c0001t0002g0004 a0001c0001t0002g0008 others(97): Show |
100 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.-31+6856delA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28675679 | ||||||
| chr1:28675781 | C | G | 3 | a0001c0001t0009g0082 a0001c0001t0009g0083 a0001c0001t0009g0231 |
3 | HG01243.hp2 HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-31+6942C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675781 | |||||||
| chr1:28675880 | G | C | 1 | a0001c0001t0002g0038 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-31+7041G>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675880 | |||||||
| chr1:28676007 | T | C | 1 | a0001c0001t0006g0119 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-31+7168T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676007 | |||||||
| chr1:28676030 | T | C | 1 | a0001c0001t0003g0240 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-31+7191T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676030 | |||||||
| chr1:28676335 | T | C | 2 | a0001c0001t0002g0048 a0001c0001t0017g0039 |
2 | NA18998.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-30-7248T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676335 | |||||||
| chr1:28676495 | A | G | 4 | a0001c0001t0009g0082 a0001c0001t0009g0083 a0001c0001t0009g0231 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-7088A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676495 | |||||||
| chr1:28676543 | C | T | 1 | a0001c0001t0010g0239 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-30-7040C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676543 | |||||||
| chr1:28676546 | T | G | 3 | a0001c0002t0016g0011 a0001c0002t0016g0085 a0001c0002t0026g0084 |
3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-30-7037T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676546 | |||||||
| chr1:28676685 | G | A | 137 | a0001c0001t0001g0127 a0001c0001t0001g0172 a0001c0001t0001g0189 others(134): Show |
138 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.-30-6898G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676685 | |||||||
| chr1:28676724 | C | CA | 96 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(93): Show |
96 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-30-6850dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28676724 | ||||||
| chr1:28676730 | A | T | 18 | a0001c0001t0001g0134 a0001c0001t0001g0143 a0001c0001t0001g0144 others(15): Show |
18 | HG00280.hp1 HG00639.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.-30-6853A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676730 | |||||||
| chr1:28676734 | T | A | 107 | a0001c0001t0001g0100 a0001c0001t0001g0166 a0001c0001t0001g0173 others(104): Show |
107 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-30-6849T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676734 | |||||||
| chr1:28676738 | T | A | 5 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0215 others(2): Show |
5 | HG02602.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30-6845T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676738 | |||||||
| chr1:28676848 | T | C | 56 | a0001c0001t0001g0112 a0001c0001t0001g0129 a0001c0001t0001g0130 others(53): Show |
57 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.-30-6735T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676848 | |||||||
| chr1:28677213 | C | G | 1 | a0001c0001t0002g0220 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-30-6370C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28677213 | |||||||
| chr1:28677398 | C | G | 1 | a0001c0001t0001g0134 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-30-6185C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28677398 | |||||||
| chr1:28677842 | T | C | 5 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0234 others(2): Show |
5 | HG01928.hp2 HG01943.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30-5741T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28677842 | |||||||
| chr1:28678022 | A | G | 4 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(1): Show |
4 | HG00438.hp1 HG02155.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-5561A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678022 | |||||||
| chr1:28678234 | A | G | 97 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(94): Show |
97 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-30-5349A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678234 | |||||||
| chr1:28678248 | A | G | 3 | a0001c0001t0003g0140 a0001c0001t0003g0141 a0001c0001t0003g0246 |
3 | NA18943.hp1 NA18947.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-30-5335A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678248 | |||||||
| chr1:28678299 | T | TTTTG | 4 | a0001c0001t0006g0202 a0001c0002t0016g0011 a0001c0002t0016g0085 others(1): Show |
4 | HG01255.hp2 HG02145.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-5260_-30-5257d others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28678299 | ||||||
| chr1:28678299 | TTTTGTTT others(1): Show |
T | 4 | a0001c0001t0001g0159 a0001c0001t0003g0099 a0001c0001t0030g0188 others(1): Show |
4 | HG01884.hp1 HG02109.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-5264_-30-5257d others(10): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28678299 | ||||||
| chr1:28678307 | G | GTT | 9 | a0001c0001t0001g0127 a0001c0001t0001g0172 a0001c0001t0001g0210 others(6): Show |
9 | HG02258.hp2 HG02809.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-30-5274_-30-5273d others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28678307 | ||||||
| chr1:28678517 | G | C | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-30-5066G>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678517 | |||||||
| chr1:28678547 | G | A | 10 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(7): Show |
10 | HG00280.hp1 HG01123.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30-5036G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678547 | |||||||
| chr1:28678586 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-30-4997G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678586 | |||||||
| chr1:28678682 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-30-4901G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678682 | |||||||
| chr1:28678822 | A | G | 272 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0015 others(269): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-30-4761A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678822 | |||||||
| chr1:28678899 | G | T | 2 | a0001c0001t0002g0201 a0001c0001t0003g0111 |
2 | HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-30-4684G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678899 | |||||||
| chr1:28678907 | G | A | 1 | a0001c0001t0002g0029 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-30-4676G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678907 | |||||||
| chr1:28678950 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0030g0188 |
2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-30-4633C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678950 | |||||||
| chr1:28678951 | G | A | 6 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0001g0238 others(3): Show |
6 | HG01070.hp2 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30-4632G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678951 | |||||||
| chr1:28678966 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-30-4617A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678966 | |||||||
| chr1:28679034 | C | T | 1 | a0001c0001t0033g0242 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-30-4549C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28679034 | |||||||
| chr1:28679119 | C | T | 1 | a0001c0001t0003g0110 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-30-4464C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28679119 | |||||||
| chr1:28679209 | G | T | 1 | a0001c0002t0016g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30-4374G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28679209 | |||||||
| chr1:28679564 | T | C | 1 | a0001c0001t0003g0111 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-30-4019T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28679564 | |||||||
| chr1:28679658 | A | G | 38 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0096 others(35): Show |
38 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.-30-3925A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28679658 | |||||||
| chr1:28679802 | C | CT | 11 | a0001c0001t0001g0129 a0001c0001t0001g0139 a0001c0001t0001g0181 others(8): Show |
11 | HG01109.hp1 HG01515.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-30-3765dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28679802 | ||||||
| chr1:28679954 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-30-3629C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28679954 | |||||||
| chr1:28680182 | A | G | 29 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0114 others(26): Show |
30 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.-30-3401A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28680182 | |||||||
| chr1:28680214 | C | CT | 101 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(98): Show |
101 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.-30-3368dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28680214 | ||||||
| chr1:28680598 | G | C | 1 | a0001c0001t0009g0082 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-30-2985G>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28680598 | |||||||
| chr1:28680661 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-30-2922G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28680661 | |||||||
| chr1:28680923 | A | G | 6 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0001g0238 others(3): Show |
6 | HG01070.hp2 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30-2660A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28680923 | |||||||
| chr1:28680995 | G | A | 1 | a0001c0001t0022g0277 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-30-2588G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28680995 | |||||||
| chr1:28681089 | G | T | 2 | a0001c0001t0003g0124 a0001c0001t0008g0092 |
2 | HG02965.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-30-2494G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28681089 | |||||||
| chr1:28681217 | G | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0114 others(26): Show |
30 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.-30-2366G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28681217 | |||||||
| chr1:28681336 | C | T | 13 | a0001c0001t0001g0100 a0001c0001t0001g0142 a0001c0001t0001g0184 others(10): Show |
13 | HG02080.hp1 NA18939.hp1 NA18947.hp1 others(10): Show |
intron_variant | MODIFIER | c.-30-2247C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28681336 | |||||||
| chr1:28681361 | G | A | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-30-2222G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28681361 | |||||||
| chr1:28681452 | G | A | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-30-2131G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28681452 | |||||||
| chr1:28681505 | C | T | 1 | a0001c0001t0003g0109 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-30-2078C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28681505 | |||||||
| chr1:28681563 | T | C | 1 | a0001c0001t0003g0135 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-30-2020T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28681563 | |||||||
| chr1:28681745 | C | T | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-30-1838C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28681745 | |||||||
| chr1:28681790 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-30-1793C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28681790 | |||||||
| chr1:28681857 | C | T | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-30-1726C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28681857 | |||||||
| chr1:28682013 | C | A | 1 | a0001c0001t0025g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-30-1570C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28682013 | |||||||
| chr1:28682426 | C | G | 3 | a0001c0001t0003g0191 a0001c0001t0011g0285 a0001c0001t0036g0252 |
3 | HG02109.hp1 HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-30-1157C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28682426 | |||||||
| chr1:28682591 | G | A | 1 | a0001c0001t0003g0111 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-30-992G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28682591 | |||||||
| chr1:28682619 | C | CA | 37 | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0287 others(34): Show |
38 | HG00597.hp1 HG00673.hp2 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.-30-943dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28682619 | ||||||
| chr1:28682913 | C | T | 3 | a0001c0001t0002g0052 a0001c0001t0002g0068 a0001c0001t0002g0072 |
3 | HG01070.hp1 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-30-670C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28682913 | |||||||
| chr1:28682973 | G | A | 2 | a0001c0001t0002g0057 a0001c0001t0002g0079 |
2 | HG02040.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.-30-610G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28682973 | |||||||
| chr1:28683057 | A | G | 2 | a0001c0001t0002g0008 a0001c0001t0002g0035 |
2 | HG00673.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.-30-526A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28683057 | |||||||
| chr1:28683248 | G | A | 56 | a0001c0001t0001g0112 a0001c0001t0001g0129 a0001c0001t0001g0130 others(53): Show |
57 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.-30-335G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28683248 | |||||||
| chr1:28683302 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30-281C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28683302 | |||||||
| chr1:28683388 | C | T | 1 | a0001c0001t0002g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-30-195C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28683388 | |||||||
| chr1:28683473 | C | T | 1 | a0001c0001t0027g0284 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-30-110C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28683473 | |||||||
| chr1:28683783 | G | C | 1 | a0001c0001t0011g0286 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.128+43G>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28683783 | |||||||
| chr1:28683888 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.128+148C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28683888 | |||||||
| chr1:28683913 | T | A | 3 | a0001c0001t0006g0119 a0001c0001t0006g0208 a0001c0001t0042g0125 |
3 | HG02257.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.128+173T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28683913 | |||||||
| chr1:28684289 | T | C | 106 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(103): Show |
106 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.128+549T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28684289 | |||||||
| chr1:28684517 | C | T | 3 | a0001c0001t0009g0082 a0001c0001t0009g0083 a0001c0001t0009g0231 |
3 | HG01243.hp2 HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.128+777C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28684517 | |||||||
| chr1:28684562 | C | CA | 107 | a0001c0001t0001g0013 a0001c0001t0001g0151 a0001c0001t0001g0181 others(104): Show |
107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.128+841dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28684562 | ||||||
| chr1:28684640 | C | T | 38 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0096 others(35): Show |
38 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.128+900C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28684640 | |||||||
| chr1:28684743 | G | T | 3 | a0001c0001t0002g0027 a0001c0001t0002g0034 a0001c0001t0002g0215 |
3 | HG01891.hp1 HG02622.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.128+1003G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28684743 | |||||||
| chr1:28685166 | G | A | 3 | a0001c0001t0002g0052 a0001c0001t0002g0068 a0001c0001t0002g0072 |
3 | HG01070.hp1 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.128+1426G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28685166 | |||||||
| chr1:28685204 | G | A | 1 | a0001c0001t0003g0016 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.128+1464G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28685204 | |||||||
| chr1:28685297 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.128+1557C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28685297 | |||||||
| chr1:28685479 | A | G | 1 | a0001c0001t0002g0038 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.128+1739A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28685479 | |||||||
| chr1:28685674 | T | C | 3 | a0001c0001t0009g0082 a0001c0001t0009g0083 a0001c0001t0009g0231 |
3 | HG01243.hp2 HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.128+1934T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28685674 | |||||||
| chr1:28685736 | G | A | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.128+1996G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28685736 | |||||||
| chr1:28685827 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.128+2087C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28685827 | |||||||
| chr1:28686361 | G | A | 38 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0096 others(35): Show |
38 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.128+2621G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28686361 | |||||||
| chr1:28686502 | G | A | 1 | a0001c0001t0003g0104 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.128+2762G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28686502 | |||||||
| chr1:28686628 | C | CA | 30 | a0001c0001t0001g0127 a0001c0001t0002g0067 a0001c0001t0003g0002 others(27): Show |
31 | HG00099.hp2 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.128+2907dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28686628 | ||||||
| chr1:28686628 | C | CAA | 105 | a0001c0001t0001g0172 a0001c0001t0001g0189 a0001c0001t0001g0190 others(102): Show |
105 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.128+2906_128+2907d others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28686628 | ||||||
| chr1:28686628 | C | CAAA | 6 | a0001c0001t0002g0032 a0001c0001t0002g0072 a0001c0001t0002g0223 others(3): Show |
6 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.128+2905_128+2907d others(5): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28686628 | ||||||
| chr1:28687004 | A | G | 106 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(103): Show |
106 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.129-3100A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687004 | |||||||
| chr1:28687130 | G | A | 1 | a0001c0001t0002g0058 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.129-2974G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687130 | |||||||
| chr1:28687131 | T | C | 1 | a0001c0001t0002g0058 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.129-2973T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687131 | |||||||
| chr1:28687334 | T | A | 31 | a0001c0001t0003g0001 a0001c0001t0003g0012 a0001c0001t0003g0016 others(28): Show |
32 | HG00099.hp1 HG00597.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.129-2770T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687334 | |||||||
| chr1:28687334 | TCA | T | 12 | a0001c0001t0001g0015 a0001c0001t0001g0142 a0001c0001t0001g0158 others(9): Show |
12 | HG00609.hp1 HG01099.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.129-2717_129-2716d others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687334 | ||||||
| chr1:28687334 | TCACA | T | 11 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0170 others(8): Show |
11 | HG00280.hp2 HG02109.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.129-2719_129-2716d others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687334 | ||||||
| chr1:28687334 | TCACACA | T | 4 | a0001c0001t0012g0168 a0001c0001t0012g0169 a0001c0001t0012g0211 others(1): Show |
4 | HG00735.hp1 HG00741.hp2 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-2721_129-2716d others(8): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687334 | ||||||
| chr1:28687336 | A | T | 3 | a0001c0001t0001g0115 a0001c0001t0006g0202 a0001c0001t0006g0206 |
3 | HG02145.hp2 HG02630.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.129-2768A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687336 | |||||||
| chr1:28687361 | C | A | 1 | a0001c0001t0011g0286 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.129-2743C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687361 | |||||||
| chr1:28687373 | C | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0238 a0001c0001t0003g0111 |
3 | HG02735.hp2 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.129-2731C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687373 | |||||||
| chr1:28687373 | C | CAAAAAAA others(2): Show |
13 | a0001c0001t0001g0137 a0001c0001t0001g0139 a0001c0001t0001g0182 others(10): Show |
13 | HG01070.hp2 HG01109.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.129-2730_129-2729i others(11): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687373 | ||||||
| chr1:28687373 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0129 a0001c0001t0001g0260 |
2 | HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.129-2730_129-2729i others(12): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687373 | ||||||
| chr1:28687375 | C | A | 23 | a0001c0001t0001g0112 a0001c0001t0001g0129 a0001c0001t0001g0137 others(20): Show |
23 | HG01070.hp2 HG01109.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.129-2729C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687375 | |||||||
| chr1:28687375 | C | CAAAAAA | 3 | a0001c0001t0001g0172 a0001c0001t0002g0087 a0001c0001t0003g0191 |
3 | HG03209.hp2 HG03579.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.129-2728_129-2727i others(8): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687375 | ||||||
| chr1:28687375 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0002g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.129-2728_129-2727i others(15): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687375 | ||||||
| chr1:28687375 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0002g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.129-2728_129-2727i others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687375 | ||||||
| chr1:28687375 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0002g0034 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.129-2728_129-2727i others(18): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687375 | ||||||
| chr1:28687377 | C | A | 35 | a0001c0001t0001g0112 a0001c0001t0001g0129 a0001c0001t0001g0137 others(32): Show |
35 | HG00741.hp2 HG01070.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.129-2727C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687377 | |||||||
| chr1:28687377 | C | CAAAAAAA others(1): Show |
7 | a0001c0001t0001g0233 a0001c0001t0002g0055 a0001c0001t0002g0056 others(4): Show |
7 | HG01496.hp2 HG03453.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.129-2726_129-2725i others(10): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687377 | ||||||
| chr1:28687377 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0002g0198 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.129-2726_129-2725i others(13): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687377 | ||||||
| chr1:28687377 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0002g0215 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.129-2726_129-2725i others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687377 | ||||||
| chr1:28687379 | C | A | 54 | a0001c0001t0001g0112 a0001c0001t0001g0129 a0001c0001t0001g0137 others(51): Show |
54 | HG00597.hp2 HG00735.hp1 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.129-2725C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687379 | |||||||
| chr1:28687379 | C | CAAAAAAA others(1): Show |
5 | a0001c0001t0002g0050 a0001c0001t0009g0082 a0001c0001t0009g0083 others(2): Show |
5 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.129-2724_129-2723i others(10): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687379 | ||||||
| chr1:28687379 | C | CAAAAAAA others(3): Show |
6 | a0001c0001t0002g0021 a0001c0001t0002g0216 a0001c0001t0002g0221 others(3): Show |
6 | HG01433.hp2 HG02135.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-2724_129-2723i others(12): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687379 | ||||||
| chr1:28687379 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0002g0022 a0001c0001t0002g0214 |
2 | HG02148.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.129-2724_129-2723i others(13): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687379 | ||||||
| chr1:28687379 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0002g0224 a0001c0001t0003g0012 a0001c0001t0045g0271 |
3 | HG01928.hp1 HG03239.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.129-2724_129-2723i others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687379 | ||||||
| chr1:28687379 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0134 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.129-2724_129-2723i others(15): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687379 | ||||||
| chr1:28687381 | C | A | 81 | a0001c0001t0001g0112 a0001c0001t0001g0129 a0001c0001t0001g0134 others(78): Show |
81 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.129-2723C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687381 | |||||||
| chr1:28687381 | C | CA | 3 | a0001c0002t0016g0011 a0001c0002t0016g0085 a0001c0002t0026g0084 |
3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.129-2722dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687381 | ||||||
| chr1:28687381 | C | CAAAA | 3 | a0001c0001t0001g0150 a0001c0001t0013g0149 a0001c0001t0043g0148 |
3 | HG00323.hp2 HG01123.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.129-2722_129-2721i others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687381 | ||||||
| chr1:28687381 | C | CAAAAAA | 3 | a0001c0001t0001g0143 a0001c0001t0001g0147 a0001c0001t0010g0101 |
3 | HG01074.hp1 HG01167.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.129-2722_129-2721i others(8): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687381 | ||||||
| chr1:28687381 | C | CAAAAAAA others(1): Show |
5 | a0001c0001t0001g0127 a0001c0001t0002g0044 a0001c0001t0002g0054 others(2): Show |
5 | HG03491.hp2 NA18995.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.129-2722_129-2721i others(10): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687381 | ||||||
| chr1:28687381 | C | CAAAAAAA others(3): Show |
10 | a0001c0001t0002g0008 a0001c0001t0002g0038 a0001c0001t0002g0045 others(7): Show |
10 | HG00673.hp1 HG00735.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.129-2722_129-2721i others(12): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687381 | ||||||
| chr1:28687381 | C | CAAAAAAA others(4): Show |
9 | a0001c0001t0002g0193 a0001c0001t0003g0001 a0001c0001t0003g0103 others(6): Show |
10 | HG00597.hp1 HG00673.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.129-2722_129-2721i others(13): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687381 | ||||||
| chr1:28687381 | C | CAAAAAAA others(5): Show |
8 | a0001c0001t0002g0004 a0001c0001t0003g0106 a0001c0001t0005g0009 others(5): Show |
8 | HG00738.hp2 HG01081.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-2722_129-2721i others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687381 | ||||||
| chr1:28687381 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0002g0032 a0001c0001t0003g0131 |
2 | HG01106.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.129-2722_129-2721i others(15): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687381 | ||||||
| chr1:28687381 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0017g0037 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.129-2722_129-2721i others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687381 | ||||||
| chr1:28687381 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0022g0277 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.129-2722_129-2721i others(17): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687381 | ||||||
| chr1:28687383 | C | A | 134 | a0001c0001t0001g0013 a0001c0001t0001g0112 a0001c0001t0001g0127 others(131): Show |
135 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.129-2721C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687383 | |||||||
| chr1:28687383 | C | CAAAAAAA others(1): Show |
5 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0002g0028 others(2): Show |
5 | HG01346.hp2 HG01361.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-2720_129-2719i others(10): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687383 | ||||||
| chr1:28687383 | C | CAAAAAAA others(2): Show |
5 | a0001c0001t0003g0002 a0001c0001t0003g0090 a0001c0001t0003g0120 others(2): Show |
6 | HG02717.hp1 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-2720_129-2719i others(11): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687383 | ||||||
| chr1:28687383 | C | CAAAAAAA others(3): Show |
5 | a0001c0001t0002g0067 a0001c0001t0002g0204 a0001c0001t0002g0220 others(2): Show |
5 | HG00099.hp2 HG00609.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-2720_129-2719i others(12): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687383 | ||||||
| chr1:28687383 | C | CAAAAAAA others(4): Show |
11 | a0001c0001t0002g0025 a0001c0001t0002g0033 a0001c0001t0002g0062 others(8): Show |
11 | HG01346.hp1 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.129-2720_129-2719i others(13): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687383 | ||||||
| chr1:28687383 | C | CAAAAAAA others(5): Show |
5 | a0001c0001t0002g0053 a0001c0001t0002g0058 a0001c0001t0002g0061 others(2): Show |
5 | HG00099.hp1 HG02615.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-2720_129-2719i others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687383 | ||||||
| chr1:28687383 | C | CAAAAAAA others(6): Show |
5 | a0001c0001t0002g0229 a0001c0001t0003g0135 a0001c0001t0028g0281 others(2): Show |
5 | HG02135.hp1 HG02738.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-2720_129-2719i others(15): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687383 | ||||||
| chr1:28687383 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0159 a0001c0001t0001g0269 a0001c0001t0018g0217 |
3 | HG01884.hp1 HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.129-2720_129-2719i others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687383 | ||||||
| chr1:28687383 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0039g0200 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.129-2720_129-2719i others(19): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687383 | ||||||
| chr1:28687385 | C | A | 201 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0017 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.129-2719C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687385 | |||||||
| chr1:28687385 | C | CAAAAAAA others(3): Show |
6 | a0001c0001t0001g0144 a0001c0001t0002g0024 a0001c0001t0002g0046 others(3): Show |
6 | HG00280.hp1 HG00733.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-2718_129-2717i others(12): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687385 | ||||||
| chr1:28687385 | C | CAAAAAAA others(4): Show |
4 | a0001c0001t0002g0031 a0001c0001t0004g0273 a0001c0001t0006g0119 others(1): Show |
4 | HG00438.hp1 HG02602.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-2718_129-2717i others(13): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687385 | ||||||
| chr1:28687385 | C | CAAAAAAA others(5): Show |
11 | a0001c0001t0001g0151 a0001c0001t0001g0189 a0001c0001t0001g0190 others(8): Show |
11 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.129-2718_129-2717i others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687385 | ||||||
| chr1:28687385 | C | CAAAAAAA others(6): Show |
3 | a0001c0001t0002g0077 a0001c0001t0003g0133 a0001c0001t0006g0206 |
3 | HG01361.hp1 HG02630.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.129-2718_129-2717i others(15): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687385 | ||||||
| chr1:28687385 | C | CAAAAAAA others(7): Show |
6 | a0001c0001t0002g0010 a0001c0001t0002g0072 a0001c0001t0002g0074 others(3): Show |
6 | HG01175.hp1 HG01255.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-2718_129-2717i others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687385 | ||||||
| chr1:28687385 | C | CAAAAAAA others(8): Show |
3 | a0001c0001t0003g0016 a0001c0001t0003g0108 a0001c0001t0003g0132 |
3 | HG02040.hp1 HG02165.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.129-2718_129-2717i others(17): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687385 | ||||||
| chr1:28687387 | C | A | 246 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0017 others(243): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.129-2717C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687387 | |||||||
| chr1:28687387 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0003g0099 a0001c0001t0034g0122 |
2 | HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.129-2710_129-2709i others(13): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | ||||||
| chr1:28687387 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0248 a0001c0001t0001g0287 |
2 | HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.129-2710_129-2709i others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | ||||||
| chr1:28687387 | C | CAAAAAAA others(6): Show |
3 | a0001c0001t0001g0249 a0001c0001t0002g0066 a0001c0001t0002g0069 |
3 | HG01175.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.129-2710_129-2709i others(15): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | ||||||
| chr1:28687387 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0145 a0001c0001t0002g0048 a0001c0001t0002g0065 |
3 | HG01123.hp1 HG01943.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.129-2710_129-2709i others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | ||||||
| chr1:28687387 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0002g0070 a0001c0003t0014g0196 |
2 | HG03098.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.129-2710_129-2709i others(18): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | ||||||
| chr1:28687387 | C | CACAAAAA others(5): Show |
1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.129-2716_129-2715i others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | ||||||
| chr1:28687387 | C | CACAAAAA others(6): Show |
1 | a0001c0001t0002g0222 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.129-2716_129-2715i others(15): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | ||||||
| chr1:28687387 | C | CACAAAAA others(7): Show |
1 | a0001c0001t0001g0146 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.129-2716_129-2715i others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | ||||||
| chr1:28687387 | C | CACAAAAA others(8): Show |
1 | a0001c0001t0003g0128 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.129-2716_129-2715i others(17): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | ||||||
| chr1:28687387 | C | CACACAAA others(7): Show |
1 | a0001c0001t0001g0270 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.129-2716_129-2715i others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | ||||||
| chr1:28687387 | C | CACACACA others(18): Show |
1 | a0001c0001t0001g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.129-2716_129-2715i others(27): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | ||||||
| chr1:28687387 | C | CACACACA others(21): Show |
1 | a0001c0001t0002g0068 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.129-2716_129-2715i others(30): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | ||||||
| chr1:28687387 | C | CACACACA others(23): Show |
1 | a0001c0001t0002g0052 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.129-2716_129-2715i others(32): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | ||||||
| chr1:28687515 | G | A | 1 | a0001c0001t0003g0111 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.129-2589G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687515 | |||||||
| chr1:28687569 | C | G | 1 | a0001c0001t0011g0285 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.129-2535C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687569 | |||||||
| chr1:28687816 | G | A | 5 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0234 others(2): Show |
5 | HG01928.hp2 HG01943.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-2288G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687816 | |||||||
| chr1:28687971 | A | G | 4 | a0001c0001t0015g0156 a0001c0001t0015g0241 a0001c0001t0015g0253 others(1): Show |
4 | HG00609.hp1 HG01099.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-2133A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687971 | |||||||
| chr1:28687988 | C | T | 3 | a0001c0001t0009g0082 a0001c0001t0009g0083 a0001c0001t0009g0231 |
3 | HG01243.hp2 HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.129-2116C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687988 | |||||||
| chr1:28688112 | C | T | 3 | a0001c0002t0016g0011 a0001c0002t0016g0085 a0001c0002t0026g0084 |
3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.129-1992C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28688112 | |||||||
| chr1:28688143 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.129-1961C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28688143 | |||||||
| chr1:28688154 | A | T | 101 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(98): Show |
101 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.129-1950A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28688154 | |||||||
| chr1:28688278 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.129-1826C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28688278 | |||||||
| chr1:28688332 | G | A | 267 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0015 others(264): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.129-1772G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28688332 | |||||||
| chr1:28688522 | C | T | 1 | a0001c0001t0003g0133 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.129-1582C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28688522 | |||||||
| chr1:28688564 | C | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0114 others(15): Show |
19 | HG00323.hp2 HG00733.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.129-1540C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28688564 | |||||||
| chr1:28688653 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.129-1451A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28688653 | |||||||
| chr1:28688721 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.129-1383A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28688721 | |||||||
| chr1:28688903 | C | CTTTTTTT others(2): Show |
134 | a0001c0001t0001g0127 a0001c0001t0001g0172 a0001c0001t0001g0189 others(131): Show |
135 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.129-1195_129-1194i others(11): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28688903 | ||||||
| chr1:28688903 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0002g0198 a0001c0001t0002g0222 a0001c0001t0002g0223 |
3 | NA18967.hp1 NA18978.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.129-1195_129-1194i others(12): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28688903 | ||||||
| chr1:28688931 | G | A | 1 | a0001c0001t0002g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.129-1173G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28688931 | |||||||
| chr1:28689355 | G | A | 12 | a0001c0001t0001g0127 a0001c0001t0001g0159 a0001c0001t0001g0172 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.129-749G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28689355 | |||||||
| chr1:28689637 | A | G | 3 | a0001c0002t0016g0011 a0001c0002t0016g0085 a0001c0002t0026g0084 |
3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.129-467A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28689637 | |||||||
| chr1:28689933 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.129-171A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28689933 | |||||||
| chr1:28689983 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.129-121A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28689983 | |||||||
| chr1:28690202 | T | TG | 14 | a0001c0001t0002g0022 a0001c0001t0002g0031 a0001c0001t0002g0033 others(11): Show |
14 | HG00438.hp1 HG00609.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.211+17dupG | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 28690202 | ||||||
| chr1:28690203 | G | GT | 142 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0017 others(139): Show |
145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.211+38dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 28690203 | ||||||
| chr1:28690203 | G | GTT | 16 | a0001c0001t0001g0013 a0001c0001t0001g0146 a0001c0001t0001g0172 others(13): Show |
16 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.211+37_211+38dupTT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 28690203 | ||||||
| chr1:28690204 | T | G | 90 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(87): Show |
90 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.211+18T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28690204 | |||||||
| chr1:28690205 | T | G | 1 | a0001c0001t0002g0075 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.211+19T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28690205 | |||||||
| chr1:28690360 | C | T | 1 | a0001c0001t0006g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.211+174C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28690360 | |||||||
| chr1:28690369 | A | G | 1 | a0001c0001t0003g0103 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.211+183A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28690369 | |||||||
| chr1:28690667 | A | G | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.211+481A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28690667 | |||||||
| chr1:28690766 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.211+580A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28690766 | |||||||
| chr1:28690853 | C | T | 3 | a0001c0001t0003g0191 a0001c0001t0011g0285 a0001c0001t0036g0252 |
3 | HG02109.hp1 HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.211+667C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28690853 | |||||||
| chr1:28690905 | G | A | 6 | a0001c0001t0014g0041 a0001c0001t0018g0043 a0001c0001t0018g0217 others(3): Show |
6 | HG02257.hp1 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-680G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28690905 | |||||||
| chr1:28690911 | T | C | 262 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0015 others(259): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.212-674T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28690911 | |||||||
| chr1:28691147 | C | T | 101 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(98): Show |
101 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.212-438C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28691147 | |||||||
| chr1:28691152 | G | A | 3 | a0001c0002t0016g0011 a0001c0002t0016g0085 a0001c0002t0026g0084 |
3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.212-433G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28691152 | |||||||
| chr1:28691334 | T | C | 1 | a0001c0001t0002g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.212-251T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28691334 | |||||||
| chr1:28691374 | A | G | 3 | a0001c0001t0006g0119 a0001c0001t0006g0208 a0001c0001t0042g0125 |
3 | HG02257.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.212-211A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28691374 | |||||||
| chr1:28691421 | G | A | 3 | a0001c0001t0003g0191 a0001c0001t0011g0285 a0001c0001t0036g0252 |
3 | HG02109.hp1 HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.212-164G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28691421 | |||||||
| chr1:28691783 | T | A | 1 | a0001c0001t0003g0135 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.336+74T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28691783 | |||||||
| chr1:28691804 | T | TTTTA | 50 | a0001c0001t0001g0003 a0001c0001t0001g0100 a0001c0001t0001g0114 others(47): Show |
51 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.336+139_336+142dup others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 28691804 | ||||||
| chr1:28691804 | T | TTTTATTT others(1): Show |
7 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0265 others(4): Show |
7 | NA18939.hp1 NA18960.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.336+135_336+142dup others(8): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 28691804 | ||||||
| chr1:28691804 | TTTTA | T | 100 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(97): Show |
100 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.336+139_336+142del others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 28691804 | ||||||
| chr1:28691804 | TTTTATTT others(1): Show |
T | 4 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0254 others(1): Show |
4 | HG02280.hp2 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.336+135_336+142del others(8): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 28691804 | ||||||
| chr1:28691804 | TTTTATTT others(9): Show |
T | 1 | a0001c0001t0001g0180 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.336+127_336+142del others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 28691804 | ||||||
| chr1:28691808 | A | T | 1 | a0001c0001t0024g0283 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.336+99A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28691808 | |||||||
| chr1:28691910 | G | A | 3 | a0001c0002t0016g0011 a0001c0002t0016g0085 a0001c0002t0026g0084 |
3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.336+201G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28691910 | |||||||
| chr1:28691946 | T | C | 106 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(103): Show |
106 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.336+237T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28691946 | |||||||
| chr1:28691958 | A | G | 1 | a0001c0001t0002g0280 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.336+249A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28691958 | |||||||
| chr1:28692016 | C | CT | 7 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0234 others(4): Show |
7 | HG01928.hp2 HG01943.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.336+321dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 28692016 | ||||||
| chr1:28692016 | C | CTT | 9 | a0001c0001t0001g0127 a0001c0001t0001g0172 a0001c0001t0001g0210 others(6): Show |
9 | HG02109.hp1 HG02258.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.336+320_336+321dup others(2): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 28692016 | ||||||
| chr1:28692203 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+494C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28692203 | |||||||
| chr1:28692295 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.336+586G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28692295 | |||||||
| chr1:28692387 | C | G | 2 | a0001c0001t0008g0092 a0001c0001t0021g0174 |
2 | HG01106.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.337-555C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28692387 | |||||||
| chr1:28692405 | G | A | 1 | a0001c0001t0002g0050 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.337-537G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28692405 | |||||||
| chr1:28692538 | A | AAAAAAAT others(27): Show |
1 | a0001c0001t0024g0283 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.337-402_337-369dup others(34): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 28692538 | ||||||
| chr1:28692561 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0030g0188 |
2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.337-381C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28692561 | |||||||
| chr1:28692737 | G | T | 1 | a0001c0001t0003g0135 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.337-205G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28692737 | |||||||
| chr1:28693211 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.440+166C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28693211 | |||||||
| chr1:28693212 | G | A | 106 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(103): Show |
106 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.440+167G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28693212 | |||||||
| chr1:28693219 | A | AT | 11 | a0001c0001t0001g0003 a0001c0001t0001g0146 a0001c0001t0001g0150 others(8): Show |
12 | HG00323.hp2 HG00673.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.440+189dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28693219 | ||||||
| chr1:28693379 | A | G | 136 | a0001c0001t0001g0127 a0001c0001t0001g0172 a0001c0001t0001g0189 others(133): Show |
137 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.440+334A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28693379 | |||||||
| chr1:28693464 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.440+419A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28693464 | |||||||
| chr1:28693580 | G | A | 1 | a0001c0001t0033g0242 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.440+535G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28693580 | |||||||
| chr1:28693602 | G | C | 106 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(103): Show |
106 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.440+557G>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28693602 | |||||||
| chr1:28693609 | C | T | 4 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(1): Show |
4 | HG00438.hp1 HG02155.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.440+564C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28693609 | |||||||
| chr1:28693626 | A | G | 101 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(98): Show |
101 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.440+581A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28693626 | |||||||
| chr1:28693843 | A | C | 4 | a0001c0001t0009g0082 a0001c0001t0009g0083 a0001c0001t0009g0231 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.440+798A>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28693843 | |||||||
| chr1:28694182 | G | A | 1 | a0001c0001t0003g0111 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.440+1137G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28694182 | |||||||
| chr1:28694190 | A | AT | 21 | a0001c0001t0001g0018 a0001c0001t0001g0177 a0001c0001t0001g0181 others(18): Show |
21 | HG00597.hp1 HG00741.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.440+1164dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28694190 | ||||||
| chr1:28694365 | A | AT | 108 | a0001c0001t0001g0096 a0001c0001t0002g0004 a0001c0001t0002g0008 others(105): Show |
108 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.440+1330dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28694365 | ||||||
| chr1:28694518 | GA | G | 99 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(96): Show |
99 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.440+1485delA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28694518 | ||||||
| chr1:28694674 | G | GT | 6 | a0001c0001t0001g0265 a0001c0001t0002g0008 a0001c0001t0002g0056 others(3): Show |
6 | HG00673.hp1 HG04115.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.440+1641dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28694674 | ||||||
| chr1:28694738 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.440+1693A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28694738 | |||||||
| chr1:28694889 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.440+1844C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28694889 | |||||||
| chr1:28694905 | G | T | 1 | a0001c0001t0012g0211 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.440+1860G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28694905 | |||||||
| chr1:28694961 | C | CT | 58 | a0001c0001t0001g0018 a0001c0001t0001g0089 a0001c0001t0001g0116 others(55): Show |
59 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.440+1937dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28694961 | ||||||
| chr1:28695045 | A | G | 1 | a0001c0001t0003g0278 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.441-1882A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695045 | |||||||
| chr1:28695113 | C | T | 1 | a0001c0001t0017g0037 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.441-1814C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695113 | |||||||
| chr1:28695293 | C | T | 3 | a0001c0002t0016g0011 a0001c0002t0016g0085 a0001c0002t0026g0084 |
3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.441-1634C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695293 | |||||||
| chr1:28695294 | G | A | 1 | a0001c0001t0006g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.441-1633G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695294 | |||||||
| chr1:28695666 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.441-1261C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695666 | |||||||
| chr1:28695721 | G | A | 1 | a0001c0001t0002g0045 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.441-1206G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695721 | |||||||
| chr1:28695745 | C | T | 3 | a0001c0001t0009g0082 a0001c0001t0009g0083 a0001c0001t0009g0231 |
3 | HG01243.hp2 HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.441-1182C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695745 | |||||||
| chr1:28695811 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.441-1116C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695811 | |||||||
| chr1:28695863 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.441-1064C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695863 | |||||||
| chr1:28695896 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.441-1031G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695896 | |||||||
| chr1:28695926 | G | A | 3 | a0001c0001t0001g0267 a0001c0005t0038g0086 a0001c0005t0040g0199 |
3 | HG01891.hp2 HG02055.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.441-1001G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695926 | |||||||
| chr1:28695938 | C | CA | 15 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0001g0146 others(12): Show |
15 | HG00609.hp1 HG01123.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.441-953dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | ||||||
| chr1:28695938 | C | CAA | 17 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0001g0192 others(14): Show |
17 | HG00099.hp1 HG00673.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.441-954_441-953dup others(2): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | ||||||
| chr1:28695938 | C | CAAA | 13 | a0001c0001t0001g0170 a0001c0001t0001g0259 a0001c0001t0003g0016 others(10): Show |
13 | HG00597.hp1 HG01106.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.441-955_441-953dup others(3): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | ||||||
| chr1:28695938 | C | CAAAA | 6 | a0001c0001t0003g0001 a0001c0001t0003g0135 a0001c0001t0003g0141 others(3): Show |
7 | HG02083.hp2 HG02132.hp1 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.441-956_441-953dup others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | ||||||
| chr1:28695938 | C | CAAAAA | 6 | a0001c0001t0003g0012 a0001c0001t0003g0107 a0001c0001t0003g0237 others(3): Show |
6 | HG01258.hp2 HG02135.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.441-957_441-953dup others(5): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | ||||||
| chr1:28695938 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0003g0108 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.441-967_441-953dup others(15): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | ||||||
| chr1:28695938 | CA | C | 42 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0096 others(39): Show |
42 | HG00280.hp1 HG00639.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.441-953delA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | ||||||
| chr1:28695938 | CAA | C | 15 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0020 others(12): Show |
16 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.441-954_441-953del others(2): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | ||||||
| chr1:28695938 | CAAAAAAA others(4): Show |
C | 17 | a0001c0001t0002g0008 a0001c0001t0002g0023 a0001c0001t0002g0031 others(14): Show |
17 | HG00438.hp1 HG00673.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.441-963_441-953del others(11): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | ||||||
| chr1:28695938 | CAAAAAAA others(5): Show |
C | 82 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0021 others(79): Show |
82 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.441-964_441-953del others(12): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | ||||||
| chr1:28695938 | CAAAAAAA others(6): Show |
C | 19 | a0001c0001t0001g0112 a0001c0001t0001g0129 a0001c0001t0001g0137 others(16): Show |
19 | HG01070.hp2 HG01109.hp1 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.441-965_441-953del others(13): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | ||||||
| chr1:28695938 | CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0238 |
2 | HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.441-966_441-953del others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | ||||||
| chr1:28695942 | A | C | 1 | a0001c0001t0001g0144 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.441-985A>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695942 | |||||||
| chr1:28695963 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0019g0275 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.441-963_441-952del others(12): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695963 | |||||||
| chr1:28695973 | A | T | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.441-954A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695973 | |||||||
| chr1:28695974 | A | AT | 10 | a0001c0001t0001g0089 a0001c0001t0001g0150 a0001c0001t0001g0172 others(7): Show |
10 | HG00323.hp2 HG01109.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.441-949dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695974 | ||||||
| chr1:28695974 | A | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0115 others(12): Show |
16 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.441-953A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695974 | |||||||
| chr1:28695975 | T | A | 6 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0003g0103 others(3): Show |
6 | HG00280.hp2 HG00673.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.441-952T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695975 | |||||||
| chr1:28696041 | ATTGT | A | 121 | a0001c0001t0001g0129 a0001c0001t0001g0139 a0001c0001t0001g0150 others(118): Show |
121 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.441-879_441-876del others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28696041 | ||||||
| chr1:28696044 | G | GTTTA | 17 | a0001c0001t0001g0114 a0001c0001t0001g0130 a0001c0001t0001g0134 others(14): Show |
17 | HG00280.hp1 HG01123.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.441-880_441-879ins others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28696044 | ||||||
| chr1:28696048 | G | A | 69 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0112 others(66): Show |
71 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.441-879G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28696048 | |||||||
| chr1:28696048 | G | GTTTA | 3 | a0001c0001t0003g0102 a0001c0001t0003g0103 a0001c0001t0012g0169 |
3 | HG00673.hp2 HG00735.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.441-847_441-844dup others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28696048 | ||||||
| chr1:28696433 | T | G | 1 | a0001c0001t0001g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.441-494T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28696433 | |||||||
| chr1:28696617 | T | A | 1 | a0001c0001t0002g0075 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.441-310T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28696617 | |||||||
| chr1:28696863 | G | A | 19 | a0001c0001t0001g0112 a0001c0001t0001g0129 a0001c0001t0001g0137 others(16): Show |
19 | HG01070.hp2 HG01109.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.441-64G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28696863 | |||||||
| chr1:28697152 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.598+68C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697152 | |||||||
| chr1:28697162 | C | CAT | 27 | a0001c0001t0002g0010 a0001c0001t0002g0051 a0001c0001t0002g0053 others(24): Show |
27 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.598+115_598+116dup others(2): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | ||||||
| chr1:28697162 | C | CATAT | 36 | a0001c0001t0001g0018 a0001c0001t0001g0254 a0001c0001t0001g0255 others(33): Show |
37 | HG00438.hp1 HG00673.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.598+113_598+116dup others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | ||||||
| chr1:28697162 | C | CATATAT | 33 | a0001c0001t0001g0114 a0001c0001t0001g0129 a0001c0001t0001g0161 others(30): Show |
33 | HG00099.hp2 HG00738.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.598+111_598+116dup others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | ||||||
| chr1:28697162 | C | CATATATA others(1): Show |
49 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(46): Show |
50 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.598+109_598+116dup others(8): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | ||||||
| chr1:28697162 | C | CATATATA others(3): Show |
26 | a0001c0001t0001g0089 a0001c0001t0001g0115 a0001c0001t0001g0166 others(23): Show |
26 | HG00438.hp2 HG00597.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.598+107_598+116dup others(10): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | ||||||
| chr1:28697162 | C | CATATATA others(5): Show |
3 | a0001c0001t0001g0173 a0001c0001t0002g0056 a0001c0001t0003g0236 |
3 | HG02896.hp1 NA18942.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.598+105_598+116dup others(12): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | ||||||
| chr1:28697162 | C | CATATATA others(7): Show |
3 | a0001c0001t0001g0130 a0001c0001t0001g0269 a0001c0001t0003g0140 |
3 | HG02809.hp1 NA18522.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.598+103_598+116dup others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | ||||||
| chr1:28697162 | C | CATATATA others(9): Show |
3 | a0001c0001t0001g0258 a0001c0001t0003g0121 a0001c0001t0003g0246 |
3 | HG02572.hp1 HG02896.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.598+101_598+116dup others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | ||||||
| chr1:28697162 | C | CATATATA others(11): Show |
1 | a0001c0001t0001g0150 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.598+99_598+116dupA others(17): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | ||||||
| chr1:28697162 | CATAT | C | 5 | a0001c0001t0001g0144 a0001c0001t0001g0160 a0001c0001t0001g0287 others(2): Show |
5 | HG00280.hp1 HG02630.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+113_598+116del others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | ||||||
| chr1:28697162 | CATATAT | C | 11 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0001g0146 others(8): Show |
11 | HG01123.hp1 HG01167.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.598+111_598+116del others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | ||||||
| chr1:28697162 | CATATATA others(1): Show |
C | 8 | a0001c0001t0001g0003 a0001c0001t0006g0119 a0001c0001t0006g0208 others(5): Show |
9 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.598+109_598+116del others(8): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | ||||||
| chr1:28697162 | CATATATA others(3): Show |
C | 12 | a0001c0001t0001g0127 a0001c0001t0001g0172 a0001c0001t0001g0210 others(9): Show |
12 | HG01074.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.598+107_598+116del others(10): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | ||||||
| chr1:28697162 | CATATATA others(5): Show |
C | 10 | a0001c0001t0001g0015 a0001c0001t0001g0159 a0001c0001t0001g0267 others(7): Show |
10 | HG00609.hp1 HG00639.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.598+105_598+116del others(12): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | ||||||
| chr1:28697162 | CATATATA others(7): Show |
C | 33 | a0001c0001t0001g0013 a0001c0001t0001g0096 a0001c0001t0001g0097 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.598+103_598+116del others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | ||||||
| chr1:28697162 | CATATATA others(9): Show |
C | 6 | a0001c0001t0003g0104 a0001c0001t0003g0106 a0001c0001t0003g0110 others(3): Show |
6 | HG00099.hp1 HG01106.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.598+101_598+116del others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | ||||||
| chr1:28697162 | CATATATA others(11): Show |
C | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 |
3 | HG00733.hp1 HG01346.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.598+99_598+116delA others(17): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | ||||||
| chr1:28697162 | CATATATA others(13): Show |
C | 2 | a0001c0001t0001g0171 a0001c0001t0004g0152 |
2 | HG01069.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.598+97_598+116delA others(19): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | ||||||
| chr1:28697162 | CATATATA others(15): Show |
C | 2 | a0001c0001t0001g0163 a0001c0001t0002g0218 |
2 | HG00597.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.598+95_598+116delA others(21): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | ||||||
| chr1:28697162 | CATATATA others(17): Show |
C | 1 | a0001c0001t0002g0058 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.598+93_598+116delA others(23): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | ||||||
| chr1:28697193 | A | G | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.598+109A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697193 | |||||||
| chr1:28697270 | G | A | 3 | a0001c0002t0016g0011 a0001c0002t0016g0085 a0001c0002t0026g0084 |
3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.598+186G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697270 | |||||||
| chr1:28697285 | T | C | 106 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(103): Show |
106 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.598+201T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697285 | |||||||
| chr1:28697400 | G | T | 1 | a0001c0001t0003g0102 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.598+316G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697400 | |||||||
| chr1:28697431 | C | T | 1 | a0001c0001t0003g0123 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.598+347C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697431 | |||||||
| chr1:28697495 | A | T | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.598+411A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697495 | |||||||
| chr1:28697496 | C | T | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.598+412C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697496 | |||||||
| chr1:28697617 | C | A | 106 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(103): Show |
106 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.598+533C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697617 | |||||||
| chr1:28697619 | A | G | 3 | a0001c0001t0003g0191 a0001c0001t0011g0285 a0001c0001t0036g0252 |
3 | HG02109.hp1 HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.598+535A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697619 | |||||||
| chr1:28697857 | C | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0210 |
2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.598+773C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697857 | |||||||
| chr1:28697867 | C | T | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | NA18939.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.598+783C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697867 | |||||||
| chr1:28697875 | C | G | 2 | a0001c0001t0001g0115 a0001c0001t0031g0272 |
2 | HG02735.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.598+791C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697875 | |||||||
| chr1:28697892 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.598+808C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697892 | |||||||
| chr1:28698274 | C | T | 21 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0090 others(18): Show |
22 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.598+1190C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698274 | |||||||
| chr1:28698391 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0030g0188 |
2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.598+1307G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698391 | |||||||
| chr1:28698394 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+1310G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698394 | |||||||
| chr1:28698396 | C | T | 97 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(94): Show |
97 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.598+1312C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698396 | |||||||
| chr1:28698441 | C | T | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.598+1357C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698441 | |||||||
| chr1:28698442 | A | G | 106 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(103): Show |
106 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.598+1358A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698442 | |||||||
| chr1:28698444 | A | G | 106 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(103): Show |
106 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.598+1360A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698444 | |||||||
| chr1:28698461 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.598+1377G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698461 | |||||||
| chr1:28698568 | G | A | 1 | a0001c0001t0002g0036 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.598+1484G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698568 | |||||||
| chr1:28698674 | C | CA | 103 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(100): Show |
103 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.598+1605dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28698674 | ||||||
| chr1:28698719 | C | T | 1 | a0001c0001t0003g0240 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.598+1635C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698719 | |||||||
| chr1:28698842 | G | A | 1 | a0001c0001t0003g0124 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.598+1758G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698842 | |||||||
| chr1:28698908 | C | A | 3 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0071 |
3 | NA18942.hp2 NA18964.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.598+1824C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698908 | |||||||
| chr1:28699235 | G | A | 101 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(98): Show |
101 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.598+2151G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28699235 | |||||||
| chr1:28699486 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.598+2402A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28699486 | |||||||
| chr1:28699515 | C | T | 2 | a0001c0001t0002g0070 a0001c0001t0002g0222 |
2 | NA19012.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.598+2431C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28699515 | |||||||
| chr1:28699517 | C | T | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.598+2433C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28699517 | |||||||
| chr1:28700058 | C | CA | 45 | a0001c0001t0001g0143 a0001c0001t0001g0184 a0001c0001t0001g0185 others(42): Show |
46 | HG00673.hp1 HG01175.hp2 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.599-2357dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28700058 | ||||||
| chr1:28700058 | CA | C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(21): Show |
25 | HG00323.hp2 HG00733.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.599-2357delA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28700058 | ||||||
| chr1:28700058 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0045g0271 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.599-2368_599-2357d others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28700058 | ||||||
| chr1:28700278 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.599-2160C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28700278 | |||||||
| chr1:28700279 | G | A | 1 | a0001c0001t0004g0162 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.599-2159G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28700279 | |||||||
| chr1:28700463 | G | A | 3 | a0001c0001t0003g0191 a0001c0001t0011g0285 a0001c0001t0036g0252 |
3 | HG02109.hp1 HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.599-1975G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28700463 | |||||||
| chr1:28700483 | C | T | 1 | a0001c0001t0003g0104 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.599-1955C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28700483 | |||||||
| chr1:28700513 | C | CA | 13 | a0001c0001t0001g0018 a0001c0001t0001g0130 a0001c0001t0001g0269 others(10): Show |
13 | HG00438.hp1 HG00609.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.599-1903dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28700513 | ||||||
| chr1:28700513 | CA | C | 84 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0096 others(81): Show |
86 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.599-1903delA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28700513 | ||||||
| chr1:28700664 | A | G | 106 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(103): Show |
106 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.599-1774A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28700664 | |||||||
| chr1:28700684 | C | CA | 24 | a0001c0001t0001g0142 a0001c0001t0002g0033 a0001c0001t0002g0221 others(21): Show |
25 | HG01255.hp2 HG02055.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.599-1738dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28700684 | ||||||
| chr1:28700799 | C | T | 3 | a0001c0002t0016g0011 a0001c0002t0016g0085 a0001c0002t0026g0084 |
3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.599-1639C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28700799 | |||||||
| chr1:28700827 | C | T | 1 | a0001c0001t0002g0036 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.599-1611C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28700827 | |||||||
| chr1:28700893 | G | T | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.599-1545G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28700893 | |||||||
| chr1:28700933 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.599-1505T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28700933 | |||||||
| chr1:28700961 | G | A | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.599-1477G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28700961 | |||||||
| chr1:28701142 | A | G | 101 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(98): Show |
101 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.599-1296A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28701142 | |||||||
| chr1:28701268 | C | CT | 35 | a0001c0001t0001g0248 a0001c0001t0003g0001 a0001c0001t0003g0012 others(32): Show |
36 | HG00099.hp1 HG00597.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.599-1153dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28701268 | ||||||
| chr1:28701268 | C | CTTTTT | 15 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0090 others(12): Show |
16 | HG02055.hp2 HG02257.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.599-1157_599-1153d others(7): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28701268 | ||||||
| chr1:28701268 | C | CTTTTTT | 101 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0002g0008 others(98): Show |
101 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.599-1158_599-1153d others(8): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28701268 | ||||||
| chr1:28701268 | C | CTTTTTTT | 20 | a0001c0001t0001g0127 a0001c0001t0001g0172 a0001c0001t0001g0210 others(17): Show |
20 | HG01261.hp1 HG01346.hp1 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.599-1159_599-1153d others(9): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28701268 | ||||||
| chr1:28701294 | T | C | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.599-1144T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28701294 | |||||||
| chr1:28701387 | A | G | 1 | a0002c0007t0002g0226 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.599-1051A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28701387 | |||||||
| chr1:28701398 | T | C | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.599-1040T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28701398 | |||||||
| chr1:28701415 | A | G | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.599-1023A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28701415 | |||||||
| chr1:28701559 | C | T | 18 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0114 others(15): Show |
19 | HG00323.hp2 HG00733.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.599-879C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28701559 | |||||||
| chr1:28701748 | C | T | 2 | a0001c0001t0003g0104 a0001c0001t0028g0281 |
2 | HG02738.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.599-690C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28701748 | |||||||
| chr1:28702680 | C | T | 3 | a0001c0002t0016g0011 a0001c0002t0016g0085 a0001c0002t0026g0084 |
3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.730+111C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28702680 | |||||||
| chr1:28702982 | A | G | 1 | a0001c0001t0006g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.730+413A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28702982 | |||||||
| chr1:28702986 | C | T | 2 | a0001c0001t0002g0064 a0001c0001t0002g0074 |
2 | HG00438.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.730+417C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28702986 | |||||||
| chr1:28703043 | A | G | 3 | a0001c0002t0016g0011 a0001c0002t0016g0085 a0001c0002t0026g0084 |
3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.730+474A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28703043 | |||||||
| chr1:28703317 | TTTA | T | 3 | a0001c0002t0016g0011 a0001c0002t0016g0085 a0001c0002t0026g0084 |
3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.730+754_730+756del others(3): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 28703317 | ||||||
| chr1:28703389 | C | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0114 others(29): Show |
33 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.731-803C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28703389 | |||||||
| chr1:28703493 | C | A | 1 | a0001c0001t0002g0075 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.731-699C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28703493 | |||||||
| chr1:28703648 | G | A | 2 | a0001c0001t0002g0048 a0001c0001t0017g0039 |
2 | NA18998.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.731-544G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28703648 | |||||||
| chr1:28703696 | A | C | 3 | a0001c0002t0016g0011 a0001c0002t0016g0085 a0001c0002t0026g0084 |
3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.731-496A>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28703696 | |||||||
| chr1:28703714 | C | G | 1 | a0001c0001t0002g0058 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.731-478C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28703714 | |||||||
| chr1:28703844 | T | C | 1 | a0001c0001t0004g0152 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.731-348T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28703844 | |||||||
| chr1:28704138 | A | G | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.731-54A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28704138 | |||||||
| chr1:28704376 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0030g0188 |
2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.868+47C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28704376 | |||||||
| chr1:28704380 | C | T | 3 | a0001c0001t0003g0002 a0001c0001t0003g0090 a0001c0001t0003g0120 |
4 | HG02717.hp1 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.868+51C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28704380 | |||||||
| chr1:28704608 | A | T | 3 | a0001c0001t0003g0016 a0001c0001t0018g0043 a0001c0001t0018g0217 |
3 | HG02572.hp2 HG02723.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.868+279A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28704608 | |||||||
| chr1:28704649 | A | G | 1 | a0001c0001t0006g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.868+320A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28704649 | |||||||
| chr1:28704666 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0269 |
2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.868+337C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28704666 | |||||||
| chr1:28704667 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0031g0272 |
2 | HG02735.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.868+338G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28704667 | |||||||
| chr1:28704686 | A | G | 2 | a0001c0001t0003g0191 a0001c0001t0011g0285 |
2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.868+357A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28704686 | |||||||
| chr1:28704788 | A | G | 4 | a0001c0001t0001g0245 a0001c0001t0001g0254 a0001c0001t0001g0261 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.868+459A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28704788 | |||||||
| chr1:28704854 | C | T | 1 | a0001c0001t0003g0278 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.868+525C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28704854 | |||||||
| chr1:28705082 | C | CA | 21 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0001g0170 others(18): Show |
21 | HG02135.hp1 HG02300.hp2 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.868+773dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28705082 | ||||||
| chr1:28705102 | A | C | 1 | a0001c0001t0003g0133 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.868+773A>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28705102 | |||||||
| chr1:28705161 | G | A | 1 | a0001c0001t0004g0273 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.868+832G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28705161 | |||||||
| chr1:28705206 | T | C | 10 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(7): Show |
10 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.868+877T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28705206 | |||||||
| chr1:28705298 | G | A | 2 | a0001c0001t0002g0064 a0001c0001t0002g0074 |
2 | HG00438.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.868+969G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28705298 | |||||||
| chr1:28705430 | C | T | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.868+1101C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28705430 | |||||||
| chr1:28705445 | C | CT | 10 | a0001c0001t0001g0150 a0001c0001t0002g0032 a0001c0001t0002g0033 others(7): Show |
10 | HG01109.hp1 HG01261.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.868+1135dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28705445 | ||||||
| chr1:28705445 | CT | C | 39 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0096 others(36): Show |
39 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.868+1135delT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28705445 | ||||||
| chr1:28705552 | C | T | 1 | a0001c0001t0039g0200 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.868+1223C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28705552 | |||||||
| chr1:28705595 | G | A | 1 | a0001c0001t0003g0109 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.868+1266G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28705595 | |||||||
| chr1:28705834 | T | C | 1 | a0001c0001t0002g0025 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.868+1505T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28705834 | |||||||
| chr1:28706011 | G | A | 19 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0090 others(16): Show |
20 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.868+1682G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706011 | |||||||
| chr1:28706068 | G | A | 10 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(7): Show |
10 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.868+1739G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706068 | |||||||
| chr1:28706071 | A | G | 17 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0090 others(14): Show |
18 | HG02055.hp2 HG02257.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.868+1742A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706071 | |||||||
| chr1:28706086 | A | G | 265 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0015 others(262): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.868+1757A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706086 | |||||||
| chr1:28706092 | T | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0269 |
2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.868+1763T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706092 | |||||||
| chr1:28706157 | A | AAAAT | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0003g0001 others(4): Show |
8 | HG00639.hp1 HG02083.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.868+1856_868+1859d others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28706157 | ||||||
| chr1:28706157 | AAAAT | A | 106 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(103): Show |
106 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.868+1856_868+1859d others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28706157 | ||||||
| chr1:28706244 | T | C | 101 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(98): Show |
101 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.868+1915T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706244 | |||||||
| chr1:28706307 | T | C | 1 | a0001c0001t0011g0285 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.868+1978T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706307 | |||||||
| chr1:28706338 | C | T | 6 | a0001c0001t0014g0041 a0001c0001t0018g0043 a0001c0001t0018g0217 others(3): Show |
6 | HG02257.hp1 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.868+2009C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706338 | |||||||
| chr1:28706413 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.868+2084T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706413 | |||||||
| chr1:28706459 | C | T | 1 | a0001c0001t0006g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.868+2130C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706459 | |||||||
| chr1:28706573 | CAGCCTGG others(35): Show |
C | 10 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(7): Show |
10 | HG00280.hp1 HG01123.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.868+2246_868+2287d others(44): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28706573 | ||||||
| chr1:28706603 | C | CA | 8 | a0001c0001t0002g0057 a0001c0001t0002g0229 a0001c0001t0006g0202 others(5): Show |
8 | HG01243.hp2 HG01884.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.868+2288dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28706603 | ||||||
| chr1:28706910 | A | G | 1 | a0001c0001t0003g0107 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.868+2581A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706910 | |||||||
| chr1:28706975 | T | TG | 28 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0021 others(25): Show |
28 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.868+2648dupG | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28706975 | ||||||
| chr1:28706977 | G | GT | 78 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0017 others(75): Show |
80 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.868+2673dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28706977 | ||||||
| chr1:28706977 | G | GTT | 19 | a0001c0001t0001g0097 a0001c0001t0001g0178 a0001c0001t0001g0184 others(16): Show |
19 | HG01255.hp2 HG01952.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.868+2672_868+2673d others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28706977 | ||||||
| chr1:28706977 | GT | G | 8 | a0001c0001t0001g0127 a0001c0001t0001g0172 a0001c0001t0001g0210 others(5): Show |
8 | HG02109.hp1 HG02258.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.868+2673delT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28706977 | ||||||
| chr1:28706978 | T | G | 67 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0025 others(64): Show |
67 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.868+2649T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706978 | |||||||
| chr1:28706990 | T | G | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG01123.hp1 HG01167.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.868+2661T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706990 | |||||||
| chr1:28707063 | A | G | 101 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(98): Show |
101 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.868+2734A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28707063 | |||||||
| chr1:28707122 | A | G | 1 | a0001c0001t0002g0070 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.868+2793A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28707122 | |||||||
| chr1:28707196 | G | A | 106 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(103): Show |
106 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.868+2867G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28707196 | |||||||
| chr1:28707229 | G | A | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.868+2900G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28707229 | |||||||
| chr1:28707261 | C | T | 4 | a0001c0001t0009g0082 a0001c0001t0009g0083 a0001c0001t0009g0231 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.868+2932C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28707261 | |||||||
| chr1:28708355 | G | A | 101 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(98): Show |
101 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.869-2165G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28708355 | |||||||
| chr1:28708607 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.869-1913A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28708607 | |||||||
| chr1:28708741 | C | T | 1 | a0001c0001t0011g0286 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.869-1779C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28708741 | |||||||
| chr1:28708794 | G | A | 1 | a0001c0001t0003g0240 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.869-1726G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28708794 | |||||||
| chr1:28708897 | C | T | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.869-1623C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28708897 | |||||||
| chr1:28708899 | A | T | 1 | a0001c0001t0030g0188 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.869-1621A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28708899 | |||||||
| chr1:28708914 | A | G | 137 | a0001c0001t0001g0127 a0001c0001t0001g0172 a0001c0001t0001g0189 others(134): Show |
138 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.869-1606A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28708914 | |||||||
| chr1:28708947 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.869-1573C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28708947 | |||||||
| chr1:28709058 | C | T | 1 | a0001c0001t0002g0077 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.869-1462C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709058 | |||||||
| chr1:28709133 | C | CA | 101 | a0001c0001t0001g0192 a0001c0001t0001g0249 a0001c0001t0001g0265 others(98): Show |
101 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.869-1371dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28709133 | ||||||
| chr1:28709133 | C | CAA | 7 | a0001c0001t0002g0044 a0001c0001t0002g0070 a0001c0001t0002g0215 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.869-1372_869-1371d others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28709133 | ||||||
| chr1:28709246 | G | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0114 others(26): Show |
30 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.869-1274G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709246 | |||||||
| chr1:28709260 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.869-1260T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709260 | |||||||
| chr1:28709371 | A | G | 1 | a0001c0001t0002g0023 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.869-1149A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709371 | |||||||
| chr1:28709502 | G | C | 1 | a0001c0001t0004g0273 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.869-1018G>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709502 | |||||||
| chr1:28709511 | A | G | 1 | a0001c0001t0002g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.869-1009A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709511 | |||||||
| chr1:28709584 | A | T | 2 | a0001c0001t0010g0113 a0001c0001t0010g0239 |
2 | HG01099.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.869-936A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709584 | |||||||
| chr1:28709585 | A | T | 54 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0089 others(51): Show |
56 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.869-935A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709585 | |||||||
| chr1:28709586 | T | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.869-934T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709586 | |||||||
| chr1:28709770 | T | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.869-750T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709770 | |||||||
| chr1:28709929 | A | G | 2 | a0001c0005t0038g0086 a0001c0005t0040g0199 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.869-591A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709929 | |||||||
| chr1:28709933 | G | A | 6 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(3): Show |
6 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.869-587G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709933 | |||||||
| chr1:28710424 | A | G | 1 | a0001c0001t0039g0200 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.869-96A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28710424 | |||||||
| chr1:28710728 | C | CT | 135 | a0001c0001t0001g0127 a0001c0001t0001g0172 a0001c0001t0001g0189 others(132): Show |
136 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.991+98dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 28710728 | ||||||
| chr1:28710783 | G | A | 1 | a0001c0001t0002g0218 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.991+141G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28710783 | |||||||
| chr1:28711157 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.991+515G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28711157 | |||||||
| chr1:28711265 | G | A | 1 | a0001c0001t0002g0218 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.991+623G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28711265 | |||||||
| chr1:28711267 | C | T | 1 | a0001c0001t0002g0071 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.991+625C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28711267 | |||||||
| chr1:28711281 | T | G | 102 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(99): Show |
102 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.991+639T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28711281 | |||||||
| chr1:28711299 | A | G | 1 | a0001c0001t0017g0039 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.991+657A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28711299 | |||||||
| chr1:28711300 | G | A | 2 | a0001c0001t0002g0070 a0001c0001t0017g0039 |
2 | NA18998.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.991+658G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28711300 | |||||||
| chr1:28711300 | G | GA | 103 | a0001c0001t0001g0100 a0001c0001t0001g0184 a0001c0001t0002g0004 others(100): Show |
103 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.991+667dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 28711300 | ||||||
| chr1:28711599 | G | T | 1 | a0001c0001t0001g0114 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.991+957G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28711599 | |||||||
| chr1:28711647 | G | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0139 a0001c0001t0004g0138 |
3 | HG01109.hp1 HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.991+1005G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28711647 | |||||||
| chr1:28711661 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.991+1019C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28711661 | |||||||
| chr1:28711952 | C | T | 5 | a0001c0001t0009g0082 a0001c0001t0009g0083 a0001c0001t0009g0231 others(2): Show |
5 | HG01070.hp2 HG01243.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.991+1310C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28711952 | |||||||
| chr1:28712098 | G | A | 102 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(99): Show |
102 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.991+1456G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712098 | |||||||
| chr1:28712108 | T | A | 1 | a0001c0001t0039g0200 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.991+1466T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712108 | |||||||
| chr1:28712150 | A | G | 5 | a0001c0001t0003g0109 a0001c0001t0003g0140 a0001c0001t0003g0141 others(2): Show |
5 | NA18943.hp1 NA18947.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.991+1508A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712150 | |||||||
| chr1:28712159 | G | A | 5 | a0001c0001t0003g0006 a0001c0001t0003g0154 a0001c0001t0003g0155 others(2): Show |
5 | HG02055.hp2 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.991+1517G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712159 | |||||||
| chr1:28712315 | C | T | 1 | a0001c0001t0002g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.991+1673C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712315 | |||||||
| chr1:28712332 | A | C | 1 | a0001c0001t0003g0110 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.991+1690A>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712332 | |||||||
| chr1:28712425 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.992-1648C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712425 | |||||||
| chr1:28712560 | C | T | 102 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(99): Show |
102 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.992-1513C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712560 | |||||||
| chr1:28712636 | T | C | 1 | a0001c0001t0018g0217 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.992-1437T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712636 | |||||||
| chr1:28712647 | C | A | 1 | a0001c0001t0003g0278 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.992-1426C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712647 | |||||||
| chr1:28712704 | A | C | 5 | a0001c0001t0009g0082 a0001c0001t0009g0083 a0001c0001t0009g0231 others(2): Show |
5 | HG01070.hp2 HG01243.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.992-1369A>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712704 | |||||||
| chr1:28712712 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.992-1361G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712712 | |||||||
| chr1:28712858 | A | G | 24 | a0001c0001t0001g0127 a0001c0001t0001g0172 a0001c0001t0001g0210 others(21): Show |
25 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.992-1215A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712858 | |||||||
| chr1:28712877 | G | A | 1 | a0001c0001t0007g0212 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.992-1196G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712877 | |||||||
| chr1:28712995 | C | CA | 196 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(193): Show |
198 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.992-1067dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 28712995 | ||||||
| chr1:28712995 | C | CAA | 39 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0096 others(36): Show |
39 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.992-1068_992-1067d others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 28712995 | ||||||
| chr1:28713012 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0269 |
2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.992-1061G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28713012 | |||||||
| chr1:28713019 | G | A | 2 | a0001c0001t0001g0263 a0001c0001t0018g0043 |
2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.992-1054G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28713019 | |||||||
| chr1:28713020 | C | T | 1 | a0001c0001t0043g0148 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.992-1053C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28713020 | |||||||
| chr1:28713035 | G | A | 1 | a0001c0001t0001g0015 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.992-1038G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28713035 | |||||||
| chr1:28713037 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.992-1036A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28713037 | |||||||
| chr1:28713157 | C | CA | 50 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(47): Show |
51 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.992-898dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 28713157 | ||||||
| chr1:28713384 | G | A | 1 | a0001c0001t0007g0212 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.992-689G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28713384 | |||||||
| chr1:28713921 | C | G | 2 | a0001c0001t0019g0136 a0001c0001t0019g0275 |
2 | HG01070.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.992-152C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28713921 | |||||||
| chr1:28714038 | T | G | 1 | a0001c0001t0002g0074 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.992-35T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28714038 |