Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4224 |
| ensemblid | ENSG00000112818.11 |
| hgncid | 7015 |
| symbol | MEP1A |
| name | meprin A subunit alpha |
| refseq_nuc | NM_005588.3 |
| refseq_prot | NP_005579.2 |
| ensembl_nuc | ENST00000230588.9 |
| ensembl_prot | ENSP00000230588.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 46793389 |
| end | 46839778 |
| strand | + |
| ver | v1.2 |
| region | chr6:46793389-46839778 |
| region5000 | chr6:46788389-46844778 |
| regionname0 | MEP1A_chr6_46793389_46839778 |
| regionname5000 | MEP1A_chr6_46788389_46844778 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 746 | 117 | 27 | 19 | 58 | 2 | 11 | 50 | MEP1A_chr6_46788389_46844778 | MEP1A | MAWIR others(741): Show |
chr6 | 46788389 | 46844778 |
| a0002 | 1/0 | 746 | 94 | 5 | 20 | 55 | 3 | 10 | 46 | MEP1A_chr6_46788389_46844778 | MEP1A | MAWIR others(741): Show |
chr6 | 46788389 | 46844778 |
| a0003 | 0/1 | 746 | 62 | 10 | 12 | 20 | 6 | 13 | 18 | MEP1A_chr6_46788389_46844778 | MEP1A | MAWIR others(741): Show |
chr6 | 46788389 | 46844778 |
| a0004 | 0/0 | 746 | 23 | 19 | 2 | 2 | 0 | 0 | 2 | MEP1A_chr6_46788389_46844778 | MEP1A | MAWIR others(741): Show |
chr6 | 46788389 | 46844778 |
| a0005 | 0/0 | 746 | 16 | 4 | 5 | 6 | 0 | 1 | 4 | MEP1A_chr6_46788389_46844778 | MEP1A | MAWIR others(741): Show |
chr6 | 46788389 | 46844778 |
| a0006 | 0/0 | 746 | 11 | 6 | 1 | 3 | 0 | 1 | 2 | MEP1A_chr6_46788389_46844778 | MEP1A | MAWIR others(741): Show |
chr6 | 46788389 | 46844778 |
| a0007 | 0/0 | 746 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | MAWIR others(741): Show |
chr6 | 46788389 | 46844778 |
| a0008 | 0/0 | 746 | 4 | 0 | 0 | 0 | 2 | 2 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | MAWIR others(741): Show |
chr6 | 46788389 | 46844778 |
| a0009 | 0/0 | 746 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | MAWIR others(741): Show |
chr6 | 46788389 | 46844778 |
| a0010 | 0/0 | 746 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | MAWIR others(741): Show |
chr6 | 46788389 | 46844778 |
| a0011 | 0/0 | 746 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | MAWIR others(741): Show |
chr6 | 46788389 | 46844778 |
| a0012 | 0/0 | 746 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | MAWIR others(741): Show |
chr6 | 46788389 | 46844778 |
| a0013 | 0/0 | 746 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | MAWIR others(741): Show |
chr6 | 46788389 | 46844778 |
| a0014 | 0/0 | 746 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | MAWIR others(741): Show |
chr6 | 46788389 | 46844778 |
| a0015 | 0/0 | 746 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | MAWIR others(741): Show |
chr6 | 46788389 | 46844778 |
| a0016 | 0/0 | 746 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | MAWIR others(741): Show |
chr6 | 46788389 | 46844778 |
| a0017 | 0/0 | 746 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | MAWIR others(741): Show |
chr6 | 46788389 | 46844778 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2238 | 115 | 27 | 19 | 58 | 2 | 9 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0001c0013 | 0/0 | 2238 | 2 | 0 | 0 | 0 | 0 | 2 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0002c0002 | 1/0 | 2238 | 93 | 5 | 19 | 55 | 3 | 10 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0002c0020 | 0/0 | 2238 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0003c0003 | 0/1 | 2238 | 62 | 10 | 12 | 20 | 6 | 13 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0004c0004 | 0/0 | 2238 | 21 | 18 | 1 | 2 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0004c0021 | 0/0 | 2238 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0004c0023 | 0/0 | 2238 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0005c0006 | 0/0 | 2238 | 10 | 4 | 5 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0005c0008 | 0/0 | 2238 | 6 | 0 | 0 | 6 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0006c0005 | 0/0 | 2238 | 11 | 6 | 1 | 3 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0007c0007 | 0/0 | 2238 | 9 | 8 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0007c0017 | 0/0 | 2238 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0008c0010 | 0/0 | 2238 | 4 | 0 | 0 | 0 | 2 | 2 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0009c0009 | 0/0 | 2238 | 4 | 4 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0010c0011 | 0/0 | 2238 | 3 | 0 | 0 | 0 | 0 | 3 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0011c0012 | 0/0 | 2238 | 2 | 2 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0012c0016 | 0/0 | 2238 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0013c0019 | 0/0 | 2238 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0014c0022 | 0/0 | 2238 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0015c0018 | 0/0 | 2238 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0016c0014 | 0/0 | 2238 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 | ||
| a0017c0015 | 0/0 | 2238 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ATGGC others(2233): Show |
chr6 | 46788389 | 46844778 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2905 | 108 | 21 | 19 | 57 | 2 | 9 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0001c0001t0005 | 0/0 | 2893 | 4 | 4 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2888): Show |
chr6 | 46788389 | 46844778 |
| a0001c0001t0006 | 0/0 | 2893 | 2 | 2 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2888): Show |
chr6 | 46788389 | 46844778 |
| a0001c0001t0008 | 0/0 | 2905 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0001c0013t0001 | 0/0 | 2905 | 2 | 0 | 0 | 0 | 0 | 2 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0002c0002t0001 | 0/0 | 2905 | 4 | 0 | 0 | 4 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0002c0002t0002 | 1/0 | 2893 | 88 | 5 | 18 | 51 | 3 | 10 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2888): Show |
chr6 | 46788389 | 46844778 |
| a0002c0002t0007 | 0/0 | 2905 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0002c0020t0002 | 0/0 | 2893 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2888): Show |
chr6 | 46788389 | 46844778 |
| a0003c0003t0003 | 0/1 | 2905 | 61 | 10 | 12 | 20 | 6 | 12 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0003c0003t0011 | 0/0 | 2905 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0004c0004t0001 | 0/0 | 2905 | 2 | 2 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0004c0004t0002 | 0/0 | 2893 | 15 | 12 | 1 | 2 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2888): Show |
chr6 | 46788389 | 46844778 |
| a0004c0004t0003 | 0/0 | 2905 | 4 | 4 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0004c0021t0002 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2888): Show |
chr6 | 46788389 | 46844778 |
| a0004c0023t0002 | 0/0 | 2893 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2888): Show |
chr6 | 46788389 | 46844778 |
| a0005c0006t0003 | 0/0 | 2905 | 10 | 4 | 5 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0005c0008t0003 | 0/0 | 2905 | 6 | 0 | 0 | 6 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0006c0005t0002 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2888): Show |
chr6 | 46788389 | 46844778 |
| a0006c0005t0003 | 0/0 | 2905 | 10 | 5 | 1 | 3 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0007c0007t0003 | 0/0 | 2905 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0007c0007t0004 | 0/0 | 2893 | 7 | 6 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2888): Show |
chr6 | 46788389 | 46844778 |
| a0007c0007t0010 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2888): Show |
chr6 | 46788389 | 46844778 |
| a0007c0017t0001 | 0/0 | 2905 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0008c0010t0001 | 0/0 | 2905 | 4 | 0 | 0 | 0 | 2 | 2 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0009c0009t0001 | 0/0 | 2905 | 4 | 4 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0010c0011t0003 | 0/0 | 2905 | 3 | 0 | 0 | 0 | 0 | 3 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0011c0012t0002 | 0/0 | 2893 | 2 | 2 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2888): Show |
chr6 | 46788389 | 46844778 |
| a0012c0016t0003 | 0/0 | 2905 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0013c0019t0002 | 0/0 | 2893 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2888): Show |
chr6 | 46788389 | 46844778 |
| a0014c0022t0001 | 0/0 | 2905 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0015c0018t0001 | 0/0 | 2905 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0016c0014t0001 | 0/0 | 2905 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| a0017c0015t0009 | 0/0 | 2905 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | ACTTG others(2900): Show |
chr6 | 46788389 | 46844778 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0001t0008g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0001c0013t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0002 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0180 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0002t0007g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0002c0020t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0150 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0003c0003t0011g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0004c0004t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0004c0004t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0004c0004t0002g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0004c0004t0002g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0004c0004t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0004c0004t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0004c0004t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0004c0004t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0004c0004t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0004c0004t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0004c0004t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0004c0004t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0004c0004t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0004c0004t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0004c0004t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0004c0004t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0004c0021t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0004c0023t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0005c0006t0003g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0005c0006t0003g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0005c0006t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0005c0006t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0005c0006t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0005c0006t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0005c0006t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0005c0006t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0005c0006t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0005c0008t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0005c0008t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0005c0008t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0005c0008t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0005c0008t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0005c0008t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0006c0005t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0006c0005t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0006c0005t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0006c0005t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0006c0005t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0006c0005t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0006c0005t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0006c0005t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0006c0005t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0006c0005t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0006c0005t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0007c0007t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0007c0007t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0007c0007t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0007c0007t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0007c0007t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0007c0007t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0007c0007t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0007c0007t0004g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0007c0007t0010g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0007c0017t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0008c0010t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0008c0010t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0008c0010t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0009c0009t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0009c0009t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0009c0009t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0009c0009t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0010c0011t0003g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0010c0011t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0011c0012t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0011c0012t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0012c0016t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0013c0019t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0014c0022t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0015c0018t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0016c0014t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| a0017c0015t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0195 | EUR | GBR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00099 | hp2 | a0003 | c0003 | t0003 | g0106 | EUR | GBR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00140 | hp1 | a0012 | c0016 | t0003 | g0098 | EUR | GBR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0026 | EUR | GBR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | FIN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00280 | hp2 | a0003 | c0003 | t0003 | g0043 | EUR | FIN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | FIN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00323 | hp2 | a0003 | c0003 | t0003 | g0103 | EUR | FIN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00408 | hp2 | a0013 | c0019 | t0002 | g0291 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00544 | hp1 | a0003 | c0003 | t0003 | g0013 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00544 | hp2 | a0014 | c0022 | t0001 | g0172 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0275 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00639 | hp1 | a0003 | c0003 | t0003 | g0305 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00639 | hp2 | a0005 | c0006 | t0003 | g0015 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0027 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00733 | hp1 | a0003 | c0003 | t0003 | g0016 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0200 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00738 | hp2 | a0003 | c0003 | t0003 | g0014 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG00741 | hp2 | a0004 | c0023 | t0002 | g0058 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01069 | hp1 | a0005 | c0006 | t0003 | g0082 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0162 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0161 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01071 | hp2 | a0005 | c0006 | t0003 | g0081 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0164 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0166 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0197 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0287 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01106 | hp2 | a0006 | c0005 | t0003 | g0135 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0159 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01167 | hp2 | a0005 | c0006 | t0003 | g0127 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0165 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01175 | hp1 | a0002 | c0002 | t0007 | g0294 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01175 | hp2 | a0005 | c0006 | t0003 | g0113 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01192 | hp1 | a0003 | c0003 | t0003 | g0100 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0022 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01243 | hp2 | a0007 | c0007 | t0004 | g0149 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01255 | hp1 | a0004 | c0004 | t0002 | g0060 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0179 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0286 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0142 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01346 | hp1 | a0003 | c0003 | t0003 | g0096 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01346 | hp2 | a0002 | c0020 | t0002 | g0143 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01358 | hp1 | a0003 | c0003 | t0003 | g0017 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0198 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01361 | hp1 | a0003 | c0003 | t0003 | g0102 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0160 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01496 | hp1 | a0003 | c0003 | t0003 | g0306 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0181 | EUR | IBS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01515 | hp2 | a0003 | c0003 | t0003 | g0014 | EUR | IBS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01516 | hp1 | a0003 | c0003 | t0003 | g0108 | EUR | IBS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01516 | hp2 | a0008 | c0010 | t0001 | g0010 | EUR | IBS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01884 | hp1 | a0004 | c0004 | t0001 | g0111 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01884 | hp2 | a0007 | c0007 | t0004 | g0039 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01891 | hp1 | a0007 | c0007 | t0003 | g0064 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01928 | hp2 | a0003 | c0003 | t0003 | g0105 | AMR | PEL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0029 | AMR | PEL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01952 | hp2 | a0003 | c0003 | t0003 | g0118 | AMR | PEL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02055 | hp2 | a0003 | c0003 | t0003 | g0042 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02056 | hp2 | a0006 | c0005 | t0003 | g0046 | EAS | KHV | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02129 | hp2 | a0005 | c0008 | t0003 | g0018 | EAS | KHV | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | KHV | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0157 | EAS | KHV | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02145 | hp1 | a0003 | c0003 | t0003 | g0094 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02145 | hp2 | a0011 | c0012 | t0002 | g0139 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02155 | hp1 | a0005 | c0008 | t0003 | g0120 | EAS | CDX | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0304 | EAS | CDX | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02257 | hp2 | a0006 | c0005 | t0003 | g0133 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02258 | hp1 | a0003 | c0003 | t0003 | g0075 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02273 | hp2 | a0003 | c0003 | t0003 | g0308 | AMR | PEL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02280 | hp1 | a0009 | c0009 | t0001 | g0055 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02280 | hp2 | a0004 | c0004 | t0002 | g0012 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02523 | hp1 | a0003 | c0003 | t0003 | g0107 | EAS | KHV | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | KHV | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02602 | hp1 | a0003 | c0003 | t0003 | g0119 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02615 | hp2 | a0006 | c0005 | t0002 | g0052 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02622 | hp1 | a0004 | c0004 | t0002 | g0061 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02622 | hp2 | a0004 | c0004 | t0003 | g0034 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02630 | hp1 | a0003 | c0003 | t0003 | g0115 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0138 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0184 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02698 | hp1 | a0003 | c0003 | t0003 | g0130 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02698 | hp2 | a0008 | c0010 | t0001 | g0001 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02723 | hp1 | a0007 | c0007 | t0004 | g0148 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0032 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02738 | hp1 | a0003 | c0003 | t0003 | g0112 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0070 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02818 | hp2 | a0003 | c0003 | t0003 | g0116 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02886 | hp2 | a0006 | c0005 | t0003 | g0134 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02896 | hp1 | a0004 | c0004 | t0002 | g0012 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02896 | hp2 | a0009 | c0009 | t0001 | g0053 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02897 | hp1 | a0003 | c0003 | t0003 | g0074 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02897 | hp2 | a0004 | c0004 | t0002 | g0063 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0144 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02965 | hp1 | a0004 | c0004 | t0003 | g0030 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0137 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02970 | hp1 | a0004 | c0004 | t0002 | g0062 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02976 | hp1 | a0007 | c0007 | t0004 | g0040 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02976 | hp2 | a0003 | c0003 | t0003 | g0095 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03041 | hp2 | a0005 | c0006 | t0003 | g0123 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03098 | hp1 | a0003 | c0003 | t0003 | g0125 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03098 | hp2 | a0004 | c0004 | t0002 | g0003 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03130 | hp1 | a0009 | c0009 | t0001 | g0056 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03130 | hp2 | a0003 | c0003 | t0003 | g0019 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03139 | hp1 | a0007 | c0007 | t0004 | g0038 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03139 | hp2 | a0009 | c0009 | t0001 | g0054 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03195 | hp1 | a0006 | c0005 | t0003 | g0065 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03209 | hp1 | a0005 | c0006 | t0003 | g0076 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03225 | hp1 | a0004 | c0004 | t0003 | g0132 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03225 | hp2 | a0007 | c0007 | t0004 | g0037 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03239 | hp2 | a0005 | c0006 | t0003 | g0018 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03453 | hp1 | a0006 | c0005 | t0003 | g0049 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0140 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03486 | hp1 | a0004 | c0004 | t0002 | g0003 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0033 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0190 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03491 | hp2 | a0001 | c0013 | t0001 | g0001 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03492 | hp1 | a0001 | c0013 | t0001 | g0001 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03492 | hp2 | a0010 | c0011 | t0003 | g0006 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03516 | hp1 | a0011 | c0012 | t0002 | g0145 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03516 | hp2 | a0004 | c0004 | t0002 | g0004 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03540 | hp1 | a0004 | c0004 | t0003 | g0035 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03579 | hp1 | a0004 | c0004 | t0002 | g0059 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03579 | hp2 | a0005 | c0006 | t0003 | g0114 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03654 | hp1 | a0003 | c0003 | t0003 | g0101 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0205 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03669 | hp1 | a0003 | c0003 | t0003 | g0093 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0295 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03688 | hp1 | a0003 | c0003 | t0003 | g0079 | SAS | STU | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0187 | SAS | STU | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0154 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0163 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03710 | hp2 | a0003 | c0003 | t0003 | g0136 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03831 | hp1 | a0003 | c0003 | t0003 | g0078 | SAS | BEB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03831 | hp2 | a0003 | c0003 | t0003 | g0099 | SAS | BEB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03834 | hp1 | a0006 | c0005 | t0003 | g0048 | SAS | BEB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03927 | hp1 | a0003 | c0003 | t0003 | g0017 | SAS | BEB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03942 | hp1 | a0016 | c0014 | t0001 | g0213 | SAS | BEB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03942 | hp2 | a0003 | c0003 | t0003 | g0007 | SAS | BEB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG04115 | hp1 | a0010 | c0011 | t0003 | g0109 | SAS | STU | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG04115 | hp2 | a0008 | c0010 | t0001 | g0261 | SAS | STU | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG04199 | hp1 | a0003 | c0003 | t0003 | g0091 | SAS | STU | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | STU | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | STU | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0141 | SAS | STU | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG04228 | hp2 | a0010 | c0011 | t0003 | g0006 | SAS | STU | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | YRI | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18522 | hp2 | a0003 | c0003 | t0003 | g0019 | AFR | YRI | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0073 | AFR | YRI | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18906 | hp2 | a0004 | c0004 | t0002 | g0004 | AFR | YRI | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18941 | hp1 | a0003 | c0003 | t0003 | g0092 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18944 | hp1 | a0003 | c0003 | t0003 | g0044 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18945 | hp1 | a0003 | c0003 | t0003 | g0016 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18946 | hp2 | a0006 | c0005 | t0003 | g0050 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0292 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0183 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18951 | hp1 | a0006 | c0005 | t0003 | g0047 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18954 | hp2 | a0005 | c0008 | t0003 | g0121 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18956 | hp2 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18960 | hp2 | a0003 | c0003 | t0003 | g0122 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18961 | hp1 | a0005 | c0008 | t0003 | g0124 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18962 | hp1 | a0003 | c0003 | t0003 | g0089 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0299 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0296 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0297 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18967 | hp2 | a0004 | c0004 | t0002 | g0088 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0290 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18972 | hp1 | a0003 | c0003 | t0003 | g0129 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18973 | hp1 | a0003 | c0003 | t0003 | g0007 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0303 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18980 | hp1 | a0003 | c0003 | t0003 | g0013 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0279 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18989 | hp2 | a0003 | c0003 | t0003 | g0097 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18990 | hp1 | a0005 | c0008 | t0003 | g0110 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18998 | hp1 | a0004 | c0004 | t0002 | g0090 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18999 | hp1 | a0005 | c0008 | t0003 | g0126 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0188 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0282 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0281 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19007 | hp1 | a0003 | c0003 | t0003 | g0080 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0276 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19010 | hp1 | a0003 | c0003 | t0003 | g0117 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19030 | hp1 | a0007 | c0007 | t0010 | g0147 | AFR | LWK | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19043 | hp1 | a0007 | c0017 | t0001 | g0051 | AFR | LWK | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | LWK | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19054 | hp2 | a0003 | c0003 | t0003 | g0085 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19059 | hp2 | a0002 | c0002 | t0002 | g0277 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19060 | hp1 | a0003 | c0003 | t0003 | g0087 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19062 | hp2 | a0003 | c0003 | t0003 | g0086 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0206 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19064 | hp2 | a0003 | c0003 | t0003 | g0128 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0285 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19072 | hp2 | a0001 | c0001 | t0008 | g0223 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19079 | hp1 | a0003 | c0003 | t0003 | g0083 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0300 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0302 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19086 | hp1 | a0003 | c0003 | t0003 | g0006 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | YRI | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA19240 | hp2 | a0005 | c0006 | t0003 | g0015 | AFR | YRI | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA20129 | hp2 | a0004 | c0004 | t0002 | g0003 | AFR | ASW | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA20752 | hp1 | a0008 | c0010 | t0001 | g0001 | EUR | TSI | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA20752 | hp2 | a0003 | c0003 | t0003 | g0104 | EUR | TSI | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA20905 | hp1 | a0003 | c0003 | t0011 | g0084 | SAS | GIH | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0284 | SAS | GIH | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0178 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG01123 | hp2 | a0003 | c0003 | t0003 | g0041 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02109 | hp1 | a0006 | c0005 | t0003 | g0045 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02109 | hp2 | a0004 | c0021 | t0002 | g0069 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02486 | hp1 | a0015 | c0018 | t0001 | g0057 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0072 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0071 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG02559 | hp2 | a0004 | c0004 | t0002 | g0004 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| HG03471 | hp2 | a0007 | c0007 | t0004 | g0036 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA18955 | hp2 | a0003 | c0003 | t0003 | g0007 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0146 | AFR | USA | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA20300 | hp2 | a0004 | c0004 | t0001 | g0307 | AFR | USA | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | LWK | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| NA21309 | hp2 | a0017 | c0015 | t0009 | g0031 | AFR | LWK | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0003 | g0150 | REF | REF | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0180 | REF | REF | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:46793456 | G | A | 1 | a0016 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.58G>A | p.Ala20Thr | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 1/14 | 68/2893 | 58/2241 | 20/746 | chr6 | 46793456 | |||
| chr6:46799146 | C | A | 1 | a0017 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.227C>A | p.Thr76Lys | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/14 | 237/2893 | 227/2241 | 76/746 | chr6 | 46799146 | |||
| chr6:46829452 | A | G | 1 | a0014 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.1025A>G | p.Gln342Arg | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/14 | 1035/2893 | 1025/2241 | 342/746 | chr6 | 46829452 | |||
| chr6:46833086 | A | G | 1 | a0015 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1157A>G | p.His386Arg | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/14 | 1167/2893 | 1157/2241 | 386/746 | chr6 | 46833086 | |||
| chr6:46833116 | A | G | 1 | a0011 | 2 | HG02145.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.1187A>G | p.Lys396Arg | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/14 | 1197/2893 | 1187/2241 | 396/746 | chr6 | 46833116 | |||
| chr6:46833334 | G | T | 9 | a0003 a0004 a0005 others(6): Show |
130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): Show |
missense_variant | MODERATE | c.1405G>T | p.Val469Leu | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/14 | 1415/2893 | 1405/2241 | 469/746 | chr6 | 46833334 | |||
| chr6:46833355 | A | G | 1 | a0006 | 11 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(8): Show |
missense_variant | MODERATE | c.1426A>G | p.Arg476Gly | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/14 | 1436/2893 | 1426/2241 | 476/746 | chr6 | 46833355 | |||
| chr6:46833377 | G | C | 1 | a0011 | 2 | HG02145.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.1448G>C | p.Arg483Thr | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/14 | 1458/2893 | 1448/2241 | 483/746 | chr6 | 46833377 | |||
| chr6:46833421 | G | A | 1 | a0013 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.1492G>A | p.Glu498Lys | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/14 | 1502/2893 | 1492/2241 | 498/746 | chr6 | 46833421 | |||
| chr6:46833477 | T | A | 1 | a0012 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.1548T>A | p.Asp516Glu | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/14 | 1558/2893 | 1548/2241 | 516/746 | chr6 | 46833477 | |||
| chr6:46833482 | G | A | 1 | a0005 | 16 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(13): Show |
missense_variant | MODERATE | c.1553G>A | p.Arg518Gln | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/14 | 1563/2893 | 1553/2241 | 518/746 | chr6 | 46833482 | |||
| chr6:46835281 | A | T | 6 | a0001 a0008 a0009 others(3): Show |
128 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
missense_variant | MODERATE | c.1816A>T | p.Thr606Ser | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/14 | 1826/2893 | 1816/2241 | 606/746 | chr6 | 46835281 | |||
| chr6:46835365 | A | G | 7 | a0001 a0007 a0008 others(4): Show |
138 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
missense_variant | MODERATE | c.1900A>G | p.Met634Val | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/14 | 1910/2893 | 1900/2241 | 634/746 | chr6 | 46835365 | |||
| chr6:46835426 | C | T | 1 | a0010 | 3 | HG03492.hp2 HG04115.hp1 HG04228.hp2 |
missense_variant | MODERATE | c.1961C>T | p.Ser654Leu | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/14 | 1971/2893 | 1961/2241 | 654/746 | chr6 | 46835426 | |||
| chr6:46839029 | G | A | 1 | a0008 | 4 | HG01516.hp2 HG02698.hp2 HG04115.hp2 others(1): Show |
missense_variant | MODERATE | c.2134G>A | p.Val712Met | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 2144/2893 | 2134/2241 | 712/746 | chr6 | 46839029 | |||
| chr6:46839072 | C | T | 4 | a0003 a0005 a0010 others(1): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(78): Show |
missense_variant | MODERATE | c.2177C>T | p.Thr726Met | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 2187/2893 | 2177/2241 | 726/746 | chr6 | 46839072 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:46809469 | C | T | 1 | a0001c0013 | 2 | HG03491.hp2 HG03492.hp1 |
synonymous_variant | LOW | c.312C>T | p.Leu104Leu | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/14 | 322/2893 | 312/2241 | 104/746 | chr6 | 46809469 | |||
| chr6:46825405 | C | T | 1 | a0004c0023 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.690C>T | p.Ala230Ala | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 8/14 | 700/2893 | 690/2241 | 230/746 | chr6 | 46825405 | |||
| chr6:46825438 | G | A | 12 | a0003c0003 a0004c0004 a0004c0023 others(9): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
synonymous_variant | LOW | c.723G>A | p.Gln241Gln | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 8/14 | 733/2893 | 723/2241 | 241/746 | chr6 | 46825438 | |||
| chr6:46833183 | A | G | 1 | a0005c0008 | 6 | HG02129.hp2 HG02155.hp1 NA18954.hp2 others(3): Show |
synonymous_variant | LOW | c.1254A>G | p.Gly418Gly | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/14 | 1264/2893 | 1254/2241 | 418/746 | chr6 | 46833183 | |||
| chr6:46834633 | G | A | 19 | a0001c0001 a0001c0013 a0003c0003 others(16): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
synonymous_variant | LOW | c.1665G>A | p.Thr555Thr | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 12/14 | 1675/2893 | 1665/2241 | 555/746 | chr6 | 46834633 | |||
| chr6:46834726 | C | T | 1 | a0002c0020 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.1758C>T | p.Asp586Asp | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 12/14 | 1768/2893 | 1758/2241 | 586/746 | chr6 | 46834726 | |||
| chr6:46839079 | C | T | 1 | a0007c0017 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.2184C>T | p.Gly728Gly | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 2194/2893 | 2184/2241 | 728/746 | chr6 | 46839079 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:46839172 | C | A | 1 | a0001c0001t0005 | 4 | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*36C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 36 | chr6 | 46839172 | ||||||
| chr6:46839202 | G | T | 9 | a0003c0003t0003 a0003c0003t0011 a0004c0004t0003 others(6): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*66G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 66 | chr6 | 46839202 | ||||||
| chr6:46839211 | G | GTTTGGGG others(5): Show |
22 | a0001c0001t0001 a0001c0001t0008 a0001c0013t0001 others(19): Show |
227 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*78_*79insGGGGCAGC others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 79 | INFO_REALIGN_3_PRIME | chr6 | 46839211 | |||||
| chr6:46839239 | C | A | 1 | a0002c0002t0007 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*103C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 103 | chr6 | 46839239 | ||||||
| chr6:46839265 | C | T | 1 | a0017c0015t0009 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*129C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 129 | chr6 | 46839265 | ||||||
| chr6:46839274 | C | A | 1 | a0001c0001t0008 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*138C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 138 | chr6 | 46839274 | ||||||
| chr6:46839303 | C | A | 22 | a0001c0001t0001 a0001c0001t0008 a0001c0013t0001 others(19): Show |
227 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*167C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 167 | chr6 | 46839303 | ||||||
| chr6:46839349 | C | A | 1 | a0003c0003t0011 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*213C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 213 | chr6 | 46839349 | ||||||
| chr6:46839387 | T | C | 2 | a0001c0001t0005 a0001c0001t0006 |
6 | HG02486.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*251T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 251 | chr6 | 46839387 | ||||||
| chr6:46839502 | A | G | 2 | a0007c0007t0004 a0007c0007t0010 |
8 | HG01243.hp2 HG01884.hp2 HG02723.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*366A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 366 | chr6 | 46839502 | ||||||
| chr6:46839655 | T | G | 1 | a0007c0007t0010 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*519T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 519 | chr6 | 46839655 | ||||||
| chr6:46839768 | T | C | 2 | a0001c0001t0005 a0001c0001t0006 |
6 | HG02486.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*632T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 632 | chr6 | 46839768 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:46793758 | G | A | 136 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0067 others(133): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.145+42G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793758 | |||||||
| chr6:46793786 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+70T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793786 | |||||||
| chr6:46793795 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+79T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793795 | |||||||
| chr6:46793797 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+81A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793797 | |||||||
| chr6:46793803 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+87T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793803 | |||||||
| chr6:46793814 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+98T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793814 | |||||||
| chr6:46793836 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+120G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793836 | |||||||
| chr6:46793838 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+122G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793838 | |||||||
| chr6:46793843 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+127G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793843 | |||||||
| chr6:46793849 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+133A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793849 | |||||||
| chr6:46793851 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+135T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793851 | |||||||
| chr6:46793867 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+151A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793867 | |||||||
| chr6:46793869 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+153A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793869 | |||||||
| chr6:46793870 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+154A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793870 | |||||||
| chr6:46793871 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+155A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793871 | |||||||
| chr6:46793877 | G | A | 6 | a0001c0001t0006g0032 a0001c0001t0006g0033 a0004c0004t0003g0030 others(3): Show |
6 | HG02622.hp2 HG02723.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+161G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793877 | |||||||
| chr6:46793914 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+198G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793914 | |||||||
| chr6:46793915 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+199C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793915 | |||||||
| chr6:46793924 | C | T | 9 | a0004c0004t0002g0003 a0004c0004t0002g0004 a0004c0004t0002g0012 others(6): Show |
14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.145+208C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793924 | |||||||
| chr6:46793953 | T | G | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+237T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793953 | |||||||
| chr6:46793961 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+245T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793961 | |||||||
| chr6:46793963 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+247T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793963 | |||||||
| chr6:46793964 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+248A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793964 | |||||||
| chr6:46793975 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+259T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793975 | |||||||
| chr6:46793998 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+282A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793998 | |||||||
| chr6:46794001 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+285G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46794001 | |||||||
| chr6:46794013 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+297G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46794013 | |||||||
| chr6:46794030 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+314T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46794030 | |||||||
| chr6:46794032 | A | AAGAAACA others(95): Show |
1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+317_145+318ins others(102): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46794032 | ||||||
| chr6:46794129 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.145+413T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46794129 | |||||||
| chr6:46794142 | T | C | 5 | a0007c0007t0004g0036 a0007c0007t0004g0037 a0007c0007t0004g0038 others(2): Show |
5 | HG01884.hp2 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.145+426T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46794142 | |||||||
| chr6:46794146 | T | C | 3 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 |
3 | HG00280.hp2 HG01123.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.145+430T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46794146 | |||||||
| chr6:46794316 | G | A | 1 | a0002c0002t0002g0154 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.145+600G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46794316 | |||||||
| chr6:46794400 | T | G | 1 | a0001c0001t0001g0155 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.145+684T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46794400 | |||||||
| chr6:46794757 | C | G | 1 | a0001c0001t0001g0151 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.145+1041C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46794757 | |||||||
| chr6:46794830 | TAG | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0309 a0001c0001t0001g0310 |
3 | HG02602.hp2 HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.145+1117_145+1118d others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46794830 | ||||||
| chr6:46795020 | C | A | 1 | a0003c0003t0003g0044 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.145+1304C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46795020 | |||||||
| chr6:46795100 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.145+1384G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46795100 | |||||||
| chr6:46795425 | C | T | 8 | a0007c0007t0004g0036 a0007c0007t0004g0037 a0007c0007t0004g0038 others(5): Show |
8 | HG01243.hp2 HG01884.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.145+1709C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46795425 | |||||||
| chr6:46795509 | T | C | 8 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(5): Show |
8 | HG02056.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.145+1793T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46795509 | |||||||
| chr6:46795695 | C | A | 4 | a0009c0009t0001g0053 a0009c0009t0001g0054 a0009c0009t0001g0055 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.145+1979C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46795695 | |||||||
| chr6:46795783 | A | G | 7 | a0007c0007t0004g0036 a0007c0007t0004g0037 a0007c0007t0004g0038 others(4): Show |
7 | HG01243.hp2 HG01884.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.145+2067A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46795783 | |||||||
| chr6:46795998 | A | T | 6 | a0001c0001t0006g0032 a0001c0001t0006g0033 a0004c0004t0003g0030 others(3): Show |
6 | HG02622.hp2 HG02723.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+2282A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46795998 | |||||||
| chr6:46796005 | G | C | 1 | a0002c0002t0002g0157 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.145+2289G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796005 | |||||||
| chr6:46796124 | C | T | 10 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0140 others(7): Show |
10 | HG01261.hp2 HG01346.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.145+2408C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796124 | |||||||
| chr6:46796174 | A | G | 1 | a0007c0007t0010g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.146-2432A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796174 | |||||||
| chr6:46796195 | C | T | 1 | a0003c0003t0003g0136 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.146-2411C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796195 | |||||||
| chr6:46796199 | G | A | 1 | a0015c0018t0001g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.146-2407G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796199 | |||||||
| chr6:46796213 | A | G | 3 | a0006c0005t0003g0133 a0006c0005t0003g0134 a0006c0005t0003g0135 |
3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.146-2393A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796213 | |||||||
| chr6:46796226 | C | T | 87 | a0001c0001t0001g0131 a0002c0002t0002g0077 a0003c0003t0003g0006 others(84): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.146-2380C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796226 | |||||||
| chr6:46796252 | CAAGT | C | 5 | a0001c0001t0005g0070 a0001c0001t0005g0071 a0001c0001t0005g0072 others(2): Show |
5 | HG02109.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.146-2353_146-2350d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796252 | |||||||
| chr6:46796520 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.146-2086T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796520 | |||||||
| chr6:46796807 | C | G | 3 | a0002c0002t0002g0302 a0002c0002t0002g0303 a0002c0002t0002g0304 |
3 | HG02155.hp2 NA18975.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.146-1799C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796807 | |||||||
| chr6:46796881 | T | G | 6 | a0001c0001t0006g0032 a0001c0001t0006g0033 a0004c0004t0003g0030 others(3): Show |
6 | HG02622.hp2 HG02723.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.146-1725T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796881 | |||||||
| chr6:46796978 | C | T | 7 | a0007c0007t0004g0036 a0007c0007t0004g0037 a0007c0007t0004g0038 others(4): Show |
7 | HG01243.hp2 HG01884.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.146-1628C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796978 | |||||||
| chr6:46797445 | G | A | 77 | a0002c0002t0002g0077 a0003c0003t0003g0006 a0003c0003t0003g0007 others(74): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.146-1161G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797445 | |||||||
| chr6:46797596 | A | C | 1 | a0001c0001t0001g0301 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.146-1010A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797596 | |||||||
| chr6:46797637 | G | A | 1 | a0003c0003t0003g0013 | 2 | HG00544.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.146-969G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797637 | |||||||
| chr6:46797697 | T | C | 9 | a0004c0004t0002g0003 a0004c0004t0002g0004 a0004c0004t0002g0012 others(6): Show |
14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.146-909T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797697 | |||||||
| chr6:46797716 | C | T | 4 | a0001c0001t0005g0070 a0001c0001t0005g0071 a0001c0001t0005g0072 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-890C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797716 | |||||||
| chr6:46797772 | TTTTCTTT others(23): Show |
T | 1 | a0006c0005t0003g0135 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.146-812_146-783del others(30): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797772 | ||||||
| chr6:46797772 | TTTTCTTT others(27): Show |
T | 2 | a0006c0005t0003g0133 a0006c0005t0003g0134 |
2 | HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.146-812_146-779del others(34): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797772 | ||||||
| chr6:46797778 | T | TTC | 4 | a0007c0007t0004g0036 a0007c0007t0004g0037 a0007c0007t0004g0148 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-826_146-825dup others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797778 | ||||||
| chr6:46797778 | TTCTTTCT others(7): Show |
T | 2 | a0003c0003t0003g0074 a0003c0003t0003g0075 |
2 | HG02258.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.146-812_146-799del others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797778 | ||||||
| chr6:46797782 | TTCTTTCT others(3): Show |
T | 1 | a0003c0003t0003g0019 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.146-812_146-803del others(10): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797782 | ||||||
| chr6:46797786 | TTCTTTC | T | 3 | a0003c0003t0003g0019 a0003c0003t0003g0116 a0004c0004t0001g0111 |
3 | HG01884.hp1 HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.146-812_146-807del others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797786 | ||||||
| chr6:46797790 | TTC | T | 8 | a0003c0003t0003g0094 a0003c0003t0003g0095 a0003c0003t0003g0115 others(5): Show |
8 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.146-812_146-811del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797790 | ||||||
| chr6:46797792 | C | CTCTT | 17 | a0002c0002t0002g0022 a0002c0002t0002g0029 a0002c0002t0002g0163 others(14): Show |
18 | HG00738.hp1 HG01081.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.146-770_146-767dup others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | ||||||
| chr6:46797792 | C | CTCTTTCT others(1): Show |
15 | a0002c0002t0001g0293 a0002c0002t0002g0026 a0002c0002t0002g0027 others(12): Show |
15 | HG00673.hp2 HG01099.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.146-774_146-767dup others(8): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | ||||||
| chr6:46797792 | C | CTCTTTCT others(5): Show |
3 | a0002c0002t0001g0193 a0002c0002t0002g0022 a0002c0002t0002g0282 |
3 | HG00438.hp1 HG02132.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.146-778_146-767dup others(12): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | ||||||
| chr6:46797792 | C | CTCTTTCT others(9): Show |
1 | a0002c0002t0001g0194 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.146-782_146-767dup others(16): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | ||||||
| chr6:46797792 | C | CTT | 3 | a0007c0007t0004g0036 a0007c0007t0004g0037 a0007c0007t0004g0148 |
3 | HG02723.hp1 HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.146-813_146-812ins others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | ||||||
| chr6:46797792 | C | T | 6 | a0002c0002t0002g0288 a0006c0005t0003g0045 a0006c0005t0003g0046 others(3): Show |
6 | HG02056.hp2 HG02109.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.146-814C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797792 | |||||||
| chr6:46797792 | CTCTT | C | 23 | a0002c0002t0002g0002 a0002c0002t0002g0026 a0002c0002t0002g0138 others(20): Show |
26 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.146-770_146-767del others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | ||||||
| chr6:46797792 | CTCTTTCT others(1): Show |
C | 21 | a0001c0001t0005g0070 a0002c0002t0002g0137 a0002c0002t0002g0144 others(18): Show |
22 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.146-774_146-767del others(8): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | ||||||
| chr6:46797792 | CTCTTTCT others(5): Show |
C | 51 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0218 others(48): Show |
54 | HG00544.hp1 HG00639.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.146-778_146-767del others(12): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | ||||||
| chr6:46797792 | CTCTTTCT others(9): Show |
C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0215 a0001c0001t0001g0222 others(19): Show |
23 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.146-782_146-767del others(16): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | ||||||
| chr6:46797792 | CTCTTTCT others(13): Show |
C | 106 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(103): Show |
118 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.146-786_146-767del others(20): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | ||||||
| chr6:46797792 | CTCTTTCT others(17): Show |
C | 2 | a0001c0001t0001g0264 a0003c0003t0003g0102 |
2 | HG01361.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.146-790_146-767del others(24): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | ||||||
| chr6:46797798 | CTT | C | 3 | a0003c0003t0003g0094 a0003c0003t0003g0095 a0003c0003t0003g0115 |
3 | HG02145.hp1 HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.146-806_146-805del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797798 | ||||||
| chr6:46797802 | CTT | C | 3 | a0003c0003t0003g0019 a0003c0003t0003g0116 a0004c0004t0001g0111 |
3 | HG01884.hp1 HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.146-802_146-801del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797802 | ||||||
| chr6:46797808 | T | TTC | 3 | a0006c0005t0003g0046 a0006c0005t0003g0047 a0006c0005t0003g0048 |
3 | HG02056.hp2 HG03834.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.146-796_146-795dup others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797808 | ||||||
| chr6:46797810 | CTT | C | 3 | a0003c0003t0003g0074 a0003c0003t0003g0075 a0006c0005t0003g0045 |
3 | HG02109.hp1 HG02258.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.146-794_146-793del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797810 | ||||||
| chr6:46797836 | T | C | 1 | a0005c0006t0003g0076 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.146-770T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797836 | |||||||
| chr6:46797840 | C | T | 2 | a0002c0002t0002g0299 a0002c0002t0002g0300 |
2 | NA18962.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.146-766C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797840 | |||||||
| chr6:46797844 | C | T | 1 | a0002c0002t0002g0300 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.146-762C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797844 | |||||||
| chr6:46797848 | T | C | 2 | a0002c0002t0002g0299 a0007c0007t0003g0064 |
2 | HG01891.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.146-758T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797848 | |||||||
| chr6:46797856 | T | C | 1 | a0002c0002t0002g0300 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.146-750T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797856 | |||||||
| chr6:46797860 | T | C | 1 | a0002c0002t0002g0300 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.146-746T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797860 | |||||||
| chr6:46797861 | A | T | 1 | a0002c0002t0002g0300 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.146-745A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797861 | |||||||
| chr6:46797868 | A | T | 1 | a0002c0002t0002g0300 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.146-738A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797868 | |||||||
| chr6:46797869 | C | T | 1 | a0002c0002t0002g0300 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.146-737C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797869 | |||||||
| chr6:46797871 | T | TTTCC | 8 | a0002c0002t0002g0159 a0002c0002t0002g0160 a0002c0002t0002g0161 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.146-679_146-676dup others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797871 | ||||||
| chr6:46797878 | C | T | 1 | a0002c0002t0002g0300 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.146-728C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797878 | |||||||
| chr6:46797881 | T | A | 1 | a0002c0002t0002g0300 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.146-725T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797881 | |||||||
| chr6:46797899 | CTTCCTTC others(25): Show |
C | 2 | a0001c0001t0001g0298 a0003c0003t0003g0130 |
2 | HG02698.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.146-676_146-645del others(32): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797899 | ||||||
| chr6:46797903 | CTTCCTTC others(21): Show |
C | 24 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(21): Show |
26 | HG00408.hp1 HG00673.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.146-675_146-648del others(28): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797903 | ||||||
| chr6:46797907 | CTTCCTTC others(17): Show |
C | 44 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0025 others(41): Show |
48 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.146-675_146-652del others(24): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797907 | ||||||
| chr6:46797911 | C | A | 4 | a0001c0001t0005g0070 a0001c0001t0005g0071 a0001c0001t0005g0072 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-695C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797911 | |||||||
| chr6:46797911 | CTTCCTTC others(13): Show |
C | 62 | a0001c0001t0001g0068 a0001c0001t0001g0156 a0001c0001t0001g0158 others(59): Show |
66 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.146-675_146-656del others(20): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797911 | ||||||
| chr6:46797915 | CTTCCTTC others(9): Show |
C | 25 | a0001c0001t0001g0151 a0001c0001t0001g0211 a0001c0001t0001g0219 others(22): Show |
25 | HG00323.hp1 HG00544.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.146-675_146-660del others(16): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797915 | ||||||
| chr6:46797919 | CTTCCTTC others(5): Show |
C | 22 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0024 others(19): Show |
25 | HG01070.hp1 HG01106.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.146-675_146-664del others(12): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797919 | ||||||
| chr6:46797923 | CTTCCTTC others(1): Show |
C | 15 | a0002c0002t0001g0289 a0002c0002t0001g0293 a0002c0002t0002g0002 others(12): Show |
17 | HG00609.hp1 HG00642.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.146-675_146-668del others(8): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797923 | ||||||
| chr6:46797927 | C | T | 1 | a0007c0007t0003g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.146-679C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797927 | |||||||
| chr6:46797927 | CTTCT | C | 14 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0209 others(11): Show |
14 | HG00280.hp1 HG00438.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.146-675_146-672del others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797927 | ||||||
| chr6:46797931 | T | C | 51 | a0001c0001t0005g0070 a0001c0001t0005g0071 a0001c0001t0005g0072 others(48): Show |
57 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.146-675T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797931 | |||||||
| chr6:46797931 | TTTCC | T | 27 | a0002c0002t0001g0193 a0002c0002t0001g0194 a0002c0002t0002g0022 others(24): Show |
29 | HG00423.hp2 HG00438.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.146-648_146-645del others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797931 | ||||||
| chr6:46797931 | TTTCCTTC others(1): Show |
T | 20 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0152 others(17): Show |
22 | HG00544.hp2 HG00741.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.146-652_146-645del others(8): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797931 | ||||||
| chr6:46797931 | TTTCCTTC others(5): Show |
T | 7 | a0002c0002t0002g0077 a0003c0003t0003g0078 a0003c0003t0003g0079 others(4): Show |
7 | HG02523.hp2 HG03688.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.146-656_146-645del others(12): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797931 | ||||||
| chr6:46797935 | C | CTTCCTTC others(5): Show |
1 | a0002c0002t0002g0157 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.146-660_146-659ins others(12): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797935 | ||||||
| chr6:46797935 | C | CTTCT | 7 | a0002c0002t0002g0140 a0002c0002t0002g0203 a0002c0002t0002g0204 others(4): Show |
7 | HG00609.hp2 HG02145.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-668_146-667ins others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797935 | ||||||
| chr6:46797935 | C | T | 43 | a0001c0001t0005g0070 a0001c0001t0005g0071 a0001c0001t0005g0072 others(40): Show |
50 | HG00140.hp2 HG00408.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.146-671C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797935 | |||||||
| chr6:46797939 | C | CTTCT | 7 | a0004c0004t0002g0003 a0004c0004t0002g0004 a0004c0004t0002g0059 others(4): Show |
11 | HG01255.hp1 HG02559.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.146-664_146-663ins others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797939 | ||||||
| chr6:46797939 | C | T | 114 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
128 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.146-667C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797939 | |||||||
| chr6:46797943 | C | T | 69 | a0001c0001t0001g0298 a0003c0003t0003g0006 a0003c0003t0003g0007 others(66): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.146-663C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797943 | |||||||
| chr6:46798000 | C | T | 1 | a0004c0021t0002g0069 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.146-606C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46798000 | |||||||
| chr6:46798103 | G | T | 3 | a0006c0005t0003g0133 a0006c0005t0003g0134 a0006c0005t0003g0135 |
3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.146-503G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46798103 | |||||||
| chr6:46798292 | C | T | 7 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(4): Show |
7 | HG02056.hp2 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-314C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46798292 | |||||||
| chr6:46798333 | T | G | 1 | a0006c0005t0003g0049 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.146-273T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46798333 | |||||||
| chr6:46798356 | T | C | 2 | a0003c0003t0003g0086 a0003c0003t0003g0087 |
2 | NA19060.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.146-250T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46798356 | |||||||
| chr6:46798378 | G | A | 5 | a0001c0001t0005g0070 a0001c0001t0005g0071 a0001c0001t0005g0072 others(2): Show |
5 | HG02109.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.146-228G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46798378 | |||||||
| chr6:46798730 | G | C | 109 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(106): Show |
124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.186+84G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 4/13 | chr6 | 46798730 | |||||||
| chr6:46798731 | G | C | 109 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(106): Show |
124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.186+85G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 4/13 | chr6 | 46798731 | |||||||
| chr6:46799437 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.262+256C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46799437 | |||||||
| chr6:46799908 | A | G | 108 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(105): Show |
123 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.262+727A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46799908 | |||||||
| chr6:46799951 | G | A | 31 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0021 others(28): Show |
36 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.262+770G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46799951 | |||||||
| chr6:46800068 | T | C | 226 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.262+887T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46800068 | |||||||
| chr6:46800250 | A | G | 1 | a0001c0001t0001g0273 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.262+1069A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46800250 | |||||||
| chr6:46800284 | C | T | 1 | a0003c0003t0003g0129 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.262+1103C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46800284 | |||||||
| chr6:46800312 | T | C | 226 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.262+1131T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46800312 | |||||||
| chr6:46800746 | C | T | 1 | a0015c0018t0001g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.262+1565C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46800746 | |||||||
| chr6:46800926 | C | T | 1 | a0001c0001t0008g0223 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.262+1745C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46800926 | |||||||
| chr6:46801089 | T | C | 88 | a0001c0001t0001g0208 a0002c0002t0002g0077 a0003c0003t0003g0006 others(85): Show |
97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.262+1908T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46801089 | |||||||
| chr6:46801173 | G | T | 1 | a0009c0009t0001g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.262+1992G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46801173 | |||||||
| chr6:46801192 | G | A | 12 | a0002c0002t0002g0077 a0003c0003t0003g0078 a0003c0003t0003g0079 others(9): Show |
12 | HG02523.hp2 HG03669.hp1 HG03688.hp1 others(9): Show |
intron_variant | MODIFIER | c.262+2011G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46801192 | |||||||
| chr6:46801273 | G | A | 1 | a0015c0018t0001g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.262+2092G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46801273 | |||||||
| chr6:46801393 | A | G | 26 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0021 others(23): Show |
31 | HG00438.hp2 HG00544.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.262+2212A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46801393 | |||||||
| chr6:46801582 | T | A | 2 | a0005c0006t0003g0081 a0005c0006t0003g0082 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.262+2401T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46801582 | |||||||
| chr6:46801815 | T | C | 97 | a0001c0001t0001g0208 a0002c0002t0002g0077 a0003c0003t0003g0006 others(94): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.262+2634T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46801815 | |||||||
| chr6:46801880 | C | T | 1 | a0004c0004t0003g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.262+2699C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46801880 | |||||||
| chr6:46801891 | C | T | 219 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(216): Show |
248 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.262+2710C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46801891 | |||||||
| chr6:46802126 | G | A | 1 | a0004c0021t0002g0069 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.262+2945G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802126 | |||||||
| chr6:46802222 | C | A | 1 | a0006c0005t0003g0050 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.262+3041C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802222 | |||||||
| chr6:46802287 | C | A | 1 | a0001c0001t0001g0224 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.262+3106C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802287 | |||||||
| chr6:46802361 | T | G | 3 | a0001c0001t0001g0152 a0001c0001t0001g0309 a0001c0001t0001g0310 |
3 | HG02602.hp2 HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.262+3180T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802361 | |||||||
| chr6:46802461 | A | G | 1 | a0003c0003t0003g0128 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.262+3280A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802461 | |||||||
| chr6:46802564 | G | T | 1 | a0006c0005t0003g0048 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.262+3383G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802564 | |||||||
| chr6:46802643 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.262+3462T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802643 | |||||||
| chr6:46802692 | C | CTGTA | 3 | a0005c0006t0003g0081 a0005c0006t0003g0082 a0005c0006t0003g0127 |
3 | HG01069.hp1 HG01071.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.262+3512_262+3515d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46802692 | ||||||
| chr6:46802711 | G | A | 3 | a0004c0004t0003g0030 a0004c0004t0003g0034 a0004c0004t0003g0035 |
3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.262+3530G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802711 | |||||||
| chr6:46802757 | G | A | 10 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(7): Show |
10 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.262+3576G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802757 | |||||||
| chr6:46802862 | G | A | 1 | a0002c0002t0002g0275 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.262+3681G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802862 | |||||||
| chr6:46802874 | T | A | 1 | a0017c0015t0009g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.262+3693T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802874 | |||||||
| chr6:46803159 | C | G | 3 | a0006c0005t0003g0133 a0006c0005t0003g0134 a0006c0005t0003g0135 |
3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.262+3978C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46803159 | |||||||
| chr6:46803162 | C | T | 5 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0140 others(2): Show |
5 | HG01074.hp2 HG02647.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.262+3981C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46803162 | |||||||
| chr6:46803183 | T | C | 1 | a0007c0007t0010g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.262+4002T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46803183 | |||||||
| chr6:46803414 | G | GTAGAATC others(339): Show |
1 | a0005c0008t0003g0126 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.262+4243_262+4244i others(348): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46803414 | ||||||
| chr6:46803458 | A | G | 1 | a0001c0001t0001g0272 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.262+4277A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46803458 | |||||||
| chr6:46803501 | A | G | 219 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(216): Show |
248 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.262+4320A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46803501 | |||||||
| chr6:46803685 | A | C | 1 | a0015c0018t0001g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.262+4504A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46803685 | |||||||
| chr6:46803738 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.262+4557T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46803738 | |||||||
| chr6:46803738 | TA | T | 111 | a0002c0002t0002g0077 a0003c0003t0003g0006 a0003c0003t0003g0007 others(108): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.262+4560delA | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46803738 | ||||||
| chr6:46803828 | A | G | 2 | a0011c0012t0002g0139 a0011c0012t0002g0145 |
2 | HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.262+4647A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46803828 | |||||||
| chr6:46804044 | T | A | 1 | a0004c0004t0003g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.262+4863T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804044 | |||||||
| chr6:46804292 | C | T | 2 | a0002c0002t0002g0201 a0002c0002t0002g0202 |
2 | NA18955.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.262+5111C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804292 | |||||||
| chr6:46804415 | A | G | 1 | a0004c0021t0002g0069 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.263-5005A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804415 | |||||||
| chr6:46804417 | C | T | 10 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(7): Show |
10 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.263-5003C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804417 | |||||||
| chr6:46804505 | C | CT | 78 | a0001c0001t0001g0208 a0002c0002t0002g0077 a0003c0003t0003g0006 others(75): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.263-4914dupT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46804505 | ||||||
| chr6:46804630 | C | T | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.263-4790C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804630 | |||||||
| chr6:46804632 | T | C | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.263-4788T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804632 | |||||||
| chr6:46804690 | A | C | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.263-4730A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804690 | |||||||
| chr6:46804700 | C | A | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.263-4720C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804700 | |||||||
| chr6:46804701 | A | T | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.263-4719A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804701 | |||||||
| chr6:46804703 | C | G | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.263-4717C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804703 | |||||||
| chr6:46804704 | T | C | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.263-4716T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804704 | |||||||
| chr6:46804705 | A | G | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.263-4715A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804705 | |||||||
| chr6:46804716 | A | T | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.263-4704A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804716 | |||||||
| chr6:46804797 | T | G | 108 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(105): Show |
123 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.263-4623T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804797 | |||||||
| chr6:46804888 | AG | A | 10 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(7): Show |
10 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.263-4530delG | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46804888 | ||||||
| chr6:46804980 | T | G | 7 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(4): Show |
7 | HG02056.hp2 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.263-4440T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804980 | |||||||
| chr6:46805143 | A | T | 1 | a0004c0004t0003g0132 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.263-4277A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805143 | |||||||
| chr6:46805187 | A | T | 3 | a0006c0005t0003g0133 a0006c0005t0003g0134 a0006c0005t0003g0135 |
3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.263-4233A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805187 | |||||||
| chr6:46805283 | G | C | 1 | a0004c0004t0002g0088 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.263-4137G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805283 | |||||||
| chr6:46805284 | T | A | 1 | a0004c0004t0002g0088 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.263-4136T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805284 | |||||||
| chr6:46805285 | T | C | 1 | a0004c0004t0002g0088 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.263-4135T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805285 | |||||||
| chr6:46805287 | C | A | 1 | a0004c0004t0002g0088 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.263-4133C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805287 | |||||||
| chr6:46805288 | G | GATCGCGT others(3): Show |
1 | a0004c0004t0002g0088 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.263-4132_263-4131i others(12): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805288 | |||||||
| chr6:46805326 | T | C | 1 | a0002c0002t0002g0276 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.263-4094T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805326 | |||||||
| chr6:46805480 | C | T | 7 | a0007c0007t0004g0036 a0007c0007t0004g0037 a0007c0007t0004g0038 others(4): Show |
7 | HG01243.hp2 HG01884.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.263-3940C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805480 | |||||||
| chr6:46805666 | T | A | 2 | a0002c0002t0002g0201 a0002c0002t0002g0202 |
2 | NA18955.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.263-3754T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805666 | |||||||
| chr6:46805670 | T | A | 2 | a0003c0003t0003g0094 a0003c0003t0003g0095 |
2 | HG02145.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.263-3750T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805670 | |||||||
| chr6:46806109 | A | T | 219 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(216): Show |
248 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.263-3311A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46806109 | |||||||
| chr6:46806311 | G | T | 1 | a0007c0007t0003g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.263-3109G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46806311 | |||||||
| chr6:46806312 | C | T | 1 | a0003c0003t0003g0125 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.263-3108C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46806312 | |||||||
| chr6:46806639 | T | A | 1 | a0007c0007t0004g0037 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.263-2781T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46806639 | |||||||
| chr6:46806887 | A | G | 1 | a0003c0003t0003g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.263-2533A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46806887 | |||||||
| chr6:46807145 | G | A | 1 | a0003c0003t0003g0096 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.263-2275G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807145 | |||||||
| chr6:46807157 | A | T | 1 | a0004c0004t0002g0088 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.263-2263A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807157 | |||||||
| chr6:46807159 | C | A | 1 | a0015c0018t0001g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.263-2261C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807159 | |||||||
| chr6:46807315 | T | C | 3 | a0001c0001t0006g0032 a0001c0001t0006g0033 a0004c0021t0002g0069 |
3 | HG02109.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.263-2105T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807315 | |||||||
| chr6:46807320 | A | C | 9 | a0004c0004t0002g0003 a0004c0004t0002g0004 a0004c0004t0002g0012 others(6): Show |
14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.263-2100A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807320 | |||||||
| chr6:46807439 | C | T | 1 | a0002c0002t0002g0200 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.263-1981C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807439 | |||||||
| chr6:46807512 | T | G | 3 | a0002c0002t0002g0026 a0002c0002t0002g0141 a0002c0002t0002g0142 |
3 | HG00140.hp2 HG01261.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.263-1908T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807512 | |||||||
| chr6:46807512 | T | TAAAG | 13 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0020 others(10): Show |
15 | HG00733.hp2 HG01074.hp1 HG02004.hp1 others(12): Show |
intron_variant | MODIFIER | c.263-1855_263-1852d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807512 | ||||||
| chr6:46807512 | T | TAAAGAAA others(1): Show |
7 | a0001c0001t0001g0021 a0001c0013t0001g0001 a0002c0002t0002g0182 others(4): Show |
7 | HG00099.hp2 HG01516.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.263-1859_263-1852d others(10): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807512 | ||||||
| chr6:46807512 | T | TAAAGAAA others(5): Show |
13 | a0001c0001t0001g0175 a0001c0001t0001g0266 a0001c0013t0001g0001 others(10): Show |
14 | HG00438.hp1 HG00642.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.263-1863_263-1852d others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807512 | ||||||
| chr6:46807512 | T | TAAAGAAA others(9): Show |
8 | a0001c0001t0001g0173 a0001c0001t0005g0072 a0002c0002t0002g0002 others(5): Show |
8 | HG02155.hp2 HG02486.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.263-1867_263-1852d others(18): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807512 | ||||||
| chr6:46807512 | T | TAAAGAAA others(13): Show |
4 | a0002c0002t0001g0289 a0002c0002t0002g0146 a0002c0002t0002g0202 others(1): Show |
4 | NA18955.hp1 NA18968.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-1871_263-1852d others(22): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807512 | ||||||
| chr6:46807512 | T | TAAAGAAA others(17): Show |
1 | a0002c0002t0002g0187 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.263-1875_263-1852d others(26): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807512 | ||||||
| chr6:46807512 | T | TAAATAAA others(13): Show |
1 | a0001c0001t0006g0032 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263-1905_263-1904i others(22): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807512 | ||||||
| chr6:46807512 | T | TAAATAAA others(9): Show |
1 | a0001c0001t0006g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.263-1905_263-1904i others(18): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807512 | ||||||
| chr6:46807512 | TAAAG | T | 4 | a0002c0002t0002g0023 a0002c0002t0002g0161 a0002c0002t0002g0162 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-1855_263-1852d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807512 | ||||||
| chr6:46807512 | TAAAGAAA others(5): Show |
T | 1 | a0002c0002t0002g0280 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.263-1863_263-1852d others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807512 | ||||||
| chr6:46807516 | G | T | 21 | a0001c0001t0001g0224 a0001c0001t0001g0274 a0001c0001t0008g0223 others(18): Show |
21 | HG01069.hp2 HG01106.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.263-1904G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807516 | |||||||
| chr6:46807520 | G | T | 15 | a0001c0001t0001g0274 a0001c0001t0008g0223 a0003c0003t0003g0086 others(12): Show |
15 | HG01069.hp2 HG01106.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.263-1900G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807520 | |||||||
| chr6:46807524 | G | T | 9 | a0001c0001t0001g0274 a0006c0005t0002g0052 a0006c0005t0003g0046 others(6): Show |
9 | HG01069.hp2 HG01106.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.263-1896G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807524 | |||||||
| chr6:46807525 | A | G | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.263-1895A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807525 | |||||||
| chr6:46807528 | G | T | 5 | a0006c0005t0002g0052 a0006c0005t0003g0049 a0006c0005t0003g0133 others(2): Show |
5 | HG01106.hp2 HG02257.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.263-1892G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807528 | |||||||
| chr6:46807529 | A | G | 1 | a0002c0002t0002g0296 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.263-1891A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807529 | |||||||
| chr6:46807541 | A | G | 1 | a0005c0008t0003g0124 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.263-1879A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807541 | |||||||
| chr6:46807553 | AAAGAAAG others(9): Show |
A | 1 | a0002c0002t0002g0300 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.263-1863_263-1848d others(18): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807553 | ||||||
| chr6:46807553 | AAAGAAAG others(17): Show |
A | 1 | a0002c0002t0002g0275 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.263-1863_263-1840d others(26): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807553 | ||||||
| chr6:46807557 | AAAGAAAG others(5): Show |
A | 5 | a0002c0002t0002g0002 a0002c0002t0002g0189 a0002c0002t0002g0205 others(2): Show |
5 | HG03654.hp2 NA18948.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.263-1859_263-1848d others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807557 | ||||||
| chr6:46807557 | AAAGAAAG others(9): Show |
A | 6 | a0002c0002t0002g0002 a0002c0002t0002g0023 a0002c0002t0002g0026 others(3): Show |
6 | NA18939.hp2 NA18943.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.263-1859_263-1844d others(18): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807557 | ||||||
| chr6:46807557 | AAAGAAAG others(33): Show |
A | 2 | a0003c0003t0003g0075 a0007c0007t0004g0148 |
2 | HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.263-1859_263-1820d others(42): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807557 | ||||||
| chr6:46807557 | AAAGAAAG others(41): Show |
A | 1 | a0007c0007t0004g0149 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.263-1859_263-1812d others(50): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807557 | ||||||
| chr6:46807561 | A | AAAGAAAG others(6): Show |
1 | a0011c0012t0002g0139 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.263-1852_263-1851i others(15): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807561 | ||||||
| chr6:46807561 | AAAGAAAG others(5): Show |
A | 2 | a0001c0001t0001g0009 a0002c0002t0002g0295 |
2 | HG03669.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.263-1855_263-1844d others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807561 | ||||||
| chr6:46807561 | AAAGAAAG others(9): Show |
A | 3 | a0001c0001t0001g0237 a0001c0001t0001g0243 a0002c0002t0002g0200 |
3 | HG00738.hp1 HG03209.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.263-1855_263-1840d others(18): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807561 | ||||||
| chr6:46807561 | AAAGAAAG others(21): Show |
A | 5 | a0001c0001t0001g0210 a0001c0001t0001g0239 a0003c0003t0003g0083 others(2): Show |
5 | HG01070.hp1 HG01081.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.263-1855_263-1828d others(30): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807561 | ||||||
| chr6:46807561 | AAAGAAAG others(25): Show |
A | 1 | a0003c0003t0003g0116 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.263-1855_263-1824d others(34): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807561 | ||||||
| chr6:46807562 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.263-1858A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807562 | |||||||
| chr6:46807563 | A | G | 1 | a0001c0001t0006g0032 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263-1857A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807563 | |||||||
| chr6:46807565 | A | AAAGAAAG others(13): Show |
2 | a0002c0002t0002g0027 a0002c0020t0002g0143 |
2 | HG00673.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.263-1852_263-1851i others(22): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807565 | ||||||
| chr6:46807565 | A | AAAGAAAG others(5): Show |
3 | a0002c0002t0002g0166 a0002c0002t0002g0195 a0013c0019t0002g0291 |
3 | HG00099.hp1 HG00408.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.263-1852_263-1851i others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807565 | ||||||
| chr6:46807565 | A | AAAGAAAG others(9): Show |
1 | a0002c0002t0002g0201 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.263-1852_263-1851i others(18): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807565 | ||||||
| chr6:46807565 | A | AAAGAAAG others(1): Show |
3 | a0002c0002t0002g0204 a0002c0002t0002g0206 a0002c0002t0002g0278 |
3 | HG00609.hp2 NA19064.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.263-1852_263-1851i others(10): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807565 | ||||||
| chr6:46807565 | A | AAAGAAAG others(5): Show |
2 | a0002c0002t0002g0163 a0002c0002t0002g0185 |
2 | HG03710.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.263-1852_263-1851i others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807565 | ||||||
| chr6:46807565 | A | G | 2 | a0002c0002t0002g0028 a0002c0002t0002g0197 |
2 | HG01081.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.263-1855A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807565 | |||||||
| chr6:46807565 | AAAGG | A | 3 | a0002c0002t0002g0179 a0002c0002t0002g0181 a0002c0002t0002g0198 |
3 | HG01255.hp2 HG01358.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.263-1800_263-1797d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807565 | ||||||
| chr6:46807565 | AAAGGAAG others(1): Show |
A | 8 | a0001c0001t0005g0073 a0002c0002t0002g0154 a0002c0002t0002g0160 others(5): Show |
8 | HG01175.hp1 HG01361.hp2 HG03704.hp2 others(5): Show |
intron_variant | MODIFIER | c.263-1804_263-1797d others(10): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807565 | ||||||
| chr6:46807566 | AAGGAAGG others(7): Show |
A | 1 | a0001c0001t0001g0009 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.263-1853_263-1840d others(16): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807566 | |||||||
| chr6:46807567 | A | G | 1 | a0001c0001t0006g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.263-1853A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807567 | |||||||
| chr6:46807567 | AGGAAGGA others(6): Show |
A | 1 | a0003c0003t0003g0006 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.263-1851_263-1839d others(15): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807567 | ||||||
| chr6:46807569 | G | A | 232 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(229): Show |
261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.263-1851G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807569 | |||||||
| chr6:46807572 | GGAAGGAA others(45): Show |
G | 3 | a0006c0005t0003g0133 a0006c0005t0003g0134 a0006c0005t0003g0135 |
3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.263-1836_263-1785d others(54): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807572 | ||||||
| chr6:46807573 | G | A | 183 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(180): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.263-1847G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807573 | |||||||
| chr6:46807576 | GGAAGGAA others(7): Show |
G | 1 | a0003c0003t0003g0108 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.263-1843_263-1830d others(16): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807576 | |||||||
| chr6:46807577 | G | A | 139 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(136): Show |
156 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.263-1843G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807577 | |||||||
| chr6:46807580 | GGAAGGAA others(37): Show |
G | 1 | a0004c0004t0003g0034 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.263-1828_263-1785d others(46): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807580 | ||||||
| chr6:46807581 | G | A | 88 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(85): Show |
98 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.263-1839G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807581 | |||||||
| chr6:46807584 | G | A | 4 | a0003c0003t0003g0006 a0007c0007t0004g0037 a0007c0007t0004g0039 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.263-1836G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807584 | |||||||
| chr6:46807585 | G | A | 36 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0024 others(33): Show |
38 | HG00099.hp2 HG00544.hp1 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.263-1835G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807585 | |||||||
| chr6:46807588 | G | A | 1 | a0003c0003t0003g0006 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.263-1832G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807588 | |||||||
| chr6:46807588 | GGAAGGAA others(29): Show |
G | 5 | a0004c0004t0002g0004 a0006c0005t0002g0052 a0006c0005t0003g0045 others(2): Show |
5 | HG02109.hp1 HG02615.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.263-1820_263-1785d others(38): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807588 | ||||||
| chr6:46807589 | G | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0212 a0001c0001t0001g0263 others(13): Show |
16 | HG00544.hp1 HG01891.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.263-1831G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807589 | |||||||
| chr6:46807592 | G | A | 2 | a0003c0003t0003g0006 a0003c0003t0003g0108 |
2 | HG01516.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.263-1828G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807592 | |||||||
| chr6:46807592 | GGAAGGAA others(25): Show |
G | 9 | a0004c0004t0002g0004 a0004c0004t0002g0012 a0004c0004t0002g0063 others(6): Show |
9 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.263-1816_263-1785d others(34): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807592 | ||||||
| chr6:46807593 | G | A | 3 | a0004c0004t0002g0012 a0004c0004t0003g0030 a0009c0009t0001g0053 |
3 | HG02280.hp2 HG02896.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.263-1827G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807593 | |||||||
| chr6:46807596 | G | A | 3 | a0003c0003t0003g0006 a0007c0007t0004g0036 a0007c0007t0004g0038 |
3 | HG03139.hp1 HG03471.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.263-1824G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807596 | |||||||
| chr6:46807596 | GGAAGGAA others(21): Show |
G | 11 | a0004c0004t0002g0003 a0004c0004t0002g0059 a0004c0004t0002g0060 others(8): Show |
12 | HG00140.hp1 HG01255.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.263-1812_263-1785d others(30): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807596 | ||||||
| chr6:46807597 | G | A | 2 | a0004c0004t0002g0012 a0009c0009t0001g0053 |
2 | HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.263-1823G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807597 | |||||||
| chr6:46807600 | GGAAGGAA others(17): Show |
G | 6 | a0001c0001t0001g0238 a0003c0003t0003g0019 a0004c0004t0002g0003 others(3): Show |
6 | HG00323.hp1 HG01167.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.263-1808_263-1785d others(26): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807600 | ||||||
| chr6:46807601 | G | A | 1 | a0004c0004t0002g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.263-1819G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807601 | |||||||
| chr6:46807604 | GGAAGGAA others(13): Show |
G | 11 | a0001c0001t0001g0209 a0001c0001t0001g0272 a0003c0003t0003g0019 others(8): Show |
11 | HG00280.hp1 HG02965.hp1 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.263-1804_263-1785d others(22): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807604 | ||||||
| chr6:46807605 | G | A | 1 | a0004c0004t0002g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.263-1815G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807605 | |||||||
| chr6:46807608 | GGAAGGAA others(9): Show |
G | 19 | a0001c0001t0001g0256 a0001c0001t0001g0271 a0002c0002t0002g0077 others(16): Show |
19 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.263-1800_263-1785d others(18): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807608 | ||||||
| chr6:46807612 | GGAAGGAA others(5): Show |
G | 34 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(31): Show |
34 | HG00738.hp2 HG01069.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.263-1794_263-1783d others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807612 | ||||||
| chr6:46807616 | GGAAGGAA others(1): Show |
G | 48 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(45): Show |
50 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.263-1796_263-1789d others(10): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807616 | ||||||
| chr6:46807620 | GGAAA | G | 36 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0151 others(33): Show |
36 | HG00280.hp2 HG00323.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.263-1796_263-1793d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807620 | ||||||
| chr6:46807624 | A | G | 59 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(56): Show |
64 | HG00099.hp2 HG00423.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.263-1796A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807624 | |||||||
| chr6:46807702 | G | GA | 4 | a0001c0001t0001g0226 a0002c0002t0002g0141 a0002c0002t0002g0277 others(1): Show |
4 | HG04204.hp2 NA18959.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.263-1712dupA | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807702 | ||||||
| chr6:46807747 | A | AAAGG | 91 | a0001c0001t0001g0025 a0001c0001t0001g0066 a0001c0001t0001g0131 others(88): Show |
97 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.263-1660_263-1657d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807747 | ||||||
| chr6:46807763 | GGAGA | G | 70 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(67): Show |
82 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.263-1656_263-1653d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807763 | |||||||
| chr6:46807763 | GGAGAAAG others(2): Show |
G | 14 | a0001c0001t0001g0210 a0001c0001t0001g0217 a0001c0001t0001g0262 others(11): Show |
16 | HG01070.hp1 HG01346.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.263-1656_263-1648d others(11): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807763 | |||||||
| chr6:46807763 | GGAGAAAG others(6): Show |
G | 2 | a0009c0009t0001g0055 a0012c0016t0003g0098 |
2 | HG00140.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.263-1656_263-1644d others(15): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807763 | |||||||
| chr6:46807764 | G | A | 42 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0068 others(39): Show |
51 | HG00733.hp1 HG00733.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.263-1656G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807764 | |||||||
| chr6:46807767 | A | G | 42 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0068 others(39): Show |
51 | HG00733.hp1 HG00733.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.263-1653A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807767 | |||||||
| chr6:46807768 | A | G | 42 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0068 others(39): Show |
51 | HG00733.hp1 HG00733.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.263-1652A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807768 | |||||||
| chr6:46807770 | G | GGAAA | 25 | a0001c0001t0001g0211 a0001c0001t0001g0229 a0001c0001t0001g0272 others(22): Show |
27 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.263-1584_263-1581d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807770 | ||||||
| chr6:46807770 | G | GGAAAGAA others(1): Show |
5 | a0001c0001t0001g0228 a0002c0002t0002g0176 a0002c0002t0002g0200 others(2): Show |
5 | HG00408.hp1 HG00738.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.263-1588_263-1581d others(10): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807770 | ||||||
| chr6:46807770 | G | GGAAAGAA others(5): Show |
4 | a0001c0001t0001g0227 a0003c0003t0003g0099 a0003c0003t0003g0100 others(1): Show |
4 | HG01192.hp1 HG03831.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-1592_263-1581d others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807770 | ||||||
| chr6:46807770 | GGAAA | G | 24 | a0002c0002t0002g0027 a0002c0002t0002g0137 a0002c0002t0002g0146 others(21): Show |
25 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.263-1584_263-1581d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807770 | ||||||
| chr6:46807770 | GGAAAGAA others(1): Show |
G | 21 | a0001c0001t0006g0033 a0002c0002t0001g0289 a0002c0002t0002g0022 others(18): Show |
24 | HG00408.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.263-1588_263-1581d others(10): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807770 | ||||||
| chr6:46807770 | GGAAAGAA others(5): Show |
G | 17 | a0002c0002t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0293 others(14): Show |
21 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.263-1592_263-1581d others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807770 | ||||||
| chr6:46807770 | GGAAAGAA others(9): Show |
G | 3 | a0002c0002t0002g0165 a0002c0002t0002g0196 a0002c0002t0002g0197 |
3 | HG01081.hp2 HG01168.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.263-1596_263-1581d others(18): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807770 | ||||||
| chr6:46807770 | GGAAAGAA others(13): Show |
G | 2 | a0002c0002t0002g0198 a0002c0002t0002g0295 |
2 | HG01358.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.263-1600_263-1581d others(22): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807770 | ||||||
| chr6:46807770 | GGAAAGAA others(17): Show |
G | 2 | a0002c0002t0002g0199 a0002c0002t0002g0304 |
2 | HG02155.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.263-1604_263-1581d others(26): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807770 | ||||||
| chr6:46807771 | G | A | 43 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0068 others(40): Show |
52 | HG00733.hp1 HG00733.hp2 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.263-1649G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807771 | |||||||
| chr6:46807771 | GA | G | 37 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(34): Show |
47 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.263-1646delA | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807771 | ||||||
| chr6:46807772 | A | G | 33 | a0001c0001t0001g0020 a0001c0001t0001g0067 a0001c0001t0001g0156 others(30): Show |
35 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.263-1648A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807772 | |||||||
| chr6:46807773 | A | G | 37 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(34): Show |
47 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.263-1647A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807773 | |||||||
| chr6:46807774 | A | G | 76 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0021 others(73): Show |
87 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.263-1646A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807774 | |||||||
| chr6:46807775 | G | A | 34 | a0001c0001t0001g0020 a0001c0001t0001g0067 a0001c0001t0001g0156 others(31): Show |
36 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.263-1645G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807775 | |||||||
| chr6:46807776 | A | AAAGAAAG others(9): Show |
1 | a0001c0001t0005g0073 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.263-1629_263-1628i others(18): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807776 | ||||||
| chr6:46807776 | A | G | 14 | a0001c0001t0001g0210 a0001c0001t0001g0217 a0001c0001t0001g0262 others(11): Show |
16 | HG01070.hp1 HG01346.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.263-1644A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807776 | |||||||
| chr6:46807777 | A | G | 14 | a0001c0001t0001g0210 a0001c0001t0001g0217 a0001c0001t0001g0262 others(11): Show |
16 | HG01070.hp1 HG01346.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.263-1643A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807777 | |||||||
| chr6:46807778 | A | G | 33 | a0001c0001t0001g0020 a0001c0001t0001g0067 a0001c0001t0001g0156 others(30): Show |
35 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.263-1642A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807778 | |||||||
| chr6:46807779 | GAAA | G | 37 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(34): Show |
47 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.263-1640_263-1638d others(5): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807779 | |||||||
| chr6:46807780 | A | AAAGAAAG others(5): Show |
1 | a0001c0001t0005g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.263-1629_263-1628i others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807780 | ||||||
| chr6:46807780 | A | G | 2 | a0009c0009t0001g0055 a0012c0016t0003g0098 |
2 | HG00140.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.263-1640A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807780 | |||||||
| chr6:46807781 | A | AAGAAAGA others(4): Show |
1 | a0001c0001t0005g0071 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.263-1629_263-1628i others(13): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807781 | ||||||
| chr6:46807781 | A | G | 2 | a0009c0009t0001g0055 a0012c0016t0003g0098 |
2 | HG00140.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.263-1639A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807781 | |||||||
| chr6:46807783 | GAAA | G | 14 | a0001c0001t0001g0210 a0001c0001t0001g0217 a0001c0001t0001g0262 others(11): Show |
16 | HG01070.hp1 HG01346.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.263-1636_263-1634d others(5): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807783 | |||||||
| chr6:46807788 | A | G | 1 | a0001c0001t0006g0032 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263-1632A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807788 | |||||||
| chr6:46807792 | A | G | 1 | a0004c0021t0002g0069 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.263-1628A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807792 | |||||||
| chr6:46807796 | A | G | 1 | a0001c0001t0006g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.263-1624A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807796 | |||||||
| chr6:46807800 | A | G | 1 | a0001c0001t0005g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.263-1620A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807800 | |||||||
| chr6:46807822 | A | AGAAAGAA others(17): Show |
1 | a0004c0004t0003g0034 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.263-1581_263-1580i others(26): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807822 | ||||||
| chr6:46807822 | A | AGAAAGAA others(13): Show |
2 | a0004c0004t0003g0030 a0004c0004t0003g0035 |
2 | HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.263-1581_263-1580i others(22): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807822 | ||||||
| chr6:46807829 | AAGAAAGA others(3): Show |
A | 1 | a0002c0002t0002g0292 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.263-1590_263-1581d others(12): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807829 | |||||||
| chr6:46807836 | A | G | 5 | a0003c0003t0003g0094 a0003c0003t0003g0095 a0005c0008t0003g0120 others(2): Show |
5 | HG02145.hp1 HG02155.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.263-1584A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807836 | |||||||
| chr6:46807840 | G | A | 57 | a0002c0002t0002g0077 a0003c0003t0003g0006 a0003c0003t0003g0007 others(54): Show |
64 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.263-1580G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807840 | |||||||
| chr6:46807840 | G | GAAGA | 18 | a0003c0003t0003g0019 a0003c0003t0003g0074 a0003c0003t0003g0075 others(15): Show |
20 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.263-1576_263-1573d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807840 | ||||||
| chr6:46808143 | C | CT | 9 | a0004c0004t0002g0003 a0004c0004t0002g0004 a0004c0004t0002g0012 others(6): Show |
14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.263-1268dupT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46808143 | ||||||
| chr6:46808293 | C | T | 1 | a0006c0005t0003g0047 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.263-1127C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46808293 | |||||||
| chr6:46808473 | C | A | 1 | a0006c0005t0003g0049 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.263-947C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46808473 | |||||||
| chr6:46808600 | G | T | 107 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(104): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.263-820G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46808600 | |||||||
| chr6:46808602 | G | A | 2 | a0007c0007t0003g0064 a0015c0018t0001g0057 |
2 | HG01891.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.263-818G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46808602 | |||||||
| chr6:46808685 | G | A | 1 | a0015c0018t0001g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.263-735G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46808685 | |||||||
| chr6:46809136 | ATTATT | A | 13 | a0004c0004t0003g0030 a0004c0004t0003g0034 a0004c0004t0003g0035 others(10): Show |
13 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.263-277_263-273del others(5): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46809136 | ||||||
| chr6:46809261 | T | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0268 |
2 | HG02135.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.263-159T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46809261 | |||||||
| chr6:46809266 | A | G | 1 | a0015c0018t0001g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.263-154A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46809266 | |||||||
| chr6:46809407 | C | T | 2 | a0003c0003t0003g0075 a0003c0003t0003g0116 |
2 | HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.263-13C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46809407 | |||||||
| chr6:46809640 | T | C | 301 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(298): Show |
339 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.380+103T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809640 | |||||||
| chr6:46809653 | CTT | C | 3 | a0003c0003t0003g0102 a0003c0003t0003g0106 a0003c0003t0003g0119 |
3 | HG00099.hp2 HG01361.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.380+117_380+118del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809653 | |||||||
| chr6:46809690 | G | GT | 8 | a0002c0002t0002g0199 a0002c0002t0002g0206 a0002c0002t0002g0207 others(5): Show |
8 | HG01261.hp1 HG04115.hp2 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.380+159dupT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr6 | 46809690 | ||||||
| chr6:46809772 | C | G | 1 | a0015c0018t0001g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.380+235C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809772 | |||||||
| chr6:46809801 | T | G | 1 | a0001c0001t0001g0228 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.380+264T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809801 | |||||||
| chr6:46809812 | G | A | 3 | a0004c0004t0003g0030 a0004c0004t0003g0034 a0004c0004t0003g0035 |
3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.380+275G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809812 | |||||||
| chr6:46809813 | T | A | 1 | a0002c0002t0002g0277 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.380+276T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809813 | |||||||
| chr6:46809814 | A | G | 1 | a0002c0002t0002g0277 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.380+277A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809814 | |||||||
| chr6:46809828 | T | A | 1 | a0004c0004t0003g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.380+291T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809828 | |||||||
| chr6:46809831 | A | T | 1 | a0004c0004t0003g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.380+294A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809831 | |||||||
| chr6:46809832 | C | T | 1 | a0004c0004t0003g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.380+295C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809832 | |||||||
| chr6:46809832 | CAT | C | 9 | a0004c0004t0002g0003 a0004c0004t0002g0004 a0004c0004t0002g0012 others(6): Show |
14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.380+300_380+301del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr6 | 46809832 | ||||||
| chr6:46809834 | T | C | 1 | a0004c0004t0003g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.380+297T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809834 | |||||||
| chr6:46809836 | TA | T | 101 | a0002c0002t0002g0077 a0003c0003t0003g0006 a0003c0003t0003g0007 others(98): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.380+300delA | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809836 | |||||||
| chr6:46809867 | A | G | 1 | a0013c0019t0002g0291 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.380+330A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809867 | |||||||
| chr6:46809966 | G | C | 219 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(216): Show |
248 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.380+429G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809966 | |||||||
| chr6:46810002 | A | T | 1 | a0002c0002t0002g0277 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.380+465A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810002 | |||||||
| chr6:46810134 | T | A | 3 | a0001c0001t0006g0032 a0001c0001t0006g0033 a0004c0021t0002g0069 |
3 | HG02109.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.380+597T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810134 | |||||||
| chr6:46810141 | T | G | 3 | a0004c0004t0003g0030 a0004c0004t0003g0034 a0004c0004t0003g0035 |
3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.380+604T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810141 | |||||||
| chr6:46810152 | G | T | 1 | a0004c0004t0002g0088 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.380+615G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810152 | |||||||
| chr6:46810219 | A | T | 1 | a0002c0002t0002g0277 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.380+682A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810219 | |||||||
| chr6:46810287 | A | T | 1 | a0002c0002t0002g0277 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.380+750A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810287 | |||||||
| chr6:46810343 | G | C | 4 | a0001c0001t0005g0070 a0001c0001t0005g0071 a0001c0001t0005g0072 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.380+806G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810343 | |||||||
| chr6:46810453 | C | A | 2 | a0003c0003t0003g0094 a0003c0003t0003g0095 |
2 | HG02145.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.380+916C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810453 | |||||||
| chr6:46810766 | C | A | 1 | a0001c0001t0001g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380+1229C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810766 | |||||||
| chr6:46810876 | C | T | 219 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(216): Show |
248 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.380+1339C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810876 | |||||||
| chr6:46810952 | T | C | 3 | a0004c0004t0003g0030 a0004c0004t0003g0034 a0004c0004t0003g0035 |
3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.380+1415T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810952 | |||||||
| chr6:46810978 | A | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0151 |
2 | HG01106.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.380+1441A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810978 | |||||||
| chr6:46810986 | T | C | 112 | a0001c0001t0001g0208 a0002c0002t0002g0077 a0003c0003t0003g0006 others(109): Show |
126 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.380+1449T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810986 | |||||||
| chr6:46811173 | T | C | 301 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(298): Show |
339 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.380+1636T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811173 | |||||||
| chr6:46811217 | T | G | 1 | a0001c0001t0001g0212 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.380+1680T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811217 | |||||||
| chr6:46811245 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.380+1708T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811245 | |||||||
| chr6:46811267 | A | T | 1 | a0004c0004t0002g0088 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.380+1730A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811267 | |||||||
| chr6:46811273 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
6 | HG01106.hp1 HG02615.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.380+1736G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811273 | |||||||
| chr6:46811432 | C | T | 1 | a0003c0003t0003g0105 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.380+1895C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811432 | |||||||
| chr6:46811496 | T | C | 1 | a0004c0004t0002g0088 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.380+1959T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811496 | |||||||
| chr6:46811497 | T | A | 1 | a0004c0004t0002g0088 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.380+1960T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811497 | |||||||
| chr6:46811687 | G | T | 1 | a0007c0017t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.380+2150G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811687 | |||||||
| chr6:46811841 | A | G | 9 | a0007c0007t0004g0036 a0007c0007t0004g0037 a0007c0007t0004g0038 others(6): Show |
9 | HG01243.hp2 HG01884.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.380+2304A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811841 | |||||||
| chr6:46811897 | C | A | 226 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.380+2360C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811897 | |||||||
| chr6:46812081 | T | G | 216 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(213): Show |
245 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.380+2544T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812081 | |||||||
| chr6:46812092 | A | C | 1 | a0001c0001t0001g0267 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.380+2555A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812092 | |||||||
| chr6:46812387 | A | G | 1 | a0003c0003t0003g0096 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.380+2850A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812387 | |||||||
| chr6:46812395 | A | C | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+2858A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812395 | |||||||
| chr6:46812397 | T | C | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+2860T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812397 | |||||||
| chr6:46812399 | T | A | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+2862T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812399 | |||||||
| chr6:46812400 | T | G | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+2863T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812400 | |||||||
| chr6:46812403 | T | C | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+2866T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812403 | |||||||
| chr6:46812404 | T | G | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+2867T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812404 | |||||||
| chr6:46812405 | A | C | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+2868A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812405 | |||||||
| chr6:46812406 | T | G | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+2869T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812406 | |||||||
| chr6:46812408 | T | G | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+2871T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812408 | |||||||
| chr6:46812454 | T | A | 1 | a0001c0001t0001g0237 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.380+2917T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812454 | |||||||
| chr6:46812515 | A | G | 219 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(216): Show |
248 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.380+2978A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812515 | |||||||
| chr6:46812608 | T | C | 9 | a0004c0004t0002g0003 a0004c0004t0002g0004 a0004c0004t0002g0012 others(6): Show |
14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.380+3071T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812608 | |||||||
| chr6:46812718 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.380+3181G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812718 | |||||||
| chr6:46813124 | C | T | 3 | a0004c0004t0003g0030 a0004c0004t0003g0034 a0004c0004t0003g0035 |
3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.380+3587C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813124 | |||||||
| chr6:46813410 | A | T | 1 | a0003c0003t0003g0075 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.380+3873A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813410 | |||||||
| chr6:46813445 | A | G | 108 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(105): Show |
123 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.380+3908A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813445 | |||||||
| chr6:46813648 | G | A | 1 | a0006c0005t0003g0065 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.380+4111G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813648 | |||||||
| chr6:46813723 | C | A | 10 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(7): Show |
10 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.380+4186C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813723 | |||||||
| chr6:46813764 | G | A | 1 | a0003c0003t0003g0105 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.380+4227G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813764 | |||||||
| chr6:46813824 | G | A | 2 | a0001c0001t0001g0068 a0006c0005t0003g0065 |
2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.380+4287G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813824 | |||||||
| chr6:46813869 | A | C | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+4332A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813869 | |||||||
| chr6:46813871 | A | C | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+4334A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813871 | |||||||
| chr6:46813875 | G | T | 1 | a0002c0002t0002g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+4338G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813875 | |||||||
| chr6:46813930 | G | T | 1 | a0003c0003t0003g0019 | 2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.380+4393G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813930 | |||||||
| chr6:46814021 | G | A | 226 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.380+4484G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814021 | |||||||
| chr6:46814032 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG00741.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.380+4495C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814032 | |||||||
| chr6:46814239 | A | C | 1 | a0007c0007t0003g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.380+4702A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814239 | |||||||
| chr6:46814270 | G | A | 4 | a0001c0001t0005g0070 a0001c0001t0005g0071 a0001c0001t0005g0072 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.380+4733G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814270 | |||||||
| chr6:46814395 | T | C | 3 | a0004c0004t0003g0030 a0004c0004t0003g0034 a0004c0004t0003g0035 |
3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.380+4858T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814395 | |||||||
| chr6:46814522 | C | T | 226 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.380+4985C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814522 | |||||||
| chr6:46814556 | G | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0222 |
2 | NA18945.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.381-4973G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814556 | |||||||
| chr6:46814664 | A | T | 1 | a0007c0007t0003g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.381-4865A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814664 | |||||||
| chr6:46814704 | G | C | 1 | a0001c0001t0001g0156 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.381-4825G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814704 | |||||||
| chr6:46814868 | GGAGTACA others(2): Show |
G | 87 | a0002c0002t0002g0077 a0003c0003t0003g0006 a0003c0003t0003g0007 others(84): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.381-4656_381-4648d others(11): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr6 | 46814868 | ||||||
| chr6:46814913 | G | C | 3 | a0002c0002t0002g0188 a0002c0002t0002g0191 a0002c0002t0002g0192 |
3 | NA18941.hp2 NA18999.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.381-4616G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814913 | |||||||
| chr6:46814945 | T | C | 3 | a0004c0004t0003g0030 a0004c0004t0003g0034 a0004c0004t0003g0035 |
3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.381-4584T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814945 | |||||||
| chr6:46815113 | T | C | 108 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(105): Show |
123 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.381-4416T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815113 | |||||||
| chr6:46815202 | C | A | 10 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(7): Show |
10 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.381-4327C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815202 | |||||||
| chr6:46815359 | A | G | 1 | a0002c0002t0002g0187 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.381-4170A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815359 | |||||||
| chr6:46815414 | G | A | 3 | a0006c0005t0003g0133 a0006c0005t0003g0134 a0006c0005t0003g0135 |
3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.381-4115G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815414 | |||||||
| chr6:46815491 | A | G | 226 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.381-4038A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815491 | |||||||
| chr6:46815509 | G | A | 220 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(217): Show |
249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.381-4020G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815509 | |||||||
| chr6:46815515 | C | T | 107 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(104): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.381-4014C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815515 | |||||||
| chr6:46815540 | C | A | 1 | a0002c0002t0002g0296 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.381-3989C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815540 | |||||||
| chr6:46815657 | A | C | 1 | a0002c0002t0002g0285 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.381-3872A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815657 | |||||||
| chr6:46815661 | C | A | 15 | a0005c0006t0003g0015 a0005c0006t0003g0018 a0005c0006t0003g0076 others(12): Show |
16 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.381-3868C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815661 | |||||||
| chr6:46815842 | A | G | 1 | a0002c0002t0002g0159 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.381-3687A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815842 | |||||||
| chr6:46815863 | T | G | 1 | a0001c0001t0001g0238 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.381-3666T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815863 | |||||||
| chr6:46815965 | C | A | 107 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(104): Show |
122 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.381-3564C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815965 | |||||||
| chr6:46816081 | C | T | 2 | a0003c0003t0003g0100 a0003c0003t0003g0104 |
2 | HG01192.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.381-3448C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46816081 | |||||||
| chr6:46816159 | A | T | 97 | a0001c0001t0001g0208 a0002c0002t0002g0077 a0003c0003t0003g0006 others(94): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.381-3370A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46816159 | |||||||
| chr6:46816204 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.381-3325C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46816204 | |||||||
| chr6:46816252 | C | T | 4 | a0001c0001t0005g0070 a0001c0001t0005g0071 a0001c0001t0005g0072 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.381-3277C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46816252 | |||||||
| chr6:46816273 | A | T | 1 | a0004c0021t0002g0069 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.381-3256A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46816273 | |||||||
| chr6:46816446 | A | G | 219 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(216): Show |
248 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.381-3083A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46816446 | |||||||
| chr6:46816773 | G | A | 11 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(8): Show |
11 | HG01106.hp2 HG01891.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.381-2756G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46816773 | |||||||
| chr6:46816873 | G | A | 10 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(7): Show |
10 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.381-2656G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46816873 | |||||||
| chr6:46816928 | A | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0268 |
2 | HG02135.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.381-2601A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46816928 | |||||||
| chr6:46816932 | A | G | 2 | a0002c0002t0002g0205 a0002c0002t0002g0295 |
2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.381-2597A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46816932 | |||||||
| chr6:46817110 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.381-2419T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817110 | |||||||
| chr6:46817185 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.381-2344G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817185 | |||||||
| chr6:46817219 | A | C | 3 | a0004c0004t0003g0030 a0004c0004t0003g0034 a0004c0004t0003g0035 |
3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.381-2310A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817219 | |||||||
| chr6:46817236 | G | T | 115 | a0002c0002t0002g0077 a0003c0003t0003g0006 a0003c0003t0003g0007 others(112): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.381-2293G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817236 | |||||||
| chr6:46817296 | A | C | 1 | a0003c0003t0003g0119 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.381-2233A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817296 | |||||||
| chr6:46817313 | G | A | 104 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(101): Show |
119 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.381-2216G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817313 | |||||||
| chr6:46817339 | A | G | 1 | a0007c0007t0003g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.381-2190A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817339 | |||||||
| chr6:46817391 | T | C | 1 | a0004c0004t0003g0132 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.381-2138T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817391 | |||||||
| chr6:46817603 | T | A | 1 | a0002c0002t0002g0287 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.381-1926T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817603 | |||||||
| chr6:46817741 | G | A | 1 | a0015c0018t0001g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.381-1788G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817741 | |||||||
| chr6:46817875 | G | A | 1 | a0003c0003t0003g0125 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.381-1654G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817875 | |||||||
| chr6:46817946 | G | C | 1 | a0014c0022t0001g0172 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.381-1583G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817946 | |||||||
| chr6:46818205 | T | A | 1 | a0002c0002t0002g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.381-1324T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818205 | |||||||
| chr6:46818400 | T | G | 1 | a0004c0021t0002g0069 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.381-1129T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818400 | |||||||
| chr6:46818446 | G | T | 114 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(111): Show |
128 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.381-1083G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818446 | |||||||
| chr6:46818490 | C | T | 1 | a0007c0007t0010g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.381-1039C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818490 | |||||||
| chr6:46818594 | T | C | 114 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(111): Show |
128 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.381-935T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818594 | |||||||
| chr6:46818626 | G | A | 1 | a0002c0002t0002g0281 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.381-903G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818626 | |||||||
| chr6:46818652 | A | G | 76 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(73): Show |
85 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.381-877A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818652 | |||||||
| chr6:46818665 | G | A | 1 | a0002c0002t0002g0198 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.381-864G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818665 | |||||||
| chr6:46818725 | T | A | 1 | a0007c0007t0003g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.381-804T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818725 | |||||||
| chr6:46818736 | C | T | 1 | a0004c0004t0003g0132 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.381-793C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818736 | |||||||
| chr6:46818854 | G | A | 1 | a0012c0016t0003g0098 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.381-675G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818854 | |||||||
| chr6:46818971 | A | G | 1 | a0007c0007t0010g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.381-558A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818971 | |||||||
| chr6:46818982 | C | CTGGGTGT others(9): Show |
114 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(111): Show |
128 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.381-545_381-544ins others(16): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr6 | 46818982 | ||||||
| chr6:46819034 | C | A | 11 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(8): Show |
11 | HG01106.hp2 HG01891.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.381-495C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46819034 | |||||||
| chr6:46819228 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.381-301G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46819228 | |||||||
| chr6:46819229 | C | A | 1 | a0015c0018t0001g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.381-300C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46819229 | |||||||
| chr6:46819438 | A | G | 2 | a0001c0001t0001g0236 a0001c0001t0001g0247 |
2 | NA18946.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.381-91A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46819438 | |||||||
| chr6:46820195 | A | T | 1 | a0007c0007t0003g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.556+491A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820195 | |||||||
| chr6:46820262 | A | G | 1 | a0002c0002t0002g0189 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.556+558A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820262 | |||||||
| chr6:46820327 | T | G | 225 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(222): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.556+623T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820327 | |||||||
| chr6:46820346 | G | T | 1 | a0001c0001t0001g0298 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.556+642G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820346 | |||||||
| chr6:46820429 | G | T | 115 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(112): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.556+725G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820429 | |||||||
| chr6:46820454 | G | A | 115 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(112): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.556+750G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820454 | |||||||
| chr6:46820480 | T | C | 1 | a0007c0007t0003g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.556+776T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820480 | |||||||
| chr6:46820588 | A | G | 2 | a0002c0002t0002g0140 a0002c0002t0002g0146 |
2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.556+884A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820588 | |||||||
| chr6:46820778 | A | G | 2 | a0002c0002t0002g0186 a0002c0002t0002g0199 |
2 | NA18947.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.556+1074A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820778 | |||||||
| chr6:46820855 | T | C | 115 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(112): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.556+1151T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820855 | |||||||
| chr6:46820906 | T | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0151 |
2 | HG01106.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.556+1202T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820906 | |||||||
| chr6:46821057 | T | C | 1 | a0015c0018t0001g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.556+1353T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46821057 | |||||||
| chr6:46821270 | A | T | 9 | a0004c0004t0002g0003 a0004c0004t0002g0004 a0004c0004t0002g0012 others(6): Show |
14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.556+1566A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46821270 | |||||||
| chr6:46821304 | C | G | 5 | a0003c0003t0003g0074 a0003c0003t0003g0094 a0003c0003t0003g0095 others(2): Show |
5 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.556+1600C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46821304 | |||||||
| chr6:46821330 | C | A | 1 | a0001c0001t0001g0248 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.556+1626C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46821330 | |||||||
| chr6:46821668 | A | C | 1 | a0007c0007t0010g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.556+1964A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46821668 | |||||||
| chr6:46821840 | G | A | 13 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(10): Show |
13 | HG01106.hp2 HG01891.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.556+2136G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46821840 | |||||||
| chr6:46821864 | C | T | 2 | a0011c0012t0002g0139 a0011c0012t0002g0145 |
2 | HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.556+2160C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46821864 | |||||||
| chr6:46821990 | C | T | 1 | a0002c0002t0002g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.556+2286C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46821990 | |||||||
| chr6:46822120 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0269 |
2 | HG01167.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.556+2416G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46822120 | |||||||
| chr6:46822334 | T | C | 5 | a0005c0006t0003g0015 a0005c0006t0003g0076 a0005c0006t0003g0113 others(2): Show |
6 | HG00639.hp2 HG01175.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.556+2630T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46822334 | |||||||
| chr6:46822375 | A | G | 1 | a0010c0011t0003g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.556+2671A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46822375 | |||||||
| chr6:46822387 | G | A | 9 | a0004c0004t0002g0003 a0004c0004t0002g0004 a0004c0004t0002g0012 others(6): Show |
14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.556+2683G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46822387 | |||||||
| chr6:46822391 | A | T | 1 | a0001c0001t0001g0266 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.556+2687A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46822391 | |||||||
| chr6:46822474 | A | T | 115 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(112): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.556+2770A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46822474 | |||||||
| chr6:46822732 | A | T | 3 | a0004c0004t0003g0030 a0004c0004t0003g0034 a0004c0004t0003g0035 |
3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.557-2540A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46822732 | |||||||
| chr6:46822989 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.557-2283A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46822989 | |||||||
| chr6:46823364 | C | T | 11 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(8): Show |
11 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.557-1908C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46823364 | |||||||
| chr6:46823417 | G | C | 1 | a0001c0001t0001g0249 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.557-1855G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46823417 | |||||||
| chr6:46823472 | C | T | 1 | a0002c0002t0002g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.557-1800C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46823472 | |||||||
| chr6:46823486 | C | T | 2 | a0001c0001t0006g0032 a0001c0001t0006g0033 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.557-1786C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46823486 | |||||||
| chr6:46823551 | G | A | 1 | a0003c0003t0003g0122 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.557-1721G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46823551 | |||||||
| chr6:46823731 | C | T | 1 | a0004c0021t0002g0069 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.557-1541C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46823731 | |||||||
| chr6:46823798 | C | T | 4 | a0009c0009t0001g0053 a0009c0009t0001g0054 a0009c0009t0001g0055 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.557-1474C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46823798 | |||||||
| chr6:46823824 | C | A | 115 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(112): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.557-1448C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46823824 | |||||||
| chr6:46824003 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.557-1269G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824003 | |||||||
| chr6:46824048 | C | T | 115 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(112): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.557-1224C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824048 | |||||||
| chr6:46824113 | T | G | 115 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(112): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.557-1159T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824113 | |||||||
| chr6:46824122 | C | T | 4 | a0001c0001t0005g0070 a0001c0001t0005g0071 a0001c0001t0005g0072 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.557-1150C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824122 | |||||||
| chr6:46824151 | A | G | 1 | a0015c0018t0001g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.557-1121A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824151 | |||||||
| chr6:46824261 | C | T | 110 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
125 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.557-1011C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824261 | |||||||
| chr6:46824365 | A | G | 2 | a0001c0001t0006g0032 a0001c0001t0006g0033 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.557-907A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824365 | |||||||
| chr6:46824408 | G | A | 8 | a0003c0003t0003g0019 a0003c0003t0003g0074 a0003c0003t0003g0075 others(5): Show |
9 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.557-864G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824408 | |||||||
| chr6:46824483 | A | C | 3 | a0004c0004t0003g0030 a0004c0004t0003g0034 a0004c0004t0003g0035 |
3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.557-789A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824483 | |||||||
| chr6:46824483 | ATATTTAA others(7): Show |
A | 3 | a0001c0001t0001g0231 a0002c0002t0002g0185 a0002c0002t0002g0187 |
3 | HG03688.hp2 NA19090.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.557-764_557-751del others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824483 | ||||||
| chr6:46824553 | TTATATAT others(29): Show |
T | 1 | a0002c0002t0002g0290 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.557-687_557-652del others(36): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824553 | ||||||
| chr6:46824567 | G | GATGTATT others(66): Show |
1 | a0002c0002t0002g0280 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.557-692_557-620dup others(73): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824567 | ||||||
| chr6:46824586 | A | T | 1 | a0002c0002t0002g0277 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.557-686A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824586 | |||||||
| chr6:46824595 | ATTAAATA others(63): Show |
A | 3 | a0004c0004t0003g0030 a0004c0004t0003g0034 a0004c0004t0003g0035 |
3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.557-643_557-574del others(70): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824595 | ||||||
| chr6:46824605 | T | A | 1 | a0007c0007t0004g0149 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.557-667T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824605 | |||||||
| chr6:46824606 | G | A | 1 | a0001c0001t0006g0032 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.557-666G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824606 | |||||||
| chr6:46824613 | AAT | A | 4 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0140 others(1): Show |
4 | HG02647.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.557-651_557-650del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824613 | ||||||
| chr6:46824632 | T | TA | 4 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0140 others(1): Show |
4 | HG02647.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.557-640_557-639ins others(1): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824632 | |||||||
| chr6:46824640 | A | G | 4 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0140 others(1): Show |
4 | HG02647.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.557-632A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824640 | |||||||
| chr6:46824653 | T | A | 4 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0140 others(1): Show |
4 | HG02647.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.557-619T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824653 | |||||||
| chr6:46824659 | A | AAATT | 4 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0140 others(1): Show |
4 | HG02647.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.557-612_557-611ins others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824659 | ||||||
| chr6:46824659 | AATGTATT others(67): Show |
A | 6 | a0001c0001t0001g0221 a0001c0001t0001g0246 a0001c0001t0001g0260 others(3): Show |
6 | HG00544.hp2 HG01243.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.557-539_557-466del others(74): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824659 | ||||||
| chr6:46824662 | G | A | 4 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0140 others(1): Show |
4 | HG02647.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.557-610G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824662 | |||||||
| chr6:46824673 | G | A | 4 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0140 others(1): Show |
4 | HG02647.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.557-599G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824673 | |||||||
| chr6:46824686 | A | T | 4 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0140 others(1): Show |
4 | HG02647.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.557-586A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824686 | |||||||
| chr6:46824692 | AAATT | A | 4 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0140 others(1): Show |
4 | HG02647.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.557-578_557-575del others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824692 | ||||||
| chr6:46824699 | G | A | 1 | a0007c0007t0010g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.557-573G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824699 | |||||||
| chr6:46824710 | G | A | 1 | a0007c0007t0010g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.557-562G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824710 | |||||||
| chr6:46824723 | A | T | 1 | a0007c0007t0010g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.557-549A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824723 | |||||||
| chr6:46824733 | T | G | 109 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(106): Show |
124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.557-539T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824733 | |||||||
| chr6:46824733 | TATGTATT others(7): Show |
T | 7 | a0007c0007t0004g0036 a0007c0007t0004g0037 a0007c0007t0004g0038 others(4): Show |
7 | HG01243.hp2 HG01884.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.557-525_557-512del others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824733 | ||||||
| chr6:46824736 | G | A | 105 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(102): Show |
120 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.557-536G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824736 | |||||||
| chr6:46824743 | AATAGATG others(9): Show |
A | 4 | a0003c0003t0003g0014 a0003c0003t0003g0099 a0003c0003t0003g0101 others(1): Show |
5 | HG00738.hp2 HG01515.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.557-525_557-510del others(16): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824743 | ||||||
| chr6:46824744 | A | T | 105 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(102): Show |
120 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.557-528A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824744 | |||||||
| chr6:46824750 | G | A | 1 | a0007c0017t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.557-522G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824750 | |||||||
| chr6:46824757 | A | AATATATA others(6): Show |
100 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(97): Show |
115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.557-512_557-500dup others(13): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824757 | ||||||
| chr6:46824759 | T | TATATATA others(41): Show |
1 | a0001c0001t0001g0067 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.557-500_557-499ins others(48): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824759 | ||||||
| chr6:46824769 | T | TTATATAT others(43): Show |
1 | a0001c0001t0001g0167 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.557-500_557-499ins others(50): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824769 | ||||||
| chr6:46824770 | T | G | 16 | a0002c0002t0002g0166 a0003c0003t0003g0014 a0003c0003t0003g0099 others(13): Show |
17 | HG00738.hp2 HG01074.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.557-502T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824770 | |||||||
| chr6:46824770 | TATGTATT others(17): Show |
T | 2 | a0001c0001t0001g0068 a0001c0001t0006g0033 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.557-499_557-476del others(24): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824770 | ||||||
| chr6:46824770 | TATGTATT others(265): Show |
T | 1 | a0001c0001t0001g0262 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.557-499_557-228del | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824770 | ||||||
| chr6:46824773 | G | A | 117 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
133 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.557-499G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824773 | |||||||
| chr6:46824780 | AATAGATG others(9): Show |
A | 73 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(70): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.557-488_557-473del others(16): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824780 | ||||||
| chr6:46824781 | A | ATAGATGT others(104): Show |
9 | a0004c0004t0002g0003 a0004c0004t0002g0004 a0004c0004t0002g0012 others(6): Show |
14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.557-463_557-462ins others(111): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824781 | ||||||
| chr6:46824781 | A | T | 16 | a0002c0002t0002g0166 a0003c0003t0003g0014 a0003c0003t0003g0099 others(13): Show |
17 | HG00738.hp2 HG01074.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.557-491A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824781 | |||||||
| chr6:46824787 | G | C | 102 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(99): Show |
117 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.557-485G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824787 | |||||||
| chr6:46824787 | GTATTTAA others(80): Show |
G | 1 | a0002c0002t0002g0166 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.557-465_557-379del others(87): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824787 | ||||||
| chr6:46824794 | A | AATATATA others(6): Show |
3 | a0001c0001t0001g0249 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | NA18982.hp1 NA19059.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.557-466_557-465ins others(13): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824794 | ||||||
| chr6:46824794 | AAT | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0151 |
5 | HG01106.hp1 HG02615.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.557-470_557-469del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824794 | ||||||
| chr6:46824794 | AATAT | A | 11 | a0003c0003t0003g0014 a0003c0003t0003g0099 a0003c0003t0003g0101 others(8): Show |
12 | HG00738.hp2 HG01243.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.557-472_557-469del others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824794 | ||||||
| chr6:46824798 | T | TATATAAA others(115): Show |
1 | a0007c0017t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.557-466_557-465ins others(122): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824798 | ||||||
| chr6:46824807 | G | T | 122 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(119): Show |
137 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.557-465G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824807 | |||||||
| chr6:46824810 | G | A | 215 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(212): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.557-462G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824810 | |||||||
| chr6:46824818 | T | A | 122 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(119): Show |
137 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.557-454T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824818 | |||||||
| chr6:46824824 | G | C | 104 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(101): Show |
119 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.557-448G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824824 | |||||||
| chr6:46824824 | GTATTTAA others(43): Show |
G | 4 | a0002c0002t0002g0144 a0002c0020t0002g0143 a0011c0012t0002g0139 others(1): Show |
4 | HG01346.hp2 HG02145.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.557-371_557-322del others(50): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824824 | ||||||
| chr6:46824831 | AATATATA others(6): Show |
A | 74 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(71): Show |
84 | HG00323.hp1 HG00408.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.557-421_557-409del others(13): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824831 | ||||||
| chr6:46824831 | AATATATA others(8): Show |
A | 1 | a0001c0001t0001g0068 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.557-433_557-419del others(15): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824831 | ||||||
| chr6:46824831 | AATATATA others(10): Show |
A | 73 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(70): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.557-435_557-419del others(17): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824831 | ||||||
| chr6:46824843 | T | TGATATAT others(17): Show |
3 | a0006c0005t0003g0133 a0006c0005t0003g0134 a0006c0005t0003g0135 |
3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.557-429_557-428ins others(24): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824843 | |||||||
| chr6:46824844 | T | A | 3 | a0006c0005t0003g0133 a0006c0005t0003g0134 a0006c0005t0003g0135 |
3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.557-428T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824844 | |||||||
| chr6:46824844 | T | TATATATT others(17): Show |
46 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0021 others(43): Show |
51 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.557-422_557-421ins others(24): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824844 | ||||||
| chr6:46824844 | T | TATATATT others(54): Show |
2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG00741.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.557-422_557-421ins others(61): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824844 | ||||||
| chr6:46824846 | T | TATATTTA others(15): Show |
1 | a0001c0001t0005g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.557-422_557-421ins others(22): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824846 | ||||||
| chr6:46824851 | A | T | 1 | a0001c0001t0001g0239 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.557-421A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824851 | |||||||
| chr6:46824857 | T | G | 96 | a0001c0001t0001g0239 a0002c0002t0002g0137 a0002c0002t0002g0138 others(93): Show |
104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.557-415T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824857 | |||||||
| chr6:46824860 | A | C | 1 | a0001c0001t0001g0239 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.557-412A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824860 | |||||||
| chr6:46824860 | A | G | 8 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0140 others(5): Show |
8 | HG01261.hp2 HG02647.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.557-412A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824860 | |||||||
| chr6:46824868 | A | T | 95 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0140 others(92): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.557-404A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824868 | |||||||
| chr6:46824871 | G | T | 1 | a0001c0001t0001g0239 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.557-401G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824871 | |||||||
| chr6:46824874 | C | A | 1 | a0001c0001t0001g0239 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.557-398C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824874 | |||||||
| chr6:46824874 | C | G | 97 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0140 others(94): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.557-398C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824874 | |||||||
| chr6:46824878 | T | C | 3 | a0006c0005t0003g0133 a0006c0005t0003g0134 a0006c0005t0003g0135 |
3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.557-394T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824878 | |||||||
| chr6:46824881 | AAT | A | 3 | a0004c0004t0003g0030 a0004c0004t0003g0034 a0004c0004t0003g0035 |
3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.557-383_557-382del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824881 | ||||||
| chr6:46824881 | AATATATA others(6): Show |
A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(91): Show |
106 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.557-371_557-359del others(13): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824881 | ||||||
| chr6:46824881 | AATATATA others(10): Show |
A | 3 | a0005c0006t0003g0081 a0005c0006t0003g0082 a0005c0006t0003g0127 |
3 | HG01069.hp1 HG01071.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.557-385_557-369del others(17): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824881 | ||||||
| chr6:46824885 | T | G | 1 | a0001c0001t0001g0239 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.557-387T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824885 | |||||||
| chr6:46824888 | A | AAATTATA others(4): Show |
1 | a0001c0001t0005g0070 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.557-384_557-383ins others(11): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824888 | |||||||
| chr6:46824888 | A | C | 1 | a0001c0001t0001g0239 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.557-384A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824888 | |||||||
| chr6:46824891 | A | T | 1 | a0001c0001t0001g0239 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.557-381A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824891 | |||||||
| chr6:46824892 | A | T | 1 | a0001c0001t0001g0239 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.557-380A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824892 | |||||||
| chr6:46824893 | T | TAGATCTA others(4): Show |
1 | a0001c0001t0005g0070 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.557-379_557-378ins others(11): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824893 | |||||||
| chr6:46824893 | TTA | T | 4 | a0009c0009t0001g0053 a0009c0009t0001g0054 a0009c0009t0001g0055 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.557-370_557-369del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824893 | ||||||
| chr6:46824894 | T | A | 2 | a0001c0001t0001g0239 a0001c0001t0005g0070 |
2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.557-378T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824894 | |||||||
| chr6:46824894 | T | TATATATA others(30): Show |
1 | a0002c0002t0002g0290 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.557-303_557-267dup others(37): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824894 | ||||||
| chr6:46824894 | T | TATATATT others(17): Show |
22 | a0001c0001t0001g0008 a0001c0001t0001g0167 a0001c0001t0001g0169 others(19): Show |
25 | HG00741.hp1 HG00741.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.557-372_557-371ins others(24): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824894 | ||||||
| chr6:46824894 | T | TATATATT others(54): Show |
3 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0007c0017t0001g0051 |
3 | HG03927.hp2 NA18943.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.557-372_557-371ins others(61): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824894 | ||||||
| chr6:46824894 | T | TATATATT others(91): Show |
11 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(8): Show |
12 | HG00280.hp1 HG00438.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.557-372_557-371ins others(98): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824894 | ||||||
| chr6:46824894 | T | TATATATT others(126): Show |
2 | a0004c0004t0002g0003 a0004c0004t0002g0060 |
4 | HG01255.hp1 HG03098.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.557-372_557-371ins others(133): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824894 | ||||||
| chr6:46824894 | T | TATATATT others(128): Show |
6 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0152 others(3): Show |
6 | HG01928.hp1 HG02004.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.557-372_557-371ins others(135): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824894 | ||||||
| chr6:46824894 | T | TATGTATT others(3): Show |
1 | a0007c0007t0010g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.557-376_557-375ins others(10): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824894 | ||||||
| chr6:46824894 | T | TATGTATT others(91): Show |
1 | a0001c0001t0001g0168 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.557-376_557-375ins others(98): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824894 | ||||||
| chr6:46824894 | TATATATA others(30): Show |
T | 1 | a0002c0002t0002g0026 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.557-303_557-267del others(37): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824894 | ||||||
| chr6:46824896 | T | TATATTTA others(15): Show |
2 | a0001c0001t0005g0071 a0001c0001t0005g0073 |
2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.557-372_557-371ins others(22): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824896 | ||||||
| chr6:46824901 | A | T | 3 | a0004c0004t0003g0030 a0004c0004t0003g0034 a0004c0004t0003g0035 |
3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.557-371A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824901 | |||||||
| chr6:46824904 | AATTATAT others(22): Show |
A | 3 | a0004c0004t0003g0030 a0004c0004t0003g0034 a0004c0004t0003g0035 |
3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.557-365_557-337del others(29): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824904 | ||||||
| chr6:46824907 | T | G | 14 | a0005c0006t0003g0081 a0005c0006t0003g0082 a0005c0006t0003g0127 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.557-365T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824907 | |||||||
| chr6:46824918 | A | T | 14 | a0005c0006t0003g0081 a0005c0006t0003g0082 a0005c0006t0003g0127 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.557-354A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824918 | |||||||
| chr6:46824924 | C | G | 14 | a0005c0006t0003g0081 a0005c0006t0003g0082 a0005c0006t0003g0127 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.557-348C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824924 | |||||||
| chr6:46824928 | T | C | 1 | a0006c0005t0003g0065 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.557-344T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824928 | |||||||
| chr6:46824944 | T | G | 8 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(5): Show |
8 | HG02056.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.557-328T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824944 | |||||||
| chr6:46824944 | TATATATT others(17): Show |
T | 5 | a0005c0006t0003g0081 a0005c0006t0003g0082 a0005c0006t0003g0127 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.557-321_557-298del others(24): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824944 | ||||||
| chr6:46824945 | ATATATTT others(54): Show |
A | 1 | a0006c0005t0003g0065 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.557-321_557-261del others(61): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824945 | ||||||
| chr6:46824955 | A | T | 8 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(5): Show |
8 | HG02056.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.557-317A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824955 | |||||||
| chr6:46824958 | GATCTATT others(104): Show |
G | 3 | a0003c0003t0003g0014 a0003c0003t0003g0101 a0003c0003t0003g0108 |
4 | HG00738.hp2 HG01515.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.557-299_557-189del | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824958 | ||||||
| chr6:46824961 | C | G | 8 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(5): Show |
8 | HG02056.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.557-311C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824961 | |||||||
| chr6:46824965 | T | C | 7 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(4): Show |
7 | HG02056.hp2 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.557-307T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824965 | |||||||
| chr6:46824969 | ATATATAT others(30): Show |
A | 1 | a0003c0003t0003g0129 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.557-266_557-230del others(37): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824969 | ||||||
| chr6:46824973 | A | T | 11 | a0007c0007t0004g0036 a0007c0007t0004g0037 a0007c0007t0004g0038 others(8): Show |
11 | HG01243.hp2 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.557-299A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824973 | |||||||
| chr6:46824982 | ATATATTT others(17): Show |
A | 7 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(4): Show |
7 | HG02056.hp2 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.557-284_557-261del others(24): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824982 | ||||||
| chr6:46824986 | ATTTAAAT others(54): Show |
A | 1 | a0007c0007t0010g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.557-284_557-224del others(61): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824986 | ||||||
| chr6:46824992 | ATAGATCT others(7): Show |
A | 3 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0272 |
3 | HG00323.hp1 HG01081.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.557-277_557-264del others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824992 | ||||||
| chr6:46824995 | GATCTATT others(67): Show |
G | 80 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(77): Show |
88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.557-266_557-193del others(74): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824995 | ||||||
| chr6:46825002 | TTA | T | 9 | a0004c0004t0002g0003 a0004c0004t0002g0004 a0004c0004t0002g0012 others(6): Show |
14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.557-269_557-268del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825002 | |||||||
| chr6:46825006 | G | A | 127 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(124): Show |
147 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.557-266G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825006 | |||||||
| chr6:46825007 | T | TATATATA others(26): Show |
1 | a0006c0005t0003g0134 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.557-258_557-257ins others(33): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46825007 | ||||||
| chr6:46825010 | A | T | 1 | a0003c0003t0003g0075 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.557-262A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825010 | |||||||
| chr6:46825015 | A | T | 3 | a0006c0005t0003g0133 a0006c0005t0003g0134 a0006c0005t0003g0135 |
3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.557-257A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825015 | |||||||
| chr6:46825016 | A | T | 1 | a0003c0003t0003g0075 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.557-256A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825016 | |||||||
| chr6:46825021 | A | ATATTTAA others(30): Show |
4 | a0001c0001t0005g0070 a0001c0001t0005g0071 a0001c0001t0005g0072 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.557-240_557-204dup others(37): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46825021 | ||||||
| chr6:46825023 | ATTTAAAT others(65): Show |
A | 1 | a0003c0003t0003g0075 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.557-247_557-176del others(72): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46825023 | ||||||
| chr6:46825032 | GATCTATT others(30): Show |
G | 21 | a0001c0001t0001g0011 a0001c0001t0001g0131 a0001c0001t0001g0158 others(18): Show |
22 | HG01243.hp1 HG02273.hp1 HG02622.hp2 others(19): Show |
intron_variant | MODIFIER | c.557-155_557-119del others(37): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46825032 | ||||||
| chr6:46825043 | A | G | 1 | a0002c0002t0002g0196 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.557-229A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825043 | |||||||
| chr6:46825047 | T | A | 121 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(118): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.557-225T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825047 | |||||||
| chr6:46825058 | G | A | 122 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(119): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.557-214G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825058 | |||||||
| chr6:46825069 | A | G | 127 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(124): Show |
145 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.557-203A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825069 | |||||||
| chr6:46825069 | A | T | 1 | a0015c0018t0001g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.557-203A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825069 | |||||||
| chr6:46825084 | T | A | 1 | a0001c0001t0001g0171 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.557-188T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825084 | |||||||
| chr6:46825095 | G | A | 114 | a0001c0001t0001g0171 a0003c0003t0003g0006 a0003c0003t0003g0007 others(111): Show |
128 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.557-177G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825095 | |||||||
| chr6:46825106 | A | G | 125 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(122): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.557-166A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825106 | |||||||
| chr6:46825623 | G | A | 3 | a0004c0004t0003g0030 a0004c0004t0003g0034 a0004c0004t0003g0035 |
3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.778+130G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 8/13 | chr6 | 46825623 | |||||||
| chr6:46825677 | G | GT | 86 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(83): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.778+189dupT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr6 | 46825677 | ||||||
| chr6:46825789 | A | G | 1 | a0003c0003t0003g0102 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.778+296A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 8/13 | chr6 | 46825789 | |||||||
| chr6:46825810 | G | A | 1 | a0007c0017t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.778+317G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 8/13 | chr6 | 46825810 | |||||||
| chr6:46825929 | G | A | 4 | a0001c0001t0005g0070 a0001c0001t0005g0071 a0001c0001t0005g0072 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.779-425G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 8/13 | chr6 | 46825929 | |||||||
| chr6:46826053 | A | G | 9 | a0004c0004t0002g0003 a0004c0004t0002g0004 a0004c0004t0002g0012 others(6): Show |
14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.779-301A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 8/13 | chr6 | 46826053 | |||||||
| chr6:46826171 | G | A | 1 | a0004c0004t0003g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.779-183G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 8/13 | chr6 | 46826171 | |||||||
| chr6:46826311 | C | G | 115 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(112): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.779-43C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 8/13 | chr6 | 46826311 | |||||||
| chr6:46826555 | AG | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0067 |
4 | HG02615.hp1 HG03540.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.928+54delG | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr6 | 46826555 | ||||||
| chr6:46826911 | G | A | 4 | a0009c0009t0001g0053 a0009c0009t0001g0054 a0009c0009t0001g0055 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.928+408G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46826911 | |||||||
| chr6:46827074 | C | A | 1 | a0001c0001t0006g0032 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.928+571C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46827074 | |||||||
| chr6:46827153 | A | G | 2 | a0002c0002t0002g0184 a0002c0002t0002g0284 |
2 | HG02683.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.928+650A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46827153 | |||||||
| chr6:46827264 | C | T | 11 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(8): Show |
11 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.928+761C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46827264 | |||||||
| chr6:46827547 | G | A | 7 | a0004c0004t0003g0030 a0004c0004t0003g0034 a0004c0004t0003g0035 others(4): Show |
7 | HG02280.hp1 HG02622.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.928+1044G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46827547 | |||||||
| chr6:46827561 | G | A | 9 | a0004c0004t0002g0003 a0004c0004t0002g0004 a0004c0004t0002g0012 others(6): Show |
14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.928+1058G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46827561 | |||||||
| chr6:46827614 | C | T | 1 | a0003c0003t0003g0108 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.928+1111C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46827614 | |||||||
| chr6:46827745 | T | G | 4 | a0009c0009t0001g0053 a0009c0009t0001g0054 a0009c0009t0001g0055 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.928+1242T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46827745 | |||||||
| chr6:46827815 | G | A | 86 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(83): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.928+1312G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46827815 | |||||||
| chr6:46827883 | T | C | 1 | a0007c0017t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.928+1380T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46827883 | |||||||
| chr6:46828123 | G | C | 1 | a0001c0001t0001g0210 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.929-1233G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46828123 | |||||||
| chr6:46828236 | G | GT | 13 | a0001c0001t0001g0237 a0001c0001t0001g0253 a0001c0001t0001g0270 others(10): Show |
13 | HG02486.hp2 HG02559.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.929-1106dupT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr6 | 46828236 | ||||||
| chr6:46828236 | G | GTT | 98 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(95): Show |
113 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.929-1107_929-1106d others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr6 | 46828236 | ||||||
| chr6:46828236 | GT | G | 9 | a0004c0004t0002g0003 a0004c0004t0002g0004 a0004c0004t0002g0012 others(6): Show |
14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.929-1106delT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr6 | 46828236 | ||||||
| chr6:46828503 | A | T | 4 | a0009c0009t0001g0053 a0009c0009t0001g0054 a0009c0009t0001g0055 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.929-853A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46828503 | |||||||
| chr6:46828529 | T | A | 9 | a0004c0004t0002g0003 a0004c0004t0002g0004 a0004c0004t0002g0012 others(6): Show |
14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.929-827T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46828529 | |||||||
| chr6:46828616 | T | A | 1 | a0015c0018t0001g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.929-740T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46828616 | |||||||
| chr6:46828631 | G | A | 4 | a0009c0009t0001g0053 a0009c0009t0001g0054 a0009c0009t0001g0055 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.929-725G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46828631 | |||||||
| chr6:46828757 | T | C | 7 | a0001c0001t0001g0158 a0001c0001t0001g0241 a0001c0001t0001g0242 others(4): Show |
7 | HG00642.hp1 HG02055.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.929-599T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46828757 | |||||||
| chr6:46828829 | T | C | 11 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(8): Show |
11 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.929-527T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46828829 | |||||||
| chr6:46828841 | G | T | 86 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(83): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.929-515G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46828841 | |||||||
| chr6:46828847 | A | T | 11 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(8): Show |
11 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.929-509A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46828847 | |||||||
| chr6:46828862 | C | G | 2 | a0002c0002t0002g0184 a0002c0002t0002g0284 |
2 | HG02683.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.929-494C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46828862 | |||||||
| chr6:46828911 | T | TATC | 113 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(110): Show |
127 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.929-443_929-442ins others(3): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr6 | 46828911 | ||||||
| chr6:46829103 | A | G | 115 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(112): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.929-253A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46829103 | |||||||
| chr6:46829285 | CTTTG | C | 9 | a0004c0004t0002g0003 a0004c0004t0002g0004 a0004c0004t0002g0012 others(6): Show |
14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.929-66_929-63delTT others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr6 | 46829285 | ||||||
| chr6:46829592 | G | A | 75 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(72): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1144+21G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46829592 | |||||||
| chr6:46829654 | A | C | 1 | a0015c0018t0001g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1144+83A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46829654 | |||||||
| chr6:46829778 | G | A | 115 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(112): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1144+207G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46829778 | |||||||
| chr6:46829783 | A | G | 2 | a0001c0001t0006g0032 a0001c0001t0006g0033 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1144+212A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46829783 | |||||||
| chr6:46829875 | A | T | 1 | a0001c0001t0001g0232 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1144+304A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46829875 | |||||||
| chr6:46829983 | C | T | 2 | a0001c0001t0006g0032 a0001c0001t0006g0033 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1144+412C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46829983 | |||||||
| chr6:46830100 | T | C | 4 | a0009c0009t0001g0053 a0009c0009t0001g0054 a0009c0009t0001g0055 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144+529T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830100 | |||||||
| chr6:46830230 | C | G | 1 | a0001c0001t0001g0151 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1144+659C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830230 | |||||||
| chr6:46830235 | C | G | 8 | a0003c0003t0003g0019 a0003c0003t0003g0074 a0003c0003t0003g0075 others(5): Show |
9 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1144+664C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830235 | |||||||
| chr6:46830247 | TAAAA | T | 41 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0001t0001g0174 others(38): Show |
44 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.1144+707_1144+710d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr6 | 46830247 | ||||||
| chr6:46830247 | TAAAAAA | T | 12 | a0001c0001t0001g0066 a0001c0001t0001g0247 a0001c0001t0001g0252 others(9): Show |
12 | HG01070.hp2 HG01106.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1144+705_1144+710d others(8): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr6 | 46830247 | ||||||
| chr6:46830247 | TAAAAAAA others(1): Show |
T | 14 | a0003c0003t0003g0042 a0003c0003t0003g0094 a0003c0003t0003g0097 others(11): Show |
14 | HG00639.hp1 HG01175.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.1144+703_1144+710d others(10): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr6 | 46830247 | ||||||
| chr6:46830247 | TAAAAAAA others(2): Show |
T | 72 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(69): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1144+702_1144+710d others(11): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr6 | 46830247 | ||||||
| chr6:46830247 | TAAAAAAA others(3): Show |
T | 13 | a0003c0003t0003g0086 a0003c0003t0003g0087 a0004c0004t0002g0060 others(10): Show |
13 | HG01069.hp1 HG01243.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.1144+701_1144+710d others(12): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr6 | 46830247 | ||||||
| chr6:46830247 | TAAAAAAA others(4): Show |
T | 1 | a0007c0007t0004g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1144+700_1144+710d others(13): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr6 | 46830247 | ||||||
| chr6:46830363 | G | T | 1 | a0002c0002t0002g0184 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1144+792G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830363 | |||||||
| chr6:46830450 | T | C | 1 | a0006c0005t0003g0065 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1144+879T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830450 | |||||||
| chr6:46830464 | T | A | 1 | a0002c0002t0002g0077 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1144+893T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830464 | |||||||
| chr6:46830681 | T | A | 4 | a0009c0009t0001g0053 a0009c0009t0001g0054 a0009c0009t0001g0055 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144+1110T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830681 | |||||||
| chr6:46830721 | G | A | 1 | a0004c0021t0002g0069 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1144+1150G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830721 | |||||||
| chr6:46830873 | T | A | 4 | a0001c0001t0005g0070 a0001c0001t0005g0071 a0001c0001t0005g0072 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144+1302T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830873 | |||||||
| chr6:46830959 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1144+1388C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830959 | |||||||
| chr6:46830998 | T | C | 4 | a0003c0003t0003g0305 a0003c0003t0003g0306 a0003c0003t0003g0308 others(1): Show |
4 | HG00639.hp1 HG01496.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144+1427T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830998 | |||||||
| chr6:46831006 | A | C | 1 | a0004c0004t0003g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1144+1435A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831006 | |||||||
| chr6:46831068 | T | G | 4 | a0003c0003t0003g0094 a0003c0003t0003g0095 a0003c0003t0003g0115 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144+1497T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831068 | |||||||
| chr6:46831171 | C | T | 1 | a0007c0007t0003g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1144+1600C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831171 | |||||||
| chr6:46831205 | T | C | 2 | a0003c0003t0003g0044 a0003c0003t0003g0107 |
2 | HG02523.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1144+1634T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831205 | |||||||
| chr6:46831206 | A | G | 1 | a0015c0018t0001g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1144+1635A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831206 | |||||||
| chr6:46831325 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1145-1749A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831325 | |||||||
| chr6:46831382 | A | G | 2 | a0007c0017t0001g0051 a0017c0015t0009g0031 |
2 | NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1145-1692A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831382 | |||||||
| chr6:46831431 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1145-1643C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831431 | |||||||
| chr6:46831461 | A | G | 4 | a0009c0009t0001g0053 a0009c0009t0001g0054 a0009c0009t0001g0055 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1145-1613A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831461 | |||||||
| chr6:46831547 | G | A | 7 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(4): Show |
7 | HG02056.hp2 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1145-1527G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831547 | |||||||
| chr6:46831584 | T | C | 6 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0256 others(3): Show |
6 | HG00642.hp1 HG02055.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1145-1490T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831584 | |||||||
| chr6:46831596 | C | A | 1 | a0001c0001t0001g0248 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1145-1478C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831596 | |||||||
| chr6:46831793 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1145-1281C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831793 | |||||||
| chr6:46831871 | A | G | 1 | a0001c0001t0008g0223 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1145-1203A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831871 | |||||||
| chr6:46832029 | TAGAG | T | 4 | a0009c0009t0001g0053 a0009c0009t0001g0054 a0009c0009t0001g0055 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1145-1041_1145-103 others(8): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr6 | 46832029 | ||||||
| chr6:46832124 | A | C | 1 | a0004c0004t0003g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1145-950A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46832124 | |||||||
| chr6:46832272 | T | C | 76 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(73): Show |
85 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1145-802T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46832272 | |||||||
| chr6:46832322 | G | C | 4 | a0009c0009t0001g0053 a0009c0009t0001g0054 a0009c0009t0001g0055 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1145-752G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46832322 | |||||||
| chr6:46832338 | T | C | 3 | a0003c0003t0003g0078 a0004c0004t0002g0088 a0004c0004t0002g0090 |
3 | HG03831.hp1 NA18967.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1145-736T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46832338 | |||||||
| chr6:46832591 | T | C | 1 | a0007c0007t0010g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1145-483T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46832591 | |||||||
| chr6:46832720 | T | C | 116 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(113): Show |
130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1145-354T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46832720 | |||||||
| chr6:46832831 | C | T | 1 | a0007c0007t0003g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1145-243C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46832831 | |||||||
| chr6:46833926 | A | G | 12 | a0002c0002t0002g0285 a0006c0005t0002g0052 a0006c0005t0003g0045 others(9): Show |
12 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1609+388A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46833926 | |||||||
| chr6:46833978 | AT | A | 88 | a0001c0001t0001g0158 a0001c0001t0001g0254 a0001c0001t0001g0269 others(85): Show |
97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1609+456delT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 46833978 | ||||||
| chr6:46834101 | C | T | 1 | a0007c0007t0004g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1610-477C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834101 | |||||||
| chr6:46834128 | G | A | 4 | a0009c0009t0001g0053 a0009c0009t0001g0054 a0009c0009t0001g0055 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1610-450G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834128 | |||||||
| chr6:46834226 | AT | A | 11 | a0001c0001t0006g0032 a0001c0001t0006g0033 a0005c0006t0003g0015 others(8): Show |
12 | HG00639.hp2 HG01175.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1610-339delT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 46834226 | ||||||
| chr6:46834227 | T | A | 52 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(49): Show |
59 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.1610-351T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834227 | |||||||
| chr6:46834275 | C | T | 1 | a0006c0005t0003g0047 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1610-303C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834275 | |||||||
| chr6:46834308 | G | A | 225 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(222): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1610-270G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834308 | |||||||
| chr6:46834385 | C | T | 1 | a0007c0007t0003g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1610-193C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834385 | |||||||
| chr6:46834426 | TTTATTTT others(12): Show |
T | 1 | a0007c0007t0003g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1610-149_1610-131d others(21): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 46834426 | ||||||
| chr6:46834431 | T | A | 1 | a0001c0001t0001g0011 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1610-147T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834431 | |||||||
| chr6:46834435 | ATATT | A | 72 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(69): Show |
77 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.1610-97_1610-94del others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 46834435 | ||||||
| chr6:46834435 | ATATTTAT others(1): Show |
A | 62 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(59): Show |
67 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.1610-101_1610-94de others(9): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 46834435 | ||||||
| chr6:46834435 | ATATTTAT others(5): Show |
A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0067 others(6): Show |
11 | HG00544.hp2 HG01106.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1610-105_1610-94de others(13): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 46834435 | ||||||
| chr6:46834435 | ATATTTAT others(9): Show |
A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0226 a0001c0001t0001g0260 |
3 | HG01891.hp2 NA18948.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1610-109_1610-94de others(17): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 46834435 | ||||||
| chr6:46834435 | ATATTTAT others(13): Show |
A | 99 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(96): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1610-113_1610-94de others(21): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 46834435 | ||||||
| chr6:46834443 | T | A | 1 | a0001c0001t0001g0011 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1610-135T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834443 | |||||||
| chr6:46834453 | A | T | 1 | a0007c0007t0003g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1610-125A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834453 | |||||||
| chr6:46834455 | T | A | 1 | a0007c0007t0003g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1610-123T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834455 | |||||||
| chr6:46834520 | A | C | 1 | a0007c0007t0004g0037 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1610-58A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834520 | |||||||
| chr6:46834767 | TTCCTGAG others(7): Show |
T | 3 | a0005c0006t0003g0081 a0005c0006t0003g0082 a0005c0006t0003g0127 |
3 | HG01069.hp1 HG01071.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1783+21_1783+34del others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 46834767 | ||||||
| chr6:46834833 | C | T | 29 | a0004c0004t0003g0030 a0004c0004t0003g0034 a0004c0004t0003g0035 others(26): Show |
29 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1783+82C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 12/13 | chr6 | 46834833 | |||||||
| chr6:46834850 | G | T | 1 | a0002c0002t0002g0277 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1783+99G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 12/13 | chr6 | 46834850 | |||||||
| chr6:46834867 | T | C | 3 | a0004c0004t0003g0030 a0004c0004t0003g0034 a0004c0004t0003g0035 |
3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1783+116T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 12/13 | chr6 | 46834867 | |||||||
| chr6:46834901 | C | T | 1 | a0002c0020t0002g0143 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1783+150C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 12/13 | chr6 | 46834901 | |||||||
| chr6:46835041 | G | A | 6 | a0006c0005t0002g0052 a0006c0005t0003g0045 a0006c0005t0003g0046 others(3): Show |
6 | HG02056.hp2 HG02109.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1784-208G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 12/13 | chr6 | 46835041 | |||||||
| chr6:46835164 | G | C | 133 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(130): Show |
153 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1784-85G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 12/13 | chr6 | 46835164 | |||||||
| chr6:46835603 | T | A | 1 | a0002c0002t0002g0195 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2084+54T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46835603 | |||||||
| chr6:46835608 | G | A | 81 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(78): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.2084+59G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46835608 | |||||||
| chr6:46835673 | G | A | 1 | a0007c0007t0003g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2084+124G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46835673 | |||||||
| chr6:46835748 | C | T | 1 | a0003c0003t0003g0125 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2084+199C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46835748 | |||||||
| chr6:46835778 | C | T | 2 | a0002c0002t0002g0141 a0002c0002t0002g0142 |
2 | HG01261.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2084+229C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46835778 | |||||||
| chr6:46835872 | T | C | 77 | a0001c0001t0001g0066 a0001c0001t0001g0265 a0001c0001t0001g0267 others(74): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.2084+323T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46835872 | |||||||
| chr6:46835877 | G | A | 4 | a0009c0009t0001g0053 a0009c0009t0001g0054 a0009c0009t0001g0055 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2084+328G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46835877 | |||||||
| chr6:46835976 | AT | A | 3 | a0009c0009t0001g0053 a0009c0009t0001g0055 a0009c0009t0001g0056 |
3 | HG02280.hp1 HG02896.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2084+429delT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 46835976 | ||||||
| chr6:46836487 | C | T | 1 | a0002c0002t0002g0181 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2084+938C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46836487 | |||||||
| chr6:46836591 | T | C | 1 | a0002c0002t0002g0188 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2084+1042T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46836591 | |||||||
| chr6:46836690 | G | T | 6 | a0001c0001t0005g0070 a0001c0001t0005g0071 a0001c0001t0005g0072 others(3): Show |
6 | HG02486.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2084+1141G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46836690 | |||||||
| chr6:46836739 | C | G | 1 | a0002c0002t0002g0286 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2084+1190C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46836739 | |||||||
| chr6:46836775 | G | A | 2 | a0001c0001t0001g0236 a0001c0001t0001g0247 |
2 | NA18946.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2084+1226G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46836775 | |||||||
| chr6:46836793 | A | AT | 73 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(70): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.2084+1260dupT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 46836793 | ||||||
| chr6:46836793 | AT | A | 124 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(121): Show |
139 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.2084+1260delT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 46836793 | ||||||
| chr6:46836873 | G | C | 1 | a0003c0003t0011g0084 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2084+1324G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46836873 | |||||||
| chr6:46836896 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0243 a0001c0001t0001g0245 others(1): Show |
6 | NA18950.hp2 NA18990.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.2084+1347G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46836896 | |||||||
| chr6:46836968 | T | A | 4 | a0004c0004t0003g0030 a0004c0004t0003g0034 a0004c0004t0003g0035 others(1): Show |
4 | HG01891.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2084+1419T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46836968 | |||||||
| chr6:46837071 | T | C | 1 | a0007c0017t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2084+1522T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837071 | |||||||
| chr6:46837229 | T | A | 3 | a0006c0005t0003g0133 a0006c0005t0003g0134 a0006c0005t0003g0135 |
3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2084+1680T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837229 | |||||||
| chr6:46837249 | G | A | 83 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0013 others(80): Show |
92 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.2084+1700G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837249 | |||||||
| chr6:46837265 | T | C | 5 | a0001c0001t0001g0211 a0009c0009t0001g0053 a0009c0009t0001g0054 others(2): Show |
5 | HG02056.hp1 HG02280.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2085-1715T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837265 | |||||||
| chr6:46837267 | A | T | 217 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(214): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.2085-1713A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837267 | |||||||
| chr6:46837503 | C | T | 203 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(200): Show |
227 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.2085-1477C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837503 | |||||||
| chr6:46837666 | C | A | 203 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(200): Show |
227 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.2085-1314C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837666 | |||||||
| chr6:46837723 | A | G | 5 | a0002c0002t0002g0161 a0002c0002t0002g0162 a0002c0002t0002g0164 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.2085-1257A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837723 | |||||||
| chr6:46837762 | A | G | 217 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(214): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.2085-1218A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837762 | |||||||
| chr6:46837791 | C | A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0309 a0001c0001t0001g0310 |
3 | HG02602.hp2 HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2085-1189C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837791 | |||||||
| chr6:46837803 | C | T | 4 | a0009c0009t0001g0053 a0009c0009t0001g0054 a0009c0009t0001g0055 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2085-1177C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837803 | |||||||
| chr6:46837832 | A | T | 1 | a0001c0001t0001g0224 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2085-1148A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837832 | |||||||
| chr6:46837842 | G | A | 4 | a0009c0009t0001g0053 a0009c0009t0001g0054 a0009c0009t0001g0055 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2085-1138G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837842 | |||||||
| chr6:46837895 | A | AT | 9 | a0001c0001t0001g0212 a0001c0001t0001g0243 a0002c0002t0002g0187 others(6): Show |
9 | HG02056.hp2 HG02280.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.2085-1071dupT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 46837895 | ||||||
| chr6:46837895 | AT | A | 11 | a0001c0001t0005g0070 a0001c0001t0005g0071 a0001c0001t0005g0072 others(8): Show |
11 | HG02486.hp1 HG02486.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2085-1071delT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 46837895 | ||||||
| chr6:46838017 | G | A | 3 | a0006c0005t0003g0133 a0006c0005t0003g0134 a0006c0005t0003g0135 |
3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2085-963G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46838017 | |||||||
| chr6:46838057 | A | AT | 6 | a0001c0001t0001g0241 a0001c0001t0001g0258 a0002c0002t0002g0185 others(3): Show |
6 | HG02970.hp2 NA18955.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.2085-907dupT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 46838057 | ||||||
| chr6:46838057 | AT | A | 25 | a0001c0001t0001g0169 a0001c0001t0001g0216 a0001c0001t0005g0070 others(22): Show |
31 | HG01099.hp2 HG01255.hp1 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.2085-907delT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 46838057 | ||||||
| chr6:46838131 | C | T | 1 | a0002c0002t0002g0288 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2085-849C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46838131 | |||||||
| chr6:46838331 | A | G | 202 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(199): Show |
226 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.2085-649A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46838331 | |||||||
| chr6:46838473 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2085-507T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46838473 | |||||||
| chr6:46838555 | G | GGTCTATA others(33): Show |
1 | a0002c0002t0002g0183 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2085-423_2085-384d others(42): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 46838555 | ||||||
| chr6:46838646 | G | A | 130 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
145 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.2085-334G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46838646 | |||||||
| chr6:46838884 | G | A | 7 | a0007c0007t0004g0036 a0007c0007t0004g0037 a0007c0007t0004g0038 others(4): Show |
7 | HG01243.hp2 HG01884.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2085-96G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46838884 | |||||||
| chr6:46838886 | G | A | 2 | a0002c0002t0002g0287 a0007c0017t0001g0051 |
2 | HG01099.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2085-94G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46838886 |