Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 135112 |
| ensemblid | ENSG00000111912.20 |
| hgncid | 21081 |
| symbol | NCOA7 |
| name | nuclear receptor coactivator 7 |
| refseq_nuc | NM_181782.5 |
| refseq_prot | NP_861447.3 |
| ensembl_nuc | ENST00000392477.7 |
| ensembl_prot | ENSP00000376269.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 125790960 |
| end | 125932034 |
| strand | + |
| ver | v1.2 |
| region | chr6:125790960-125932034 |
| region5000 | chr6:125785960-125937034 |
| regionname0 | NCOA7_chr6_125790960_125932034 |
| regionname5000 | NCOA7_chr6_125785960_125937034 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 942 | 127 | 25 | 28 | 54 | 7 | 13 | 48 | NCOA7_chr6_125785960_125937034 | NCOA7 | MDTKE others(937): Show |
chr6 | 125785960 | 125937034 |
| a0002 | 1/1 | 942 | 88 | 22 | 15 | 30 | 7 | 12 | 26 | NCOA7_chr6_125785960_125937034 | NCOA7 | MDTKE others(937): Show |
chr6 | 125785960 | 125937034 |
| a0003 | 0/0 | 942 | 47 | 19 | 3 | 19 | 2 | 4 | 16 | NCOA7_chr6_125785960_125937034 | NCOA7 | MDTKE others(937): Show |
chr6 | 125785960 | 125937034 |
| a0004 | 0/0 | 942 | 3 | 1 | 0 | 2 | 0 | 0 | 2 | NCOA7_chr6_125785960_125937034 | NCOA7 | MDTKE others(937): Show |
chr6 | 125785960 | 125937034 |
| a0005 | 0/0 | 942 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | MDTKE others(937): Show |
chr6 | 125785960 | 125937034 |
| a0006 | 0/0 | 942 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | MDTKE others(937): Show |
chr6 | 125785960 | 125937034 |
| a0007 | 0/0 | 942 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | MDTKE others(937): Show |
chr6 | 125785960 | 125937034 |
| a0008 | 0/0 | 16 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | MDTKE others(11): Show |
chr6 | 125785960 | 125937034 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2826 | 124 | 23 | 28 | 54 | 7 | 12 | NCOA7_chr6_125785960_125937034 | NCOA7 | ATGGA others(2821): Show |
chr6 | 125785960 | 125937034 | ||
| a0001c0007 | 0/0 | 2826 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | ATGGA others(2821): Show |
chr6 | 125785960 | 125937034 | ||
| a0001c0009 | 0/0 | 2826 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | ATGGA others(2821): Show |
chr6 | 125785960 | 125937034 | ||
| a0001c0010 | 0/0 | 2826 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | ATGGA others(2821): Show |
chr6 | 125785960 | 125937034 | ||
| a0002c0002 | 1/1 | 2826 | 83 | 17 | 15 | 30 | 7 | 12 | NCOA7_chr6_125785960_125937034 | NCOA7 | ATGGA others(2821): Show |
chr6 | 125785960 | 125937034 | ||
| a0002c0004 | 0/0 | 2826 | 4 | 4 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | ATGGA others(2821): Show |
chr6 | 125785960 | 125937034 | ||
| a0002c0008 | 0/0 | 2826 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | ATGGA others(2821): Show |
chr6 | 125785960 | 125937034 | ||
| a0003c0003 | 0/0 | 2826 | 47 | 19 | 3 | 19 | 2 | 4 | NCOA7_chr6_125785960_125937034 | NCOA7 | ATGGA others(2821): Show |
chr6 | 125785960 | 125937034 | ||
| a0004c0005 | 0/0 | 2826 | 2 | 0 | 0 | 2 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | ATGGA others(2821): Show |
chr6 | 125785960 | 125937034 | ||
| a0004c0013 | 0/0 | 2826 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | ATGGA others(2821): Show |
chr6 | 125785960 | 125937034 | ||
| a0005c0006 | 0/0 | 2826 | 2 | 0 | 2 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | ATGGA others(2821): Show |
chr6 | 125785960 | 125937034 | ||
| a0006c0011 | 0/0 | 2826 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | ATGGA others(2821): Show |
chr6 | 125785960 | 125937034 | ||
| a0007c0012 | 0/0 | 2826 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | ATGGA others(2821): Show |
chr6 | 125785960 | 125937034 | ||
| a0008c0014 | 0/0 | 2826 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | ATGGA others(2821): Show |
chr6 | 125785960 | 125937034 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6264 | 77 | 4 | 23 | 32 | 6 | 12 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0001c0001t0002 | 0/0 | 6264 | 7 | 3 | 3 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0001c0001t0004 | 0/0 | 6265 | 19 | 4 | 1 | 14 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6260): Show |
chr6 | 125785960 | 125937034 |
| a0001c0001t0005 | 0/0 | 6265 | 5 | 3 | 1 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6260): Show |
chr6 | 125785960 | 125937034 |
| a0001c0001t0006 | 0/0 | 6264 | 5 | 5 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0001c0001t0007 | 0/0 | 6264 | 2 | 1 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0001c0001t0009 | 0/0 | 6265 | 3 | 0 | 0 | 3 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6260): Show |
chr6 | 125785960 | 125937034 |
| a0001c0001t0011 | 0/0 | 6265 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6260): Show |
chr6 | 125785960 | 125937034 |
| a0001c0001t0016 | 0/0 | 6264 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0001c0001t0017 | 0/0 | 6264 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0001c0001t0024 | 0/0 | 6264 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0001c0001t0025 | 0/0 | 6265 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6260): Show |
chr6 | 125785960 | 125937034 |
| a0001c0001t0026 | 0/0 | 6264 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0001c0007t0001 | 0/0 | 6264 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0001c0009t0022 | 0/0 | 6264 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0001c0010t0005 | 0/0 | 6265 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6260): Show |
chr6 | 125785960 | 125937034 |
| a0002c0002t0001 | 0/1 | 6264 | 13 | 5 | 3 | 1 | 2 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0002c0002t0002 | 1/0 | 6264 | 55 | 5 | 12 | 23 | 4 | 10 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0002c0002t0004 | 0/0 | 6265 | 2 | 1 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6260): Show |
chr6 | 125785960 | 125937034 |
| a0002c0002t0005 | 0/0 | 6265 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6260): Show |
chr6 | 125785960 | 125937034 |
| a0002c0002t0007 | 0/0 | 6264 | 2 | 1 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0002c0002t0008 | 0/0 | 6264 | 4 | 0 | 0 | 4 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0002c0002t0010 | 0/0 | 6264 | 2 | 2 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0002c0002t0011 | 0/0 | 6265 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6260): Show |
chr6 | 125785960 | 125937034 |
| a0002c0002t0012 | 0/0 | 6264 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0002c0002t0014 | 0/0 | 6264 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0002c0002t0023 | 0/0 | 6264 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0002c0004t0002 | 0/0 | 6264 | 4 | 4 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0002c0008t0015 | 0/0 | 6264 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0003c0003t0003 | 0/0 | 6253 | 43 | 17 | 3 | 17 | 2 | 4 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6248): Show |
chr6 | 125785960 | 125937034 |
| a0003c0003t0018 | 0/0 | 6253 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6248): Show |
chr6 | 125785960 | 125937034 |
| a0003c0003t0019 | 0/0 | 6253 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6248): Show |
chr6 | 125785960 | 125937034 |
| a0003c0003t0020 | 0/0 | 6253 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6248): Show |
chr6 | 125785960 | 125937034 |
| a0003c0003t0021 | 0/0 | 6253 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6248): Show |
chr6 | 125785960 | 125937034 |
| a0004c0005t0003 | 0/0 | 6253 | 2 | 0 | 0 | 2 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6248): Show |
chr6 | 125785960 | 125937034 |
| a0004c0013t0013 | 0/0 | 6253 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6248): Show |
chr6 | 125785960 | 125937034 |
| a0005c0006t0002 | 0/0 | 6264 | 2 | 0 | 2 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6259): Show |
chr6 | 125785960 | 125937034 |
| a0006c0011t0003 | 0/0 | 6253 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6248): Show |
chr6 | 125785960 | 125937034 |
| a0007c0012t0003 | 0/0 | 6253 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6248): Show |
chr6 | 125785960 | 125937034 |
| a0008c0014t0003 | 0/0 | 6253 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | GAGAG others(6248): Show |
chr6 | 125785960 | 125937034 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0005g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0005g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0006g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0006g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0007g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0009g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0009g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0009g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0011g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0016g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0017g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0024g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0025g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0001t0026g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0007t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0009t0022g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0001c0010t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0007g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0007g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0008g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0008g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0008g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0008g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0010g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0010g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0011g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0012g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0014g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0002t0023g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0004t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0004t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0004t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0004t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0002c0008t0015g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0018g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0019g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0020g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0003c0003t0021g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0004c0005t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0004c0005t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0004c0013t0013g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0005c0006t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0006c0011t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0007c0012t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| a0008c0014t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0180 | EUR | GBR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | GBR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0055 | EUR | GBR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | GBR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | FIN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00280 | hp2 | a0003 | c0003 | t0003 | g0051 | EUR | FIN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0228 | EUR | FIN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | FIN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0232 | EAS | CHS | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | CHS | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0063 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0214 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0079 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0087 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00738 | hp1 | a0005 | c0006 | t0002 | g0001 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0017 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01071 | hp2 | a0005 | c0006 | t0002 | g0001 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01106 | hp2 | a0003 | c0003 | t0003 | g0247 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0218 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0106 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01175 | hp1 | a0003 | c0003 | t0003 | g0138 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01192 | hp2 | a0003 | c0003 | t0003 | g0134 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0077 | AMR | CLM | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0071 | AMR | CLM | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0064 | AMR | CLM | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0181 | AMR | CLM | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0076 | AMR | CLM | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0145 | EUR | IBS | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01515 | hp2 | a0002 | c0002 | t0007 | g0154 | EUR | IBS | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0144 | EUR | IBS | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0153 | EUR | IBS | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01884 | hp1 | a0003 | c0003 | t0003 | g0147 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01891 | hp2 | a0001 | c0001 | t0026 | g0260 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0088 | AMR | PEL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PEL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0094 | AMR | PEL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02027 | hp2 | a0003 | c0003 | t0003 | g0119 | EAS | KHV | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0131 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02080 | hp1 | a0003 | c0003 | t0003 | g0116 | EAS | KHV | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | KHV | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | KHV | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02135 | hp2 | a0003 | c0003 | t0019 | g0210 | EAS | KHV | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02257 | hp1 | a0006 | c0011 | t0003 | g0129 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0267 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0237 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0233 | AMR | PEL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02523 | hp1 | a0007 | c0012 | t0003 | g0113 | EAS | KHV | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02523 | hp2 | a0002 | c0002 | t0023 | g0074 | EAS | KHV | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02572 | hp1 | a0002 | c0002 | t0010 | g0133 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0090 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02615 | hp1 | a0003 | c0003 | t0003 | g0035 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02615 | hp2 | a0002 | c0004 | t0002 | g0152 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02630 | hp1 | a0002 | c0004 | t0002 | g0028 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02630 | hp2 | a0003 | c0003 | t0003 | g0124 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02647 | hp1 | a0003 | c0003 | t0003 | g0130 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0085 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0053 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02717 | hp1 | a0003 | c0003 | t0003 | g0139 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02717 | hp2 | a0002 | c0002 | t0005 | g0252 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0049 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02723 | hp2 | a0003 | c0003 | t0020 | g0122 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02735 | hp2 | a0001 | c0007 | t0001 | g0047 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02809 | hp1 | a0003 | c0003 | t0003 | g0140 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02818 | hp1 | a0002 | c0002 | t0010 | g0141 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02818 | hp2 | a0003 | c0003 | t0003 | g0005 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0146 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02896 | hp2 | a0003 | c0003 | t0003 | g0030 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02922 | hp1 | a0002 | c0008 | t0015 | g0261 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02965 | hp1 | a0002 | c0004 | t0002 | g0161 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02965 | hp2 | a0001 | c0010 | t0005 | g0162 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02976 | hp1 | a0003 | c0003 | t0003 | g0034 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02976 | hp2 | a0001 | c0009 | t0022 | g0262 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03017 | hp1 | a0003 | c0003 | t0003 | g0109 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03041 | hp1 | a0002 | c0002 | t0007 | g0004 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03041 | hp2 | a0003 | c0003 | t0003 | g0029 | AFR | GWD | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03098 | hp1 | a0003 | c0003 | t0003 | g0149 | AFR | MSL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0016 | AFR | MSL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03139 | hp1 | a0003 | c0003 | t0003 | g0127 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0033 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03195 | hp1 | a0004 | c0013 | t0013 | g0263 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03195 | hp2 | a0003 | c0003 | t0003 | g0148 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0258 | AFR | MSL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03239 | hp1 | a0002 | c0002 | t0012 | g0143 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03239 | hp2 | a0003 | c0003 | t0003 | g0104 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | MSL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0259 | AFR | MSL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0057 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03490 | hp2 | a0003 | c0003 | t0003 | g0205 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0081 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0058 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03516 | hp1 | a0002 | c0002 | t0004 | g0137 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | ESN | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0082 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03669 | hp2 | a0008 | c0014 | t0003 | g0248 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0061 | SAS | BEB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0062 | SAS | BEB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0084 | SAS | BEB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0060 | SAS | STU | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | STU | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0222 | SAS | STU | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG04228 | hp2 | a0003 | c0003 | t0003 | g0249 | SAS | STU | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0037 | AFR | YRI | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18522 | hp2 | a0002 | c0004 | t0002 | g0031 | AFR | YRI | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | YRI | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18906 | hp2 | a0001 | c0001 | t0011 | g0158 | AFR | YRI | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18939 | hp2 | a0003 | c0003 | t0003 | g0115 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18940 | hp2 | a0002 | c0002 | t0008 | g0056 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18943 | hp1 | a0001 | c0001 | t0025 | g0010 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18943 | hp2 | a0001 | c0001 | t0024 | g0150 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18946 | hp1 | a0003 | c0003 | t0003 | g0208 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18946 | hp2 | a0001 | c0001 | t0007 | g0080 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18949 | hp1 | a0001 | c0001 | t0017 | g0246 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18950 | hp1 | a0003 | c0003 | t0003 | g0111 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18951 | hp2 | a0003 | c0003 | t0003 | g0217 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18960 | hp1 | a0003 | c0003 | t0021 | g0207 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18960 | hp2 | a0001 | c0001 | t0009 | g0187 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0156 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18968 | hp2 | a0002 | c0002 | t0008 | g0066 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0236 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18972 | hp2 | a0003 | c0003 | t0003 | g0078 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18973 | hp1 | a0003 | c0003 | t0003 | g0118 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18978 | hp1 | a0004 | c0005 | t0003 | g0027 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18986 | hp1 | a0001 | c0001 | t0005 | g0265 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18987 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18995 | hp1 | a0003 | c0003 | t0003 | g0125 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19000 | hp2 | a0003 | c0003 | t0003 | g0256 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19003 | hp1 | a0002 | c0002 | t0008 | g0052 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19003 | hp2 | a0001 | c0001 | t0009 | g0174 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19010 | hp1 | a0003 | c0003 | t0003 | g0117 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19010 | hp2 | a0002 | c0002 | t0008 | g0089 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19011 | hp2 | a0003 | c0003 | t0003 | g0206 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19055 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19055 | hp2 | a0003 | c0003 | t0003 | g0226 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19060 | hp2 | a0003 | c0003 | t0003 | g0112 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19062 | hp2 | a0002 | c0002 | t0004 | g0204 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19070 | hp2 | a0004 | c0005 | t0003 | g0021 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19077 | hp1 | a0003 | c0003 | t0003 | g0123 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19078 | hp1 | a0001 | c0001 | t0009 | g0189 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19078 | hp2 | a0003 | c0003 | t0003 | g0126 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19084 | hp2 | a0003 | c0003 | t0003 | g0251 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19240 | hp1 | a0003 | c0003 | t0003 | g0105 | AFR | YRI | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | YRI | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0070 | AFR | ASW | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA20129 | hp2 | a0003 | c0003 | t0018 | g0128 | AFR | ASW | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0227 | EUR | TSI | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | TSI | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA20805 | hp1 | a0003 | c0003 | t0003 | g0120 | EUR | TSI | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | TSI | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0234 | SAS | GIH | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | GIH | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0091 | AMR | CLM | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0050 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02109 | hp2 | a0003 | c0003 | t0003 | g0114 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02486 | hp1 | a0003 | c0003 | t0003 | g0019 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02486 | hp2 | a0001 | c0001 | t0016 | g0231 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0059 | AFR | ACB | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA20300 | hp1 | a0002 | c0002 | t0014 | g0015 | AFR | USA | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA20300 | hp2 | a0002 | c0002 | t0011 | g0048 | AFR | USA | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA21309 | hp1 | a0003 | c0003 | t0003 | g0142 | AFR | LWK | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0253 | AFR | LWK | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0151 | REF | REF | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0110 | REF | REF | NCOA7_chr6_125785960_125937034 | NCOA7 | chr6 | 125785960 | 125937034 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:125815403 | C | T | 1 | a0008 | 1 | HG03669.hp2 | stop_gained&splice_region_variant | HIGH | c.49C>T | p.Arg17* | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/16 | 221/6264 | 49/2829 | 17/942 | chr6 | 125815403 | |||
| chr6:125882430 | C | T | 1 | a0007 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.578C>T | p.Ala193Val | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/16 | 750/6264 | 578/2829 | 193/942 | chr6 | 125882430 | |||
| chr6:125889039 | A | C | 1 | a0006 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.985A>C | p.Asn329His | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 9/16 | 1157/6264 | 985/2829 | 329/942 | chr6 | 125889039 | |||
| chr6:125889249 | T | G | 2 | a0001 a0004 |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
missense_variant | MODERATE | c.1195T>G | p.Ser399Ala | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 9/16 | 1367/6264 | 1195/2829 | 399/942 | chr6 | 125889249 | |||
| chr6:125889651 | G | A | 1 | a0005 | 2 | HG00738.hp1 HG01071.hp2 |
missense_variant | MODERATE | c.1597G>A | p.Gly533Arg | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 9/16 | 1769/6264 | 1597/2829 | 533/942 | chr6 | 125889651 | |||
| chr6:125928768 | T | G | 5 | a0003 a0004 a0006 others(2): Show |
53 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(50): Show |
missense_variant | MODERATE | c.2826T>G | p.Asp942Glu | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 2998/6264 | 2826/2829 | 942/942 | chr6 | 125928768 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:125855023 | G | C | 1 | a0001c0007 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.54G>C | p.Leu18Leu | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/16 | 226/6264 | 54/2829 | 18/942 | chr6 | 125855023 | |||
| chr6:125881137 | A | G | 1 | a0004c0013 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.507A>G | p.Leu169Leu | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/16 | 679/6264 | 507/2829 | 169/942 | chr6 | 125881137 | |||
| chr6:125885332 | T | C | 1 | a0002c0008 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.873T>C | p.Asp291Asp | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/16 | 1045/6264 | 873/2829 | 291/942 | chr6 | 125885332 | |||
| chr6:125889140 | C | T | 1 | a0001c0010 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.1086C>T | p.Pro362Pro | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 9/16 | 1258/6264 | 1086/2829 | 362/942 | chr6 | 125889140 | |||
| chr6:125920999 | C | T | 1 | a0002c0004 | 4 | HG02615.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
synonymous_variant | LOW | c.2301C>T | p.Asp767Asp | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/16 | 2473/6264 | 2301/2829 | 767/942 | chr6 | 125920999 | |||
| chr6:125922720 | A | G | 1 | a0001c0009 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.2409A>G | p.Pro803Pro | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/16 | 2581/6264 | 2409/2829 | 803/942 | chr6 | 125922720 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:125790994 | G | A | 1 | a0002c0002t0012 | 1 | HG03239.hp1 | 5_prime_UTR_variant | MODIFIER | c.-138G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/16 | 24361 | chr6 | 125790994 | ||||||
| chr6:125815296 | C | T | 4 | a0001c0001t0006 a0001c0001t0011 a0001c0001t0026 others(1): Show |
8 | HG01891.hp2 HG02257.hp2 HG02723.hp1 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-59C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/16 | chr6 | 125815296 | |||||||
| chr6:125928810 | G | A | 1 | a0004c0013t0013 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*39G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 39 | chr6 | 125928810 | ||||||
| chr6:125929249 | T | A | 2 | a0002c0002t0014 a0002c0008t0015 |
2 | HG02922.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*478T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 478 | chr6 | 125929249 | ||||||
| chr6:125929249 | T | TA | 1 | a0001c0001t0009 | 3 | NA18960.hp2 NA19003.hp2 NA19078.hp1 |
3_prime_UTR_variant | MODIFIER | c.*478_*479insA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 479 | chr6 | 125929249 | ||||||
| chr6:125929250 | T | A | 9 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0016 others(6): Show |
99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*479T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 479 | chr6 | 125929250 | ||||||
| chr6:125929250 | T | TA | 13 | a0001c0001t0005 a0001c0010t0005 a0002c0002t0005 others(10): Show |
60 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*479_*480insA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 480 | chr6 | 125929250 | ||||||
| chr6:125929251 | T | A | 27 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(24): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*480T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 480 | chr6 | 125929251 | ||||||
| chr6:125929252 | T | A | 28 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(25): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*481T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 481 | chr6 | 125929252 | ||||||
| chr6:125929253 | A | T | 1 | a0002c0002t0008 | 4 | NA18940.hp2 NA18968.hp2 NA19003.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*482A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 482 | chr6 | 125929253 | ||||||
| chr6:125929285 | A | T | 1 | a0001c0001t0017 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*514A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 514 | chr6 | 125929285 | ||||||
| chr6:125929301 | C | T | 1 | a0001c0001t0016 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*530C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 530 | chr6 | 125929301 | ||||||
| chr6:125929306 | G | GT | 5 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0025 others(2): Show |
24 | HG00597.hp2 HG00639.hp2 HG02055.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*543dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 544 | INFO_REALIGN_3_PRIME | chr6 | 125929306 | |||||
| chr6:125929435 | G | A | 1 | a0003c0003t0018 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*664G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 664 | chr6 | 125929435 | ||||||
| chr6:125929436 | ATAGGTCT others(5): Show |
A | 10 | a0003c0003t0003 a0003c0003t0018 a0003c0003t0019 others(7): Show |
53 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*666_*677delTAGGTC others(6): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 666 | chr6 | 125929436 | ||||||
| chr6:125929581 | C | G | 1 | a0003c0003t0021 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*810C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 810 | chr6 | 125929581 | ||||||
| chr6:125929894 | T | A | 1 | a0001c0001t0025 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1123T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 1123 | chr6 | 125929894 | ||||||
| chr6:125930124 | G | A | 1 | a0001c0009t0022 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1353G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 1353 | chr6 | 125930124 | ||||||
| chr6:125930267 | G | A | 1 | a0003c0003t0019 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1496G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 1496 | chr6 | 125930267 | ||||||
| chr6:125931308 | T | A | 1 | a0002c0002t0010 | 2 | HG02572.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2537T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 2537 | chr6 | 125931308 | ||||||
| chr6:125931487 | T | C | 27 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(24): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*2716T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 2716 | chr6 | 125931487 | ||||||
| chr6:125931531 | C | A | 9 | a0001c0001t0024 a0003c0003t0003 a0003c0003t0018 others(6): Show |
52 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2760C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 2760 | chr6 | 125931531 | ||||||
| chr6:125931739 | G | C | 1 | a0002c0002t0014 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2968G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 16/16 | 2968 | chr6 | 125931739 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:125791120 | C | T | 1 | a0001c0001t0006g0267 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-65+53C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125791120 | |||||||
| chr6:125791178 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-65+111C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125791178 | |||||||
| chr6:125791238 | C | T | 2 | a0001c0001t0001g0264 a0001c0001t0005g0265 |
2 | NA18961.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-65+171C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125791238 | |||||||
| chr6:125791303 | T | C | 44 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0041 others(41): Show |
44 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.-65+236T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125791303 | |||||||
| chr6:125791309 | G | A | 3 | a0001c0001t0006g0049 a0001c0001t0007g0050 a0002c0002t0011g0048 |
3 | HG02109.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-65+242G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125791309 | |||||||
| chr6:125791810 | C | T | 1 | a0001c0001t0006g0267 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-65+743C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125791810 | |||||||
| chr6:125791974 | G | A | 2 | a0001c0001t0006g0049 a0002c0002t0011g0048 |
2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-65+907G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125791974 | |||||||
| chr6:125792009 | G | GTA | 44 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0041 others(41): Show |
44 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.-65+945_-65+946dup others(2): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125792009 | ||||||
| chr6:125792078 | A | T | 12 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(9): Show |
12 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-65+1011A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125792078 | |||||||
| chr6:125792205 | G | C | 1 | a0001c0001t0007g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-65+1138G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125792205 | |||||||
| chr6:125792245 | A | C | 6 | a0001c0001t0006g0258 a0001c0001t0006g0259 a0001c0001t0026g0260 others(3): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-65+1178A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125792245 | |||||||
| chr6:125792309 | A | G | 1 | a0001c0001t0006g0267 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-65+1242A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125792309 | |||||||
| chr6:125792327 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-65+1260A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125792327 | |||||||
| chr6:125792446 | A | G | 32 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(29): Show |
32 | HG00639.hp2 HG00741.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.-65+1379A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125792446 | |||||||
| chr6:125792578 | A | G | 44 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0041 others(41): Show |
44 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.-65+1511A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125792578 | |||||||
| chr6:125792676 | G | A | 54 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0041 others(51): Show |
54 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.-65+1609G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125792676 | |||||||
| chr6:125792725 | A | T | 2 | a0002c0002t0001g0255 a0003c0003t0003g0256 |
2 | NA18985.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-65+1658A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125792725 | |||||||
| chr6:125792778 | GA | G | 44 | a0001c0001t0001g0006 a0001c0001t0001g0041 a0001c0001t0001g0042 others(41): Show |
44 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.-65+1722delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125792778 | ||||||
| chr6:125793106 | A | G | 20 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(17): Show |
20 | HG00741.hp2 HG02055.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.-65+2039A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125793106 | |||||||
| chr6:125793151 | GA | G | 6 | a0001c0001t0006g0258 a0001c0001t0006g0259 a0001c0001t0026g0260 others(3): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-65+2091delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125793151 | ||||||
| chr6:125793507 | C | T | 2 | a0002c0002t0002g0253 a0002c0002t0005g0252 |
2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-65+2440C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125793507 | |||||||
| chr6:125793527 | T | A | 29 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(26): Show |
29 | HG00639.hp2 HG00741.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-65+2460T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125793527 | |||||||
| chr6:125793575 | C | G | 1 | a0003c0003t0003g0251 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-65+2508C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125793575 | |||||||
| chr6:125794006 | A | G | 1 | a0001c0001t0007g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-65+2939A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125794006 | |||||||
| chr6:125794072 | C | A | 4 | a0002c0002t0002g0016 a0002c0002t0002g0033 a0003c0003t0003g0034 others(1): Show |
4 | HG02615.hp1 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-65+3005C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125794072 | |||||||
| chr6:125794098 | C | G | 32 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(29): Show |
32 | HG00639.hp2 HG00741.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.-65+3031C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125794098 | |||||||
| chr6:125794237 | A | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0159 a0001c0001t0001g0165 others(97): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.-65+3170A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125794237 | |||||||
| chr6:125794675 | T | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0159 a0001c0001t0001g0165 others(97): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.-65+3608T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125794675 | |||||||
| chr6:125794949 | A | G | 1 | a0001c0001t0004g0032 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-65+3882A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125794949 | |||||||
| chr6:125794984 | C | CAT | 155 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.-65+3918_-65+3919i others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125794984 | ||||||
| chr6:125795131 | G | T | 32 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(29): Show |
32 | HG00639.hp2 HG00741.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.-65+4064G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125795131 | |||||||
| chr6:125795267 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0257 |
2 | HG01175.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.-65+4200G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125795267 | |||||||
| chr6:125795285 | G | C | 1 | a0001c0001t0006g0267 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-65+4218G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125795285 | |||||||
| chr6:125795422 | TC | T | 4 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0002c0002t0002g0002 others(1): Show |
5 | NA18949.hp2 NA18957.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-65+4359delC | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125795422 | ||||||
| chr6:125795608 | G | C | 44 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0041 others(41): Show |
44 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.-65+4541G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125795608 | |||||||
| chr6:125795718 | G | A | 1 | a0001c0001t0011g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-65+4651G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125795718 | |||||||
| chr6:125795722 | G | A | 1 | a0003c0003t0003g0051 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-65+4655G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125795722 | |||||||
| chr6:125795726 | C | T | 1 | a0002c0002t0002g0253 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-65+4659C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125795726 | |||||||
| chr6:125795742 | G | C | 1 | a0001c0001t0002g0160 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-65+4675G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125795742 | |||||||
| chr6:125795807 | A | G | 97 | a0001c0001t0001g0003 a0001c0001t0001g0159 a0001c0001t0001g0165 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.-65+4740A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125795807 | |||||||
| chr6:125795819 | C | T | 32 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(29): Show |
32 | HG00639.hp2 HG00741.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.-65+4752C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125795819 | |||||||
| chr6:125796028 | G | C | 1 | a0001c0001t0006g0037 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-65+4961G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796028 | |||||||
| chr6:125796038 | T | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | NA19000.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-65+4971T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796038 | |||||||
| chr6:125796081 | C | T | 1 | a0002c0004t0002g0152 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-65+5014C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796081 | |||||||
| chr6:125796095 | T | C | 13 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(10): Show |
13 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.-65+5028T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796095 | |||||||
| chr6:125796097 | C | G | 13 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(10): Show |
13 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.-65+5030C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796097 | |||||||
| chr6:125796106 | C | A | 1 | a0001c0001t0001g0168 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-65+5039C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796106 | |||||||
| chr6:125796146 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-65+5079C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796146 | |||||||
| chr6:125796187 | A | G | 1 | a0001c0001t0006g0267 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-65+5120A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796187 | |||||||
| chr6:125796230 | G | A | 20 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(17): Show |
20 | HG00741.hp2 HG02055.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.-65+5163G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796230 | |||||||
| chr6:125796337 | C | T | 13 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(10): Show |
13 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.-65+5270C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796337 | |||||||
| chr6:125796362 | A | T | 13 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(10): Show |
13 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.-65+5295A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796362 | |||||||
| chr6:125796364 | T | A | 3 | a0001c0001t0002g0039 a0001c0001t0004g0038 a0001c0001t0004g0040 |
3 | HG01243.hp2 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-65+5297T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796364 | |||||||
| chr6:125796457 | C | A | 14 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.-65+5390C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796457 | |||||||
| chr6:125796608 | C | A | 2 | a0001c0010t0005g0162 a0002c0004t0002g0161 |
2 | HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-65+5541C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796608 | |||||||
| chr6:125796633 | C | A | 7 | a0001c0001t0006g0258 a0001c0001t0006g0259 a0001c0001t0007g0050 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-65+5566C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796633 | |||||||
| chr6:125796656 | A | AT | 12 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0040 others(9): Show |
12 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-65+5605dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125796656 | ||||||
| chr6:125796656 | A | ATT | 10 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(7): Show |
10 | HG02630.hp1 HG02809.hp2 NA18978.hp1 others(7): Show |
intron_variant | MODIFIER | c.-65+5604_-65+5605d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125796656 | ||||||
| chr6:125796656 | A | G | 1 | a0001c0001t0024g0150 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-65+5589A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796656 | |||||||
| chr6:125796656 | AT | A | 14 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(11): Show |
14 | HG00639.hp2 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-65+5605delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125796656 | ||||||
| chr6:125796694 | G | A | 212 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(209): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-65+5627G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796694 | |||||||
| chr6:125796739 | C | T | 1 | a0001c0001t0006g0267 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-65+5672C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796739 | |||||||
| chr6:125796841 | G | C | 14 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.-65+5774G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125796841 | |||||||
| chr6:125797066 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(6): Show |
9 | HG00639.hp2 HG01884.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.-65+5999G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125797066 | |||||||
| chr6:125797131 | C | G | 5 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(2): Show |
5 | NA18949.hp1 NA18957.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.-65+6064C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125797131 | |||||||
| chr6:125797265 | T | C | 1 | a0003c0003t0003g0104 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-65+6198T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125797265 | |||||||
| chr6:125797272 | T | C | 23 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(20): Show |
23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-65+6205T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125797272 | |||||||
| chr6:125797395 | A | T | 6 | a0001c0001t0006g0258 a0001c0001t0006g0259 a0001c0001t0026g0260 others(3): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-65+6328A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125797395 | |||||||
| chr6:125797717 | A | G | 23 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(20): Show |
23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-65+6650A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125797717 | |||||||
| chr6:125797748 | G | A | 41 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(38): Show |
41 | HG00639.hp2 HG01884.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.-65+6681G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125797748 | |||||||
| chr6:125797795 | A | T | 6 | a0001c0001t0006g0258 a0001c0001t0006g0259 a0001c0001t0026g0260 others(3): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-65+6728A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125797795 | |||||||
| chr6:125797938 | A | G | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG02027.hp1 HG02080.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.-65+6871A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125797938 | |||||||
| chr6:125798393 | T | C | 1 | a0003c0003t0003g0105 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-65+7326T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125798393 | |||||||
| chr6:125798615 | T | G | 9 | a0001c0001t0006g0049 a0001c0001t0006g0258 a0001c0001t0006g0259 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-65+7548T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125798615 | |||||||
| chr6:125798676 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-65+7609G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125798676 | |||||||
| chr6:125798786 | T | C | 2 | a0001c0001t0006g0049 a0002c0002t0011g0048 |
2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-65+7719T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125798786 | |||||||
| chr6:125798922 | C | T | 2 | a0001c0001t0001g0238 a0001c0001t0005g0237 |
2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-65+7855C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125798922 | |||||||
| chr6:125799089 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(6): Show |
9 | HG00639.hp2 HG01884.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.-65+8022C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125799089 | |||||||
| chr6:125799260 | C | CT | 9 | a0001c0001t0006g0049 a0001c0001t0006g0258 a0001c0001t0006g0259 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-65+8195dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125799260 | ||||||
| chr6:125799282 | C | T | 23 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(20): Show |
23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-65+8215C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125799282 | |||||||
| chr6:125799366 | G | C | 1 | a0001c0001t0001g0170 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-65+8299G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125799366 | |||||||
| chr6:125799443 | CT | C | 170 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0054 others(167): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-65+8392delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125799443 | ||||||
| chr6:125799479 | G | A | 2 | a0001c0001t0004g0038 a0001c0001t0004g0040 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-65+8412G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125799479 | |||||||
| chr6:125799567 | A | G | 23 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(20): Show |
23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-65+8500A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125799567 | |||||||
| chr6:125799568 | T | G | 1 | a0001c0010t0005g0162 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-65+8501T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125799568 | |||||||
| chr6:125799643 | G | T | 1 | a0001c0007t0001g0047 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-65+8576G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125799643 | |||||||
| chr6:125799684 | C | T | 66 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0001g0083 others(63): Show |
68 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.-65+8617C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125799684 | |||||||
| chr6:125799844 | G | A | 156 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(153): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.-65+8777G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125799844 | |||||||
| chr6:125799882 | A | G | 1 | a0002c0002t0001g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-65+8815A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125799882 | |||||||
| chr6:125800201 | A | G | 1 | a0001c0001t0011g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-65+9134A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800201 | |||||||
| chr6:125800228 | C | T | 5 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0002c0004t0002g0031 others(2): Show |
5 | HG02055.hp2 HG02486.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-65+9161C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800228 | |||||||
| chr6:125800384 | G | A | 23 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(20): Show |
23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-65+9317G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800384 | |||||||
| chr6:125800441 | T | G | 1 | a0001c0001t0001g0171 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-65+9374T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800441 | |||||||
| chr6:125800458 | T | C | 1 | a0002c0002t0002g0107 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-65+9391T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800458 | |||||||
| chr6:125800516 | C | T | 1 | a0002c0002t0002g0253 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-65+9449C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800516 | |||||||
| chr6:125800598 | G | C | 1 | a0002c0002t0002g0055 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-65+9531G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800598 | |||||||
| chr6:125800704 | A | G | 1 | a0001c0001t0016g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-65+9637A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800704 | |||||||
| chr6:125800730 | T | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0054 others(196): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.-65+9663T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800730 | |||||||
| chr6:125800843 | A | G | 23 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(20): Show |
23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-65+9776A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800843 | |||||||
| chr6:125800886 | G | A | 1 | a0001c0001t0016g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-65+9819G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125800886 | |||||||
| chr6:125801082 | C | T | 1 | a0001c0001t0006g0267 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-65+10015C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125801082 | |||||||
| chr6:125801083 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-65+10016G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125801083 | |||||||
| chr6:125801134 | C | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0159 others(84): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.-65+10067C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125801134 | |||||||
| chr6:125801418 | A | G | 13 | a0002c0002t0002g0107 a0002c0002t0002g0144 a0002c0002t0002g0145 others(10): Show |
13 | HG01175.hp1 HG01515.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.-65+10351A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125801418 | |||||||
| chr6:125801471 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(6): Show |
9 | HG00639.hp2 HG01884.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.-65+10404G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125801471 | |||||||
| chr6:125801731 | T | G | 2 | a0003c0003t0003g0147 a0003c0003t0003g0148 |
2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-65+10664T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125801731 | |||||||
| chr6:125801819 | A | C | 1 | a0001c0001t0006g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-65+10752A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125801819 | |||||||
| chr6:125801887 | C | T | 9 | a0002c0002t0002g0095 a0002c0002t0002g0096 a0002c0002t0002g0097 others(6): Show |
9 | NA18944.hp1 NA18978.hp2 NA18982.hp2 others(6): Show |
intron_variant | MODIFIER | c.-65+10820C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125801887 | |||||||
| chr6:125802157 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-65+11090A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125802157 | |||||||
| chr6:125802187 | A | G | 6 | a0001c0001t0006g0258 a0001c0001t0006g0259 a0001c0001t0026g0260 others(3): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-65+11120A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125802187 | |||||||
| chr6:125802270 | G | A | 1 | a0001c0001t0006g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-65+11203G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125802270 | |||||||
| chr6:125802338 | C | G | 1 | a0002c0002t0001g0094 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-65+11271C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125802338 | |||||||
| chr6:125802658 | T | G | 1 | a0002c0008t0015g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-65+11591T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125802658 | |||||||
| chr6:125802875 | T | A | 1 | a0001c0001t0011g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-65+11808T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125802875 | |||||||
| chr6:125802890 | A | G | 23 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(20): Show |
23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-65+11823A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125802890 | |||||||
| chr6:125803012 | A | G | 1 | a0001c0001t0006g0267 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-65+11945A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125803012 | |||||||
| chr6:125803024 | G | C | 23 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(20): Show |
23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-65+11957G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125803024 | |||||||
| chr6:125803359 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-64-11932T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125803359 | |||||||
| chr6:125803648 | A | G | 1 | a0001c0001t0001g0229 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-64-11643A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125803648 | |||||||
| chr6:125803826 | C | T | 24 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(21): Show |
24 | HG00323.hp1 HG01884.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.-64-11465C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125803826 | |||||||
| chr6:125803944 | AT | A | 24 | a0001c0001t0004g0018 a0001c0001t0004g0022 a0001c0001t0004g0023 others(21): Show |
24 | HG01884.hp1 HG02486.hp1 HG02615.hp1 others(21): Show |
intron_variant | MODIFIER | c.-64-11335delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125803944 | ||||||
| chr6:125804075 | G | T | 1 | a0002c0002t0001g0228 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-64-11216G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125804075 | |||||||
| chr6:125804388 | A | G | 9 | a0001c0001t0006g0049 a0001c0001t0006g0258 a0001c0001t0006g0259 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-64-10903A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125804388 | |||||||
| chr6:125804443 | A | T | 1 | a0002c0002t0004g0137 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-64-10848A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125804443 | |||||||
| chr6:125804547 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-64-10744A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125804547 | |||||||
| chr6:125804672 | T | C | 1 | a0002c0002t0002g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-64-10619T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125804672 | |||||||
| chr6:125804880 | G | A | 1 | a0001c0001t0006g0037 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-64-10411G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125804880 | |||||||
| chr6:125805087 | C | CT | 99 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0086 others(96): Show |
100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.-64-10176dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125805087 | ||||||
| chr6:125805087 | C | CTT | 19 | a0001c0001t0001g0159 a0001c0001t0001g0168 a0001c0001t0001g0172 others(16): Show |
19 | HG00544.hp2 HG01192.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.-64-10177_-64-1017 others(6): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125805087 | ||||||
| chr6:125805087 | C | CTTT | 11 | a0001c0001t0001g0006 a0001c0001t0004g0009 a0001c0001t0004g0011 others(8): Show |
11 | HG00639.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-64-10178_-64-1017 others(7): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125805087 | ||||||
| chr6:125805087 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0002g0160 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-64-10194_-64-1017 others(23): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125805087 | ||||||
| chr6:125805087 | CT | C | 5 | a0001c0001t0001g0041 a0001c0007t0001g0047 a0002c0002t0007g0004 others(2): Show |
5 | HG00323.hp2 HG02735.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-64-10176delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125805087 | ||||||
| chr6:125805087 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0006g0049 a0002c0002t0011g0048 |
2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-64-10185_-64-1017 others(14): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125805087 | ||||||
| chr6:125805470 | G | A | 23 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(20): Show |
23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-64-9821G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125805470 | |||||||
| chr6:125805537 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-64-9754G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125805537 | |||||||
| chr6:125805606 | A | G | 1 | a0001c0001t0002g0160 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-64-9685A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125805606 | |||||||
| chr6:125805837 | A | G | 1 | a0002c0002t0002g0222 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-64-9454A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125805837 | |||||||
| chr6:125805866 | T | C | 1 | a0001c0001t0001g0264 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-64-9425T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125805866 | |||||||
| chr6:125806036 | G | A | 23 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(20): Show |
23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-64-9255G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125806036 | |||||||
| chr6:125806055 | T | C | 23 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(20): Show |
23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-64-9236T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125806055 | |||||||
| chr6:125806109 | G | C | 1 | a0002c0002t0002g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-64-9182G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125806109 | |||||||
| chr6:125806138 | C | G | 2 | a0002c0002t0007g0004 a0003c0003t0003g0005 |
2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-64-9153C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125806138 | |||||||
| chr6:125806147 | C | T | 23 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(20): Show |
23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-64-9144C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125806147 | |||||||
| chr6:125806270 | G | C | 1 | a0003c0003t0003g0138 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-64-9021G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125806270 | |||||||
| chr6:125806592 | C | T | 1 | a0001c0001t0011g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-64-8699C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125806592 | |||||||
| chr6:125806975 | G | A | 1 | a0002c0002t0002g0002 | 2 | NA19079.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-64-8316G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125806975 | |||||||
| chr6:125807106 | C | G | 23 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(20): Show |
23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-64-8185C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125807106 | |||||||
| chr6:125807358 | T | C | 1 | a0002c0002t0002g0107 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-64-7933T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125807358 | |||||||
| chr6:125807378 | G | A | 1 | a0002c0002t0002g0254 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-64-7913G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125807378 | |||||||
| chr6:125807464 | T | G | 1 | a0002c0002t0002g0254 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-64-7827T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125807464 | |||||||
| chr6:125807576 | A | C | 23 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(20): Show |
23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-64-7715A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125807576 | |||||||
| chr6:125807619 | T | G | 3 | a0001c0001t0006g0258 a0001c0001t0006g0259 a0001c0001t0026g0260 |
3 | HG01891.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-64-7672T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125807619 | |||||||
| chr6:125807670 | A | G | 3 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0002c0002t0010g0133 |
3 | HG01891.hp1 HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-64-7621A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125807670 | |||||||
| chr6:125807727 | T | A | 7 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0011 others(4): Show |
7 | HG00639.hp2 NA18940.hp1 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.-64-7564T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125807727 | |||||||
| chr6:125807951 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-64-7340C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125807951 | |||||||
| chr6:125807983 | A | G | 1 | a0001c0001t0002g0227 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-64-7308A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125807983 | |||||||
| chr6:125808207 | A | T | 3 | a0001c0001t0001g0083 a0002c0002t0002g0053 a0002c0002t0002g0082 |
3 | HG02698.hp1 HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-64-7084A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125808207 | |||||||
| chr6:125808389 | C | G | 1 | a0002c0002t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-64-6902C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125808389 | |||||||
| chr6:125808577 | T | G | 2 | a0002c0002t0002g0057 a0002c0002t0002g0058 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-64-6714T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125808577 | |||||||
| chr6:125808779 | G | A | 3 | a0002c0002t0002g0057 a0002c0002t0002g0058 a0002c0002t0002g0084 |
3 | HG03490.hp1 HG03492.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-64-6512G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125808779 | |||||||
| chr6:125808825 | C | T | 1 | a0003c0003t0003g0051 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-64-6466C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125808825 | |||||||
| chr6:125808968 | G | T | 1 | a0001c0001t0011g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-64-6323G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125808968 | |||||||
| chr6:125809022 | G | A | 10 | a0001c0001t0006g0049 a0001c0001t0006g0258 a0001c0001t0006g0259 others(7): Show |
10 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-64-6269G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125809022 | |||||||
| chr6:125809159 | G | C | 1 | a0001c0001t0011g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-64-6132G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125809159 | |||||||
| chr6:125809171 | G | C | 1 | a0001c0001t0011g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-64-6120G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125809171 | |||||||
| chr6:125809309 | C | T | 1 | a0002c0002t0010g0133 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-64-5982C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125809309 | |||||||
| chr6:125809502 | A | G | 5 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0002c0004t0002g0031 others(2): Show |
5 | HG02055.hp2 HG02486.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-64-5789A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125809502 | |||||||
| chr6:125809506 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-64-5785G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125809506 | |||||||
| chr6:125809671 | A | G | 1 | a0001c0001t0016g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-64-5620A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125809671 | |||||||
| chr6:125810009 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-64-5282C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125810009 | |||||||
| chr6:125810217 | G | A | 10 | a0001c0001t0006g0049 a0001c0001t0006g0258 a0001c0001t0006g0259 others(7): Show |
10 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-64-5074G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125810217 | |||||||
| chr6:125810466 | C | T | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-64-4825C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125810466 | |||||||
| chr6:125810504 | G | A | 1 | a0002c0002t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-64-4787G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125810504 | |||||||
| chr6:125810561 | A | G | 3 | a0002c0002t0001g0181 a0002c0002t0002g0180 a0002c0002t0002g0218 |
3 | HG00099.hp1 HG01109.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-64-4730A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125810561 | |||||||
| chr6:125810636 | T | C | 2 | a0002c0002t0002g0095 a0002c0002t0002g0096 |
2 | NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-64-4655T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125810636 | |||||||
| chr6:125810792 | G | A | 35 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(32): Show |
35 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.-64-4499G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125810792 | |||||||
| chr6:125811071 | A | C | 1 | a0004c0005t0003g0027 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-64-4220A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125811071 | |||||||
| chr6:125811193 | C | T | 2 | a0001c0001t0006g0258 a0001c0001t0006g0259 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-64-4098C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125811193 | |||||||
| chr6:125811323 | G | A | 10 | a0001c0001t0006g0049 a0001c0001t0006g0258 a0001c0001t0006g0259 others(7): Show |
10 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-64-3968G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125811323 | |||||||
| chr6:125811538 | G | A | 25 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(22): Show |
25 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(22): Show |
intron_variant | MODIFIER | c.-64-3753G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125811538 | |||||||
| chr6:125811672 | G | C | 25 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(22): Show |
25 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(22): Show |
intron_variant | MODIFIER | c.-64-3619G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125811672 | |||||||
| chr6:125811859 | G | A | 1 | a0003c0003t0020g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-64-3432G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125811859 | |||||||
| chr6:125811877 | T | C | 1 | a0002c0002t0004g0137 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-64-3414T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125811877 | |||||||
| chr6:125811895 | G | A | 25 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(22): Show |
25 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(22): Show |
intron_variant | MODIFIER | c.-64-3396G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125811895 | |||||||
| chr6:125812243 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(189): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.-64-3048A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125812243 | |||||||
| chr6:125812335 | C | G | 1 | a0002c0002t0002g0107 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-64-2956C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125812335 | |||||||
| chr6:125812493 | T | C | 2 | a0001c0009t0022g0262 a0002c0008t0015g0261 |
2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-64-2798T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125812493 | |||||||
| chr6:125812667 | C | T | 1 | a0001c0001t0011g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-64-2624C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125812667 | |||||||
| chr6:125812677 | A | G | 10 | a0001c0001t0006g0049 a0001c0001t0006g0258 a0001c0001t0006g0259 others(7): Show |
10 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-64-2614A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125812677 | |||||||
| chr6:125812734 | T | C | 24 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(21): Show |
24 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.-64-2557T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125812734 | |||||||
| chr6:125812816 | C | T | 1 | a0003c0003t0003g0130 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-64-2475C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125812816 | |||||||
| chr6:125812918 | A | G | 1 | a0003c0003t0003g0217 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-64-2373A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125812918 | |||||||
| chr6:125812941 | C | G | 1 | a0002c0002t0001g0255 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-64-2350C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125812941 | |||||||
| chr6:125813204 | C | T | 1 | a0001c0001t0002g0227 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-64-2087C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125813204 | |||||||
| chr6:125813228 | A | G | 6 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(3): Show |
6 | NA18982.hp1 NA18985.hp2 NA19068.hp1 others(3): Show |
intron_variant | MODIFIER | c.-64-2063A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125813228 | |||||||
| chr6:125813449 | A | AT | 13 | a0001c0001t0002g0216 a0001c0001t0006g0049 a0001c0001t0006g0258 others(10): Show |
13 | HG01891.hp2 HG01981.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-64-1822dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125813449 | ||||||
| chr6:125813449 | AT | A | 8 | a0001c0001t0001g0235 a0001c0001t0004g0018 a0001c0001t0004g0020 others(5): Show |
8 | HG01517.hp2 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-64-1822delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125813449 | ||||||
| chr6:125813458 | T | C | 9 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(6): Show |
9 | HG00639.hp2 HG01884.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.-64-1833T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125813458 | |||||||
| chr6:125813669 | C | T | 1 | a0001c0001t0011g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-64-1622C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125813669 | |||||||
| chr6:125813755 | T | G | 1 | a0002c0002t0002g0055 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-64-1536T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125813755 | |||||||
| chr6:125813790 | G | A | 155 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(152): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.-64-1501G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125813790 | |||||||
| chr6:125813923 | A | ATTT | 201 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0054 others(198): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.-64-1366_-64-1365i others(5): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr6 | 125813923 | ||||||
| chr6:125814223 | T | C | 202 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0054 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-64-1068T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814223 | |||||||
| chr6:125814278 | C | T | 1 | a0001c0010t0005g0162 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-64-1013C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814278 | |||||||
| chr6:125814301 | T | C | 201 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0054 others(198): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.-64-990T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814301 | |||||||
| chr6:125814370 | G | A | 5 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0267 others(2): Show |
5 | HG02109.hp1 HG02257.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-64-921G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814370 | |||||||
| chr6:125814424 | G | A | 5 | a0001c0001t0006g0258 a0001c0001t0006g0259 a0001c0001t0026g0260 others(2): Show |
5 | HG01891.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-64-867G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814424 | |||||||
| chr6:125814434 | G | T | 1 | a0001c0001t0001g0215 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-64-857G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814434 | |||||||
| chr6:125814452 | C | G | 1 | a0002c0004t0002g0152 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-64-839C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814452 | |||||||
| chr6:125814591 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-64-700C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814591 | |||||||
| chr6:125814681 | A | G | 27 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(24): Show |
27 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-64-610A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814681 | |||||||
| chr6:125814702 | G | T | 26 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(23): Show |
26 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-64-589G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814702 | |||||||
| chr6:125814736 | A | G | 1 | a0002c0002t0001g0081 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-64-555A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814736 | |||||||
| chr6:125814747 | C | G | 72 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0001g0083 others(69): Show |
73 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.-64-544C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814747 | |||||||
| chr6:125814856 | A | G | 4 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0002c0002t0002g0002 others(1): Show |
5 | NA18949.hp2 NA18957.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-64-435A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814856 | |||||||
| chr6:125814963 | T | A | 1 | a0001c0001t0001g0042 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-64-328T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125814963 | |||||||
| chr6:125815031 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-64-260G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125815031 | |||||||
| chr6:125815127 | T | C | 9 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(6): Show |
9 | HG00639.hp2 HG01884.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.-64-164T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125815127 | |||||||
| chr6:125815137 | A | G | 1 | a0002c0002t0004g0137 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-64-154A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125815137 | |||||||
| chr6:125815279 | C | T | 23 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(20): Show |
23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-64-12C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 1/15 | chr6 | 125815279 | |||||||
| chr6:125815967 | A | C | 4 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0002c0002t0002g0002 others(1): Show |
5 | NA18949.hp2 NA18957.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.50+563A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125815967 | |||||||
| chr6:125816686 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.50+1282G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125816686 | |||||||
| chr6:125816768 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.50+1364A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125816768 | |||||||
| chr6:125816778 | C | A | 1 | a0002c0002t0002g0055 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.50+1374C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125816778 | |||||||
| chr6:125816861 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0007g0080 |
2 | NA18946.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.50+1457C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125816861 | |||||||
| chr6:125816886 | C | T | 3 | a0002c0004t0002g0031 a0002c0004t0002g0161 a0003c0003t0003g0019 |
3 | HG02486.hp1 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.50+1482C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125816886 | |||||||
| chr6:125816933 | T | A | 10 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(7): Show |
10 | HG00639.hp2 HG01884.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.50+1529T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125816933 | |||||||
| chr6:125816935 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0044 others(1): Show |
4 | HG00323.hp2 HG00738.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.50+1531C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125816935 | |||||||
| chr6:125816998 | A | G | 23 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0004g0022 others(20): Show |
23 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.50+1594A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125816998 | |||||||
| chr6:125817201 | G | T | 2 | a0001c0001t0002g0132 a0001c0001t0002g0136 |
2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.50+1797G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125817201 | |||||||
| chr6:125817472 | G | A | 1 | a0002c0002t0002g0107 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.50+2068G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125817472 | |||||||
| chr6:125817835 | T | C | 1 | a0001c0001t0004g0155 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.50+2431T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125817835 | |||||||
| chr6:125817936 | G | A | 1 | a0002c0002t0002g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.50+2532G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125817936 | |||||||
| chr6:125817941 | G | C | 3 | a0001c0001t0002g0039 a0001c0001t0004g0038 a0001c0001t0004g0040 |
3 | HG01243.hp2 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.50+2537G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125817941 | |||||||
| chr6:125817975 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.50+2571C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125817975 | |||||||
| chr6:125817980 | C | T | 1 | a0002c0008t0015g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50+2576C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125817980 | |||||||
| chr6:125818022 | C | G | 1 | a0002c0002t0004g0137 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.50+2618C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125818022 | |||||||
| chr6:125818062 | G | A | 1 | a0002c0002t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.50+2658G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125818062 | |||||||
| chr6:125818098 | T | C | 2 | a0001c0001t0004g0018 a0001c0001t0004g0020 |
2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.50+2694T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125818098 | |||||||
| chr6:125818589 | G | A | 2 | a0002c0002t0010g0133 a0002c0002t0010g0141 |
2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.50+3185G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125818589 | |||||||
| chr6:125818594 | AG | A | 4 | a0001c0001t0002g0160 a0002c0002t0007g0004 a0002c0008t0015g0261 others(1): Show |
4 | HG02280.hp2 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.50+3191delG | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125818594 | |||||||
| chr6:125818715 | A | G | 6 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0011g0158 others(3): Show |
6 | HG02055.hp2 HG02486.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.50+3311A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125818715 | |||||||
| chr6:125818871 | T | C | 1 | a0001c0009t0022g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.50+3467T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125818871 | |||||||
| chr6:125818873 | C | A | 1 | a0002c0002t0002g0253 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.50+3469C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125818873 | |||||||
| chr6:125818919 | A | T | 1 | a0003c0003t0003g0119 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.50+3515A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125818919 | |||||||
| chr6:125819046 | A | G | 1 | a0005c0006t0002g0001 | 2 | HG00738.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.50+3642A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125819046 | |||||||
| chr6:125819141 | A | T | 2 | a0001c0001t0002g0132 a0001c0001t0002g0136 |
2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.50+3737A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125819141 | |||||||
| chr6:125819239 | C | T | 155 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(152): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.50+3835C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125819239 | |||||||
| chr6:125819255 | A | G | 9 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(6): Show |
9 | HG00639.hp2 HG02922.hp1 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.50+3851A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125819255 | |||||||
| chr6:125819341 | A | G | 1 | a0002c0002t0002g0234 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.50+3937A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125819341 | |||||||
| chr6:125819551 | A | G | 160 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(157): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.50+4147A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125819551 | |||||||
| chr6:125819896 | C | G | 1 | a0001c0001t0007g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.50+4492C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125819896 | |||||||
| chr6:125820055 | T | C | 204 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0054 others(201): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.50+4651T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125820055 | |||||||
| chr6:125820198 | A | G | 2 | a0001c0001t0002g0132 a0001c0001t0002g0136 |
2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.50+4794A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125820198 | |||||||
| chr6:125820297 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.50+4893G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125820297 | |||||||
| chr6:125820424 | A | G | 19 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(16): Show |
19 | HG00639.hp2 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.50+5020A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125820424 | |||||||
| chr6:125820814 | A | G | 2 | a0003c0003t0003g0029 a0003c0003t0003g0030 |
2 | HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.50+5410A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125820814 | |||||||
| chr6:125820877 | G | T | 1 | a0002c0008t0015g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50+5473G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125820877 | |||||||
| chr6:125820914 | T | C | 201 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0054 others(198): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.50+5510T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125820914 | |||||||
| chr6:125820958 | T | C | 1 | a0001c0009t0022g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.50+5554T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125820958 | |||||||
| chr6:125821108 | T | C | 10 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0258 others(7): Show |
10 | HG01891.hp2 HG02257.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.50+5704T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125821108 | |||||||
| chr6:125821199 | G | C | 7 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(4): Show |
7 | NA18978.hp1 NA18982.hp1 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.50+5795G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125821199 | |||||||
| chr6:125821340 | G | A | 2 | a0002c0002t0007g0004 a0003c0003t0003g0005 |
2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.50+5936G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125821340 | |||||||
| chr6:125821430 | T | G | 202 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0054 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.50+6026T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125821430 | |||||||
| chr6:125821504 | G | C | 1 | a0003c0003t0003g0138 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.50+6100G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125821504 | |||||||
| chr6:125821507 | C | A | 2 | a0001c0001t0002g0132 a0001c0001t0002g0136 |
2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.50+6103C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125821507 | |||||||
| chr6:125821640 | T | C | 1 | a0001c0001t0002g0160 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.50+6236T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125821640 | |||||||
| chr6:125821700 | A | G | 3 | a0003c0003t0003g0127 a0003c0003t0003g0130 a0003c0003t0018g0128 |
3 | HG02647.hp1 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.50+6296A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125821700 | |||||||
| chr6:125821713 | C | A | 1 | a0002c0002t0002g0061 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.50+6309C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125821713 | |||||||
| chr6:125821755 | C | T | 2 | a0002c0002t0007g0004 a0003c0003t0003g0005 |
2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.50+6351C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125821755 | |||||||
| chr6:125822158 | C | T | 3 | a0001c0001t0006g0258 a0001c0001t0006g0259 a0001c0001t0026g0260 |
3 | HG01891.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.50+6754C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125822158 | |||||||
| chr6:125822225 | T | C | 1 | a0001c0001t0002g0160 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.50+6821T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125822225 | |||||||
| chr6:125822535 | A | G | 216 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(213): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.50+7131A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125822535 | |||||||
| chr6:125822612 | T | C | 4 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0267 others(1): Show |
4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.50+7208T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125822612 | |||||||
| chr6:125822619 | T | G | 2 | a0003c0003t0003g0029 a0003c0003t0003g0030 |
2 | HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.50+7215T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125822619 | |||||||
| chr6:125822641 | A | G | 1 | a0002c0002t0014g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.50+7237A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125822641 | |||||||
| chr6:125822898 | G | A | 16 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(13): Show |
16 | HG01884.hp1 HG02630.hp1 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.50+7494G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125822898 | |||||||
| chr6:125822935 | C | CA | 10 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0172 others(7): Show |
10 | HG00544.hp1 HG00544.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.50+7546dupA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125822935 | ||||||
| chr6:125822937 | A | G | 15 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(12): Show |
15 | HG01884.hp1 HG02630.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.50+7533A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125822937 | |||||||
| chr6:125822954 | C | A | 1 | a0001c0001t0001g0229 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.50+7550C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125822954 | |||||||
| chr6:125822994 | GA | G | 200 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0054 others(197): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.50+7600delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125822994 | ||||||
| chr6:125823178 | C | CG | 5 | a0003c0003t0003g0117 a0003c0003t0003g0118 a0003c0003t0003g0123 others(2): Show |
5 | NA18973.hp1 NA18995.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.50+7775dupG | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125823178 | ||||||
| chr6:125823244 | A | G | 10 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0258 others(7): Show |
10 | HG01891.hp2 HG02257.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.50+7840A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125823244 | |||||||
| chr6:125823803 | T | C | 3 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0004g0224 |
3 | NA18961.hp2 NA18987.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.50+8399T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125823803 | |||||||
| chr6:125824071 | T | A | 2 | a0003c0003t0003g0147 a0003c0003t0003g0148 |
2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.50+8667T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824071 | |||||||
| chr6:125824213 | T | A | 2 | a0001c0001t0004g0155 a0001c0001t0004g0156 |
2 | NA18949.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.50+8809T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824213 | |||||||
| chr6:125824221 | A | G | 2 | a0001c0001t0004g0155 a0001c0001t0004g0156 |
2 | NA18949.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.50+8817A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824221 | |||||||
| chr6:125824238 | C | A | 1 | a0001c0001t0001g0173 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.50+8834C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824238 | |||||||
| chr6:125824255 | A | T | 1 | a0002c0002t0002g0079 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.50+8851A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824255 | |||||||
| chr6:125824303 | A | T | 1 | a0003c0003t0003g0116 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.50+8899A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824303 | |||||||
| chr6:125824332 | C | T | 2 | a0002c0002t0007g0004 a0003c0003t0003g0005 |
2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.50+8928C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824332 | |||||||
| chr6:125824751 | A | C | 201 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0054 others(198): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.50+9347A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824751 | |||||||
| chr6:125824820 | G | C | 157 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(154): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.50+9416G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824820 | |||||||
| chr6:125824851 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.50+9447C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824851 | |||||||
| chr6:125824877 | G | A | 1 | a0001c0001t0016g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.50+9473G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824877 | |||||||
| chr6:125824918 | C | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0007t0001g0047 |
3 | HG01074.hp2 HG01123.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.50+9514C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824918 | |||||||
| chr6:125824934 | G | C | 1 | a0002c0002t0001g0255 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.50+9530G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125824934 | |||||||
| chr6:125825174 | C | CA | 21 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(18): Show |
21 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.50+9789dupA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125825174 | ||||||
| chr6:125825174 | C | CAA | 7 | a0001c0001t0001g0044 a0001c0001t0004g0018 a0001c0001t0004g0020 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.50+9788_50+9789dup others(2): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125825174 | ||||||
| chr6:125825174 | C | CAAA | 17 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(14): Show |
17 | HG01884.hp1 HG02630.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.50+9787_50+9789dup others(3): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125825174 | ||||||
| chr6:125825209 | A | C | 182 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0054 others(179): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.50+9805A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125825209 | |||||||
| chr6:125825239 | G | A | 170 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0054 others(167): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.50+9835G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125825239 | |||||||
| chr6:125825293 | G | A | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | NA18995.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.50+9889G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125825293 | |||||||
| chr6:125825565 | A | G | 80 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0001g0083 others(77): Show |
82 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.50+10161A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125825565 | |||||||
| chr6:125826051 | C | T | 85 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0041 others(82): Show |
86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.50+10647C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826051 | |||||||
| chr6:125826091 | C | T | 1 | a0002c0002t0002g0214 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.50+10687C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826091 | |||||||
| chr6:125826130 | A | T | 1 | a0001c0001t0002g0160 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.50+10726A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826130 | |||||||
| chr6:125826336 | G | GA | 15 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(12): Show |
15 | HG02615.hp1 HG02630.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.50+10945dupA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125826336 | ||||||
| chr6:125826336 | GA | G | 82 | a0001c0001t0001g0006 a0001c0001t0001g0073 a0001c0001t0001g0075 others(79): Show |
84 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.50+10945delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125826336 | ||||||
| chr6:125826350 | G | A | 1 | a0003c0003t0003g0019 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.50+10946G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826350 | |||||||
| chr6:125826369 | C | T | 1 | a0003c0003t0003g0140 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.50+10965C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826369 | |||||||
| chr6:125826413 | A | G | 15 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.50+11009A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826413 | |||||||
| chr6:125826459 | A | C | 1 | a0003c0003t0003g0115 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.50+11055A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826459 | |||||||
| chr6:125826771 | G | A | 1 | a0002c0002t0002g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.50+11367G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826771 | |||||||
| chr6:125826839 | G | T | 1 | a0004c0013t0013g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.50+11435G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826839 | |||||||
| chr6:125826926 | G | A | 1 | a0001c0001t0009g0187 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.50+11522G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826926 | |||||||
| chr6:125826928 | T | G | 83 | a0001c0001t0001g0006 a0001c0001t0001g0073 a0001c0001t0001g0075 others(80): Show |
85 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.50+11524T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826928 | |||||||
| chr6:125826972 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.50+11568C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125826972 | |||||||
| chr6:125827172 | G | A | 132 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0041 others(129): Show |
134 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.50+11768G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125827172 | |||||||
| chr6:125827188 | C | CA | 20 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0026g0260 others(17): Show |
20 | HG00738.hp2 HG01517.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.50+11812dupA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125827188 | ||||||
| chr6:125827188 | CA | C | 91 | a0001c0001t0001g0006 a0001c0001t0001g0073 a0001c0001t0001g0075 others(88): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.50+11812delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125827188 | ||||||
| chr6:125827188 | CAA | C | 6 | a0001c0001t0001g0178 a0001c0001t0002g0132 a0001c0001t0002g0136 others(3): Show |
6 | HG00741.hp2 HG01891.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.50+11811_50+11812d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125827188 | ||||||
| chr6:125827188 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0188 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.50+11801_50+11812d others(14): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125827188 | ||||||
| chr6:125827188 | CAAAAAAA others(6): Show |
C | 69 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0086 others(66): Show |
70 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.50+11800_50+11812d others(15): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125827188 | ||||||
| chr6:125827188 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0220 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.50+11799_50+11812d others(16): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125827188 | ||||||
| chr6:125827294 | A | G | 1 | a0002c0002t0010g0141 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.50+11890A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125827294 | |||||||
| chr6:125827475 | G | A | 1 | a0005c0006t0002g0001 | 2 | HG00738.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.50+12071G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125827475 | |||||||
| chr6:125827583 | A | G | 1 | a0002c0002t0014g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.50+12179A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125827583 | |||||||
| chr6:125827686 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.50+12282G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125827686 | |||||||
| chr6:125827828 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0045 |
2 | HG00738.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.50+12424A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125827828 | |||||||
| chr6:125827922 | T | A | 203 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(200): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.50+12518T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125827922 | |||||||
| chr6:125827981 | C | T | 132 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0041 others(129): Show |
134 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.50+12577C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125827981 | |||||||
| chr6:125828058 | C | T | 2 | a0001c0001t0006g0258 a0001c0001t0006g0259 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.50+12654C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125828058 | |||||||
| chr6:125828101 | G | A | 1 | a0003c0003t0003g0030 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.50+12697G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125828101 | |||||||
| chr6:125828163 | G | A | 4 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0267 others(1): Show |
4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.50+12759G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125828163 | |||||||
| chr6:125828281 | G | T | 2 | a0002c0002t0002g0087 a0002c0002t0002g0233 |
2 | HG00735.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.50+12877G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125828281 | |||||||
| chr6:125828478 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.50+13074G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125828478 | |||||||
| chr6:125828506 | C | A | 1 | a0002c0002t0014g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.50+13102C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125828506 | |||||||
| chr6:125828691 | G | A | 2 | a0002c0002t0001g0153 a0002c0002t0007g0154 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.50+13287G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125828691 | |||||||
| chr6:125828804 | T | C | 3 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 |
3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.50+13400T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125828804 | |||||||
| chr6:125828846 | C | T | 2 | a0003c0003t0003g0034 a0003c0003t0003g0035 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.50+13442C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125828846 | |||||||
| chr6:125829024 | A | G | 2 | a0002c0002t0007g0004 a0003c0003t0003g0005 |
2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.50+13620A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125829024 | |||||||
| chr6:125829350 | T | C | 6 | a0002c0002t0002g0144 a0002c0002t0002g0145 a0002c0002t0012g0143 others(3): Show |
6 | HG01175.hp1 HG01515.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.50+13946T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125829350 | |||||||
| chr6:125829414 | C | A | 1 | a0001c0001t0016g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.50+14010C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125829414 | |||||||
| chr6:125829766 | C | CT | 70 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0086 others(67): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.50+14362_50+14363i others(3): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125829766 | |||||||
| chr6:125829767 | A | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0086 others(67): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.50+14363A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125829767 | |||||||
| chr6:125829789 | C | T | 1 | a0002c0002t0002g0077 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.50+14385C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125829789 | |||||||
| chr6:125829854 | T | G | 70 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0086 others(67): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.50+14450T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125829854 | |||||||
| chr6:125829912 | C | G | 3 | a0002c0002t0002g0016 a0003c0003t0003g0034 a0003c0003t0003g0035 |
3 | HG02615.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.50+14508C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125829912 | |||||||
| chr6:125829954 | G | A | 7 | a0001c0001t0004g0065 a0002c0002t0002g0067 a0002c0002t0002g0068 others(4): Show |
7 | HG00597.hp2 HG02132.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.50+14550G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125829954 | |||||||
| chr6:125829959 | A | T | 1 | a0002c0002t0014g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.50+14555A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125829959 | |||||||
| chr6:125830258 | C | A | 1 | a0002c0002t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.50+14854C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125830258 | |||||||
| chr6:125830472 | T | C | 2 | a0002c0002t0002g0057 a0002c0002t0002g0058 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.50+15068T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125830472 | |||||||
| chr6:125830721 | T | TTA | 3 | a0001c0001t0004g0038 a0001c0001t0004g0040 a0003c0003t0003g0109 |
3 | HG03017.hp1 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.50+15333_50+15334d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830721 | ||||||
| chr6:125830721 | TTA | T | 16 | a0001c0001t0001g0006 a0001c0001t0001g0165 a0001c0001t0001g0166 others(13): Show |
16 | HG00639.hp2 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.50+15333_50+15334d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830721 | ||||||
| chr6:125830733 | A | ATGTGTGT others(3): Show |
3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0235 |
3 | HG03491.hp1 HG03492.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.50+15330_50+15331i others(12): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830733 | ||||||
| chr6:125830733 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.50+15329A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125830733 | |||||||
| chr6:125830735 | A | ATG | 10 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0185 others(7): Show |
10 | HG01109.hp2 HG01256.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.50+15332_50+15333i others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830735 | ||||||
| chr6:125830735 | A | ATGTG | 12 | a0001c0001t0001g0054 a0001c0001t0001g0183 a0001c0001t0001g0192 others(9): Show |
12 | HG00140.hp2 HG01069.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.50+15332_50+15333i others(6): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830735 | ||||||
| chr6:125830735 | A | ATGTGTG | 11 | a0001c0001t0001g0108 a0001c0001t0001g0171 a0001c0001t0001g0186 others(8): Show |
11 | HG00099.hp2 HG01074.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.50+15332_50+15333i others(8): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830735 | ||||||
| chr6:125830735 | A | ATGTGTGT others(1): Show |
5 | a0001c0001t0001g0086 a0001c0001t0001g0170 a0001c0001t0001g0172 others(2): Show |
5 | HG00642.hp2 HG01192.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.50+15332_50+15333i others(10): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830735 | ||||||
| chr6:125830735 | A | ATGTGTGT others(3): Show |
5 | a0001c0001t0001g0159 a0001c0001t0001g0198 a0001c0001t0001g0215 others(2): Show |
5 | HG00735.hp2 HG01243.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.50+15332_50+15333i others(12): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830735 | ||||||
| chr6:125830735 | A | ATGTGTGT others(5): Show |
6 | a0001c0001t0001g0003 a0001c0001t0001g0199 a0001c0001t0001g0200 others(3): Show |
7 | HG00544.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.50+15332_50+15333i others(14): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830735 | ||||||
| chr6:125830735 | A | ATGTGTGT others(7): Show |
2 | a0001c0001t0001g0201 a0001c0001t0001g0245 |
2 | HG03927.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.50+15332_50+15333i others(16): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830735 | ||||||
| chr6:125830735 | A | G | 7 | a0001c0001t0001g0121 a0001c0001t0001g0168 a0001c0001t0001g0188 others(4): Show |
7 | HG00597.hp1 HG01106.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.50+15331A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125830735 | |||||||
| chr6:125830735 | ATATGTGT others(5): Show |
A | 1 | a0001c0001t0016g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.50+15333_50+15344d others(14): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830735 | ||||||
| chr6:125830737 | A | ATG | 3 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0011g0158 |
3 | HG02055.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.50+15355_50+15356d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830737 | ||||||
| chr6:125830737 | A | ATGTGTGT others(9): Show |
1 | a0001c0001t0009g0187 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.50+15341_50+15356d others(18): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830737 | ||||||
| chr6:125830737 | A | G | 171 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0041 others(168): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.50+15333A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125830737 | |||||||
| chr6:125830739 | G | A | 1 | a0001c0001t0005g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.50+15335G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125830739 | |||||||
| chr6:125830751 | G | GTGTGTGT others(1): Show |
3 | a0001c0001t0006g0258 a0001c0001t0006g0259 a0001c0001t0026g0260 |
3 | HG01891.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.50+15354_50+15355i others(10): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830751 | ||||||
| chr6:125830753 | G | GTGTGTA | 11 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
11 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.50+15354_50+15355i others(8): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830753 | ||||||
| chr6:125830757 | G | GTA | 15 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(12): Show |
15 | HG02109.hp1 HG02615.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.50+15354_50+15355i others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830757 | ||||||
| chr6:125830759 | G | A | 76 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0001g0083 others(73): Show |
78 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.50+15355G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125830759 | |||||||
| chr6:125830759 | GTA | G | 4 | a0001c0001t0001g0238 a0001c0001t0005g0007 a0001c0001t0005g0237 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.50+15357_50+15358d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125830759 | ||||||
| chr6:125830761 | A | G | 181 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0041 others(178): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.50+15357A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125830761 | |||||||
| chr6:125831218 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.50+15814C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125831218 | |||||||
| chr6:125831338 | A | G | 12 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(9): Show |
12 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.50+15934A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125831338 | |||||||
| chr6:125831388 | T | A | 14 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(11): Show |
14 | HG02615.hp1 HG02630.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.50+15984T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125831388 | |||||||
| chr6:125831430 | T | C | 5 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0179 others(2): Show |
5 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.50+16026T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125831430 | |||||||
| chr6:125831526 | C | A | 3 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 |
3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.50+16122C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125831526 | |||||||
| chr6:125831649 | A | G | 102 | a0001c0001t0001g0006 a0001c0001t0001g0073 a0001c0001t0001g0075 others(99): Show |
104 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.50+16245A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125831649 | |||||||
| chr6:125831666 | TA | T | 9 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(6): Show |
9 | HG00639.hp2 HG03225.hp2 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.50+16267delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125831666 | ||||||
| chr6:125831708 | C | T | 2 | a0003c0003t0003g0147 a0003c0003t0003g0148 |
2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.50+16304C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125831708 | |||||||
| chr6:125831975 | A | G | 1 | a0002c0002t0014g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.50+16571A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125831975 | |||||||
| chr6:125832107 | T | C | 70 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0001g0083 others(67): Show |
72 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.50+16703T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125832107 | |||||||
| chr6:125832333 | C | T | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.50+16929C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125832333 | |||||||
| chr6:125832337 | A | G | 4 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0267 others(1): Show |
4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.50+16933A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125832337 | |||||||
| chr6:125832461 | A | G | 1 | a0002c0002t0002g0233 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.50+17057A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125832461 | |||||||
| chr6:125832470 | C | A | 1 | a0001c0001t0004g0008 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.50+17066C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125832470 | |||||||
| chr6:125832647 | G | T | 1 | a0002c0002t0001g0135 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.50+17243G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125832647 | |||||||
| chr6:125832664 | A | G | 3 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 |
3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.50+17260A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125832664 | |||||||
| chr6:125833018 | A | G | 12 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(9): Show |
12 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.50+17614A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125833018 | |||||||
| chr6:125833094 | G | C | 2 | a0002c0002t0002g0163 a0002c0002t0002g0254 |
2 | NA18963.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.50+17690G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125833094 | |||||||
| chr6:125833158 | T | C | 3 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 |
3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.50+17754T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125833158 | |||||||
| chr6:125833208 | A | G | 1 | a0004c0013t0013g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.50+17804A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125833208 | |||||||
| chr6:125833329 | G | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0086 others(67): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.50+17925G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125833329 | |||||||
| chr6:125833592 | G | A | 1 | a0003c0003t0019g0210 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.50+18188G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125833592 | |||||||
| chr6:125833593 | A | AG | 121 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0043 others(118): Show |
122 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.50+18196dupG | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125833593 | ||||||
| chr6:125833601 | A | G | 1 | a0001c0001t0009g0189 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.50+18197A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125833601 | |||||||
| chr6:125833799 | G | A | 1 | a0002c0002t0014g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.50+18395G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125833799 | |||||||
| chr6:125834088 | AT | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0086 others(68): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.50+18685delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125834088 | |||||||
| chr6:125834091 | A | G | 71 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0086 others(68): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.50+18687A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125834091 | |||||||
| chr6:125834156 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.50+18752T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125834156 | |||||||
| chr6:125834170 | CAA | C | 15 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.50+18768_50+18769d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125834170 | ||||||
| chr6:125834367 | A | G | 1 | a0001c0001t0009g0189 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.50+18963A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125834367 | |||||||
| chr6:125834381 | A | G | 1 | a0001c0001t0005g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.50+18977A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125834381 | |||||||
| chr6:125834433 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(6): Show |
9 | HG00639.hp2 HG03225.hp2 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.50+19029G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125834433 | |||||||
| chr6:125834843 | G | C | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.50+19439G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125834843 | |||||||
| chr6:125834848 | A | G | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.50+19444A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125834848 | |||||||
| chr6:125835203 | A | G | 3 | a0002c0002t0002g0163 a0002c0002t0002g0164 a0002c0002t0002g0254 |
3 | NA18951.hp1 NA18963.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.50+19799A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125835203 | |||||||
| chr6:125835307 | C | T | 1 | a0002c0008t0015g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.51-19713C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125835307 | |||||||
| chr6:125835353 | A | G | 1 | a0001c0001t0001g0195 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.51-19667A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125835353 | |||||||
| chr6:125835426 | T | C | 14 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(11): Show |
14 | HG02615.hp1 HG02630.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.51-19594T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125835426 | |||||||
| chr6:125835464 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.51-19556G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125835464 | |||||||
| chr6:125835601 | G | A | 1 | a0002c0002t0014g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.51-19419G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125835601 | |||||||
| chr6:125835797 | G | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0086 others(67): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.51-19223G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125835797 | |||||||
| chr6:125835807 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.51-19213G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125835807 | |||||||
| chr6:125835811 | G | A | 4 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0267 others(1): Show |
4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.51-19209G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125835811 | |||||||
| chr6:125835893 | G | A | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-19127G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125835893 | |||||||
| chr6:125836032 | C | T | 203 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(200): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.51-18988C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125836032 | |||||||
| chr6:125836082 | G | A | 1 | a0002c0002t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.51-18938G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125836082 | |||||||
| chr6:125836410 | A | G | 2 | a0003c0003t0003g0114 a0006c0011t0003g0129 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.51-18610A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125836410 | |||||||
| chr6:125836682 | G | A | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-18338G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125836682 | |||||||
| chr6:125836863 | G | T | 2 | a0001c0001t0001g0230 a0001c0001t0009g0174 |
2 | NA18964.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.51-18157G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125836863 | |||||||
| chr6:125837111 | G | C | 26 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(23): Show |
26 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.51-17909G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125837111 | |||||||
| chr6:125837210 | CT | C | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-17809delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125837210 | |||||||
| chr6:125837305 | G | A | 1 | a0002c0008t0015g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.51-17715G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125837305 | |||||||
| chr6:125837332 | G | A | 1 | a0003c0003t0003g0140 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.51-17688G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125837332 | |||||||
| chr6:125837449 | C | T | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-17571C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125837449 | |||||||
| chr6:125837604 | T | G | 1 | a0002c0002t0002g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.51-17416T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125837604 | |||||||
| chr6:125837813 | C | T | 1 | a0003c0003t0003g0226 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.51-17207C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125837813 | |||||||
| chr6:125837971 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.51-17049T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125837971 | |||||||
| chr6:125838017 | C | G | 105 | a0001c0001t0001g0006 a0001c0001t0001g0073 a0001c0001t0001g0075 others(102): Show |
107 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.51-17003C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125838017 | |||||||
| chr6:125838038 | G | T | 2 | a0002c0002t0007g0004 a0003c0003t0003g0005 |
2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.51-16982G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125838038 | |||||||
| chr6:125838506 | G | A | 15 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.51-16514G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125838506 | |||||||
| chr6:125838595 | A | C | 1 | a0001c0001t0002g0039 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.51-16425A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125838595 | |||||||
| chr6:125838604 | G | T | 3 | a0001c0001t0001g0191 a0001c0001t0001g0197 a0001c0001t0001g0250 |
3 | HG02132.hp2 NA18939.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.51-16416G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125838604 | |||||||
| chr6:125838924 | G | A | 1 | a0002c0002t0002g0254 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.51-16096G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125838924 | |||||||
| chr6:125839101 | C | T | 1 | a0002c0002t0005g0252 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.51-15919C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125839101 | |||||||
| chr6:125839188 | G | A | 15 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.51-15832G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125839188 | |||||||
| chr6:125839447 | G | C | 12 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(9): Show |
12 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.51-15573G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125839447 | |||||||
| chr6:125839472 | C | T | 6 | a0002c0002t0001g0135 a0003c0003t0003g0134 a0003c0003t0003g0139 others(3): Show |
6 | HG01192.hp2 HG01884.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.51-15548C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125839472 | |||||||
| chr6:125839537 | C | T | 1 | a0002c0002t0002g0055 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.51-15483C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125839537 | |||||||
| chr6:125839570 | C | T | 1 | a0001c0001t0026g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.51-15450C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125839570 | |||||||
| chr6:125839682 | A | C | 220 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.51-15338A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125839682 | |||||||
| chr6:125839749 | A | T | 3 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 |
3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.51-15271A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125839749 | |||||||
| chr6:125839988 | C | G | 2 | a0003c0003t0003g0208 a0003c0003t0021g0207 |
2 | NA18946.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.51-15032C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125839988 | |||||||
| chr6:125840027 | G | A | 1 | a0002c0002t0002g0218 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.51-14993G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125840027 | |||||||
| chr6:125840230 | G | T | 1 | a0001c0001t0001g0178 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.51-14790G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125840230 | |||||||
| chr6:125840366 | GA | G | 3 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 |
3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.51-14648delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840366 | ||||||
| chr6:125840488 | T | C | 15 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.51-14532T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125840488 | |||||||
| chr6:125840576 | T | A | 1 | a0002c0002t0002g0061 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.51-14444T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125840576 | |||||||
| chr6:125840867 | GGTTTTTT others(10): Show |
G | 3 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0010t0005g0162 |
3 | HG02055.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.51-14152_51-14136d others(19): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125840867 | |||||||
| chr6:125840867 | GGTTTTTT others(11): Show |
G | 7 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0038 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.51-14152_51-14135d others(20): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125840867 | |||||||
| chr6:125840867 | GGTTTTTT others(14): Show |
G | 1 | a0001c0001t0005g0017 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.51-14152_51-14132d others(23): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125840867 | |||||||
| chr6:125840868 | G | GTT | 5 | a0001c0001t0004g0008 a0001c0001t0004g0013 a0002c0002t0004g0137 others(2): Show |
5 | HG02080.hp1 HG03516.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.51-14111_51-14110d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | G | GTTTTT | 9 | a0002c0002t0001g0255 a0002c0002t0002g0055 a0002c0002t0002g0057 others(6): Show |
10 | HG00140.hp1 HG00738.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.51-14114_51-14110d others(7): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | G | GTTTTTT | 17 | a0001c0001t0001g0073 a0001c0001t0001g0092 a0001c0001t0001g0209 others(14): Show |
17 | HG00544.hp1 HG01257.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.51-14115_51-14110d others(8): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | G | GTTTTTTT | 9 | a0001c0001t0001g0075 a0001c0001t0001g0083 a0001c0001t0004g0156 others(6): Show |
9 | HG02004.hp1 HG02293.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.51-14116_51-14110d others(9): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | G | GTTTTTTT others(2): Show |
5 | a0002c0002t0002g0016 a0002c0002t0002g0082 a0002c0002t0002g0101 others(2): Show |
5 | HG03098.hp2 HG03669.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.51-14118_51-14110d others(11): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | G | GTTTTTTT others(3): Show |
2 | a0001c0001t0004g0009 a0001c0001t0005g0085 |
2 | HG02647.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.51-14119_51-14110d others(12): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | G | GTTTTTTT others(4): Show |
3 | a0001c0001t0024g0150 a0002c0002t0002g0076 a0002c0002t0002g0214 |
3 | HG00642.hp1 HG01261.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.51-14120_51-14110d others(13): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | G | GTTTTTTT others(5): Show |
6 | a0002c0002t0001g0228 a0002c0002t0002g0061 a0002c0002t0002g0062 others(3): Show |
6 | HG00323.hp1 HG02293.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.51-14121_51-14110d others(14): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | G | GTTTTTTT others(6): Show |
5 | a0002c0002t0002g0060 a0002c0002t0002g0068 a0002c0002t0002g0087 others(2): Show |
5 | HG00735.hp1 HG01981.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.51-14122_51-14110d others(15): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | G | GTTTTTTT others(8): Show |
3 | a0002c0002t0002g0053 a0002c0002t0007g0004 a0003c0003t0003g0005 |
3 | HG02698.hp1 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.51-14124_51-14110d others(17): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | G | GTTTTTTT others(9): Show |
1 | a0002c0002t0002g0079 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.51-14125_51-14110d others(18): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | G | GTTTTTTT others(11): Show |
3 | a0001c0001t0006g0037 a0002c0002t0002g0095 a0002c0002t0002g0096 |
3 | NA18522.hp1 NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.51-14127_51-14110d others(20): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | G | GTTTTTTT others(12): Show |
1 | a0002c0002t0007g0154 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.51-14128_51-14110d others(21): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | G | GTTTTTTT others(13): Show |
1 | a0002c0002t0001g0153 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.51-14129_51-14110d others(22): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | G | GTTTTTTT others(22): Show |
1 | a0002c0002t0002g0098 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.51-14138_51-14110d others(31): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | GT | G | 23 | a0001c0001t0004g0011 a0001c0009t0022g0262 a0002c0002t0001g0181 others(20): Show |
23 | HG00099.hp1 HG00639.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.51-14110delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | GTT | G | 15 | a0001c0001t0001g0006 a0002c0002t0001g0059 a0002c0002t0001g0135 others(12): Show |
15 | HG00280.hp2 HG01192.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.51-14111_51-14110d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | GTTT | G | 13 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0025g0010 others(10): Show |
13 | HG01891.hp1 HG02145.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.51-14112_51-14110d others(5): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | GTTTT | G | 8 | a0001c0001t0002g0160 a0001c0001t0004g0065 a0001c0001t0004g0224 others(5): Show |
8 | HG00597.hp2 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.51-14113_51-14110d others(6): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | GTTTTTTT others(5): Show |
G | 2 | a0002c0002t0002g0063 a0002c0002t0005g0252 |
2 | HG00639.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.51-14121_51-14110d others(14): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | GTTTTTTT others(6): Show |
G | 3 | a0001c0001t0001g0044 a0003c0003t0003g0111 a0003c0003t0003g0115 |
3 | HG03831.hp1 NA18939.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.51-14122_51-14110d others(15): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | GTTTTTTT others(7): Show |
G | 11 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
12 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.51-14123_51-14110d others(16): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | GTTTTTTT others(8): Show |
G | 2 | a0001c0001t0006g0267 a0001c0001t0007g0050 |
2 | HG02109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.51-14124_51-14110d others(17): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | GTTTTTTT others(9): Show |
G | 2 | a0001c0001t0002g0039 a0001c0001t0026g0260 |
2 | HG01243.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.51-14125_51-14110d others(18): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | GTTTTTTT others(10): Show |
G | 4 | a0001c0001t0006g0258 a0001c0001t0006g0259 a0003c0003t0003g0139 others(1): Show |
4 | HG02717.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.51-14126_51-14110d others(19): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | GTTTTTTT others(11): Show |
G | 1 | a0004c0005t0003g0027 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.51-14127_51-14110d others(20): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | GTTTTTTT others(12): Show |
G | 7 | a0001c0001t0004g0022 a0001c0001t0004g0024 a0001c0001t0004g0025 others(4): Show |
7 | HG03490.hp2 NA18982.hp1 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.51-14128_51-14110d others(21): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | GTTTTTTT others(13): Show |
G | 17 | a0001c0001t0001g0086 a0001c0001t0001g0159 a0001c0001t0001g0168 others(14): Show |
17 | HG00642.hp2 HG01106.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.51-14129_51-14110d others(22): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | GTTTTTTT others(14): Show |
G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0108 others(52): Show |
56 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.51-14130_51-14110d others(23): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840868 | GTTTTTTT others(15): Show |
G | 1 | a0002c0002t0014g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.51-14131_51-14110d others(24): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125840868 | ||||||
| chr6:125840997 | A | G | 122 | a0001c0001t0001g0006 a0001c0001t0001g0073 a0001c0001t0001g0075 others(119): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.51-14023A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125840997 | |||||||
| chr6:125841026 | G | A | 1 | a0003c0003t0003g0030 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.51-13994G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841026 | |||||||
| chr6:125841136 | T | C | 150 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0041 others(147): Show |
152 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.51-13884T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841136 | |||||||
| chr6:125841137 | G | A | 14 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(11): Show |
14 | HG02615.hp1 HG02630.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.51-13883G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841137 | |||||||
| chr6:125841153 | G | A | 2 | a0003c0003t0003g0124 a0003c0003t0003g0149 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.51-13867G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841153 | |||||||
| chr6:125841179 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.51-13841C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841179 | |||||||
| chr6:125841186 | GGCC | G | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-13833_51-13831d others(5): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841186 | |||||||
| chr6:125841191 | A | AT | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-13829_51-13828i others(3): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841191 | |||||||
| chr6:125841192 | C | G | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-13828C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841192 | |||||||
| chr6:125841193 | C | T | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-13827C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841193 | |||||||
| chr6:125841212 | G | A | 3 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 |
3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.51-13808G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841212 | |||||||
| chr6:125841510 | G | A | 2 | a0001c0001t0004g0038 a0001c0001t0004g0040 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.51-13510G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841510 | |||||||
| chr6:125841551 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.51-13469C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841551 | |||||||
| chr6:125841991 | G | A | 1 | a0002c0002t0008g0066 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.51-13029G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125841991 | |||||||
| chr6:125842030 | TAA | T | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-12989_51-12988d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842030 | |||||||
| chr6:125842262 | C | T | 3 | a0002c0002t0001g0181 a0002c0002t0002g0180 a0002c0002t0002g0218 |
3 | HG00099.hp1 HG01109.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.51-12758C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842262 | |||||||
| chr6:125842294 | C | T | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-12726C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842294 | |||||||
| chr6:125842295 | G | T | 1 | a0001c0001t0001g0223 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.51-12725G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842295 | |||||||
| chr6:125842321 | T | C | 1 | a0004c0013t0013g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.51-12699T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842321 | |||||||
| chr6:125842391 | C | T | 93 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0001g0083 others(90): Show |
95 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.51-12629C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842391 | |||||||
| chr6:125842444 | C | T | 1 | a0002c0002t0012g0143 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.51-12576C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842444 | |||||||
| chr6:125842453 | A | G | 11 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
11 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.51-12567A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842453 | |||||||
| chr6:125842496 | G | A | 1 | a0002c0002t0002g0055 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.51-12524G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842496 | |||||||
| chr6:125842649 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.51-12371C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842649 | |||||||
| chr6:125842711 | T | C | 1 | a0001c0001t0001g0194 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.51-12309T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842711 | |||||||
| chr6:125842736 | C | T | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-12284C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842736 | |||||||
| chr6:125842794 | A | C | 2 | a0003c0003t0003g0124 a0003c0003t0003g0149 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.51-12226A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125842794 | |||||||
| chr6:125843030 | G | A | 1 | a0002c0002t0001g0059 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.51-11990G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125843030 | |||||||
| chr6:125843438 | G | C | 4 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0267 others(1): Show |
4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.51-11582G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125843438 | |||||||
| chr6:125843458 | T | C | 1 | a0001c0001t0017g0246 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.51-11562T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125843458 | |||||||
| chr6:125843558 | T | C | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-11462T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125843558 | |||||||
| chr6:125843674 | A | G | 1 | a0002c0002t0007g0004 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.51-11346A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125843674 | |||||||
| chr6:125843721 | G | A | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-11299G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125843721 | |||||||
| chr6:125843787 | C | G | 1 | a0002c0002t0002g0033 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.51-11233C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125843787 | |||||||
| chr6:125843857 | G | A | 133 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0041 others(130): Show |
135 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.51-11163G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125843857 | |||||||
| chr6:125843914 | C | T | 1 | a0002c0002t0014g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.51-11106C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125843914 | |||||||
| chr6:125844122 | A | C | 1 | a0002c0002t0005g0252 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.51-10898A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125844122 | |||||||
| chr6:125844254 | T | C | 1 | a0003c0003t0003g0142 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.51-10766T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125844254 | |||||||
| chr6:125844319 | G | A | 214 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.51-10701G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125844319 | |||||||
| chr6:125844574 | G | T | 131 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0041 others(128): Show |
133 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.51-10446G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125844574 | |||||||
| chr6:125844775 | C | A | 1 | a0001c0001t0001g0178 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.51-10245C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125844775 | |||||||
| chr6:125845166 | A | G | 1 | a0004c0005t0003g0027 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.51-9854A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125845166 | |||||||
| chr6:125845239 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.51-9781C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125845239 | |||||||
| chr6:125845272 | T | A | 1 | a0002c0002t0001g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.51-9748T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125845272 | |||||||
| chr6:125845504 | G | A | 12 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(9): Show |
12 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.51-9516G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125845504 | |||||||
| chr6:125845721 | C | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(69): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.51-9299C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125845721 | |||||||
| chr6:125845786 | G | A | 2 | a0002c0002t0002g0087 a0002c0002t0002g0233 |
2 | HG00735.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.51-9234G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125845786 | |||||||
| chr6:125845833 | C | T | 4 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0267 others(1): Show |
4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.51-9187C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125845833 | |||||||
| chr6:125845983 | A | G | 16 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(13): Show |
16 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.51-9037A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125845983 | |||||||
| chr6:125846305 | T | C | 1 | a0001c0009t0022g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.51-8715T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125846305 | |||||||
| chr6:125846326 | G | T | 75 | a0001c0001t0001g0075 a0001c0001t0001g0083 a0001c0001t0001g0092 others(72): Show |
77 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.51-8694G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125846326 | |||||||
| chr6:125846361 | A | T | 1 | a0002c0002t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.51-8659A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125846361 | |||||||
| chr6:125846361 | AT | A | 6 | a0001c0001t0006g0259 a0002c0002t0002g0145 a0002c0002t0007g0004 others(3): Show |
6 | HG01515.hp1 HG02109.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.51-8641delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125846361 | ||||||
| chr6:125846361 | ATT | A | 33 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(30): Show |
33 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.51-8642_51-8641del others(2): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125846361 | ||||||
| chr6:125846361 | ATTT | A | 92 | a0001c0001t0001g0006 a0001c0001t0001g0075 a0001c0001t0001g0083 others(89): Show |
94 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.51-8643_51-8641del others(3): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125846361 | ||||||
| chr6:125846361 | ATTTT | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(72): Show |
76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.51-8644_51-8641del others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125846361 | ||||||
| chr6:125846363 | T | A | 3 | a0001c0001t0006g0259 a0002c0002t0007g0004 a0003c0003t0003g0005 |
3 | HG02818.hp2 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.51-8657T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125846363 | |||||||
| chr6:125846364 | T | A | 26 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(23): Show |
26 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.51-8656T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125846364 | |||||||
| chr6:125846365 | T | A | 18 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(15): Show |
18 | HG00639.hp2 HG02280.hp1 HG03225.hp1 others(15): Show |
intron_variant | MODIFIER | c.51-8655T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125846365 | |||||||
| chr6:125847078 | A | G | 2 | a0001c0001t0026g0260 a0004c0013t0013g0263 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.51-7942A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125847078 | |||||||
| chr6:125847113 | T | A | 1 | a0001c0001t0001g0191 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.51-7907T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125847113 | |||||||
| chr6:125847154 | A | G | 1 | a0007c0012t0003g0113 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.51-7866A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125847154 | |||||||
| chr6:125847355 | T | C | 1 | a0002c0002t0002g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.51-7665T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125847355 | |||||||
| chr6:125847459 | C | T | 203 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(200): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.51-7561C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125847459 | |||||||
| chr6:125847590 | G | A | 1 | a0001c0001t0007g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.51-7430G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125847590 | |||||||
| chr6:125847792 | A | G | 4 | a0001c0001t0001g0073 a0001c0001t0001g0168 a0001c0001t0001g0225 others(1): Show |
4 | NA18943.hp2 NA18950.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.51-7228A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125847792 | |||||||
| chr6:125848093 | C | A | 2 | a0001c0001t0006g0258 a0001c0001t0006g0259 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.51-6927C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125848093 | |||||||
| chr6:125848102 | AC | A | 4 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0267 others(1): Show |
4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.51-6916delC | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125848102 | ||||||
| chr6:125848443 | G | A | 4 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 others(1): Show |
4 | HG01891.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.51-6577G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125848443 | |||||||
| chr6:125848488 | A | G | 1 | a0001c0009t0022g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.51-6532A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125848488 | |||||||
| chr6:125848549 | G | C | 16 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(13): Show |
16 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.51-6471G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125848549 | |||||||
| chr6:125848592 | T | C | 1 | a0002c0002t0001g0059 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.51-6428T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125848592 | |||||||
| chr6:125848855 | A | G | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-6165A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125848855 | |||||||
| chr6:125849471 | G | A | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-5549G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125849471 | |||||||
| chr6:125849607 | A | G | 1 | a0002c0002t0002g0097 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.51-5413A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125849607 | |||||||
| chr6:125849622 | G | A | 10 | a0002c0002t0001g0059 a0002c0002t0002g0107 a0002c0002t0002g0144 others(7): Show |
10 | HG01175.hp1 HG01515.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.51-5398G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125849622 | |||||||
| chr6:125849717 | T | C | 4 | a0002c0002t0008g0052 a0002c0002t0008g0056 a0002c0002t0008g0066 others(1): Show |
4 | NA18940.hp2 NA18968.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.51-5303T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125849717 | |||||||
| chr6:125849963 | T | G | 2 | a0001c0001t0026g0260 a0004c0013t0013g0263 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.51-5057T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125849963 | |||||||
| chr6:125850064 | G | A | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.51-4956G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125850064 | |||||||
| chr6:125851216 | A | G | 62 | a0002c0002t0001g0059 a0002c0002t0001g0131 a0002c0002t0001g0135 others(59): Show |
62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.51-3804A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125851216 | |||||||
| chr6:125851335 | C | T | 17 | a0002c0002t0001g0135 a0002c0002t0010g0133 a0002c0002t0010g0141 others(14): Show |
17 | HG01192.hp2 HG01884.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.51-3685C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125851335 | |||||||
| chr6:125851489 | C | T | 1 | a0002c0004t0002g0152 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.51-3531C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125851489 | |||||||
| chr6:125851679 | G | T | 16 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(13): Show |
16 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.51-3341G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125851679 | |||||||
| chr6:125851835 | C | T | 4 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 others(1): Show |
4 | HG01891.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.51-3185C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125851835 | |||||||
| chr6:125851850 | T | C | 10 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(7): Show |
10 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.51-3170T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125851850 | |||||||
| chr6:125851890 | C | CT | 14 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.51-3119dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | 125851890 | ||||||
| chr6:125852131 | G | A | 1 | a0002c0008t0015g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.51-2889G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125852131 | |||||||
| chr6:125852884 | T | A | 2 | a0001c0001t0026g0260 a0004c0013t0013g0263 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.51-2136T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125852884 | |||||||
| chr6:125852896 | C | T | 1 | a0002c0002t0002g0180 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.51-2124C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125852896 | |||||||
| chr6:125853069 | T | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(131): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.51-1951T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853069 | |||||||
| chr6:125853482 | G | A | 16 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(13): Show |
16 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.51-1538G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853482 | |||||||
| chr6:125853528 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.51-1492T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853528 | |||||||
| chr6:125853568 | C | G | 134 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(131): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.51-1452C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853568 | |||||||
| chr6:125853601 | A | G | 172 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0041 others(169): Show |
173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.51-1419A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853601 | |||||||
| chr6:125853620 | A | G | 3 | a0002c0002t0001g0181 a0002c0002t0002g0180 a0002c0002t0002g0218 |
3 | HG00099.hp1 HG01109.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.51-1400A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853620 | |||||||
| chr6:125853673 | G | T | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0179 |
3 | HG00280.hp1 HG00733.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.51-1347G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853673 | |||||||
| chr6:125853713 | A | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(131): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.51-1307A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853713 | |||||||
| chr6:125853939 | A | G | 197 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(194): Show |
198 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.51-1081A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853939 | |||||||
| chr6:125853947 | G | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(131): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.51-1073G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853947 | |||||||
| chr6:125853954 | A | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0201 a0001c0001t0001g0202 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.51-1066A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125853954 | |||||||
| chr6:125854039 | A | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(69): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.51-981A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125854039 | |||||||
| chr6:125854339 | C | G | 1 | a0003c0003t0003g0030 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.51-681C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125854339 | |||||||
| chr6:125854447 | C | T | 1 | a0002c0002t0001g0094 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.51-573C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125854447 | |||||||
| chr6:125854737 | A | G | 4 | a0001c0001t0001g0073 a0001c0001t0001g0168 a0001c0001t0001g0225 others(1): Show |
4 | NA18943.hp2 NA18950.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.51-283A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125854737 | |||||||
| chr6:125854948 | C | T | 2 | a0001c0009t0022g0262 a0002c0002t0014g0015 |
2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.51-72C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | chr6 | 125854948 | |||||||
| chr6:125855281 | A | T | 1 | a0001c0001t0002g0132 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.271+41A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125855281 | |||||||
| chr6:125855424 | T | C | 1 | a0007c0012t0003g0113 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.271+184T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125855424 | |||||||
| chr6:125855544 | C | A | 23 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(20): Show |
23 | HG00639.hp2 HG01891.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.271+304C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125855544 | |||||||
| chr6:125855646 | G | T | 1 | a0002c0002t0002g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.271+406G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125855646 | |||||||
| chr6:125855650 | AAAAAAC | A | 4 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 others(1): Show |
4 | HG01891.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.271+426_271+431del others(6): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125855650 | ||||||
| chr6:125855651 | A | C | 1 | a0002c0002t0002g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.271+411A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125855651 | |||||||
| chr6:125855672 | C | CA | 6 | a0001c0001t0001g0257 a0001c0001t0002g0216 a0001c0001t0017g0246 others(3): Show |
6 | HG01175.hp2 HG01981.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.271+441dupA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125855672 | ||||||
| chr6:125855673 | A | C | 1 | a0001c0001t0009g0189 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.271+433A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125855673 | |||||||
| chr6:125855828 | T | C | 4 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0267 others(1): Show |
4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+588T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125855828 | |||||||
| chr6:125855874 | G | A | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.271+634G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125855874 | |||||||
| chr6:125856189 | G | A | 1 | a0001c0001t0007g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.271+949G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125856189 | |||||||
| chr6:125856261 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.271+1021A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125856261 | |||||||
| chr6:125856298 | A | G | 161 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0041 others(158): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.271+1058A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125856298 | |||||||
| chr6:125856362 | GT | G | 99 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0041 others(96): Show |
100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.271+1130delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125856362 | ||||||
| chr6:125856454 | A | G | 2 | a0003c0003t0003g0139 a0003c0003t0003g0140 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.271+1214A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125856454 | |||||||
| chr6:125856609 | C | T | 1 | a0004c0013t0013g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.271+1369C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125856609 | |||||||
| chr6:125856786 | C | G | 3 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 |
3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.271+1546C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125856786 | |||||||
| chr6:125856831 | T | C | 11 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
11 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.271+1591T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125856831 | |||||||
| chr6:125856882 | G | A | 2 | a0003c0003t0003g0147 a0003c0003t0003g0148 |
2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.271+1642G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125856882 | |||||||
| chr6:125857000 | G | A | 62 | a0002c0002t0001g0059 a0002c0002t0001g0131 a0002c0002t0001g0135 others(59): Show |
62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.271+1760G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857000 | |||||||
| chr6:125857288 | A | T | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.271+2048A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857288 | |||||||
| chr6:125857292 | C | T | 11 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(8): Show |
11 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.271+2052C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857292 | |||||||
| chr6:125857428 | CAT | C | 12 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0004g0018 others(9): Show |
12 | HG00741.hp2 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.271+2201_271+2202d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125857428 | ||||||
| chr6:125857439 | A | T | 1 | a0001c0001t0001g0003 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.271+2199A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857439 | |||||||
| chr6:125857439 | ATAT | A | 11 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
11 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.271+2201_271+2203d others(5): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125857439 | ||||||
| chr6:125857441 | A | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(73): Show |
77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.271+2201A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857441 | |||||||
| chr6:125857441 | AT | A | 61 | a0001c0001t0001g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(58): Show |
61 | HG00639.hp2 HG01175.hp1 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.271+2212delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125857441 | ||||||
| chr6:125857441 | ATT | A | 6 | a0002c0002t0001g0146 a0002c0002t0007g0004 a0003c0003t0003g0005 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.271+2211_271+2212d others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125857441 | ||||||
| chr6:125857443 | T | A | 26 | a0001c0009t0022g0262 a0002c0002t0001g0255 a0002c0002t0002g0068 others(23): Show |
26 | HG00280.hp2 HG00544.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.271+2203T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857443 | |||||||
| chr6:125857545 | C | T | 3 | a0002c0002t0001g0091 a0002c0002t0001g0094 a0002c0002t0002g0076 |
3 | HG01123.hp1 HG01261.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.271+2305C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857545 | |||||||
| chr6:125857859 | T | G | 28 | a0002c0002t0001g0255 a0002c0002t0004g0204 a0003c0003t0003g0051 others(25): Show |
28 | HG00280.hp2 HG01106.hp2 HG02027.hp2 others(25): Show |
intron_variant | MODIFIER | c.271+2619T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857859 | |||||||
| chr6:125857878 | A | G | 1 | a0002c0002t0008g0052 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.271+2638A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857878 | |||||||
| chr6:125857924 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.271+2684G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857924 | |||||||
| chr6:125857963 | G | A | 1 | a0003c0003t0003g0005 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.271+2723G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857963 | |||||||
| chr6:125857965 | G | A | 72 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(69): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.271+2725G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125857965 | |||||||
| chr6:125858213 | A | G | 3 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 |
3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.271+2973A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125858213 | |||||||
| chr6:125858231 | T | C | 1 | a0001c0010t0005g0162 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.271+2991T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125858231 | |||||||
| chr6:125858416 | A | T | 2 | a0003c0003t0003g0139 a0003c0003t0003g0140 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.271+3176A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125858416 | |||||||
| chr6:125858698 | T | C | 1 | a0001c0009t0022g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.271+3458T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125858698 | |||||||
| chr6:125859061 | A | C | 1 | a0001c0010t0005g0162 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.271+3821A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125859061 | |||||||
| chr6:125859485 | G | T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0041 others(85): Show |
89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.271+4245G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125859485 | |||||||
| chr6:125859787 | T | C | 1 | a0001c0001t0002g0039 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.271+4547T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125859787 | |||||||
| chr6:125860114 | G | A | 1 | a0001c0001t0006g0037 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.271+4874G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125860114 | |||||||
| chr6:125860145 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.271+4905G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125860145 | |||||||
| chr6:125860473 | G | A | 1 | a0002c0002t0005g0252 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.271+5233G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125860473 | |||||||
| chr6:125860559 | G | A | 1 | a0002c0002t0005g0252 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.271+5319G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125860559 | |||||||
| chr6:125860701 | C | T | 2 | a0001c0001t0026g0260 a0004c0013t0013g0263 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.271+5461C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125860701 | |||||||
| chr6:125860714 | A | G | 2 | a0002c0002t0007g0004 a0003c0003t0003g0005 |
2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.271+5474A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125860714 | |||||||
| chr6:125860810 | T | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0041 others(84): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.271+5570T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125860810 | |||||||
| chr6:125861081 | T | A | 2 | a0002c0002t0001g0153 a0002c0002t0007g0154 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.271+5841T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125861081 | |||||||
| chr6:125861265 | A | G | 1 | a0002c0002t0005g0252 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.271+6025A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125861265 | |||||||
| chr6:125861416 | G | A | 4 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0267 others(1): Show |
4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+6176G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125861416 | |||||||
| chr6:125861464 | T | A | 4 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0267 others(1): Show |
4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+6224T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125861464 | |||||||
| chr6:125861898 | G | A | 3 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 |
3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.271+6658G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125861898 | |||||||
| chr6:125861898 | GTGGTGGC others(4285): Show |
G | 62 | a0002c0002t0001g0059 a0002c0002t0001g0131 a0002c0002t0001g0135 others(59): Show |
62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.271+6679_272-8679d others(2): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125861898 | ||||||
| chr6:125861901 | G | A | 2 | a0001c0001t0001g0046 a0001c0007t0001g0047 |
2 | HG01074.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.271+6661G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125861901 | |||||||
| chr6:125862037 | C | CA | 22 | a0001c0001t0004g0011 a0002c0002t0001g0081 a0002c0002t0001g0091 others(19): Show |
22 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.271+6824dupA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125862037 | ||||||
| chr6:125862037 | CA | C | 23 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0002g0132 others(20): Show |
23 | HG00323.hp1 HG00741.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.271+6824delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125862037 | ||||||
| chr6:125862037 | CAAAAAA | C | 16 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(13): Show |
16 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.271+6819_271+6824d others(8): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125862037 | ||||||
| chr6:125862037 | CAAAAAAA others(2): Show |
C | 69 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(66): Show |
70 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.271+6816_271+6824d others(11): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125862037 | ||||||
| chr6:125862037 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0179 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.271+6815_271+6824d others(12): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125862037 | ||||||
| chr6:125862059 | A | G | 14 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.271+6819A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125862059 | |||||||
| chr6:125862093 | A | G | 3 | a0002c0002t0002g0163 a0002c0002t0002g0164 a0002c0002t0002g0254 |
3 | NA18951.hp1 NA18963.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.271+6853A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125862093 | |||||||
| chr6:125862539 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.271+7299G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125862539 | |||||||
| chr6:125862597 | T | C | 3 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 |
3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.271+7357T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125862597 | |||||||
| chr6:125862638 | T | C | 1 | a0001c0001t0004g0040 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.271+7398T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125862638 | |||||||
| chr6:125863076 | G | T | 2 | a0001c0001t0026g0260 a0004c0013t0013g0263 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.271+7836G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125863076 | |||||||
| chr6:125863205 | C | T | 1 | a0002c0002t0011g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.271+7965C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125863205 | |||||||
| chr6:125863265 | G | A | 2 | a0001c0001t0006g0258 a0001c0001t0006g0259 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.271+8025G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125863265 | |||||||
| chr6:125863610 | GGAAAAAT others(20): Show |
G | 1 | a0001c0001t0004g0014 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.271+8371_271+8397d others(29): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125863610 | |||||||
| chr6:125864013 | G | A | 2 | a0001c0001t0001g0191 a0001c0001t0001g0250 |
2 | NA18939.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.271+8773G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125864013 | |||||||
| chr6:125864039 | T | C | 173 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(170): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.271+8799T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125864039 | |||||||
| chr6:125864063 | A | G | 3 | a0002c0002t0001g0153 a0002c0002t0001g0228 a0002c0002t0007g0154 |
3 | HG00323.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.271+8823A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125864063 | |||||||
| chr6:125864171 | G | A | 11 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
11 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.271+8931G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125864171 | |||||||
| chr6:125864391 | T | G | 2 | a0001c0001t0026g0260 a0004c0013t0013g0263 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.271+9151T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125864391 | |||||||
| chr6:125864702 | G | A | 1 | a0002c0008t0015g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.271+9462G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125864702 | |||||||
| chr6:125865328 | G | C | 25 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(22): Show |
25 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.272-9561G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125865328 | |||||||
| chr6:125865488 | C | T | 2 | a0001c0001t0006g0258 a0001c0001t0006g0259 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.272-9401C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125865488 | |||||||
| chr6:125865694 | C | G | 1 | a0002c0002t0002g0084 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.272-9195C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125865694 | |||||||
| chr6:125865839 | T | TTTTCTTT others(5): Show |
1 | a0002c0008t0015g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.272-9038_272-9027d others(14): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125865839 | ||||||
| chr6:125865942 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.272-8947C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125865942 | |||||||
| chr6:125866011 | A | G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG00140.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.272-8878A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125866011 | |||||||
| chr6:125866062 | T | G | 32 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(29): Show |
32 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.272-8827T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125866062 | |||||||
| chr6:125866338 | GA | G | 6 | a0002c0002t0007g0004 a0002c0002t0014g0015 a0002c0008t0015g0261 others(3): Show |
6 | HG02615.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.272-8541delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125866338 | ||||||
| chr6:125866439 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.272-8450A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125866439 | |||||||
| chr6:125866487 | T | C | 7 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0005g0007 others(4): Show |
7 | HG00741.hp2 HG01884.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.272-8402T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125866487 | |||||||
| chr6:125866550 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.272-8339G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125866550 | |||||||
| chr6:125866610 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.272-8279A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125866610 | |||||||
| chr6:125866712 | A | T | 1 | a0001c0001t0004g0014 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.272-8177A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125866712 | |||||||
| chr6:125866973 | T | A | 31 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(28): Show |
31 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.272-7916T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125866973 | |||||||
| chr6:125867098 | A | T | 31 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(28): Show |
31 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.272-7791A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867098 | |||||||
| chr6:125867099 | T | C | 32 | a0001c0001t0001g0006 a0001c0001t0001g0178 a0001c0001t0001g0238 others(29): Show |
32 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.272-7790T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867099 | |||||||
| chr6:125867157 | C | T | 2 | a0001c0001t0001g0178 a0001c0001t0005g0017 |
2 | HG00741.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.272-7732C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867157 | |||||||
| chr6:125867284 | C | T | 1 | a0001c0001t0004g0014 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.272-7605C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867284 | |||||||
| chr6:125867342 | G | C | 62 | a0002c0002t0001g0059 a0002c0002t0001g0131 a0002c0002t0001g0135 others(59): Show |
62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.272-7547G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867342 | |||||||
| chr6:125867396 | A | G | 6 | a0002c0002t0007g0004 a0002c0002t0014g0015 a0002c0008t0015g0261 others(3): Show |
6 | HG02615.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.272-7493A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867396 | |||||||
| chr6:125867406 | T | C | 1 | a0002c0002t0005g0252 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.272-7483T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867406 | |||||||
| chr6:125867407 | T | A | 1 | a0002c0002t0005g0252 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.272-7482T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867407 | |||||||
| chr6:125867511 | G | A | 2 | a0001c0001t0001g0245 a0001c0001t0017g0246 |
2 | NA18949.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.272-7378G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867511 | |||||||
| chr6:125867747 | G | A | 1 | a0001c0001t0006g0267 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.272-7142G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867747 | |||||||
| chr6:125867843 | G | T | 1 | a0001c0001t0007g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.272-7046G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125867843 | |||||||
| chr6:125868002 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.272-6887T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868002 | |||||||
| chr6:125868026 | C | T | 5 | a0002c0002t0007g0004 a0002c0002t0014g0015 a0003c0003t0003g0005 others(2): Show |
5 | HG02615.hp1 HG02818.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.272-6863C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868026 | |||||||
| chr6:125868102 | A | G | 4 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0044 others(1): Show |
4 | HG00323.hp2 HG00738.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.272-6787A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868102 | |||||||
| chr6:125868155 | A | T | 3 | a0001c0001t0004g0018 a0001c0001t0004g0020 a0001c0001t0011g0158 |
3 | HG02055.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.272-6734A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868155 | |||||||
| chr6:125868188 | A | C | 3 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0025 |
3 | NA18985.hp2 NA19068.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.272-6701A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868188 | |||||||
| chr6:125868295 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.272-6594G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868295 | |||||||
| chr6:125868501 | A | G | 8 | a0002c0002t0002g0062 a0002c0002t0002g0063 a0002c0002t0002g0064 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.272-6388A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868501 | |||||||
| chr6:125868513 | A | G | 4 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0267 others(1): Show |
4 | HG02257.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.272-6376A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868513 | |||||||
| chr6:125868751 | A | G | 2 | a0002c0002t0002g0016 a0002c0002t0002g0033 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.272-6138A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868751 | |||||||
| chr6:125868841 | T | A | 1 | a0001c0001t0001g0215 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.272-6048T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868841 | |||||||
| chr6:125868857 | T | A | 7 | a0002c0002t0002g0107 a0002c0002t0002g0144 a0002c0002t0002g0145 others(4): Show |
7 | HG01175.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.272-6032T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868857 | |||||||
| chr6:125868914 | G | A | 1 | a0001c0001t0024g0150 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.272-5975G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125868914 | |||||||
| chr6:125869061 | C | T | 25 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(22): Show |
25 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.272-5828C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125869061 | |||||||
| chr6:125869207 | C | G | 1 | a0007c0012t0003g0113 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.272-5682C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125869207 | |||||||
| chr6:125869280 | C | G | 1 | a0001c0001t0001g0235 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.272-5609C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125869280 | |||||||
| chr6:125869329 | C | A | 1 | a0002c0002t0005g0252 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.272-5560C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125869329 | |||||||
| chr6:125869407 | T | C | 3 | a0002c0002t0014g0015 a0003c0003t0003g0034 a0003c0003t0003g0035 |
3 | HG02615.hp1 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.272-5482T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125869407 | |||||||
| chr6:125869442 | C | G | 88 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(85): Show |
88 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(85): Show |
intron_variant | MODIFIER | c.272-5447C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125869442 | |||||||
| chr6:125869748 | A | G | 73 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(70): Show |
74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.272-5141A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125869748 | |||||||
| chr6:125869794 | C | T | 3 | a0001c0001t0006g0049 a0001c0001t0006g0267 a0002c0002t0011g0048 |
3 | HG02257.hp2 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.272-5095C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125869794 | |||||||
| chr6:125870057 | C | T | 25 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(22): Show |
25 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.272-4832C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125870057 | |||||||
| chr6:125870074 | A | G | 25 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(22): Show |
25 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.272-4815A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125870074 | |||||||
| chr6:125870122 | G | A | 1 | a0002c0008t0015g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.272-4767G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125870122 | |||||||
| chr6:125870248 | C | T | 93 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(90): Show |
93 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.272-4641C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125870248 | |||||||
| chr6:125870587 | T | C | 199 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(196): Show |
200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.272-4302T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125870587 | |||||||
| chr6:125870650 | C | G | 1 | a0001c0001t0026g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.272-4239C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125870650 | |||||||
| chr6:125870888 | C | T | 73 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(70): Show |
74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.272-4001C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125870888 | |||||||
| chr6:125870890 | C | T | 1 | a0002c0002t0001g0081 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.272-3999C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125870890 | |||||||
| chr6:125871014 | A | G | 32 | a0001c0001t0001g0006 a0001c0001t0001g0178 a0001c0001t0001g0238 others(29): Show |
32 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.272-3875A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125871014 | |||||||
| chr6:125871277 | G | T | 1 | a0001c0001t0001g0184 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.272-3612G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125871277 | |||||||
| chr6:125871281 | GAGCACCA others(6): Show |
G | 93 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(90): Show |
93 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.272-3602_272-3590d others(15): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125871281 | ||||||
| chr6:125871336 | G | A | 2 | a0002c0002t0007g0004 a0003c0003t0003g0005 |
2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.272-3553G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125871336 | |||||||
| chr6:125871448 | C | G | 1 | a0002c0002t0002g0069 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.272-3441C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125871448 | |||||||
| chr6:125871998 | GA | G | 84 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(81): Show |
84 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.272-2871delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | 125871998 | ||||||
| chr6:125871999 | A | G | 1 | a0002c0002t0002g0214 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.272-2890A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125871999 | |||||||
| chr6:125872066 | A | G | 1 | a0002c0002t0002g0098 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.272-2823A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125872066 | |||||||
| chr6:125872273 | C | T | 1 | a0001c0001t0026g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.272-2616C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125872273 | |||||||
| chr6:125872343 | A | G | 3 | a0002c0002t0014g0015 a0003c0003t0003g0034 a0003c0003t0003g0035 |
3 | HG02615.hp1 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.272-2546A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125872343 | |||||||
| chr6:125872413 | C | G | 1 | a0002c0002t0002g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.272-2476C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125872413 | |||||||
| chr6:125872673 | A | G | 1 | a0004c0013t0013g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.272-2216A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125872673 | |||||||
| chr6:125872962 | G | C | 2 | a0001c0001t0004g0038 a0001c0001t0004g0040 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.272-1927G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125872962 | |||||||
| chr6:125872963 | T | C | 5 | a0002c0002t0007g0004 a0002c0002t0014g0015 a0003c0003t0003g0005 others(2): Show |
5 | HG02615.hp1 HG02818.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.272-1926T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125872963 | |||||||
| chr6:125873143 | G | A | 7 | a0002c0002t0002g0107 a0002c0002t0002g0144 a0002c0002t0002g0145 others(4): Show |
7 | HG01175.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.272-1746G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125873143 | |||||||
| chr6:125873626 | G | A | 1 | a0002c0002t0001g0228 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.272-1263G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125873626 | |||||||
| chr6:125873688 | A | G | 1 | a0002c0002t0002g0164 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.272-1201A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125873688 | |||||||
| chr6:125874274 | G | A | 1 | a0002c0002t0002g0002 | 2 | NA19079.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.272-615G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125874274 | |||||||
| chr6:125874284 | C | T | 1 | a0003c0003t0003g0138 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.272-605C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125874284 | |||||||
| chr6:125874297 | C | G | 1 | a0001c0001t0004g0011 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.272-592C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125874297 | |||||||
| chr6:125874354 | G | A | 123 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0041 others(120): Show |
123 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.272-535G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | chr6 | 125874354 | |||||||
| chr6:125874996 | T | C | 9 | a0001c0001t0001g0086 a0001c0001t0001g0172 a0001c0001t0001g0211 others(6): Show |
9 | HG00140.hp2 HG00642.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.351+28T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125874996 | |||||||
| chr6:125875274 | C | T | 1 | a0002c0002t0001g0026 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.351+306C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125875274 | |||||||
| chr6:125875903 | C | T | 24 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(21): Show |
24 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.351+935C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125875903 | |||||||
| chr6:125876097 | G | A | 1 | a0004c0013t0013g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.351+1129G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125876097 | |||||||
| chr6:125876100 | G | A | 1 | a0002c0002t0002g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.351+1132G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125876100 | |||||||
| chr6:125876223 | C | G | 1 | a0001c0001t0026g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.351+1255C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125876223 | |||||||
| chr6:125876252 | T | C | 1 | a0001c0001t0007g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.351+1284T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125876252 | |||||||
| chr6:125876294 | A | G | 1 | a0002c0002t0007g0004 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.351+1326A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125876294 | |||||||
| chr6:125876333 | G | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0044 others(1): Show |
4 | HG00323.hp2 HG00738.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+1365G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125876333 | |||||||
| chr6:125876558 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.351+1590A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125876558 | |||||||
| chr6:125876601 | TA | T | 11 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
11 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.352-1645delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 125876601 | ||||||
| chr6:125876798 | G | A | 3 | a0002c0002t0002g0097 a0002c0002t0002g0100 a0002c0002t0002g0102 |
3 | NA18978.hp2 NA18982.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.352-1465G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125876798 | |||||||
| chr6:125877178 | G | C | 24 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(21): Show |
24 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.352-1085G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125877178 | |||||||
| chr6:125877462 | A | C | 1 | a0002c0002t0007g0004 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.352-801A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125877462 | |||||||
| chr6:125877536 | A | AG | 4 | a0002c0002t0007g0004 a0002c0002t0014g0015 a0003c0003t0003g0034 others(1): Show |
4 | HG02615.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-726dupG | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr6 | 125877536 | ||||||
| chr6:125877592 | C | T | 2 | a0002c0002t0002g0090 a0002c0002t0002g0214 |
2 | HG00642.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.352-671C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125877592 | |||||||
| chr6:125877923 | G | A | 1 | a0001c0001t0026g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.352-340G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125877923 | |||||||
| chr6:125877954 | C | G | 1 | a0002c0008t0015g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.352-309C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125877954 | |||||||
| chr6:125877994 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.352-269A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125877994 | |||||||
| chr6:125878031 | A | G | 1 | a0001c0001t0005g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.352-232A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125878031 | |||||||
| chr6:125878234 | A | G | 1 | a0001c0001t0004g0040 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.352-29A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 4/15 | chr6 | 125878234 | |||||||
| chr6:125878563 | G | A | 62 | a0002c0002t0001g0059 a0002c0002t0001g0131 a0002c0002t0001g0135 others(59): Show |
62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.459+193G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125878563 | |||||||
| chr6:125878683 | C | A | 1 | a0003c0003t0003g0134 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.459+313C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125878683 | |||||||
| chr6:125878686 | T | C | 1 | a0002c0002t0002g0106 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.459+316T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125878686 | |||||||
| chr6:125878716 | C | T | 62 | a0002c0002t0001g0059 a0002c0002t0001g0131 a0002c0002t0001g0135 others(59): Show |
62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.459+346C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125878716 | |||||||
| chr6:125878992 | T | A | 3 | a0001c0001t0006g0258 a0001c0001t0006g0259 a0001c0009t0022g0262 |
3 | HG02976.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.459+622T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125878992 | |||||||
| chr6:125878994 | G | T | 3 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0025 |
3 | NA18985.hp2 NA19068.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.459+624G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125878994 | |||||||
| chr6:125879049 | T | A | 1 | a0002c0008t0015g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.459+679T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125879049 | |||||||
| chr6:125879129 | T | C | 1 | a0002c0002t0002g0062 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.459+759T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125879129 | |||||||
| chr6:125879174 | T | C | 3 | a0003c0003t0003g0104 a0003c0003t0003g0138 a0003c0003t0003g0142 |
3 | HG01175.hp1 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.459+804T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125879174 | |||||||
| chr6:125879200 | CATTGACC others(3): Show |
C | 1 | a0001c0001t0026g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.459+836_459+845del others(10): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr6 | 125879200 | ||||||
| chr6:125879486 | A | G | 1 | a0003c0003t0003g0117 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.459+1116A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125879486 | |||||||
| chr6:125879492 | T | A | 91 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(88): Show |
91 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.459+1122T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125879492 | |||||||
| chr6:125879651 | T | C | 1 | a0003c0003t0003g0116 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.459+1281T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125879651 | |||||||
| chr6:125879740 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0201 |
3 | HG01167.hp1 HG01169.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.460-1350G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125879740 | |||||||
| chr6:125880012 | G | A | 196 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(193): Show |
197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.460-1078G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125880012 | |||||||
| chr6:125880079 | G | T | 8 | a0001c0001t0001g0173 a0001c0001t0001g0192 a0001c0001t0001g0193 others(5): Show |
8 | NA18944.hp2 NA18963.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.460-1011G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125880079 | |||||||
| chr6:125880176 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.460-914G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125880176 | |||||||
| chr6:125880360 | A | T | 1 | a0005c0006t0002g0001 | 2 | HG00738.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.460-730A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125880360 | |||||||
| chr6:125880448 | C | T | 2 | a0001c0001t0006g0258 a0001c0001t0006g0259 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.460-642C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125880448 | |||||||
| chr6:125880517 | ATATTTTA others(3): Show |
A | 1 | a0001c0001t0026g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.460-556_460-547del others(10): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr6 | 125880517 | ||||||
| chr6:125880598 | G | T | 3 | a0002c0002t0014g0015 a0003c0003t0003g0034 a0003c0003t0003g0035 |
3 | HG02615.hp1 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.460-492G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125880598 | |||||||
| chr6:125880944 | G | A | 1 | a0002c0002t0002g0082 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.460-146G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125880944 | |||||||
| chr6:125880992 | A | G | 62 | a0002c0002t0001g0059 a0002c0002t0001g0131 a0002c0002t0001g0135 others(59): Show |
62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.460-98A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 5/15 | chr6 | 125880992 | |||||||
| chr6:125881229 | A | T | 1 | a0002c0002t0005g0252 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.573+26A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | chr6 | 125881229 | |||||||
| chr6:125881337 | G | A | 1 | a0002c0002t0002g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.573+134G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | chr6 | 125881337 | |||||||
| chr6:125881670 | CA | C | 10 | a0001c0001t0001g0159 a0001c0001t0001g0165 a0001c0001t0001g0239 others(7): Show |
10 | HG01106.hp2 HG01243.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.573+487delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr6 | 125881670 | ||||||
| chr6:125881670 | CAA | C | 156 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0041 others(153): Show |
157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.573+486_573+487del others(2): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr6 | 125881670 | ||||||
| chr6:125881670 | CAAA | C | 31 | a0001c0001t0001g0006 a0001c0001t0001g0178 a0001c0001t0001g0238 others(28): Show |
31 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.573+485_573+487del others(3): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr6 | 125881670 | ||||||
| chr6:125881736 | G | A | 196 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(193): Show |
197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.573+533G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | chr6 | 125881736 | |||||||
| chr6:125881772 | T | A | 26 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(23): Show |
26 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.573+569T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | chr6 | 125881772 | |||||||
| chr6:125881773 | A | T | 1 | a0003c0003t0003g0105 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.573+570A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | chr6 | 125881773 | |||||||
| chr6:125881862 | T | C | 1 | a0002c0002t0002g0107 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.574-564T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | chr6 | 125881862 | |||||||
| chr6:125881886 | C | T | 1 | a0002c0002t0002g0157 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.574-540C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | chr6 | 125881886 | |||||||
| chr6:125882103 | C | A | 1 | a0001c0001t0001g0199 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.574-323C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | chr6 | 125882103 | |||||||
| chr6:125882105 | C | T | 1 | a0002c0002t0002g0067 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.574-321C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | chr6 | 125882105 | |||||||
| chr6:125882230 | G | GA | 12 | a0001c0001t0006g0258 a0001c0001t0006g0259 a0001c0001t0006g0267 others(9): Show |
12 | HG01192.hp2 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.574-186dupA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr6 | 125882230 | ||||||
| chr6:125882277 | A | G | 1 | a0001c0009t0022g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.574-149A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 6/15 | chr6 | 125882277 | |||||||
| chr6:125882834 | A | G | 1 | a0002c0002t0002g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.699+283A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125882834 | |||||||
| chr6:125883057 | G | C | 191 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(188): Show |
192 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.699+506G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125883057 | |||||||
| chr6:125883156 | T | C | 1 | a0001c0001t0026g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.699+605T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125883156 | |||||||
| chr6:125883187 | C | G | 91 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(88): Show |
91 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.699+636C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125883187 | |||||||
| chr6:125883263 | A | G | 1 | a0001c0001t0005g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.699+712A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125883263 | |||||||
| chr6:125883324 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.699+773G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125883324 | |||||||
| chr6:125883398 | A | G | 24 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(21): Show |
24 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.699+847A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125883398 | |||||||
| chr6:125883713 | C | CT | 6 | a0002c0002t0002g0214 a0002c0002t0002g0233 a0002c0002t0008g0056 others(3): Show |
6 | HG00642.hp1 HG02257.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.699+1185dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr6 | 125883713 | ||||||
| chr6:125883713 | CT | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.699+1185delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr6 | 125883713 | ||||||
| chr6:125883753 | C | G | 1 | a0002c0002t0002g0214 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.699+1202C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125883753 | |||||||
| chr6:125883902 | A | G | 1 | a0002c0002t0010g0141 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.700-1257A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125883902 | |||||||
| chr6:125884010 | C | T | 1 | a0001c0001t0016g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.700-1149C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125884010 | |||||||
| chr6:125884171 | T | C | 1 | a0002c0008t0015g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.700-988T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125884171 | |||||||
| chr6:125884319 | A | G | 2 | a0002c0002t0002g0063 a0002c0002t0002g0079 |
2 | HG00639.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.700-840A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125884319 | |||||||
| chr6:125884330 | T | C | 4 | a0001c0001t0006g0258 a0001c0001t0006g0259 a0001c0001t0006g0267 others(1): Show |
4 | HG02257.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.700-829T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125884330 | |||||||
| chr6:125884443 | T | G | 73 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(70): Show |
74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.700-716T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125884443 | |||||||
| chr6:125884799 | C | A | 1 | a0001c0001t0001g0239 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.700-360C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125884799 | |||||||
| chr6:125884863 | G | A | 1 | a0001c0001t0026g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.700-296G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125884863 | |||||||
| chr6:125884897 | A | G | 1 | a0001c0009t0022g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.700-262A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125884897 | |||||||
| chr6:125884898 | C | G | 3 | a0002c0002t0014g0015 a0003c0003t0003g0034 a0003c0003t0003g0035 |
3 | HG02615.hp1 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.700-261C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125884898 | |||||||
| chr6:125884921 | T | C | 1 | a0002c0008t0015g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.700-238T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 7/15 | chr6 | 125884921 | |||||||
| chr6:125885508 | A | G | 3 | a0002c0002t0014g0015 a0003c0003t0003g0034 a0003c0003t0003g0035 |
3 | HG02615.hp1 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.884+165A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125885508 | |||||||
| chr6:125885517 | A | G | 1 | a0002c0008t0015g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.884+174A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125885517 | |||||||
| chr6:125885542 | A | C | 62 | a0002c0002t0001g0059 a0002c0002t0001g0131 a0002c0002t0001g0135 others(59): Show |
62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.884+199A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125885542 | |||||||
| chr6:125885799 | G | A | 196 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(193): Show |
197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.884+456G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125885799 | |||||||
| chr6:125885871 | T | C | 1 | a0003c0003t0003g0148 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.884+528T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125885871 | |||||||
| chr6:125885917 | C | T | 3 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 |
3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.884+574C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125885917 | |||||||
| chr6:125886040 | C | T | 24 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(21): Show |
24 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.884+697C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125886040 | |||||||
| chr6:125886061 | A | G | 1 | a0001c0001t0002g0160 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.884+718A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125886061 | |||||||
| chr6:125886080 | A | G | 1 | a0001c0001t0026g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.884+737A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125886080 | |||||||
| chr6:125886144 | C | T | 1 | a0002c0002t0004g0204 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.884+801C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125886144 | |||||||
| chr6:125886160 | A | G | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0179 |
3 | HG00280.hp1 HG00733.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.884+817A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125886160 | |||||||
| chr6:125886164 | G | GA | 75 | a0001c0001t0001g0083 a0001c0001t0001g0201 a0001c0001t0005g0007 others(72): Show |
75 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(72): Show |
intron_variant | MODIFIER | c.884+839dupA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 125886164 | ||||||
| chr6:125886164 | G | GAA | 20 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0043 others(17): Show |
20 | HG00323.hp2 HG00738.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.884+838_884+839dup others(2): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 125886164 | ||||||
| chr6:125886164 | G | GAAA | 6 | a0001c0001t0001g0042 a0001c0001t0001g0169 a0001c0001t0002g0039 others(3): Show |
6 | HG00741.hp1 HG01243.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.884+837_884+839dup others(3): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 125886164 | ||||||
| chr6:125886771 | A | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.884+1428A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125886771 | |||||||
| chr6:125886903 | C | T | 31 | a0001c0001t0001g0006 a0001c0001t0001g0178 a0001c0001t0001g0238 others(28): Show |
31 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.884+1560C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125886903 | |||||||
| chr6:125886910 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0045 |
2 | HG00738.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.884+1567A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125886910 | |||||||
| chr6:125887112 | C | T | 1 | a0003c0003t0003g0119 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.884+1769C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125887112 | |||||||
| chr6:125887411 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.885-1528A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125887411 | |||||||
| chr6:125887883 | A | G | 62 | a0002c0002t0001g0059 a0002c0002t0001g0131 a0002c0002t0001g0135 others(59): Show |
62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.885-1056A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125887883 | |||||||
| chr6:125888099 | G | A | 90 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(87): Show |
90 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(87): Show |
intron_variant | MODIFIER | c.885-840G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125888099 | |||||||
| chr6:125888267 | A | T | 1 | a0001c0001t0002g0039 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.885-672A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125888267 | |||||||
| chr6:125888315 | G | A | 1 | a0003c0003t0003g0205 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.885-624G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125888315 | |||||||
| chr6:125888386 | A | C | 1 | a0001c0001t0026g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.885-553A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125888386 | |||||||
| chr6:125888442 | T | G | 1 | a0003c0003t0003g0147 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.885-497T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125888442 | |||||||
| chr6:125888505 | T | C | 2 | a0001c0001t0001g0209 a0001c0001t0007g0080 |
2 | NA18946.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.885-434T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125888505 | |||||||
| chr6:125888530 | ATGTT | A | 62 | a0002c0002t0001g0059 a0002c0002t0001g0131 a0002c0002t0001g0135 others(59): Show |
62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.885-406_885-403del others(4): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr6 | 125888530 | ||||||
| chr6:125888599 | T | C | 2 | a0002c0002t0002g0090 a0002c0002t0002g0214 |
2 | HG00642.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.885-340T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125888599 | |||||||
| chr6:125888680 | T | C | 1 | a0002c0002t0001g0081 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.885-259T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 8/15 | chr6 | 125888680 | |||||||
| chr6:125890040 | T | G | 1 | a0001c0001t0001g0221 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1927+59T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 9/15 | chr6 | 125890040 | |||||||
| chr6:125890168 | G | A | 264 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(261): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.1927+187G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 9/15 | chr6 | 125890168 | |||||||
| chr6:125890265 | G | A | 1 | a0004c0005t0003g0021 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1927+284G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 9/15 | chr6 | 125890265 | |||||||
| chr6:125890416 | A | T | 2 | a0002c0002t0002g0144 a0002c0002t0002g0145 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1928-226A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 9/15 | chr6 | 125890416 | |||||||
| chr6:125890513 | C | T | 62 | a0002c0002t0001g0059 a0002c0002t0001g0131 a0002c0002t0001g0135 others(59): Show |
62 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.1928-129C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 9/15 | chr6 | 125890513 | |||||||
| chr6:125890629 | G | A | 1 | a0002c0002t0001g0181 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1928-13G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 9/15 | chr6 | 125890629 | |||||||
| chr6:125891106 | T | C | 1 | a0004c0013t0013g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2096+296T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125891106 | |||||||
| chr6:125891552 | A | G | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0179 |
3 | HG00280.hp1 HG00733.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.2096+742A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125891552 | |||||||
| chr6:125891768 | T | G | 1 | a0002c0008t0015g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2096+958T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125891768 | |||||||
| chr6:125891771 | T | C | 3 | a0002c0002t0014g0015 a0003c0003t0003g0034 a0003c0003t0003g0035 |
3 | HG02615.hp1 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2096+961T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125891771 | |||||||
| chr6:125891825 | C | A | 1 | a0001c0001t0007g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2096+1015C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125891825 | |||||||
| chr6:125891951 | G | A | 2 | a0001c0001t0001g0238 a0001c0001t0005g0237 |
2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2096+1141G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125891951 | |||||||
| chr6:125892452 | C | T | 1 | a0003c0003t0003g0051 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2096+1642C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125892452 | |||||||
| chr6:125892566 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2096+1756C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125892566 | |||||||
| chr6:125892589 | G | A | 12 | a0002c0002t0001g0026 a0002c0002t0001g0059 a0002c0002t0001g0131 others(9): Show |
12 | HG01175.hp1 HG01515.hp1 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.2096+1779G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125892589 | |||||||
| chr6:125892630 | C | T | 2 | a0002c0002t0002g0163 a0002c0002t0002g0254 |
2 | NA18963.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2096+1820C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125892630 | |||||||
| chr6:125892653 | G | A | 1 | a0001c0001t0009g0187 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2096+1843G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125892653 | |||||||
| chr6:125892765 | C | T | 1 | a0003c0003t0003g0005 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2096+1955C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125892765 | |||||||
| chr6:125892951 | C | G | 1 | a0001c0009t0022g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2096+2141C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125892951 | |||||||
| chr6:125892979 | T | G | 31 | a0001c0001t0001g0006 a0001c0001t0001g0178 a0001c0001t0001g0238 others(28): Show |
31 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.2096+2169T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125892979 | |||||||
| chr6:125893263 | C | T | 3 | a0002c0002t0014g0015 a0003c0003t0003g0034 a0003c0003t0003g0035 |
3 | HG02615.hp1 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2096+2453C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125893263 | |||||||
| chr6:125893446 | TA | T | 3 | a0002c0002t0014g0015 a0003c0003t0003g0034 a0003c0003t0003g0035 |
3 | HG02615.hp1 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2096+2641delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125893446 | ||||||
| chr6:125893478 | A | C | 73 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(70): Show |
74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.2096+2668A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125893478 | |||||||
| chr6:125893589 | G | T | 1 | a0001c0001t0002g0039 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2096+2779G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125893589 | |||||||
| chr6:125893592 | C | T | 63 | a0002c0002t0001g0026 a0002c0002t0001g0059 a0002c0002t0001g0131 others(60): Show |
63 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(60): Show |
intron_variant | MODIFIER | c.2096+2782C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125893592 | |||||||
| chr6:125893666 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2096+2856C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125893666 | |||||||
| chr6:125893846 | C | T | 3 | a0001c0001t0006g0258 a0001c0001t0006g0259 a0001c0001t0006g0267 |
3 | HG02257.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2096+3036C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125893846 | |||||||
| chr6:125893859 | C | T | 3 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 |
3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2096+3049C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125893859 | |||||||
| chr6:125893903 | A | G | 3 | a0002c0002t0014g0015 a0003c0003t0003g0034 a0003c0003t0003g0035 |
3 | HG02615.hp1 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2096+3093A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125893903 | |||||||
| chr6:125893955 | T | C | 63 | a0002c0002t0001g0026 a0002c0002t0001g0059 a0002c0002t0001g0131 others(60): Show |
63 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(60): Show |
intron_variant | MODIFIER | c.2096+3145T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125893955 | |||||||
| chr6:125894004 | C | T | 1 | a0002c0002t0002g0063 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2096+3194C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125894004 | |||||||
| chr6:125894051 | A | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(71): Show |
75 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.2096+3241A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125894051 | |||||||
| chr6:125894150 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(71): Show |
75 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.2096+3340C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125894150 | |||||||
| chr6:125894275 | G | A | 1 | a0002c0008t0015g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2096+3465G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125894275 | |||||||
| chr6:125894329 | G | A | 1 | a0003c0003t0003g0005 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2096+3519G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125894329 | |||||||
| chr6:125894340 | G | C | 73 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(70): Show |
74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.2096+3530G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125894340 | |||||||
| chr6:125894764 | T | G | 1 | a0001c0001t0006g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2096+3954T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125894764 | |||||||
| chr6:125894879 | G | A | 168 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0041 others(165): Show |
169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.2096+4069G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125894879 | |||||||
| chr6:125894901 | C | A | 67 | a0001c0001t0001g0178 a0001c0001t0001g0238 a0001c0001t0005g0007 others(64): Show |
67 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(64): Show |
intron_variant | MODIFIER | c.2096+4091C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125894901 | |||||||
| chr6:125894985 | T | A | 1 | a0001c0001t0005g0085 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2096+4175T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125894985 | |||||||
| chr6:125895006 | G | C | 1 | a0002c0002t0002g0222 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2096+4196G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125895006 | |||||||
| chr6:125895043 | A | G | 4 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 others(1): Show |
4 | HG01891.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2096+4233A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125895043 | |||||||
| chr6:125895229 | G | A | 1 | a0002c0002t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2096+4419G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125895229 | |||||||
| chr6:125895257 | C | G | 92 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0073 others(89): Show |
93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.2096+4447C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125895257 | |||||||
| chr6:125895961 | A | G | 1 | a0001c0001t0016g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2096+5151A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125895961 | |||||||
| chr6:125895965 | A | ATG | 5 | a0001c0001t0002g0039 a0002c0002t0001g0091 a0002c0002t0001g0094 others(2): Show |
5 | HG01123.hp1 HG01243.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.2096+5179_2096+518 others(6): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125895965 | ||||||
| chr6:125895965 | A | G | 3 | a0001c0001t0001g0075 a0001c0001t0001g0083 a0001c0001t0001g0092 |
3 | HG02145.hp2 HG02293.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2096+5155A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125895965 | |||||||
| chr6:125895965 | ATG | A | 53 | a0001c0001t0026g0260 a0002c0002t0010g0133 a0002c0002t0010g0141 others(50): Show |
53 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.2096+5179_2096+518 others(6): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125895965 | ||||||
| chr6:125895965 | ATGTG | A | 14 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 others(11): Show |
14 | HG01891.hp1 HG02027.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2096+5177_2096+518 others(8): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125895965 | ||||||
| chr6:125895981 | G | C | 1 | a0002c0002t0007g0004 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2096+5171G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125895981 | |||||||
| chr6:125896142 | G | A | 1 | a0002c0002t0004g0204 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2096+5332G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125896142 | |||||||
| chr6:125896176 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2096+5366T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125896176 | |||||||
| chr6:125896446 | G | T | 1 | a0002c0002t0007g0004 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2096+5636G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125896446 | |||||||
| chr6:125896540 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2096+5730C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125896540 | |||||||
| chr6:125897053 | A | G | 3 | a0001c0001t0006g0258 a0001c0001t0006g0259 a0001c0001t0006g0267 |
3 | HG02257.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2096+6243A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125897053 | |||||||
| chr6:125897454 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(204): Show |
208 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.2096+6644T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125897454 | |||||||
| chr6:125897696 | T | G | 1 | a0003c0003t0018g0128 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2096+6886T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125897696 | |||||||
| chr6:125897765 | C | T | 1 | a0001c0001t0002g0216 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2096+6955C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125897765 | |||||||
| chr6:125897815 | C | G | 171 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0041 others(168): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.2096+7005C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125897815 | |||||||
| chr6:125897900 | T | C | 3 | a0002c0002t0010g0133 a0002c0002t0010g0141 a0003c0003t0003g0005 |
3 | HG02572.hp1 HG02818.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2096+7090T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125897900 | |||||||
| chr6:125898119 | C | G | 2 | a0002c0002t0002g0087 a0002c0002t0002g0233 |
2 | HG00735.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2096+7309C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125898119 | |||||||
| chr6:125898248 | G | T | 52 | a0002c0002t0010g0133 a0002c0002t0010g0141 a0003c0003t0003g0005 others(49): Show |
52 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.2096+7438G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125898248 | |||||||
| chr6:125898582 | A | G | 10 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0258 others(7): Show |
10 | HG02109.hp1 HG02257.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2096+7772A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125898582 | |||||||
| chr6:125898680 | C | G | 63 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0258 others(60): Show |
63 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(60): Show |
intron_variant | MODIFIER | c.2096+7870C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125898680 | |||||||
| chr6:125898850 | A | G | 3 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0025 |
3 | NA18985.hp2 NA19068.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2096+8040A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125898850 | |||||||
| chr6:125899077 | A | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0075 others(72): Show |
76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.2096+8267A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125899077 | |||||||
| chr6:125899709 | C | T | 63 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0258 others(60): Show |
63 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(60): Show |
intron_variant | MODIFIER | c.2096+8899C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125899709 | |||||||
| chr6:125899843 | A | G | 1 | a0002c0002t0002g0077 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2096+9033A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125899843 | |||||||
| chr6:125899862 | G | A | 90 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0075 others(87): Show |
91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2096+9052G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125899862 | |||||||
| chr6:125900070 | G | C | 1 | a0001c0001t0001g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2096+9260G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125900070 | |||||||
| chr6:125900373 | A | G | 1 | a0002c0002t0002g0062 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2096+9563A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125900373 | |||||||
| chr6:125900385 | A | C | 3 | a0002c0002t0010g0133 a0002c0002t0010g0141 a0003c0003t0003g0005 |
3 | HG02572.hp1 HG02818.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2096+9575A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125900385 | |||||||
| chr6:125900455 | G | A | 12 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0258 others(9): Show |
12 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2096+9645G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125900455 | |||||||
| chr6:125900611 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2096+9801C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125900611 | |||||||
| chr6:125900676 | G | A | 1 | a0002c0002t0001g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2096+9866G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125900676 | |||||||
| chr6:125901149 | C | T | 1 | a0002c0002t0007g0004 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2096+10339C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125901149 | |||||||
| chr6:125901286 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2096+10476G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125901286 | |||||||
| chr6:125901371 | C | G | 3 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 |
3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2096+10561C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125901371 | |||||||
| chr6:125901440 | G | A | 2 | a0002c0002t0014g0015 a0002c0008t0015g0261 |
2 | HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2096+10630G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125901440 | |||||||
| chr6:125901466 | G | C | 1 | a0001c0001t0026g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2096+10656G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125901466 | |||||||
| chr6:125901541 | C | G | 1 | a0003c0003t0003g0251 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2096+10731C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125901541 | |||||||
| chr6:125901571 | A | T | 1 | a0001c0001t0007g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2096+10761A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125901571 | |||||||
| chr6:125901886 | G | A | 114 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0041 others(111): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2096+11076G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125901886 | |||||||
| chr6:125901927 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0041 others(101): Show |
105 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.2096+11117G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125901927 | |||||||
| chr6:125902412 | G | A | 54 | a0002c0002t0010g0133 a0002c0002t0010g0141 a0003c0003t0003g0005 others(51): Show |
54 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(51): Show |
intron_variant | MODIFIER | c.2096+11602G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125902412 | |||||||
| chr6:125902481 | G | GT | 6 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.2096+11685dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125902481 | ||||||
| chr6:125902496 | A | T | 202 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(199): Show |
203 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.2096+11686A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125902496 | |||||||
| chr6:125902508 | G | T | 1 | a0002c0002t0002g0222 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2096+11698G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125902508 | |||||||
| chr6:125902571 | G | A | 1 | a0001c0001t0004g0032 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2096+11761G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125902571 | |||||||
| chr6:125902757 | G | C | 53 | a0002c0002t0010g0133 a0002c0002t0010g0141 a0003c0003t0003g0005 others(50): Show |
53 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.2096+11947G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125902757 | |||||||
| chr6:125902798 | G | A | 91 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0075 others(88): Show |
92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.2096+11988G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125902798 | |||||||
| chr6:125902879 | G | T | 1 | a0001c0009t0022g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2096+12069G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125902879 | |||||||
| chr6:125903125 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2097-12208G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125903125 | |||||||
| chr6:125903570 | A | G | 3 | a0001c0001t0001g0075 a0001c0001t0001g0083 a0001c0001t0001g0092 |
3 | HG02145.hp2 HG02293.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2097-11763A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125903570 | |||||||
| chr6:125903709 | C | CT | 92 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0075 others(89): Show |
93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.2097-11610dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125903709 | ||||||
| chr6:125903722 | T | C | 10 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0258 others(7): Show |
10 | HG02109.hp1 HG02257.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2097-11611T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125903722 | |||||||
| chr6:125903793 | C | T | 1 | a0002c0002t0002g0069 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2097-11540C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125903793 | |||||||
| chr6:125903825 | C | T | 6 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0258 others(3): Show |
6 | HG02109.hp1 HG02257.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2097-11508C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125903825 | |||||||
| chr6:125903849 | G | A | 1 | a0002c0002t0007g0004 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2097-11484G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125903849 | |||||||
| chr6:125904153 | C | G | 1 | a0001c0001t0006g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2097-11180C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125904153 | |||||||
| chr6:125904288 | G | A | 2 | a0002c0002t0010g0133 a0002c0002t0010g0141 |
2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2097-11045G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125904288 | |||||||
| chr6:125904500 | C | A | 2 | a0003c0003t0003g0117 a0003c0003t0003g0125 |
2 | NA18995.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2097-10833C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125904500 | |||||||
| chr6:125904727 | C | T | 1 | a0003c0003t0003g0206 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2097-10606C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125904727 | |||||||
| chr6:125905136 | A | C | 2 | a0001c0001t0009g0187 a0001c0001t0009g0189 |
2 | NA18960.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.2097-10197A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125905136 | |||||||
| chr6:125905238 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2097-10095G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125905238 | |||||||
| chr6:125905253 | A | AT | 79 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(76): Show |
79 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.2097-10060dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125905253 | ||||||
| chr6:125905253 | AT | A | 5 | a0001c0001t0004g0013 a0001c0001t0006g0049 a0002c0002t0002g0101 others(2): Show |
5 | HG02723.hp1 HG03239.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.2097-10060delT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125905253 | ||||||
| chr6:125905330 | C | A | 54 | a0002c0002t0010g0133 a0002c0002t0010g0141 a0003c0003t0003g0005 others(51): Show |
54 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(51): Show |
intron_variant | MODIFIER | c.2097-10003C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125905330 | |||||||
| chr6:125905513 | C | T | 10 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0258 others(7): Show |
10 | HG02109.hp1 HG02257.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2097-9820C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125905513 | |||||||
| chr6:125905681 | A | G | 64 | a0001c0001t0001g0006 a0001c0001t0006g0037 a0001c0001t0006g0049 others(61): Show |
64 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(61): Show |
intron_variant | MODIFIER | c.2097-9652A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125905681 | |||||||
| chr6:125905701 | C | G | 1 | a0003c0003t0003g0126 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2097-9632C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125905701 | |||||||
| chr6:125905975 | G | A | 52 | a0003c0003t0003g0005 a0003c0003t0003g0019 a0003c0003t0003g0029 others(49): Show |
52 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.2097-9358G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125905975 | |||||||
| chr6:125906246 | G | T | 1 | a0001c0001t0004g0065 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2097-9087G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125906246 | |||||||
| chr6:125906309 | C | T | 1 | a0003c0003t0003g0117 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2097-9024C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125906309 | |||||||
| chr6:125906314 | G | A | 1 | a0002c0002t0007g0004 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2097-9019G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125906314 | |||||||
| chr6:125906610 | G | T | 3 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0160 |
3 | HG01891.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2097-8723G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125906610 | |||||||
| chr6:125906690 | T | A | 1 | a0002c0002t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2097-8643T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125906690 | |||||||
| chr6:125906920 | C | T | 2 | a0001c0001t0002g0175 a0001c0001t0002g0216 |
2 | HG01069.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.2097-8413C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125906920 | |||||||
| chr6:125906953 | A | G | 1 | a0001c0001t0007g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2097-8380A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125906953 | |||||||
| chr6:125907082 | A | T | 6 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0258 others(3): Show |
6 | HG02109.hp1 HG02257.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2097-8251A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907082 | |||||||
| chr6:125907249 | G | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(168): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.2097-8084G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907249 | |||||||
| chr6:125907352 | G | C | 152 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0054 others(149): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.2097-7981G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907352 | |||||||
| chr6:125907366 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0054 others(101): Show |
105 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.2097-7967G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907366 | |||||||
| chr6:125907387 | G | A | 3 | a0001c0001t0006g0258 a0001c0001t0006g0259 a0001c0001t0006g0267 |
3 | HG02257.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2097-7946G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907387 | |||||||
| chr6:125907389 | C | CT | 105 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0054 others(102): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.2097-7942dupT | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125907389 | ||||||
| chr6:125907399 | A | G | 1 | a0001c0009t0022g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2097-7934A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907399 | |||||||
| chr6:125907440 | C | T | 1 | a0003c0003t0003g0019 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2097-7893C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907440 | |||||||
| chr6:125907521 | A | G | 1 | a0001c0001t0005g0237 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2097-7812A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907521 | |||||||
| chr6:125907524 | C | T | 2 | a0002c0002t0014g0015 a0002c0008t0015g0261 |
2 | HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2097-7809C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907524 | |||||||
| chr6:125907673 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2097-7660G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907673 | |||||||
| chr6:125907781 | C | T | 1 | a0002c0002t0002g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2097-7552C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125907781 | |||||||
| chr6:125908434 | T | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(168): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.2097-6899T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125908434 | |||||||
| chr6:125908546 | T | C | 1 | a0001c0001t0006g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2097-6787T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125908546 | |||||||
| chr6:125908668 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2097-6665G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125908668 | |||||||
| chr6:125908983 | A | G | 1 | a0002c0002t0011g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2097-6350A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125908983 | |||||||
| chr6:125908988 | GCATTCTC others(4): Show |
G | 1 | a0002c0002t0002g0180 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2097-6340_2097-633 others(15): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125908988 | ||||||
| chr6:125909210 | A | G | 1 | a0001c0009t0022g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2097-6123A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125909210 | |||||||
| chr6:125909299 | C | T | 198 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(195): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.2097-6034C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125909299 | |||||||
| chr6:125909472 | T | G | 4 | a0003c0003t0003g0078 a0003c0003t0003g0116 a0003c0003t0003g0208 others(1): Show |
4 | HG02080.hp1 NA18946.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.2097-5861T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125909472 | |||||||
| chr6:125909644 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2097-5689A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125909644 | |||||||
| chr6:125909679 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2097-5654G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125909679 | |||||||
| chr6:125909740 | G | A | 2 | a0001c0001t0001g0200 a0002c0002t0002g0090 |
2 | HG02572.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.2097-5593G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125909740 | |||||||
| chr6:125909771 | C | T | 1 | a0002c0002t0007g0004 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2097-5562C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125909771 | |||||||
| chr6:125909937 | A | G | 1 | a0002c0002t0002g0098 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2097-5396A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125909937 | |||||||
| chr6:125910604 | T | G | 1 | a0001c0009t0022g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2097-4729T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125910604 | |||||||
| chr6:125910825 | A | G | 24 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0011 others(21): Show |
24 | HG00597.hp2 HG00639.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.2097-4508A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125910825 | |||||||
| chr6:125910917 | G | A | 157 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0054 others(154): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.2097-4416G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125910917 | |||||||
| chr6:125910999 | G | A | 52 | a0003c0003t0003g0005 a0003c0003t0003g0019 a0003c0003t0003g0029 others(49): Show |
52 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.2097-4334G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125910999 | |||||||
| chr6:125911031 | G | A | 1 | a0002c0002t0002g0157 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2097-4302G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125911031 | |||||||
| chr6:125911053 | A | G | 6 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0258 others(3): Show |
6 | HG02109.hp1 HG02257.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2097-4280A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125911053 | |||||||
| chr6:125911072 | G | A | 52 | a0003c0003t0003g0005 a0003c0003t0003g0019 a0003c0003t0003g0029 others(49): Show |
52 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.2097-4261G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125911072 | |||||||
| chr6:125911302 | C | T | 4 | a0003c0003t0003g0051 a0003c0003t0003g0104 a0003c0003t0003g0138 others(1): Show |
4 | HG00280.hp2 HG01175.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2097-4031C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125911302 | |||||||
| chr6:125911648 | A | G | 1 | a0002c0008t0015g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2097-3685A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125911648 | |||||||
| chr6:125911743 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2097-3590C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125911743 | |||||||
| chr6:125911891 | A | G | 2 | a0002c0002t0002g0053 a0002c0002t0002g0082 |
2 | HG02698.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.2097-3442A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125911891 | |||||||
| chr6:125912186 | C | A | 1 | a0003c0003t0003g0019 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2097-3147C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125912186 | |||||||
| chr6:125912248 | T | A | 1 | a0001c0007t0001g0047 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2097-3085T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125912248 | |||||||
| chr6:125912360 | CTCCATAT | C | 51 | a0003c0003t0003g0005 a0003c0003t0003g0019 a0003c0003t0003g0029 others(48): Show |
51 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(48): Show |
intron_variant | MODIFIER | c.2097-2971_2097-296 others(11): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr6 | 125912360 | ||||||
| chr6:125912399 | T | A | 1 | a0002c0002t0004g0204 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2097-2934T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125912399 | |||||||
| chr6:125912545 | G | A | 157 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0054 others(154): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.2097-2788G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125912545 | |||||||
| chr6:125912606 | A | C | 1 | a0001c0001t0001g0225 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2097-2727A>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125912606 | |||||||
| chr6:125912651 | G | A | 1 | a0001c0009t0022g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2097-2682G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125912651 | |||||||
| chr6:125912664 | G | A | 157 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0054 others(154): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.2097-2669G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125912664 | |||||||
| chr6:125913173 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2097-2160A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125913173 | |||||||
| chr6:125913271 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2097-2062G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125913271 | |||||||
| chr6:125913489 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2097-1844C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125913489 | |||||||
| chr6:125913603 | C | T | 2 | a0001c0001t0004g0024 a0001c0001t0004g0032 |
2 | NA18982.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2097-1730C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125913603 | |||||||
| chr6:125913887 | G | A | 6 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0258 others(3): Show |
6 | HG02109.hp1 HG02257.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2097-1446G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125913887 | |||||||
| chr6:125913921 | G | A | 1 | a0004c0013t0013g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2097-1412G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125913921 | |||||||
| chr6:125914037 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2097-1296C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125914037 | |||||||
| chr6:125914054 | T | A | 1 | a0003c0003t0003g0051 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2097-1279T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125914054 | |||||||
| chr6:125914111 | T | C | 2 | a0002c0002t0014g0015 a0002c0008t0015g0261 |
2 | HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2097-1222T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125914111 | |||||||
| chr6:125914170 | G | A | 264 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(261): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.2097-1163G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125914170 | |||||||
| chr6:125914281 | C | T | 53 | a0003c0003t0003g0005 a0003c0003t0003g0019 a0003c0003t0003g0029 others(50): Show |
53 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.2097-1052C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125914281 | |||||||
| chr6:125914708 | A | G | 52 | a0003c0003t0003g0005 a0003c0003t0003g0019 a0003c0003t0003g0029 others(49): Show |
52 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.2097-625A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125914708 | |||||||
| chr6:125914720 | A | G | 53 | a0003c0003t0003g0005 a0003c0003t0003g0019 a0003c0003t0003g0029 others(50): Show |
53 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.2097-613A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125914720 | |||||||
| chr6:125914778 | G | A | 2 | a0001c0001t0001g0178 a0002c0002t0005g0252 |
2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2097-555G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 10/15 | chr6 | 125914778 | |||||||
| chr6:125915538 | G | C | 5 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0258 others(2): Show |
5 | HG02257.hp2 HG02723.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2244+58G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125915538 | |||||||
| chr6:125915585 | G | T | 1 | a0001c0001t0001g0238 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2244+105G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125915585 | |||||||
| chr6:125915660 | A | G | 53 | a0003c0003t0003g0005 a0003c0003t0003g0019 a0003c0003t0003g0029 others(50): Show |
53 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.2244+180A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125915660 | |||||||
| chr6:125915978 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2244+498G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125915978 | |||||||
| chr6:125915981 | A | G | 53 | a0003c0003t0003g0005 a0003c0003t0003g0019 a0003c0003t0003g0029 others(50): Show |
53 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.2244+501A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125915981 | |||||||
| chr6:125916339 | A | G | 7 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0012 others(4): Show |
7 | NA18940.hp1 NA18943.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.2244+859A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125916339 | |||||||
| chr6:125916374 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2244+894G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125916374 | |||||||
| chr6:125916428 | G | A | 1 | a0004c0013t0013g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2244+948G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125916428 | |||||||
| chr6:125916759 | A | G | 55 | a0001c0001t0001g0186 a0002c0002t0001g0059 a0003c0003t0003g0005 others(52): Show |
55 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(52): Show |
intron_variant | MODIFIER | c.2244+1279A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125916759 | |||||||
| chr6:125916837 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2244+1357A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125916837 | |||||||
| chr6:125917164 | C | T | 117 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(114): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.2244+1684C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125917164 | |||||||
| chr6:125917196 | T | TAGAATCT others(3390): Show |
1 | a0001c0001t0006g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244+1732_2244+173 others(3401): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr6 | 125917196 | ||||||
| chr6:125917196 | T | TAGAATCT others(3394): Show |
1 | a0001c0001t0006g0258 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2244+1732_2244+173 others(3405): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr6 | 125917196 | ||||||
| chr6:125917196 | T | TAGAATCT others(3393): Show |
1 | a0001c0001t0006g0267 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2244+1732_2244+173 others(3404): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr6 | 125917196 | ||||||
| chr6:125917196 | T | TAGAATCT others(3444): Show |
1 | a0001c0001t0006g0037 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2244+1732_2244+173 others(3455): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr6 | 125917196 | ||||||
| chr6:125917196 | T | TAGAATCT others(2634): Show |
1 | a0001c0001t0007g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2244+1732_2244+173 others(2645): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr6 | 125917196 | ||||||
| chr6:125917196 | T | TAGAATCT others(3495): Show |
1 | a0001c0001t0006g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2244+1732_2244+173 others(3506): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr6 | 125917196 | ||||||
| chr6:125917400 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2244+1920A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125917400 | |||||||
| chr6:125917521 | A | G | 12 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(9): Show |
12 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.2244+2041A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125917521 | |||||||
| chr6:125917871 | A | G | 53 | a0003c0003t0003g0005 a0003c0003t0003g0019 a0003c0003t0003g0029 others(50): Show |
53 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.2244+2391A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125917871 | |||||||
| chr6:125918050 | C | T | 1 | a0002c0002t0007g0004 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2244+2570C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125918050 | |||||||
| chr6:125918246 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2245-2697T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125918246 | |||||||
| chr6:125918270 | T | C | 1 | a0003c0003t0003g0125 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2245-2673T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125918270 | |||||||
| chr6:125918438 | A | G | 1 | a0002c0002t0007g0004 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2245-2505A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125918438 | |||||||
| chr6:125918814 | G | A | 1 | a0004c0013t0013g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2245-2129G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125918814 | |||||||
| chr6:125918946 | G | A | 6 | a0001c0001t0006g0037 a0001c0001t0006g0049 a0001c0001t0006g0258 others(3): Show |
6 | HG02109.hp1 HG02257.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2245-1997G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125918946 | |||||||
| chr6:125919094 | G | A | 4 | a0002c0004t0002g0028 a0002c0004t0002g0031 a0002c0004t0002g0152 others(1): Show |
4 | HG02615.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2245-1849G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125919094 | |||||||
| chr6:125919664 | AAC | A | 52 | a0003c0003t0003g0005 a0003c0003t0003g0019 a0003c0003t0003g0029 others(49): Show |
52 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.2245-1275_2245-127 others(6): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr6 | 125919664 | ||||||
| chr6:125919748 | G | A | 52 | a0003c0003t0003g0005 a0003c0003t0003g0019 a0003c0003t0003g0029 others(49): Show |
52 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.2245-1195G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125919748 | |||||||
| chr6:125920588 | G | A | 264 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(261): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.2245-355G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125920588 | |||||||
| chr6:125920837 | G | A | 1 | a0001c0001t0016g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2245-106G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125920837 | |||||||
| chr6:125920860 | G | A | 2 | a0001c0001t0009g0187 a0001c0001t0009g0189 |
2 | NA18960.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.2245-83G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 11/15 | chr6 | 125920860 | |||||||
| chr6:125921129 | G | C | 1 | a0001c0001t0004g0008 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2370+61G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125921129 | |||||||
| chr6:125921131 | C | G | 1 | a0001c0001t0004g0008 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2370+63C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125921131 | |||||||
| chr6:125921171 | A | G | 1 | a0001c0001t0004g0008 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2370+103A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125921171 | |||||||
| chr6:125921327 | T | G | 1 | a0001c0001t0026g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2370+259T>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125921327 | |||||||
| chr6:125921920 | A | G | 1 | a0001c0001t0026g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2371-762A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125921920 | |||||||
| chr6:125921921 | T | A | 1 | a0001c0001t0004g0008 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2371-761T>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125921921 | |||||||
| chr6:125921924 | C | T | 1 | a0001c0001t0004g0008 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2371-758C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125921924 | |||||||
| chr6:125921982 | G | T | 1 | a0001c0001t0004g0008 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2371-700G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125921982 | |||||||
| chr6:125922009 | A | T | 1 | a0002c0002t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2371-673A>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125922009 | |||||||
| chr6:125922114 | G | A | 1 | a0004c0013t0013g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2371-568G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125922114 | |||||||
| chr6:125922197 | T | C | 1 | a0003c0003t0018g0128 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2371-485T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125922197 | |||||||
| chr6:125922241 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2371-441G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125922241 | |||||||
| chr6:125922445 | C | G | 114 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(111): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2371-237C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 12/15 | chr6 | 125922445 | |||||||
| chr6:125922839 | G | A | 1 | a0003c0003t0003g0005 | 1 | HG02818.hp2 | splice_region_variant&intron_variant | LOW | c.2523+5G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125922839 | |||||||
| chr6:125923217 | C | G | 1 | a0002c0002t0002g0084 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2523+383C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125923217 | |||||||
| chr6:125923362 | G | A | 1 | a0001c0001t0026g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2523+528G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125923362 | |||||||
| chr6:125923481 | G | T | 2 | a0001c0009t0022g0262 a0002c0002t0007g0004 |
2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2523+647G>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125923481 | |||||||
| chr6:125923507 | G | A | 2 | a0002c0002t0002g0090 a0002c0002t0002g0214 |
2 | HG00642.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2523+673G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125923507 | |||||||
| chr6:125923535 | A | G | 1 | a0002c0002t0002g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2523+701A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125923535 | |||||||
| chr6:125923536 | T | C | 169 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(166): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.2523+702T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125923536 | |||||||
| chr6:125924301 | A | G | 53 | a0003c0003t0003g0005 a0003c0003t0003g0019 a0003c0003t0003g0029 others(50): Show |
53 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.2523+1467A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125924301 | |||||||
| chr6:125924498 | C | A | 52 | a0003c0003t0003g0005 a0003c0003t0003g0019 a0003c0003t0003g0029 others(49): Show |
52 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.2523+1664C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125924498 | |||||||
| chr6:125924699 | C | A | 52 | a0003c0003t0003g0005 a0003c0003t0003g0019 a0003c0003t0003g0029 others(49): Show |
52 | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.2523+1865C>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125924699 | |||||||
| chr6:125924772 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2523+1938G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125924772 | |||||||
| chr6:125924825 | ACT | A | 3 | a0001c0001t0006g0258 a0001c0001t0006g0259 a0001c0001t0006g0267 |
3 | HG02257.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2523+1996_2523+199 others(6): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr6 | 125924825 | ||||||
| chr6:125924914 | G | C | 1 | a0004c0013t0013g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2523+2080G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125924914 | |||||||
| chr6:125925005 | C | T | 1 | a0001c0001t0026g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2523+2171C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125925005 | |||||||
| chr6:125925572 | A | G | 25 | a0002c0002t0002g0067 a0002c0002t0002g0068 a0002c0002t0002g0069 others(22): Show |
25 | HG00544.hp1 HG02132.hp1 HG02135.hp1 others(22): Show |
intron_variant | MODIFIER | c.2524-2091A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125925572 | |||||||
| chr6:125925778 | C | G | 1 | a0003c0003t0003g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2524-1885C>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125925778 | |||||||
| chr6:125926132 | G | A | 2 | a0002c0002t0010g0133 a0002c0002t0010g0141 |
2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2524-1531G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125926132 | |||||||
| chr6:125926139 | C | T | 1 | a0002c0002t0002g0103 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2524-1524C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125926139 | |||||||
| chr6:125926204 | G | A | 7 | a0002c0002t0002g0016 a0002c0002t0002g0033 a0002c0002t0002g0253 others(4): Show |
7 | HG02615.hp2 HG02630.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2524-1459G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125926204 | |||||||
| chr6:125926260 | T | C | 264 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(261): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.2524-1403T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125926260 | |||||||
| chr6:125926311 | CA | C | 53 | a0001c0001t0001g0170 a0002c0002t0001g0228 a0003c0003t0003g0005 others(50): Show |
53 | HG00280.hp2 HG00323.hp1 HG01106.hp2 others(50): Show |
intron_variant | MODIFIER | c.2524-1339delA | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr6 | 125926311 | ||||||
| chr6:125926324 | A | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0213 |
2 | HG01106.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.2524-1339A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125926324 | |||||||
| chr6:125926404 | T | C | 1 | a0001c0001t0004g0065 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2524-1259T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125926404 | |||||||
| chr6:125926865 | A | G | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0179 |
3 | HG00280.hp1 HG00733.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.2524-798A>G | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125926865 | |||||||
| chr6:125926971 | C | T | 1 | a0004c0013t0013g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2524-692C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125926971 | |||||||
| chr6:125927073 | C | T | 2 | a0001c0001t0004g0038 a0001c0001t0004g0040 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2524-590C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125927073 | |||||||
| chr6:125927228 | T | C | 113 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(110): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.2524-435T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125927228 | |||||||
| chr6:125927450 | G | A | 194 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0036 others(191): Show |
195 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.2524-213G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 13/15 | chr6 | 125927450 | |||||||
| chr6:125927799 | G | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0241 |
2 | HG00597.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.2619+41G>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 14/15 | chr6 | 125927799 | |||||||
| chr6:125927878 | G | A | 12 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(9): Show |
12 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.2619+120G>A | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 14/15 | chr6 | 125927878 | |||||||
| chr6:125927999 | T | C | 1 | a0001c0001t0002g0039 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2620-175T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 14/15 | chr6 | 125927999 | |||||||
| chr6:125928393 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2693+146C>T | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 15/15 | chr6 | 125928393 | |||||||
| chr6:125928448 | T | C | 1 | a0001c0001t0005g0017 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2694-188T>C | NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 15/15 | chr6 | 125928448 |