Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79670 |
| ensemblid | ENSG00000083223.18 |
| hgncid | 25817 |
| symbol | TUT7 |
| name | terminal uridylyl transferase 7 |
| refseq_nuc | NM_024617.4 |
| refseq_prot | NP_078893.2 |
| ensembl_nuc | ENST00000375963.8 |
| ensembl_prot | ENSP00000365130.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 86287733 |
| end | 86354410 |
| strand | - |
| ver | v1.2 |
| region | chr9:86287733-86354410 |
| region5000 | chr9:86282733-86359410 |
| regionname0 | TUT7_chr9_86287733_86354410 |
| regionname5000 | TUT7_chr9_86282733_86359410 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1494 | 178 | 39 | 36 | 74 | 8 | 21 | 62 | TUT7_chr9_86282733_86359410 | TUT7 | MGDTA others(1489): Show |
chr9 | 86282733 | 86359410 |
| a0002 | 1/1 | 1495 | 163 | 38 | 28 | 73 | 7 | 15 | 55 | TUT7_chr9_86282733_86359410 | TUT7 | MGDTA others(1490): Show |
chr9 | 86282733 | 86359410 |
| a0003 | 0/0 | 1494 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | MGDTA others(1489): Show |
chr9 | 86282733 | 86359410 |
| a0004 | 0/0 | 1494 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | MGDTA others(1489): Show |
chr9 | 86282733 | 86359410 |
| a0005 | 0/0 | 1495 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | MGDTA others(1490): Show |
chr9 | 86282733 | 86359410 |
| a0006 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | MGDTA others(1489): Show |
chr9 | 86282733 | 86359410 |
| a0007 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | MGDTA others(1489): Show |
chr9 | 86282733 | 86359410 |
| a0008 | 0/0 | 1495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | MGDTA others(1490): Show |
chr9 | 86282733 | 86359410 |
| a0009 | 0/0 | 1495 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | MGDTA others(1490): Show |
chr9 | 86282733 | 86359410 |
| a0010 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | MGDTA others(1489): Show |
chr9 | 86282733 | 86359410 |
| a0011 | 0/0 | 1495 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | MGDTA others(1490): Show |
chr9 | 86282733 | 86359410 |
| a0012 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | MGDTA others(1489): Show |
chr9 | 86282733 | 86359410 |
| a0013 | 0/0 | 1495 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | MGDTA others(1490): Show |
chr9 | 86282733 | 86359410 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4482 | 170 | 33 | 35 | 74 | 8 | 20 | TUT7_chr9_86282733_86359410 | TUT7 | ATGGG others(4477): Show |
chr9 | 86282733 | 86359410 | ||
| a0001c0006 | 0/0 | 4482 | 4 | 4 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | ATGGG others(4477): Show |
chr9 | 86282733 | 86359410 | ||
| a0001c0009 | 0/0 | 4482 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | ATGGG others(4477): Show |
chr9 | 86282733 | 86359410 | ||
| a0001c0012 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | ATGGG others(4477): Show |
chr9 | 86282733 | 86359410 | ||
| a0001c0013 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | ATGGG others(4477): Show |
chr9 | 86282733 | 86359410 | ||
| a0001c0014 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | ATGGG others(4477): Show |
chr9 | 86282733 | 86359410 | ||
| a0002c0002 | 1/1 | 4485 | 121 | 17 | 24 | 59 | 7 | 12 | TUT7_chr9_86282733_86359410 | TUT7 | ATGGG others(4480): Show |
chr9 | 86282733 | 86359410 | ||
| a0002c0003 | 0/0 | 4485 | 42 | 21 | 4 | 14 | 0 | 3 | TUT7_chr9_86282733_86359410 | TUT7 | ATGGG others(4480): Show |
chr9 | 86282733 | 86359410 | ||
| a0003c0004 | 0/0 | 4482 | 6 | 6 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | ATGGG others(4477): Show |
chr9 | 86282733 | 86359410 | ||
| a0004c0005 | 0/0 | 4482 | 5 | 4 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | ATGGG others(4477): Show |
chr9 | 86282733 | 86359410 | ||
| a0005c0007 | 0/0 | 4485 | 2 | 0 | 1 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | ATGGG others(4480): Show |
chr9 | 86282733 | 86359410 | ||
| a0006c0016 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | ATGGG others(4477): Show |
chr9 | 86282733 | 86359410 | ||
| a0007c0017 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | ATGGG others(4477): Show |
chr9 | 86282733 | 86359410 | ||
| a0008c0011 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | ATGGG others(4480): Show |
chr9 | 86282733 | 86359410 | ||
| a0009c0018 | 0/0 | 4485 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | ATGGG others(4480): Show |
chr9 | 86282733 | 86359410 | ||
| a0010c0015 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | ATGGG others(4477): Show |
chr9 | 86282733 | 86359410 | ||
| a0011c0008 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | ATGGG others(4480): Show |
chr9 | 86282733 | 86359410 | ||
| a0012c0010 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | ATGGG others(4477): Show |
chr9 | 86282733 | 86359410 | ||
| a0013c0019 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | ATGGG others(4480): Show |
chr9 | 86282733 | 86359410 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5600 | 136 | 26 | 20 | 72 | 2 | 16 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5595): Show |
chr9 | 86282733 | 86359410 |
| a0001c0001t0002 | 0/0 | 5600 | 28 | 1 | 15 | 2 | 6 | 4 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5595): Show |
chr9 | 86282733 | 86359410 |
| a0001c0001t0003 | 0/0 | 5600 | 3 | 3 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5595): Show |
chr9 | 86282733 | 86359410 |
| a0001c0001t0004 | 0/0 | 5600 | 2 | 2 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5595): Show |
chr9 | 86282733 | 86359410 |
| a0001c0001t0010 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5595): Show |
chr9 | 86282733 | 86359410 |
| a0001c0006t0001 | 0/0 | 5600 | 4 | 4 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5595): Show |
chr9 | 86282733 | 86359410 |
| a0001c0009t0001 | 0/0 | 5600 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5595): Show |
chr9 | 86282733 | 86359410 |
| a0001c0012t0008 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5595): Show |
chr9 | 86282733 | 86359410 |
| a0001c0013t0001 | 0/0 | 5600 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5595): Show |
chr9 | 86282733 | 86359410 |
| a0001c0014t0011 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5595): Show |
chr9 | 86282733 | 86359410 |
| a0002c0002t0001 | 0/1 | 5603 | 114 | 16 | 21 | 58 | 7 | 11 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5598): Show |
chr9 | 86282733 | 86359410 |
| a0002c0002t0002 | 1/0 | 5603 | 3 | 0 | 2 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5598): Show |
chr9 | 86282733 | 86359410 |
| a0002c0002t0005 | 0/0 | 5603 | 2 | 0 | 1 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5598): Show |
chr9 | 86282733 | 86359410 |
| a0002c0002t0006 | 0/0 | 5603 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5598): Show |
chr9 | 86282733 | 86359410 |
| a0002c0002t0009 | 0/0 | 5603 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5598): Show |
chr9 | 86282733 | 86359410 |
| a0002c0003t0001 | 0/0 | 5603 | 41 | 21 | 4 | 14 | 0 | 2 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5598): Show |
chr9 | 86282733 | 86359410 |
| a0002c0003t0007 | 0/0 | 5603 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5598): Show |
chr9 | 86282733 | 86359410 |
| a0003c0004t0001 | 0/0 | 5600 | 6 | 6 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5595): Show |
chr9 | 86282733 | 86359410 |
| a0004c0005t0001 | 0/0 | 5600 | 5 | 4 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5595): Show |
chr9 | 86282733 | 86359410 |
| a0005c0007t0001 | 0/0 | 5603 | 2 | 0 | 1 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5598): Show |
chr9 | 86282733 | 86359410 |
| a0006c0016t0001 | 0/0 | 5600 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5595): Show |
chr9 | 86282733 | 86359410 |
| a0007c0017t0001 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5595): Show |
chr9 | 86282733 | 86359410 |
| a0008c0011t0001 | 0/0 | 5603 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5598): Show |
chr9 | 86282733 | 86359410 |
| a0009c0018t0001 | 0/0 | 5603 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5598): Show |
chr9 | 86282733 | 86359410 |
| a0010c0015t0004 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5595): Show |
chr9 | 86282733 | 86359410 |
| a0011c0008t0001 | 0/0 | 5603 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5598): Show |
chr9 | 86282733 | 86359410 |
| a0012c0010t0001 | 0/0 | 5600 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5595): Show |
chr9 | 86282733 | 86359410 |
| a0013c0019t0001 | 0/0 | 5603 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | AGGAA others(5598): Show |
chr9 | 86282733 | 86359410 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0006 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0002g0002 | 0/0 | 8 | 0 | 5 | 0 | 1 | 2 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0001t0010g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0006t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0006t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0006t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0006t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0009t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0012t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0013t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0001c0014t0011g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0001 | 0/0 | 11 | 5 | 2 | 3 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0002g0198 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0005g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0002t0009g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0002c0003t0007g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0003c0004t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0003c0004t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0003c0004t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0003c0004t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0003c0004t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0003c0004t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0004c0005t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0004c0005t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0004c0005t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0005c0007t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0005c0007t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0006c0016t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0007c0017t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0008c0011t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0009c0018t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0010c0015t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0011c0008t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0012c0010t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| a0013c0019t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0005 | c0007 | t0001 | g0197 | EUR | GBR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0048 | EUR | GBR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0027 | EUR | GBR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0188 | EUR | FIN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0046 | EUR | FIN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | CHS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | CHS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | CHS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | CHS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | CHS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0257 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0221 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00733 | hp1 | a0002 | c0003 | t0001 | g0267 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00735 | hp1 | a0002 | c0003 | t0001 | g0266 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0199 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0175 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0189 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0190 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0191 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01109 | hp2 | a0002 | c0003 | t0001 | g0282 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0258 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0171 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0225 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0032 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01243 | hp1 | a0004 | c0005 | t0001 | g0037 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0208 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01255 | hp2 | a0002 | c0003 | t0001 | g0289 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0177 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0228 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0176 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01261 | hp1 | a0002 | c0002 | t0005 | g0227 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0186 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0244 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01433 | hp1 | a0005 | c0007 | t0001 | g0259 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0043 | EUR | IBS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0028 | EUR | IBS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0028 | EUR | IBS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01884 | hp2 | a0001 | c0014 | t0011 | g0294 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0206 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0238 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02040 | hp2 | a0002 | c0003 | t0001 | g0262 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02055 | hp2 | a0002 | c0003 | t0001 | g0290 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0268 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | CDX | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02257 | hp1 | a0002 | c0003 | t0001 | g0035 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02257 | hp2 | a0003 | c0004 | t0001 | g0273 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02258 | hp2 | a0001 | c0001 | t0010 | g0160 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02280 | hp1 | a0002 | c0003 | t0001 | g0035 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0196 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0170 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02451 | hp1 | a0002 | c0003 | t0001 | g0038 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02602 | hp1 | a0006 | c0016 | t0001 | g0153 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0179 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02615 | hp1 | a0007 | c0017 | t0001 | g0096 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02615 | hp2 | a0003 | c0004 | t0001 | g0274 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02622 | hp1 | a0001 | c0006 | t0001 | g0090 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0147 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02630 | hp1 | a0002 | c0003 | t0001 | g0013 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02630 | hp2 | a0002 | c0003 | t0001 | g0246 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0205 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02698 | hp2 | a0002 | c0003 | t0001 | g0034 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02717 | hp1 | a0002 | c0003 | t0001 | g0038 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02723 | hp2 | a0008 | c0011 | t0001 | g0286 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0261 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0270 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02818 | hp2 | a0002 | c0003 | t0001 | g0288 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02886 | hp1 | a0003 | c0004 | t0001 | g0271 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0209 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02895 | hp2 | a0001 | c0006 | t0001 | g0091 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0284 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0293 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02897 | hp1 | a0002 | c0003 | t0001 | g0285 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02897 | hp2 | a0001 | c0006 | t0001 | g0089 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0216 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02965 | hp1 | a0004 | c0005 | t0001 | g0036 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0230 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02970 | hp2 | a0002 | c0003 | t0001 | g0291 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02976 | hp2 | a0002 | c0002 | t0006 | g0173 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03017 | hp1 | a0009 | c0018 | t0001 | g0202 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0087 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03041 | hp2 | a0004 | c0005 | t0001 | g0036 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03130 | hp2 | a0002 | c0003 | t0001 | g0287 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03139 | hp1 | a0002 | c0003 | t0001 | g0039 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03139 | hp2 | a0002 | c0003 | t0001 | g0269 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03195 | hp1 | a0004 | c0005 | t0001 | g0280 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0085 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03209 | hp1 | a0010 | c0015 | t0004 | g0086 | AFR | MSL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0063 | AFR | MSL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03225 | hp1 | a0001 | c0012 | t0008 | g0151 | AFR | MSL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0030 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03453 | hp1 | a0002 | c0003 | t0001 | g0279 | AFR | MSL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0245 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03516 | hp2 | a0002 | c0003 | t0001 | g0169 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03540 | hp1 | a0002 | c0003 | t0001 | g0040 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03540 | hp2 | a0003 | c0004 | t0001 | g0272 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0172 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0210 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0229 | SAS | BEB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03942 | hp1 | a0002 | c0002 | t0009 | g0167 | SAS | BEB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03942 | hp2 | a0002 | c0003 | t0001 | g0034 | SAS | BEB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0201 | SAS | STU | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | STU | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG04184 | hp1 | a0001 | c0013 | t0001 | g0072 | SAS | BEB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0223 | SAS | BEB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | STU | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG04228 | hp1 | a0002 | c0003 | t0007 | g0148 | SAS | STU | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0174 | SAS | STU | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | YRI | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0222 | AFR | YRI | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | CHB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18747 | hp1 | a0002 | c0003 | t0001 | g0247 | EAS | CHB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | CHB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18906 | hp1 | a0003 | c0004 | t0001 | g0276 | AFR | YRI | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18948 | hp2 | a0002 | c0002 | t0005 | g0203 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18950 | hp1 | a0002 | c0003 | t0001 | g0253 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18957 | hp1 | a0002 | c0003 | t0001 | g0265 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18959 | hp1 | a0002 | c0003 | t0001 | g0264 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18963 | hp2 | a0002 | c0003 | t0001 | g0137 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18967 | hp2 | a0011 | c0008 | t0001 | g0168 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18978 | hp2 | a0002 | c0003 | t0001 | g0254 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18992 | hp2 | a0002 | c0003 | t0001 | g0252 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18998 | hp1 | a0002 | c0003 | t0001 | g0263 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18999 | hp1 | a0002 | c0003 | t0001 | g0255 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19005 | hp2 | a0002 | c0003 | t0001 | g0165 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19007 | hp1 | a0012 | c0010 | t0001 | g0132 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | LWK | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0193 | AFR | LWK | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19062 | hp1 | a0013 | c0019 | t0001 | g0256 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19070 | hp1 | a0002 | c0003 | t0001 | g0251 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19074 | hp2 | a0002 | c0003 | t0001 | g0033 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19080 | hp1 | a0002 | c0003 | t0001 | g0033 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | YRI | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0122 | AFR | YRI | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA20129 | hp1 | a0003 | c0004 | t0001 | g0275 | AFR | ASW | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA20129 | hp2 | a0002 | c0003 | t0001 | g0283 | AFR | ASW | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | TSI | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | TSI | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0224 | EUR | TSI | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0149 | EUR | TSI | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | GIH | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01123 | hp1 | a0001 | c0009 | t0001 | g0069 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02109 | hp2 | a0001 | c0006 | t0001 | g0088 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG03471 | hp2 | a0002 | c0003 | t0001 | g0292 | AFR | MSL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG06807 | hp1 | a0002 | c0003 | t0001 | g0013 | AFR | USA | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | USA | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA20300 | hp1 | a0004 | c0005 | t0001 | g0037 | AFR | USA | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | USA | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0217 | AFR | LWK | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0166 | AFR | LWK | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0211 | REF | REF | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0198 | REF | REF | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:86301359 | T | C | 1 | a0001 | 4 | HG02109.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
missense_variant | MODERATE | c.4337A>G | p.Lys1446Arg | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/27 | 4508/5603 | 4337/4488 | 1446/1495 | chr9 | 86301359 | |||
| chr9:86301593 | C | T | 1 | a0009 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.4103G>A | p.Arg1368Gln | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/27 | 4274/5603 | 4103/4488 | 1368/1495 | chr9 | 86301593 | |||
| chr9:86309220 | C | G | 1 | a0001 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.3652G>C | p.Asp1218His | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 21/27 | 3823/5603 | 3652/4488 | 1218/1495 | chr9 | 86309220 | |||
| chr9:86322456 | C | A | 1 | a0008 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.2897G>T | p.Ser966Ile | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/27 | 3068/5603 | 2897/4488 | 966/1495 | chr9 | 86322456 | |||
| chr9:86322456 | C | T | 1 | a0001 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.2897G>A | p.Ser966Asn | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/27 | 3068/5603 | 2897/4488 | 966/1495 | chr9 | 86322456 | |||
| chr9:86322457 | T | G | 1 | a0008 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.2896A>C | p.Ser966Arg | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/27 | 3067/5603 | 2896/4488 | 966/1495 | chr9 | 86322457 | |||
| chr9:86322936 | ATTT | A | 7 | a0001 a0003 a0004 others(4): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
disruptive_inframe_deletion | MODERATE | c.2811_2813delAAA | p.Lys937del | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 13/27 | 2984/5603 | 2811/4488 | 937/1495 | chr9 | 86322936 | |||
| chr9:86323133 | T | C | 1 | a0010 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.2617A>G | p.Met873Val | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 13/27 | 2788/5603 | 2617/4488 | 873/1495 | chr9 | 86323133 | |||
| chr9:86323171 | G | A | 1 | a0006 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.2579C>T | p.Pro860Leu | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 13/27 | 2750/5603 | 2579/4488 | 860/1495 | chr9 | 86323171 | |||
| chr9:86323199 | C | T | 1 | a0012 | 1 | NA19007.hp1 | missense_variant | MODERATE | c.2551G>A | p.Asp851Asn | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 13/27 | 2722/5603 | 2551/4488 | 851/1495 | chr9 | 86323199 | |||
| chr9:86323541 | T | C | 1 | a0007 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.2209A>G | p.Lys737Glu | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 13/27 | 2380/5603 | 2209/4488 | 737/1495 | chr9 | 86323541 | |||
| chr9:86323753 | G | A | 1 | a0005 | 2 | HG00099.hp1 HG01433.hp1 |
missense_variant | MODERATE | c.1997C>T | p.Thr666Ile | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 13/27 | 2168/5603 | 1997/4488 | 666/1495 | chr9 | 86323753 | |||
| chr9:86346438 | G | A | 1 | a0003 | 6 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
missense_variant | MODERATE | c.563C>T | p.Thr188Ile | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 3/27 | 734/5603 | 563/4488 | 188/1495 | chr9 | 86346438 | |||
| chr9:86346438 | G | C | 1 | a0013 | 1 | NA19062.hp1 | missense_variant | MODERATE | c.563C>G | p.Thr188Ser | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 3/27 | 734/5603 | 563/4488 | 188/1495 | chr9 | 86346438 | |||
| chr9:86346444 | C | T | 1 | a0011 | 1 | NA18967.hp2 | missense_variant | MODERATE | c.557G>A | p.Arg186Gln | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 3/27 | 728/5603 | 557/4488 | 186/1495 | chr9 | 86346444 | |||
| chr9:86353148 | T | A | 1 | a0004 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
missense_variant | MODERATE | c.52A>T | p.Thr18Ser | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/27 | 223/5603 | 52/4488 | 18/1495 | chr9 | 86353148 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:86304865 | G | T | 1 | a0001c0014 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.3969C>A | p.Pro1323Pro | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/27 | 4140/5603 | 3969/4488 | 1323/1495 | chr9 | 86304865 | |||
| chr9:86345023 | C | T | 15 | a0001c0001 a0001c0006 a0001c0009 others(12): Show |
237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
synonymous_variant | LOW | c.951G>A | p.Leu317Leu | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/27 | 1122/5603 | 951/4488 | 317/1495 | chr9 | 86345023 | |||
| chr9:86346419 | C | T | 1 | a0001c0009 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.582G>A | p.Glu194Glu | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 3/27 | 753/5603 | 582/4488 | 194/1495 | chr9 | 86346419 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:86287748 | C | T | 26 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(23): Show |
330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
3_prime_UTR_variant | MODIFIER | c.*929G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 929 | chr9 | 86287748 | ||||||
| chr9:86287976 | T | C | 1 | a0002c0002t0009 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*701A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 701 | chr9 | 86287976 | ||||||
| chr9:86288160 | C | T | 1 | a0001c0014t0011 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*517G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 517 | chr9 | 86288160 | ||||||
| chr9:86288232 | T | C | 1 | a0002c0002t0005 | 2 | HG01261.hp1 NA18948.hp2 |
3_prime_UTR_variant | MODIFIER | c.*445A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 445 | chr9 | 86288232 | ||||||
| chr9:86288240 | C | T | 1 | a0001c0001t0003 | 3 | HG02280.hp2 HG02486.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*437G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 437 | chr9 | 86288240 | ||||||
| chr9:86288305 | C | T | 1 | a0001c0012t0008 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*372G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 372 | chr9 | 86288305 | ||||||
| chr9:86288452 | T | A | 26 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(23): Show |
330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
3_prime_UTR_variant | MODIFIER | c.*225A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 225 | chr9 | 86288452 | ||||||
| chr9:86288500 | C | G | 1 | a0002c0003t0007 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*177G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 177 | chr9 | 86288500 | ||||||
| chr9:86288562 | C | T | 3 | a0001c0001t0003 a0001c0001t0004 a0010c0015t0004 |
6 | HG02280.hp2 HG02486.hp2 HG03041.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*115G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 115 | chr9 | 86288562 | ||||||
| chr9:86288603 | T | C | 1 | a0001c0001t0010 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*74A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 74 | chr9 | 86288603 | ||||||
| chr9:86288638 | C | T | 1 | a0002c0002t0006 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*39G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 39 | chr9 | 86288638 | ||||||
| chr9:86354355 | G | A | 1 | a0001c0014t0011 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-116C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 1/27 | 1156 | chr9 | 86354355 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:86288932 | T | A | 1 | a0002c0003t0001g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4421-188A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86288932 | |||||||
| chr9:86289092 | T | C | 3 | a0002c0002t0001g0063 a0004c0005t0001g0037 a0004c0005t0001g0280 |
4 | HG01243.hp1 HG03195.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.4421-348A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86289092 | |||||||
| chr9:86289146 | C | T | 4 | a0002c0003t0001g0033 a0002c0003t0001g0253 a0002c0003t0001g0255 others(1): Show |
5 | NA18950.hp1 NA18999.hp1 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.4421-402G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86289146 | |||||||
| chr9:86289235 | A | C | 18 | a0001c0001t0001g0278 a0002c0003t0001g0033 a0002c0003t0001g0034 others(15): Show |
20 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.4421-491T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86289235 | |||||||
| chr9:86289404 | A | C | 1 | a0004c0005t0001g0036 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.4421-660T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86289404 | |||||||
| chr9:86289553 | G | A | 1 | a0002c0002t0001g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4421-809C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86289553 | |||||||
| chr9:86289554 | TAAGA | T | 134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(131): Show |
164 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.4421-814_4421-811d others(6): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86289554 | |||||||
| chr9:86289697 | A | G | 18 | a0001c0001t0001g0278 a0002c0003t0001g0033 a0002c0003t0001g0034 others(15): Show |
20 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.4421-953T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86289697 | |||||||
| chr9:86289742 | CA | C | 5 | a0001c0001t0001g0093 a0001c0001t0001g0110 a0001c0001t0001g0111 others(2): Show |
5 | HG03453.hp1 NA18948.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.4421-999delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86289742 | |||||||
| chr9:86290033 | A | G | 1 | a0002c0002t0001g0236 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.4421-1289T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290033 | |||||||
| chr9:86290073 | G | A | 2 | a0004c0005t0001g0037 a0004c0005t0001g0280 |
3 | HG01243.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4421-1329C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290073 | |||||||
| chr9:86290092 | C | G | 5 | a0002c0002t0001g0032 a0002c0002t0001g0147 a0002c0002t0001g0225 others(2): Show |
6 | HG01168.hp2 HG01169.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.4421-1348G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290092 | |||||||
| chr9:86290323 | T | C | 1 | a0001c0012t0008g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4421-1579A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290323 | |||||||
| chr9:86290415 | G | A | 99 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0011 others(96): Show |
122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.4421-1671C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290415 | |||||||
| chr9:86290686 | C | CA | 45 | a0001c0001t0001g0059 a0001c0001t0001g0071 a0001c0001t0001g0075 others(42): Show |
47 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.4421-1943dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290686 | |||||||
| chr9:86290686 | CA | C | 7 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0106 others(4): Show |
8 | HG00323.hp1 HG01070.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.4421-1943delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290686 | |||||||
| chr9:86290779 | C | T | 1 | a0001c0012t0008g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4421-2035G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290779 | |||||||
| chr9:86290822 | T | G | 48 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0024 others(45): Show |
55 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.4421-2078A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290822 | |||||||
| chr9:86290909 | C | A | 1 | a0001c0001t0001g0123 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4421-2165G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290909 | |||||||
| chr9:86290929 | A | G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0139 a0001c0001t0001g0145 |
3 | HG02723.hp1 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4421-2185T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290929 | |||||||
| chr9:86291165 | T | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0099 a0001c0001t0001g0101 |
4 | HG01928.hp2 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.4421-2421A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86291165 | |||||||
| chr9:86291368 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4421-2624G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86291368 | |||||||
| chr9:86291464 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01192.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.4421-2720C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86291464 | |||||||
| chr9:86291521 | G | A | 2 | a0004c0005t0001g0037 a0004c0005t0001g0280 |
3 | HG01243.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4421-2777C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86291521 | |||||||
| chr9:86291572 | C | CA | 7 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0120 others(4): Show |
7 | HG01255.hp1 HG02129.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.4421-2829dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86291572 | |||||||
| chr9:86291572 | CA | C | 9 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0161 others(6): Show |
9 | HG01070.hp1 HG01167.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.4421-2829delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86291572 | |||||||
| chr9:86291736 | C | T | 1 | a0001c0014t0011g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4421-2992G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86291736 | |||||||
| chr9:86291780 | C | G | 272 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.4421-3036G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86291780 | |||||||
| chr9:86291795 | T | C | 1 | a0002c0003t0007g0148 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4421-3051A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86291795 | |||||||
| chr9:86291905 | T | C | 1 | a0002c0003t0001g0039 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4421-3161A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86291905 | |||||||
| chr9:86292049 | A | T | 1 | a0002c0002t0001g0186 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4421-3305T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86292049 | |||||||
| chr9:86292239 | T | C | 2 | a0002c0003t0001g0252 a0002c0003t0001g0254 |
2 | NA18978.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.4421-3495A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86292239 | |||||||
| chr9:86292290 | A | C | 1 | a0002c0002t0001g0178 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.4421-3546T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86292290 | |||||||
| chr9:86292417 | A | G | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.4421-3673T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86292417 | |||||||
| chr9:86292468 | C | CA | 16 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0058 others(13): Show |
18 | HG00621.hp1 HG02109.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.4421-3725dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86292468 | |||||||
| chr9:86292475 | A | G | 1 | a0001c0001t0002g0048 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4421-3731T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86292475 | |||||||
| chr9:86292607 | T | TA | 5 | a0001c0001t0001g0042 a0001c0001t0001g0092 a0001c0001t0001g0139 others(2): Show |
7 | HG01109.hp1 HG01516.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.4421-3864dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86292607 | |||||||
| chr9:86292607 | TA | T | 14 | a0001c0001t0001g0066 a0001c0001t0001g0077 a0001c0001t0001g0126 others(11): Show |
14 | HG00323.hp2 HG00544.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.4421-3864delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86292607 | |||||||
| chr9:86293340 | T | A | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.4421-4596A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86293340 | |||||||
| chr9:86293533 | C | A | 1 | a0004c0005t0001g0280 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4421-4789G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86293533 | |||||||
| chr9:86293621 | T | C | 1 | a0001c0001t0010g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4421-4877A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86293621 | |||||||
| chr9:86293886 | T | C | 101 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0011 others(98): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.4421-5142A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86293886 | |||||||
| chr9:86293888 | G | A | 1 | a0001c0012t0008g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4421-5144C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86293888 | |||||||
| chr9:86293965 | G | A | 2 | a0002c0003t0001g0247 a0002c0003t0001g0262 |
2 | HG02040.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.4421-5221C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86293965 | |||||||
| chr9:86294026 | G | A | 1 | a0002c0002t0001g0204 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.4421-5282C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294026 | |||||||
| chr9:86294026 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4421-5282C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294026 | |||||||
| chr9:86294038 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4421-5294C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294038 | |||||||
| chr9:86294052 | A | C | 1 | a0002c0002t0001g0226 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.4421-5308T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294052 | |||||||
| chr9:86294274 | C | CA | 12 | a0001c0001t0001g0278 a0001c0001t0002g0043 a0001c0001t0002g0044 others(9): Show |
12 | HG00099.hp2 HG00323.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.4421-5531dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294274 | |||||||
| chr9:86294274 | CA | C | 118 | a0001c0001t0001g0023 a0001c0001t0001g0071 a0001c0001t0001g0104 others(115): Show |
144 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.4421-5531delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294274 | |||||||
| chr9:86294274 | CAA | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
148 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.4421-5532_4421-553 others(6): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294274 | |||||||
| chr9:86294328 | G | T | 1 | a0006c0016t0001g0153 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4421-5584C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294328 | |||||||
| chr9:86294366 | A | G | 1 | a0001c0012t0008g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4421-5622T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294366 | |||||||
| chr9:86294440 | G | T | 140 | a0001c0001t0001g0123 a0001c0001t0001g0278 a0002c0002t0001g0001 others(137): Show |
168 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.4421-5696C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294440 | |||||||
| chr9:86294442 | T | C | 1 | a0002c0002t0001g0222 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4421-5698A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294442 | |||||||
| chr9:86294586 | T | TA | 274 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.4421-5843dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294586 | |||||||
| chr9:86294715 | A | T | 1 | a0001c0001t0001g0092 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4421-5971T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294715 | |||||||
| chr9:86294745 | TTTA | T | 2 | a0002c0002t0001g0164 a0002c0003t0001g0035 |
3 | HG02257.hp1 HG02280.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.4421-6004_4421-600 others(7): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294745 | |||||||
| chr9:86294822 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4421-6078A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294822 | |||||||
| chr9:86294847 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4421-6103G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294847 | |||||||
| chr9:86294978 | A | T | 139 | a0001c0001t0001g0278 a0002c0002t0001g0001 a0002c0002t0001g0007 others(136): Show |
167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.4421-6234T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294978 | |||||||
| chr9:86295122 | TCAAA | T | 7 | a0002c0003t0001g0013 a0002c0003t0001g0035 a0002c0003t0001g0040 others(4): Show |
9 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.4420+6150_4420+615 others(8): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86295122 | |||||||
| chr9:86295154 | C | T | 2 | a0003c0004t0001g0271 a0003c0004t0001g0272 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.4420+6122G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86295154 | |||||||
| chr9:86295246 | T | C | 139 | a0001c0001t0001g0278 a0002c0002t0001g0001 a0002c0002t0001g0007 others(136): Show |
167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.4420+6030A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86295246 | |||||||
| chr9:86295344 | G | A | 115 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0011 others(112): Show |
139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.4420+5932C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86295344 | |||||||
| chr9:86295413 | G | A | 1 | a0002c0003t0001g0283 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4420+5863C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86295413 | |||||||
| chr9:86295643 | T | C | 18 | a0001c0001t0001g0278 a0002c0003t0001g0033 a0002c0003t0001g0034 others(15): Show |
20 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.4420+5633A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86295643 | |||||||
| chr9:86295823 | GAATA | G | 139 | a0001c0001t0001g0278 a0002c0002t0001g0001 a0002c0002t0001g0007 others(136): Show |
167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.4420+5449_4420+545 others(8): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86295823 | |||||||
| chr9:86296150 | T | C | 1 | a0002c0002t0001g0031 | 2 | NA18981.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.4420+5126A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86296150 | |||||||
| chr9:86296154 | G | A | 18 | a0001c0001t0001g0278 a0002c0003t0001g0033 a0002c0003t0001g0034 others(15): Show |
20 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.4420+5122C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86296154 | |||||||
| chr9:86296493 | C | G | 104 | a0001c0001t0001g0074 a0001c0001t0001g0079 a0001c0001t0001g0081 others(101): Show |
127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.4420+4783G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86296493 | |||||||
| chr9:86296636 | G | A | 6 | a0002c0002t0001g0178 a0002c0002t0001g0181 a0002c0002t0001g0182 others(3): Show |
6 | HG00544.hp1 HG02074.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.4420+4640C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86296636 | |||||||
| chr9:86296870 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4420+4406C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86296870 | |||||||
| chr9:86296954 | G | A | 1 | a0002c0003t0001g0283 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4420+4322C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86296954 | |||||||
| chr9:86297079 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4420+4197T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297079 | |||||||
| chr9:86297086 | T | C | 1 | a0002c0003t0001g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4420+4190A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297086 | |||||||
| chr9:86297154 | G | A | 1 | a0002c0002t0001g0209 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4420+4122C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297154 | |||||||
| chr9:86297256 | C | G | 1 | a0001c0001t0010g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4420+4020G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297256 | |||||||
| chr9:86297380 | G | C | 1 | a0002c0002t0001g0217 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4420+3896C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297380 | |||||||
| chr9:86297447 | C | T | 6 | a0003c0004t0001g0271 a0003c0004t0001g0272 a0003c0004t0001g0273 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4420+3829G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297447 | |||||||
| chr9:86297623 | T | C | 1 | a0001c0001t0010g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4420+3653A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297623 | |||||||
| chr9:86297665 | A | C | 1 | a0002c0002t0001g0186 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4420+3611T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297665 | |||||||
| chr9:86297850 | C | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
104 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.4420+3426G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297850 | |||||||
| chr9:86297921 | C | CTTTTTTT | 6 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0123 others(3): Show |
8 | HG01069.hp1 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.4420+3348_4420+335 others(11): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297921 | |||||||
| chr9:86297921 | C | CTTTTTTT others(1): Show |
112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
140 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.4420+3347_4420+335 others(12): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297921 | |||||||
| chr9:86297921 | C | CTTTTTTT others(2): Show |
14 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0001g0097 others(11): Show |
14 | HG00438.hp1 HG02109.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.4420+3346_4420+335 others(13): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297921 | |||||||
| chr9:86297921 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0010g0160 a0001c0006t0001g0090 a0002c0003t0001g0262 others(1): Show |
4 | HG02040.hp2 HG02258.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.4420+3345_4420+335 others(14): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297921 | |||||||
| chr9:86297921 | C | CTTTTTTT others(4): Show |
20 | a0001c0001t0001g0278 a0002c0002t0001g0225 a0002c0003t0001g0033 others(17): Show |
23 | HG00733.hp1 HG00735.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.4420+3344_4420+335 others(15): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297921 | |||||||
| chr9:86297921 | C | CTTTTTTT others(5): Show |
33 | a0002c0002t0001g0032 a0002c0002t0001g0147 a0002c0002t0001g0166 others(30): Show |
36 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.4420+3343_4420+335 others(16): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297921 | |||||||
| chr9:86297921 | C | CTTTTTTT others(6): Show |
63 | a0002c0002t0001g0001 a0002c0002t0001g0027 a0002c0002t0001g0028 others(60): Show |
78 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.4420+3342_4420+335 others(17): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297921 | |||||||
| chr9:86297921 | C | CTTTTTTT others(7): Show |
17 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(14): Show |
24 | HG00544.hp2 HG00738.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.4420+3341_4420+335 others(18): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297921 | |||||||
| chr9:86297921 | C | CTTTTTTT others(8): Show |
2 | a0002c0002t0001g0195 a0002c0002t0001g0240 |
2 | NA18990.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.4420+3354_4420+335 others(19): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297921 | |||||||
| chr9:86297954 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0125 |
5 | HG01123.hp2 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.4420+3322G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297954 | |||||||
| chr9:86298058 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0081 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.4420+3218C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86298058 | |||||||
| chr9:86298189 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4420+3087T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86298189 | |||||||
| chr9:86298196 | T | C | 274 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.4420+3080A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86298196 | |||||||
| chr9:86298591 | G | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(129): Show |
160 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.4420+2685C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86298591 | |||||||
| chr9:86298747 | T | G | 1 | a0001c0001t0001g0095 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4420+2529A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86298747 | |||||||
| chr9:86298861 | T | G | 1 | a0001c0001t0001g0277 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.4420+2415A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86298861 | |||||||
| chr9:86298944 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4420+2332A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86298944 | |||||||
| chr9:86299088 | G | A | 139 | a0001c0001t0001g0278 a0002c0002t0001g0001 a0002c0002t0001g0007 others(136): Show |
167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.4420+2188C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86299088 | |||||||
| chr9:86299219 | G | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0083 |
4 | HG02165.hp2 NA19007.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.4420+2057C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86299219 | |||||||
| chr9:86299222 | T | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4420+2054A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86299222 | |||||||
| chr9:86299335 | AACTTTCA others(7): Show |
A | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.4420+1927_4420+194 others(18): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86299335 | |||||||
| chr9:86299435 | A | G | 13 | a0002c0003t0001g0038 a0002c0003t0001g0039 a0002c0003t0001g0282 others(10): Show |
14 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.4420+1841T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86299435 | |||||||
| chr9:86299484 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.4420+1792T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86299484 | |||||||
| chr9:86299624 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4420+1652A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86299624 | |||||||
| chr9:86299639 | G | T | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.4420+1637C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86299639 | |||||||
| chr9:86299779 | G | A | 1 | a0002c0003t0001g0262 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4420+1497C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86299779 | |||||||
| chr9:86299899 | T | C | 1 | a0002c0002t0001g0171 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.4420+1377A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86299899 | |||||||
| chr9:86300651 | A | T | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(97): Show |
127 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.4420+625T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86300651 | |||||||
| chr9:86300927 | G | A | 6 | a0003c0004t0001g0271 a0003c0004t0001g0272 a0003c0004t0001g0273 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4420+349C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86300927 | |||||||
| chr9:86300980 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4420+296A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86300980 | |||||||
| chr9:86301614 | T | C | 1 | a0002c0002t0001g0183 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4095-13A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86301614 | |||||||
| chr9:86301660 | G | A | 6 | a0002c0003t0001g0013 a0002c0003t0001g0035 a0002c0003t0001g0040 others(3): Show |
8 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.4095-59C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86301660 | |||||||
| chr9:86301898 | A | T | 1 | a0002c0002t0001g0194 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4095-297T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86301898 | |||||||
| chr9:86301899 | A | C | 1 | a0002c0002t0001g0194 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4095-298T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86301899 | |||||||
| chr9:86301930 | C | T | 1 | a0002c0002t0001g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4095-329G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86301930 | |||||||
| chr9:86302082 | G | A | 13 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0059 others(10): Show |
14 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.4095-481C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86302082 | |||||||
| chr9:86302257 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0250 |
2 | HG00741.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.4095-656C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86302257 | |||||||
| chr9:86302302 | T | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01192.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.4095-701A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86302302 | |||||||
| chr9:86302309 | A | C | 5 | a0001c0001t0003g0020 a0001c0001t0003g0122 a0001c0001t0004g0085 others(2): Show |
6 | HG02280.hp2 HG02486.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4095-708T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86302309 | |||||||
| chr9:86302331 | TACAA | T | 138 | a0001c0001t0001g0278 a0002c0002t0001g0001 a0002c0002t0001g0007 others(135): Show |
166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.4095-734_4095-731d others(6): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86302331 | |||||||
| chr9:86302423 | A | T | 18 | a0001c0001t0001g0278 a0002c0003t0001g0033 a0002c0003t0001g0034 others(15): Show |
20 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.4094+663T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86302423 | |||||||
| chr9:86302617 | C | CT | 131 | a0001c0001t0001g0108 a0001c0001t0001g0115 a0001c0001t0001g0278 others(128): Show |
159 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.4094+468dupA | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86302617 | |||||||
| chr9:86302763 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4094+323G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86302763 | |||||||
| chr9:86302832 | C | A | 1 | a0002c0003t0001g0269 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4094+254G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86302832 | |||||||
| chr9:86303228 | C | G | 1 | a0002c0003t0001g0169 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3979-27G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86303228 | |||||||
| chr9:86303518 | A | G | 1 | a0002c0003t0001g0279 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3979-317T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86303518 | |||||||
| chr9:86303623 | T | G | 1 | a0002c0002t0001g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3979-422A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86303623 | |||||||
| chr9:86303679 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0144 |
3 | NA18943.hp1 NA18973.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.3979-478C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86303679 | |||||||
| chr9:86304024 | TAGAC | T | 13 | a0002c0003t0001g0038 a0002c0003t0001g0039 a0002c0003t0001g0282 others(10): Show |
14 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3979-827_3979-824d others(6): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86304024 | |||||||
| chr9:86304146 | GAT | G | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.3978+708_3978+709d others(4): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86304146 | |||||||
| chr9:86304186 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3978+670A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86304186 | |||||||
| chr9:86304257 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01192.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.3978+599C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86304257 | |||||||
| chr9:86304415 | T | G | 2 | a0001c0001t0002g0056 a0001c0001t0002g0057 |
2 | NA18943.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.3978+441A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86304415 | |||||||
| chr9:86304521 | G | T | 1 | a0002c0002t0001g0172 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3978+335C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86304521 | |||||||
| chr9:86304538 | C | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
134 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.3978+318G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86304538 | |||||||
| chr9:86304660 | A | G | 1 | a0002c0002t0001g0235 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3978+196T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86304660 | |||||||
| chr9:86304689 | G | A | 6 | a0002c0002t0001g0178 a0002c0002t0001g0181 a0002c0002t0001g0182 others(3): Show |
6 | HG00544.hp1 HG02074.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.3978+167C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86304689 | |||||||
| chr9:86304733 | A | T | 291 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(288): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.3978+123T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86304733 | |||||||
| chr9:86305033 | C | T | 1 | a0001c0001t0001g0024 | 2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.3887-86G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 23/26 | chr9 | 86305033 | |||||||
| chr9:86305179 | C | T | 18 | a0001c0001t0001g0278 a0002c0003t0001g0033 a0002c0003t0001g0034 others(15): Show |
20 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.3886+13G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 23/26 | chr9 | 86305179 | |||||||
| chr9:86305313 | C | T | 13 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0059 others(10): Show |
14 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.3839-74G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86305313 | |||||||
| chr9:86305401 | T | G | 1 | a0001c0001t0001g0076 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3839-162A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86305401 | |||||||
| chr9:86305588 | G | A | 1 | a0001c0001t0010g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3839-349C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86305588 | |||||||
| chr9:86306055 | A | T | 13 | a0002c0003t0001g0038 a0002c0003t0001g0039 a0002c0003t0001g0282 others(10): Show |
14 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3839-816T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306055 | |||||||
| chr9:86306295 | G | A | 1 | a0002c0002t0001g0187 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3839-1056C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306295 | |||||||
| chr9:86306305 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0281 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3839-1066C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306305 | |||||||
| chr9:86306313 | T | C | 139 | a0001c0001t0001g0278 a0002c0002t0001g0001 a0002c0002t0001g0007 others(136): Show |
167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.3839-1074A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306313 | |||||||
| chr9:86306375 | G | A | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.3839-1136C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306375 | |||||||
| chr9:86306668 | T | A | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.3839-1429A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306668 | |||||||
| chr9:86306730 | C | T | 1 | a0002c0003t0001g0264 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3839-1491G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306730 | |||||||
| chr9:86306800 | C | G | 59 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0011 others(56): Show |
78 | HG00099.hp1 HG00544.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.3839-1561G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306800 | |||||||
| chr9:86306806 | A | G | 101 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0011 others(98): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.3839-1567T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306806 | |||||||
| chr9:86306819 | G | A | 1 | a0002c0002t0001g0224 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3839-1580C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306819 | |||||||
| chr9:86306933 | G | A | 274 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.3838+1496C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306933 | |||||||
| chr9:86306980 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0281 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3838+1449G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306980 | |||||||
| chr9:86307039 | G | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0077 |
2 | HG01069.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.3838+1390C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86307039 | |||||||
| chr9:86307359 | A | G | 3 | a0002c0002t0001g0201 a0002c0002t0001g0223 a0002c0002t0001g0245 |
3 | HG03491.hp2 HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.3838+1070T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86307359 | |||||||
| chr9:86307542 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0250 |
2 | HG00741.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.3838+887A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86307542 | |||||||
| chr9:86307884 | C | T | 13 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0059 others(10): Show |
14 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.3838+545G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86307884 | |||||||
| chr9:86308059 | A | G | 1 | a0005c0007t0001g0259 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3838+370T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86308059 | |||||||
| chr9:86308098 | G | C | 1 | a0002c0003t0001g0279 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3838+331C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86308098 | |||||||
| chr9:86308136 | C | A | 24 | a0001c0001t0001g0278 a0002c0003t0001g0013 a0002c0003t0001g0033 others(21): Show |
28 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.3838+293G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86308136 | |||||||
| chr9:86308358 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3838+71C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86308358 | |||||||
| chr9:86308371 | T | C | 9 | a0001c0001t0001g0278 a0002c0003t0001g0033 a0002c0003t0001g0165 others(6): Show |
10 | NA18950.hp1 NA18978.hp2 NA18992.hp2 others(7): Show |
intron_variant | MODIFIER | c.3838+58A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86308371 | |||||||
| chr9:86308383 | T | G | 6 | a0002c0003t0001g0013 a0002c0003t0001g0035 a0002c0003t0001g0040 others(3): Show |
8 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.3838+46A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86308383 | |||||||
| chr9:86308965 | G | C | 1 | a0002c0002t0001g0183 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3660+247C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 21/26 | chr9 | 86308965 | |||||||
| chr9:86309142 | A | C | 274 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.3660+70T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 21/26 | chr9 | 86309142 | |||||||
| chr9:86309154 | T | C | 7 | a0001c0001t0001g0026 a0001c0001t0001g0068 a0001c0001t0001g0105 others(4): Show |
8 | HG01106.hp2 HG02129.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.3660+58A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 21/26 | chr9 | 86309154 | |||||||
| chr9:86309424 | A | G | 1 | a0002c0002t0001g0210 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3582+39T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 20/26 | chr9 | 86309424 | |||||||
| chr9:86310061 | A | G | 4 | a0002c0002t0001g0231 a0002c0002t0001g0232 a0002c0002t0001g0233 others(1): Show |
4 | NA18975.hp1 NA18991.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.3379-44T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 18/26 | chr9 | 86310061 | |||||||
| chr9:86310070 | C | CT | 265 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(262): Show |
322 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.3379-54dupA | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 18/26 | chr9 | 86310070 | |||||||
| chr9:86310391 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0104 |
3 | NA18953.hp1 NA18978.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.3378+315A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 18/26 | chr9 | 86310391 | |||||||
| chr9:86310605 | C | A | 1 | a0001c0012t0008g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3378+101G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 18/26 | chr9 | 86310605 | |||||||
| chr9:86310619 | ATG | A | 274 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.3378+85_3378+86del others(2): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 18/26 | chr9 | 86310619 | |||||||
| chr9:86310859 | A | G | 31 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0029 others(28): Show |
34 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.3275-50T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86310859 | |||||||
| chr9:86311194 | T | C | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.3275-385A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311194 | |||||||
| chr9:86311462 | G | A | 101 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0011 others(98): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.3275-653C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311462 | |||||||
| chr9:86311560 | T | C | 2 | a0004c0005t0001g0037 a0004c0005t0001g0280 |
3 | HG01243.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3275-751A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311560 | |||||||
| chr9:86311589 | T | TCCCTCTC | 138 | a0001c0001t0001g0278 a0002c0002t0001g0001 a0002c0002t0001g0007 others(135): Show |
166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.3275-787_3275-781d others(9): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311589 | |||||||
| chr9:86311632 | A | ACGGTCTC others(10): Show |
130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
157 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.3275-840_3275-824d others(19): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311632 | |||||||
| chr9:86311632 | ACGGTCTC others(10): Show |
A | 1 | a0002c0002t0001g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3275-840_3275-824d others(19): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311632 | |||||||
| chr9:86311651 | G | GGTCTCCC others(10): Show |
1 | a0003c0004t0001g0272 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3275-843_3275-842i others(19): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311651 | |||||||
| chr9:86311668 | G | A | 2 | a0002c0003t0001g0269 a0002c0003t0001g0270 |
2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3275-859C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311668 | |||||||
| chr9:86311672 | C | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01192.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.3275-863G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311672 | |||||||
| chr9:86311721 | C | A | 2 | a0001c0001t0002g0046 a0001c0001t0002g0052 |
2 | HG00323.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.3275-912G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311721 | |||||||
| chr9:86311744 | C | T | 2 | a0001c0001t0010g0160 a0002c0002t0006g0173 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3275-935G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311744 | |||||||
| chr9:86311745 | G | A | 3 | a0001c0001t0003g0020 a0001c0001t0003g0122 a0001c0001t0004g0087 |
4 | HG02280.hp2 HG02486.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3275-936C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311745 | |||||||
| chr9:86311766 | C | T | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.3275-957G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311766 | |||||||
| chr9:86311812 | G | C | 139 | a0001c0001t0001g0278 a0002c0002t0001g0001 a0002c0002t0001g0007 others(136): Show |
167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.3275-1003C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311812 | |||||||
| chr9:86311826 | T | G | 1 | a0002c0003t0001g0137 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.3275-1017A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311826 | |||||||
| chr9:86311837 | G | C | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.3275-1028C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311837 | |||||||
| chr9:86311855 | C | T | 9 | a0001c0001t0001g0023 a0001c0001t0001g0062 a0001c0001t0001g0084 others(6): Show |
10 | HG02572.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.3275-1046G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311855 | |||||||
| chr9:86311885 | G | T | 1 | a0001c0001t0001g0019 | 2 | HG02071.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.3275-1076C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311885 | |||||||
| chr9:86311926 | A | G | 139 | a0001c0001t0001g0278 a0002c0002t0001g0001 a0002c0002t0001g0007 others(136): Show |
167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.3275-1117T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311926 | |||||||
| chr9:86311943 | G | C | 18 | a0001c0001t0001g0278 a0002c0003t0001g0033 a0002c0003t0001g0034 others(15): Show |
20 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.3275-1134C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311943 | |||||||
| chr9:86311953 | G | A | 3 | a0004c0005t0001g0036 a0004c0005t0001g0037 a0004c0005t0001g0280 |
5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3275-1144C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311953 | |||||||
| chr9:86312032 | C | T | 2 | a0002c0002t0001g0209 a0002c0002t0001g0258 |
2 | HG01167.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3275-1223G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312032 | |||||||
| chr9:86312045 | G | A | 2 | a0001c0001t0001g0080 a0006c0016t0001g0153 |
2 | HG02602.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.3275-1236C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312045 | |||||||
| chr9:86312179 | G | A | 1 | a0001c0001t0010g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3275-1370C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312179 | |||||||
| chr9:86312185 | T | C | 1 | a0001c0001t0010g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3275-1376A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312185 | |||||||
| chr9:86312246 | G | A | 1 | a0002c0002t0001g0184 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3275-1437C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312246 | |||||||
| chr9:86312276 | C | T | 1 | a0002c0003t0001g0289 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3275-1467G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312276 | |||||||
| chr9:86312433 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0059 |
4 | NA18953.hp2 NA18955.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.3275-1624G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312433 | |||||||
| chr9:86312451 | C | T | 3 | a0002c0002t0001g0174 a0002c0002t0001g0175 a0002c0002t0009g0167 |
3 | HG00738.hp2 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3275-1642G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312451 | |||||||
| chr9:86312456 | C | A | 1 | a0002c0002t0005g0227 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3275-1647G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312456 | |||||||
| chr9:86312473 | C | T | 139 | a0001c0001t0001g0278 a0002c0002t0001g0001 a0002c0002t0001g0007 others(136): Show |
167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.3275-1664G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312473 | |||||||
| chr9:86312474 | A | G | 274 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.3275-1665T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312474 | |||||||
| chr9:86312478 | G | A | 1 | a0002c0003t0001g0279 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3275-1669C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312478 | |||||||
| chr9:86312501 | C | T | 139 | a0001c0001t0001g0278 a0002c0002t0001g0001 a0002c0002t0001g0007 others(136): Show |
167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.3275-1692G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312501 | |||||||
| chr9:86312510 | G | A | 3 | a0003c0004t0001g0271 a0003c0004t0001g0272 a0003c0004t0001g0273 |
3 | HG02257.hp2 HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3275-1701C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312510 | |||||||
| chr9:86312522 | C | T | 1 | a0001c0012t0008g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3275-1713G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312522 | |||||||
| chr9:86312633 | C | T | 2 | a0002c0002t0001g0229 a0002c0002t0001g0261 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.3275-1824G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312633 | |||||||
| chr9:86312634 | A | G | 274 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.3275-1825T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312634 | |||||||
| chr9:86312653 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3275-1844C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312653 | |||||||
| chr9:86312665 | T | C | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.3275-1856A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312665 | |||||||
| chr9:86312910 | C | T | 1 | a0004c0005t0001g0036 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3275-2101G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312910 | |||||||
| chr9:86313005 | C | G | 1 | a0002c0003t0001g0169 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3275-2196G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313005 | |||||||
| chr9:86313126 | T | TAATA | 108 | a0001c0001t0001g0026 a0001c0001t0001g0070 a0001c0001t0001g0078 others(105): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.3275-2321_3275-231 others(8): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313126 | |||||||
| chr9:86313126 | T | TAATAAAT others(1): Show |
4 | a0002c0002t0001g0012 a0002c0002t0001g0172 a0002c0002t0001g0222 others(1): Show |
6 | HG03491.hp2 HG03654.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.3275-2325_3275-231 others(12): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313126 | |||||||
| chr9:86313126 | T | TAATAAAT others(5): Show |
1 | a0005c0007t0001g0259 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3275-2329_3275-231 others(16): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313126 | |||||||
| chr9:86313126 | TAATA | T | 70 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0022 others(67): Show |
89 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.3275-2321_3275-231 others(8): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313126 | |||||||
| chr9:86313126 | TAATAAAT others(1): Show |
T | 3 | a0001c0001t0001g0105 a0001c0001t0010g0160 a0001c0012t0008g0151 |
3 | HG02258.hp2 HG03225.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.3275-2325_3275-231 others(12): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313126 | |||||||
| chr9:86313126 | TAATAAAT others(5): Show |
T | 1 | a0002c0003t0001g0034 | 2 | HG02698.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.3275-2329_3275-231 others(16): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313126 | |||||||
| chr9:86313150 | A | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0104 |
3 | NA18953.hp1 NA18978.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.3275-2341T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313150 | |||||||
| chr9:86313183 | G | A | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.3275-2374C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313183 | |||||||
| chr9:86313200 | A | G | 1 | a0002c0003t0001g0251 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3275-2391T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313200 | |||||||
| chr9:86313283 | G | T | 1 | a0002c0003t0001g0169 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3275-2474C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313283 | |||||||
| chr9:86313417 | G | A | 2 | a0001c0001t0001g0278 a0002c0003t0001g0251 |
2 | NA18997.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.3275-2608C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313417 | |||||||
| chr9:86313485 | G | C | 1 | a0002c0003t0001g0292 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3275-2676C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313485 | |||||||
| chr9:86313576 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0070 others(1): Show |
7 | HG00280.hp2 HG01123.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.3275-2767A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313576 | |||||||
| chr9:86313646 | G | C | 139 | a0001c0001t0001g0278 a0002c0002t0001g0001 a0002c0002t0001g0007 others(136): Show |
167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.3275-2837C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313646 | |||||||
| chr9:86313760 | C | A | 1 | a0002c0002t0001g0221 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3275-2951G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313760 | |||||||
| chr9:86313763 | A | T | 1 | a0002c0002t0001g0239 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3275-2954T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313763 | |||||||
| chr9:86314016 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3274+3203C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314016 | |||||||
| chr9:86314017 | C | T | 1 | a0007c0017t0001g0096 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3274+3202G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314017 | |||||||
| chr9:86314075 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0144 |
3 | NA18943.hp1 NA18973.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.3274+3144T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314075 | |||||||
| chr9:86314390 | C | CA | 137 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0011 others(134): Show |
165 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.3274+2828dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314390 | |||||||
| chr9:86314593 | T | G | 1 | a0002c0002t0001g0205 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3274+2626A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314593 | |||||||
| chr9:86314595 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01192.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.3274+2624C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314595 | |||||||
| chr9:86314679 | C | G | 3 | a0002c0002t0001g0174 a0002c0002t0001g0175 a0002c0002t0009g0167 |
3 | HG00738.hp2 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3274+2540G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314679 | |||||||
| chr9:86314809 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3274+2410C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314809 | |||||||
| chr9:86314829 | T | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3274+2390A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314829 | |||||||
| chr9:86314847 | C | T | 1 | a0002c0002t0001g0217 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3274+2372G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314847 | |||||||
| chr9:86314894 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0125 |
5 | HG01123.hp2 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3274+2325T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314894 | |||||||
| chr9:86315009 | C | T | 1 | a0002c0003t0001g0279 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3274+2210G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86315009 | |||||||
| chr9:86315107 | AC | A | 6 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0002c0002t0001g0223 others(3): Show |
6 | HG01192.hp1 HG01884.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.3274+2111delG | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86315107 | |||||||
| chr9:86315243 | G | A | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(106): Show |
136 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.3274+1976C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86315243 | |||||||
| chr9:86315299 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3274+1920G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86315299 | |||||||
| chr9:86315310 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3274+1909G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86315310 | |||||||
| chr9:86315763 | T | A | 1 | a0002c0002t0001g0185 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3274+1456A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86315763 | |||||||
| chr9:86315763 | T | TA | 136 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(133): Show |
166 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.3274+1455dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86315763 | |||||||
| chr9:86315806 | A | G | 3 | a0002c0003t0001g0263 a0002c0003t0001g0264 a0002c0003t0001g0265 |
3 | NA18957.hp1 NA18959.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.3274+1413T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86315806 | |||||||
| chr9:86315929 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3274+1290C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86315929 | |||||||
| chr9:86315994 | C | T | 1 | a0002c0003t0001g0288 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3274+1225G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86315994 | |||||||
| chr9:86316028 | G | A | 1 | a0004c0005t0001g0036 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3274+1191C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316028 | |||||||
| chr9:86316073 | C | T | 1 | a0002c0002t0001g0200 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3274+1146G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316073 | |||||||
| chr9:86316141 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3274+1078G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316141 | |||||||
| chr9:86316194 | C | T | 1 | a0002c0002t0001g0221 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3274+1025G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316194 | |||||||
| chr9:86316586 | C | T | 1 | a0002c0002t0001g0175 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3274+633G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316586 | |||||||
| chr9:86316713 | C | G | 1 | a0001c0001t0010g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3274+506G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316713 | |||||||
| chr9:86316789 | A | G | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(151): Show |
194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.3274+430T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316789 | |||||||
| chr9:86316882 | CAACT | C | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG00558.hp2 HG00597.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.3274+333_3274+336d others(6): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316882 | |||||||
| chr9:86316898 | AACGAT | A | 6 | a0002c0003t0001g0013 a0002c0003t0001g0035 a0002c0003t0001g0040 others(3): Show |
8 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.3274+316_3274+320d others(7): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316898 | |||||||
| chr9:86316909 | A | G | 1 | a0012c0010t0001g0132 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3274+310T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316909 | |||||||
| chr9:86316946 | T | G | 1 | a0001c0014t0011g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3274+273A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316946 | |||||||
| chr9:86317077 | A | AT | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
128 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.3274+141dupA | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86317077 | |||||||
| chr9:86317287 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01192.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.3217-11C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86317287 | |||||||
| chr9:86317298 | G | T | 1 | a0002c0002t0001g0258 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3217-22C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86317298 | |||||||
| chr9:86317311 | A | G | 17 | a0002c0002t0001g0030 a0002c0002t0001g0164 a0002c0002t0001g0200 others(14): Show |
18 | HG01261.hp1 HG02040.hp1 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.3217-35T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86317311 | |||||||
| chr9:86317348 | T | C | 1 | a0005c0007t0001g0197 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3217-72A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86317348 | |||||||
| chr9:86317442 | T | G | 1 | a0002c0003t0001g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3217-166A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86317442 | |||||||
| chr9:86317451 | T | C | 1 | a0002c0002t0001g0216 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3217-175A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86317451 | |||||||
| chr9:86317841 | G | A | 1 | a0004c0005t0001g0036 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3217-565C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86317841 | |||||||
| chr9:86318066 | T | C | 1 | a0002c0002t0001g0170 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3217-790A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318066 | |||||||
| chr9:86318193 | C | T | 1 | a0002c0002t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3216+765G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318193 | |||||||
| chr9:86318330 | A | G | 3 | a0002c0003t0001g0013 a0002c0003t0001g0040 a0002c0003t0001g0279 |
4 | HG02630.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.3216+628T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318330 | |||||||
| chr9:86318411 | C | G | 1 | a0001c0001t0001g0127 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3216+547G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318411 | |||||||
| chr9:86318420 | A | G | 13 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0059 others(10): Show |
14 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.3216+538T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318420 | |||||||
| chr9:86318475 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG03017.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.3216+483C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318475 | |||||||
| chr9:86318542 | T | C | 3 | a0001c0001t0001g0117 a0001c0001t0001g0156 a0001c0001t0001g0157 |
3 | NA18956.hp2 NA18974.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3216+416A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318542 | |||||||
| chr9:86318688 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3216+270T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318688 | |||||||
| chr9:86318757 | A | G | 209 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.3216+201T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318757 | |||||||
| chr9:86318758 | G | A | 13 | a0002c0003t0001g0038 a0002c0003t0001g0039 a0002c0003t0001g0282 others(10): Show |
14 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3216+200C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318758 | |||||||
| chr9:86318759 | T | G | 13 | a0002c0003t0001g0038 a0002c0003t0001g0039 a0002c0003t0001g0282 others(10): Show |
14 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3216+199A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318759 | |||||||
| chr9:86318764 | G | T | 13 | a0002c0003t0001g0038 a0002c0003t0001g0039 a0002c0003t0001g0282 others(10): Show |
14 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3216+194C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318764 | |||||||
| chr9:86319331 | A | G | 1 | a0001c0012t0008g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3115+253T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 15/26 | chr9 | 86319331 | |||||||
| chr9:86319419 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3115+165G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 15/26 | chr9 | 86319419 | |||||||
| chr9:86319484 | G | A | 1 | a0002c0002t0001g0237 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3115+100C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 15/26 | chr9 | 86319484 | |||||||
| chr9:86319709 | G | T | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
236 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.3029-39C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86319709 | |||||||
| chr9:86319723 | G | C | 1 | a0002c0002t0001g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3029-53C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86319723 | |||||||
| chr9:86319923 | C | A | 13 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0059 others(10): Show |
14 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.3029-253G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86319923 | |||||||
| chr9:86319932 | A | C | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.3029-262T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86319932 | |||||||
| chr9:86320009 | C | T | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.3029-339G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320009 | |||||||
| chr9:86320067 | G | A | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.3029-397C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320067 | |||||||
| chr9:86320257 | C | CA | 8 | a0001c0001t0001g0118 a0002c0002t0001g0215 a0002c0003t0001g0246 others(5): Show |
8 | HG02257.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3029-588dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320257 | |||||||
| chr9:86320257 | C | CAA | 19 | a0001c0001t0001g0121 a0001c0001t0002g0002 a0001c0001t0002g0008 others(16): Show |
29 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.3029-589_3029-588d others(4): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320257 | |||||||
| chr9:86320257 | CA | C | 16 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0059 others(13): Show |
17 | HG00323.hp1 HG02109.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.3029-588delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320257 | |||||||
| chr9:86320258 | A | C | 2 | a0002c0002t0001g0230 a0002c0002t0001g0293 |
2 | HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3029-588T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320258 | |||||||
| chr9:86320259 | A | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
6 | HG03017.hp2 HG04115.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.3029-589T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320259 | |||||||
| chr9:86320304 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3029-634G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320304 | |||||||
| chr9:86320308 | T | G | 1 | a0002c0002t0001g0216 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3029-638A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320308 | |||||||
| chr9:86320343 | C | T | 1 | a0002c0002t0001g0164 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3029-673G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320343 | |||||||
| chr9:86320470 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3029-800G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320470 | |||||||
| chr9:86320473 | T | C | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.3029-803A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320473 | |||||||
| chr9:86320500 | T | C | 1 | a0002c0002t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3029-830A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320500 | |||||||
| chr9:86320522 | T | C | 17 | a0002c0002t0001g0029 a0002c0002t0001g0149 a0002c0002t0001g0174 others(14): Show |
18 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.3029-852A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320522 | |||||||
| chr9:86320764 | T | C | 1 | a0002c0002t0001g0217 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3029-1094A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320764 | |||||||
| chr9:86320848 | A | G | 2 | a0002c0003t0001g0269 a0002c0003t0001g0270 |
2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3029-1178T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320848 | |||||||
| chr9:86320857 | G | C | 291 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(288): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.3029-1187C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320857 | |||||||
| chr9:86320895 | T | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
6 | HG03017.hp2 HG04115.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.3029-1225A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320895 | |||||||
| chr9:86321075 | G | A | 13 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0059 others(10): Show |
14 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.3028+1250C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86321075 | |||||||
| chr9:86321127 | C | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0250 a0001c0014t0011g0294 |
3 | HG00741.hp1 HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.3028+1198G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86321127 | |||||||
| chr9:86321190 | T | TA | 16 | a0001c0001t0002g0053 a0002c0003t0001g0033 a0002c0003t0001g0034 others(13): Show |
18 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.3028+1134dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86321190 | |||||||
| chr9:86321190 | TA | T | 6 | a0001c0001t0001g0082 a0001c0001t0001g0102 a0001c0001t0001g0123 others(3): Show |
6 | HG00323.hp2 HG00639.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3028+1134delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86321190 | |||||||
| chr9:86321235 | T | C | 5 | a0002c0003t0001g0282 a0002c0003t0001g0283 a0002c0003t0001g0284 others(2): Show |
5 | HG01109.hp2 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3028+1090A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86321235 | |||||||
| chr9:86321312 | G | A | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.3028+1013C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86321312 | |||||||
| chr9:86321445 | C | T | 2 | a0002c0002t0002g0176 a0002c0002t0002g0177 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3028+880G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86321445 | |||||||
| chr9:86321580 | T | C | 1 | a0002c0002t0001g0224 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3028+745A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86321580 | |||||||
| chr9:86321628 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.3028+697A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86321628 | |||||||
| chr9:86321729 | A | T | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(151): Show |
194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.3028+596T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86321729 | |||||||
| chr9:86322037 | C | T | 3 | a0001c0006t0001g0088 a0001c0006t0001g0089 a0001c0006t0001g0091 |
3 | HG02109.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3028+288G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86322037 | |||||||
| chr9:86322092 | T | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0125 |
5 | HG01123.hp2 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3028+233A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86322092 | |||||||
| chr9:86322174 | C | A | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(106): Show |
136 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.3028+151G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86322174 | |||||||
| chr9:86322512 | C | T | 1 | a0002c0002t0001g0175 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2878-37G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 13/26 | chr9 | 86322512 | |||||||
| chr9:86322702 | T | A | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.2877+171A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 13/26 | chr9 | 86322702 | |||||||
| chr9:86322781 | T | C | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.2877+92A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 13/26 | chr9 | 86322781 | |||||||
| chr9:86324061 | A | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
5 | HG01928.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1790-101T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 12/26 | chr9 | 86324061 | |||||||
| chr9:86324253 | T | C | 1 | a0002c0002t0001g0218 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1790-293A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 12/26 | chr9 | 86324253 | |||||||
| chr9:86324254 | C | T | 9 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(6): Show |
9 | HG00558.hp2 HG00597.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1790-294G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 12/26 | chr9 | 86324254 | |||||||
| chr9:86324609 | T | C | 3 | a0001c0001t0001g0068 a0001c0001t0001g0119 a0001c0001t0001g0131 |
3 | HG01106.hp2 NA19081.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1790-649A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 12/26 | chr9 | 86324609 | |||||||
| chr9:86324617 | GA | G | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(150): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1790-658delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 12/26 | chr9 | 86324617 | |||||||
| chr9:86324821 | T | C | 2 | a0002c0002t0001g0219 a0002c0002t0001g0220 |
2 | NA18969.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1789+513A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 12/26 | chr9 | 86324821 | |||||||
| chr9:86325086 | C | T | 2 | a0004c0005t0001g0037 a0004c0005t0001g0280 |
3 | HG01243.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1789+248G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 12/26 | chr9 | 86325086 | |||||||
| chr9:86325148 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1789+186C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 12/26 | chr9 | 86325148 | |||||||
| chr9:86325277 | A | G | 1 | a0002c0002t0001g0221 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1789+57T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 12/26 | chr9 | 86325277 | |||||||
| chr9:86325312 | T | C | 1 | a0001c0001t0001g0277 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1789+22A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 12/26 | chr9 | 86325312 | |||||||
| chr9:86325654 | T | C | 2 | a0002c0002t0001g0032 a0002c0002t0001g0225 |
3 | HG01168.hp2 HG01169.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1609-140A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86325654 | |||||||
| chr9:86325708 | T | C | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1609-194A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86325708 | |||||||
| chr9:86325875 | G | A | 1 | a0002c0003t0001g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1609-361C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86325875 | |||||||
| chr9:86326082 | C | A | 1 | a0002c0002t0001g0221 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1609-568G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86326082 | |||||||
| chr9:86326086 | G | A | 1 | a0002c0003t0001g0279 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1609-572C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86326086 | |||||||
| chr9:86326149 | T | C | 1 | a0002c0002t0001g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1609-635A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86326149 | |||||||
| chr9:86326152 | T | C | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.1609-638A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86326152 | |||||||
| chr9:86326245 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1609-731A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86326245 | |||||||
| chr9:86326634 | C | A | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(150): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1609-1120G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86326634 | |||||||
| chr9:86326798 | AC | A | 3 | a0002c0003t0001g0013 a0002c0003t0001g0040 a0002c0003t0001g0279 |
4 | HG02630.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-1285delG | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86326798 | |||||||
| chr9:86326829 | A | C | 1 | a0001c0001t0002g0056 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1609-1315T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86326829 | |||||||
| chr9:86326856 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1609-1342A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86326856 | |||||||
| chr9:86327156 | T | G | 7 | a0001c0001t0001g0023 a0001c0001t0001g0062 a0001c0001t0001g0126 others(4): Show |
8 | HG02572.hp1 HG02615.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1608+1184A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86327156 | |||||||
| chr9:86327442 | T | C | 1 | a0008c0011t0001g0286 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1608+898A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86327442 | |||||||
| chr9:86327523 | A | G | 2 | a0001c0001t0003g0020 a0001c0001t0003g0122 |
3 | HG02280.hp2 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1608+817T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86327523 | |||||||
| chr9:86327639 | C | T | 1 | a0005c0007t0001g0197 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1608+701G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86327639 | |||||||
| chr9:86327642 | C | T | 1 | a0001c0001t0010g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1608+698G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86327642 | |||||||
| chr9:86327759 | A | G | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(151): Show |
194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1608+581T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86327759 | |||||||
| chr9:86327776 | C | T | 1 | a0002c0002t0001g0170 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1608+564G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86327776 | |||||||
| chr9:86327840 | C | T | 1 | a0003c0004t0001g0273 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1608+500G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86327840 | |||||||
| chr9:86328085 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0250 |
2 | HG00741.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1608+255A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86328085 | |||||||
| chr9:86328090 | T | C | 13 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0059 others(10): Show |
14 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.1608+250A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86328090 | |||||||
| chr9:86328256 | T | C | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1608+84A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86328256 | |||||||
| chr9:86328534 | T | A | 1 | a0001c0001t0001g0120 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1456-42A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86328534 | |||||||
| chr9:86328619 | A | C | 2 | a0004c0005t0001g0037 a0004c0005t0001g0280 |
3 | HG01243.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1456-127T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86328619 | |||||||
| chr9:86328817 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1456-325C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86328817 | |||||||
| chr9:86328842 | T | C | 1 | a0001c0001t0001g0017 | 2 | HG03491.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1456-350A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86328842 | |||||||
| chr9:86329032 | T | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
130 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1456-540A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86329032 | |||||||
| chr9:86329070 | A | G | 13 | a0002c0003t0001g0038 a0002c0003t0001g0039 a0002c0003t0001g0282 others(10): Show |
14 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1456-578T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86329070 | |||||||
| chr9:86329248 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0250 |
2 | HG00741.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1456-756C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86329248 | |||||||
| chr9:86329280 | T | C | 1 | a0002c0002t0001g0268 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1456-788A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86329280 | |||||||
| chr9:86329299 | G | A | 1 | a0001c0001t0001g0018 | 2 | HG00280.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1456-807C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86329299 | |||||||
| chr9:86329391 | C | T | 1 | a0001c0014t0011g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1456-899G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86329391 | |||||||
| chr9:86329511 | G | A | 1 | a0002c0002t0006g0173 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1456-1019C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86329511 | |||||||
| chr9:86329523 | C | CA | 4 | a0002c0003t0001g0246 a0004c0005t0001g0036 a0004c0005t0001g0037 others(1): Show |
6 | HG01243.hp1 HG02630.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1456-1032dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86329523 | |||||||
| chr9:86329523 | CA | C | 150 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1456-1032delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86329523 | |||||||
| chr9:86329683 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0281 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1456-1191T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86329683 | |||||||
| chr9:86330015 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1456-1523A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86330015 | |||||||
| chr9:86330091 | C | T | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(151): Show |
194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1456-1599G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86330091 | |||||||
| chr9:86330134 | T | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
6 | HG03017.hp2 HG04115.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.1456-1642A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86330134 | |||||||
| chr9:86330223 | A | C | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1456-1731T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86330223 | |||||||
| chr9:86330299 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1456-1807T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86330299 | |||||||
| chr9:86330331 | A | G | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
161 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.1456-1839T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86330331 | |||||||
| chr9:86330351 | T | G | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1456-1859A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86330351 | |||||||
| chr9:86330745 | T | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
161 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.1456-2253A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86330745 | |||||||
| chr9:86330880 | CT | C | 6 | a0002c0003t0001g0013 a0002c0003t0001g0035 a0002c0003t0001g0040 others(3): Show |
8 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1456-2389delA | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86330880 | |||||||
| chr9:86331083 | T | A | 3 | a0004c0005t0001g0036 a0004c0005t0001g0037 a0004c0005t0001g0280 |
5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1456-2591A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86331083 | |||||||
| chr9:86331192 | C | T | 13 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0059 others(10): Show |
14 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.1456-2700G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86331192 | |||||||
| chr9:86331227 | A | AT | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
161 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.1456-2736dupA | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86331227 | |||||||
| chr9:86331236 | C | T | 1 | a0002c0002t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1456-2744G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86331236 | |||||||
| chr9:86331323 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0144 |
3 | NA18943.hp1 NA18973.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1456-2831A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86331323 | |||||||
| chr9:86331450 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1456-2958C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86331450 | |||||||
| chr9:86331806 | A | C | 3 | a0002c0003t0001g0247 a0002c0003t0001g0262 a0002c0003t0007g0148 |
3 | HG02040.hp2 HG04228.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1456-3314T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86331806 | |||||||
| chr9:86331808 | A | C | 1 | a0001c0001t0001g0098 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1456-3316T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86331808 | |||||||
| chr9:86332332 | T | G | 1 | a0002c0002t0001g0149 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1456-3840A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86332332 | |||||||
| chr9:86332339 | C | T | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1456-3847G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86332339 | |||||||
| chr9:86332359 | TA | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
129 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1456-3868delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86332359 | |||||||
| chr9:86332623 | A | G | 1 | a0002c0002t0001g0231 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1456-4131T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86332623 | |||||||
| chr9:86332755 | T | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
129 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1456-4263A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86332755 | |||||||
| chr9:86333021 | T | C | 1 | a0002c0002t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1455+4398A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333021 | |||||||
| chr9:86333182 | A | G | 1 | a0004c0005t0001g0036 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1455+4237T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333182 | |||||||
| chr9:86333486 | G | C | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1455+3933C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333486 | |||||||
| chr9:86333522 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1455+3897C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333522 | |||||||
| chr9:86333556 | A | T | 1 | a0001c0001t0002g0045 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1455+3863T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333556 | |||||||
| chr9:86333630 | T | A | 17 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0062 others(14): Show |
22 | HG01123.hp2 HG02109.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.1455+3789A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333630 | |||||||
| chr9:86333773 | T | C | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1455+3646A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333773 | |||||||
| chr9:86333809 | T | C | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1455+3610A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333809 | |||||||
| chr9:86333833 | TTA | T | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1455+3584_1455+358 others(6): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333833 | |||||||
| chr9:86333848 | T | C | 3 | a0004c0005t0001g0036 a0004c0005t0001g0037 a0004c0005t0001g0280 |
5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1455+3571A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333848 | |||||||
| chr9:86333881 | G | C | 1 | a0001c0012t0008g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1455+3538C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333881 | |||||||
| chr9:86334073 | T | C | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1455+3346A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86334073 | |||||||
| chr9:86334207 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1455+3212G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86334207 | |||||||
| chr9:86334236 | T | C | 1 | a0002c0002t0001g0222 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1455+3183A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86334236 | |||||||
| chr9:86334331 | G | A | 1 | a0002c0002t0001g0223 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1455+3088C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86334331 | |||||||
| chr9:86334364 | G | A | 6 | a0002c0003t0001g0013 a0002c0003t0001g0035 a0002c0003t0001g0040 others(3): Show |
8 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1455+3055C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86334364 | |||||||
| chr9:86334614 | G | A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0059 others(3): Show |
7 | HG03017.hp2 HG03540.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.1455+2805C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86334614 | |||||||
| chr9:86334617 | T | C | 6 | a0003c0004t0001g0271 a0003c0004t0001g0272 a0003c0004t0001g0273 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1455+2802A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86334617 | |||||||
| chr9:86334708 | T | G | 3 | a0004c0005t0001g0036 a0004c0005t0001g0037 a0004c0005t0001g0280 |
5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1455+2711A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86334708 | |||||||
| chr9:86334949 | T | C | 1 | a0002c0003t0001g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1455+2470A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86334949 | |||||||
| chr9:86335162 | G | A | 1 | a0001c0001t0001g0024 | 2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1455+2257C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86335162 | |||||||
| chr9:86335283 | T | C | 6 | a0003c0004t0001g0271 a0003c0004t0001g0272 a0003c0004t0001g0273 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1455+2136A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86335283 | |||||||
| chr9:86335474 | A | C | 1 | a0002c0002t0001g0234 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1455+1945T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86335474 | |||||||
| chr9:86335542 | A | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1455+1877T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86335542 | |||||||
| chr9:86335795 | A | G | 1 | a0001c0012t0008g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1455+1624T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86335795 | |||||||
| chr9:86335988 | T | C | 1 | a0001c0001t0010g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1455+1431A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86335988 | |||||||
| chr9:86336094 | C | A | 1 | a0002c0002t0001g0249 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1455+1325G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86336094 | |||||||
| chr9:86336498 | C | T | 6 | a0002c0003t0001g0013 a0002c0003t0001g0035 a0002c0003t0001g0040 others(3): Show |
8 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1455+921G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86336498 | |||||||
| chr9:86336558 | T | C | 1 | a0002c0002t0001g0224 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1455+861A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86336558 | |||||||
| chr9:86336613 | G | C | 1 | a0001c0001t0001g0130 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1455+806C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86336613 | |||||||
| chr9:86336721 | T | G | 1 | a0011c0008t0001g0168 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1455+698A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86336721 | |||||||
| chr9:86336923 | C | T | 190 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.1455+496G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86336923 | |||||||
| chr9:86336972 | T | G | 1 | a0001c0001t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1455+447A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86336972 | |||||||
| chr9:86337103 | C | T | 1 | a0001c0014t0011g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1455+316G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86337103 | |||||||
| chr9:86337149 | T | C | 6 | a0003c0004t0001g0271 a0003c0004t0001g0272 a0003c0004t0001g0273 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1455+270A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86337149 | |||||||
| chr9:86337257 | A | G | 3 | a0002c0002t0001g0007 a0002c0002t0001g0194 a0002c0002t0001g0195 |
6 | NA18942.hp2 NA18946.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.1455+162T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86337257 | |||||||
| chr9:86337331 | G | A | 2 | a0002c0002t0001g0032 a0002c0002t0001g0225 |
3 | HG01168.hp2 HG01169.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1455+88C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86337331 | |||||||
| chr9:86337366 | T | A | 1 | a0001c0001t0001g0131 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1455+53A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86337366 | |||||||
| chr9:86337398 | A | C | 3 | a0001c0001t0002g0014 a0001c0001t0002g0043 a0001c0001t0002g0044 |
4 | HG00639.hp2 HG00738.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1455+21T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86337398 | |||||||
| chr9:86337648 | T | C | 1 | a0002c0002t0001g0226 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1336-110A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86337648 | |||||||
| chr9:86337705 | G | A | 3 | a0004c0005t0001g0036 a0004c0005t0001g0037 a0004c0005t0001g0280 |
5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1336-167C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86337705 | |||||||
| chr9:86337719 | T | A | 1 | a0001c0001t0001g0080 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1336-181A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86337719 | |||||||
| chr9:86337860 | G | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
6 | HG03017.hp2 HG04115.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.1336-322C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86337860 | |||||||
| chr9:86337870 | C | T | 3 | a0004c0005t0001g0036 a0004c0005t0001g0037 a0004c0005t0001g0280 |
5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1336-332G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86337870 | |||||||
| chr9:86337958 | T | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0139 a0001c0001t0001g0145 |
3 | HG02723.hp1 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1336-420A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86337958 | |||||||
| chr9:86337962 | C | T | 3 | a0004c0005t0001g0036 a0004c0005t0001g0037 a0004c0005t0001g0280 |
5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1336-424G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86337962 | |||||||
| chr9:86338158 | A | G | 5 | a0002c0003t0001g0282 a0002c0003t0001g0283 a0002c0003t0001g0284 others(2): Show |
5 | HG01109.hp2 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1336-620T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86338158 | |||||||
| chr9:86338210 | CT | C | 13 | a0001c0001t0001g0081 a0001c0001t0001g0092 a0001c0001t0001g0145 others(10): Show |
13 | HG01167.hp1 HG01257.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.1335+612delA | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86338210 | |||||||
| chr9:86338210 | CTTTTTTT others(4): Show |
C | 2 | a0002c0002t0001g0229 a0002c0002t0001g0261 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1335+602_1335+612d others(13): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86338210 | |||||||
| chr9:86338275 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0144 |
3 | NA18943.hp1 NA18973.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1335+548C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86338275 | |||||||
| chr9:86338322 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1335+501A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86338322 | |||||||
| chr9:86338514 | G | T | 1 | a0007c0017t0001g0096 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1335+309C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86338514 | |||||||
| chr9:86338607 | C | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
137 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1335+216G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86338607 | |||||||
| chr9:86338639 | C | T | 22 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(19): Show |
34 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.1335+184G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86338639 | |||||||
| chr9:86338720 | T | C | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
3 | HG02135.hp2 NA18946.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1335+103A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86338720 | |||||||
| chr9:86338772 | A | G | 1 | a0001c0012t0008g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1335+51T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86338772 | |||||||
| chr9:86339042 | C | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0082 |
3 | HG02071.hp2 NA18969.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1209-93G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 8/26 | chr9 | 86339042 | |||||||
| chr9:86339079 | A | C | 1 | a0001c0001t0001g0095 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1209-130T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 8/26 | chr9 | 86339079 | |||||||
| chr9:86339138 | C | T | 1 | a0001c0014t0011g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1209-189G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 8/26 | chr9 | 86339138 | |||||||
| chr9:86339254 | T | C | 5 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
5 | HG02135.hp2 NA18946.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.1209-305A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 8/26 | chr9 | 86339254 | |||||||
| chr9:86339449 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1209-500G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 8/26 | chr9 | 86339449 | |||||||
| chr9:86339789 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
130 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1208+247G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 8/26 | chr9 | 86339789 | |||||||
| chr9:86339964 | T | C | 3 | a0002c0002t0001g0147 a0002c0002t0001g0230 a0002c0002t0001g0293 |
3 | HG02622.hp2 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1208+72A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 8/26 | chr9 | 86339964 | |||||||
| chr9:86340014 | A | T | 3 | a0004c0005t0001g0036 a0004c0005t0001g0037 a0004c0005t0001g0280 |
5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1208+22T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 8/26 | chr9 | 86340014 | |||||||
| chr9:86340188 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1139-83A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 7/26 | chr9 | 86340188 | |||||||
| chr9:86340462 | C | T | 21 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(18): Show |
33 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.1139-357G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 7/26 | chr9 | 86340462 | |||||||
| chr9:86340628 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1138+374A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 7/26 | chr9 | 86340628 | |||||||
| chr9:86340874 | T | C | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1138+128A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 7/26 | chr9 | 86340874 | |||||||
| chr9:86341102 | C | T | 11 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0170 others(8): Show |
13 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.1087-49G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86341102 | |||||||
| chr9:86341252 | G | C | 1 | a0001c0001t0001g0142 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1087-199C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86341252 | |||||||
| chr9:86341363 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1087-310T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86341363 | |||||||
| chr9:86341416 | A | G | 13 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0059 others(10): Show |
14 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.1087-363T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86341416 | |||||||
| chr9:86341433 | T | C | 6 | a0003c0004t0001g0271 a0003c0004t0001g0272 a0003c0004t0001g0273 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1087-380A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86341433 | |||||||
| chr9:86341448 | G | A | 1 | a0003c0004t0001g0273 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1087-395C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86341448 | |||||||
| chr9:86341517 | T | G | 1 | a0002c0002t0001g0187 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1087-464A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86341517 | |||||||
| chr9:86341733 | C | T | 13 | a0002c0003t0001g0038 a0002c0003t0001g0039 a0002c0003t0001g0282 others(10): Show |
14 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1087-680G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86341733 | |||||||
| chr9:86341931 | G | A | 1 | a0002c0002t0001g0242 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1087-878C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86341931 | |||||||
| chr9:86342019 | G | A | 4 | a0002c0002t0001g0231 a0002c0002t0001g0232 a0002c0002t0001g0233 others(1): Show |
4 | NA18975.hp1 NA18991.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1087-966C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342019 | |||||||
| chr9:86342067 | G | C | 6 | a0002c0003t0001g0013 a0002c0003t0001g0035 a0002c0003t0001g0040 others(3): Show |
8 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1086+1008C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342067 | |||||||
| chr9:86342092 | C | T | 18 | a0001c0001t0001g0278 a0002c0003t0001g0033 a0002c0003t0001g0034 others(15): Show |
20 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.1086+983G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342092 | |||||||
| chr9:86342172 | A | AT | 3 | a0004c0005t0001g0036 a0004c0005t0001g0037 a0004c0005t0001g0280 |
5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1086+902dupA | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342172 | |||||||
| chr9:86342393 | T | G | 4 | a0002c0002t0001g0234 a0002c0002t0001g0235 a0002c0002t0001g0236 others(1): Show |
4 | HG00544.hp2 NA18952.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.1086+682A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342393 | |||||||
| chr9:86342691 | A | G | 1 | a0002c0002t0001g0196 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1086+384T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342691 | |||||||
| chr9:86342757 | C | T | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1086+318G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342757 | |||||||
| chr9:86342770 | C | T | 3 | a0002c0002t0001g0007 a0002c0002t0001g0194 a0002c0002t0001g0195 |
6 | NA18942.hp2 NA18946.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.1086+305G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342770 | |||||||
| chr9:86342934 | T | G | 4 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0001g0190 others(1): Show |
4 | HG00323.hp1 HG01070.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1086+141A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342934 | |||||||
| chr9:86342942 | T | C | 2 | a0001c0001t0002g0056 a0001c0001t0002g0057 |
2 | NA18943.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1086+133A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342942 | |||||||
| chr9:86342951 | G | C | 1 | a0002c0002t0001g0238 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1086+124C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342951 | |||||||
| chr9:86343317 | T | C | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.998-154A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86343317 | |||||||
| chr9:86343488 | T | C | 11 | a0002c0002t0001g0012 a0002c0002t0001g0239 a0002c0002t0001g0240 others(8): Show |
13 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.998-325A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86343488 | |||||||
| chr9:86343831 | C | T | 2 | a0004c0005t0001g0037 a0004c0005t0001g0280 |
3 | HG01243.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.998-668G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86343831 | |||||||
| chr9:86343865 | T | C | 2 | a0004c0005t0001g0037 a0004c0005t0001g0280 |
3 | HG01243.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.998-702A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86343865 | |||||||
| chr9:86343916 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.998-753T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86343916 | |||||||
| chr9:86344020 | T | G | 1 | a0002c0003t0001g0137 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.998-857A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344020 | |||||||
| chr9:86344071 | A | G | 1 | a0002c0002t0001g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.997+906T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344071 | |||||||
| chr9:86344075 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
138 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.997+902A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344075 | |||||||
| chr9:86344504 | C | T | 18 | a0001c0001t0001g0278 a0002c0003t0001g0033 a0002c0003t0001g0034 others(15): Show |
20 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.997+473G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344504 | |||||||
| chr9:86344588 | C | CT | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
157 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.997+388dupA | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344588 | |||||||
| chr9:86344663 | G | A | 1 | a0001c0001t0001g0025 | 2 | NA18947.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.997+314C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344663 | |||||||
| chr9:86344723 | A | G | 1 | a0002c0003t0001g0269 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.997+254T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344723 | |||||||
| chr9:86344734 | C | T | 3 | a0004c0005t0001g0036 a0004c0005t0001g0037 a0004c0005t0001g0280 |
5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.997+243G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344734 | |||||||
| chr9:86344846 | C | CA | 18 | a0001c0001t0001g0278 a0002c0003t0001g0033 a0002c0003t0001g0034 others(15): Show |
20 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.997+130dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344846 | |||||||
| chr9:86344881 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.997+96C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344881 | |||||||
| chr9:86344888 | A | C | 1 | a0002c0002t0009g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.997+89T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344888 | |||||||
| chr9:86345348 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.820-194A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 4/26 | chr9 | 86345348 | |||||||
| chr9:86345446 | C | T | 1 | a0002c0003t0001g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.819+223G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 4/26 | chr9 | 86345446 | |||||||
| chr9:86345466 | A | C | 13 | a0002c0003t0001g0038 a0002c0003t0001g0039 a0002c0003t0001g0282 others(10): Show |
14 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.819+203T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 4/26 | chr9 | 86345466 | |||||||
| chr9:86345517 | T | G | 3 | a0004c0005t0001g0036 a0004c0005t0001g0037 a0004c0005t0001g0280 |
5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.819+152A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 4/26 | chr9 | 86345517 | |||||||
| chr9:86346195 | C | A | 3 | a0004c0005t0001g0036 a0004c0005t0001g0037 a0004c0005t0001g0280 |
5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+104G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 3/26 | chr9 | 86346195 | |||||||
| chr9:86346281 | T | C | 2 | a0002c0003t0001g0013 a0002c0003t0001g0040 |
3 | HG02630.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.702+18A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 3/26 | chr9 | 86346281 | |||||||
| chr9:86346800 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0140 a0001c0001t0001g0141 others(1): Show |
5 | HG00621.hp2 NA18612.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.521-320C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86346800 | |||||||
| chr9:86346845 | T | C | 1 | a0002c0002t0001g0243 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.521-365A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86346845 | |||||||
| chr9:86346913 | C | T | 5 | a0001c0001t0001g0084 a0001c0001t0003g0020 a0001c0001t0004g0085 others(2): Show |
6 | HG02280.hp2 HG02486.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.521-433G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86346913 | |||||||
| chr9:86347023 | T | C | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG00558.hp2 HG00597.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.521-543A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86347023 | |||||||
| chr9:86347063 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.521-583C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86347063 | |||||||
| chr9:86347252 | C | A | 1 | a0002c0002t0001g0244 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.521-772G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86347252 | |||||||
| chr9:86347552 | C | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(22): Show |
36 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.521-1072G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86347552 | |||||||
| chr9:86347560 | T | G | 1 | a0002c0002t0001g0245 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.521-1080A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86347560 | |||||||
| chr9:86347578 | G | C | 1 | a0003c0004t0001g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.521-1098C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86347578 | |||||||
| chr9:86347588 | G | T | 6 | a0002c0003t0001g0013 a0002c0003t0001g0035 a0002c0003t0001g0040 others(3): Show |
8 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.521-1108C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86347588 | |||||||
| chr9:86347680 | A | T | 1 | a0002c0002t0009g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.521-1200T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86347680 | |||||||
| chr9:86347880 | AT | A | 9 | a0002c0003t0001g0013 a0002c0003t0001g0035 a0002c0003t0001g0040 others(6): Show |
13 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.521-1401delA | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86347880 | |||||||
| chr9:86348093 | C | T | 30 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0029 others(27): Show |
33 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.521-1613G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86348093 | |||||||
| chr9:86348451 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.521-1971A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86348451 | |||||||
| chr9:86348515 | G | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0144 |
3 | NA18943.hp1 NA18973.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.521-2035C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86348515 | |||||||
| chr9:86348658 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.521-2178G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86348658 | |||||||
| chr9:86348662 | A | G | 1 | a0002c0003t0001g0251 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.521-2182T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86348662 | |||||||
| chr9:86348708 | C | T | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG00558.hp2 HG00597.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.521-2228G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86348708 | |||||||
| chr9:86348803 | T | A | 1 | a0001c0001t0001g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.521-2323A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86348803 | |||||||
| chr9:86348852 | T | C | 1 | a0002c0003t0001g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.521-2372A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86348852 | |||||||
| chr9:86349033 | T | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
221 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.521-2553A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86349033 | |||||||
| chr9:86349065 | G | A | 1 | a0002c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.521-2585C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86349065 | |||||||
| chr9:86349077 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.521-2597C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86349077 | |||||||
| chr9:86349392 | C | T | 2 | a0002c0003t0001g0013 a0002c0003t0001g0040 |
3 | HG02630.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.521-2912G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86349392 | |||||||
| chr9:86349573 | GA | G | 3 | a0004c0005t0001g0036 a0004c0005t0001g0037 a0004c0005t0001g0280 |
5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.521-3094delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86349573 | |||||||
| chr9:86349603 | A | G | 3 | a0004c0005t0001g0036 a0004c0005t0001g0037 a0004c0005t0001g0280 |
5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.520+3077T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86349603 | |||||||
| chr9:86349712 | T | C | 1 | a0002c0002t0001g0249 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.520+2968A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86349712 | |||||||
| chr9:86349792 | C | G | 1 | a0002c0002t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.520+2888G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86349792 | |||||||
| chr9:86349823 | G | T | 9 | a0001c0001t0001g0278 a0002c0003t0001g0033 a0002c0003t0001g0165 others(6): Show |
10 | NA18950.hp1 NA18978.hp2 NA18992.hp2 others(7): Show |
intron_variant | MODIFIER | c.520+2857C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86349823 | |||||||
| chr9:86349892 | C | T | 1 | a0002c0002t0001g0164 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.520+2788G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86349892 | |||||||
| chr9:86350006 | T | C | 6 | a0003c0004t0001g0271 a0003c0004t0001g0272 a0003c0004t0001g0273 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.520+2674A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86350006 | |||||||
| chr9:86350202 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.520+2478C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86350202 | |||||||
| chr9:86350511 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0250 |
2 | HG00741.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.520+2169G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86350511 | |||||||
| chr9:86350518 | G | A | 3 | a0004c0005t0001g0036 a0004c0005t0001g0037 a0004c0005t0001g0280 |
5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.520+2162C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86350518 | |||||||
| chr9:86350684 | A | T | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
161 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.520+1996T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86350684 | |||||||
| chr9:86350701 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.520+1979T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86350701 | |||||||
| chr9:86350753 | T | C | 2 | a0004c0005t0001g0037 a0004c0005t0001g0280 |
3 | HG01243.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.520+1927A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86350753 | |||||||
| chr9:86350771 | C | T | 1 | a0002c0002t0001g0149 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.520+1909G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86350771 | |||||||
| chr9:86351000 | G | T | 1 | a0002c0002t0001g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.520+1680C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351000 | |||||||
| chr9:86351074 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.520+1606G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351074 | |||||||
| chr9:86351132 | C | CA | 30 | a0001c0001t0001g0250 a0001c0001t0001g0278 a0001c0014t0011g0294 others(27): Show |
33 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.520+1547dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351132 | |||||||
| chr9:86351132 | CA | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.520+1547delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351132 | |||||||
| chr9:86351177 | T | C | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.520+1503A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351177 | |||||||
| chr9:86351217 | C | A | 1 | a0002c0002t0001g0268 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.520+1463G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351217 | |||||||
| chr9:86351392 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
6 | HG03017.hp2 HG04115.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.520+1288G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351392 | |||||||
| chr9:86351422 | C | A | 6 | a0002c0003t0001g0013 a0002c0003t0001g0035 a0002c0003t0001g0040 others(3): Show |
8 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.520+1258G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351422 | |||||||
| chr9:86351431 | G | A | 6 | a0003c0004t0001g0271 a0003c0004t0001g0272 a0003c0004t0001g0273 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.520+1249C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351431 | |||||||
| chr9:86351455 | A | G | 3 | a0004c0005t0001g0036 a0004c0005t0001g0037 a0004c0005t0001g0280 |
5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.520+1225T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351455 | |||||||
| chr9:86351477 | G | A | 3 | a0004c0005t0001g0036 a0004c0005t0001g0037 a0004c0005t0001g0280 |
5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.520+1203C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351477 | |||||||
| chr9:86351519 | C | T | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(15): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.520+1161G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351519 | |||||||
| chr9:86351620 | T | C | 1 | a0001c0001t0001g0277 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.520+1060A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351620 | |||||||
| chr9:86351639 | C | T | 1 | a0001c0014t0011g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.520+1041G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351639 | |||||||
| chr9:86351859 | T | C | 2 | a0004c0005t0001g0037 a0004c0005t0001g0280 |
3 | HG01243.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.520+821A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351859 | |||||||
| chr9:86351892 | T | C | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.520+788A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351892 | |||||||
| chr9:86352385 | A | G | 21 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0014 others(18): Show |
33 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.520+295T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86352385 | |||||||
| chr9:86352440 | C | A | 3 | a0004c0005t0001g0036 a0004c0005t0001g0037 a0004c0005t0001g0280 |
5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.520+240G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86352440 | |||||||
| chr9:86353494 | G | A | 4 | a0002c0003t0001g0013 a0002c0003t0001g0035 a0002c0003t0001g0040 others(1): Show |
6 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31-264C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 1/26 | chr9 | 86353494 | |||||||
| chr9:86353536 | T | C | 3 | a0004c0005t0001g0036 a0004c0005t0001g0037 a0004c0005t0001g0280 |
5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31-306A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 1/26 | chr9 | 86353536 | |||||||
| chr9:86353618 | G | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | NA18966.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.-31-388C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 1/26 | chr9 | 86353618 | |||||||
| chr9:86353763 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-32+508C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 1/26 | chr9 | 86353763 | |||||||
| chr9:86353929 | C | G | 2 | a0002c0003t0001g0013 a0002c0003t0001g0040 |
3 | HG02630.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-32+342G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 1/26 | chr9 | 86353929 | |||||||
| chr9:86353955 | CG | C | 14 | a0002c0002t0001g0293 a0002c0003t0001g0038 a0002c0003t0001g0039 others(11): Show |
15 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-32+315delC | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 1/26 | chr9 | 86353955 | |||||||
| chr9:86354093 | C | T | 1 | a0002c0003t0001g0039 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-32+178G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 1/26 | chr9 | 86354093 |