Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 144455 |
| ensemblid | ENSG00000165891.16 |
| hgncid | 23820 |
| symbol | E2F7 |
| name | E2F transcription factor 7 |
| refseq_nuc | NM_203394.3 |
| refseq_prot | NP_976328.2 |
| ensembl_nuc | ENST00000322886.12 |
| ensembl_prot | ENSP00000323246.7 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 77021251 |
| end | 77065569 |
| strand | - |
| ver | v1.2 |
| region | chr12:77021251-77065569 |
| region5000 | chr12:77016251-77070569 |
| regionname0 | E2F7_chr12_77021251_77065569 |
| regionname5000 | E2F7_chr12_77016251_77070569 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 911 | 327 | 56 | 68 | 161 | 8 | 33 | 125 | E2F7_chr12_77016251_77070569 | E2F7 | MEVNC others(906): Show |
chr12 | 77016251 | 77070569 |
| a0002 | 1/0 | 911 | 40 | 32 | 4 | 0 | 0 | 3 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | MEVNC others(906): Show |
chr12 | 77016251 | 77070569 |
| a0003 | 0/0 | 911 | 11 | 1 | 7 | 0 | 1 | 2 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | MEVNC others(906): Show |
chr12 | 77016251 | 77070569 |
| a0004 | 0/0 | 911 | 5 | 0 | 0 | 5 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | MEVNC others(906): Show |
chr12 | 77016251 | 77070569 |
| a0005 | 0/0 | 911 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | MEVNC others(906): Show |
chr12 | 77016251 | 77070569 |
| a0006 | 0/0 | 911 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | E2F7_chr12_77016251_77070569 | E2F7 | MEVNC others(906): Show |
chr12 | 77016251 | 77070569 |
| a0007 | 0/0 | 911 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | MEVNC others(906): Show |
chr12 | 77016251 | 77070569 |
| a0008 | 0/0 | 911 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | MEVNC others(906): Show |
chr12 | 77016251 | 77070569 |
| a0009 | 0/0 | 911 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | MEVNC others(906): Show |
chr12 | 77016251 | 77070569 |
| a0010 | 0/0 | 911 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | MEVNC others(906): Show |
chr12 | 77016251 | 77070569 |
| a0011 | 0/0 | 911 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | MEVNC others(906): Show |
chr12 | 77016251 | 77070569 |
| a0012 | 0/0 | 911 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | MEVNC others(906): Show |
chr12 | 77016251 | 77070569 |
| a0013 | 0/0 | 911 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | MEVNC others(906): Show |
chr12 | 77016251 | 77070569 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2733 | 250 | 37 | 47 | 132 | 5 | 29 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0001c0002 | 0/0 | 2733 | 60 | 7 | 19 | 28 | 2 | 4 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0001c0004 | 0/0 | 2733 | 11 | 9 | 1 | 0 | 1 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0001c0009 | 0/0 | 2733 | 2 | 2 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0001c0012 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0001c0013 | 0/0 | 2733 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0001c0018 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0001c0023 | 0/1 | 2733 | 1 | 0 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0002c0003 | 1/0 | 2733 | 29 | 25 | 0 | 0 | 0 | 3 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0002c0006 | 0/0 | 2733 | 6 | 2 | 4 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0002c0008 | 0/0 | 2733 | 4 | 4 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0002c0024 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0003c0005 | 0/0 | 2733 | 10 | 1 | 6 | 0 | 1 | 2 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0003c0014 | 0/0 | 2733 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0004c0007 | 0/0 | 2733 | 5 | 0 | 0 | 5 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0005c0011 | 0/0 | 2733 | 2 | 0 | 0 | 0 | 1 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0006c0010 | 0/0 | 2733 | 2 | 0 | 0 | 2 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0007c0021 | 0/0 | 2733 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0008c0016 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0009c0022 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0010c0020 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0011c0015 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0012c0019 | 0/0 | 2733 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 | ||
| a0013c0017 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | ATGGA others(2728): Show |
chr12 | 77016251 | 77070569 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5726 | 156 | 21 | 20 | 91 | 5 | 19 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0001t0002 | 0/0 | 5726 | 74 | 11 | 19 | 36 | 0 | 8 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0001t0003 | 0/0 | 5726 | 2 | 1 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0001t0005 | 0/0 | 5725 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5720): Show |
chr12 | 77016251 | 77070569 |
| a0001c0001t0006 | 0/0 | 5726 | 4 | 1 | 3 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0001t0007 | 0/0 | 5726 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0001t0008 | 0/0 | 5726 | 2 | 0 | 1 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0001t0009 | 0/0 | 5726 | 2 | 0 | 0 | 2 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0001t0011 | 0/0 | 5726 | 2 | 0 | 0 | 2 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0001t0017 | 0/0 | 5726 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0001t0020 | 0/0 | 5726 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0001t0021 | 0/0 | 5726 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0001t0022 | 0/0 | 5726 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0001t0023 | 0/0 | 5726 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0001t0024 | 0/0 | 5726 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0002t0001 | 0/0 | 5726 | 21 | 6 | 4 | 9 | 1 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0002t0002 | 0/0 | 5726 | 34 | 1 | 13 | 16 | 1 | 3 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0002t0012 | 0/0 | 5726 | 2 | 0 | 0 | 2 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0002t0016 | 0/0 | 5726 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0002t0018 | 0/0 | 5726 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0002t0019 | 0/0 | 5726 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0004t0001 | 0/0 | 5726 | 9 | 7 | 1 | 0 | 1 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0004t0005 | 0/0 | 5725 | 2 | 2 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5720): Show |
chr12 | 77016251 | 77070569 |
| a0001c0009t0015 | 0/0 | 5726 | 2 | 2 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0012t0001 | 0/0 | 5726 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0013t0001 | 0/0 | 5726 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0018t0001 | 0/0 | 5726 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0001c0023t0002 | 0/1 | 5726 | 1 | 0 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0002c0003t0001 | 0/0 | 5726 | 9 | 8 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0002c0003t0002 | 0/0 | 5726 | 6 | 4 | 0 | 0 | 0 | 2 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0002c0003t0003 | 0/0 | 5726 | 9 | 9 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0002c0003t0005 | 1/0 | 5725 | 1 | 0 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5720): Show |
chr12 | 77016251 | 77070569 |
| a0002c0003t0010 | 0/0 | 5726 | 2 | 2 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0002c0003t0014 | 0/0 | 5726 | 2 | 2 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0002c0006t0001 | 0/0 | 5726 | 4 | 0 | 4 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0002c0006t0002 | 0/0 | 5726 | 2 | 2 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0002c0008t0001 | 0/0 | 5726 | 2 | 2 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0002c0008t0005 | 0/0 | 5725 | 2 | 2 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5720): Show |
chr12 | 77016251 | 77070569 |
| a0002c0024t0001 | 0/0 | 5726 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0003c0005t0004 | 0/0 | 5726 | 6 | 0 | 4 | 0 | 1 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0003c0005t0007 | 0/0 | 5726 | 2 | 1 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0003c0005t0013 | 0/0 | 5726 | 2 | 0 | 2 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0003c0014t0004 | 0/0 | 5726 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0004c0007t0001 | 0/0 | 5726 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0004c0007t0002 | 0/0 | 5726 | 4 | 0 | 0 | 4 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0005c0011t0001 | 0/0 | 5726 | 2 | 0 | 0 | 0 | 1 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0006c0010t0001 | 0/0 | 5726 | 2 | 0 | 0 | 2 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0007c0021t0005 | 0/0 | 5725 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5720): Show |
chr12 | 77016251 | 77070569 |
| a0008c0016t0001 | 0/0 | 5726 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0009c0022t0002 | 0/0 | 5726 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0010c0020t0001 | 0/0 | 5726 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0011c0015t0001 | 0/0 | 5726 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0012c0019t0002 | 0/0 | 5726 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| a0013c0017t0001 | 0/0 | 5726 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | GACTA others(5721): Show |
chr12 | 77016251 | 77070569 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 19 | 0 | 3 | 13 | 0 | 3 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 4 | 0 | 2 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0002 | 0/0 | 9 | 1 | 8 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0005 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0011 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0006g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0007g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0008g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0008g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0009g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0011g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0011g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0017g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0020g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0021g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0022g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0023g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0001t0024g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0001g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0001g0013 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0008 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0012g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0012g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0016g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0018g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0002t0019g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0004t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0004t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0004t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0004t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0004t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0004t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0004t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0004t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0004t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0009t0015g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0009t0015g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0012t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0013t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0018t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0001c0023t0002g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0003t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0003t0002g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0003t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0003t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0003t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0003t0003g0004 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0003t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0003t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0003t0005g0180 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0003t0010g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0003t0014g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0003t0014g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0006t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0006t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0006t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0008t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0008t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0008t0005g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0002c0024t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0003c0005t0004g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0003c0005t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0003c0005t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0003c0005t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0003c0005t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0003c0005t0007g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0003c0005t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0003c0005t0013g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0003c0014t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0004c0007t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0004c0007t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0004c0007t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0004c0007t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0005c0011t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0005c0011t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0006c0010t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0006c0010t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0007c0021t0005g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0008c0016t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0009c0022t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0010c0020t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0011c0015t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0012c0019t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| a0013c0017t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0283 | EUR | GBR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | FIN | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00280 | hp2 | a0005 | c0011 | t0001 | g0137 | EUR | FIN | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | FIN | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00408 | hp2 | a0004 | c0007 | t0002 | g0172 | EAS | CHS | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | CHS | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00673 | hp1 | a0001 | c0001 | t0024 | g0094 | EAS | CHS | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00673 | hp2 | a0004 | c0007 | t0001 | g0075 | EAS | CHS | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00733 | hp1 | a0003 | c0005 | t0013 | g0046 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0081 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00738 | hp1 | a0003 | c0014 | t0004 | g0052 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00738 | hp2 | a0002 | c0006 | t0001 | g0015 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01069 | hp1 | a0003 | c0005 | t0004 | g0048 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01069 | hp2 | a0001 | c0002 | t0018 | g0228 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0211 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01071 | hp1 | a0003 | c0005 | t0004 | g0019 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01081 | hp1 | a0001 | c0001 | t0022 | g0093 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0229 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01106 | hp2 | a0001 | c0001 | t0017 | g0056 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01175 | hp1 | a0003 | c0005 | t0004 | g0053 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0063 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01192 | hp2 | a0001 | c0004 | t0001 | g0273 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0085 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01255 | hp1 | a0003 | c0005 | t0013 | g0046 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0057 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01256 | hp2 | a0001 | c0013 | t0001 | g0201 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01261 | hp1 | a0007 | c0021 | t0005 | g0179 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01261 | hp2 | a0001 | c0001 | t0008 | g0049 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01346 | hp2 | a0001 | c0001 | t0021 | g0187 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0224 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01361 | hp2 | a0002 | c0006 | t0001 | g0015 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0184 | EUR | IBS | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01891 | hp1 | a0003 | c0005 | t0007 | g0284 | AFR | ACB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01891 | hp2 | a0002 | c0003 | t0001 | g0150 | AFR | ACB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01928 | hp1 | a0001 | c0002 | t0016 | g0051 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01928 | hp2 | a0001 | c0001 | t0006 | g0020 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0080 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0020 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01978 | hp1 | a0002 | c0006 | t0001 | g0015 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0126 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01993 | hp1 | a0002 | c0006 | t0001 | g0246 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02027 | hp2 | a0004 | c0007 | t0002 | g0108 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | ACB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02055 | hp2 | a0002 | c0008 | t0005 | g0037 | AFR | ACB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02080 | hp1 | a0004 | c0007 | t0002 | g0030 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0225 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | ACB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02145 | hp2 | a0001 | c0004 | t0005 | g0125 | AFR | ACB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02155 | hp1 | a0001 | c0002 | t0012 | g0078 | EAS | CDX | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0135 | EAS | CDX | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02165 | hp1 | a0004 | c0007 | t0002 | g0030 | EAS | CDX | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CDX | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02257 | hp1 | a0002 | c0008 | t0001 | g0158 | AFR | ACB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | ACB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02258 | hp1 | a0001 | c0004 | t0005 | g0250 | AFR | ACB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02258 | hp2 | a0002 | c0006 | t0002 | g0038 | AFR | ACB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ACB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02300 | hp1 | a0003 | c0005 | t0004 | g0055 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PEL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0227 | AFR | ACB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02523 | hp1 | a0009 | c0022 | t0002 | g0077 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02602 | hp1 | a0003 | c0005 | t0007 | g0276 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0013 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02615 | hp1 | a0001 | c0001 | t0023 | g0248 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02622 | hp1 | a0002 | c0003 | t0002 | g0149 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02622 | hp2 | a0002 | c0003 | t0003 | g0004 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0127 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02630 | hp2 | a0001 | c0009 | t0015 | g0138 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0247 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02683 | hp2 | a0002 | c0003 | t0001 | g0144 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0277 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02717 | hp2 | a0001 | c0004 | t0001 | g0042 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02723 | hp2 | a0002 | c0003 | t0001 | g0151 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02809 | hp2 | a0001 | c0004 | t0001 | g0042 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02818 | hp1 | a0002 | c0003 | t0002 | g0039 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0134 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0185 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02895 | hp1 | a0011 | c0015 | t0001 | g0162 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02895 | hp2 | a0002 | c0003 | t0014 | g0152 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02897 | hp2 | a0002 | c0003 | t0014 | g0140 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | ESN | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02922 | hp2 | a0001 | c0018 | t0001 | g0208 | AFR | ESN | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0260 | AFR | ESN | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02976 | hp1 | a0002 | c0003 | t0003 | g0142 | AFR | ESN | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02976 | hp2 | a0002 | c0003 | t0001 | g0034 | AFR | ESN | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0275 | AFR | MSL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03130 | hp2 | a0002 | c0008 | t0005 | g0037 | AFR | ESN | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03139 | hp1 | a0001 | c0004 | t0001 | g0157 | AFR | ESN | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03139 | hp2 | a0002 | c0006 | t0002 | g0038 | AFR | ESN | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03209 | hp1 | a0002 | c0003 | t0003 | g0004 | AFR | MSL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03209 | hp2 | a0001 | c0004 | t0001 | g0156 | AFR | MSL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03225 | hp1 | a0002 | c0003 | t0001 | g0146 | AFR | MSL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03225 | hp2 | a0002 | c0003 | t0001 | g0034 | AFR | MSL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | MSL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03453 | hp2 | a0002 | c0003 | t0010 | g0036 | AFR | MSL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | MSL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03490 | hp1 | a0002 | c0003 | t0002 | g0035 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03491 | hp1 | a0001 | c0001 | t0008 | g0050 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03492 | hp2 | a0002 | c0003 | t0002 | g0035 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03516 | hp1 | a0002 | c0003 | t0003 | g0004 | AFR | ESN | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03516 | hp2 | a0001 | c0009 | t0015 | g0249 | AFR | ESN | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03579 | hp2 | a0002 | c0003 | t0010 | g0036 | AFR | MSL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03669 | hp2 | a0012 | c0019 | t0002 | g0264 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | STU | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | STU | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03704 | hp1 | a0003 | c0005 | t0004 | g0019 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | BEB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03927 | hp1 | a0001 | c0001 | t0007 | g0215 | SAS | BEB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0079 | SAS | BEB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0242 | SAS | BEB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0188 | SAS | STU | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | STU | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0261 | SAS | BEB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | STU | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | STU | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG04228 | hp1 | a0005 | c0011 | t0001 | g0136 | SAS | STU | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0279 | SAS | STU | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18522 | hp1 | a0002 | c0003 | t0003 | g0004 | AFR | YRI | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18522 | hp2 | a0001 | c0001 | t0020 | g0205 | AFR | YRI | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | CHB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18747 | hp1 | a0001 | c0001 | t0009 | g0027 | EAS | CHB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0270 | EAS | CHB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18906 | hp1 | a0002 | c0024 | t0001 | g0147 | AFR | YRI | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18906 | hp2 | a0002 | c0003 | t0001 | g0143 | AFR | YRI | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18941 | hp1 | a0001 | c0001 | t0011 | g0265 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18952 | hp2 | a0001 | c0002 | t0012 | g0257 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18966 | hp1 | a0001 | c0012 | t0001 | g0060 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18980 | hp1 | a0001 | c0002 | t0019 | g0171 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18983 | hp1 | a0013 | c0017 | t0001 | g0092 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19004 | hp2 | a0006 | c0010 | t0001 | g0173 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19011 | hp2 | a0001 | c0001 | t0009 | g0027 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19030 | hp1 | a0002 | c0003 | t0001 | g0145 | AFR | LWK | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0155 | AFR | LWK | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19043 | hp2 | a0001 | c0004 | t0001 | g0245 | AFR | LWK | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19072 | hp1 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19084 | hp1 | a0001 | c0001 | t0011 | g0263 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19087 | hp1 | a0006 | c0010 | t0001 | g0168 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA19240 | hp2 | a0002 | c0003 | t0003 | g0004 | AFR | YRI | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA20752 | hp1 | a0001 | c0004 | t0001 | g0212 | EUR | TSI | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA20752 | hp2 | a0003 | c0005 | t0004 | g0054 | EUR | TSI | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | GIH | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | GIH | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | ACB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02109 | hp2 | a0008 | c0016 | t0001 | g0161 | AFR | ACB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02486 | hp1 | a0002 | c0003 | t0001 | g0139 | AFR | ACB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02559 | hp1 | a0002 | c0003 | t0003 | g0159 | AFR | ACB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG02559 | hp2 | a0010 | c0020 | t0001 | g0189 | AFR | ACB | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG03471 | hp2 | a0002 | c0003 | t0003 | g0004 | AFR | MSL | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG06807 | hp1 | a0002 | c0003 | t0002 | g0039 | AFR | USA | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| HG06807 | hp2 | a0002 | c0003 | t0003 | g0004 | AFR | USA | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA20300 | hp1 | a0002 | c0008 | t0001 | g0148 | AFR | USA | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0058 | AFR | USA | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | LWK | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| NA21309 | hp2 | a0002 | c0003 | t0002 | g0141 | AFR | LWK | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| homoSapiens | chm13v2 | a0001 | c0023 | t0002 | g0197 | REF | REF | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0005 | g0180 | REF | REF | E2F7_chr12_77016251_77070569 | E2F7 | chr12 | 77016251 | 77070569 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:77024094 | T | C | 1 | a0010 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.2657A>G | p.Lys886Arg | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 2882/5725 | 2657/2736 | 886/911 | chr12 | 77024094 | |||
| chr12:77025561 | A | T | 1 | a0003 | 11 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(8): Show |
missense_variant | MODERATE | c.2562T>A | p.His854Gln | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/13 | 2787/5725 | 2562/2736 | 854/911 | chr12 | 77025561 | |||
| chr12:77025757 | C | T | 1 | a0012 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.2366G>A | p.Gly789Glu | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/13 | 2591/5725 | 2366/2736 | 789/911 | chr12 | 77025757 | |||
| chr12:77025923 | A | G | 1 | a0013 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.2200T>C | p.Ser734Pro | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/13 | 2425/5725 | 2200/2736 | 734/911 | chr12 | 77025923 | |||
| chr12:77027946 | T | C | 1 | a0007 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.2077A>G | p.Lys693Glu | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 11/13 | 2302/5725 | 2077/2736 | 693/911 | chr12 | 77027946 | |||
| chr12:77028089 | C | G | 1 | a0008 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.1934G>C | p.Arg645Thr | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 11/13 | 2159/5725 | 1934/2736 | 645/911 | chr12 | 77028089 | |||
| chr12:77029839 | T | C | 1 | a0004 | 5 | HG00408.hp2 HG00673.hp2 HG02027.hp2 others(2): Show |
missense_variant | MODERATE | c.1876A>G | p.Met626Val | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/13 | 2101/5725 | 1876/2736 | 626/911 | chr12 | 77029839 | |||
| chr12:77029931 | C | T | 1 | a0011 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.1784G>A | p.Arg595His | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/13 | 2009/5725 | 1784/2736 | 595/911 | chr12 | 77029931 | |||
| chr12:77030298 | G | T | 1 | a0009 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.1417C>A | p.Pro473Thr | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/13 | 1642/5725 | 1417/2736 | 473/911 | chr12 | 77030298 | |||
| chr12:77033913 | T | C | 1 | a0006 | 2 | NA19004.hp2 NA19087.hp1 |
missense_variant | MODERATE | c.1253A>G | p.Glu418Gly | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 8/13 | 1478/5725 | 1253/2736 | 418/911 | chr12 | 77033913 | |||
| chr12:77046043 | G | C | 1 | a0005 | 2 | HG00280.hp2 HG04228.hp1 |
missense_variant | MODERATE | c.824C>G | p.Pro275Arg | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 5/13 | 1049/5725 | 824/2736 | 275/911 | chr12 | 77046043 | |||
| chr12:77056010 | A | G | 11 | a0001 a0003 a0004 others(8): Show |
351 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
missense_variant | MODERATE | c.214T>C | p.Phe72Leu | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/13 | 439/5725 | 214/2736 | 72/911 | chr12 | 77056010 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:77025594 | G | A | 1 | a0001c0009 | 2 | HG02630.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.2529C>T | p.Tyr843Tyr | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/13 | 2754/5725 | 2529/2736 | 843/911 | chr12 | 77025594 | |||
| chr12:77025813 | A | G | 2 | a0003c0005 a0003c0014 |
11 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(8): Show |
synonymous_variant | LOW | c.2310T>C | p.Ser770Ser | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/13 | 2535/5725 | 2310/2736 | 770/911 | chr12 | 77025813 | |||
| chr12:77025822 | C | T | 1 | a0001c0018 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.2301G>A | p.Pro767Pro | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/13 | 2526/5725 | 2301/2736 | 767/911 | chr12 | 77025822 | |||
| chr12:77027998 | A | C | 2 | a0001c0004 a0002c0008 |
15 | HG01192.hp2 HG02055.hp2 HG02145.hp2 others(12): Show |
synonymous_variant | LOW | c.2025T>G | p.Val675Val | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 11/13 | 2250/5725 | 2025/2736 | 675/911 | chr12 | 77027998 | |||
| chr12:77030005 | C | T | 1 | a0002c0024 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.1710G>A | p.Gly570Gly | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/13 | 1935/5725 | 1710/2736 | 570/911 | chr12 | 77030005 | |||
| chr12:77033873 | C | T | 1 | a0003c0014 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.1293G>A | p.Pro431Pro | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 8/13 | 1518/5725 | 1293/2736 | 431/911 | chr12 | 77033873 | |||
| chr12:77044656 | T | C | 6 | a0001c0002 a0001c0013 a0002c0006 others(3): Show |
72 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(69): Show |
synonymous_variant | LOW | c.969A>G | p.Pro323Pro | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 6/13 | 1194/5725 | 969/2736 | 323/911 | chr12 | 77044656 | |||
| chr12:77046231 | C | G | 1 | a0001c0013 | 1 | HG01256.hp2 | synonymous_variant | LOW | c.636G>C | p.Arg212Arg | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 5/13 | 861/5725 | 636/2736 | 212/911 | chr12 | 77046231 | |||
| chr12:77064600 | G | T | 1 | a0001c0012 | 1 | NA18966.hp1 | synonymous_variant | LOW | c.36C>A | p.Ile12Ile | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/13 | 261/5725 | 36/2736 | 12/911 | chr12 | 77064600 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:77021596 | G | A | 1 | a0001c0001t0022 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2419C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 2419 | chr12 | 77021596 | ||||||
| chr12:77021929 | T | C | 1 | a0001c0001t0023 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2086A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 2086 | chr12 | 77021929 | ||||||
| chr12:77022089 | G | A | 1 | a0001c0002t0012 | 2 | HG02155.hp1 NA18952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1926C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 1926 | chr12 | 77022089 | ||||||
| chr12:77022116 | G | C | 1 | a0001c0001t0024 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1899C>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 1899 | chr12 | 77022116 | ||||||
| chr12:77022187 | C | T | 5 | a0001c0001t0007 a0003c0005t0004 a0003c0005t0007 others(2): Show |
12 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1828G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 1828 | chr12 | 77022187 | ||||||
| chr12:77022317 | T | C | 1 | a0002c0003t0010 | 2 | HG03453.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1698A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 1698 | chr12 | 77022317 | ||||||
| chr12:77023034 | C | T | 1 | a0003c0005t0013 | 2 | HG00733.hp1 HG01255.hp1 |
3_prime_UTR_variant | MODIFIER | c.*981G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 981 | chr12 | 77023034 | ||||||
| chr12:77023058 | A | G | 1 | a0001c0001t0011 | 2 | NA18941.hp1 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*957T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 957 | chr12 | 77023058 | ||||||
| chr12:77023090 | T | C | 1 | a0001c0002t0019 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*925A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 925 | chr12 | 77023090 | ||||||
| chr12:77023106 | C | T | 1 | a0001c0009t0015 | 2 | HG02630.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*909G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 909 | chr12 | 77023106 | ||||||
| chr12:77023194 | C | T | 1 | a0001c0001t0021 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*821G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 821 | chr12 | 77023194 | ||||||
| chr12:77023380 | A | C | 1 | a0001c0001t0020 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*635T>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 635 | chr12 | 77023380 | ||||||
| chr12:77023564 | G | A | 15 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(12): Show |
136 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*451C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 451 | chr12 | 77023564 | ||||||
| chr12:77023729 | G | T | 15 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(12): Show |
136 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*286C>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 286 | chr12 | 77023729 | ||||||
| chr12:77023750 | G | GC | 48 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(45): Show |
386 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(383): Show |
3_prime_UTR_variant | MODIFIER | c.*264_*265insG | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 264 | chr12 | 77023750 | ||||||
| chr12:77023894 | A | G | 1 | a0001c0002t0018 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*121T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 121 | chr12 | 77023894 | ||||||
| chr12:77023910 | G | C | 1 | a0002c0003t0014 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*105C>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 105 | chr12 | 77023910 | ||||||
| chr12:77023925 | C | T | 3 | a0001c0001t0003 a0002c0003t0003 a0002c0003t0010 |
13 | HG01192.hp1 HG02451.hp2 HG02559.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*90G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 90 | chr12 | 77023925 | ||||||
| chr12:77023926 | G | A | 1 | a0001c0009t0015 | 2 | HG02630.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*89C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 89 | chr12 | 77023926 | ||||||
| chr12:77023996 | C | G | 1 | a0001c0001t0009 | 2 | NA18747.hp1 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*19G>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 13/13 | 19 | chr12 | 77023996 | ||||||
| chr12:77065432 | C | G | 1 | a0001c0001t0006 | 4 | HG01255.hp2 HG01928.hp2 HG01943.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-88G>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 1/13 | 797 | chr12 | 77065432 | ||||||
| chr12:77065439 | C | T | 1 | a0001c0001t0017 | 1 | HG01106.hp2 | 5_prime_UTR_variant | MODIFIER | c.-95G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 1/13 | 804 | chr12 | 77065439 | ||||||
| chr12:77065524 | C | G | 4 | a0001c0001t0008 a0001c0002t0016 a0003c0005t0004 others(1): Show |
10 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-180G>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 1/13 | 889 | chr12 | 77065524 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:77024192 | A | C | 5 | a0001c0001t0001g0154 a0001c0001t0001g0167 a0001c0002t0001g0021 others(2): Show |
7 | HG02257.hp2 HG02486.hp2 HG02886.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.2566-7T>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/12 | chr12 | 77024192 | |||||||
| chr12:77024195 | GA | G | 3 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0007g0215 |
3 | HG00642.hp2 HG01106.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2566-11delT | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/12 | chr12 | 77024195 | |||||||
| chr12:77024257 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0117 |
4 | NA18953.hp1 NA18970.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.2566-72A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/12 | chr12 | 77024257 | |||||||
| chr12:77024440 | C | T | 2 | a0001c0009t0015g0138 a0001c0009t0015g0249 |
2 | HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2566-255G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/12 | chr12 | 77024440 | |||||||
| chr12:77024458 | G | A | 5 | a0001c0001t0002g0190 a0001c0001t0002g0191 a0001c0001t0002g0203 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2566-273C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/12 | chr12 | 77024458 | |||||||
| chr12:77024471 | C | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0132 |
2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2566-286G>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/12 | chr12 | 77024471 | |||||||
| chr12:77024483 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2566-298A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/12 | chr12 | 77024483 | |||||||
| chr12:77024580 | C | T | 1 | a0002c0003t0001g0034 | 2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2566-395G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/12 | chr12 | 77024580 | |||||||
| chr12:77024733 | C | T | 5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0132 others(2): Show |
5 | HG01109.hp2 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2566-548G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/12 | chr12 | 77024733 | |||||||
| chr12:77024736 | T | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2566-551A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/12 | chr12 | 77024736 | |||||||
| chr12:77024897 | C | A | 10 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0132 others(7): Show |
11 | HG01109.hp2 HG02257.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2565+661G>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/12 | chr12 | 77024897 | |||||||
| chr12:77024902 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2565+656A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/12 | chr12 | 77024902 | |||||||
| chr12:77024957 | T | C | 5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0132 others(2): Show |
5 | HG01109.hp2 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2565+601A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/12 | chr12 | 77024957 | |||||||
| chr12:77024996 | C | T | 279 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(276): Show |
387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.2565+562G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/12 | chr12 | 77024996 | |||||||
| chr12:77025032 | G | GTATAGAT others(18): Show |
4 | a0001c0001t0001g0047 a0001c0001t0001g0131 a0002c0003t0001g0150 others(1): Show |
5 | HG01496.hp1 HG01891.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2565+501_2565+525d others(27): Show |
E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/12 | chr12 | 77025032 | |||||||
| chr12:77025037 | G | A | 4 | a0001c0004t0001g0042 a0001c0004t0001g0156 a0001c0004t0001g0245 others(1): Show |
5 | HG02257.hp1 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2565+521C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/12 | chr12 | 77025037 | |||||||
| chr12:77025142 | C | T | 10 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0132 others(7): Show |
11 | HG01109.hp2 HG02257.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2565+416G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/12 | chr12 | 77025142 | |||||||
| chr12:77025294 | C | T | 9 | a0003c0005t0004g0019 a0003c0005t0004g0048 a0003c0005t0004g0053 others(6): Show |
11 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.2565+264G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/12 | chr12 | 77025294 | |||||||
| chr12:77025295 | G | A | 1 | a0001c0001t0011g0265 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2565+263C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 12/12 | chr12 | 77025295 | |||||||
| chr12:77026069 | C | T | 10 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0132 others(7): Show |
11 | HG01109.hp2 HG02257.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2141-87G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 11/12 | chr12 | 77026069 | |||||||
| chr12:77026089 | A | G | 1 | a0003c0005t0013g0046 | 2 | HG00733.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.2141-107T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 11/12 | chr12 | 77026089 | |||||||
| chr12:77026629 | A | C | 1 | a0001c0002t0001g0185 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2141-647T>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 11/12 | chr12 | 77026629 | |||||||
| chr12:77026899 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2141-917A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 11/12 | chr12 | 77026899 | |||||||
| chr12:77026909 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2141-927G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 11/12 | chr12 | 77026909 | |||||||
| chr12:77026910 | G | A | 4 | a0001c0004t0001g0042 a0001c0004t0001g0156 a0001c0004t0001g0245 others(1): Show |
5 | HG02257.hp1 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2141-928C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 11/12 | chr12 | 77026910 | |||||||
| chr12:77026930 | T | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(219): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.2141-948A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 11/12 | chr12 | 77026930 | |||||||
| chr12:77027012 | G | A | 4 | a0001c0004t0001g0127 a0001c0004t0001g0134 a0001c0004t0001g0157 others(1): Show |
4 | HG02630.hp1 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2140+871C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 11/12 | chr12 | 77027012 | |||||||
| chr12:77027043 | G | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0132 |
3 | HG01109.hp2 HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2140+840C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 11/12 | chr12 | 77027043 | |||||||
| chr12:77027266 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2140+617G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 11/12 | chr12 | 77027266 | |||||||
| chr12:77027307 | C | T | 33 | a0001c0001t0002g0005 a0001c0001t0002g0011 a0001c0001t0002g0023 others(30): Show |
49 | HG01099.hp2 HG01106.hp2 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.2140+576G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 11/12 | chr12 | 77027307 | |||||||
| chr12:77027497 | C | G | 2 | a0001c0001t0001g0131 a0011c0015t0001g0162 |
2 | HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2140+386G>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 11/12 | chr12 | 77027497 | |||||||
| chr12:77027608 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(211): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.2140+275G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 11/12 | chr12 | 77027608 | |||||||
| chr12:77027648 | A | C | 1 | a0001c0001t0001g0199 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2140+235T>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 11/12 | chr12 | 77027648 | |||||||
| chr12:77027788 | G | T | 2 | a0001c0009t0015g0138 a0001c0009t0015g0249 |
2 | HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2140+95C>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 11/12 | chr12 | 77027788 | |||||||
| chr12:77028192 | ATCTC | A | 33 | a0001c0001t0002g0005 a0001c0001t0002g0011 a0001c0001t0002g0023 others(30): Show |
49 | HG01099.hp2 HG01106.hp2 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.1885-58_1885-55del others(4): Show |
E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/12 | chr12 | 77028192 | |||||||
| chr12:77028356 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1885-218A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/12 | chr12 | 77028356 | |||||||
| chr12:77028439 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1885-301C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/12 | chr12 | 77028439 | |||||||
| chr12:77028473 | C | CTT | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(86): Show |
123 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1885-337_1885-336d others(4): Show |
E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/12 | chr12 | 77028473 | |||||||
| chr12:77028530 | C | T | 6 | a0001c0001t0001g0047 a0001c0001t0001g0131 a0001c0001t0001g0165 others(3): Show |
7 | HG01496.hp1 HG01891.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1885-392G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/12 | chr12 | 77028530 | |||||||
| chr12:77028543 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(83): Show |
119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1885-405G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/12 | chr12 | 77028543 | |||||||
| chr12:77028569 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1885-431T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/12 | chr12 | 77028569 | |||||||
| chr12:77028578 | C | T | 2 | a0001c0001t0002g0255 a0002c0003t0002g0039 |
3 | HG02818.hp1 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1885-440G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/12 | chr12 | 77028578 | |||||||
| chr12:77028699 | T | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(219): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1885-561A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/12 | chr12 | 77028699 | |||||||
| chr12:77028769 | G | A | 2 | a0001c0001t0001g0131 a0011c0015t0001g0162 |
2 | HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1885-631C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/12 | chr12 | 77028769 | |||||||
| chr12:77028839 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1885-701C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/12 | chr12 | 77028839 | |||||||
| chr12:77028879 | T | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0234 |
4 | HG00558.hp1 HG02071.hp2 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1885-741A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/12 | chr12 | 77028879 | |||||||
| chr12:77028950 | C | A | 102 | a0001c0001t0001g0047 a0001c0001t0001g0131 a0001c0001t0001g0165 others(99): Show |
140 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.1885-812G>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/12 | chr12 | 77028950 | |||||||
| chr12:77029031 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1884+800A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/12 | chr12 | 77029031 | |||||||
| chr12:77029032 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1884+799C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/12 | chr12 | 77029032 | |||||||
| chr12:77029207 | T | C | 2 | a0001c0001t0002g0059 a0001c0001t0002g0153 |
2 | HG02280.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1884+624A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/12 | chr12 | 77029207 | |||||||
| chr12:77029351 | G | A | 5 | a0001c0001t0002g0190 a0001c0001t0002g0191 a0001c0001t0002g0203 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1884+480C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/12 | chr12 | 77029351 | |||||||
| chr12:77029404 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1884+427A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/12 | chr12 | 77029404 | |||||||
| chr12:77029437 | C | A | 1 | a0001c0001t0001g0254 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1884+394G>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/12 | chr12 | 77029437 | |||||||
| chr12:77029450 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1884+381G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 10/12 | chr12 | 77029450 | |||||||
| chr12:77030351 | G | A | 5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0132 others(2): Show |
5 | HG01109.hp2 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1383-19C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77030351 | |||||||
| chr12:77030355 | C | T | 94 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0011 others(91): Show |
131 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.1383-23G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77030355 | |||||||
| chr12:77030356 | G | T | 2 | a0001c0001t0001g0131 a0011c0015t0001g0162 |
2 | HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1383-24C>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77030356 | |||||||
| chr12:77030464 | G | C | 1 | a0001c0001t0003g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1383-132C>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77030464 | |||||||
| chr12:77030631 | C | G | 1 | a0002c0003t0001g0145 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1383-299G>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77030631 | |||||||
| chr12:77030867 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1383-535G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77030867 | |||||||
| chr12:77030910 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1383-578A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77030910 | |||||||
| chr12:77030926 | C | T | 2 | a0001c0001t0002g0278 a0001c0001t0002g0280 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1383-594G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77030926 | |||||||
| chr12:77031024 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1383-692G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77031024 | |||||||
| chr12:77031070 | C | T | 9 | a0003c0005t0004g0019 a0003c0005t0004g0048 a0003c0005t0004g0053 others(6): Show |
11 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.1383-738G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77031070 | |||||||
| chr12:77031179 | C | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0132 |
3 | HG01109.hp2 HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1383-847G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77031179 | |||||||
| chr12:77031330 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0236 |
2 | NA18993.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1383-998C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77031330 | |||||||
| chr12:77031411 | C | A | 33 | a0001c0001t0002g0005 a0001c0001t0002g0011 a0001c0001t0002g0023 others(30): Show |
49 | HG01099.hp2 HG01106.hp2 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.1383-1079G>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77031411 | |||||||
| chr12:77031435 | GT | G | 60 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(57): Show |
83 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.1383-1104delA | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77031435 | |||||||
| chr12:77031556 | G | A | 65 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(62): Show |
88 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.1383-1224C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77031556 | |||||||
| chr12:77031573 | G | A | 33 | a0001c0001t0002g0005 a0001c0001t0002g0011 a0001c0001t0002g0023 others(30): Show |
49 | HG01099.hp2 HG01106.hp2 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.1383-1241C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77031573 | |||||||
| chr12:77031589 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1383-1257A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77031589 | |||||||
| chr12:77031610 | C | T | 5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0132 others(2): Show |
5 | HG01109.hp2 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1383-1278G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77031610 | |||||||
| chr12:77031822 | C | T | 5 | a0001c0001t0001g0214 a0001c0004t0001g0042 a0001c0004t0001g0156 others(2): Show |
6 | HG00642.hp2 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1382+1228G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77031822 | |||||||
| chr12:77031879 | C | T | 1 | a0001c0001t0002g0090 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1382+1171G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77031879 | |||||||
| chr12:77031898 | A | G | 2 | a0001c0001t0001g0047 a0002c0003t0001g0150 |
3 | HG01496.hp1 HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1382+1152T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77031898 | |||||||
| chr12:77031945 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1382+1105T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77031945 | |||||||
| chr12:77031962 | C | T | 52 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(49): Show |
73 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1382+1088G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77031962 | |||||||
| chr12:77032077 | T | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(269): Show |
380 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.1382+973A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77032077 | |||||||
| chr12:77032078 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1382+972C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77032078 | |||||||
| chr12:77032168 | C | T | 2 | a0001c0002t0001g0021 a0001c0002t0001g0022 |
4 | HG02257.hp2 HG02896.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1382+882G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77032168 | |||||||
| chr12:77032282 | A | G | 3 | a0001c0002t0002g0016 a0001c0002t0002g0211 a0001c0002t0016g0051 |
5 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1382+768T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77032282 | |||||||
| chr12:77032295 | A | G | 24 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0024 others(21): Show |
38 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1382+755T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77032295 | |||||||
| chr12:77032412 | T | C | 59 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(56): Show |
80 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.1382+638A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77032412 | |||||||
| chr12:77032479 | G | A | 1 | a0001c0004t0001g0157 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1382+571C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77032479 | |||||||
| chr12:77032809 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1382+241C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77032809 | |||||||
| chr12:77032996 | G | A | 127 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0024 others(124): Show |
179 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.1382+54C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77032996 | |||||||
| chr12:77033038 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1382+12A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 9/12 | chr12 | 77033038 | |||||||
| chr12:77033213 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1310-91A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 8/12 | chr12 | 77033213 | |||||||
| chr12:77033376 | G | A | 33 | a0001c0001t0002g0005 a0001c0001t0002g0011 a0001c0001t0002g0023 others(30): Show |
49 | HG01099.hp2 HG01106.hp2 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.1310-254C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 8/12 | chr12 | 77033376 | |||||||
| chr12:77033384 | C | T | 204 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(201): Show |
281 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(278): Show |
intron_variant | MODIFIER | c.1310-262G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 8/12 | chr12 | 77033384 | |||||||
| chr12:77033409 | G | A | 1 | a0001c0001t0023g0248 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1310-287C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 8/12 | chr12 | 77033409 | |||||||
| chr12:77033675 | C | T | 52 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(49): Show |
73 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1309+182G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 8/12 | chr12 | 77033675 | |||||||
| chr12:77033756 | AGTCAGTT others(25): Show |
A | 1 | a0001c0001t0001g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1309+69_1309+100de others(33): Show |
E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 8/12 | chr12 | 77033756 | |||||||
| chr12:77034138 | T | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0219 |
2 | HG02015.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1124-96A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77034138 | |||||||
| chr12:77034171 | C | T | 104 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0132 others(101): Show |
143 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.1124-129G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77034171 | |||||||
| chr12:77034224 | C | CT | 6 | a0001c0001t0001g0186 a0001c0001t0001g0192 a0001c0001t0001g0199 others(3): Show |
6 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1124-183dupA | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77034224 | |||||||
| chr12:77034453 | T | G | 5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0132 others(2): Show |
5 | HG01109.hp2 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1124-411A>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77034453 | |||||||
| chr12:77034661 | G | A | 5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0132 others(2): Show |
5 | HG01109.hp2 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1124-619C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77034661 | |||||||
| chr12:77034913 | A | C | 1 | a0001c0001t0005g0155 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1124-871T>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77034913 | |||||||
| chr12:77035021 | C | A | 1 | a0001c0001t0001g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1124-979G>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77035021 | |||||||
| chr12:77035190 | T | C | 2 | a0001c0001t0020g0205 a0002c0003t0001g0151 |
2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1124-1148A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77035190 | |||||||
| chr12:77035396 | G | T | 1 | a0001c0002t0002g0269 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1124-1354C>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77035396 | |||||||
| chr12:77035405 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1124-1363G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77035405 | |||||||
| chr12:77035482 | T | A | 1 | a0001c0002t0001g0185 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1124-1440A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77035482 | |||||||
| chr12:77035599 | A | G | 3 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0007g0215 |
3 | HG00642.hp2 HG01106.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1124-1557T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77035599 | |||||||
| chr12:77035622 | G | A | 279 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(276): Show |
387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.1124-1580C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77035622 | |||||||
| chr12:77035631 | A | G | 1 | a0002c0003t0001g0143 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1124-1589T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77035631 | |||||||
| chr12:77035901 | TA | T | 100 | a0001c0001t0001g0154 a0001c0001t0001g0186 a0001c0001t0001g0192 others(97): Show |
137 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.1124-1860delT | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77035901 | |||||||
| chr12:77035915 | T | TGG | 64 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(61): Show |
95 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.1124-1875_1124-187 others(6): Show |
E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77035915 | |||||||
| chr12:77035979 | A | AG | 207 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(204): Show |
284 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.1124-1938_1124-193 others(5): Show |
E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77035979 | |||||||
| chr12:77035980 | T | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(204): Show |
284 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.1124-1938A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77035980 | |||||||
| chr12:77035983 | A | ACT | 207 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(204): Show |
284 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.1124-1942_1124-194 others(6): Show |
E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77035983 | |||||||
| chr12:77035987 | A | AGACACAG others(4): Show |
207 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(204): Show |
284 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.1124-1946_1124-194 others(15): Show |
E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77035987 | |||||||
| chr12:77035988 | T | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(204): Show |
284 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.1124-1946A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77035988 | |||||||
| chr12:77035991 | A | AACTG | 207 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(204): Show |
284 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.1124-1950_1124-194 others(8): Show |
E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77035991 | |||||||
| chr12:77035994 | A | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(204): Show |
284 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.1124-1952T>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77035994 | |||||||
| chr12:77035996 | T | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(204): Show |
284 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.1124-1954A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77035996 | |||||||
| chr12:77036183 | A | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0091 a0001c0001t0001g0117 |
5 | NA18953.hp1 NA18970.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.1124-2141T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77036183 | |||||||
| chr12:77036356 | T | C | 35 | a0001c0001t0001g0186 a0001c0001t0001g0192 a0001c0001t0001g0199 others(32): Show |
45 | HG00558.hp2 HG00733.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.1124-2314A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77036356 | |||||||
| chr12:77036474 | A | G | 2 | a0001c0001t0001g0047 a0002c0003t0001g0150 |
3 | HG01496.hp1 HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1124-2432T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77036474 | |||||||
| chr12:77036488 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1124-2446C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77036488 | |||||||
| chr12:77036534 | C | CA | 144 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0024 others(141): Show |
198 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.1124-2493dupT | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77036534 | |||||||
| chr12:77036713 | G | A | 1 | a0002c0003t0001g0143 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1124-2671C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77036713 | |||||||
| chr12:77036726 | G | A | 9 | a0003c0005t0004g0019 a0003c0005t0004g0048 a0003c0005t0004g0053 others(6): Show |
11 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.1124-2684C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77036726 | |||||||
| chr12:77036744 | A | AT | 14 | a0001c0001t0002g0255 a0001c0002t0002g0079 a0001c0004t0001g0212 others(11): Show |
17 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1124-2703dupA | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77036744 | |||||||
| chr12:77036744 | AT | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0024 others(22): Show |
39 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1124-2703delA | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77036744 | |||||||
| chr12:77036766 | G | C | 1 | a0001c0002t0002g0079 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1124-2724C>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77036766 | |||||||
| chr12:77036890 | C | T | 1 | a0001c0018t0001g0208 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1124-2848G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77036890 | |||||||
| chr12:77036940 | G | A | 5 | a0001c0001t0002g0190 a0001c0001t0002g0191 a0001c0001t0002g0203 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1124-2898C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77036940 | |||||||
| chr12:77036984 | C | T | 2 | a0001c0001t0002g0191 a0002c0003t0002g0149 |
2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1124-2942G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77036984 | |||||||
| chr12:77036989 | T | C | 24 | a0001c0001t0001g0186 a0001c0001t0001g0192 a0001c0001t0001g0199 others(21): Show |
33 | HG00558.hp2 HG00733.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1124-2947A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77036989 | |||||||
| chr12:77036995 | C | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0074 a0001c0001t0001g0128 others(7): Show |
14 | HG02132.hp1 HG02280.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1124-2953G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77036995 | |||||||
| chr12:77037061 | C | T | 8 | a0003c0005t0004g0019 a0003c0005t0004g0048 a0003c0005t0004g0053 others(5): Show |
9 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1124-3019G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77037061 | |||||||
| chr12:77037085 | A | G | 11 | a0001c0001t0001g0154 a0001c0002t0001g0021 a0001c0002t0001g0022 others(8): Show |
13 | HG01192.hp2 HG02257.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1124-3043T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77037085 | |||||||
| chr12:77037174 | G | C | 1 | a0001c0001t0023g0248 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1124-3132C>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77037174 | |||||||
| chr12:77037203 | G | C | 18 | a0001c0001t0001g0154 a0001c0001t0001g0165 a0001c0001t0001g0166 others(15): Show |
21 | HG01192.hp2 HG02257.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.1124-3161C>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77037203 | |||||||
| chr12:77037228 | T | C | 210 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(207): Show |
287 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.1124-3186A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77037228 | |||||||
| chr12:77037441 | A | C | 1 | a0001c0002t0001g0260 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1124-3399T>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77037441 | |||||||
| chr12:77037548 | C | A | 5 | a0001c0001t0002g0190 a0001c0001t0002g0191 a0001c0001t0002g0203 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1124-3506G>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77037548 | |||||||
| chr12:77037902 | G | A | 24 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0024 others(21): Show |
38 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1124-3860C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77037902 | |||||||
| chr12:77038016 | T | A | 103 | a0001c0001t0001g0186 a0001c0001t0001g0192 a0001c0001t0001g0199 others(100): Show |
142 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.1124-3974A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77038016 | |||||||
| chr12:77038026 | A | G | 1 | a0002c0003t0001g0034 | 2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1124-3984T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77038026 | |||||||
| chr12:77038233 | T | C | 3 | a0003c0005t0004g0053 a0003c0005t0004g0055 a0003c0005t0007g0276 |
3 | HG01175.hp1 HG02300.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1124-4191A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77038233 | |||||||
| chr12:77038244 | G | A | 208 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(205): Show |
285 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(282): Show |
intron_variant | MODIFIER | c.1124-4202C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77038244 | |||||||
| chr12:77038300 | C | T | 2 | a0001c0001t0020g0205 a0002c0003t0001g0151 |
2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1124-4258G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77038300 | |||||||
| chr12:77038514 | G | A | 24 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0024 others(21): Show |
38 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1124-4472C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77038514 | |||||||
| chr12:77038704 | G | C | 1 | a0002c0024t0001g0147 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1123+4361C>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77038704 | |||||||
| chr12:77038743 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(62): Show |
96 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1123+4322A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77038743 | |||||||
| chr12:77038878 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0169 |
2 | NA18954.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1123+4187G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77038878 | |||||||
| chr12:77038907 | G | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(274): Show |
385 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.1123+4158C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77038907 | |||||||
| chr12:77039076 | G | A | 1 | a0001c0002t0001g0022 | 2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1123+3989C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77039076 | |||||||
| chr12:77039122 | G | C | 50 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(47): Show |
71 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.1123+3943C>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77039122 | |||||||
| chr12:77039281 | A | G | 1 | a0001c0001t0002g0193 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1123+3784T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77039281 | |||||||
| chr12:77039545 | T | A | 1 | a0001c0001t0001g0282 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1123+3520A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77039545 | |||||||
| chr12:77039740 | C | T | 1 | a0007c0021t0005g0179 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1123+3325G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77039740 | |||||||
| chr12:77039953 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1123+3112A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77039953 | |||||||
| chr12:77040032 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1123+3033C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77040032 | |||||||
| chr12:77040167 | T | C | 1 | a0003c0005t0004g0054 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1123+2898A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77040167 | |||||||
| chr12:77040184 | T | G | 1 | a0001c0001t0002g0178 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1123+2881A>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77040184 | |||||||
| chr12:77040251 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1123+2814C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77040251 | |||||||
| chr12:77040908 | A | C | 47 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(44): Show |
65 | HG00323.hp2 HG01192.hp1 HG01192.hp2 others(62): Show |
intron_variant | MODIFIER | c.1123+2157T>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77040908 | |||||||
| chr12:77040922 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1123+2143T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77040922 | |||||||
| chr12:77041060 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1123+2005C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77041060 | |||||||
| chr12:77041173 | C | T | 1 | a0001c0002t0002g0283 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1123+1892G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77041173 | |||||||
| chr12:77041202 | C | G | 1 | a0001c0001t0003g0123 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1123+1863G>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77041202 | |||||||
| chr12:77041202 | C | T | 52 | a0001c0001t0001g0167 a0001c0001t0001g0266 a0001c0001t0001g0271 others(49): Show |
70 | HG00609.hp1 HG00733.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.1123+1863G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77041202 | |||||||
| chr12:77041213 | C | T | 9 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0002g0040 others(6): Show |
11 | HG01074.hp2 HG01261.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1123+1852G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77041213 | |||||||
| chr12:77041416 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1123+1649G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77041416 | |||||||
| chr12:77041755 | C | T | 1 | a0001c0001t0002g0261 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1123+1310G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77041755 | |||||||
| chr12:77041760 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1123+1305G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77041760 | |||||||
| chr12:77041890 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1123+1175T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77041890 | |||||||
| chr12:77041928 | G | A | 1 | a0001c0002t0002g0262 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1123+1137C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77041928 | |||||||
| chr12:77042011 | A | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0024 others(74): Show |
105 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1123+1054T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77042011 | |||||||
| chr12:77042062 | G | A | 1 | a0001c0002t0002g0081 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1123+1003C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77042062 | |||||||
| chr12:77042264 | T | C | 68 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(65): Show |
95 | HG00323.hp2 HG00558.hp2 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.1123+801A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77042264 | |||||||
| chr12:77042280 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1123+785C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77042280 | |||||||
| chr12:77042360 | C | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0061 a0001c0001t0001g0062 |
5 | HG00323.hp2 HG02735.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.1123+705G>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77042360 | |||||||
| chr12:77042368 | C | T | 222 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(219): Show |
302 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(299): Show |
intron_variant | MODIFIER | c.1123+697G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77042368 | |||||||
| chr12:77042588 | C | T | 1 | a0001c0002t0001g0185 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1123+477G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77042588 | |||||||
| chr12:77042727 | CTGCTAAT others(34): Show |
C | 1 | a0001c0001t0002g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1123+297_1123+337d others(43): Show |
E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77042727 | |||||||
| chr12:77042882 | G | A | 1 | a0001c0002t0001g0185 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1123+183C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 7/12 | chr12 | 77042882 | |||||||
| chr12:77043454 | A | C | 156 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0024 others(153): Show |
209 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.989-255T>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 6/12 | chr12 | 77043454 | |||||||
| chr12:77043467 | G | A | 1 | a0001c0002t0002g0283 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.989-268C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 6/12 | chr12 | 77043467 | |||||||
| chr12:77043495 | T | C | 223 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(220): Show |
303 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(300): Show |
intron_variant | MODIFIER | c.989-296A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 6/12 | chr12 | 77043495 | |||||||
| chr12:77043564 | C | T | 4 | a0001c0001t0001g0128 a0001c0004t0001g0127 a0001c0004t0001g0134 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-365G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 6/12 | chr12 | 77043564 | |||||||
| chr12:77043602 | T | C | 69 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(66): Show |
96 | HG00323.hp2 HG00558.hp2 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.989-403A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 6/12 | chr12 | 77043602 | |||||||
| chr12:77043658 | G | A | 1 | a0001c0001t0003g0123 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.989-459C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 6/12 | chr12 | 77043658 | |||||||
| chr12:77043774 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.989-575A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 6/12 | chr12 | 77043774 | |||||||
| chr12:77043940 | C | T | 13 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0061 others(10): Show |
19 | HG00323.hp2 HG01192.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.988+697G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 6/12 | chr12 | 77043940 | |||||||
| chr12:77044319 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.988+318C>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 6/12 | chr12 | 77044319 | |||||||
| chr12:77044383 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.988+254G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 6/12 | chr12 | 77044383 | |||||||
| chr12:77044426 | C | A | 1 | a0001c0001t0001g0256 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.988+211G>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 6/12 | chr12 | 77044426 | |||||||
| chr12:77044429 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.988+208G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 6/12 | chr12 | 77044429 | |||||||
| chr12:77044525 | G | A | 1 | a0003c0005t0007g0284 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.988+112C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 6/12 | chr12 | 77044525 | |||||||
| chr12:77044614 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.988+23A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 6/12 | chr12 | 77044614 | |||||||
| chr12:77044827 | T | C | 122 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(119): Show |
168 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.830-32A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 5/12 | chr12 | 77044827 | |||||||
| chr12:77044933 | A | G | 6 | a0001c0001t0001g0128 a0001c0001t0002g0153 a0001c0004t0001g0127 others(3): Show |
6 | HG02280.hp1 HG02280.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.830-138T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 5/12 | chr12 | 77044933 | |||||||
| chr12:77045049 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.830-254G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 5/12 | chr12 | 77045049 | |||||||
| chr12:77045121 | A | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0266 |
2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.830-326T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 5/12 | chr12 | 77045121 | |||||||
| chr12:77045135 | G | C | 2 | a0001c0001t0002g0191 a0002c0003t0002g0149 |
2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.830-340C>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 5/12 | chr12 | 77045135 | |||||||
| chr12:77045220 | T | C | 42 | a0001c0002t0001g0009 a0001c0002t0001g0026 a0001c0002t0001g0104 others(39): Show |
55 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.830-425A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 5/12 | chr12 | 77045220 | |||||||
| chr12:77045374 | G | A | 1 | a0001c0002t0002g0126 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.830-579C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 5/12 | chr12 | 77045374 | |||||||
| chr12:77045422 | G | C | 1 | a0001c0002t0002g0259 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.829+616C>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 5/12 | chr12 | 77045422 | |||||||
| chr12:77045571 | C | T | 67 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(64): Show |
94 | HG00323.hp2 HG00558.hp2 HG00733.hp2 others(91): Show |
intron_variant | MODIFIER | c.829+467G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 5/12 | chr12 | 77045571 | |||||||
| chr12:77045577 | C | T | 4 | a0001c0001t0001g0128 a0001c0004t0001g0127 a0001c0004t0001g0134 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.829+461G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 5/12 | chr12 | 77045577 | |||||||
| chr12:77045599 | C | T | 1 | a0001c0004t0005g0250 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.829+439G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 5/12 | chr12 | 77045599 | |||||||
| chr12:77045634 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.829+404T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 5/12 | chr12 | 77045634 | |||||||
| chr12:77045703 | T | G | 1 | a0001c0002t0001g0185 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.829+335A>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 5/12 | chr12 | 77045703 | |||||||
| chr12:77045718 | C | A | 1 | a0001c0001t0001g0069 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.829+320G>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 5/12 | chr12 | 77045718 | |||||||
| chr12:77045860 | G | A | 1 | a0001c0009t0015g0138 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.829+178C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 5/12 | chr12 | 77045860 | |||||||
| chr12:77045916 | A | G | 3 | a0001c0001t0001g0186 a0001c0001t0001g0192 a0001c0001t0001g0199 |
3 | HG01123.hp2 HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.829+122T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 5/12 | chr12 | 77045916 | |||||||
| chr12:77045940 | T | C | 11 | a0001c0002t0001g0013 a0001c0002t0001g0021 a0001c0002t0001g0022 others(8): Show |
17 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.829+98A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 5/12 | chr12 | 77045940 | |||||||
| chr12:77046381 | A | T | 1 | a0001c0001t0001g0223 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.539-53T>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77046381 | |||||||
| chr12:77046405 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.539-77T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77046405 | |||||||
| chr12:77046511 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.539-183G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77046511 | |||||||
| chr12:77046801 | T | A | 67 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(64): Show |
94 | HG00323.hp2 HG00558.hp2 HG00733.hp2 others(91): Show |
intron_variant | MODIFIER | c.539-473A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77046801 | |||||||
| chr12:77046872 | G | T | 1 | a0001c0001t0021g0187 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.539-544C>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77046872 | |||||||
| chr12:77046882 | A | G | 5 | a0001c0001t0002g0068 a0001c0001t0002g0116 a0001c0001t0006g0020 others(2): Show |
6 | HG01255.hp2 HG01928.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.539-554T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77046882 | |||||||
| chr12:77046894 | A | C | 3 | a0001c0004t0001g0042 a0001c0004t0001g0245 a0002c0008t0001g0158 |
4 | HG02257.hp1 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.539-566T>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77046894 | |||||||
| chr12:77046970 | G | A | 68 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(65): Show |
95 | HG00323.hp2 HG00558.hp2 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.539-642C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77046970 | |||||||
| chr12:77047021 | G | C | 1 | a0001c0001t0003g0123 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.539-693C>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77047021 | |||||||
| chr12:77047101 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | NA18964.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.539-773C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77047101 | |||||||
| chr12:77047195 | G | T | 1 | a0010c0020t0001g0189 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.539-867C>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77047195 | |||||||
| chr12:77047338 | A | G | 6 | a0001c0001t0001g0128 a0001c0001t0002g0153 a0001c0004t0001g0127 others(3): Show |
6 | HG02280.hp1 HG02280.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.539-1010T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77047338 | |||||||
| chr12:77047400 | C | G | 1 | a0001c0002t0002g0247 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.539-1072G>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77047400 | |||||||
| chr12:77047464 | G | A | 1 | a0003c0005t0013g0046 | 2 | HG00733.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.539-1136C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77047464 | |||||||
| chr12:77047554 | A | T | 1 | a0004c0007t0002g0172 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.539-1226T>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77047554 | |||||||
| chr12:77047585 | T | C | 68 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(65): Show |
95 | HG00323.hp2 HG00558.hp2 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.539-1257A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77047585 | |||||||
| chr12:77047600 | A | T | 1 | a0001c0001t0001g0234 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.539-1272T>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77047600 | |||||||
| chr12:77047618 | T | C | 6 | a0001c0001t0002g0274 a0001c0001t0002g0275 a0001c0001t0002g0278 others(3): Show |
6 | HG01099.hp2 HG01106.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.539-1290A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77047618 | |||||||
| chr12:77047780 | C | T | 5 | a0001c0001t0001g0175 a0001c0001t0002g0040 a0001c0001t0002g0178 others(2): Show |
7 | HG01074.hp2 HG01891.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.539-1452G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77047780 | |||||||
| chr12:77047781 | G | A | 4 | a0001c0001t0001g0128 a0001c0004t0001g0127 a0001c0004t0001g0134 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.539-1453C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77047781 | |||||||
| chr12:77047798 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.539-1470C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77047798 | |||||||
| chr12:77047906 | A | C | 16 | a0001c0001t0001g0128 a0001c0001t0001g0154 a0001c0001t0002g0153 others(13): Show |
22 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.539-1578T>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77047906 | |||||||
| chr12:77047906 | A | T | 1 | a0001c0001t0001g0089 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.539-1578T>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77047906 | |||||||
| chr12:77048114 | A | C | 1 | a0001c0001t0001g0233 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.539-1786T>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77048114 | |||||||
| chr12:77048184 | G | A | 1 | a0001c0009t0015g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.539-1856C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77048184 | |||||||
| chr12:77048224 | C | T | 191 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(188): Show |
265 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.539-1896G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77048224 | |||||||
| chr12:77048509 | T | C | 11 | a0001c0002t0001g0013 a0001c0002t0001g0021 a0001c0002t0001g0022 others(8): Show |
17 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.538+2067A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77048509 | |||||||
| chr12:77048552 | C | T | 66 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(63): Show |
93 | HG00323.hp2 HG00558.hp2 HG00733.hp2 others(90): Show |
intron_variant | MODIFIER | c.538+2024G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77048552 | |||||||
| chr12:77048630 | C | T | 1 | a0001c0002t0002g0247 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.538+1946G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77048630 | |||||||
| chr12:77048631 | G | A | 9 | a0003c0005t0004g0019 a0003c0005t0004g0048 a0003c0005t0004g0053 others(6): Show |
11 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.538+1945C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77048631 | |||||||
| chr12:77049137 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0266 |
2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.538+1439G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77049137 | |||||||
| chr12:77049311 | G | A | 1 | a0010c0020t0001g0189 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.538+1265C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77049311 | |||||||
| chr12:77049468 | G | A | 22 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0061 others(19): Show |
28 | HG00323.hp2 HG01192.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.538+1108C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77049468 | |||||||
| chr12:77049511 | G | T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0024 others(18): Show |
34 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.538+1065C>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77049511 | |||||||
| chr12:77049607 | G | A | 1 | a0001c0004t0001g0212 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.538+969C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77049607 | |||||||
| chr12:77049880 | C | G | 24 | a0001c0001t0001g0121 a0001c0001t0001g0164 a0001c0001t0001g0186 others(21): Show |
33 | HG00558.hp2 HG00733.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.538+696G>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77049880 | |||||||
| chr12:77049909 | T | C | 43 | a0001c0001t0001g0244 a0001c0002t0001g0009 a0001c0002t0001g0026 others(40): Show |
56 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.538+667A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77049909 | |||||||
| chr12:77049989 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.538+587T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77049989 | |||||||
| chr12:77049992 | T | C | 1 | a0001c0001t0002g0191 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.538+584A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77049992 | |||||||
| chr12:77050044 | G | A | 1 | a0001c0001t0001g0243 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.538+532C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77050044 | |||||||
| chr12:77050094 | C | CT | 6 | a0001c0001t0001g0128 a0001c0001t0002g0153 a0001c0004t0001g0127 others(3): Show |
6 | HG02280.hp1 HG02280.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.538+481dupA | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77050094 | |||||||
| chr12:77050205 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.538+371A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77050205 | |||||||
| chr12:77050333 | T | C | 69 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(66): Show |
96 | HG00323.hp2 HG00558.hp2 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.538+243A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77050333 | |||||||
| chr12:77050475 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.538+101C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77050475 | |||||||
| chr12:77050477 | T | C | 1 | a0001c0001t0011g0265 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.538+99A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 4/12 | chr12 | 77050477 | |||||||
| chr12:77050759 | T | C | 2 | a0001c0001t0001g0133 a0002c0003t0001g0139 |
2 | HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.370-15A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77050759 | |||||||
| chr12:77050771 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.370-27C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77050771 | |||||||
| chr12:77051053 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.370-309G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77051053 | |||||||
| chr12:77051284 | G | T | 1 | a0001c0001t0006g0057 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.370-540C>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77051284 | |||||||
| chr12:77051300 | A | C | 1 | a0002c0003t0001g0150 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.370-556T>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77051300 | |||||||
| chr12:77051306 | A | G | 10 | a0001c0002t0001g0013 a0001c0002t0001g0021 a0001c0002t0001g0022 others(7): Show |
16 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.370-562T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77051306 | |||||||
| chr12:77051315 | G | A | 2 | a0001c0002t0001g0260 a0002c0006t0002g0038 |
3 | HG02258.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.370-571C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77051315 | |||||||
| chr12:77051475 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0266 |
2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.370-731G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77051475 | |||||||
| chr12:77051602 | A | G | 8 | a0001c0001t0001g0128 a0001c0001t0002g0153 a0001c0002t0002g0247 others(5): Show |
8 | HG02280.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.370-858T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77051602 | |||||||
| chr12:77051682 | A | G | 10 | a0001c0002t0001g0013 a0001c0002t0001g0021 a0001c0002t0001g0022 others(7): Show |
16 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.370-938T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77051682 | |||||||
| chr12:77051766 | G | T | 1 | a0001c0001t0001g0088 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.370-1022C>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77051766 | |||||||
| chr12:77051806 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.370-1062G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77051806 | |||||||
| chr12:77051948 | T | A | 45 | a0001c0001t0001g0083 a0001c0001t0001g0165 a0001c0001t0001g0166 others(42): Show |
62 | HG00609.hp1 HG01074.hp2 HG01099.hp2 others(59): Show |
intron_variant | MODIFIER | c.370-1204A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77051948 | |||||||
| chr12:77051975 | A | T | 1 | a0001c0001t0011g0263 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.370-1231T>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77051975 | |||||||
| chr12:77051990 | T | A | 1 | a0001c0009t0015g0138 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.370-1246A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77051990 | |||||||
| chr12:77052318 | T | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0266 |
2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.370-1574A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77052318 | |||||||
| chr12:77052519 | T | A | 43 | a0001c0001t0001g0043 a0001c0001t0001g0238 a0001c0002t0001g0009 others(40): Show |
57 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.370-1775A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77052519 | |||||||
| chr12:77052520 | C | G | 43 | a0001c0001t0001g0043 a0001c0001t0001g0238 a0001c0002t0001g0009 others(40): Show |
57 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.370-1776G>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77052520 | |||||||
| chr12:77052564 | G | A | 2 | a0001c0002t0002g0229 a0001c0002t0018g0228 |
2 | HG01069.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.370-1820C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77052564 | |||||||
| chr12:77052578 | C | T | 69 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(66): Show |
96 | HG00323.hp2 HG00558.hp2 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.370-1834G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77052578 | |||||||
| chr12:77052586 | A | G | 1 | a0001c0001t0001g0029 | 2 | NA19009.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.370-1842T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77052586 | |||||||
| chr12:77052679 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.370-1935C>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77052679 | |||||||
| chr12:77052696 | A | G | 1 | a0001c0001t0003g0123 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.370-1952T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77052696 | |||||||
| chr12:77052769 | T | C | 222 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(219): Show |
302 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(299): Show |
intron_variant | MODIFIER | c.370-2025A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77052769 | |||||||
| chr12:77052823 | C | CA | 7 | a0001c0001t0001g0234 a0001c0001t0001g0285 a0001c0002t0002g0253 others(4): Show |
14 | HG02071.hp2 HG02559.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.370-2080dupT | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77052823 | |||||||
| chr12:77052834 | C | A | 1 | a0001c0009t0015g0138 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.370-2090G>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77052834 | |||||||
| chr12:77052875 | G | A | 11 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0132 others(8): Show |
11 | HG01109.hp1 HG01109.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.370-2131C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77052875 | |||||||
| chr12:77052950 | T | A | 279 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(276): Show |
387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.370-2206A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77052950 | |||||||
| chr12:77052982 | T | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.370-2238A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77052982 | |||||||
| chr12:77053016 | C | T | 3 | a0001c0001t0001g0160 a0001c0001t0005g0155 a0001c0004t0001g0156 |
3 | HG01243.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.370-2272G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77053016 | |||||||
| chr12:77053034 | T | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0069 a0001c0001t0001g0071 others(5): Show |
12 | HG02135.hp1 HG02523.hp2 NA18941.hp2 others(9): Show |
intron_variant | MODIFIER | c.370-2290A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77053034 | |||||||
| chr12:77053104 | T | C | 6 | a0001c0002t0001g0184 a0001c0013t0001g0201 a0002c0006t0001g0015 others(3): Show |
8 | HG00280.hp2 HG00738.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.370-2360A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77053104 | |||||||
| chr12:77053152 | T | G | 1 | a0002c0024t0001g0147 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.370-2408A>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77053152 | |||||||
| chr12:77053267 | G | A | 3 | a0001c0004t0001g0042 a0001c0004t0001g0245 a0002c0008t0001g0158 |
4 | HG02257.hp1 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-2523C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77053267 | |||||||
| chr12:77053290 | G | A | 1 | a0001c0001t0002g0275 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.370-2546C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77053290 | |||||||
| chr12:77053442 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.369+2413G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77053442 | |||||||
| chr12:77053626 | C | T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0024 others(18): Show |
34 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.369+2229G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77053626 | |||||||
| chr12:77053683 | A | G | 9 | a0001c0002t0001g0013 a0001c0002t0001g0021 a0001c0002t0001g0022 others(6): Show |
15 | HG00639.hp2 HG00738.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.369+2172T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77053683 | |||||||
| chr12:77053779 | A | G | 71 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(68): Show |
98 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.369+2076T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77053779 | |||||||
| chr12:77053827 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.369+2028T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77053827 | |||||||
| chr12:77053882 | C | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0072 a0001c0001t0001g0222 |
3 | HG00280.hp1 HG01346.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.369+1973G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77053882 | |||||||
| chr12:77053926 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0266 |
2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.369+1929A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77053926 | |||||||
| chr12:77054030 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.369+1825G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77054030 | |||||||
| chr12:77054090 | G | A | 1 | a0001c0001t0001g0232 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.369+1765C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77054090 | |||||||
| chr12:77054211 | C | A | 8 | a0001c0001t0001g0121 a0001c0001t0002g0041 a0001c0001t0002g0086 others(5): Show |
9 | HG00558.hp2 HG01123.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.369+1644G>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77054211 | |||||||
| chr12:77054254 | A | C | 2 | a0001c0004t0001g0042 a0002c0008t0001g0158 |
3 | HG02257.hp1 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.369+1601T>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77054254 | |||||||
| chr12:77054328 | T | A | 23 | a0001c0001t0001g0028 a0001c0001t0001g0121 a0001c0001t0001g0192 others(20): Show |
33 | HG00558.hp2 HG00733.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.369+1527A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77054328 | |||||||
| chr12:77054338 | C | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(93): Show |
140 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.369+1517G>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77054338 | |||||||
| chr12:77054399 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0222 |
2 | HG00280.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.369+1456T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77054399 | |||||||
| chr12:77054436 | A | T | 3 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0007g0215 |
3 | HG00642.hp2 HG01106.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.369+1419T>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77054436 | |||||||
| chr12:77054501 | A | T | 1 | a0001c0001t0001g0199 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.369+1354T>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77054501 | |||||||
| chr12:77054661 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.369+1194G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77054661 | |||||||
| chr12:77054785 | A | G | 38 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0024 others(35): Show |
53 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.369+1070T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77054785 | |||||||
| chr12:77054832 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.369+1023A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77054832 | |||||||
| chr12:77054834 | T | A | 1 | a0002c0003t0001g0151 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.369+1021A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77054834 | |||||||
| chr12:77055125 | C | T | 1 | a0001c0002t0001g0184 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.369+730G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77055125 | |||||||
| chr12:77055355 | C | CT | 11 | a0001c0001t0001g0047 a0001c0001t0001g0071 a0001c0001t0001g0160 others(8): Show |
14 | HG01243.hp2 HG01496.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.369+499dupA | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77055355 | |||||||
| chr12:77055355 | CT | C | 21 | a0001c0001t0001g0106 a0001c0001t0001g0209 a0001c0001t0001g0233 others(18): Show |
22 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.369+499delA | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77055355 | |||||||
| chr12:77055457 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.369+398G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77055457 | |||||||
| chr12:77055508 | A | T | 1 | a0001c0004t0001g0042 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.369+347T>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77055508 | |||||||
| chr12:77055589 | T | A | 1 | a0001c0001t0001g0031 | 2 | NA18965.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.369+266A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77055589 | |||||||
| chr12:77055714 | C | G | 4 | a0001c0001t0001g0160 a0001c0001t0002g0153 a0008c0016t0001g0161 others(1): Show |
4 | HG01243.hp2 HG02109.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+141G>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77055714 | |||||||
| chr12:77055734 | T | C | 36 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0251 others(33): Show |
44 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.369+121A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77055734 | |||||||
| chr12:77055775 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.369+80A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77055775 | |||||||
| chr12:77055833 | C | T | 1 | a0001c0004t0001g0245 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.369+22G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 3/12 | chr12 | 77055833 | |||||||
| chr12:77056383 | G | A | 7 | a0001c0001t0001g0160 a0001c0001t0002g0153 a0001c0001t0005g0155 others(4): Show |
7 | HG01243.hp2 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-253C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77056383 | |||||||
| chr12:77056401 | T | C | 1 | a0001c0001t0002g0045 | 2 | NA18945.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.94-271A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77056401 | |||||||
| chr12:77056424 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0234 |
4 | HG00558.hp1 HG02071.hp2 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-294C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77056424 | |||||||
| chr12:77056434 | G | A | 1 | a0004c0007t0002g0108 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.94-304C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77056434 | |||||||
| chr12:77056506 | G | A | 9 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0002t0016g0051 others(6): Show |
10 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.94-376C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77056506 | |||||||
| chr12:77056633 | C | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(198): Show |
273 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.94-503G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77056633 | |||||||
| chr12:77056664 | A | T | 1 | a0001c0018t0001g0208 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.94-534T>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77056664 | |||||||
| chr12:77056682 | G | T | 1 | a0001c0001t0002g0213 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.94-552C>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77056682 | |||||||
| chr12:77056685 | T | A | 1 | a0001c0004t0001g0245 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.94-555A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77056685 | |||||||
| chr12:77056773 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.94-643G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77056773 | |||||||
| chr12:77056847 | T | C | 2 | a0001c0001t0001g0266 a0001c0001t0002g0267 |
2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.94-717A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77056847 | |||||||
| chr12:77056851 | G | A | 1 | a0001c0001t0001g0243 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.94-721C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77056851 | |||||||
| chr12:77056887 | A | C | 82 | a0001c0001t0001g0047 a0001c0001t0001g0164 a0001c0001t0001g0165 others(79): Show |
101 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.94-757T>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77056887 | |||||||
| chr12:77056888 | C | CT | 8 | a0001c0001t0001g0268 a0001c0001t0001g0271 a0001c0001t0002g0163 others(5): Show |
8 | HG01070.hp2 HG01256.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.94-759dupA | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77056888 | |||||||
| chr12:77056888 | C | CTT | 74 | a0001c0001t0001g0047 a0001c0001t0001g0164 a0001c0001t0001g0165 others(71): Show |
94 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.94-760_94-759dupAA | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77056888 | |||||||
| chr12:77056888 | CT | C | 9 | a0001c0001t0001g0109 a0001c0001t0001g0117 a0001c0001t0001g0120 others(6): Show |
9 | HG00280.hp2 HG02897.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.94-759delA | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77056888 | |||||||
| chr12:77056914 | G | T | 9 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0002t0016g0051 others(6): Show |
10 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.94-784C>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77056914 | |||||||
| chr12:77056985 | C | T | 3 | a0001c0002t0002g0018 a0001c0002t0002g0252 a0001c0002t0002g0253 |
5 | NA18984.hp2 NA19005.hp1 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-855G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77056985 | |||||||
| chr12:77057239 | T | A | 2 | a0002c0003t0014g0140 a0002c0003t0014g0152 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.94-1109A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77057239 | |||||||
| chr12:77057370 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(85): Show |
137 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.94-1240G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77057370 | |||||||
| chr12:77057395 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.94-1265C>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77057395 | |||||||
| chr12:77057605 | C | T | 4 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(1): Show |
4 | HG02486.hp2 HG02970.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-1475G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77057605 | |||||||
| chr12:77057626 | A | G | 1 | a0001c0002t0002g0252 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.94-1496T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77057626 | |||||||
| chr12:77057716 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.94-1586C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77057716 | |||||||
| chr12:77057923 | G | T | 1 | a0001c0001t0002g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.94-1793C>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77057923 | |||||||
| chr12:77058112 | T | C | 9 | a0001c0001t0002g0274 a0001c0001t0002g0275 a0001c0001t0002g0278 others(6): Show |
10 | HG00733.hp1 HG01099.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.94-1982A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77058112 | |||||||
| chr12:77058226 | A | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(167): Show |
232 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.94-2096T>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77058226 | |||||||
| chr12:77058241 | G | A | 1 | a0001c0013t0001g0201 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.94-2111C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77058241 | |||||||
| chr12:77058361 | G | A | 3 | a0001c0001t0001g0160 a0008c0016t0001g0161 a0011c0015t0001g0162 |
3 | HG01243.hp2 HG02109.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.94-2231C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77058361 | |||||||
| chr12:77058364 | G | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(116): Show |
171 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.94-2234C>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77058364 | |||||||
| chr12:77058442 | C | T | 2 | a0001c0001t0002g0124 a0001c0001t0003g0123 |
2 | HG01192.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.94-2312G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77058442 | |||||||
| chr12:77058443 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(253): Show |
351 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.94-2313A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77058443 | |||||||
| chr12:77058515 | C | A | 1 | a0001c0001t0001g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.94-2385G>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77058515 | |||||||
| chr12:77058573 | T | C | 4 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(1): Show |
4 | HG02486.hp2 HG02970.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-2443A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77058573 | |||||||
| chr12:77058850 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.94-2720G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77058850 | |||||||
| chr12:77059025 | T | A | 2 | a0001c0001t0002g0277 a0003c0005t0007g0276 |
2 | HG02602.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.94-2895A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77059025 | |||||||
| chr12:77059095 | G | A | 4 | a0001c0001t0001g0160 a0001c0001t0002g0153 a0008c0016t0001g0161 others(1): Show |
4 | HG01243.hp2 HG02109.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-2965C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77059095 | |||||||
| chr12:77059131 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(249): Show |
347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.94-3001A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77059131 | |||||||
| chr12:77059446 | G | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(193): Show |
268 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.94-3316C>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77059446 | |||||||
| chr12:77059528 | G | A | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG01257.hp2 HG01258.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.94-3398C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77059528 | |||||||
| chr12:77059534 | C | T | 1 | a0001c0004t0005g0250 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.94-3404G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77059534 | |||||||
| chr12:77059694 | A | G | 1 | a0001c0009t0015g0138 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.94-3564T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77059694 | |||||||
| chr12:77059823 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0002g0023 |
3 | NA18954.hp2 NA18955.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.94-3693G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77059823 | |||||||
| chr12:77059960 | C | CA | 95 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(92): Show |
148 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.94-3831dupT | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77059960 | |||||||
| chr12:77059960 | C | CAA | 14 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0114 others(11): Show |
15 | HG02056.hp1 HG02818.hp2 HG03453.hp1 others(12): Show |
intron_variant | MODIFIER | c.94-3832_94-3831dup others(2): Show |
E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77059960 | |||||||
| chr12:77059960 | CA | C | 38 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0017 others(35): Show |
57 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.94-3831delT | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77059960 | |||||||
| chr12:77059960 | CAA | C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0202 a0001c0001t0001g0206 others(10): Show |
16 | HG01070.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.94-3832_94-3831del others(2): Show |
E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77059960 | |||||||
| chr12:77059960 | CAAA | C | 40 | a0001c0001t0001g0047 a0001c0001t0001g0251 a0001c0001t0001g0254 others(37): Show |
48 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.94-3833_94-3831del others(3): Show |
E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77059960 | |||||||
| chr12:77060024 | G | T | 30 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0182 others(27): Show |
40 | HG00323.hp1 HG00558.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.94-3894C>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77060024 | |||||||
| chr12:77060046 | C | T | 4 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(1): Show |
4 | HG02486.hp2 HG02970.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-3916G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77060046 | |||||||
| chr12:77060211 | G | A | 1 | a0001c0004t0001g0245 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.94-4081C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77060211 | |||||||
| chr12:77060226 | A | G | 1 | a0001c0004t0001g0042 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.94-4096T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77060226 | |||||||
| chr12:77060473 | C | T | 5 | a0001c0001t0001g0066 a0001c0001t0006g0020 a0001c0001t0006g0057 others(2): Show |
6 | HG01255.hp2 HG01928.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.93+4070G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77060473 | |||||||
| chr12:77060602 | C | T | 1 | a0001c0001t0002g0065 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.93+3941G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77060602 | |||||||
| chr12:77060621 | GC | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(112): Show |
167 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.93+3921delG | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77060621 | |||||||
| chr12:77060627 | C | T | 1 | a0001c0004t0001g0245 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.93+3916G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77060627 | |||||||
| chr12:77060733 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.93+3810T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77060733 | |||||||
| chr12:77061029 | C | G | 1 | a0001c0001t0001g0064 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.93+3514G>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77061029 | |||||||
| chr12:77061106 | G | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(250): Show |
348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.93+3437C>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77061106 | |||||||
| chr12:77061183 | C | T | 5 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0002g0040 others(2): Show |
6 | HG01074.hp2 HG01261.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.93+3360G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77061183 | |||||||
| chr12:77061241 | T | G | 1 | a0001c0002t0002g0247 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.93+3302A>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77061241 | |||||||
| chr12:77061285 | A | G | 2 | a0001c0001t0002g0174 a0001c0001t0002g0176 |
2 | NA18985.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.93+3258T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77061285 | |||||||
| chr12:77061459 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.93+3084A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77061459 | |||||||
| chr12:77061479 | G | A | 1 | a0002c0008t0001g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.93+3064C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77061479 | |||||||
| chr12:77061525 | G | T | 1 | a0001c0009t0015g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.93+3018C>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77061525 | |||||||
| chr12:77061747 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(109): Show |
164 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.93+2796A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77061747 | |||||||
| chr12:77061774 | T | A | 56 | a0001c0001t0001g0047 a0001c0001t0001g0164 a0001c0001t0001g0165 others(53): Show |
66 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.93+2769A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77061774 | |||||||
| chr12:77061857 | C | T | 10 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(7): Show |
10 | HG01109.hp2 HG01978.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.93+2686G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77061857 | |||||||
| chr12:77061882 | T | C | 2 | a0001c0001t0002g0032 a0001c0001t0002g0033 |
4 | NA18957.hp1 NA18967.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+2661A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77061882 | |||||||
| chr12:77062068 | GC | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(109): Show |
164 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.93+2474delG | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77062068 | |||||||
| chr12:77062249 | T | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0202 a0001c0001t0001g0206 others(6): Show |
13 | HG02055.hp1 HG02145.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.93+2294A>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77062249 | |||||||
| chr12:77062269 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.93+2274G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77062269 | |||||||
| chr12:77062270 | G | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0202 a0001c0001t0001g0206 others(7): Show |
13 | HG00140.hp1 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.93+2273C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77062270 | |||||||
| chr12:77062454 | C | G | 1 | a0001c0001t0023g0248 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.93+2089G>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77062454 | |||||||
| chr12:77062594 | GT | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(94): Show |
146 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.93+1948delA | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77062594 | |||||||
| chr12:77062887 | T | TA | 6 | a0001c0001t0001g0160 a0001c0001t0002g0241 a0001c0004t0001g0245 others(3): Show |
6 | HG01243.hp2 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.93+1655dupT | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77062887 | |||||||
| chr12:77062887 | TA | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(87): Show |
139 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.93+1655delT | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77062887 | |||||||
| chr12:77062899 | A | AC | 54 | a0001c0001t0001g0047 a0001c0001t0001g0164 a0001c0001t0001g0165 others(51): Show |
64 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.93+1643_93+1644ins others(1): Show |
E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77062899 | |||||||
| chr12:77063008 | T | C | 10 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(7): Show |
10 | HG01109.hp2 HG01978.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.93+1535A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77063008 | |||||||
| chr12:77063052 | C | T | 55 | a0001c0001t0001g0047 a0001c0001t0001g0164 a0001c0001t0001g0165 others(52): Show |
65 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.93+1491G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77063052 | |||||||
| chr12:77063091 | C | T | 1 | a0002c0003t0001g0139 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.93+1452G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77063091 | |||||||
| chr12:77063095 | G | A | 2 | a0001c0018t0001g0208 a0011c0015t0001g0162 |
2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.93+1448C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77063095 | |||||||
| chr12:77063124 | A | G | 1 | a0001c0009t0015g0138 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.93+1419T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77063124 | |||||||
| chr12:77063134 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.93+1409C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77063134 | |||||||
| chr12:77063176 | C | T | 1 | a0001c0002t0002g0247 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.93+1367G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77063176 | |||||||
| chr12:77063221 | T | A | 1 | a0001c0001t0001g0122 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.93+1322A>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77063221 | |||||||
| chr12:77063420 | C | T | 55 | a0001c0001t0001g0047 a0001c0001t0001g0164 a0001c0001t0001g0165 others(52): Show |
65 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.93+1123G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77063420 | |||||||
| chr12:77063533 | A | G | 4 | a0002c0006t0001g0015 a0002c0006t0001g0246 a0005c0011t0001g0136 others(1): Show |
6 | HG00280.hp2 HG00738.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.93+1010T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77063533 | |||||||
| chr12:77063550 | CCA | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(83): Show |
135 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.93+991_93+992delTG | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77063550 | |||||||
| chr12:77063619 | C | T | 1 | a0001c0001t0002g0163 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.93+924G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77063619 | |||||||
| chr12:77063659 | A | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(83): Show |
122 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.93+884T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77063659 | |||||||
| chr12:77063690 | G | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0202 a0001c0001t0001g0206 others(5): Show |
11 | HG02055.hp1 HG02145.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.93+853C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77063690 | |||||||
| chr12:77063742 | C | A | 9 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0002t0016g0051 others(6): Show |
10 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.93+801G>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77063742 | |||||||
| chr12:77063942 | T | C | 1 | a0001c0002t0002g0242 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.93+601A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77063942 | |||||||
| chr12:77063983 | G | C | 1 | a0001c0002t0002g0135 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.93+560C>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77063983 | |||||||
| chr12:77063992 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0061 a0001c0001t0001g0062 |
5 | HG00323.hp2 HG02735.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+551T>C | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77063992 | |||||||
| chr12:77064117 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(99): Show |
153 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.93+426G>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77064117 | |||||||
| chr12:77064220 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0202 a0001c0001t0001g0206 others(6): Show |
13 | HG02055.hp1 HG02145.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.93+323C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77064220 | |||||||
| chr12:77064483 | A | T | 1 | a0001c0001t0001g0243 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.93+60T>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 2/12 | chr12 | 77064483 | |||||||
| chr12:77064663 | G | T | 3 | a0001c0001t0002g0059 a0001c0002t0001g0021 a0001c0002t0001g0022 |
5 | HG02257.hp2 HG02896.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1-28C>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 1/12 | chr12 | 77064663 | |||||||
| chr12:77064717 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1-82A>G | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 1/12 | chr12 | 77064717 | |||||||
| chr12:77064827 | A | T | 40 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0017 others(37): Show |
59 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.1-192T>A | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 1/12 | chr12 | 77064827 | |||||||
| chr12:77065068 | G | A | 42 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0017 others(39): Show |
61 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.-1+277C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 1/12 | chr12 | 77065068 | |||||||
| chr12:77065098 | G | A | 1 | a0001c0001t0001g0047 | 2 | HG01496.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-1+247C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 1/12 | chr12 | 77065098 | |||||||
| chr12:77065286 | G | A | 46 | a0001c0001t0001g0047 a0001c0001t0001g0251 a0001c0001t0001g0254 others(43): Show |
53 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.-1+59C>T | E2F7 | ENSG00000165891.16 | transcript | ENST00000322886.12 | protein_coding | 1/12 | chr12 | 77065286 |