Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 389206 |
| ensemblid | ENSG00000188848.17 |
| hgncid | 23815 |
| symbol | BEND4 |
| name | BEN domain containing 4 |
| refseq_nuc | NM_207406.4 |
| refseq_prot | NP_997289.2 |
| ensembl_nuc | ENST00000502486.6 |
| ensembl_prot | ENSP00000421169.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 42110853 |
| end | 42152655 |
| strand | - |
| ver | v1.2 |
| region | chr4:42110853-42152655 |
| region5000 | chr4:42105853-42157655 |
| regionname0 | BEND4_chr4_42110853_42152655 |
| regionname5000 | BEND4_chr4_42105853_42157655 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 534 | 216 | 84 | 47 | 42 | 10 | 31 | 30 | BEND4_chr4_42105853_42157655 | BEND4 | MEEEM others(529): Show |
chr4 | 42105853 | 42157655 |
| a0002 | 0/0 | 534 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | MEEEM others(529): Show |
chr4 | 42105853 | 42157655 |
| a0003 | 0/0 | 534 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | MEEEM others(529): Show |
chr4 | 42105853 | 42157655 |
| a0004 | 0/0 | 534 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | MEEEM others(529): Show |
chr4 | 42105853 | 42157655 |
| a0005 | 0/0 | 534 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | MEEEM others(529): Show |
chr4 | 42105853 | 42157655 |
| a0006 | 0/0 | 534 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | MEEEM others(529): Show |
chr4 | 42105853 | 42157655 |
| a0007 | 0/0 | 534 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | MEEEM others(529): Show |
chr4 | 42105853 | 42157655 |
| a0008 | 0/0 | 534 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | MEEEM others(529): Show |
chr4 | 42105853 | 42157655 |
| a0009 | 0/0 | 534 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | MEEEM others(529): Show |
chr4 | 42105853 | 42157655 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1602 | 211 | 83 | 46 | 42 | 8 | 30 | BEND4_chr4_42105853_42157655 | BEND4 | ATGGA others(1597): Show |
chr4 | 42105853 | 42157655 | ||
| a0001c0003 | 0/0 | 1602 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | ATGGA others(1597): Show |
chr4 | 42105853 | 42157655 | ||
| a0001c0004 | 0/0 | 1602 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | ATGGA others(1597): Show |
chr4 | 42105853 | 42157655 | ||
| a0001c0008 | 0/0 | 1602 | 1 | 0 | 0 | 0 | 1 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | ATGGA others(1597): Show |
chr4 | 42105853 | 42157655 | ||
| a0001c0010 | 0/0 | 1602 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | ATGGA others(1597): Show |
chr4 | 42105853 | 42157655 | ||
| a0001c0012 | 0/0 | 1602 | 1 | 0 | 0 | 0 | 1 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | ATGGA others(1597): Show |
chr4 | 42105853 | 42157655 | ||
| a0002c0002 | 0/0 | 1602 | 3 | 3 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | ATGGA others(1597): Show |
chr4 | 42105853 | 42157655 | ||
| a0003c0007 | 0/0 | 1602 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | ATGGA others(1597): Show |
chr4 | 42105853 | 42157655 | ||
| a0004c0005 | 0/0 | 1602 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | ATGGA others(1597): Show |
chr4 | 42105853 | 42157655 | ||
| a0005c0014 | 0/0 | 1602 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | ATGGA others(1597): Show |
chr4 | 42105853 | 42157655 | ||
| a0006c0011 | 0/0 | 1602 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | ATGGA others(1597): Show |
chr4 | 42105853 | 42157655 | ||
| a0007c0006 | 0/0 | 1602 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | ATGGA others(1597): Show |
chr4 | 42105853 | 42157655 | ||
| a0008c0013 | 0/0 | 1602 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | ATGGA others(1597): Show |
chr4 | 42105853 | 42157655 | ||
| a0009c0009 | 0/0 | 1602 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | ATGGA others(1597): Show |
chr4 | 42105853 | 42157655 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 8627 | 74 | 5 | 25 | 22 | 3 | 17 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8622): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0002 | 0/0 | 8628 | 35 | 10 | 6 | 8 | 1 | 10 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0003 | 0/0 | 8628 | 14 | 11 | 1 | 0 | 2 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0004 | 0/0 | 8628 | 12 | 7 | 2 | 2 | 1 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0005 | 0/0 | 8628 | 11 | 11 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0006 | 0/0 | 8628 | 9 | 9 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0007 | 0/0 | 8628 | 10 | 10 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0008 | 0/0 | 8628 | 8 | 0 | 4 | 3 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0009 | 0/0 | 8628 | 6 | 6 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0010 | 0/0 | 8628 | 5 | 5 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0011 | 0/0 | 8628 | 4 | 0 | 0 | 4 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0012 | 0/0 | 8628 | 3 | 0 | 3 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0013 | 0/0 | 8627 | 2 | 0 | 1 | 0 | 1 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8622): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0014 | 0/0 | 8628 | 2 | 2 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0015 | 0/0 | 8628 | 2 | 2 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0016 | 0/0 | 8628 | 2 | 2 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0018 | 0/0 | 8627 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8622): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0019 | 0/0 | 8627 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8622): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0020 | 0/0 | 8627 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8622): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0021 | 0/0 | 8627 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8622): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0022 | 0/0 | 8614 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8609): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0023 | 0/0 | 8627 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8622): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0024 | 0/0 | 8628 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0025 | 0/0 | 8628 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0026 | 0/0 | 8628 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0027 | 0/0 | 8628 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0029 | 0/0 | 8628 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0001t0031 | 0/0 | 8627 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8622): Show |
chr4 | 42105853 | 42157655 |
| a0001c0003t0011 | 0/0 | 8628 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0004t0006 | 0/0 | 8628 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0008t0032 | 0/0 | 8628 | 1 | 0 | 0 | 0 | 1 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0010t0028 | 0/0 | 8628 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0001c0012t0001 | 0/0 | 8627 | 1 | 0 | 0 | 0 | 1 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8622): Show |
chr4 | 42105853 | 42157655 |
| a0002c0002t0017 | 0/0 | 8634 | 2 | 2 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8629): Show |
chr4 | 42105853 | 42157655 |
| a0002c0002t0030 | 0/0 | 8634 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8629): Show |
chr4 | 42105853 | 42157655 |
| a0003c0007t0001 | 0/0 | 8627 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8622): Show |
chr4 | 42105853 | 42157655 |
| a0004c0005t0009 | 0/0 | 8628 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0005c0014t0005 | 0/0 | 8628 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0006c0011t0002 | 0/0 | 8628 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0007c0006t0008 | 0/0 | 8628 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0008c0013t0002 | 0/0 | 8628 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| a0009c0009t0004 | 0/0 | 8628 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | GTTTC others(8623): Show |
chr4 | 42105853 | 42157655 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 21 | 1 | 6 | 10 | 3 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0064 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0002 | 0/0 | 10 | 3 | 2 | 2 | 0 | 3 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0003g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0004g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0005g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0005g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0005g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0006g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0007g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0007g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0007g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0007g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0008g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0008g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0008g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0008g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0008g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0008g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0009g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0009g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0010g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0010g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0010g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0011g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0011g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0011g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0012g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0013g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0013g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0014g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0015g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0015g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0016g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0016g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0018g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0019g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0020g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0021g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0022g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0023g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0024g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0025g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0026g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0027g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0029g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0001t0031g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0003t0011g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0004t0006g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0008t0032g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0010t0028g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0001c0012t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0002c0002t0017g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0002c0002t0030g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0003c0007t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0004c0005t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0005c0014t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0006c0011t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0007c0006t0008g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0008c0013t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| a0009c0009t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0012 | t0001 | g0039 | EUR | GBR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG00140 | hp2 | a0001 | c0001 | t0013 | g0035 | EUR | GBR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG00621 | hp2 | a0001 | c0001 | t0011 | g0140 | EAS | CHS | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG00642 | hp2 | a0001 | c0001 | t0008 | g0010 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG00735 | hp1 | a0001 | c0001 | t0012 | g0008 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0097 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01069 | hp2 | a0001 | c0001 | t0008 | g0010 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01074 | hp1 | a0001 | c0001 | t0031 | g0159 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01081 | hp2 | a0001 | c0001 | t0012 | g0008 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01099 | hp1 | a0001 | c0001 | t0012 | g0008 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0095 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01109 | hp2 | a0001 | c0001 | t0008 | g0010 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01167 | hp2 | a0001 | c0004 | t0006 | g0115 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01255 | hp1 | a0001 | c0001 | t0020 | g0076 | AMR | CLM | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | CLM | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01257 | hp1 | a0001 | c0001 | t0022 | g0056 | AMR | CLM | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0154 | AMR | CLM | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01361 | hp2 | a0001 | c0001 | t0013 | g0036 | AMR | CLM | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01496 | hp1 | a0003 | c0007 | t0001 | g0057 | AMR | CLM | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01515 | hp1 | a0001 | c0008 | t0032 | g0161 | EUR | IBS | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0103 | EUR | IBS | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01884 | hp1 | a0002 | c0002 | t0017 | g0024 | AFR | ACB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | ACB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0028 | AFR | ACB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01981 | hp2 | a0001 | c0001 | t0008 | g0150 | AMR | PEL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02055 | hp2 | a0002 | c0002 | t0017 | g0024 | AFR | ACB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02056 | hp1 | a0001 | c0001 | t0018 | g0071 | EAS | KHV | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02074 | hp1 | a0001 | c0001 | t0011 | g0027 | EAS | KHV | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02074 | hp2 | a0001 | c0001 | t0023 | g0069 | EAS | KHV | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0157 | AFR | ACB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | ACB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | ACB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02280 | hp1 | a0004 | c0005 | t0009 | g0160 | AFR | ACB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0116 | AFR | ACB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0102 | AFR | ACB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | ACB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02572 | hp2 | a0001 | c0001 | t0026 | g0098 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0003 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02622 | hp2 | a0001 | c0001 | t0016 | g0123 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0100 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02630 | hp2 | a0001 | c0001 | t0010 | g0032 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0003 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02647 | hp2 | a0005 | c0014 | t0005 | g0158 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0109 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0125 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02735 | hp1 | a0001 | c0003 | t0011 | g0029 | SAS | PJL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02738 | hp1 | a0006 | c0011 | t0002 | g0134 | SAS | PJL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02818 | hp2 | a0001 | c0010 | t0028 | g0121 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02886 | hp1 | a0001 | c0001 | t0015 | g0096 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02896 | hp1 | a0001 | c0001 | t0014 | g0012 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02896 | hp2 | a0001 | c0001 | t0010 | g0033 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0034 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0114 | AFR | ESN | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0107 | AFR | ESN | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | ESN | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0108 | AFR | ESN | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0156 | AFR | ESN | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | ESN | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02976 | hp2 | a0001 | c0001 | t0016 | g0133 | AFR | ESN | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0047 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0162 | AFR | MSL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | MSL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03139 | hp1 | a0001 | c0001 | t0014 | g0012 | AFR | ESN | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ESN | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0104 | AFR | ESN | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03195 | hp2 | a0002 | c0002 | t0030 | g0132 | AFR | ESN | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0106 | AFR | MSL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | MSL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03225 | hp1 | a0001 | c0001 | t0010 | g0099 | AFR | MSL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03239 | hp1 | a0001 | c0001 | t0021 | g0086 | SAS | PJL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | MSL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03453 | hp2 | a0001 | c0001 | t0010 | g0030 | AFR | MSL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | MSL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0141 | AFR | MSL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0111 | AFR | ESN | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0105 | AFR | GWD | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0118 | AFR | MSL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | STU | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | STU | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03710 | hp2 | a0001 | c0001 | t0008 | g0083 | SAS | PJL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | BEB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | BEB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | STU | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG04115 | hp2 | a0007 | c0006 | t0008 | g0153 | SAS | STU | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG04184 | hp1 | a0001 | c0001 | t0024 | g0135 | SAS | BEB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | STU | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG04228 | hp1 | a0008 | c0013 | t0002 | g0084 | SAS | STU | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | STU | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | YRI | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | YRI | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | YRI | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA18906 | hp2 | a0001 | c0001 | t0027 | g0145 | AFR | YRI | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA18950 | hp2 | a0001 | c0001 | t0011 | g0027 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA18993 | hp2 | a0001 | c0001 | t0008 | g0147 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA19007 | hp2 | a0001 | c0001 | t0008 | g0151 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA19030 | hp1 | a0001 | c0001 | t0025 | g0101 | AFR | LWK | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | LWK | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0011 | AFR | LWK | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | LWK | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA19066 | hp1 | a0001 | c0001 | t0019 | g0055 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA19076 | hp2 | a0001 | c0001 | t0011 | g0152 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA19089 | hp2 | a0001 | c0001 | t0008 | g0149 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0011 | AFR | YRI | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA19240 | hp2 | a0009 | c0009 | t0004 | g0117 | AFR | YRI | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0018 | EUR | TSI | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0148 | EUR | TSI | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0018 | EUR | TSI | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG01123 | hp2 | a0001 | c0001 | t0029 | g0142 | AMR | CLM | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0112 | AFR | ACB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0003 | AFR | ACB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0028 | AFR | ACB | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | MSL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | MSL | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG06807 | hp1 | a0001 | c0001 | t0015 | g0094 | AFR | USA | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0113 | AFR | USA | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA20300 | hp1 | a0001 | c0001 | t0009 | g0011 | AFR | USA | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | USA | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | LWK | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0064 | REF | REF | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | BEND4_chr4_42105853_42157655 | BEND4 | chr4 | 42105853 | 42157655 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:42117528 | G | A | 1 | a0003 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.1595C>T | p.Ser532Phe | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 1952/8627 | 1595/1605 | 532/534 | chr4 | 42117528 | |||
| chr4:42117567 | G | C | 1 | a0002 | 3 | HG01884.hp1 HG02055.hp2 HG03195.hp2 |
missense_variant | MODERATE | c.1556C>G | p.Ser519Cys | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 1913/8627 | 1556/1605 | 519/534 | chr4 | 42117567 | |||
| chr4:42117582 | A | G | 1 | a0007 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.1541T>C | p.Ile514Thr | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 1898/8627 | 1541/1605 | 514/534 | chr4 | 42117582 | |||
| chr4:42125642 | T | A | 1 | a0009 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.1087A>T | p.Met363Leu | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/6 | 1444/8627 | 1087/1605 | 363/534 | chr4 | 42125642 | |||
| chr4:42143521 | C | T | 1 | a0004 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.961G>A | p.Gly321Ser | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/6 | 1318/8627 | 961/1605 | 321/534 | chr4 | 42143521 | |||
| chr4:42143789 | T | C | 1 | a0006 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.693A>G | p.Ile231Met | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/6 | 1050/8627 | 693/1605 | 231/534 | chr4 | 42143789 | |||
| chr4:42143907 | T | C | 1 | a0008 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.575A>G | p.Asn192Ser | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/6 | 932/8627 | 575/1605 | 192/534 | chr4 | 42143907 | |||
| chr4:42151885 | G | C | 1 | a0005 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.259C>G | p.Pro87Ala | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/6 | 616/8627 | 259/1605 | 87/534 | chr4 | 42151885 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:42117704 | G | A | 1 | a0001c0008 | 1 | HG01515.hp1 | synonymous_variant | LOW | c.1419C>T | p.Pro473Pro | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 1776/8627 | 1419/1605 | 473/534 | chr4 | 42117704 | |||
| chr4:42125661 | G | A | 1 | a0001c0010 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.1068C>T | p.Thr356Thr | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/6 | 1425/8627 | 1068/1605 | 356/534 | chr4 | 42125661 | |||
| chr4:42143588 | C | T | 1 | a0001c0004 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.894G>A | p.Thr298Thr | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/6 | 1251/8627 | 894/1605 | 298/534 | chr4 | 42143588 | |||
| chr4:42143882 | G | A | 1 | a0001c0012 | 1 | HG00140.hp1 | synonymous_variant | LOW | c.600C>T | p.Cys200Cys | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/6 | 957/8627 | 600/1605 | 200/534 | chr4 | 42143882 | |||
| chr4:42151760 | C | G | 1 | a0001c0003 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.384G>C | p.Ser128Ser | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/6 | 741/8627 | 384/1605 | 128/534 | chr4 | 42151760 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:42110890 | A | G | 19 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(16): Show |
84 | HG00621.hp2 HG00735.hp1 HG00738.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*6628T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 6628 | chr4 | 42110890 | ||||||
| chr4:42111066 | T | C | 1 | a0001c0001t0027 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6452A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 6452 | chr4 | 42111066 | ||||||
| chr4:42111091 | A | C | 1 | a0001c0001t0003 | 14 | HG01099.hp2 HG02109.hp2 HG02258.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*6427T>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 6427 | chr4 | 42111091 | ||||||
| chr4:42111224 | C | T | 31 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(28): Show |
141 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*6294G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 6294 | chr4 | 42111224 | ||||||
| chr4:42111232 | A | T | 8 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0011 others(5): Show |
30 | HG00621.hp2 HG00738.hp2 HG01123.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*6286T>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 6286 | chr4 | 42111232 | ||||||
| chr4:42111716 | A | G | 1 | a0002c0002t0017 | 2 | HG01884.hp1 HG02055.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5802T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 5802 | chr4 | 42111716 | ||||||
| chr4:42111783 | C | A | 2 | a0001c0001t0007 a0001c0001t0026 |
11 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5735G>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 5735 | chr4 | 42111783 | ||||||
| chr4:42111873 | G | A | 2 | a0001c0001t0015 a0001c0001t0027 |
3 | HG02886.hp1 HG06807.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5645C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 5645 | chr4 | 42111873 | ||||||
| chr4:42111923 | A | G | 4 | a0001c0001t0003 a0001c0001t0005 a0001c0010t0028 others(1): Show |
27 | HG01099.hp2 HG02109.hp2 HG02258.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*5595T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 5595 | chr4 | 42111923 | ||||||
| chr4:42112311 | C | T | 1 | a0001c0001t0020 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5207G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 5207 | chr4 | 42112311 | ||||||
| chr4:42112423 | T | C | 1 | a0001c0001t0014 | 2 | HG02896.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5095A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 5095 | chr4 | 42112423 | ||||||
| chr4:42112548 | A | G | 3 | a0001c0001t0008 a0001c0001t0019 a0007c0006t0008 |
10 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4970T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 4970 | chr4 | 42112548 | ||||||
| chr4:42112654 | T | G | 18 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(15): Show |
96 | HG00642.hp2 HG00735.hp1 HG00738.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*4864A>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 4864 | chr4 | 42112654 | ||||||
| chr4:42112704 | T | C | 1 | a0001c0008t0032 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4814A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 4814 | chr4 | 42112704 | ||||||
| chr4:42112927 | G | A | 2 | a0001c0001t0004 a0009c0009t0004 |
13 | HG00738.hp2 HG01257.hp2 HG01516.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4591C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 4591 | chr4 | 42112927 | ||||||
| chr4:42112937 | C | T | 2 | a0001c0001t0003 a0001c0010t0028 |
15 | HG01099.hp2 HG02109.hp2 HG02258.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4581G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 4581 | chr4 | 42112937 | ||||||
| chr4:42113618 | A | T | 1 | a0001c0001t0025 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3900T>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 3900 | chr4 | 42113618 | ||||||
| chr4:42113696 | A | G | 2 | a0002c0002t0017 a0002c0002t0030 |
3 | HG01884.hp1 HG02055.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3822T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 3822 | chr4 | 42113696 | ||||||
| chr4:42113784 | G | A | 1 | a0001c0001t0013 | 2 | HG00140.hp2 HG01361.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3734C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 3734 | chr4 | 42113784 | ||||||
| chr4:42113793 | C | T | 4 | a0001c0001t0004 a0001c0001t0006 a0001c0004t0006 others(1): Show |
23 | HG00738.hp2 HG01167.hp2 HG01257.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3725G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 3725 | chr4 | 42113793 | ||||||
| chr4:42114053 | T | C | 1 | a0001c0001t0021 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3465A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 3465 | chr4 | 42114053 | ||||||
| chr4:42114093 | T | G | 10 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(7): Show |
61 | HG00735.hp1 HG00738.hp1 HG01074.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*3425A>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 3425 | chr4 | 42114093 | ||||||
| chr4:42114099 | T | C | 9 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0012 others(6): Show |
51 | HG00735.hp1 HG00738.hp1 HG01074.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*3419A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 3419 | chr4 | 42114099 | ||||||
| chr4:42114170 | T | G | 2 | a0001c0001t0006 a0001c0004t0006 |
10 | HG01167.hp2 HG02109.hp1 HG02922.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3348A>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 3348 | chr4 | 42114170 | ||||||
| chr4:42114196 | G | A | 1 | a0001c0001t0025 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3322C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 3322 | chr4 | 42114196 | ||||||
| chr4:42114410 | C | T | 2 | a0001c0001t0015 a0001c0001t0027 |
3 | HG02886.hp1 HG06807.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3108G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 3108 | chr4 | 42114410 | ||||||
| chr4:42114511 | A | G | 1 | a0001c0001t0018 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3007T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 3007 | chr4 | 42114511 | ||||||
| chr4:42114670 | AATGACAG others(6): Show |
A | 1 | a0001c0001t0022 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2835_*2847delCGGA others(9): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 2835 | chr4 | 42114670 | ||||||
| chr4:42114687 | C | T | 1 | a0001c0001t0007 | 10 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2831G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 2831 | chr4 | 42114687 | ||||||
| chr4:42114777 | C | G | 8 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0012 others(5): Show |
50 | HG00735.hp1 HG00738.hp1 HG01074.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*2741G>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 2741 | chr4 | 42114777 | ||||||
| chr4:42114796 | C | T | 2 | a0001c0001t0014 a0001c0001t0016 |
4 | HG02622.hp2 HG02896.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2722G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 2722 | chr4 | 42114796 | ||||||
| chr4:42114804 | G | A | 2 | a0001c0001t0004 a0009c0009t0004 |
13 | HG00738.hp2 HG01257.hp2 HG01516.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2714C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 2714 | chr4 | 42114804 | ||||||
| chr4:42114928 | T | C | 1 | a0001c0001t0023 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2590A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 2590 | chr4 | 42114928 | ||||||
| chr4:42114990 | G | C | 1 | a0001c0001t0024 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2528C>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 2528 | chr4 | 42114990 | ||||||
| chr4:42115053 | G | T | 3 | a0001c0001t0004 a0001c0008t0032 a0009c0009t0004 |
14 | HG00738.hp2 HG01257.hp2 HG01515.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2465C>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 2465 | chr4 | 42115053 | ||||||
| chr4:42115062 | C | G | 8 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0011 others(5): Show |
24 | HG00621.hp2 HG01123.hp2 HG01515.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2456G>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 2456 | chr4 | 42115062 | ||||||
| chr4:42115118 | A | C | 2 | a0002c0002t0017 a0002c0002t0030 |
3 | HG01884.hp1 HG02055.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2400T>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 2400 | chr4 | 42115118 | ||||||
| chr4:42115156 | C | T | 20 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(17): Show |
88 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*2362G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 2362 | chr4 | 42115156 | ||||||
| chr4:42115312 | C | T | 3 | a0001c0001t0003 a0001c0001t0005 a0005c0014t0005 |
26 | HG01099.hp2 HG02109.hp2 HG02258.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2206G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 2206 | chr4 | 42115312 | ||||||
| chr4:42115360 | T | TGGAGCA | 2 | a0002c0002t0017 a0002c0002t0030 |
3 | HG01884.hp1 HG02055.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2152_*2157dupTGCT others(2): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 2157 | chr4 | 42115360 | ||||||
| chr4:42115457 | T | C | 21 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(18): Show |
79 | HG00621.hp2 HG00642.hp2 HG01069.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2061A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 2061 | chr4 | 42115457 | ||||||
| chr4:42115483 | G | A | 3 | a0001c0001t0011 a0001c0001t0029 a0001c0003t0011 |
6 | HG00621.hp2 HG01123.hp2 HG02074.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2035C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 2035 | chr4 | 42115483 | ||||||
| chr4:42115542 | G | A | 20 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(17): Show |
80 | HG00621.hp2 HG00642.hp2 HG00738.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1976C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 1976 | chr4 | 42115542 | ||||||
| chr4:42115549 | T | G | 3 | a0001c0001t0011 a0001c0001t0029 a0001c0003t0011 |
6 | HG00621.hp2 HG01123.hp2 HG02074.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1969A>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 1969 | chr4 | 42115549 | ||||||
| chr4:42115615 | G | A | 1 | a0001c0001t0016 | 2 | HG02622.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1903C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 1903 | chr4 | 42115615 | ||||||
| chr4:42115616 | G | C | 4 | a0001c0001t0003 a0001c0001t0005 a0001c0010t0028 others(1): Show |
27 | HG01099.hp2 HG02109.hp2 HG02258.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1902C>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 1902 | chr4 | 42115616 | ||||||
| chr4:42115631 | T | C | 2 | a0001c0001t0008 a0007c0006t0008 |
9 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1887A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 1887 | chr4 | 42115631 | ||||||
| chr4:42115673 | A | G | 1 | a0001c0001t0016 | 2 | HG02622.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1845T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 1845 | chr4 | 42115673 | ||||||
| chr4:42115727 | G | T | 1 | a0001c0001t0016 | 2 | HG02622.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1791C>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 1791 | chr4 | 42115727 | ||||||
| chr4:42115856 | T | TA | 31 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(28): Show |
141 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*1661_*1662insT | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 1661 | chr4 | 42115856 | ||||||
| chr4:42116158 | T | A | 3 | a0001c0001t0011 a0001c0001t0029 a0001c0003t0011 |
6 | HG00621.hp2 HG01123.hp2 HG02074.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1360A>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 1360 | chr4 | 42116158 | ||||||
| chr4:42116409 | G | A | 1 | a0001c0001t0029 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1109C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 1109 | chr4 | 42116409 | ||||||
| chr4:42116410 | G | A | 2 | a0002c0002t0017 a0002c0002t0030 |
3 | HG01884.hp1 HG02055.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1108C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 1108 | chr4 | 42116410 | ||||||
| chr4:42116463 | G | A | 4 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0016 others(1): Show |
28 | HG01099.hp2 HG02109.hp2 HG02258.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1055C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 1055 | chr4 | 42116463 | ||||||
| chr4:42116645 | G | A | 5 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(2): Show |
38 | HG01099.hp2 HG01884.hp2 HG02109.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*873C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 873 | chr4 | 42116645 | ||||||
| chr4:42116768 | A | G | 1 | a0001c0008t0032 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*750T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 750 | chr4 | 42116768 | ||||||
| chr4:42116883 | T | C | 1 | a0001c0001t0012 | 3 | HG00735.hp1 HG01081.hp2 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*635A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 635 | chr4 | 42116883 | ||||||
| chr4:42117182 | C | A | 2 | a0002c0002t0017 a0002c0002t0030 |
3 | HG01884.hp1 HG02055.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*336G>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 6/6 | 336 | chr4 | 42117182 | ||||||
| chr4:42152325 | G | C | 1 | a0001c0001t0031 | 1 | HG01074.hp1 | 5_prime_UTR_variant | MODIFIER | c.-182C>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/6 | 182 | chr4 | 42152325 | ||||||
| chr4:42152595 | T | C | 3 | a0001c0001t0009 a0001c0008t0032 a0004c0005t0009 |
8 | HG01515.hp1 HG01891.hp1 HG02280.hp1 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-297A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 1/6 | chr4 | 42152595 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:42117934 | TA | T | 102 | a0001c0001t0001g0015 a0001c0001t0002g0002 a0001c0001t0002g0009 others(99): Show |
143 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(140): Show |
intron_variant | MODIFIER | c.1388-200delT | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42117934 | |||||||
| chr4:42118088 | A | G | 21 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(18): Show |
29 | HG01099.hp2 HG02109.hp2 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.1388-353T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42118088 | |||||||
| chr4:42118120 | C | G | 7 | a0001c0001t0008g0010 a0001c0001t0008g0083 a0001c0001t0008g0147 others(4): Show |
9 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1388-385G>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42118120 | |||||||
| chr4:42118138 | T | C | 1 | a0001c0001t0007g0006 | 3 | HG01884.hp2 HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1388-403A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42118138 | |||||||
| chr4:42118172 | G | A | 7 | a0001c0001t0008g0010 a0001c0001t0008g0083 a0001c0001t0008g0147 others(4): Show |
9 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1388-437C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42118172 | |||||||
| chr4:42118210 | G | A | 1 | a0001c0001t0024g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1388-475C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42118210 | |||||||
| chr4:42118321 | G | A | 26 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(23): Show |
36 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.1388-586C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42118321 | |||||||
| chr4:42118344 | A | C | 7 | a0001c0001t0008g0010 a0001c0001t0008g0083 a0001c0001t0008g0147 others(4): Show |
9 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1388-609T>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42118344 | |||||||
| chr4:42118370 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1388-635G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42118370 | |||||||
| chr4:42118449 | G | T | 1 | a0001c0001t0006g0141 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1388-714C>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42118449 | |||||||
| chr4:42118465 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1388-730T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42118465 | |||||||
| chr4:42118492 | A | G | 101 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0025 others(98): Show |
141 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(138): Show |
intron_variant | MODIFIER | c.1388-757T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42118492 | |||||||
| chr4:42118627 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1388-892A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42118627 | |||||||
| chr4:42118907 | G | A | 3 | a0001c0001t0015g0094 a0001c0001t0015g0096 a0001c0001t0027g0145 |
3 | HG02886.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1387+1147C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42118907 | |||||||
| chr4:42119090 | C | G | 2 | a0002c0002t0017g0024 a0002c0002t0030g0132 |
3 | HG01884.hp1 HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1387+964G>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42119090 | |||||||
| chr4:42119117 | A | C | 20 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(17): Show |
28 | HG01099.hp2 HG02109.hp2 HG02258.hp1 others(25): Show |
intron_variant | MODIFIER | c.1387+937T>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42119117 | |||||||
| chr4:42119206 | C | T | 22 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(19): Show |
31 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.1387+848G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42119206 | |||||||
| chr4:42119395 | G | C | 79 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0025 others(76): Show |
110 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.1387+659C>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42119395 | |||||||
| chr4:42119597 | T | C | 6 | a0001c0001t0007g0003 a0001c0001t0007g0006 a0001c0001t0007g0014 others(3): Show |
11 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1387+457A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42119597 | |||||||
| chr4:42119603 | T | C | 1 | a0001c0001t0024g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1387+451A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42119603 | |||||||
| chr4:42119757 | G | A | 7 | a0001c0001t0008g0010 a0001c0001t0008g0083 a0001c0001t0008g0147 others(4): Show |
9 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1387+297C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42119757 | |||||||
| chr4:42119835 | C | T | 1 | a0001c0001t0026g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1387+219G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42119835 | |||||||
| chr4:42119856 | A | T | 21 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(18): Show |
30 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1387+198T>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42119856 | |||||||
| chr4:42119868 | C | T | 7 | a0001c0001t0008g0010 a0001c0001t0008g0083 a0001c0001t0008g0147 others(4): Show |
9 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1387+186G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42119868 | |||||||
| chr4:42119886 | T | G | 1 | a0001c0001t0008g0149 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1387+168A>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 5/5 | chr4 | 42119886 | |||||||
| chr4:42120388 | C | G | 8 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(5): Show |
13 | HG01099.hp2 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1147-94G>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42120388 | |||||||
| chr4:42120581 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1147-287C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42120581 | |||||||
| chr4:42120583 | C | T | 1 | a0009c0009t0004g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1147-289G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42120583 | |||||||
| chr4:42120585 | G | A | 2 | a0001c0001t0016g0123 a0001c0001t0016g0133 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1147-291C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42120585 | |||||||
| chr4:42120832 | GA | G | 22 | a0001c0001t0002g0009 a0001c0001t0002g0051 a0001c0001t0002g0082 others(19): Show |
28 | HG00738.hp1 HG01243.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1147-539delT | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42120832 | |||||||
| chr4:42120869 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1147-575A>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42120869 | |||||||
| chr4:42121002 | G | A | 1 | a0001c0001t0003g0046 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1147-708C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42121002 | |||||||
| chr4:42121231 | G | A | 1 | a0001c0001t0026g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1147-937C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42121231 | |||||||
| chr4:42121232 | G | C | 3 | a0001c0001t0015g0094 a0001c0001t0015g0096 a0001c0001t0027g0145 |
3 | HG02886.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1147-938C>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42121232 | |||||||
| chr4:42121314 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1147-1020C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42121314 | |||||||
| chr4:42121346 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0061 |
2 | HG03710.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1147-1052C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42121346 | |||||||
| chr4:42121498 | T | C | 86 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0025 others(83): Show |
122 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(119): Show |
intron_variant | MODIFIER | c.1147-1204A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42121498 | |||||||
| chr4:42121547 | T | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0075 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1147-1253A>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42121547 | |||||||
| chr4:42121641 | T | C | 2 | a0001c0001t0014g0012 a0001c0008t0032g0161 |
3 | HG01515.hp1 HG02896.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1147-1347A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42121641 | |||||||
| chr4:42121711 | A | C | 56 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0025 others(53): Show |
83 | HG00621.hp2 HG00735.hp1 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.1147-1417T>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42121711 | |||||||
| chr4:42121733 | G | A | 1 | a0001c0001t0025g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1147-1439C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42121733 | |||||||
| chr4:42121746 | A | T | 1 | a0001c0001t0006g0141 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1147-1452T>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42121746 | |||||||
| chr4:42121843 | T | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0050 a0001c0001t0001g0068 |
5 | HG01071.hp1 HG01358.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-1549A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42121843 | |||||||
| chr4:42121875 | C | T | 66 | a0001c0001t0001g0074 a0001c0001t0001g0126 a0001c0001t0002g0002 others(63): Show |
97 | HG00621.hp1 HG00735.hp1 HG00738.hp2 others(94): Show |
intron_variant | MODIFIER | c.1147-1581G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42121875 | |||||||
| chr4:42122212 | C | A | 1 | a0001c0001t0014g0012 | 2 | HG02896.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1147-1918G>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42122212 | |||||||
| chr4:42122345 | A | G | 39 | a0001c0001t0001g0052 a0001c0001t0001g0126 a0001c0001t0002g0002 others(36): Show |
58 | HG00621.hp2 HG00735.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1147-2051T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42122345 | |||||||
| chr4:42122445 | A | G | 8 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(5): Show |
13 | HG01099.hp2 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1147-2151T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42122445 | |||||||
| chr4:42122735 | A | C | 43 | a0001c0001t0001g0052 a0001c0001t0001g0126 a0001c0001t0002g0002 others(40): Show |
67 | HG00621.hp2 HG00735.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.1147-2441T>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42122735 | |||||||
| chr4:42123125 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1146+2458T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123125 | |||||||
| chr4:42123129 | C | T | 2 | a0001c0001t0002g0025 a0001c0001t0002g0127 |
3 | NA18944.hp2 NA18962.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1146+2454G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123129 | |||||||
| chr4:42123367 | A | C | 1 | a0001c0001t0026g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1146+2216T>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123367 | |||||||
| chr4:42123474 | G | T | 1 | a0001c0001t0003g0018 | 2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1146+2109C>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123474 | |||||||
| chr4:42123505 | T | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0061 |
2 | HG03710.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1146+2078A>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123505 | |||||||
| chr4:42123517 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1146+2066G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123517 | |||||||
| chr4:42123538 | C | T | 5 | a0001c0001t0010g0030 a0001c0001t0010g0032 a0001c0001t0010g0033 others(2): Show |
5 | HG02630.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1146+2045G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123538 | |||||||
| chr4:42123604 | A | G | 103 | a0001c0001t0001g0052 a0001c0001t0001g0126 a0001c0001t0002g0002 others(100): Show |
143 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(140): Show |
intron_variant | MODIFIER | c.1146+1979T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123604 | |||||||
| chr4:42123633 | T | C | 5 | a0001c0001t0016g0123 a0001c0001t0016g0133 a0001c0001t0025g0101 others(2): Show |
6 | HG01884.hp1 HG02055.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1146+1950A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123633 | |||||||
| chr4:42123693 | A | AG | 2 | a0001c0001t0005g0019 a0001c0001t0005g0022 |
4 | HG02451.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146+1889dupC | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123693 | |||||||
| chr4:42123694 | G | GA | 5 | a0001c0001t0001g0043 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
5 | HG01361.hp2 HG03225.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1146+1888dupT | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123694 | |||||||
| chr4:42123694 | G | GAA | 10 | a0001c0001t0001g0044 a0001c0001t0001g0129 a0001c0001t0003g0005 others(7): Show |
15 | HG01099.hp2 HG02027.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1146+1887_1146+188 others(6): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123694 | |||||||
| chr4:42123694 | G | GAAAAA | 4 | a0001c0001t0007g0014 a0001c0001t0007g0047 a0001c0001t0015g0094 others(1): Show |
5 | HG02886.hp1 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1146+1884_1146+188 others(9): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123694 | |||||||
| chr4:42123694 | G | GAAAAAAA others(5): Show |
1 | a0007c0006t0008g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1146+1888_1146+188 others(16): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123694 | |||||||
| chr4:42123694 | G | GAAAAAAA others(6): Show |
2 | a0001c0001t0008g0010 a0001c0001t0008g0083 |
4 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146+1888_1146+188 others(17): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123694 | |||||||
| chr4:42123694 | G | GAAAAAAA others(7): Show |
1 | a0001c0001t0008g0150 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1146+1888_1146+188 others(18): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123694 | |||||||
| chr4:42123695 | A | G | 8 | a0001c0001t0002g0110 a0001c0001t0005g0021 a0001c0001t0005g0107 others(5): Show |
9 | HG02258.hp2 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1146+1888T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123695 | |||||||
| chr4:42123696 | A | AAAAAAAA others(2): Show |
4 | a0001c0001t0016g0123 a0001c0001t0016g0133 a0002c0002t0017g0024 others(1): Show |
5 | HG01884.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1146+1886_1146+188 others(13): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123696 | |||||||
| chr4:42123700 | A | AAAAACAA others(7): Show |
18 | a0001c0001t0004g0020 a0001c0001t0004g0023 a0001c0001t0004g0097 others(15): Show |
22 | HG00738.hp2 HG01167.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1146+1882_1146+188 others(18): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123700 | |||||||
| chr4:42123701 | A | AAACAAAA others(10): Show |
1 | a0001c0001t0002g0130 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1146+1881_1146+188 others(21): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123701 | |||||||
| chr4:42123702 | A | AACAAAAA others(9): Show |
35 | a0001c0001t0001g0052 a0001c0001t0001g0126 a0001c0001t0002g0002 others(32): Show |
52 | HG00621.hp2 HG00735.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1146+1880_1146+188 others(20): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123702 | |||||||
| chr4:42123703 | A | AAACAAAA others(7): Show |
1 | a0001c0001t0008g0149 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1146+1879_1146+188 others(18): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123703 | |||||||
| chr4:42123703 | A | AAACAAAA others(6): Show |
2 | a0001c0001t0008g0147 a0001c0001t0008g0151 |
2 | NA18993.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1146+1879_1146+188 others(17): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123703 | |||||||
| chr4:42123703 | A | ACAAAAAA others(8): Show |
2 | a0001c0001t0002g0009 a0001c0001t0002g0136 |
4 | HG01255.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146+1879_1146+188 others(19): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123703 | |||||||
| chr4:42123704 | A | ACAAAAAA others(8): Show |
1 | a0001c0001t0004g0157 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1146+1878_1146+187 others(19): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123704 | |||||||
| chr4:42123705 | A | C | 18 | a0001c0001t0004g0020 a0001c0001t0004g0023 a0001c0001t0004g0097 others(15): Show |
22 | HG00738.hp2 HG01167.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1146+1878T>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123705 | |||||||
| chr4:42123706 | A | C | 1 | a0001c0010t0028g0121 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1146+1877T>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123706 | |||||||
| chr4:42123718 | C | A | 6 | a0001c0001t0014g0012 a0001c0001t0016g0123 a0001c0001t0016g0133 others(3): Show |
8 | HG01884.hp1 HG02055.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1146+1865G>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123718 | |||||||
| chr4:42123729 | G | T | 103 | a0001c0001t0001g0052 a0001c0001t0001g0126 a0001c0001t0002g0002 others(100): Show |
143 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(140): Show |
intron_variant | MODIFIER | c.1146+1854C>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123729 | |||||||
| chr4:42123825 | G | A | 1 | a0001c0001t0010g0099 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1146+1758C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123825 | |||||||
| chr4:42123828 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1146+1755C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123828 | |||||||
| chr4:42123884 | C | T | 1 | a0001c0004t0006g0115 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1146+1699G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123884 | |||||||
| chr4:42123902 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1146+1681C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123902 | |||||||
| chr4:42123946 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1146+1637C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123946 | |||||||
| chr4:42123984 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1146+1599G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42123984 | |||||||
| chr4:42124008 | G | T | 7 | a0001c0001t0008g0010 a0001c0001t0008g0083 a0001c0001t0008g0147 others(4): Show |
9 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1146+1575C>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42124008 | |||||||
| chr4:42124184 | A | G | 103 | a0001c0001t0001g0052 a0001c0001t0001g0126 a0001c0001t0002g0002 others(100): Show |
143 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(140): Show |
intron_variant | MODIFIER | c.1146+1399T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42124184 | |||||||
| chr4:42124326 | T | C | 13 | a0001c0001t0008g0010 a0001c0001t0008g0083 a0001c0001t0008g0147 others(10): Show |
17 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1146+1257A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42124326 | |||||||
| chr4:42124552 | G | T | 1 | a0001c0001t0002g0026 | 2 | HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1146+1031C>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42124552 | |||||||
| chr4:42124714 | C | G | 4 | a0001c0001t0016g0123 a0001c0001t0016g0133 a0002c0002t0017g0024 others(1): Show |
5 | HG01884.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1146+869G>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42124714 | |||||||
| chr4:42124720 | T | C | 1 | a0001c0001t0002g0092 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1146+863A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42124720 | |||||||
| chr4:42124860 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1146+723T>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42124860 | |||||||
| chr4:42124907 | A | G | 103 | a0001c0001t0001g0052 a0001c0001t0001g0126 a0001c0001t0002g0002 others(100): Show |
143 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(140): Show |
intron_variant | MODIFIER | c.1146+676T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42124907 | |||||||
| chr4:42124999 | A | C | 1 | a0009c0009t0004g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1146+584T>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42124999 | |||||||
| chr4:42125185 | T | A | 13 | a0001c0001t0008g0010 a0001c0001t0008g0083 a0001c0001t0008g0147 others(10): Show |
17 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1146+398A>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42125185 | |||||||
| chr4:42125212 | A | G | 103 | a0001c0001t0001g0052 a0001c0001t0001g0126 a0001c0001t0002g0002 others(100): Show |
143 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(140): Show |
intron_variant | MODIFIER | c.1146+371T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42125212 | |||||||
| chr4:42125304 | C | T | 13 | a0001c0001t0008g0010 a0001c0001t0008g0083 a0001c0001t0008g0147 others(10): Show |
17 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1146+279G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 4/5 | chr4 | 42125304 | |||||||
| chr4:42125991 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1055-317A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42125991 | |||||||
| chr4:42126004 | G | C | 4 | a0001c0001t0009g0011 a0001c0001t0009g0028 a0001c0001t0009g0162 others(1): Show |
7 | HG01891.hp1 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1055-330C>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42126004 | |||||||
| chr4:42126068 | C | CA | 7 | a0001c0001t0008g0010 a0001c0001t0008g0083 a0001c0001t0008g0147 others(4): Show |
9 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1055-395dupT | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42126068 | |||||||
| chr4:42126208 | G | C | 1 | a0009c0009t0004g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1055-534C>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42126208 | |||||||
| chr4:42126233 | G | T | 1 | a0001c0001t0002g0137 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1055-559C>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42126233 | |||||||
| chr4:42126306 | T | C | 1 | a0001c0001t0009g0011 | 3 | NA19043.hp1 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1055-632A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42126306 | |||||||
| chr4:42126629 | T | C | 5 | a0001c0001t0007g0003 a0001c0001t0007g0006 a0001c0001t0007g0014 others(2): Show |
10 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1055-955A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42126629 | |||||||
| chr4:42126650 | A | G | 11 | a0001c0001t0002g0110 a0001c0001t0005g0019 a0001c0001t0005g0021 others(8): Show |
15 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1055-976T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42126650 | |||||||
| chr4:42126738 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1055-1064C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42126738 | |||||||
| chr4:42126832 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1055-1158C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42126832 | |||||||
| chr4:42126856 | AAAAACAA others(3): Show |
A | 2 | a0001c0001t0001g0048 a0001c0010t0028g0121 |
2 | HG01433.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1055-1192_1055-118 others(14): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42126856 | |||||||
| chr4:42126958 | T | C | 1 | a0001c0001t0014g0012 | 2 | HG02896.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1055-1284A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42126958 | |||||||
| chr4:42126965 | G | C | 2 | a0001c0001t0015g0096 a0001c0008t0032g0161 |
2 | HG01515.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1055-1291C>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42126965 | |||||||
| chr4:42127409 | T | C | 8 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(5): Show |
13 | HG01099.hp2 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1055-1735A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42127409 | |||||||
| chr4:42127468 | C | A | 20 | a0001c0001t0004g0020 a0001c0001t0004g0023 a0001c0001t0004g0097 others(17): Show |
24 | HG00738.hp2 HG01167.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.1055-1794G>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42127468 | |||||||
| chr4:42127471 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1055-1797G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42127471 | |||||||
| chr4:42127545 | A | G | 1 | a0001c0001t0015g0096 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1055-1871T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42127545 | |||||||
| chr4:42127667 | G | A | 11 | a0001c0001t0002g0110 a0001c0001t0005g0019 a0001c0001t0005g0021 others(8): Show |
15 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1055-1993C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42127667 | |||||||
| chr4:42127763 | G | A | 5 | a0001c0001t0010g0030 a0001c0001t0010g0032 a0001c0001t0010g0033 others(2): Show |
5 | HG02630.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1055-2089C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42127763 | |||||||
| chr4:42127865 | T | C | 5 | a0001c0001t0016g0123 a0001c0001t0016g0133 a0001c0001t0025g0101 others(2): Show |
6 | HG01884.hp1 HG02055.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1055-2191A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42127865 | |||||||
| chr4:42127980 | C | T | 98 | a0001c0001t0001g0126 a0001c0001t0002g0002 a0001c0001t0002g0009 others(95): Show |
138 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(135): Show |
intron_variant | MODIFIER | c.1055-2306G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42127980 | |||||||
| chr4:42127986 | G | T | 2 | a0001c0001t0015g0096 a0001c0008t0032g0161 |
2 | HG01515.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1055-2312C>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42127986 | |||||||
| chr4:42128182 | C | T | 2 | a0001c0001t0002g0025 a0001c0001t0002g0127 |
3 | NA18944.hp2 NA18962.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1055-2508G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42128182 | |||||||
| chr4:42128315 | C | T | 1 | a0001c0001t0005g0109 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1055-2641G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42128315 | |||||||
| chr4:42128439 | C | G | 5 | a0001c0001t0007g0003 a0001c0001t0007g0006 a0001c0001t0007g0014 others(2): Show |
10 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1055-2765G>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42128439 | |||||||
| chr4:42128619 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1055-2945C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42128619 | |||||||
| chr4:42128766 | T | TACAA | 14 | a0001c0001t0001g0087 a0001c0001t0002g0110 a0001c0001t0005g0019 others(11): Show |
19 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1055-3096_1055-309 others(8): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42128766 | |||||||
| chr4:42128775 | A | C | 1 | a0001c0001t0003g0125 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1055-3101T>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42128775 | |||||||
| chr4:42128793 | G | A | 4 | a0001c0001t0016g0123 a0001c0001t0016g0133 a0002c0002t0017g0024 others(1): Show |
5 | HG01884.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055-3119C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42128793 | |||||||
| chr4:42128809 | G | A | 11 | a0001c0001t0002g0110 a0001c0001t0005g0019 a0001c0001t0005g0021 others(8): Show |
15 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1055-3135C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42128809 | |||||||
| chr4:42128828 | C | T | 7 | a0001c0001t0008g0010 a0001c0001t0008g0083 a0001c0001t0008g0147 others(4): Show |
9 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1055-3154G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42128828 | |||||||
| chr4:42128858 | C | G | 1 | a0001c0001t0001g0049 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1055-3184G>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42128858 | |||||||
| chr4:42129034 | C | T | 98 | a0001c0001t0001g0126 a0001c0001t0002g0002 a0001c0001t0002g0009 others(95): Show |
138 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(135): Show |
intron_variant | MODIFIER | c.1055-3360G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42129034 | |||||||
| chr4:42129063 | A | G | 7 | a0001c0001t0008g0010 a0001c0001t0008g0083 a0001c0001t0008g0147 others(4): Show |
9 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1055-3389T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42129063 | |||||||
| chr4:42129198 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1055-3524G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42129198 | |||||||
| chr4:42129236 | C | G | 2 | a0001c0001t0013g0035 a0001c0001t0013g0036 |
2 | HG00140.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1055-3562G>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42129236 | |||||||
| chr4:42129326 | A | G | 2 | a0002c0002t0017g0024 a0002c0002t0030g0132 |
3 | HG01884.hp1 HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1055-3652T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42129326 | |||||||
| chr4:42129329 | T | C | 10 | a0001c0001t0002g0110 a0001c0001t0005g0019 a0001c0001t0005g0021 others(7): Show |
13 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1055-3655A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42129329 | |||||||
| chr4:42129634 | GGGGAAAG others(4): Show |
G | 1 | a0001c0001t0002g0124 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1055-3971_1055-396 others(15): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42129634 | |||||||
| chr4:42129684 | C | T | 98 | a0001c0001t0001g0126 a0001c0001t0002g0002 a0001c0001t0002g0009 others(95): Show |
138 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(135): Show |
intron_variant | MODIFIER | c.1055-4010G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42129684 | |||||||
| chr4:42129805 | C | G | 16 | a0001c0001t0002g0110 a0001c0001t0005g0019 a0001c0001t0005g0021 others(13): Show |
21 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1055-4131G>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42129805 | |||||||
| chr4:42129974 | G | C | 1 | a0001c0001t0001g0079 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1055-4300C>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42129974 | |||||||
| chr4:42130256 | G | A | 1 | a0001c0003t0011g0029 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1055-4582C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42130256 | |||||||
| chr4:42130276 | C | A | 3 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 |
3 | HG02145.hp1 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1055-4602G>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42130276 | |||||||
| chr4:42130363 | C | A | 1 | a0001c0001t0001g0063 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1055-4689G>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42130363 | |||||||
| chr4:42130373 | G | A | 1 | a0001c0001t0007g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1055-4699C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42130373 | |||||||
| chr4:42130412 | G | A | 11 | a0001c0001t0002g0110 a0001c0001t0005g0019 a0001c0001t0005g0021 others(8): Show |
15 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1055-4738C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42130412 | |||||||
| chr4:42130445 | A | C | 11 | a0001c0001t0002g0110 a0001c0001t0005g0019 a0001c0001t0005g0021 others(8): Show |
15 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1055-4771T>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42130445 | |||||||
| chr4:42130458 | C | A | 1 | a0001c0001t0001g0063 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1055-4784G>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42130458 | |||||||
| chr4:42130475 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0075 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1055-4801C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42130475 | |||||||
| chr4:42130479 | C | CA | 44 | a0001c0001t0001g0078 a0001c0001t0001g0126 a0001c0001t0002g0002 others(41): Show |
70 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.1055-4806dupT | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42130479 | |||||||
| chr4:42130479 | C | CAA | 13 | a0001c0001t0002g0119 a0001c0001t0002g0127 a0001c0001t0002g0130 others(10): Show |
14 | HG01175.hp1 HG01257.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1055-4807_1055-480 others(6): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42130479 | |||||||
| chr4:42130479 | C | CAAA | 14 | a0001c0001t0004g0023 a0001c0001t0004g0097 a0001c0001t0004g0103 others(11): Show |
17 | HG00738.hp2 HG01167.hp2 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.1055-4808_1055-480 others(7): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42130479 | |||||||
| chr4:42130501 | T | A | 1 | a0001c0001t0004g0103 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1055-4827A>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42130501 | |||||||
| chr4:42130593 | A | C | 1 | a0001c0001t0005g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1055-4919T>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42130593 | |||||||
| chr4:42130677 | G | A | 3 | a0001c0001t0009g0028 a0001c0001t0009g0162 a0004c0005t0009g0160 |
4 | HG01891.hp1 HG02280.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1055-5003C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42130677 | |||||||
| chr4:42130712 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1055-5038C>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42130712 | |||||||
| chr4:42130727 | G | A | 5 | a0001c0001t0007g0003 a0001c0001t0007g0006 a0001c0001t0007g0014 others(2): Show |
10 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1055-5053C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42130727 | |||||||
| chr4:42130820 | T | C | 15 | a0001c0001t0002g0110 a0001c0001t0005g0019 a0001c0001t0005g0021 others(12): Show |
20 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1055-5146A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42130820 | |||||||
| chr4:42130895 | CGA | C | 96 | a0001c0001t0001g0126 a0001c0001t0002g0002 a0001c0001t0002g0009 others(93): Show |
136 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(133): Show |
intron_variant | MODIFIER | c.1055-5223_1055-522 others(6): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42130895 | |||||||
| chr4:42130933 | G | A | 15 | a0001c0001t0002g0110 a0001c0001t0005g0019 a0001c0001t0005g0021 others(12): Show |
20 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1055-5259C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42130933 | |||||||
| chr4:42131017 | G | A | 11 | a0001c0001t0002g0110 a0001c0001t0005g0019 a0001c0001t0005g0021 others(8): Show |
15 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1055-5343C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42131017 | |||||||
| chr4:42131064 | T | C | 7 | a0001c0001t0008g0010 a0001c0001t0008g0083 a0001c0001t0008g0147 others(4): Show |
9 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1055-5390A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42131064 | |||||||
| chr4:42131356 | C | T | 2 | a0001c0001t0015g0094 a0001c0001t0027g0145 |
2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1055-5682G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42131356 | |||||||
| chr4:42131441 | A | G | 7 | a0001c0001t0008g0010 a0001c0001t0008g0083 a0001c0001t0008g0147 others(4): Show |
9 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1055-5767T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42131441 | |||||||
| chr4:42131578 | CTCTT | C | 1 | a0001c0001t0003g0018 | 2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1055-5908_1055-590 others(8): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42131578 | |||||||
| chr4:42131930 | T | C | 26 | a0001c0001t0004g0020 a0001c0001t0004g0023 a0001c0001t0004g0097 others(23): Show |
30 | HG00738.hp2 HG01167.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.1055-6256A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42131930 | |||||||
| chr4:42132009 | A | G | 7 | a0001c0001t0008g0010 a0001c0001t0008g0083 a0001c0001t0008g0147 others(4): Show |
9 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1055-6335T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42132009 | |||||||
| chr4:42132049 | C | T | 98 | a0001c0001t0001g0126 a0001c0001t0002g0002 a0001c0001t0002g0009 others(95): Show |
138 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(135): Show |
intron_variant | MODIFIER | c.1055-6375G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42132049 | |||||||
| chr4:42132055 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1055-6381G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42132055 | |||||||
| chr4:42132154 | A | G | 8 | a0001c0001t0004g0020 a0001c0001t0004g0023 a0001c0001t0004g0105 others(5): Show |
10 | HG01257.hp2 HG02145.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1055-6480T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42132154 | |||||||
| chr4:42132219 | G | A | 4 | a0001c0001t0005g0107 a0001c0001t0005g0108 a0001c0001t0005g0111 others(1): Show |
4 | HG02922.hp2 HG02970.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1055-6545C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42132219 | |||||||
| chr4:42132319 | A | G | 15 | a0001c0001t0002g0110 a0001c0001t0005g0019 a0001c0001t0005g0021 others(12): Show |
20 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1055-6645T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42132319 | |||||||
| chr4:42132380 | T | C | 3 | a0001c0001t0008g0147 a0001c0001t0008g0149 a0001c0001t0008g0151 |
3 | NA18993.hp2 NA19007.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1055-6706A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42132380 | |||||||
| chr4:42132386 | C | G | 7 | a0001c0001t0008g0010 a0001c0001t0008g0083 a0001c0001t0008g0147 others(4): Show |
9 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1055-6712G>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42132386 | |||||||
| chr4:42132440 | A | ATTAT | 84 | a0001c0001t0001g0126 a0001c0001t0002g0002 a0001c0001t0002g0009 others(81): Show |
120 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(117): Show |
intron_variant | MODIFIER | c.1055-6770_1055-676 others(8): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42132440 | |||||||
| chr4:42132440 | A | ATTATTTA others(1): Show |
14 | a0001c0001t0002g0110 a0001c0001t0005g0019 a0001c0001t0005g0021 others(11): Show |
18 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1055-6774_1055-676 others(12): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42132440 | |||||||
| chr4:42132504 | G | A | 1 | a0001c0001t0007g0102 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1055-6830C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42132504 | |||||||
| chr4:42132514 | G | A | 7 | a0001c0001t0008g0010 a0001c0001t0008g0083 a0001c0001t0008g0147 others(4): Show |
9 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1055-6840C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42132514 | |||||||
| chr4:42132722 | G | C | 3 | a0001c0001t0010g0099 a0001c0001t0015g0096 a0001c0008t0032g0161 |
3 | HG01515.hp1 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1055-7048C>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42132722 | |||||||
| chr4:42132777 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG00609.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.1055-7103C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42132777 | |||||||
| chr4:42132793 | C | A | 1 | a0009c0009t0004g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1055-7119G>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42132793 | |||||||
| chr4:42132835 | A | G | 1 | a0001c0001t0002g0009 | 3 | HG02717.hp1 HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1055-7161T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42132835 | |||||||
| chr4:42133002 | C | T | 98 | a0001c0001t0001g0126 a0001c0001t0002g0002 a0001c0001t0002g0009 others(95): Show |
138 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(135): Show |
intron_variant | MODIFIER | c.1055-7328G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42133002 | |||||||
| chr4:42133042 | C | T | 3 | a0001c0001t0010g0032 a0001c0001t0010g0033 a0001c0001t0010g0034 |
3 | HG02630.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1055-7368G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42133042 | |||||||
| chr4:42133371 | T | G | 1 | a0001c0001t0001g0081 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1055-7697A>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42133371 | |||||||
| chr4:42133400 | C | T | 3 | a0001c0001t0010g0099 a0001c0001t0015g0096 a0001c0008t0032g0161 |
3 | HG01515.hp1 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1055-7726G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42133400 | |||||||
| chr4:42133438 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1055-7764T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42133438 | |||||||
| chr4:42133637 | G | A | 5 | a0001c0001t0011g0027 a0001c0001t0011g0140 a0001c0001t0011g0152 others(2): Show |
6 | HG00621.hp2 HG01123.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1055-7963C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42133637 | |||||||
| chr4:42133651 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1055-7977C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42133651 | |||||||
| chr4:42133703 | A | C | 1 | a0001c0001t0002g0122 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1055-8029T>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42133703 | |||||||
| chr4:42134317 | T | A | 1 | a0001c0001t0003g0143 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1055-8643A>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42134317 | |||||||
| chr4:42134599 | T | G | 1 | a0009c0009t0004g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1054+8829A>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42134599 | |||||||
| chr4:42134661 | G | A | 1 | a0001c0001t0006g0141 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1054+8767C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42134661 | |||||||
| chr4:42134715 | T | C | 1 | a0001c0001t0006g0141 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1054+8713A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42134715 | |||||||
| chr4:42134724 | C | A | 1 | a0001c0001t0002g0130 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1054+8704G>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42134724 | |||||||
| chr4:42135188 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1054+8240G>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42135188 | |||||||
| chr4:42135222 | C | T | 25 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(22): Show |
40 | HG00735.hp1 HG01074.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.1054+8206G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42135222 | |||||||
| chr4:42135254 | A | T | 1 | a0001c0001t0008g0149 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1054+8174T>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42135254 | |||||||
| chr4:42135286 | C | A | 1 | a0001c0001t0023g0069 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1054+8142G>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42135286 | |||||||
| chr4:42135407 | T | A | 1 | a0001c0003t0011g0029 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1054+8021A>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42135407 | |||||||
| chr4:42135439 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1054+7989A>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42135439 | |||||||
| chr4:42135539 | G | A | 1 | a0007c0006t0008g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1054+7889C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42135539 | |||||||
| chr4:42135569 | G | A | 1 | a0001c0001t0006g0104 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1054+7859C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42135569 | |||||||
| chr4:42135636 | G | A | 84 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(81): Show |
118 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(115): Show |
intron_variant | MODIFIER | c.1054+7792C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42135636 | |||||||
| chr4:42135647 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1054+7781G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42135647 | |||||||
| chr4:42135700 | G | A | 2 | a0001c0001t0015g0094 a0001c0001t0027g0145 |
2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1054+7728C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42135700 | |||||||
| chr4:42135785 | CCAAA | C | 7 | a0001c0001t0009g0011 a0001c0001t0009g0028 a0001c0001t0009g0162 others(4): Show |
10 | HG01515.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1054+7639_1054+764 others(8): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42135785 | |||||||
| chr4:42135796 | T | C | 1 | a0001c0001t0014g0012 | 2 | HG02896.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1054+7632A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42135796 | |||||||
| chr4:42135934 | C | T | 2 | a0001c0001t0003g0016 a0001c0001t0003g0017 |
4 | HG02258.hp1 HG02622.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054+7494G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42135934 | |||||||
| chr4:42135937 | A | G | 1 | a0001c0001t0002g0144 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1054+7491T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42135937 | |||||||
| chr4:42135945 | T | G | 2 | a0001c0001t0015g0094 a0001c0001t0027g0145 |
2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1054+7483A>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42135945 | |||||||
| chr4:42136146 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0075 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1054+7282T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42136146 | |||||||
| chr4:42136687 | C | T | 7 | a0001c0001t0009g0011 a0001c0001t0009g0028 a0001c0001t0009g0162 others(4): Show |
10 | HG01515.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1054+6741G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42136687 | |||||||
| chr4:42136760 | C | T | 1 | a0001c0001t0024g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1054+6668G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42136760 | |||||||
| chr4:42136797 | A | G | 1 | a0001c0001t0006g0118 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1054+6631T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42136797 | |||||||
| chr4:42136846 | C | A | 1 | a0001c0001t0010g0030 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1054+6582G>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42136846 | |||||||
| chr4:42136938 | G | A | 1 | a0001c0001t0018g0071 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1054+6490C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42136938 | |||||||
| chr4:42137115 | A | G | 83 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(80): Show |
117 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(114): Show |
intron_variant | MODIFIER | c.1054+6313T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42137115 | |||||||
| chr4:42137276 | C | T | 1 | a0001c0001t0010g0030 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1054+6152G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42137276 | |||||||
| chr4:42137561 | C | T | 2 | a0001c0001t0005g0107 a0001c0001t0005g0108 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1054+5867G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42137561 | |||||||
| chr4:42137652 | A | T | 1 | a0001c0001t0004g0105 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1054+5776T>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42137652 | |||||||
| chr4:42137666 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1054+5762T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42137666 | |||||||
| chr4:42137724 | G | A | 3 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 |
3 | HG02145.hp1 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1054+5704C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42137724 | |||||||
| chr4:42137935 | A | G | 1 | a0001c0001t0010g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1054+5493T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42137935 | |||||||
| chr4:42138043 | C | G | 7 | a0001c0001t0009g0011 a0001c0001t0009g0028 a0001c0001t0009g0162 others(4): Show |
10 | HG01515.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1054+5385G>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42138043 | |||||||
| chr4:42138050 | A | G | 36 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(33): Show |
54 | HG00642.hp2 HG00735.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.1054+5378T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42138050 | |||||||
| chr4:42138097 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1054+5331C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42138097 | |||||||
| chr4:42138192 | A | T | 1 | a0007c0006t0008g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1054+5236T>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42138192 | |||||||
| chr4:42138371 | T | G | 36 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(33): Show |
54 | HG00642.hp2 HG00735.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.1054+5057A>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42138371 | |||||||
| chr4:42138372 | T | A | 36 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(33): Show |
54 | HG00642.hp2 HG00735.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.1054+5056A>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42138372 | |||||||
| chr4:42138373 | C | A | 36 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(33): Show |
54 | HG00642.hp2 HG00735.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.1054+5055G>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42138373 | |||||||
| chr4:42138656 | A | C | 36 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(33): Show |
54 | HG00642.hp2 HG00735.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.1054+4772T>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42138656 | |||||||
| chr4:42138827 | A | G | 1 | a0006c0011t0002g0134 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1054+4601T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42138827 | |||||||
| chr4:42138881 | G | A | 1 | a0001c0001t0002g0131 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1054+4547C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42138881 | |||||||
| chr4:42138942 | T | TAGCTTAC others(6): Show |
1 | a0001c0001t0008g0149 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1054+4473_1054+448 others(17): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42138942 | |||||||
| chr4:42139019 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1054+4409C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42139019 | |||||||
| chr4:42139020 | T | G | 3 | a0001c0001t0003g0095 a0001c0001t0015g0094 a0001c0001t0027g0145 |
3 | HG01099.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1054+4408A>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42139020 | |||||||
| chr4:42139139 | A | G | 1 | a0001c0001t0014g0012 | 2 | HG02896.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1054+4289T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42139139 | |||||||
| chr4:42139347 | T | C | 1 | a0001c0001t0026g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1054+4081A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42139347 | |||||||
| chr4:42139371 | C | T | 7 | a0001c0001t0009g0011 a0001c0001t0009g0028 a0001c0001t0009g0162 others(4): Show |
10 | HG01515.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1054+4057G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42139371 | |||||||
| chr4:42139566 | T | TC | 8 | a0001c0001t0002g0148 a0001c0001t0008g0010 a0001c0001t0008g0147 others(5): Show |
10 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1054+3861dupG | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42139566 | |||||||
| chr4:42139592 | A | G | 7 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(4): Show |
12 | HG00738.hp2 HG01099.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.1054+3836T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42139592 | |||||||
| chr4:42139651 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1054+3777C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42139651 | |||||||
| chr4:42139654 | A | G | 36 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(33): Show |
54 | HG00642.hp2 HG00735.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.1054+3774T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42139654 | |||||||
| chr4:42139716 | T | G | 3 | a0001c0001t0010g0032 a0001c0001t0010g0033 a0001c0001t0010g0034 |
3 | HG02630.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1054+3712A>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42139716 | |||||||
| chr4:42139850 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1054+3578A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42139850 | |||||||
| chr4:42140096 | G | C | 3 | a0001c0001t0002g0137 a0001c0001t0002g0138 a0001c0001t0002g0139 |
3 | HG00738.hp1 HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1054+3332C>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42140096 | |||||||
| chr4:42140144 | C | T | 1 | a0001c0001t0003g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1054+3284G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42140144 | |||||||
| chr4:42140392 | G | T | 1 | a0001c0001t0008g0149 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1054+3036C>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42140392 | |||||||
| chr4:42140450 | C | T | 3 | a0001c0001t0004g0020 a0001c0001t0004g0105 a0001c0001t0004g0106 |
4 | HG03139.hp2 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1054+2978G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42140450 | |||||||
| chr4:42140647 | A | T | 1 | a0001c0001t0001g0042 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1054+2781T>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42140647 | |||||||
| chr4:42140676 | G | A | 1 | a0001c0001t0020g0076 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1054+2752C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42140676 | |||||||
| chr4:42140752 | A | G | 27 | a0001c0001t0002g0110 a0001c0001t0004g0020 a0001c0001t0004g0105 others(24): Show |
33 | HG01167.hp2 HG02109.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.1054+2676T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42140752 | |||||||
| chr4:42140991 | T | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA18973.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1054+2437A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42140991 | |||||||
| chr4:42141017 | CT | C | 7 | a0001c0001t0009g0011 a0001c0001t0009g0028 a0001c0001t0009g0162 others(4): Show |
10 | HG01515.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1054+2410delA | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42141017 | |||||||
| chr4:42141115 | T | C | 2 | a0001c0001t0004g0023 a0001c0001t0026g0098 |
3 | HG02572.hp2 NA18973.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1054+2313A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42141115 | |||||||
| chr4:42141268 | T | C | 1 | a0001c0001t0026g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1054+2160A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42141268 | |||||||
| chr4:42141300 | A | T | 1 | a0001c0001t0001g0041 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1054+2128T>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42141300 | |||||||
| chr4:42141404 | G | C | 1 | a0001c0001t0002g0082 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1054+2024C>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42141404 | |||||||
| chr4:42141433 | A | G | 2 | a0001c0001t0015g0094 a0001c0001t0027g0145 |
2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1054+1995T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42141433 | |||||||
| chr4:42141449 | T | C | 1 | a0002c0002t0030g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1054+1979A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42141449 | |||||||
| chr4:42141507 | G | A | 1 | a0001c0001t0014g0012 | 2 | HG02896.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1054+1921C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42141507 | |||||||
| chr4:42141694 | C | T | 37 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(34): Show |
55 | HG00642.hp2 HG00735.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.1054+1734G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42141694 | |||||||
| chr4:42141766 | A | G | 1 | a0001c0001t0014g0012 | 2 | HG02896.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1054+1662T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42141766 | |||||||
| chr4:42142024 | C | A | 1 | a0001c0001t0001g0038 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1054+1404G>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42142024 | |||||||
| chr4:42142065 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1054+1363C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42142065 | |||||||
| chr4:42142079 | A | G | 27 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(24): Show |
42 | HG00735.hp1 HG01074.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.1054+1349T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42142079 | |||||||
| chr4:42142081 | T | A | 27 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(24): Show |
42 | HG00735.hp1 HG01074.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.1054+1347A>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42142081 | |||||||
| chr4:42142095 | C | T | 7 | a0001c0001t0009g0011 a0001c0001t0009g0028 a0001c0001t0009g0162 others(4): Show |
10 | HG01515.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1054+1333G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42142095 | |||||||
| chr4:42142457 | T | TA | 7 | a0001c0001t0009g0011 a0001c0001t0009g0028 a0001c0001t0009g0162 others(4): Show |
10 | HG01515.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1054+970dupT | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42142457 | |||||||
| chr4:42142465 | AT | A | 83 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(80): Show |
116 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(113): Show |
intron_variant | MODIFIER | c.1054+962delA | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42142465 | |||||||
| chr4:42142465 | ATATATAT | A | 1 | a0001c0001t0014g0012 | 2 | HG02896.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1054+956_1054+962d others(9): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42142465 | |||||||
| chr4:42142466 | T | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0091 others(1): Show |
4 | HG01358.hp2 HG02132.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1054+962A>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42142466 | |||||||
| chr4:42142468 | T | A | 12 | a0001c0001t0002g0009 a0001c0001t0002g0136 a0001c0001t0002g0137 others(9): Show |
15 | HG00621.hp2 HG00738.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.1054+960A>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42142468 | |||||||
| chr4:42142636 | C | CA | 13 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0087 others(10): Show |
15 | HG00642.hp1 HG00642.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.1054+791dupT | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42142636 | |||||||
| chr4:42142636 | CA | C | 17 | a0001c0001t0002g0110 a0001c0001t0005g0019 a0001c0001t0005g0021 others(14): Show |
22 | HG01167.hp2 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1054+791delT | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42142636 | |||||||
| chr4:42142677 | TA | T | 13 | a0001c0001t0002g0148 a0001c0001t0003g0005 a0001c0001t0003g0016 others(10): Show |
20 | HG00738.hp2 HG01099.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.1054+750delT | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42142677 | |||||||
| chr4:42142875 | G | T | 1 | a0001c0001t0001g0040 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1054+553C>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42142875 | |||||||
| chr4:42142949 | A | G | 38 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(35): Show |
56 | HG00642.hp2 HG00735.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.1054+479T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42142949 | |||||||
| chr4:42143045 | G | A | 2 | a0001c0001t0008g0151 a0001c0001t0011g0152 |
2 | NA19007.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1054+383C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42143045 | |||||||
| chr4:42143054 | C | T | 1 | a0001c0001t0006g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1054+374G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42143054 | |||||||
| chr4:42143214 | C | T | 9 | a0001c0001t0002g0110 a0001c0001t0005g0021 a0001c0001t0005g0022 others(6): Show |
11 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1054+214G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42143214 | |||||||
| chr4:42143234 | T | G | 1 | a0001c0001t0002g0082 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1054+194A>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42143234 | |||||||
| chr4:42143285 | T | C | 1 | a0001c0001t0010g0030 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1054+143A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42143285 | |||||||
| chr4:42143417 | T | C | 1 | a0001c0001t0008g0083 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1054+11A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 3/5 | chr4 | 42143417 | |||||||
| chr4:42144519 | G | T | 1 | a0001c0001t0002g0009 | 3 | HG02717.hp1 HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.488-525C>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42144519 | |||||||
| chr4:42144640 | T | C | 95 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(92): Show |
132 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(129): Show |
intron_variant | MODIFIER | c.488-646A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42144640 | |||||||
| chr4:42144674 | T | G | 2 | a0001c0001t0013g0035 a0001c0001t0013g0036 |
2 | HG00140.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.488-680A>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42144674 | |||||||
| chr4:42145357 | G | C | 1 | a0007c0006t0008g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.488-1363C>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42145357 | |||||||
| chr4:42145443 | T | C | 2 | a0001c0001t0001g0085 a0001c0001t0021g0086 |
2 | HG01175.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.488-1449A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42145443 | |||||||
| chr4:42145560 | C | T | 1 | a0001c0001t0004g0023 | 2 | NA18973.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.488-1566G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42145560 | |||||||
| chr4:42145569 | G | A | 8 | a0001c0001t0002g0148 a0001c0001t0008g0010 a0001c0001t0008g0147 others(5): Show |
10 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.488-1575C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42145569 | |||||||
| chr4:42145689 | C | CA | 20 | a0001c0001t0001g0087 a0001c0001t0002g0009 a0001c0001t0002g0136 others(17): Show |
29 | HG00621.hp2 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.488-1696dupT | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42145689 | |||||||
| chr4:42145689 | CA | C | 41 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(38): Show |
61 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.488-1696delT | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42145689 | |||||||
| chr4:42145716 | T | C | 1 | a0001c0001t0014g0012 | 2 | HG02896.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.488-1722A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42145716 | |||||||
| chr4:42145748 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.488-1754A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42145748 | |||||||
| chr4:42145835 | G | C | 7 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0017 others(4): Show |
12 | HG00738.hp2 HG01099.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.488-1841C>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42145835 | |||||||
| chr4:42146279 | C | T | 2 | a0001c0001t0007g0006 a0001c0001t0026g0098 |
4 | HG01884.hp2 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-2285G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42146279 | |||||||
| chr4:42146468 | C | T | 1 | a0001c0010t0028g0121 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.488-2474G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42146468 | |||||||
| chr4:42146477 | G | A | 1 | a0001c0001t0002g0144 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.488-2483C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42146477 | |||||||
| chr4:42146504 | A | T | 1 | a0001c0001t0006g0118 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.488-2510T>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42146504 | |||||||
| chr4:42146557 | A | G | 1 | a0001c0001t0006g0118 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.488-2563T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42146557 | |||||||
| chr4:42146586 | A | AT | 54 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(51): Show |
77 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.488-2593dupA | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42146586 | |||||||
| chr4:42146590 | TTTTACTT others(4): Show |
T | 2 | a0001c0001t0007g0006 a0001c0001t0026g0098 |
4 | HG01884.hp2 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-2607_488-2597d others(13): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42146590 | |||||||
| chr4:42146657 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.488-2663A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42146657 | |||||||
| chr4:42146685 | T | G | 12 | a0001c0001t0002g0009 a0001c0001t0002g0136 a0001c0001t0002g0137 others(9): Show |
15 | HG00621.hp2 HG00738.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.488-2691A>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42146685 | |||||||
| chr4:42146828 | G | A | 8 | a0001c0001t0002g0148 a0001c0001t0008g0010 a0001c0001t0008g0147 others(5): Show |
10 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.488-2834C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42146828 | |||||||
| chr4:42147060 | G | C | 16 | a0001c0001t0002g0110 a0001c0001t0005g0019 a0001c0001t0005g0021 others(13): Show |
21 | HG01167.hp2 HG02109.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.488-3066C>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42147060 | |||||||
| chr4:42147095 | T | G | 1 | a0001c0001t0014g0012 | 2 | HG02896.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.488-3101A>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42147095 | |||||||
| chr4:42147179 | T | A | 1 | a0001c0001t0001g0090 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.488-3185A>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42147179 | |||||||
| chr4:42147242 | G | A | 12 | a0001c0001t0002g0009 a0001c0001t0002g0136 a0001c0001t0002g0137 others(9): Show |
15 | HG00621.hp2 HG00738.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.488-3248C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42147242 | |||||||
| chr4:42147335 | C | G | 2 | a0001c0001t0007g0006 a0001c0001t0026g0098 |
4 | HG01884.hp2 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-3341G>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42147335 | |||||||
| chr4:42147418 | A | T | 1 | a0001c0001t0001g0038 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.488-3424T>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42147418 | |||||||
| chr4:42147481 | C | CT | 9 | a0001c0001t0001g0037 a0001c0001t0003g0005 a0001c0001t0003g0016 others(6): Show |
14 | HG00738.hp2 HG01099.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.488-3488dupA | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42147481 | |||||||
| chr4:42147481 | CT | C | 46 | a0001c0001t0001g0091 a0001c0001t0001g0126 a0001c0001t0001g0128 others(43): Show |
67 | HG00642.hp2 HG00735.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.488-3488delA | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42147481 | |||||||
| chr4:42147605 | A | G | 2 | a0001c0001t0003g0100 a0001c0001t0025g0101 |
2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.488-3611T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42147605 | |||||||
| chr4:42147652 | C | A | 1 | a0001c0001t0010g0030 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.488-3658G>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42147652 | |||||||
| chr4:42147745 | G | A | 1 | a0001c0001t0007g0102 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.488-3751C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42147745 | |||||||
| chr4:42147749 | A | T | 1 | a0001c0001t0003g0016 | 2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.488-3755T>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42147749 | |||||||
| chr4:42147963 | C | T | 1 | a0001c0001t0011g0140 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.487+3694G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42147963 | |||||||
| chr4:42147978 | G | A | 2 | a0001c0001t0010g0099 a0001c0001t0015g0096 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.487+3679C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42147978 | |||||||
| chr4:42148011 | T | C | 2 | a0001c0001t0003g0100 a0001c0001t0025g0101 |
2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.487+3646A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42148011 | |||||||
| chr4:42148058 | G | T | 1 | a0001c0001t0009g0011 | 3 | NA19043.hp1 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.487+3599C>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42148058 | |||||||
| chr4:42148136 | ATTAAT | A | 22 | a0001c0001t0002g0110 a0001c0001t0004g0020 a0001c0001t0004g0105 others(19): Show |
28 | HG01167.hp2 HG02109.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.487+3516_487+3520d others(7): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42148136 | |||||||
| chr4:42148181 | T | C | 1 | a0001c0001t0005g0116 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.487+3476A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42148181 | |||||||
| chr4:42148196 | C | G | 92 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(89): Show |
128 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(125): Show |
intron_variant | MODIFIER | c.487+3461G>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42148196 | |||||||
| chr4:42148251 | T | A | 2 | a0001c0001t0015g0094 a0001c0001t0027g0145 |
2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.487+3406A>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42148251 | |||||||
| chr4:42148595 | C | T | 1 | a0001c0001t0002g0146 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.487+3062G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42148595 | |||||||
| chr4:42148627 | T | C | 1 | a0001c0001t0012g0008 | 3 | HG00735.hp1 HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.487+3030A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42148627 | |||||||
| chr4:42148757 | A | G | 92 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(89): Show |
128 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(125): Show |
intron_variant | MODIFIER | c.487+2900T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42148757 | |||||||
| chr4:42149066 | C | T | 1 | a0001c0001t0004g0154 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.487+2591G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42149066 | |||||||
| chr4:42149087 | C | A | 1 | a0001c0001t0006g0118 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.487+2570G>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42149087 | |||||||
| chr4:42149095 | G | A | 54 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(51): Show |
77 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.487+2562C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42149095 | |||||||
| chr4:42149191 | A | AC | 16 | a0001c0001t0001g0013 a0001c0001t0002g0009 a0001c0001t0002g0120 others(13): Show |
21 | HG00621.hp2 HG00738.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.487+2465dupG | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42149191 | |||||||
| chr4:42149289 | C | G | 92 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(89): Show |
128 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(125): Show |
intron_variant | MODIFIER | c.487+2368G>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42149289 | |||||||
| chr4:42149448 | C | T | 4 | a0001c0001t0007g0102 a0001c0001t0010g0032 a0001c0001t0010g0033 others(1): Show |
4 | HG02451.hp1 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+2209G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42149448 | |||||||
| chr4:42149553 | G | C | 2 | a0001c0001t0003g0100 a0001c0001t0025g0101 |
2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.487+2104C>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42149553 | |||||||
| chr4:42149697 | G | T | 1 | a0001c0001t0004g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.487+1960C>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42149697 | |||||||
| chr4:42149815 | A | G | 12 | a0001c0001t0002g0009 a0001c0001t0002g0136 a0001c0001t0002g0137 others(9): Show |
15 | HG00621.hp2 HG00738.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.487+1842T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42149815 | |||||||
| chr4:42149985 | A | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0136 a0001c0001t0002g0137 others(2): Show |
7 | HG00738.hp1 HG01255.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.487+1672T>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42149985 | |||||||
| chr4:42150140 | A | T | 2 | a0001c0001t0013g0035 a0001c0001t0013g0036 |
2 | HG00140.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.487+1517T>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42150140 | |||||||
| chr4:42150170 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.487+1487G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42150170 | |||||||
| chr4:42150205 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.487+1452C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42150205 | |||||||
| chr4:42150334 | C | A | 25 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(22): Show |
40 | HG00735.hp1 HG01074.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.487+1323G>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42150334 | |||||||
| chr4:42150359 | TCAAA | T | 94 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(91): Show |
130 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(127): Show |
intron_variant | MODIFIER | c.487+1294_487+1297d others(6): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42150359 | |||||||
| chr4:42150488 | G | A | 13 | a0001c0001t0002g0009 a0001c0001t0002g0136 a0001c0001t0002g0137 others(10): Show |
16 | HG00621.hp2 HG00738.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.487+1169C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42150488 | |||||||
| chr4:42150533 | A | G | 95 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(92): Show |
132 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(129): Show |
intron_variant | MODIFIER | c.487+1124T>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42150533 | |||||||
| chr4:42150571 | T | G | 2 | a0001c0001t0003g0100 a0001c0001t0025g0101 |
2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.487+1086A>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42150571 | |||||||
| chr4:42150587 | G | A | 1 | a0001c0001t0002g0146 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.487+1070C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42150587 | |||||||
| chr4:42150603 | T | C | 1 | a0009c0009t0004g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.487+1054A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42150603 | |||||||
| chr4:42150670 | T | G | 4 | a0001c0001t0007g0102 a0001c0001t0010g0032 a0001c0001t0010g0033 others(1): Show |
4 | HG02451.hp1 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+987A>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42150670 | |||||||
| chr4:42150702 | G | C | 8 | a0001c0001t0002g0148 a0001c0001t0008g0010 a0001c0001t0008g0147 others(5): Show |
10 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.487+955C>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42150702 | |||||||
| chr4:42150745 | T | C | 1 | a0001c0001t0004g0103 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.487+912A>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42150745 | |||||||
| chr4:42150751 | G | C | 93 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(90): Show |
129 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(126): Show |
intron_variant | MODIFIER | c.487+906C>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42150751 | |||||||
| chr4:42151055 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.487+602C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42151055 | |||||||
| chr4:42151064 | C | A | 23 | a0001c0001t0002g0110 a0001c0001t0004g0020 a0001c0001t0004g0105 others(20): Show |
29 | HG01167.hp2 HG02109.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.487+593G>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42151064 | |||||||
| chr4:42151217 | G | A | 1 | a0001c0001t0004g0154 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.487+440C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42151217 | |||||||
| chr4:42151242 | G | A | 53 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(50): Show |
76 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.487+415C>T | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42151242 | |||||||
| chr4:42151344 | CGGG | C | 94 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(91): Show |
130 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(127): Show |
intron_variant | MODIFIER | c.487+310_487+312del others(3): Show |
BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42151344 | |||||||
| chr4:42151394 | C | G | 3 | a0001c0001t0010g0032 a0001c0001t0010g0033 a0001c0001t0010g0034 |
3 | HG02630.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.487+263G>C | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42151394 | |||||||
| chr4:42151396 | G | C | 3 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 |
3 | HG02145.hp1 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.487+261C>G | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42151396 | |||||||
| chr4:42151490 | G | T | 1 | a0001c0001t0001g0031 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.487+167C>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42151490 | |||||||
| chr4:42151538 | C | T | 1 | a0001c0001t0010g0030 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.487+119G>A | BEND4 | ENSG00000188848.17 | transcript | ENST00000502486.6 | protein_coding | 2/5 | chr4 | 42151538 |