Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 199870 |
| ensemblid | ENSG00000009780.16 |
| hgncid | 28530 |
| symbol | FAM76A |
| name | family with sequence similarity 76 member A |
| refseq_nuc | NM_152660.3 |
| refseq_prot | NP_689873.1 |
| ensembl_nuc | ENST00000373954.11 |
| ensembl_prot | ENSP00000363065.5 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 27725961 |
| end | 27763116 |
| strand | + |
| ver | v1.2 |
| region | chr1:27725961-27763116 |
| region5000 | chr1:27720961-27768116 |
| regionname0 | FAM76A_chr1_27725961_27763116 |
| regionname5000 | FAM76A_chr1_27720961_27768116 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 307 | 258 | 88 | 38 | 100 | 4 | 28 | 66 | FAM76A_chr1_27720961_27768116 | FAM76A | MAALY others(302): Show |
chr1 | 27720961 | 27768116 |
| a0002 | 0/0 | 307 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | MAALY others(302): Show |
chr1 | 27720961 | 27768116 |
| a0003 | 0/0 | 307 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | MAALY others(302): Show |
chr1 | 27720961 | 27768116 |
| a0004 | 0/0 | 307 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | MAALY others(302): Show |
chr1 | 27720961 | 27768116 |
| a0005 | 0/0 | 307 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | MAALY others(302): Show |
chr1 | 27720961 | 27768116 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 921 | 152 | 33 | 30 | 64 | 4 | 21 | FAM76A_chr1_27720961_27768116 | FAM76A | ATGGC others(916): Show |
chr1 | 27720961 | 27768116 | ||
| a0001c0002 | 0/0 | 921 | 105 | 54 | 8 | 36 | 0 | 7 | FAM76A_chr1_27720961_27768116 | FAM76A | ATGGC others(916): Show |
chr1 | 27720961 | 27768116 | ||
| a0001c0007 | 0/0 | 921 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | ATGGC others(916): Show |
chr1 | 27720961 | 27768116 | ||
| a0002c0003 | 0/0 | 921 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | ATGGC others(916): Show |
chr1 | 27720961 | 27768116 | ||
| a0003c0004 | 0/0 | 921 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | ATGGC others(916): Show |
chr1 | 27720961 | 27768116 | ||
| a0004c0005 | 0/0 | 921 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | ATGGC others(916): Show |
chr1 | 27720961 | 27768116 | ||
| a0005c0006 | 0/0 | 921 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | ATGGC others(916): Show |
chr1 | 27720961 | 27768116 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3578 | 115 | 25 | 26 | 48 | 2 | 14 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3573): Show |
chr1 | 27720961 | 27768116 |
| a0001c0001t0005 | 0/0 | 3579 | 9 | 4 | 1 | 4 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3574): Show |
chr1 | 27720961 | 27768116 |
| a0001c0001t0006 | 0/0 | 3579 | 8 | 0 | 1 | 7 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3574): Show |
chr1 | 27720961 | 27768116 |
| a0001c0001t0007 | 0/0 | 3577 | 6 | 1 | 0 | 1 | 2 | 2 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3572): Show |
chr1 | 27720961 | 27768116 |
| a0001c0001t0010 | 0/0 | 3580 | 3 | 1 | 0 | 1 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3575): Show |
chr1 | 27720961 | 27768116 |
| a0001c0001t0011 | 0/0 | 3578 | 3 | 0 | 0 | 0 | 0 | 3 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3573): Show |
chr1 | 27720961 | 27768116 |
| a0001c0001t0014 | 0/0 | 3578 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3573): Show |
chr1 | 27720961 | 27768116 |
| a0001c0001t0015 | 0/0 | 3579 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3574): Show |
chr1 | 27720961 | 27768116 |
| a0001c0001t0029 | 0/0 | 3578 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3573): Show |
chr1 | 27720961 | 27768116 |
| a0001c0001t0032 | 0/0 | 3578 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3573): Show |
chr1 | 27720961 | 27768116 |
| a0001c0001t0033 | 0/0 | 3578 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3573): Show |
chr1 | 27720961 | 27768116 |
| a0001c0001t0041 | 0/0 | 3579 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3574): Show |
chr1 | 27720961 | 27768116 |
| a0001c0001t0042 | 0/0 | 3580 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3575): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0002 | 0/0 | 3581 | 45 | 9 | 1 | 29 | 0 | 6 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3576): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0003 | 0/0 | 3579 | 12 | 10 | 2 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3574): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0004 | 0/0 | 3582 | 11 | 8 | 3 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3577): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0008 | 0/0 | 3581 | 4 | 4 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3576): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0009 | 0/0 | 3580 | 4 | 3 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3575): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0012 | 0/0 | 3581 | 3 | 3 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3576): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0013 | 0/0 | 3582 | 3 | 1 | 0 | 2 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3577): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0016 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3578): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0017 | 0/0 | 3580 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3575): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0018 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3576): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0019 | 0/0 | 3580 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3575): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0020 | 0/0 | 3580 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3575): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0021 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3576): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0022 | 0/0 | 3580 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3575): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0023 | 0/0 | 3580 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3575): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0024 | 0/0 | 3580 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3575): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0025 | 0/0 | 3578 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3573): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0026 | 0/0 | 3582 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3577): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0027 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3577): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0028 | 0/0 | 3579 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3574): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0030 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3576): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0031 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3576): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0034 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3577): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0035 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3576): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0037 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3574): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0038 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3578): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0039 | 0/0 | 3582 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3577): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0040 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3578): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0043 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3576): Show |
chr1 | 27720961 | 27768116 |
| a0001c0002t0044 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3576): Show |
chr1 | 27720961 | 27768116 |
| a0001c0007t0008 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3576): Show |
chr1 | 27720961 | 27768116 |
| a0002c0003t0010 | 0/0 | 3580 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3575): Show |
chr1 | 27720961 | 27768116 |
| a0003c0004t0036 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3576): Show |
chr1 | 27720961 | 27768116 |
| a0004c0005t0001 | 0/0 | 3578 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3573): Show |
chr1 | 27720961 | 27768116 |
| a0005c0006t0001 | 0/0 | 3578 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | GCCTG others(3573): Show |
chr1 | 27720961 | 27768116 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0007g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0007g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0007g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0007g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0010g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0010g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0010g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0011g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0011g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0011g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0014g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0014g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0015g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0029g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0032g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0033g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0041g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0001t0042g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0003g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0004g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0004g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0008g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0008g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0008g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0008g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0009g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0009g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0009g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0012g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0012g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0012g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0013g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0013g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0013g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0016g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0017g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0018g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0019g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0020g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0021g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0022g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0023g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0024g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0025g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0026g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0027g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0028g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0030g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0031g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0034g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0035g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0037g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0038g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0039g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0040g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0043g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0002t0044g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0001c0007t0008g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0002c0003t0010g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0003c0004t0036g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0004c0005t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| a0005c0006t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG00609 | hp2 | a0001 | c0001 | t0006 | g0111 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG00621 | hp1 | a0001 | c0001 | t0006 | g0143 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG00639 | hp2 | a0001 | c0002 | t0003 | g0027 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG00741 | hp1 | a0001 | c0001 | t0042 | g0110 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0185 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0026 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01069 | hp2 | a0001 | c0002 | t0004 | g0015 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01071 | hp1 | a0001 | c0002 | t0004 | g0015 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01106 | hp1 | a0001 | c0002 | t0003 | g0071 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0134 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01243 | hp1 | a0001 | c0002 | t0019 | g0074 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01243 | hp2 | a0001 | c0002 | t0004 | g0016 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01255 | hp1 | a0001 | c0001 | t0015 | g0201 | AMR | CLM | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01255 | hp2 | a0001 | c0002 | t0026 | g0033 | AMR | CLM | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01515 | hp1 | a0001 | c0001 | t0007 | g0009 | EUR | IBS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01515 | hp2 | a0001 | c0001 | t0007 | g0155 | EUR | IBS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01884 | hp1 | a0001 | c0002 | t0003 | g0002 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0036 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01891 | hp1 | a0001 | c0002 | t0004 | g0213 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02055 | hp1 | a0001 | c0002 | t0021 | g0075 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02055 | hp2 | a0001 | c0002 | t0016 | g0208 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02074 | hp1 | a0001 | c0001 | t0006 | g0184 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02129 | hp1 | a0001 | c0002 | t0013 | g0004 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02145 | hp2 | a0001 | c0002 | t0003 | g0073 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CDX | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | CDX | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CDX | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CDX | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02257 | hp1 | a0001 | c0002 | t0003 | g0076 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02257 | hp2 | a0001 | c0002 | t0004 | g0211 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02258 | hp1 | a0001 | c0002 | t0012 | g0024 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02258 | hp2 | a0001 | c0002 | t0027 | g0217 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02280 | hp1 | a0001 | c0001 | t0010 | g0084 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02451 | hp1 | a0001 | c0002 | t0037 | g0230 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02451 | hp2 | a0001 | c0002 | t0044 | g0038 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0160 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02572 | hp1 | a0001 | c0002 | t0008 | g0215 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02572 | hp2 | a0001 | c0002 | t0013 | g0032 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02615 | hp1 | a0001 | c0002 | t0020 | g0018 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02615 | hp2 | a0001 | c0001 | t0032 | g0129 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02622 | hp2 | a0001 | c0002 | t0004 | g0206 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0067 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0034 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02647 | hp2 | a0001 | c0002 | t0030 | g0212 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0064 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02698 | hp1 | a0001 | c0001 | t0011 | g0197 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02698 | hp2 | a0001 | c0001 | t0007 | g0106 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0070 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02723 | hp1 | a0001 | c0002 | t0003 | g0002 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02723 | hp2 | a0001 | c0002 | t0004 | g0205 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02738 | hp2 | a0001 | c0001 | t0010 | g0098 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02809 | hp1 | a0001 | c0002 | t0009 | g0069 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02809 | hp2 | a0001 | c0002 | t0009 | g0008 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02818 | hp2 | a0001 | c0002 | t0003 | g0002 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02886 | hp1 | a0001 | c0002 | t0038 | g0042 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0043 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02896 | hp1 | a0001 | c0002 | t0012 | g0081 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02897 | hp2 | a0001 | c0002 | t0012 | g0025 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0056 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0002 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02970 | hp2 | a0001 | c0002 | t0008 | g0216 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0061 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03098 | hp1 | a0003 | c0004 | t0036 | g0096 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03098 | hp2 | a0001 | c0002 | t0040 | g0209 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03130 | hp2 | a0001 | c0002 | t0018 | g0051 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03139 | hp1 | a0001 | c0002 | t0008 | g0219 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0193 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03195 | hp1 | a0001 | c0002 | t0004 | g0204 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03195 | hp2 | a0001 | c0002 | t0031 | g0019 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03209 | hp2 | a0001 | c0002 | t0017 | g0066 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0214 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0045 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03453 | hp2 | a0001 | c0002 | t0034 | g0035 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0223 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0048 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03669 | hp2 | a0001 | c0001 | t0029 | g0174 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03704 | hp2 | a0001 | c0001 | t0011 | g0180 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03831 | hp2 | a0001 | c0001 | t0007 | g0113 | SAS | BEB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03834 | hp1 | a0001 | c0002 | t0025 | g0057 | SAS | BEB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03942 | hp1 | a0001 | c0001 | t0011 | g0179 | SAS | BEB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | STU | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | STU | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0046 | SAS | STU | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | YRI | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18522 | hp2 | a0001 | c0002 | t0022 | g0020 | AFR | YRI | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0080 | EAS | CHB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0203 | AFR | YRI | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0002 | AFR | YRI | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18944 | hp2 | a0001 | c0001 | t0014 | g0232 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18945 | hp2 | a0004 | c0005 | t0001 | g0014 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18946 | hp1 | a0001 | c0002 | t0009 | g0039 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18946 | hp2 | a0001 | c0001 | t0007 | g0167 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18950 | hp1 | a0001 | c0001 | t0006 | g0153 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18950 | hp2 | a0001 | c0001 | t0006 | g0138 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18952 | hp2 | a0001 | c0002 | t0043 | g0007 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18956 | hp1 | a0001 | c0001 | t0041 | g0233 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18978 | hp2 | a0001 | c0002 | t0039 | g0079 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18993 | hp1 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0175 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA18999 | hp2 | a0005 | c0006 | t0001 | g0186 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19000 | hp1 | a0001 | c0002 | t0028 | g0221 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0151 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0207 | AFR | LWK | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0130 | AFR | LWK | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19043 | hp2 | a0001 | c0002 | t0035 | g0077 | AFR | LWK | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19076 | hp1 | a0001 | c0002 | t0024 | g0054 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19076 | hp2 | a0001 | c0001 | t0010 | g0152 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19078 | hp2 | a0001 | c0002 | t0013 | g0078 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19091 | hp1 | a0001 | c0001 | t0014 | g0231 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA20129 | hp1 | a0001 | c0002 | t0023 | g0053 | AFR | ASW | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA20129 | hp2 | a0001 | c0002 | t0003 | g0072 | AFR | ASW | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02109 | hp1 | a0001 | c0002 | t0004 | g0016 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02109 | hp2 | a0002 | c0003 | t0010 | g0097 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02486 | hp2 | a0001 | c0007 | t0008 | g0220 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02559 | hp1 | a0001 | c0002 | t0009 | g0008 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG02559 | hp2 | a0001 | c0001 | t0033 | g0105 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG03471 | hp2 | a0001 | c0002 | t0008 | g0218 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG06807 | hp1 | a0001 | c0002 | t0003 | g0028 | AFR | USA | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| HG06807 | hp2 | a0001 | c0002 | t0004 | g0210 | AFR | USA | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | LWK | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0030 | AFR | LWK | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:27744718 | A | G | 1 | a0005 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.419A>G | p.Lys140Arg | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/9 | 539/3579 | 419/924 | 140/307 | chr1 | 27744718 | |||
| chr1:27744774 | C | G | 1 | a0004 | 1 | NA18945.hp2 | missense_variant | MODERATE | c.475C>G | p.Gln159Glu | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/9 | 595/3579 | 475/924 | 159/307 | chr1 | 27744774 | |||
| chr1:27755244 | A | G | 1 | a0003 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.649A>G | p.Ile217Val | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/9 | 769/3579 | 649/924 | 217/307 | chr1 | 27755244 | |||
| chr1:27760541 | G | T | 1 | a0002 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.884G>T | p.Ser295Ile | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1004/3579 | 884/924 | 295/307 | chr1 | 27760541 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:27734063 | A | G | 2 | a0001c0002 a0001c0007 |
106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
synonymous_variant | LOW | c.234A>G | p.Ala78Ala | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/9 | 354/3579 | 234/924 | 78/307 | chr1 | 27734063 | |||
| chr1:27734174 | T | C | 1 | a0001c0007 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.345T>C | p.Asp115Asp | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/9 | 465/3579 | 345/924 | 115/307 | chr1 | 27734174 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:27725981 | C | T | 1 | a0001c0002t0044 | 1 | HG02451.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-100C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/9 | chr1 | 27725981 | |||||||
| chr1:27760715 | G | A | 1 | a0001c0002t0016 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*134G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 134 | chr1 | 27760715 | ||||||
| chr1:27760774 | T | C | 2 | a0001c0002t0017 a0001c0002t0018 |
2 | HG03130.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*193T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 193 | chr1 | 27760774 | ||||||
| chr1:27760778 | T | C | 1 | a0001c0001t0011 | 3 | HG02698.hp1 HG03704.hp2 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*197T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 197 | chr1 | 27760778 | ||||||
| chr1:27760806 | C | T | 1 | a0001c0002t0043 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*225C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 225 | chr1 | 27760806 | ||||||
| chr1:27760877 | C | CT | 6 | a0001c0001t0005 a0001c0001t0041 a0001c0001t0042 others(3): Show |
24 | HG00741.hp1 HG00741.hp2 HG01069.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*319dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 320 | INFO_REALIGN_3_PRIME | chr1 | 27760877 | |||||
| chr1:27760877 | CT | C | 13 | a0001c0001t0007 a0001c0002t0002 a0001c0002t0012 others(10): Show |
64 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*319delT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 319 | INFO_REALIGN_3_PRIME | chr1 | 27760877 | |||||
| chr1:27760877 | CTT | C | 6 | a0001c0002t0008 a0001c0002t0009 a0001c0002t0017 others(3): Show |
12 | HG02055.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*318_*319delTT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 318 | INFO_REALIGN_3_PRIME | chr1 | 27760877 | |||||
| chr1:27760877 | CTTT | C | 2 | a0001c0002t0003 a0001c0002t0019 |
13 | HG00639.hp2 HG01106.hp1 HG01243.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*317_*319delTTT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 317 | INFO_REALIGN_3_PRIME | chr1 | 27760877 | |||||
| chr1:27760946 | G | GT | 18 | a0001c0001t0006 a0001c0001t0042 a0001c0002t0002 others(15): Show |
87 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*382dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 383 | INFO_REALIGN_3_PRIME | chr1 | 27760946 | |||||
| chr1:27760946 | G | GTT | 9 | a0001c0002t0008 a0001c0002t0019 a0001c0002t0021 others(6): Show |
12 | HG01243.hp1 HG01255.hp2 HG02055.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*381_*382dupTT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 383 | INFO_REALIGN_3_PRIME | chr1 | 27760946 | |||||
| chr1:27760952 | T | G | 1 | a0001c0001t0029 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*371T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 371 | chr1 | 27760952 | ||||||
| chr1:27760952 | T | TG | 5 | a0001c0002t0004 a0001c0002t0016 a0001c0002t0020 others(2): Show |
15 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*371_*372insG | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 372 | chr1 | 27760952 | ||||||
| chr1:27761124 | G | A | 2 | a0001c0001t0014 a0001c0001t0041 |
3 | NA18944.hp2 NA18956.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*543G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 543 | chr1 | 27761124 | ||||||
| chr1:27761261 | GA | G | 47 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(44): Show |
262 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(259): Show |
3_prime_UTR_variant | MODIFIER | c.*689delA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 689 | INFO_REALIGN_3_PRIME | chr1 | 27761261 | |||||
| chr1:27761450 | T | G | 1 | a0001c0002t0012 | 3 | HG02258.hp1 HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*869T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 869 | chr1 | 27761450 | ||||||
| chr1:27761640 | T | C | 1 | a0001c0002t0023 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1059T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1059 | chr1 | 27761640 | ||||||
| chr1:27761809 | C | T | 1 | a0001c0001t0029 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1228C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1228 | chr1 | 27761809 | ||||||
| chr1:27761907 | A | G | 4 | a0001c0002t0004 a0001c0002t0016 a0001c0002t0030 others(1): Show |
14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1326A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1326 | chr1 | 27761907 | ||||||
| chr1:27761964 | C | CAA | 9 | a0001c0001t0010 a0001c0002t0004 a0001c0002t0023 others(6): Show |
21 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1398_*1399dupAA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1400 | INFO_REALIGN_3_PRIME | chr1 | 27761964 | |||||
| chr1:27761964 | C | CAAA | 22 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0008 others(19): Show |
87 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1397_*1399dupAAA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1400 | INFO_REALIGN_3_PRIME | chr1 | 27761964 | |||||
| chr1:27762072 | C | A | 31 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0004 others(28): Show |
106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*1491C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1491 | chr1 | 27762072 | ||||||
| chr1:27762084 | T | G | 1 | a0001c0001t0032 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1503T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1503 | chr1 | 27762084 | ||||||
| chr1:27762157 | A | G | 31 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0004 others(28): Show |
106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*1576A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1576 | chr1 | 27762157 | ||||||
| chr1:27762482 | T | C | 1 | a0001c0001t0033 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1901T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1901 | chr1 | 27762482 | ||||||
| chr1:27762524 | G | C | 4 | a0001c0002t0004 a0001c0002t0016 a0001c0002t0030 others(1): Show |
14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1943G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1943 | chr1 | 27762524 | ||||||
| chr1:27762556 | A | G | 3 | a0001c0002t0008 a0001c0002t0027 a0001c0007t0008 |
6 | HG02258.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1975A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1975 | chr1 | 27762556 | ||||||
| chr1:27762740 | T | C | 1 | a0001c0002t0034 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2159T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 2159 | chr1 | 27762740 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:27726165 | C | G | 3 | a0001c0001t0014g0231 a0001c0001t0014g0232 a0001c0001t0041g0233 |
3 | NA18944.hp2 NA18956.hp1 NA19091.hp1 |
splice_region_variant&intron_variant | LOW | c.81+4C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27726165 | |||||||
| chr1:27726186 | G | C | 1 | a0001c0001t0001g0017 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.81+25G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27726186 | |||||||
| chr1:27726329 | G | A | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.81+168G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27726329 | |||||||
| chr1:27726381 | C | T | 1 | a0001c0002t0037g0230 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.81+220C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27726381 | |||||||
| chr1:27726509 | C | T | 3 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 |
3 | HG02818.hp1 HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.81+348C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27726509 | |||||||
| chr1:27726628 | A | AT | 6 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(3): Show |
6 | HG02056.hp1 HG03225.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+483dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 27726628 | ||||||
| chr1:27726629 | T | A | 2 | a0001c0002t0022g0020 a0001c0002t0031g0019 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.81+468T>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27726629 | |||||||
| chr1:27726694 | A | C | 6 | a0001c0002t0008g0215 a0001c0002t0008g0216 a0001c0002t0008g0218 others(3): Show |
6 | HG02258.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+533A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27726694 | |||||||
| chr1:27726752 | C | T | 1 | a0001c0001t0005g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.81+591C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27726752 | |||||||
| chr1:27726800 | G | A | 80 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(77): Show |
92 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.81+639G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27726800 | |||||||
| chr1:27726966 | C | T | 12 | a0001c0002t0004g0015 a0001c0002t0004g0016 a0001c0002t0004g0204 others(9): Show |
14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.82-506C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27726966 | |||||||
| chr1:27727083 | T | C | 1 | a0001c0002t0002g0021 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.82-389T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27727083 | |||||||
| chr1:27727136 | T | C | 1 | a0001c0002t0002g0022 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.82-336T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27727136 | |||||||
| chr1:27727615 | A | G | 1 | a0001c0001t0007g0203 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.146+79A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27727615 | |||||||
| chr1:27727800 | AT | A | 116 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(113): Show |
129 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.146+289delT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27727800 | ||||||
| chr1:27727800 | ATT | A | 22 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0085 others(19): Show |
22 | HG02080.hp1 HG02109.hp2 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.146+288_146+289del others(2): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27727800 | ||||||
| chr1:27727800 | ATTT | A | 17 | a0001c0002t0002g0080 a0001c0002t0004g0015 a0001c0002t0004g0016 others(14): Show |
19 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.146+287_146+289del others(3): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27727800 | ||||||
| chr1:27727800 | ATTTT | A | 68 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(65): Show |
80 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.146+286_146+289del others(4): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27727800 | ||||||
| chr1:27727800 | ATTTTT | A | 5 | a0001c0002t0002g0026 a0001c0002t0003g0027 a0001c0002t0003g0028 others(2): Show |
5 | HG00639.hp2 HG01069.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.146+285_146+289del others(5): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27727800 | ||||||
| chr1:27727822 | T | G | 2 | a0001c0002t0002g0023 a0001c0002t0028g0221 |
2 | NA18977.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.146+286T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27727822 | |||||||
| chr1:27727883 | C | G | 12 | a0001c0002t0003g0002 a0001c0002t0003g0027 a0001c0002t0003g0028 others(9): Show |
17 | HG00639.hp2 HG01106.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.146+347C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27727883 | |||||||
| chr1:27727916 | T | G | 1 | a0001c0001t0001g0082 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.146+380T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27727916 | |||||||
| chr1:27728084 | G | A | 80 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(77): Show |
92 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.146+548G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728084 | |||||||
| chr1:27728198 | T | G | 2 | a0001c0002t0022g0020 a0001c0002t0031g0019 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.146+662T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728198 | |||||||
| chr1:27728303 | C | T | 77 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(74): Show |
89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.146+767C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728303 | |||||||
| chr1:27728359 | CT | C | 7 | a0001c0001t0001g0083 a0001c0001t0001g0102 a0001c0001t0001g0103 others(4): Show |
7 | HG00639.hp1 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.146+830delT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27728359 | ||||||
| chr1:27728445 | C | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0011g0197 |
3 | HG01192.hp2 HG01258.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.146+909C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728445 | |||||||
| chr1:27728509 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.146+973C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728509 | |||||||
| chr1:27728510 | G | A | 1 | a0001c0001t0010g0084 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.146+974G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728510 | |||||||
| chr1:27728551 | C | T | 1 | a0001c0001t0005g0193 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.146+1015C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728551 | |||||||
| chr1:27728656 | T | G | 1 | a0001c0002t0008g0215 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.146+1120T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728656 | |||||||
| chr1:27728690 | G | A | 27 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(24): Show |
32 | HG00639.hp2 HG01106.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.146+1154G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728690 | |||||||
| chr1:27728708 | A | T | 92 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(89): Show |
106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.146+1172A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728708 | |||||||
| chr1:27728774 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.146+1238T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728774 | |||||||
| chr1:27728846 | C | A | 77 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(74): Show |
89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.146+1310C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728846 | |||||||
| chr1:27728905 | G | C | 1 | a0001c0001t0007g0106 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.146+1369G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728905 | |||||||
| chr1:27728959 | G | C | 6 | a0001c0002t0004g0015 a0001c0002t0004g0204 a0001c0002t0004g0205 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.146+1423G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728959 | |||||||
| chr1:27728990 | G | A | 80 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(77): Show |
92 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.146+1454G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728990 | |||||||
| chr1:27729040 | A | AT | 29 | a0001c0001t0001g0202 a0001c0002t0002g0029 a0001c0002t0002g0030 others(26): Show |
34 | HG00639.hp2 HG01106.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.146+1513dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27729040 | ||||||
| chr1:27729113 | G | A | 2 | a0001c0002t0022g0020 a0001c0002t0031g0019 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.146+1577G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27729113 | |||||||
| chr1:27729395 | G | A | 80 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(77): Show |
92 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.146+1859G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27729395 | |||||||
| chr1:27729495 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.146+1959C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27729495 | |||||||
| chr1:27729529 | C | CA | 92 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(89): Show |
106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.146+2003dupA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27729529 | ||||||
| chr1:27729635 | C | A | 80 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(77): Show |
92 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.146+2099C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27729635 | |||||||
| chr1:27729831 | A | G | 198 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(195): Show |
221 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(218): Show |
intron_variant | MODIFIER | c.146+2295A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27729831 | |||||||
| chr1:27730135 | A | G | 80 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(77): Show |
92 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.147-2468A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730135 | |||||||
| chr1:27730181 | C | CT | 74 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(71): Show |
86 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.147-2412dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27730181 | ||||||
| chr1:27730255 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.147-2348C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730255 | |||||||
| chr1:27730256 | G | A | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG01169.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.147-2347G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730256 | |||||||
| chr1:27730280 | A | C | 1 | a0001c0002t0003g0076 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147-2323A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730280 | |||||||
| chr1:27730318 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.147-2285C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730318 | |||||||
| chr1:27730373 | A | G | 44 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(41): Show |
51 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.147-2230A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730373 | |||||||
| chr1:27730454 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.147-2149G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730454 | |||||||
| chr1:27730767 | CT | C | 4 | a0001c0002t0012g0024 a0001c0002t0012g0025 a0001c0002t0012g0081 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.147-1833delT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27730767 | ||||||
| chr1:27730822 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0006g0134 |
2 | HG01175.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.147-1781T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730822 | |||||||
| chr1:27730822 | T | G | 1 | a0001c0001t0001g0228 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.147-1781T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730822 | |||||||
| chr1:27730824 | G | T | 80 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(77): Show |
92 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.147-1779G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730824 | |||||||
| chr1:27730914 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.147-1689G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730914 | |||||||
| chr1:27731058 | G | A | 3 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0009g0039 |
3 | HG02080.hp2 NA18946.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.147-1545G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731058 | |||||||
| chr1:27731079 | A | T | 2 | a0001c0002t0035g0077 a0001c0002t0037g0230 |
2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.147-1524A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731079 | |||||||
| chr1:27731198 | A | AT | 5 | a0001c0001t0001g0101 a0001c0001t0001g0187 a0001c0001t0001g0188 others(2): Show |
5 | HG01433.hp1 HG02486.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.147-1381dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27731198 | ||||||
| chr1:27731198 | AT | A | 24 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(21): Show |
26 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.147-1381delT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27731198 | ||||||
| chr1:27731198 | ATT | A | 61 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(58): Show |
73 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.147-1382_147-1381d others(4): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27731198 | ||||||
| chr1:27731198 | ATTT | A | 11 | a0001c0002t0002g0026 a0001c0002t0002g0043 a0001c0002t0002g0044 others(8): Show |
11 | HG01069.hp1 HG02155.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.147-1383_147-1381d others(5): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27731198 | ||||||
| chr1:27731200 | T | A | 5 | a0001c0002t0002g0036 a0001c0002t0002g0037 a0001c0002t0002g0067 others(2): Show |
5 | HG01884.hp2 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.147-1403T>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731200 | |||||||
| chr1:27731201 | T | A | 61 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(58): Show |
73 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.147-1402T>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731201 | |||||||
| chr1:27731202 | T | A | 11 | a0001c0002t0002g0026 a0001c0002t0002g0043 a0001c0002t0002g0044 others(8): Show |
11 | HG01069.hp1 HG02155.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.147-1401T>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731202 | |||||||
| chr1:27731222 | T | C | 2 | a0001c0002t0022g0020 a0001c0002t0031g0019 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.147-1381T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731222 | |||||||
| chr1:27731227 | A | G | 12 | a0001c0002t0003g0002 a0001c0002t0003g0027 a0001c0002t0003g0028 others(9): Show |
17 | HG00639.hp2 HG01106.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.147-1376A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731227 | |||||||
| chr1:27731268 | A | G | 1 | a0005c0006t0001g0186 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.147-1335A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731268 | |||||||
| chr1:27731352 | C | T | 1 | a0001c0002t0002g0045 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.147-1251C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731352 | |||||||
| chr1:27731907 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.147-696C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731907 | |||||||
| chr1:27731915 | G | A | 1 | a0001c0001t0042g0110 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.147-688G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731915 | |||||||
| chr1:27731970 | C | T | 1 | a0001c0001t0005g0185 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.147-633C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731970 | |||||||
| chr1:27732423 | G | A | 77 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(74): Show |
89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.147-180G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27732423 | |||||||
| chr1:27732479 | G | T | 77 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(74): Show |
89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.147-124G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27732479 | |||||||
| chr1:27732940 | G | GT | 5 | a0001c0001t0001g0100 a0001c0001t0001g0183 a0001c0001t0001g0224 others(2): Show |
5 | HG02074.hp1 HG03225.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+296dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 27732940 | ||||||
| chr1:27732946 | T | G | 1 | a0001c0001t0006g0138 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.201+289T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | chr1 | 27732946 | |||||||
| chr1:27732986 | A | T | 6 | a0001c0002t0008g0215 a0001c0002t0008g0216 a0001c0002t0008g0218 others(3): Show |
6 | HG02258.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.201+329A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | chr1 | 27732986 | |||||||
| chr1:27732998 | G | A | 77 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(74): Show |
89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.201+341G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | chr1 | 27732998 | |||||||
| chr1:27733212 | G | A | 1 | a0001c0001t0006g0111 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.201+555G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | chr1 | 27733212 | |||||||
| chr1:27733225 | C | T | 77 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(74): Show |
89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.201+568C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | chr1 | 27733225 | |||||||
| chr1:27733228 | G | A | 2 | a0001c0002t0022g0020 a0001c0002t0031g0019 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.201+571G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | chr1 | 27733228 | |||||||
| chr1:27733231 | A | G | 1 | a0001c0002t0017g0066 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.201+574A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | chr1 | 27733231 | |||||||
| chr1:27733447 | C | G | 77 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(74): Show |
89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.202-584C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | chr1 | 27733447 | |||||||
| chr1:27733569 | C | T | 1 | a0001c0001t0032g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.202-462C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | chr1 | 27733569 | |||||||
| chr1:27733726 | G | C | 1 | a0001c0001t0001g0139 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.202-305G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | chr1 | 27733726 | |||||||
| chr1:27734352 | C | T | 1 | a0001c0002t0002g0041 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.354+169C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27734352 | |||||||
| chr1:27734375 | G | A | 1 | a0001c0002t0012g0024 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.354+192G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27734375 | |||||||
| chr1:27734419 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.354+236C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27734419 | |||||||
| chr1:27735008 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.354+825A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27735008 | |||||||
| chr1:27735492 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.354+1309G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27735492 | |||||||
| chr1:27735545 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.354+1362A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27735545 | |||||||
| chr1:27735564 | T | C | 92 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(89): Show |
106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.354+1381T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27735564 | |||||||
| chr1:27735596 | G | C | 92 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(89): Show |
106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.354+1413G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27735596 | |||||||
| chr1:27735668 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.354+1485C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27735668 | |||||||
| chr1:27735880 | A | T | 92 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(89): Show |
106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.354+1697A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27735880 | |||||||
| chr1:27736147 | C | G | 1 | a0001c0002t0044g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.354+1964C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27736147 | |||||||
| chr1:27736149 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.354+1966G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27736149 | |||||||
| chr1:27736179 | G | A | 92 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(89): Show |
106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.354+1996G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27736179 | |||||||
| chr1:27736182 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0005g0193 a0001c0001t0005g0214 |
3 | HG02896.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.354+1999C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27736182 | |||||||
| chr1:27736183 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.354+2000G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27736183 | |||||||
| chr1:27736511 | C | T | 77 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(74): Show |
89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.354+2328C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27736511 | |||||||
| chr1:27736719 | C | G | 1 | a0001c0001t0001g0085 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.354+2536C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27736719 | |||||||
| chr1:27736832 | C | T | 1 | a0001c0001t0006g0134 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.354+2649C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27736832 | |||||||
| chr1:27736972 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG00609.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.354+2789G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27736972 | |||||||
| chr1:27737239 | G | A | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.354+3056G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737239 | |||||||
| chr1:27737276 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.354+3093T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737276 | |||||||
| chr1:27737277 | A | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.354+3094A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737277 | |||||||
| chr1:27737455 | C | A | 12 | a0001c0002t0004g0015 a0001c0002t0004g0016 a0001c0002t0004g0204 others(9): Show |
14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.354+3272C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737455 | |||||||
| chr1:27737543 | T | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0086 a0001c0001t0001g0144 others(1): Show |
5 | HG00558.hp2 HG00621.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+3360T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737543 | |||||||
| chr1:27737589 | C | T | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.354+3406C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737589 | |||||||
| chr1:27737694 | A | T | 1 | a0001c0001t0001g0144 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.354+3511A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737694 | |||||||
| chr1:27737719 | A | G | 92 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(89): Show |
106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.354+3536A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737719 | |||||||
| chr1:27737853 | AAAC | A | 27 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(24): Show |
34 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.354+3685_354+3687d others(5): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27737853 | ||||||
| chr1:27737866 | AAC | A | 12 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0047 others(9): Show |
12 | HG00621.hp2 HG00673.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.354+3685_354+3686d others(4): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27737866 | ||||||
| chr1:27737867 | AC | A | 4 | a0001c0002t0002g0026 a0001c0002t0002g0043 a0001c0002t0002g0046 others(1): Show |
4 | HG01069.hp1 HG02895.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.354+3685delC | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737867 | |||||||
| chr1:27737868 | C | A | 3 | a0001c0001t0001g0112 a0001c0002t0002g0045 a0001c0002t0038g0042 |
3 | HG01928.hp2 HG02886.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.354+3685C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737868 | |||||||
| chr1:27737868 | C | CA | 40 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0083 others(37): Show |
42 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.354+3709dupA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27737868 | ||||||
| chr1:27737868 | C | CAA | 5 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.354+3708_354+3709d others(4): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27737868 | ||||||
| chr1:27737868 | CAA | C | 16 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(13): Show |
17 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.354+3708_354+3709d others(4): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27737868 | ||||||
| chr1:27737868 | CAAA | C | 28 | a0001c0001t0006g0111 a0001c0002t0003g0002 a0001c0002t0003g0027 others(25): Show |
34 | HG00609.hp2 HG00639.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.354+3707_354+3709d others(5): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27737868 | ||||||
| chr1:27737868 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0005g0185 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.354+3699_354+3709d others(13): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27737868 | ||||||
| chr1:27737870 | A | AC | 4 | a0001c0001t0001g0095 a0001c0001t0001g0178 a0001c0001t0010g0084 others(1): Show |
4 | HG02080.hp1 HG02280.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.354+3687_354+3688i others(3): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737870 | |||||||
| chr1:27737871 | A | C | 9 | a0001c0001t0001g0101 a0001c0001t0001g0132 a0001c0001t0010g0098 others(6): Show |
9 | HG02109.hp2 HG02698.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.354+3688A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737871 | |||||||
| chr1:27737874 | A | C | 13 | a0001c0002t0004g0015 a0001c0002t0004g0016 a0001c0002t0004g0204 others(10): Show |
15 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.354+3691A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737874 | |||||||
| chr1:27737877 | A | C | 13 | a0001c0002t0004g0015 a0001c0002t0004g0016 a0001c0002t0004g0204 others(10): Show |
15 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.354+3694A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737877 | |||||||
| chr1:27737880 | A | C | 12 | a0001c0002t0004g0015 a0001c0002t0004g0016 a0001c0002t0004g0204 others(9): Show |
14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.354+3697A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737880 | |||||||
| chr1:27737883 | A | C | 12 | a0001c0002t0004g0015 a0001c0002t0004g0016 a0001c0002t0004g0204 others(9): Show |
14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.354+3700A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737883 | |||||||
| chr1:27737886 | A | C | 6 | a0001c0002t0012g0024 a0001c0002t0012g0025 a0001c0002t0012g0081 others(3): Show |
6 | HG02258.hp1 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.354+3703A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737886 | |||||||
| chr1:27737916 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.354+3733G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737916 | |||||||
| chr1:27737937 | C | T | 1 | a0001c0002t0034g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.354+3754C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737937 | |||||||
| chr1:27737978 | A | G | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.354+3795A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737978 | |||||||
| chr1:27738218 | G | A | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.354+4035G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27738218 | |||||||
| chr1:27738476 | C | CA | 12 | a0001c0002t0003g0002 a0001c0002t0003g0027 a0001c0002t0003g0028 others(9): Show |
17 | HG00639.hp2 HG01106.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.354+4303dupA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27738476 | ||||||
| chr1:27738484 | A | T | 1 | a0001c0002t0008g0218 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.354+4301A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27738484 | |||||||
| chr1:27738487 | T | A | 60 | a0001c0001t0001g0158 a0001c0001t0001g0198 a0001c0002t0002g0001 others(57): Show |
72 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.354+4304T>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27738487 | |||||||
| chr1:27738693 | C | T | 1 | a0001c0001t0005g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.354+4510C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27738693 | |||||||
| chr1:27739028 | A | C | 1 | a0001c0001t0001g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.354+4845A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27739028 | |||||||
| chr1:27739218 | T | C | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.354+5035T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27739218 | |||||||
| chr1:27739411 | T | C | 1 | a0001c0002t0002g0045 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.354+5228T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27739411 | |||||||
| chr1:27739434 | G | T | 1 | a0001c0001t0001g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.355-5220G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27739434 | |||||||
| chr1:27739809 | A | G | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.355-4845A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27739809 | |||||||
| chr1:27739820 | C | CAATA | 92 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(89): Show |
106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.355-4826_355-4823d others(6): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27739820 | ||||||
| chr1:27739840 | T | TA | 90 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(87): Show |
104 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.355-4806dupA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27739840 | ||||||
| chr1:27739964 | G | A | 1 | a0001c0001t0005g0193 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.355-4690G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27739964 | |||||||
| chr1:27739970 | A | T | 1 | a0001c0001t0001g0128 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.355-4684A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27739970 | |||||||
| chr1:27739991 | A | G | 6 | a0001c0002t0008g0215 a0001c0002t0008g0216 a0001c0002t0008g0218 others(3): Show |
6 | HG02258.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.355-4663A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27739991 | |||||||
| chr1:27740062 | A | T | 1 | a0001c0002t0038g0042 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.355-4592A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27740062 | |||||||
| chr1:27740151 | C | G | 44 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(41): Show |
51 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.355-4503C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27740151 | |||||||
| chr1:27740249 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.355-4405G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27740249 | |||||||
| chr1:27740443 | T | G | 12 | a0001c0002t0004g0015 a0001c0002t0004g0016 a0001c0002t0004g0204 others(9): Show |
14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.355-4211T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27740443 | |||||||
| chr1:27740665 | C | T | 1 | a0001c0001t0005g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.355-3989C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27740665 | |||||||
| chr1:27740669 | T | A | 1 | a0001c0001t0001g0159 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.355-3985T>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27740669 | |||||||
| chr1:27740787 | G | A | 1 | a0001c0001t0005g0160 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.355-3867G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27740787 | |||||||
| chr1:27741027 | G | A | 92 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(89): Show |
106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.355-3627G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741027 | |||||||
| chr1:27741089 | G | A | 1 | a0001c0002t0003g0070 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.355-3565G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741089 | |||||||
| chr1:27741132 | C | CA | 7 | a0001c0001t0001g0013 a0001c0001t0001g0148 a0001c0001t0001g0149 others(4): Show |
8 | HG01109.hp1 HG01891.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.355-3510dupA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27741132 | ||||||
| chr1:27741193 | A | AT | 69 | a0001c0001t0001g0017 a0001c0001t0001g0087 a0001c0001t0001g0088 others(66): Show |
77 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.355-3439dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27741193 | ||||||
| chr1:27741193 | A | ATT | 37 | a0001c0001t0007g0106 a0001c0001t0011g0197 a0001c0002t0002g0022 others(34): Show |
43 | HG00621.hp2 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.355-3440_355-3439d others(4): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27741193 | ||||||
| chr1:27741193 | A | ATTT | 9 | a0001c0002t0002g0034 a0001c0002t0002g0065 a0001c0002t0003g0076 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.355-3441_355-3439d others(5): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27741193 | ||||||
| chr1:27741199 | T | C | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.355-3455T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741199 | |||||||
| chr1:27741298 | A | G | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0156 |
3 | HG02622.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.355-3356A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741298 | |||||||
| chr1:27741370 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0007g0009 |
2 | HG01515.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.355-3284G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741370 | |||||||
| chr1:27741394 | A | C | 2 | a0001c0002t0022g0020 a0001c0002t0031g0019 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.355-3260A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741394 | |||||||
| chr1:27741557 | A | T | 2 | a0001c0002t0002g0061 a0001c0002t0002g0064 |
2 | HG02683.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.355-3097A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741557 | |||||||
| chr1:27741558 | A | T | 93 | a0001c0001t0006g0138 a0001c0002t0002g0001 a0001c0002t0002g0004 others(90): Show |
107 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.355-3096A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741558 | |||||||
| chr1:27741756 | G | A | 1 | a0001c0002t0022g0020 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.355-2898G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741756 | |||||||
| chr1:27741867 | AGT | A | 12 | a0001c0002t0004g0015 a0001c0002t0004g0016 a0001c0002t0004g0204 others(9): Show |
14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.355-2785_355-2784d others(4): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27741867 | ||||||
| chr1:27741879 | T | C | 1 | a0001c0001t0006g0111 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.355-2775T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741879 | |||||||
| chr1:27741896 | AG | A | 87 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(84): Show |
101 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.355-2757delG | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741896 | |||||||
| chr1:27741897 | G | A | 3 | a0001c0002t0002g0062 a0001c0002t0022g0020 a0001c0002t0031g0019 |
3 | HG02056.hp2 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.355-2757G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741897 | |||||||
| chr1:27742063 | C | T | 1 | a0001c0002t0022g0020 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.355-2591C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27742063 | |||||||
| chr1:27742233 | A | C | 1 | a0001c0001t0001g0093 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.355-2421A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27742233 | |||||||
| chr1:27742313 | G | T | 1 | a0001c0002t0031g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.355-2341G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27742313 | |||||||
| chr1:27742556 | T | C | 1 | a0001c0001t0001g0228 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.355-2098T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27742556 | |||||||
| chr1:27742637 | T | C | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.355-2017T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27742637 | |||||||
| chr1:27742782 | G | A | 77 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(74): Show |
89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.355-1872G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27742782 | |||||||
| chr1:27742794 | C | T | 1 | a0001c0002t0022g0020 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.355-1860C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27742794 | |||||||
| chr1:27742935 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.355-1719C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27742935 | |||||||
| chr1:27742936 | G | A | 2 | a0001c0002t0035g0077 a0001c0002t0037g0230 |
2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.355-1718G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27742936 | |||||||
| chr1:27743018 | G | C | 1 | a0001c0001t0001g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.355-1636G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27743018 | |||||||
| chr1:27743257 | T | C | 1 | a0001c0002t0002g0045 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.355-1397T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27743257 | |||||||
| chr1:27743382 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.355-1272G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27743382 | |||||||
| chr1:27743488 | G | A | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.355-1166G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27743488 | |||||||
| chr1:27743767 | GA | G | 11 | a0001c0002t0004g0015 a0001c0002t0004g0016 a0001c0002t0004g0204 others(8): Show |
13 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.355-874delA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27743767 | ||||||
| chr1:27743781 | C | T | 75 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(72): Show |
87 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.355-873C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27743781 | |||||||
| chr1:27743961 | T | C | 1 | a0001c0002t0002g0052 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.355-693T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27743961 | |||||||
| chr1:27743962 | G | A | 1 | a0001c0002t0002g0052 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.355-692G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27743962 | |||||||
| chr1:27744355 | C | T | 12 | a0001c0002t0004g0015 a0001c0002t0004g0016 a0001c0002t0004g0204 others(9): Show |
14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.355-299C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27744355 | |||||||
| chr1:27744428 | G | A | 1 | a0001c0002t0035g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.355-226G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27744428 | |||||||
| chr1:27744460 | G | A | 1 | a0001c0002t0003g0076 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.355-194G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27744460 | |||||||
| chr1:27744548 | A | C | 1 | a0001c0001t0007g0155 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.355-106A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27744548 | |||||||
| chr1:27744596 | C | T | 1 | a0001c0001t0010g0084 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.355-58C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27744596 | |||||||
| chr1:27745175 | G | C | 3 | a0001c0002t0020g0018 a0001c0002t0022g0020 a0001c0002t0031g0019 |
3 | HG02615.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.512+364G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27745175 | |||||||
| chr1:27745258 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.512+447C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27745258 | |||||||
| chr1:27745302 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.512+491C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27745302 | |||||||
| chr1:27745325 | C | T | 89 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(86): Show |
103 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.512+514C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27745325 | |||||||
| chr1:27745728 | G | C | 92 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(89): Show |
106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.512+917G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27745728 | |||||||
| chr1:27746048 | A | G | 89 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(86): Show |
103 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.512+1237A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27746048 | |||||||
| chr1:27746083 | TA | T | 36 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(33): Show |
43 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.512+1275delA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 27746083 | ||||||
| chr1:27746197 | T | G | 92 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(89): Show |
106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.512+1386T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27746197 | |||||||
| chr1:27746451 | G | A | 3 | a0001c0002t0012g0024 a0001c0002t0012g0025 a0001c0002t0012g0081 |
3 | HG02258.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.512+1640G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27746451 | |||||||
| chr1:27746595 | TG | T | 6 | a0001c0002t0004g0015 a0001c0002t0004g0204 a0001c0002t0004g0205 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.512+1785delG | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27746595 | |||||||
| chr1:27746663 | G | T | 2 | a0001c0002t0022g0020 a0001c0002t0031g0019 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.512+1852G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27746663 | |||||||
| chr1:27746689 | C | T | 4 | a0001c0002t0012g0024 a0001c0002t0012g0025 a0001c0002t0012g0081 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.512+1878C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27746689 | |||||||
| chr1:27746723 | T | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0145 |
2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.512+1912T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27746723 | |||||||
| chr1:27746903 | C | T | 3 | a0001c0002t0012g0024 a0001c0002t0012g0025 a0001c0002t0012g0081 |
3 | HG02258.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.512+2092C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27746903 | |||||||
| chr1:27747009 | A | C | 1 | a0001c0001t0001g0154 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.513-2059A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747009 | |||||||
| chr1:27747138 | T | C | 1 | a0001c0001t0001g0164 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.513-1930T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747138 | |||||||
| chr1:27747146 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.513-1922A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747146 | |||||||
| chr1:27747155 | G | T | 89 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(86): Show |
103 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.513-1913G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747155 | |||||||
| chr1:27747253 | A | C | 2 | a0001c0002t0022g0020 a0001c0002t0031g0019 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.513-1815A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747253 | |||||||
| chr1:27747379 | C | T | 19 | a0001c0001t0001g0006 a0001c0001t0001g0082 a0001c0001t0001g0087 others(16): Show |
21 | HG00558.hp1 HG00673.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.513-1689C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747379 | |||||||
| chr1:27747520 | T | C | 75 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(72): Show |
87 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.513-1548T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747520 | |||||||
| chr1:27747609 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.513-1459C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747609 | |||||||
| chr1:27747745 | G | A | 2 | a0001c0002t0022g0020 a0001c0002t0031g0019 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.513-1323G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747745 | |||||||
| chr1:27747813 | G | A | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.513-1255G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747813 | |||||||
| chr1:27747944 | C | G | 1 | a0001c0001t0029g0174 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.513-1124C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747944 | |||||||
| chr1:27747956 | T | C | 2 | a0001c0002t0022g0020 a0001c0002t0031g0019 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.513-1112T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747956 | |||||||
| chr1:27748074 | C | T | 1 | a0001c0002t0002g0052 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.513-994C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748074 | |||||||
| chr1:27748120 | G | GT | 64 | a0001c0001t0001g0082 a0001c0001t0001g0114 a0001c0001t0001g0125 others(61): Show |
76 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.513-925dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 27748120 | ||||||
| chr1:27748120 | G | GTT | 25 | a0001c0002t0002g0007 a0001c0002t0002g0022 a0001c0002t0002g0030 others(22): Show |
25 | HG00621.hp2 HG00673.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.513-926_513-925dup others(2): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 27748120 | ||||||
| chr1:27748126 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.513-942T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748126 | |||||||
| chr1:27748130 | T | G | 6 | a0001c0001t0001g0140 a0001c0001t0001g0145 a0001c0001t0001g0146 others(3): Show |
6 | HG02280.hp2 HG02622.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.513-938T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748130 | |||||||
| chr1:27748148 | C | T | 12 | a0001c0002t0004g0015 a0001c0002t0004g0016 a0001c0002t0004g0204 others(9): Show |
14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.513-920C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748148 | |||||||
| chr1:27748226 | C | T | 2 | a0001c0002t0002g0026 a0001c0002t0002g0043 |
2 | HG01069.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.513-842C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748226 | |||||||
| chr1:27748375 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.513-693C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748375 | |||||||
| chr1:27748426 | A | G | 75 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(72): Show |
87 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.513-642A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748426 | |||||||
| chr1:27748469 | G | GT | 8 | a0001c0001t0001g0104 a0001c0001t0001g0154 a0001c0001t0001g0188 others(5): Show |
8 | HG02055.hp1 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.513-579dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 27748469 | ||||||
| chr1:27748469 | GT | G | 45 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(42): Show |
52 | HG00544.hp1 HG00597.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.513-579delT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 27748469 | ||||||
| chr1:27748469 | GTT | G | 6 | a0001c0002t0017g0066 a0001c0002t0020g0018 a0001c0002t0022g0020 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.513-580_513-579del others(2): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 27748469 | ||||||
| chr1:27748568 | G | GC | 236 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
263 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(260): Show |
intron_variant | MODIFIER | c.513-495dupC | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 27748568 | ||||||
| chr1:27748608 | C | T | 3 | a0001c0002t0020g0018 a0001c0002t0022g0020 a0001c0002t0031g0019 |
3 | HG02615.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.513-460C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748608 | |||||||
| chr1:27748622 | C | T | 1 | a0001c0002t0002g0068 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.513-446C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748622 | |||||||
| chr1:27748748 | C | T | 89 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(86): Show |
103 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.513-320C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748748 | |||||||
| chr1:27748770 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0127 |
2 | NA18945.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.513-298C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748770 | |||||||
| chr1:27748856 | G | T | 1 | a0001c0002t0022g0020 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.513-212G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748856 | |||||||
| chr1:27748895 | C | G | 1 | a0001c0002t0009g0069 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.513-173C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748895 | |||||||
| chr1:27748946 | A | G | 1 | a0001c0002t0004g0015 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.513-122A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748946 | |||||||
| chr1:27748963 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.513-105A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748963 | |||||||
| chr1:27748991 | A | G | 1 | a0001c0002t0003g0070 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.513-77A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748991 | |||||||
| chr1:27749179 | G | A | 3 | a0001c0001t0001g0099 a0001c0001t0005g0193 a0001c0001t0005g0214 |
3 | HG02896.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.599+25G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27749179 | |||||||
| chr1:27749463 | G | A | 77 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(74): Show |
89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.599+309G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27749463 | |||||||
| chr1:27749466 | C | G | 3 | a0001c0001t0001g0135 a0001c0001t0001g0166 a0001c0001t0007g0167 |
3 | HG01934.hp1 HG02004.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.599+312C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27749466 | |||||||
| chr1:27749484 | C | T | 1 | a0001c0002t0031g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.599+330C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27749484 | |||||||
| chr1:27749651 | C | T | 2 | a0001c0002t0035g0077 a0001c0002t0037g0230 |
2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.599+497C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27749651 | |||||||
| chr1:27749795 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0005g0193 |
2 | HG02896.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.599+641G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27749795 | |||||||
| chr1:27749875 | G | A | 92 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(89): Show |
106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.599+721G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27749875 | |||||||
| chr1:27749952 | C | T | 77 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(74): Show |
89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.599+798C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27749952 | |||||||
| chr1:27750024 | A | G | 2 | a0001c0002t0022g0020 a0001c0002t0031g0019 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.599+870A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27750024 | |||||||
| chr1:27750149 | C | A | 4 | a0001c0002t0012g0024 a0001c0002t0012g0025 a0001c0002t0012g0081 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.599+995C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27750149 | |||||||
| chr1:27750314 | A | G | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.599+1160A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27750314 | |||||||
| chr1:27750677 | C | A | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.599+1523C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27750677 | |||||||
| chr1:27750901 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.599+1747G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27750901 | |||||||
| chr1:27751099 | G | C | 12 | a0001c0002t0004g0015 a0001c0002t0004g0016 a0001c0002t0004g0204 others(9): Show |
14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.599+1945G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27751099 | |||||||
| chr1:27751147 | C | CA | 28 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(25): Show |
33 | HG00639.hp2 HG01106.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.599+2002dupA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 27751147 | ||||||
| chr1:27751498 | CT | C | 38 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(35): Show |
43 | HG00639.hp2 HG01106.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.599+2359delT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 27751498 | ||||||
| chr1:27751994 | G | A | 2 | a0001c0002t0035g0077 a0001c0002t0037g0230 |
2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.599+2840G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27751994 | |||||||
| chr1:27752070 | A | G | 1 | a0001c0002t0002g0045 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.599+2916A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752070 | |||||||
| chr1:27752130 | C | CG | 3 | a0001c0002t0012g0024 a0001c0002t0012g0025 a0001c0002t0012g0081 |
3 | HG02258.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.599+2976_599+2977i others(3): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752130 | |||||||
| chr1:27752131 | A | G | 1 | a0001c0002t0044g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.599+2977A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752131 | |||||||
| chr1:27752131 | A | T | 3 | a0001c0002t0012g0024 a0001c0002t0012g0025 a0001c0002t0012g0081 |
3 | HG02258.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.599+2977A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752131 | |||||||
| chr1:27752254 | C | T | 36 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(33): Show |
43 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.600-2941C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752254 | |||||||
| chr1:27752343 | C | A | 92 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(89): Show |
106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.600-2852C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752343 | |||||||
| chr1:27752565 | G | A | 2 | a0001c0002t0002g0036 a0001c0002t0002g0037 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.600-2630G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752565 | |||||||
| chr1:27752589 | G | A | 12 | a0001c0002t0004g0015 a0001c0002t0004g0016 a0001c0002t0004g0204 others(9): Show |
14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.600-2606G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752589 | |||||||
| chr1:27752605 | C | T | 1 | a0001c0002t0002g0068 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.600-2590C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752605 | |||||||
| chr1:27752743 | A | G | 1 | a0001c0001t0005g0185 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.600-2452A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752743 | |||||||
| chr1:27752954 | G | T | 1 | a0001c0002t0034g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.600-2241G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752954 | |||||||
| chr1:27753032 | C | T | 2 | a0001c0002t0035g0077 a0001c0002t0037g0230 |
2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.600-2163C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27753032 | |||||||
| chr1:27753381 | T | C | 8 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0094 others(5): Show |
8 | NA18939.hp2 NA18944.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.600-1814T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27753381 | |||||||
| chr1:27753629 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.600-1566G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27753629 | |||||||
| chr1:27753850 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.600-1345T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27753850 | |||||||
| chr1:27753894 | A | G | 1 | a0001c0001t0007g0155 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.600-1301A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27753894 | |||||||
| chr1:27753916 | A | C | 1 | a0001c0001t0001g0168 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.600-1279A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27753916 | |||||||
| chr1:27754014 | T | G | 2 | a0001c0002t0002g0044 a0001c0002t0002g0080 |
2 | HG02155.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.600-1181T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27754014 | |||||||
| chr1:27754099 | C | CT | 8 | a0001c0001t0001g0162 a0001c0001t0005g0123 a0001c0001t0006g0151 others(5): Show |
8 | HG01109.hp1 HG02886.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.600-1072dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 27754099 | ||||||
| chr1:27754099 | CT | C | 46 | a0001c0001t0001g0188 a0001c0002t0002g0026 a0001c0002t0002g0029 others(43): Show |
52 | HG00639.hp2 HG01069.hp1 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.600-1072delT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 27754099 | ||||||
| chr1:27754100 | T | C | 2 | a0001c0001t0011g0179 a0001c0001t0011g0197 |
2 | HG02698.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.600-1095T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27754100 | |||||||
| chr1:27754167 | C | T | 6 | a0001c0002t0004g0015 a0001c0002t0004g0204 a0001c0002t0004g0205 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.600-1028C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27754167 | |||||||
| chr1:27754249 | G | T | 2 | a0001c0001t0001g0135 a0001c0001t0007g0167 |
2 | HG01934.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.600-946G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27754249 | |||||||
| chr1:27754365 | C | A | 75 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(72): Show |
87 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.600-830C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27754365 | |||||||
| chr1:27754704 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.600-491G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27754704 | |||||||
| chr1:27755346 | T | C | 2 | a0001c0002t0035g0077 a0001c0002t0037g0230 |
2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.735+16T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27755346 | |||||||
| chr1:27755478 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.735+148A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27755478 | |||||||
| chr1:27755665 | C | G | 1 | a0001c0002t0031g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.735+335C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27755665 | |||||||
| chr1:27755829 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.735+499C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27755829 | |||||||
| chr1:27755918 | A | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0170 a0004c0005t0001g0014 |
3 | HG01099.hp2 HG01106.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.735+588A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27755918 | |||||||
| chr1:27755951 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.735+621G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27755951 | |||||||
| chr1:27756096 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.735+766A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27756096 | |||||||
| chr1:27756346 | G | A | 1 | a0001c0002t0018g0051 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.735+1016G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27756346 | |||||||
| chr1:27756409 | A | G | 3 | a0001c0001t0014g0231 a0001c0001t0014g0232 a0001c0001t0041g0233 |
3 | NA18944.hp2 NA18956.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.735+1079A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27756409 | |||||||
| chr1:27756458 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.735+1128T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27756458 | |||||||
| chr1:27756510 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.735+1180C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27756510 | |||||||
| chr1:27756654 | A | G | 12 | a0001c0002t0004g0015 a0001c0002t0004g0016 a0001c0002t0004g0204 others(9): Show |
14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.735+1324A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27756654 | |||||||
| chr1:27756722 | T | C | 39 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(36): Show |
46 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.735+1392T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27756722 | |||||||
| chr1:27757188 | C | CT | 72 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0100 others(69): Show |
84 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.735+1883dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 27757188 | ||||||
| chr1:27757188 | C | CTT | 18 | a0001c0001t0001g0198 a0001c0002t0002g0022 a0001c0002t0002g0037 others(15): Show |
18 | HG00621.hp2 HG00639.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.735+1882_735+1883d others(4): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 27757188 | ||||||
| chr1:27757188 | CT | C | 8 | a0001c0001t0001g0099 a0001c0001t0001g0119 a0001c0001t0001g0150 others(5): Show |
8 | HG00408.hp2 HG02615.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.735+1883delT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 27757188 | ||||||
| chr1:27757342 | G | A | 8 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0031 others(5): Show |
8 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.735+2012G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757342 | |||||||
| chr1:27757611 | C | T | 1 | a0001c0001t0010g0152 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.736-1915C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757611 | |||||||
| chr1:27757684 | A | T | 89 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(86): Show |
103 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.736-1842A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757684 | |||||||
| chr1:27757688 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.736-1838C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757688 | |||||||
| chr1:27757698 | C | T | 1 | a0001c0002t0002g0063 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.736-1828C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757698 | |||||||
| chr1:27757714 | T | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0083 a0001c0001t0001g0089 others(3): Show |
7 | HG00609.hp1 HG00639.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.736-1812T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757714 | |||||||
| chr1:27757728 | C | G | 89 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(86): Show |
103 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.736-1798C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757728 | |||||||
| chr1:27757803 | T | C | 3 | a0001c0001t0001g0083 a0001c0001t0001g0102 a0001c0001t0006g0184 |
3 | HG00639.hp1 HG02074.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.736-1723T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757803 | |||||||
| chr1:27757833 | T | C | 84 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(81): Show |
98 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.736-1693T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757833 | |||||||
| chr1:27757850 | G | A | 1 | a0001c0002t0002g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.736-1676G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757850 | |||||||
| chr1:27757894 | G | A | 12 | a0001c0002t0004g0015 a0001c0002t0004g0016 a0001c0002t0004g0204 others(9): Show |
14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.736-1632G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757894 | |||||||
| chr1:27757896 | G | A | 6 | a0001c0002t0004g0015 a0001c0002t0004g0204 a0001c0002t0004g0205 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.736-1630G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757896 | |||||||
| chr1:27757933 | T | C | 92 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(89): Show |
106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.736-1593T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757933 | |||||||
| chr1:27757976 | CA | C | 93 | a0001c0001t0001g0101 a0001c0002t0002g0001 a0001c0002t0002g0004 others(90): Show |
107 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.736-1536delA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 27757976 | ||||||
| chr1:27758038 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.736-1488C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758038 | |||||||
| chr1:27758056 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.736-1470T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758056 | |||||||
| chr1:27758060 | G | A | 89 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(86): Show |
103 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.736-1466G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758060 | |||||||
| chr1:27758224 | C | T | 89 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(86): Show |
103 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.736-1302C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758224 | |||||||
| chr1:27758262 | G | A | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG01169.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.736-1264G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758262 | |||||||
| chr1:27758272 | T | A | 89 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(86): Show |
103 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.736-1254T>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758272 | |||||||
| chr1:27758329 | C | A | 2 | a0001c0002t0002g0030 a0001c0002t0026g0033 |
2 | HG01255.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.736-1197C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758329 | |||||||
| chr1:27758514 | T | A | 1 | a0001c0002t0008g0216 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.736-1012T>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758514 | |||||||
| chr1:27758590 | C | T | 2 | a0001c0001t0005g0169 a0001c0001t0006g0151 |
2 | NA18993.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.736-936C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758590 | |||||||
| chr1:27758647 | G | A | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.736-879G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758647 | |||||||
| chr1:27758679 | G | GT | 39 | a0001c0001t0001g0083 a0001c0001t0001g0100 a0001c0001t0001g0102 others(36): Show |
39 | HG00621.hp1 HG00639.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.736-827dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 27758679 | ||||||
| chr1:27758689 | T | G | 86 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(83): Show |
100 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.736-837T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758689 | |||||||
| chr1:27758699 | T | G | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.736-827T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758699 | |||||||
| chr1:27758788 | G | T | 1 | a0001c0001t0001g0133 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.736-738G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758788 | |||||||
| chr1:27758876 | T | G | 1 | a0001c0001t0001g0158 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.736-650T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758876 | |||||||
| chr1:27759201 | G | A | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.736-325G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27759201 | |||||||
| chr1:27759248 | T | C | 1 | a0001c0001t0015g0201 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.736-278T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27759248 | |||||||
| chr1:27759765 | G | GGTTTTTT others(5): Show |
1 | a0001c0002t0027g0217 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.837+139_837+150dup others(12): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759765 | ||||||
| chr1:27759765 | G | GGTTTTTT others(6): Show |
3 | a0001c0002t0020g0018 a0001c0002t0022g0020 a0001c0002t0031g0019 |
3 | HG02615.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.837+150_837+162dup others(13): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759765 | ||||||
| chr1:27759776 | T | TTTTGTTT others(7): Show |
1 | a0001c0002t0002g0045 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.837+151_837+152ins others(14): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759776 | ||||||
| chr1:27759776 | T | TTTTGTTT others(7): Show |
3 | a0001c0002t0002g0026 a0001c0002t0002g0043 a0001c0002t0038g0042 |
3 | HG01069.hp1 HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.837+151_837+152ins others(14): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759776 | ||||||
| chr1:27759779 | G | GTTTTTTG others(6): Show |
3 | a0001c0002t0002g0061 a0001c0002t0002g0064 a0001c0002t0025g0057 |
3 | HG02683.hp1 HG03017.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.837+158_837+159ins others(13): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759779 | ||||||
| chr1:27759779 | G | GTTTTTTT others(6): Show |
1 | a0001c0002t0044g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.837+159_837+160ins others(13): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759779 | ||||||
| chr1:27759779 | G | GTTTTTTT others(5): Show |
1 | a0001c0002t0023g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.837+162_837+163ins others(12): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759779 | ||||||
| chr1:27759779 | G | GTTTTTTT others(6): Show |
40 | a0001c0002t0002g0004 a0001c0002t0002g0023 a0001c0002t0002g0030 others(37): Show |
47 | HG00597.hp1 HG00639.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.837+162_837+163ins others(13): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759779 | ||||||
| chr1:27759779 | G | GTTTTTTT others(7): Show |
11 | a0001c0002t0002g0021 a0001c0002t0002g0029 a0001c0002t0002g0034 others(8): Show |
11 | HG00408.hp1 HG01106.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.837+162_837+163ins others(14): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759779 | ||||||
| chr1:27759779 | G | T | 5 | a0001c0002t0002g0026 a0001c0002t0002g0043 a0001c0002t0002g0045 others(2): Show |
5 | HG01069.hp1 HG02258.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.837+152G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | chr1 | 27759779 | |||||||
| chr1:27759780 | T | TTTTTTTT others(6): Show |
4 | a0001c0002t0009g0069 a0001c0002t0012g0024 a0001c0002t0012g0025 others(1): Show |
4 | HG02258.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+162_837+163ins others(13): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759780 | ||||||
| chr1:27759781 | T | TTTTTTGT others(6): Show |
12 | a0001c0002t0004g0015 a0001c0002t0004g0016 a0001c0002t0004g0204 others(9): Show |
14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.837+159_837+160ins others(13): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759781 | ||||||
| chr1:27759875 | C | T | 77 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0007 others(74): Show |
89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.837+248C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | chr1 | 27759875 | |||||||
| chr1:27759938 | A | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0165 |
2 | HG00408.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.837+311A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | chr1 | 27759938 | |||||||
| chr1:27759973 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.837+346A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | chr1 | 27759973 | |||||||
| chr1:27760017 | C | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG01169.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.837+390C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | chr1 | 27760017 | |||||||
| chr1:27760090 | G | A | 1 | a0001c0002t0023g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.838-405G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | chr1 | 27760090 | |||||||
| chr1:27760283 | T | C | 12 | a0001c0002t0004g0015 a0001c0002t0004g0016 a0001c0002t0004g0204 others(9): Show |
14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.838-212T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | chr1 | 27760283 | |||||||
| chr1:27760444 | C | A | 234 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(231): Show |
261 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(258): Show |
intron_variant | MODIFIER | c.838-51C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | chr1 | 27760444 |