Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2926 |
| ensemblid | ENSG00000132463.15 |
| hgncid | 4610 |
| symbol | GRSF1 |
| name | G-rich RNA sequence binding factor 1 |
| refseq_nuc | NM_002092.4 |
| refseq_prot | NP_002083.4 |
| ensembl_nuc | ENST00000254799.11 |
| ensembl_prot | ENSP00000254799.6 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 70815783 |
| end | 70839890 |
| strand | - |
| ver | v1.2 |
| region | chr4:70815783-70839890 |
| region5000 | chr4:70810783-70844890 |
| regionname0 | GRSF1_chr4_70815783_70839890 |
| regionname5000 | GRSF1_chr4_70810783_70844890 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 480 | 321 | 84 | 53 | 137 | 10 | 36 | 103 | GRSF1_chr4_70810783_70844890 | GRSF1 | MAGTR others(475): Show |
chr4 | 70810783 | 70844890 |
| a0002 | 1/0 | 480 | 4 | 3 | 0 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | MAGTR others(475): Show |
chr4 | 70810783 | 70844890 |
| a0003 | 0/0 | 480 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | MAGTR others(475): Show |
chr4 | 70810783 | 70844890 |
| a0004 | 0/0 | 480 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | MAGTR others(475): Show |
chr4 | 70810783 | 70844890 |
| a0005 | 0/0 | 480 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | MAGTR others(475): Show |
chr4 | 70810783 | 70844890 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1440 | 315 | 79 | 52 | 137 | 10 | 36 | GRSF1_chr4_70810783_70844890 | GRSF1 | ATGGC others(1435): Show |
chr4 | 70810783 | 70844890 | ||
| a0001c0003 | 0/0 | 1440 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ATGGC others(1435): Show |
chr4 | 70810783 | 70844890 | ||
| a0001c0004 | 0/0 | 1440 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ATGGC others(1435): Show |
chr4 | 70810783 | 70844890 | ||
| a0001c0005 | 0/0 | 1440 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ATGGC others(1435): Show |
chr4 | 70810783 | 70844890 | ||
| a0001c0009 | 0/0 | 1440 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ATGGC others(1435): Show |
chr4 | 70810783 | 70844890 | ||
| a0002c0002 | 1/0 | 1440 | 4 | 3 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ATGGC others(1435): Show |
chr4 | 70810783 | 70844890 | ||
| a0003c0007 | 0/0 | 1440 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ATGGC others(1435): Show |
chr4 | 70810783 | 70844890 | ||
| a0004c0006 | 0/0 | 1440 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ATGGC others(1435): Show |
chr4 | 70810783 | 70844890 | ||
| a0005c0008 | 0/0 | 1440 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ATGGC others(1435): Show |
chr4 | 70810783 | 70844890 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6609 | 161 | 28 | 41 | 64 | 7 | 21 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0002 | 0/0 | 6610 | 44 | 1 | 4 | 37 | 0 | 2 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6605): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0003 | 0/0 | 6610 | 13 | 13 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6605): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0004 | 0/0 | 6610 | 13 | 2 | 1 | 5 | 0 | 5 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6605): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0005 | 0/0 | 6609 | 12 | 0 | 0 | 12 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0006 | 0/0 | 6610 | 11 | 8 | 0 | 0 | 0 | 3 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6605): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0007 | 0/0 | 6609 | 10 | 0 | 1 | 6 | 0 | 3 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0008 | 0/0 | 6609 | 6 | 0 | 0 | 6 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0009 | 0/0 | 6610 | 6 | 6 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6605): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0011 | 0/0 | 6610 | 3 | 3 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6605): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0012 | 0/0 | 6610 | 3 | 0 | 0 | 0 | 3 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6605): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0013 | 0/0 | 6609 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0014 | 0/0 | 6610 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6605): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0015 | 0/0 | 6604 | 2 | 1 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6599): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0016 | 0/0 | 6610 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6605): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0017 | 0/0 | 6610 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6605): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0018 | 0/0 | 6609 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0019 | 0/0 | 6610 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6605): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0020 | 0/0 | 6609 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0021 | 0/0 | 6609 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0022 | 0/0 | 6610 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6605): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0023 | 0/0 | 6609 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0024 | 0/0 | 6609 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0025 | 0/0 | 6609 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0026 | 0/0 | 6609 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0027 | 0/0 | 6609 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0028 | 0/0 | 6609 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0029 | 0/0 | 6610 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6605): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0030 | 0/1 | 6609 | 1 | 0 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0031 | 0/0 | 6609 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0032 | 0/0 | 6610 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6605): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0033 | 0/0 | 6609 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0034 | 0/0 | 6609 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0035 | 0/0 | 6609 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0036 | 0/0 | 6609 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0037 | 0/0 | 6604 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6599): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0038 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6601): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0039 | 0/0 | 6610 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6605): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0040 | 0/0 | 6610 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6605): Show |
chr4 | 70810783 | 70844890 |
| a0001c0001t0042 | 0/0 | 6610 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6605): Show |
chr4 | 70810783 | 70844890 |
| a0001c0003t0001 | 0/0 | 6609 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0004t0003 | 0/0 | 6610 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6605): Show |
chr4 | 70810783 | 70844890 |
| a0001c0005t0001 | 0/0 | 6609 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0001c0009t0001 | 0/0 | 6609 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0002c0002t0010 | 1/0 | 6610 | 4 | 3 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6605): Show |
chr4 | 70810783 | 70844890 |
| a0003c0007t0001 | 0/0 | 6609 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| a0004c0006t0041 | 0/0 | 6610 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6605): Show |
chr4 | 70810783 | 70844890 |
| a0005c0008t0001 | 0/0 | 6609 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | ACTTC others(6604): Show |
chr4 | 70810783 | 70844890 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 23 | 7 | 1 | 12 | 0 | 3 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 1 | 1 | 2 | 4 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0004 | 0/0 | 6 | 2 | 2 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0012 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0014 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0002 | 0/0 | 15 | 0 | 3 | 11 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0003g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0003g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0005g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0005g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0006g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0006g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0007g0013 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0007g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0007g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0007g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0007g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0007g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0007g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0007g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0008g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0008g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0008g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0008g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0008g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0009g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0009g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0009g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0011g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0011g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0012g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0012g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0012g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0013g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0013g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0014g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0015g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0015g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0016g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0017g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0018g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0019g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0020g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0021g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0022g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0023g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0024g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0025g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0026g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0027g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0028g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0029g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0030g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0031g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0032g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0033g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0034g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0035g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0036g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0037g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0038g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0039g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0040g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0001t0042g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0003t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0004t0003g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0005t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0001c0009t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0002c0002t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0002c0002t0010g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0002c0002t0010g0224 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0002c0002t0010g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0003c0007t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0004c0006t0041g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| a0005c0008t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | GBR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG00323 | hp1 | a0001 | c0001 | t0012 | g0056 | EUR | FIN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | CHS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG00597 | hp1 | a0001 | c0001 | t0026 | g0167 | EAS | CHS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG00609 | hp1 | a0001 | c0001 | t0008 | g0164 | EAS | CHS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG00639 | hp2 | a0003 | c0007 | t0001 | g0117 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG00673 | hp2 | a0001 | c0001 | t0018 | g0156 | EAS | CHS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0182 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01106 | hp1 | a0001 | c0001 | t0023 | g0096 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01167 | hp2 | a0001 | c0001 | t0015 | g0073 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01361 | hp1 | a0001 | c0001 | t0028 | g0186 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01515 | hp2 | a0001 | c0001 | t0012 | g0055 | EUR | IBS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01517 | hp1 | a0001 | c0001 | t0012 | g0054 | EUR | IBS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | IBS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01884 | hp1 | a0001 | c0001 | t0017 | g0046 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0068 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0018 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01975 | hp2 | a0001 | c0009 | t0001 | g0221 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02027 | hp1 | a0001 | c0001 | t0008 | g0162 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02040 | hp1 | a0001 | c0001 | t0035 | g0053 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02056 | hp2 | a0001 | c0001 | t0008 | g0171 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02080 | hp1 | a0001 | c0001 | t0008 | g0036 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0213 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0070 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02148 | hp2 | a0001 | c0001 | t0025 | g0136 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02155 | hp2 | a0001 | c0001 | t0022 | g0201 | EAS | CDX | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02257 | hp1 | a0001 | c0001 | t0020 | g0134 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02258 | hp1 | a0001 | c0001 | t0040 | g0195 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02258 | hp2 | a0001 | c0001 | t0013 | g0103 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02280 | hp2 | a0001 | c0001 | t0037 | g0075 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02300 | hp1 | a0001 | c0001 | t0036 | g0084 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02451 | hp1 | a0001 | c0001 | t0021 | g0165 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02572 | hp2 | a0001 | c0001 | t0042 | g0058 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0069 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0067 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02622 | hp2 | a0001 | c0001 | t0011 | g0020 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02630 | hp1 | a0001 | c0001 | t0013 | g0105 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0037 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02647 | hp1 | a0001 | c0001 | t0009 | g0017 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02723 | hp1 | a0001 | c0001 | t0027 | g0174 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02723 | hp2 | a0001 | c0001 | t0038 | g0194 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0219 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0051 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0017 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02818 | hp1 | a0001 | c0001 | t0016 | g0019 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02818 | hp2 | a0001 | c0001 | t0015 | g0074 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0060 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02886 | hp2 | a0001 | c0001 | t0014 | g0042 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0150 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02922 | hp1 | a0002 | c0002 | t0010 | g0222 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02965 | hp1 | a0001 | c0001 | t0032 | g0111 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03017 | hp2 | a0001 | c0001 | t0006 | g0072 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03130 | hp1 | a0001 | c0001 | t0029 | g0153 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03130 | hp2 | a0004 | c0006 | t0041 | g0193 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03139 | hp2 | a0001 | c0001 | t0016 | g0019 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03195 | hp1 | a0001 | c0001 | t0011 | g0066 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0020 | AFR | MSL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | MSL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0178 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03453 | hp2 | a0001 | c0001 | t0039 | g0064 | AFR | MSL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03486 | hp1 | a0001 | c0005 | t0001 | g0140 | AFR | MSL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0065 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03540 | hp2 | a0001 | c0004 | t0003 | g0039 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0037 | AFR | MSL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | MSL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03654 | hp2 | a0001 | c0001 | t0031 | g0181 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0191 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03688 | hp2 | a0001 | c0001 | t0006 | g0071 | SAS | STU | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03710 | hp1 | a0001 | c0001 | t0007 | g0155 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03831 | hp1 | a0001 | c0001 | t0007 | g0050 | SAS | BEB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03834 | hp2 | a0001 | c0001 | t0007 | g0013 | SAS | BEB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | STU | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0177 | SAS | STU | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | STU | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | YRI | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18522 | hp2 | a0001 | c0004 | t0003 | g0039 | AFR | YRI | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18747 | hp1 | a0001 | c0001 | t0033 | g0087 | EAS | CHB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0059 | AFR | YRI | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18906 | hp2 | a0002 | c0002 | t0010 | g0225 | AFR | YRI | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18941 | hp1 | a0001 | c0001 | t0007 | g0126 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18956 | hp1 | a0005 | c0008 | t0001 | g0220 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18961 | hp2 | a0001 | c0001 | t0007 | g0149 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18962 | hp1 | a0001 | c0001 | t0007 | g0013 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18963 | hp1 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18963 | hp2 | a0001 | c0001 | t0005 | g0129 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18969 | hp1 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18987 | hp1 | a0001 | c0001 | t0005 | g0124 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18987 | hp2 | a0001 | c0001 | t0005 | g0172 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18995 | hp2 | a0001 | c0001 | t0007 | g0175 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18997 | hp1 | a0001 | c0001 | t0019 | g0176 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19005 | hp1 | a0001 | c0001 | t0007 | g0013 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19005 | hp2 | a0001 | c0001 | t0005 | g0025 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19009 | hp2 | a0001 | c0001 | t0008 | g0036 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | LWK | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | LWK | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | LWK | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19060 | hp2 | a0001 | c0001 | t0005 | g0147 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19063 | hp2 | a0001 | c0001 | t0007 | g0148 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19070 | hp2 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19077 | hp1 | a0001 | c0001 | t0005 | g0025 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19081 | hp2 | a0001 | c0001 | t0024 | g0100 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19086 | hp2 | a0001 | c0001 | t0008 | g0161 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | YRI | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA19240 | hp2 | a0001 | c0001 | t0014 | g0042 | AFR | YRI | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | ASW | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | GIH | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA20905 | hp2 | a0001 | c0001 | t0034 | g0139 | SAS | GIH | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01123 | hp1 | a0001 | c0001 | t0007 | g0157 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0214 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG03471 | hp2 | a0002 | c0002 | t0010 | g0223 | AFR | MSL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | USA | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| HG06807 | hp2 | a0001 | c0001 | t0009 | g0018 | AFR | USA | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0030 | g0142 | REF | REF | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0010 | g0224 | REF | REF | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70836188 | T | A | 1 | a0004 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.484A>T | p.Thr162Ser | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/10 | 547/6610 | 484/1443 | 162/480 | chr4 | 70836188 | |||
| chr4:70836307 | T | C | 1 | a0003 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.365A>G | p.Lys122Arg | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/10 | 428/6610 | 365/1443 | 122/480 | chr4 | 70836307 | |||
| chr4:70839521 | G | A | 1 | a0005 | 1 | NA18956.hp1 | missense_variant | MODERATE | c.307C>T | p.Pro103Ser | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/10 | 370/6610 | 307/1443 | 103/480 | chr4 | 70839521 | |||
| chr4:70839545 | A | G | 4 | a0001 a0003 a0004 others(1): Show |
323 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(320): Show |
missense_variant | MODERATE | c.283T>C | p.Ser95Pro | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/10 | 346/6610 | 283/1443 | 95/480 | chr4 | 70839545 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70825327 | A | G | 1 | a0001c0003 | 2 | HG02630.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.1362T>C | p.Val454Val | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/10 | 1425/6610 | 1362/1443 | 454/480 | chr4 | 70825327 | |||
| chr4:70826183 | G | A | 1 | a0001c0004 | 2 | HG03540.hp2 NA18522.hp2 |
synonymous_variant | LOW | c.1198C>T | p.Leu400Leu | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/10 | 1261/6610 | 1198/1443 | 400/480 | chr4 | 70826183 | |||
| chr4:70827946 | A | C | 1 | a0001c0005 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.1041T>G | p.Ala347Ala | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/10 | 1104/6610 | 1041/1443 | 347/480 | chr4 | 70827946 | |||
| chr4:70839537 | G | A | 1 | a0001c0009 | 1 | HG01975.hp2 | synonymous_variant | LOW | c.291C>T | p.Leu97Leu | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/10 | 354/6610 | 291/1443 | 97/480 | chr4 | 70839537 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70816075 | G | C | 2 | a0001c0001t0009 a0001c0001t0042 |
7 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4812C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 8244 | chr4 | 70816075 | ||||||
| chr4:70816346 | CA | C | 27 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(24): Show |
221 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*4540delT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7972 | chr4 | 70816346 | ||||||
| chr4:70816366 | G | A | 1 | a0001c0001t0004 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4521C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7953 | chr4 | 70816366 | ||||||
| chr4:70816367 | A | G | 1 | a0001c0001t0029 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4520T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7952 | chr4 | 70816367 | ||||||
| chr4:70816437 | A | G | 1 | a0001c0001t0028 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4450T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7882 | chr4 | 70816437 | ||||||
| chr4:70816675 | G | A | 3 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0042 |
10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4212C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7644 | chr4 | 70816675 | ||||||
| chr4:70816687 | A | G | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(35): Show |
289 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*4200T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7632 | chr4 | 70816687 | ||||||
| chr4:70816711 | C | T | 3 | a0001c0001t0015 a0001c0001t0037 a0001c0001t0038 |
4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4176G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7608 | chr4 | 70816711 | ||||||
| chr4:70816735 | A | G | 1 | a0001c0001t0012 | 3 | HG00323.hp1 HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4152T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7584 | chr4 | 70816735 | ||||||
| chr4:70816810 | T | C | 34 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(31): Show |
284 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(281): Show |
3_prime_UTR_variant | MODIFIER | c.*4077A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7509 | chr4 | 70816810 | ||||||
| chr4:70816852 | G | A | 1 | a0001c0001t0005 | 12 | NA18963.hp1 NA18963.hp2 NA18969.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4035C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7467 | chr4 | 70816852 | ||||||
| chr4:70816941 | T | C | 1 | a0001c0001t0012 | 3 | HG00323.hp1 HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3946A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7378 | chr4 | 70816941 | ||||||
| chr4:70817023 | CCACT | C | 3 | a0001c0001t0015 a0001c0001t0037 a0001c0001t0038 |
4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3860_*3863delAGTG | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7292 | chr4 | 70817023 | ||||||
| chr4:70817081 | A | T | 1 | a0001c0001t0027 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3806T>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7238 | chr4 | 70817081 | ||||||
| chr4:70817101 | T | C | 1 | a0001c0001t0011 | 3 | HG02622.hp2 HG03195.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3786A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7218 | chr4 | 70817101 | ||||||
| chr4:70817167 | G | C | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(28): Show |
274 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(271): Show |
3_prime_UTR_variant | MODIFIER | c.*3720C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7152 | chr4 | 70817167 | ||||||
| chr4:70817214 | TGC | T | 2 | a0001c0001t0015 a0001c0001t0037 |
3 | HG01167.hp2 HG02280.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3671_*3672delGC | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7103 | chr4 | 70817214 | ||||||
| chr4:70817216 | C | CT | 5 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(2): Show |
18 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3670dupA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7102 | chr4 | 70817216 | ||||||
| chr4:70817269 | C | T | 2 | a0001c0001t0015 a0001c0001t0037 |
3 | HG01167.hp2 HG02280.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3618G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7050 | chr4 | 70817269 | ||||||
| chr4:70817287 | G | A | 1 | a0001c0001t0042 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3600C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7032 | chr4 | 70817287 | ||||||
| chr4:70817471 | T | G | 1 | a0001c0001t0031 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3416A>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6848 | chr4 | 70817471 | ||||||
| chr4:70817522 | A | G | 1 | a0001c0001t0026 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3365T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6797 | chr4 | 70817522 | ||||||
| chr4:70817615 | T | C | 2 | a0001c0001t0013 a0001c0001t0032 |
3 | HG02258.hp2 HG02630.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3272A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6704 | chr4 | 70817615 | ||||||
| chr4:70817888 | G | A | 2 | a0001c0001t0015 a0001c0001t0037 |
3 | HG01167.hp2 HG02280.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2999C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6431 | chr4 | 70817888 | ||||||
| chr4:70817912 | G | A | 1 | a0001c0001t0038 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2975C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6407 | chr4 | 70817912 | ||||||
| chr4:70817966 | T | C | 2 | a0001c0001t0017 a0001c0001t0033 |
2 | HG01884.hp1 NA18747.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2921A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6353 | chr4 | 70817966 | ||||||
| chr4:70818118 | A | G | 3 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0022 |
47 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*2769T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6201 | chr4 | 70818118 | ||||||
| chr4:70818142 | G | A | 1 | a0001c0001t0014 | 2 | HG02886.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2745C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6177 | chr4 | 70818142 | ||||||
| chr4:70818152 | C | T | 1 | a0001c0001t0025 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2735G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6167 | chr4 | 70818152 | ||||||
| chr4:70818163 | C | T | 1 | a0001c0001t0018 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2724G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6156 | chr4 | 70818163 | ||||||
| chr4:70818273 | T | G | 1 | a0001c0001t0019 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2614A>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6046 | chr4 | 70818273 | ||||||
| chr4:70818644 | C | G | 1 | a0001c0001t0015 | 2 | HG01167.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2243G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 5675 | chr4 | 70818644 | ||||||
| chr4:70818694 | G | A | 4 | a0001c0001t0006 a0001c0001t0011 a0001c0001t0016 others(1): Show |
17 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2193C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 5625 | chr4 | 70818694 | ||||||
| chr4:70818699 | C | A | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(35): Show |
289 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*2188G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 5620 | chr4 | 70818699 | ||||||
| chr4:70818741 | G | A | 46 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(43): Show |
323 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*2146C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 5578 | chr4 | 70818741 | ||||||
| chr4:70818885 | G | A | 1 | a0001c0001t0009 | 6 | HG01891.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2002C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 5434 | chr4 | 70818885 | ||||||
| chr4:70818904 | A | G | 1 | a0001c0001t0009 | 6 | HG01891.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1983T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 5415 | chr4 | 70818904 | ||||||
| chr4:70819095 | G | T | 1 | a0001c0001t0023 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1792C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 5224 | chr4 | 70819095 | ||||||
| chr4:70819255 | C | G | 1 | a0001c0001t0022 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1632G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 5064 | chr4 | 70819255 | ||||||
| chr4:70819321 | T | C | 1 | a0001c0001t0008 | 6 | HG00609.hp1 HG02027.hp1 HG02056.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1566A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4998 | chr4 | 70819321 | ||||||
| chr4:70819375 | C | A | 34 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(31): Show |
284 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(281): Show |
3_prime_UTR_variant | MODIFIER | c.*1512G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4944 | chr4 | 70819375 | ||||||
| chr4:70819430 | C | T | 1 | a0001c0001t0016 | 2 | HG02818.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1457G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4889 | chr4 | 70819430 | ||||||
| chr4:70819486 | T | C | 1 | a0001c0001t0034 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1401A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4833 | chr4 | 70819486 | ||||||
| chr4:70819619 | A | G | 1 | a0001c0001t0021 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1268T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4700 | chr4 | 70819619 | ||||||
| chr4:70819663 | T | C | 1 | a0004c0006t0041 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1224A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4656 | chr4 | 70819663 | ||||||
| chr4:70819811 | A | G | 1 | a0001c0001t0039 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1076T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4508 | chr4 | 70819811 | ||||||
| chr4:70819830 | T | C | 1 | a0001c0001t0035 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1057A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4489 | chr4 | 70819830 | ||||||
| chr4:70819863 | G | GA | 3 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0042 |
10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1023dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4455 | chr4 | 70819863 | ||||||
| chr4:70819924 | A | C | 1 | a0001c0001t0020 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*963T>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4395 | chr4 | 70819924 | ||||||
| chr4:70819982 | G | A | 2 | a0001c0001t0009 a0001c0001t0042 |
7 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*905C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4337 | chr4 | 70819982 | ||||||
| chr4:70820108 | T | C | 1 | a0001c0001t0036 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*779A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4211 | chr4 | 70820108 | ||||||
| chr4:70820129 | A | T | 3 | a0001c0001t0007 a0001c0001t0018 a0001c0001t0019 |
12 | HG00673.hp2 HG01123.hp1 HG03710.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*758T>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4190 | chr4 | 70820129 | ||||||
| chr4:70820169 | T | C | 3 | a0001c0001t0015 a0001c0001t0037 a0001c0001t0038 |
4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*718A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4150 | chr4 | 70820169 | ||||||
| chr4:70820529 | C | G | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(34): Show |
288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*358G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 3790 | chr4 | 70820529 | ||||||
| chr4:70820733 | T | C | 3 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0042 |
10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*154A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 3586 | chr4 | 70820733 | ||||||
| chr4:70839850 | C | G | 1 | a0001c0001t0017 | 1 | HG01884.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/10 | 23 | chr4 | 70839850 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70820883 | T | C | 1 | a0001c0001t0007g0157 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.*26-22A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70820883 | |||||||
| chr4:70821109 | T | C | 1 | a0001c0001t0007g0050 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.*26-248A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821109 | |||||||
| chr4:70821164 | C | T | 10 | a0001c0001t0007g0013 a0001c0001t0007g0050 a0001c0001t0007g0126 others(7): Show |
12 | HG00673.hp2 HG01123.hp1 HG03710.hp1 others(9): Show |
intron_variant | MODIFIER | c.*26-303G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821164 | |||||||
| chr4:70821235 | C | T | 3 | a0001c0001t0012g0054 a0001c0001t0012g0055 a0001c0001t0012g0056 |
3 | HG00323.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.*26-374G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821235 | |||||||
| chr4:70821407 | G | A | 3 | a0001c0001t0015g0073 a0001c0001t0015g0074 a0001c0001t0037g0075 |
3 | HG01167.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.*26-546C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821407 | |||||||
| chr4:70821426 | A | AAAAT | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.*26-569_*26-566dup others(4): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821426 | |||||||
| chr4:70821463 | G | A | 2 | a0001c0001t0003g0216 a0001c0001t0003g0217 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.*26-602C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821463 | |||||||
| chr4:70821478 | C | T | 1 | a0001c0001t0009g0017 | 2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.*26-617G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821478 | |||||||
| chr4:70821553 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.*26-692G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821553 | |||||||
| chr4:70821566 | A | G | 4 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(1): Show |
6 | HG01891.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.*26-705T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821566 | |||||||
| chr4:70821598 | TC | T | 4 | a0001c0001t0015g0073 a0001c0001t0015g0074 a0001c0001t0037g0075 others(1): Show |
4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.*26-738delG | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821598 | |||||||
| chr4:70821601 | G | A | 1 | a0001c0001t0040g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*26-740C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821601 | |||||||
| chr4:70821607 | C | CA | 16 | a0001c0001t0001g0052 a0001c0001t0001g0086 a0001c0001t0001g0088 others(13): Show |
16 | HG00323.hp1 HG00597.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.*26-747dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821607 | |||||||
| chr4:70821673 | C | CT | 5 | a0001c0001t0003g0216 a0001c0001t0003g0217 a0001c0001t0006g0067 others(2): Show |
6 | HG02615.hp2 HG03209.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.*26-813dupA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821673 | |||||||
| chr4:70821673 | CT | C | 11 | a0001c0001t0001g0101 a0001c0001t0001g0106 a0001c0001t0001g0143 others(8): Show |
11 | HG01167.hp2 HG01884.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.*26-813delA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821673 | |||||||
| chr4:70821673 | CTT | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
278 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.*26-814_*26-813del others(2): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821673 | |||||||
| chr4:70821831 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.*26-970T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821831 | |||||||
| chr4:70821962 | C | T | 1 | a0001c0001t0040g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*26-1101G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821962 | |||||||
| chr4:70822110 | C | T | 1 | a0001c0001t0006g0072 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.*26-1249G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822110 | |||||||
| chr4:70822149 | G | A | 1 | a0001c0001t0040g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*26-1288C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822149 | |||||||
| chr4:70822149 | G | C | 1 | a0001c0001t0012g0056 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.*26-1288C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822149 | |||||||
| chr4:70822312 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0027g0174 |
2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.*26-1451C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822312 | |||||||
| chr4:70822358 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.*26-1497C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822358 | |||||||
| chr4:70822475 | T | C | 1 | a0001c0001t0013g0105 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.*26-1614A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822475 | |||||||
| chr4:70822482 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.*26-1621G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822482 | |||||||
| chr4:70822542 | C | T | 4 | a0001c0001t0015g0073 a0001c0001t0015g0074 a0001c0001t0037g0075 others(1): Show |
4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.*26-1681G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822542 | |||||||
| chr4:70822583 | CAAAAAAA others(1): Show |
C | 8 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(5): Show |
10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.*25+1703_*25+1710d others(10): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822583 | |||||||
| chr4:70822593 | AAAAAAAA others(6): Show |
A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
274 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.*25+1688_*25+1700d others(15): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822593 | |||||||
| chr4:70822604 | AAC | A | 22 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(19): Show |
30 | HG02145.hp1 HG02145.hp2 HG02486.hp2 others(27): Show |
intron_variant | MODIFIER | c.*25+1688_*25+1689d others(4): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822604 | |||||||
| chr4:70822699 | G | A | 3 | a0001c0001t0015g0073 a0001c0001t0015g0074 a0001c0001t0037g0075 |
3 | HG01167.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.*25+1595C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822699 | |||||||
| chr4:70822758 | T | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0026 others(26): Show |
43 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.*25+1536A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822758 | |||||||
| chr4:70822767 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.*25+1527C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822767 | |||||||
| chr4:70823065 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.*25+1229G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823065 | |||||||
| chr4:70823136 | C | T | 3 | a0001c0001t0003g0045 a0001c0001t0003g0215 a0001c0001t0003g0218 |
4 | HG02717.hp1 NA19030.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.*25+1158G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823136 | |||||||
| chr4:70823172 | G | C | 13 | a0001c0001t0006g0008 a0001c0001t0006g0063 a0001c0001t0006g0065 others(10): Show |
17 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.*25+1122C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823172 | |||||||
| chr4:70823247 | A | T | 3 | a0001c0001t0015g0073 a0001c0001t0015g0074 a0001c0001t0037g0075 |
3 | HG01167.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.*25+1047T>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823247 | |||||||
| chr4:70823249 | T | C | 1 | a0001c0001t0040g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*25+1045A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823249 | |||||||
| chr4:70823264 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.*25+1030C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823264 | |||||||
| chr4:70823431 | A | T | 2 | a0001c0001t0001g0098 a0001c0001t0004g0092 |
2 | NA19004.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.*25+863T>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823431 | |||||||
| chr4:70823481 | CT | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.*25+812delA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823481 | |||||||
| chr4:70823700 | T | C | 10 | a0001c0001t0007g0013 a0001c0001t0007g0050 a0001c0001t0007g0126 others(7): Show |
12 | HG00673.hp2 HG01123.hp1 HG03710.hp1 others(9): Show |
intron_variant | MODIFIER | c.*25+594A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823700 | |||||||
| chr4:70823754 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0141 |
2 | NA18971.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.*25+540G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823754 | |||||||
| chr4:70823809 | G | A | 1 | a0001c0001t0001g0035 | 2 | NA18969.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.*25+485C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823809 | |||||||
| chr4:70823812 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.*25+482C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823812 | |||||||
| chr4:70823903 | C | T | 8 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(5): Show |
10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.*25+391G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823903 | |||||||
| chr4:70823968 | A | C | 1 | a0001c0001t0037g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.*25+326T>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823968 | |||||||
| chr4:70823968 | ATC | A | 2 | a0001c0001t0002g0210 a0001c0001t0014g0042 |
3 | HG02809.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.*25+324_*25+325del others(2): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823968 | |||||||
| chr4:70823974 | C | CT | 10 | a0001c0001t0006g0065 a0001c0001t0009g0017 a0001c0001t0009g0018 others(7): Show |
12 | HG01517.hp1 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.*25+319dupA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823974 | |||||||
| chr4:70823974 | C | CTTT | 23 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0121 others(20): Show |
28 | HG00673.hp2 HG01123.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.*25+319_*25+320ins others(3): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823974 | |||||||
| chr4:70823974 | C | CTTTT | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
189 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.*25+319_*25+320ins others(4): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823974 | |||||||
| chr4:70823974 | C | CTTTTT | 27 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0091 others(24): Show |
49 | HG00408.hp2 HG00597.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.*25+319_*25+320ins others(5): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823974 | |||||||
| chr4:70823976 | C | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
318 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.*25+318G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823976 | |||||||
| chr4:70824002 | G | A | 27 | a0001c0001t0001g0189 a0001c0001t0002g0002 a0001c0001t0002g0007 others(24): Show |
49 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.*25+292C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70824002 | |||||||
| chr4:70824054 | G | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.*25+240C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70824054 | |||||||
| chr4:70824066 | G | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
284 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.*25+228C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70824066 | |||||||
| chr4:70824124 | T | A | 1 | a0001c0001t0001g0163 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.*25+170A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70824124 | |||||||
| chr4:70824205 | G | C | 1 | a0001c0001t0017g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.*25+89C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70824205 | |||||||
| chr4:70824273 | A | T | 1 | a0001c0001t0038g0194 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.*25+21T>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70824273 | |||||||
| chr4:70824504 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.1394-136T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824504 | |||||||
| chr4:70824539 | C | T | 1 | a0001c0001t0004g0219 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1394-171G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824539 | |||||||
| chr4:70824647 | G | C | 4 | a0001c0001t0015g0073 a0001c0001t0015g0074 a0001c0001t0037g0075 others(1): Show |
4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1394-279C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824647 | |||||||
| chr4:70824651 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
323 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.1394-283A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824651 | |||||||
| chr4:70824675 | C | T | 8 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(5): Show |
10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.1394-307G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824675 | |||||||
| chr4:70824714 | C | T | 8 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(5): Show |
10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.1394-346G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824714 | |||||||
| chr4:70824729 | G | A | 1 | a0001c0001t0035g0053 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1394-361C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824729 | |||||||
| chr4:70824762 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
284 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.1394-394C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824762 | |||||||
| chr4:70824859 | T | G | 11 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(8): Show |
15 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1393+437A>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824859 | |||||||
| chr4:70824945 | T | C | 1 | a0001c0001t0017g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1393+351A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824945 | |||||||
| chr4:70824965 | G | A | 13 | a0001c0001t0006g0008 a0001c0001t0006g0063 a0001c0001t0006g0065 others(10): Show |
17 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.1393+331C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824965 | |||||||
| chr4:70824984 | C | T | 3 | a0001c0001t0015g0073 a0001c0001t0015g0074 a0001c0001t0037g0075 |
3 | HG01167.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1393+312G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824984 | |||||||
| chr4:70824991 | A | G | 1 | a0001c0001t0002g0200 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1393+305T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824991 | |||||||
| chr4:70825025 | A | G | 1 | a0001c0001t0037g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1393+271T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70825025 | |||||||
| chr4:70825111 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
284 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.1393+185T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70825111 | |||||||
| chr4:70825143 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1393+153A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70825143 | |||||||
| chr4:70825197 | T | C | 24 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(21): Show |
32 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.1393+99A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70825197 | |||||||
| chr4:70825438 | GACAA | G | 4 | a0001c0001t0015g0073 a0001c0001t0015g0074 a0001c0001t0037g0075 others(1): Show |
4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1258-11_1258-8delT others(3): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/9 | chr4 | 70825438 | |||||||
| chr4:70825565 | G | T | 13 | a0001c0001t0006g0008 a0001c0001t0006g0063 a0001c0001t0006g0065 others(10): Show |
17 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.1258-134C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/9 | chr4 | 70825565 | |||||||
| chr4:70825566 | C | T | 13 | a0001c0001t0006g0008 a0001c0001t0006g0063 a0001c0001t0006g0065 others(10): Show |
17 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.1258-135G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/9 | chr4 | 70825566 | |||||||
| chr4:70825822 | C | G | 4 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(1): Show |
6 | HG01891.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1257+302G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/9 | chr4 | 70825822 | |||||||
| chr4:70825823 | T | G | 1 | a0001c0001t0005g0123 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1257+301A>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/9 | chr4 | 70825823 | |||||||
| chr4:70825918 | C | T | 1 | a0001c0001t0017g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1257+206G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/9 | chr4 | 70825918 | |||||||
| chr4:70825931 | C | CA | 24 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(21): Show |
32 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.1257+192dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/9 | chr4 | 70825931 | |||||||
| chr4:70826026 | C | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.1257+98G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/9 | chr4 | 70826026 | |||||||
| chr4:70826068 | C | A | 2 | a0001c0001t0001g0189 a0001c0001t0027g0174 |
2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1257+56G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/9 | chr4 | 70826068 | |||||||
| chr4:70826113 | C | T | 1 | a0001c0001t0039g0064 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1257+11G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/9 | chr4 | 70826113 | |||||||
| chr4:70826258 | A | G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0062 a0001c0001t0001g0088 others(6): Show |
12 | HG00639.hp2 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.1136-13T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826258 | |||||||
| chr4:70826278 | A | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0188 |
2 | HG02622.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1136-33T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826278 | |||||||
| chr4:70826287 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1136-42A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826287 | |||||||
| chr4:70826346 | T | C | 1 | a0001c0001t0029g0153 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1136-101A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826346 | |||||||
| chr4:70826457 | G | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.1136-212C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826457 | |||||||
| chr4:70826457 | G | T | 1 | a0001c0001t0001g0169 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1136-212C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826457 | |||||||
| chr4:70826496 | G | GA | 4 | a0001c0001t0015g0073 a0001c0001t0015g0074 a0001c0001t0037g0075 others(1): Show |
4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1136-252dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826496 | |||||||
| chr4:70826521 | T | C | 10 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0029 others(7): Show |
15 | HG01934.hp2 HG01978.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.1136-276A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826521 | |||||||
| chr4:70826528 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
323 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.1136-283A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826528 | |||||||
| chr4:70826536 | G | GA | 14 | a0001c0001t0003g0045 a0001c0001t0003g0061 a0001c0001t0003g0215 others(11): Show |
17 | HG00673.hp2 HG01123.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.1136-292dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826536 | |||||||
| chr4:70826566 | G | A | 5 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(2): Show |
7 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1136-321C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826566 | |||||||
| chr4:70826592 | C | A | 1 | a0001c0001t0009g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1136-347G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826592 | |||||||
| chr4:70826672 | T | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0141 |
2 | NA18971.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1136-427A>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826672 | |||||||
| chr4:70826753 | T | A | 2 | a0001c0001t0004g0178 a0001c0001t0004g0191 |
2 | HG03239.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1136-508A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826753 | |||||||
| chr4:70826787 | G | A | 1 | a0001c0001t0017g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1136-542C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826787 | |||||||
| chr4:70827181 | G | A | 10 | a0001c0001t0007g0013 a0001c0001t0007g0050 a0001c0001t0007g0126 others(7): Show |
12 | HG00673.hp2 HG01123.hp1 HG03710.hp1 others(9): Show |
intron_variant | MODIFIER | c.1135+671C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827181 | |||||||
| chr4:70827196 | G | T | 1 | a0001c0001t0017g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1135+656C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827196 | |||||||
| chr4:70827203 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1135+649C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827203 | |||||||
| chr4:70827220 | G | A | 1 | a0001c0001t0037g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1135+632C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827220 | |||||||
| chr4:70827235 | C | G | 1 | a0001c0001t0005g0123 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1135+617G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827235 | |||||||
| chr4:70827250 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1135+602A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827250 | |||||||
| chr4:70827287 | C | CA | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
270 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.1135+564dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827287 | |||||||
| chr4:70827287 | C | CAA | 8 | a0001c0001t0001g0062 a0001c0001t0001g0109 a0001c0001t0001g0112 others(5): Show |
8 | HG00609.hp1 HG01952.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1135+563_1135+564d others(4): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827287 | |||||||
| chr4:70827505 | C | T | 9 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0028 others(6): Show |
13 | HG00609.hp2 HG01255.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1135+347G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827505 | |||||||
| chr4:70827598 | C | G | 1 | a0001c0001t0040g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1135+254G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827598 | |||||||
| chr4:70827607 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1135+245T>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827607 | |||||||
| chr4:70827636 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1135+216G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827636 | |||||||
| chr4:70827643 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0159 |
2 | HG01106.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1135+209G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827643 | |||||||
| chr4:70827697 | T | A | 3 | a0001c0001t0012g0054 a0001c0001t0012g0055 a0001c0001t0012g0056 |
3 | HG00323.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1135+155A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827697 | |||||||
| chr4:70828082 | T | C | 2 | a0001c0001t0001g0189 a0001c0001t0027g0174 |
2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.951-46A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828082 | |||||||
| chr4:70828542 | G | GGACT | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
284 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.951-510_951-507dup others(4): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828542 | |||||||
| chr4:70828736 | A | AT | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
137 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.951-701dupA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828736 | |||||||
| chr4:70828736 | A | ATT | 5 | a0001c0001t0001g0022 a0001c0001t0001g0088 a0001c0001t0001g0120 others(2): Show |
6 | HG01123.hp2 HG01978.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.951-702_951-701dup others(2): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828736 | |||||||
| chr4:70828736 | AT | A | 8 | a0001c0001t0001g0189 a0001c0001t0003g0043 a0001c0001t0003g0044 others(5): Show |
10 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.951-701delA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828736 | |||||||
| chr4:70828746 | T | G | 2 | a0001c0001t0001g0189 a0001c0001t0027g0174 |
2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.951-710A>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828746 | |||||||
| chr4:70828749 | T | G | 2 | a0001c0001t0001g0189 a0001c0001t0027g0174 |
2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.951-713A>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828749 | |||||||
| chr4:70828763 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
274 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.951-727C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828763 | |||||||
| chr4:70828803 | T | C | 1 | a0001c0001t0004g0182 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.951-767A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828803 | |||||||
| chr4:70828874 | A | G | 2 | a0001c0001t0011g0020 a0001c0001t0011g0066 |
3 | HG02622.hp2 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.951-838T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828874 | |||||||
| chr4:70828883 | G | A | 2 | a0001c0001t0015g0073 a0001c0001t0015g0074 |
2 | HG01167.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.951-847C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828883 | |||||||
| chr4:70828887 | G | A | 4 | a0001c0001t0015g0073 a0001c0001t0015g0074 a0001c0001t0037g0075 others(1): Show |
4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.951-851C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828887 | |||||||
| chr4:70828987 | C | T | 3 | a0001c0001t0015g0073 a0001c0001t0015g0074 a0001c0001t0037g0075 |
3 | HG01167.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.951-951G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828987 | |||||||
| chr4:70829014 | T | C | 1 | a0001c0001t0001g0024 | 2 | HG02132.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.951-978A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829014 | |||||||
| chr4:70829053 | T | C | 8 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(5): Show |
10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.951-1017A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829053 | |||||||
| chr4:70829131 | T | C | 1 | a0001c0001t0031g0181 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.951-1095A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829131 | |||||||
| chr4:70829184 | C | T | 1 | a0001c0001t0040g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.951-1148G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829184 | |||||||
| chr4:70829350 | GT | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
285 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.951-1315delA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829350 | |||||||
| chr4:70829360 | T | C | 1 | a0001c0001t0033g0087 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.951-1324A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829360 | |||||||
| chr4:70829426 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.951-1390G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829426 | |||||||
| chr4:70829442 | G | A | 1 | a0001c0001t0038g0194 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.951-1406C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829442 | |||||||
| chr4:70829458 | C | A | 2 | a0001c0001t0001g0189 a0001c0001t0027g0174 |
2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.951-1422G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829458 | |||||||
| chr4:70829760 | G | A | 4 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(1): Show |
6 | HG01891.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.951-1724C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829760 | |||||||
| chr4:70829820 | C | T | 1 | a0001c0001t0038g0194 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.950+1719G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829820 | |||||||
| chr4:70829824 | G | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
206 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.950+1715C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829824 | |||||||
| chr4:70829904 | G | T | 1 | a0001c0001t0011g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.950+1635C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829904 | |||||||
| chr4:70830032 | G | A | 8 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(5): Show |
10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.950+1507C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830032 | |||||||
| chr4:70830056 | C | T | 1 | a0001c0001t0040g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.950+1483G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830056 | |||||||
| chr4:70830098 | G | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG00735.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.950+1441C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830098 | |||||||
| chr4:70830157 | G | A | 1 | a0001c0001t0040g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.950+1382C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830157 | |||||||
| chr4:70830180 | C | A | 1 | a0001c0001t0006g0070 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.950+1359G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830180 | |||||||
| chr4:70830181 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG02004.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.950+1358C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830181 | |||||||
| chr4:70830199 | G | A | 1 | a0001c0001t0040g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.950+1340C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830199 | |||||||
| chr4:70830275 | C | T | 4 | a0001c0001t0015g0073 a0001c0001t0015g0074 a0001c0001t0037g0075 others(1): Show |
4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.950+1264G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830275 | |||||||
| chr4:70830350 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.950+1189G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830350 | |||||||
| chr4:70830358 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.950+1181A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830358 | |||||||
| chr4:70830403 | C | T | 1 | a0001c0001t0038g0194 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.950+1136G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830403 | |||||||
| chr4:70830404 | C | A | 1 | a0001c0001t0038g0194 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.950+1135G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830404 | |||||||
| chr4:70830426 | C | G | 9 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(6): Show |
11 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.950+1113G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830426 | |||||||
| chr4:70830446 | T | TA | 19 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0138 others(16): Show |
23 | HG00673.hp2 HG01123.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.950+1092dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830446 | |||||||
| chr4:70830459 | A | C | 1 | a0001c0001t0038g0194 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.950+1080T>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830459 | |||||||
| chr4:70830461 | A | C | 9 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(6): Show |
11 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.950+1078T>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830461 | |||||||
| chr4:70830475 | C | G | 11 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(8): Show |
15 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.950+1064G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830475 | |||||||
| chr4:70830542 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.950+997C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830542 | |||||||
| chr4:70830780 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
323 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.950+759T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830780 | |||||||
| chr4:70830791 | C | A | 8 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(5): Show |
10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.950+748G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830791 | |||||||
| chr4:70830810 | G | A | 28 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0026 others(25): Show |
42 | HG00323.hp2 HG00609.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.950+729C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830810 | |||||||
| chr4:70830876 | T | C | 1 | a0001c0001t0017g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.950+663A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830876 | |||||||
| chr4:70830967 | C | A | 1 | a0001c0001t0003g0217 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.950+572G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830967 | |||||||
| chr4:70830999 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
274 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.950+540A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830999 | |||||||
| chr4:70831123 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.950+416G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831123 | |||||||
| chr4:70831140 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.950+399T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831140 | |||||||
| chr4:70831148 | G | C | 2 | a0002c0002t0010g0222 a0002c0002t0010g0223 |
2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.950+391C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831148 | |||||||
| chr4:70831212 | G | A | 14 | a0001c0001t0006g0008 a0001c0001t0006g0063 a0001c0001t0006g0065 others(11): Show |
18 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.950+327C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831212 | |||||||
| chr4:70831269 | C | G | 1 | a0002c0002t0010g0222 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.950+270G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831269 | |||||||
| chr4:70831301 | G | C | 13 | a0001c0001t0006g0008 a0001c0001t0006g0063 a0001c0001t0006g0065 others(10): Show |
17 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.950+238C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831301 | |||||||
| chr4:70831355 | C | CA | 5 | a0001c0001t0001g0114 a0001c0001t0003g0045 a0001c0001t0003g0061 others(2): Show |
6 | HG00408.hp1 HG02717.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.950+183dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831355 | |||||||
| chr4:70831432 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.950+107G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831432 | |||||||
| chr4:70831476 | G | T | 1 | a0001c0001t0040g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.950+63C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831476 | |||||||
| chr4:70831479 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.950+60G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831479 | |||||||
| chr4:70831519 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.950+20A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831519 | |||||||
| chr4:70831679 | G | A | 3 | a0001c0001t0001g0130 a0001c0001t0001g0144 a0005c0008t0001g0220 |
3 | NA18956.hp1 NA19057.hp2 NA19081.hp1 |
splice_region_variant&intron_variant | LOW | c.815-5C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70831679 | |||||||
| chr4:70831710 | C | CT | 8 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(5): Show |
10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.815-37dupA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70831710 | |||||||
| chr4:70831793 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
284 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.815-119A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70831793 | |||||||
| chr4:70831832 | G | T | 1 | a0001c0001t0001g0082 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.815-158C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70831832 | |||||||
| chr4:70831863 | A | T | 1 | a0001c0001t0027g0174 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.815-189T>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70831863 | |||||||
| chr4:70831910 | G | GT | 12 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(9): Show |
14 | HG00323.hp1 HG01167.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.815-237dupA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70831910 | |||||||
| chr4:70831910 | GT | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
300 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.815-237delA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70831910 | |||||||
| chr4:70831975 | C | T | 10 | a0001c0001t0007g0013 a0001c0001t0007g0050 a0001c0001t0007g0126 others(7): Show |
12 | HG00673.hp2 HG01123.hp1 HG03710.hp1 others(9): Show |
intron_variant | MODIFIER | c.815-301G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70831975 | |||||||
| chr4:70832112 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0027g0174 |
2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.814+195G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70832112 | |||||||
| chr4:70832147 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.814+160A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70832147 | |||||||
| chr4:70832232 | C | T | 3 | a0001c0001t0003g0216 a0001c0001t0003g0217 a0001c0004t0003g0039 |
4 | HG03209.hp2 HG03540.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.814+75G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70832232 | |||||||
| chr4:70832233 | T | A | 3 | a0001c0001t0003g0044 a0001c0001t0003g0213 a0001c0001t0003g0214 |
4 | HG02145.hp1 HG02486.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.814+74A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70832233 | |||||||
| chr4:70832243 | T | C | 1 | a0001c0009t0001g0221 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.814+64A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70832243 | |||||||
| chr4:70832282 | C | T | 2 | a0002c0002t0010g0222 a0002c0002t0010g0223 |
2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.814+25G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70832282 | |||||||
| chr4:70832466 | C | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
323 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.671-16G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 3/9 | chr4 | 70832466 | |||||||
| chr4:70832504 | C | T | 1 | a0001c0001t0038g0194 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.671-54G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 3/9 | chr4 | 70832504 | |||||||
| chr4:70833079 | T | C | 11 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(8): Show |
15 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.670+39A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 3/9 | chr4 | 70833079 | |||||||
| chr4:70833281 | T | C | 1 | a0001c0001t0038g0194 | 1 | HG02723.hp2 | splice_region_variant&intron_variant | LOW | c.515-8A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70833281 | |||||||
| chr4:70833383 | T | C | 4 | a0001c0001t0015g0073 a0001c0001t0015g0074 a0001c0001t0037g0075 others(1): Show |
4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.515-110A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70833383 | |||||||
| chr4:70833614 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.515-341A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70833614 | |||||||
| chr4:70833634 | T | A | 23 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0015 others(20): Show |
45 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.515-361A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70833634 | |||||||
| chr4:70833688 | C | T | 8 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(5): Show |
10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.515-415G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70833688 | |||||||
| chr4:70833756 | TA | T | 8 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(5): Show |
10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.515-484delT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70833756 | |||||||
| chr4:70833794 | C | T | 1 | a0001c0001t0021g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.515-521G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70833794 | |||||||
| chr4:70833810 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.515-537G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70833810 | |||||||
| chr4:70834138 | T | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.515-865A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834138 | |||||||
| chr4:70834174 | C | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.515-901G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834174 | |||||||
| chr4:70834219 | A | T | 1 | a0001c0001t0036g0084 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.515-946T>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834219 | |||||||
| chr4:70834258 | CA | C | 23 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0015 others(20): Show |
45 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.515-986delT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834258 | |||||||
| chr4:70834390 | ATGTC | A | 4 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0213 others(1): Show |
6 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.515-1121_515-1118d others(6): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834390 | |||||||
| chr4:70834530 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
244 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.515-1257A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834530 | |||||||
| chr4:70834611 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.515-1338T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834611 | |||||||
| chr4:70834637 | T | C | 2 | a0001c0001t0001g0143 a0001c0005t0001g0140 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.515-1364A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834637 | |||||||
| chr4:70834778 | C | T | 13 | a0001c0001t0006g0008 a0001c0001t0006g0063 a0001c0001t0006g0065 others(10): Show |
17 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.514+1380G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834778 | |||||||
| chr4:70834912 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.514+1246G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834912 | |||||||
| chr4:70834924 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.514+1234G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834924 | |||||||
| chr4:70835009 | T | C | 9 | a0001c0001t0001g0141 a0001c0001t0009g0017 a0001c0001t0009g0018 others(6): Show |
11 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.514+1149A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835009 | |||||||
| chr4:70835136 | A | G | 2 | a0001c0001t0006g0067 a0001c0001t0006g0068 |
2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.514+1022T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835136 | |||||||
| chr4:70835147 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.514+1011C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835147 | |||||||
| chr4:70835218 | C | G | 8 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(5): Show |
10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.514+940G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835218 | |||||||
| chr4:70835391 | C | T | 1 | a0001c0001t0004g0150 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.514+767G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835391 | |||||||
| chr4:70835424 | G | A | 1 | a0001c0001t0017g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.514+734C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835424 | |||||||
| chr4:70835428 | C | CA | 14 | a0001c0001t0001g0049 a0001c0001t0001g0146 a0001c0001t0002g0007 others(11): Show |
19 | HG00408.hp2 HG00438.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.514+729dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835428 | |||||||
| chr4:70835442 | C | A | 1 | a0001c0001t0001g0116 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.514+716G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835442 | |||||||
| chr4:70835443 | C | A | 1 | a0001c0001t0001g0116 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.514+715G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835443 | |||||||
| chr4:70835444 | T | A | 1 | a0001c0001t0001g0116 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.514+714A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835444 | |||||||
| chr4:70835446 | C | A | 1 | a0001c0001t0001g0116 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.514+712G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835446 | |||||||
| chr4:70835448 | T | A | 1 | a0001c0001t0001g0116 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.514+710A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835448 | |||||||
| chr4:70835449 | AGTATGAT others(306): Show |
A | 1 | a0001c0001t0001g0116 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.514+396_514+708del | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835449 | |||||||
| chr4:70835460 | T | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(214): Show |
319 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.514+698A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835460 | |||||||
| chr4:70835461 | T | A | 4 | a0001c0001t0001g0010 a0001c0001t0015g0073 a0001c0001t0015g0074 others(1): Show |
4 | HG01167.hp2 HG01515.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.514+697A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835461 | |||||||
| chr4:70835488 | A | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
277 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(274): Show |
intron_variant | MODIFIER | c.514+670T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835488 | |||||||
| chr4:70835585 | T | C | 13 | a0001c0001t0006g0008 a0001c0001t0006g0063 a0001c0001t0006g0065 others(10): Show |
17 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.514+573A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835585 | |||||||
| chr4:70835595 | T | C | 8 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(5): Show |
10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.514+563A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835595 | |||||||
| chr4:70835631 | C | T | 13 | a0001c0001t0006g0008 a0001c0001t0006g0063 a0001c0001t0006g0065 others(10): Show |
17 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.514+527G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835631 | |||||||
| chr4:70835663 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
214 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.514+495C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835663 | |||||||
| chr4:70835677 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.514+481C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835677 | |||||||
| chr4:70835682 | C | A | 8 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(5): Show |
10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.514+476G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835682 | |||||||
| chr4:70835693 | G | A | 8 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(5): Show |
10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.514+465C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835693 | |||||||
| chr4:70835731 | G | T | 1 | a0001c0001t0001g0163 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.514+427C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835731 | |||||||
| chr4:70835795 | C | T | 4 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0213 others(1): Show |
6 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.514+363G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835795 | |||||||
| chr4:70835825 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.514+333A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835825 | |||||||
| chr4:70835873 | G | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0151 a0001c0001t0001g0152 others(4): Show |
9 | HG02615.hp1 HG02630.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.514+285C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835873 | |||||||
| chr4:70836016 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.514+142C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70836016 | |||||||
| chr4:70836125 | A | T | 1 | a0001c0001t0003g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.514+33T>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70836125 | |||||||
| chr4:70836406 | A | T | 1 | a0001c0001t0009g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.358-92T>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836406 | |||||||
| chr4:70836541 | GGTTT | G | 22 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0015 others(19): Show |
44 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.358-231_358-228del others(4): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836541 | |||||||
| chr4:70836584 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
215 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.358-270T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836584 | |||||||
| chr4:70836586 | T | A | 3 | a0001c0001t0003g0044 a0001c0001t0003g0213 a0001c0001t0003g0214 |
4 | HG02145.hp1 HG02486.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-272A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836586 | |||||||
| chr4:70836660 | G | A | 3 | a0001c0001t0015g0073 a0001c0001t0015g0074 a0001c0001t0037g0075 |
3 | HG01167.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.358-346C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836660 | |||||||
| chr4:70836674 | T | C | 1 | a0001c0001t0006g0072 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.358-360A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836674 | |||||||
| chr4:70836731 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0004g0077 |
2 | NA18999.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.358-417A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836731 | |||||||
| chr4:70836839 | G | A | 1 | a0001c0001t0038g0194 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.358-525C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836839 | |||||||
| chr4:70836876 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.358-562G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836876 | |||||||
| chr4:70836896 | T | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
323 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.358-582A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836896 | |||||||
| chr4:70836932 | C | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
284 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.358-618G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836932 | |||||||
| chr4:70836967 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
206 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.358-653A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836967 | |||||||
| chr4:70837030 | T | G | 8 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(5): Show |
10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.358-716A>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837030 | |||||||
| chr4:70837147 | G | A | 4 | a0001c0001t0015g0073 a0001c0001t0015g0074 a0001c0001t0037g0075 others(1): Show |
4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-833C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837147 | |||||||
| chr4:70837194 | A | C | 1 | a0001c0001t0004g0150 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.358-880T>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837194 | |||||||
| chr4:70837337 | G | A | 1 | a0001c0001t0017g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.358-1023C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837337 | |||||||
| chr4:70837368 | G | T | 2 | a0001c0001t0002g0079 a0001c0001t0002g0080 |
2 | NA18967.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.358-1054C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837368 | |||||||
| chr4:70837393 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.358-1079A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837393 | |||||||
| chr4:70837446 | C | T | 1 | a0001c0001t0011g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.358-1132G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837446 | |||||||
| chr4:70837483 | G | C | 1 | a0001c0001t0004g0182 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.358-1169C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837483 | |||||||
| chr4:70837563 | C | CA | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
252 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.358-1250dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837563 | |||||||
| chr4:70837563 | C | CAA | 27 | a0001c0001t0001g0038 a0001c0001t0001g0118 a0001c0001t0001g0119 others(24): Show |
34 | HG00642.hp1 HG00673.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.358-1251_358-1250d others(4): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837563 | |||||||
| chr4:70837664 | G | T | 6 | a0001c0001t0005g0025 a0001c0001t0005g0122 a0001c0001t0005g0123 others(3): Show |
7 | NA18969.hp1 NA18987.hp1 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.358-1350C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837664 | |||||||
| chr4:70837695 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.358-1381A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837695 | |||||||
| chr4:70837792 | C | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
273 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.358-1478G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837792 | |||||||
| chr4:70837812 | A | AT | 5 | a0001c0001t0001g0121 a0001c0001t0003g0043 a0001c0001t0003g0044 others(2): Show |
7 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.358-1499dupA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837812 | |||||||
| chr4:70837841 | T | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.358-1527A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837841 | |||||||
| chr4:70837887 | G | A | 9 | a0001c0001t0001g0057 a0001c0001t0009g0017 a0001c0001t0009g0018 others(6): Show |
11 | HG00323.hp1 HG00735.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.358-1573C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837887 | |||||||
| chr4:70838038 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.357+1433A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838038 | |||||||
| chr4:70838219 | C | CA | 59 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(56): Show |
96 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.357+1251dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838219 | |||||||
| chr4:70838219 | C | CAA | 37 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0026 others(34): Show |
47 | HG00140.hp1 HG00140.hp2 HG01258.hp2 others(44): Show |
intron_variant | MODIFIER | c.357+1250_357+1251d others(4): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838219 | |||||||
| chr4:70838219 | C | CAAA | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(66): Show |
113 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.357+1249_357+1251d others(5): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838219 | |||||||
| chr4:70838219 | C | CAAAA | 12 | a0001c0001t0001g0185 a0001c0001t0001g0187 a0001c0001t0001g0188 others(9): Show |
14 | HG00642.hp2 HG01361.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.357+1248_357+1251d others(6): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838219 | |||||||
| chr4:70838219 | C | CAAAAAAA others(3): Show |
4 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0059 others(1): Show |
6 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.357+1242_357+1251d others(12): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838219 | |||||||
| chr4:70838219 | C | CAAAAAAA others(4): Show |
4 | a0001c0001t0009g0060 a0001c0001t0012g0054 a0001c0001t0012g0055 others(1): Show |
4 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+1241_357+1251d others(13): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838219 | |||||||
| chr4:70838219 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0057 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.357+1238_357+1251d others(16): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838219 | |||||||
| chr4:70838219 | CAA | C | 11 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(8): Show |
12 | HG01167.hp2 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.357+1250_357+1251d others(4): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838219 | |||||||
| chr4:70838219 | CAAA | C | 5 | a0001c0001t0006g0008 a0001c0001t0006g0063 a0001c0001t0006g0065 others(2): Show |
8 | HG02818.hp1 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.357+1249_357+1251d others(5): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838219 | |||||||
| chr4:70838289 | G | A | 23 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0015 others(20): Show |
45 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.357+1182C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838289 | |||||||
| chr4:70838289 | G | C | 1 | a0001c0001t0009g0060 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.357+1182C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838289 | |||||||
| chr4:70838311 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
260 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.357+1160G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838311 | |||||||
| chr4:70838316 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0190 |
4 | HG01081.hp2 HG02109.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+1155A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838316 | |||||||
| chr4:70838327 | G | GA | 23 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0015 others(20): Show |
45 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.357+1143dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838327 | |||||||
| chr4:70838341 | G | A | 11 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(8): Show |
15 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.357+1130C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838341 | |||||||
| chr4:70838463 | T | C | 1 | a0005c0008t0001g0220 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.357+1008A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838463 | |||||||
| chr4:70838558 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.357+913T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838558 | |||||||
| chr4:70838844 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.357+627C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838844 | |||||||
| chr4:70838953 | C | T | 10 | a0001c0001t0001g0057 a0001c0001t0003g0061 a0001c0001t0009g0017 others(7): Show |
12 | HG00323.hp1 HG00735.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.357+518G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838953 | |||||||
| chr4:70838988 | A | G | 1 | a0001c0004t0003g0039 | 2 | HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.357+483T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838988 | |||||||
| chr4:70839038 | G | A | 1 | a0001c0001t0004g0191 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.357+433C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70839038 | |||||||
| chr4:70839051 | G | T | 1 | a0004c0006t0041g0193 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.357+420C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70839051 | |||||||
| chr4:70839174 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.357+297A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70839174 | |||||||
| chr4:70839248 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
260 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.357+223G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70839248 | |||||||
| chr4:70839279 | C | G | 4 | a0001c0001t0001g0057 a0001c0001t0012g0054 a0001c0001t0012g0055 others(1): Show |
4 | HG00323.hp1 HG00735.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+192G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70839279 | |||||||
| chr4:70839337 | G | A | 1 | a0001c0001t0004g0219 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.357+134C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70839337 | |||||||
| chr4:70839390 | C | G | 1 | a0001c0001t0035g0053 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.357+81G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70839390 | |||||||
| chr4:70839408 | C | CG | 6 | a0001c0001t0001g0016 a0001c0001t0001g0048 a0001c0001t0001g0049 others(3): Show |
7 | HG00438.hp2 HG01433.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.357+62dupC | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70839408 | |||||||
| chr4:70839414 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.357+57G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70839414 |