Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26747 |
| ensemblid | ENSG00000083635.8 |
| hgncid | 8057 |
| symbol | NUFIP1 |
| name | nuclear FMR1 interacting protein 1 |
| refseq_nuc | NM_012345.3 |
| refseq_prot | NP_036477.2 |
| ensembl_nuc | ENST00000379161.5 |
| ensembl_prot | ENSP00000368459.4 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 44939249 |
| end | 44989471 |
| strand | - |
| ver | v1.2 |
| region | chr13:44939249-44989471 |
| region5000 | chr13:44934249-44994471 |
| regionname0 | NUFIP1_chr13_44939249_44989471 |
| regionname5000 | NUFIP1_chr13_44934249_44994471 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 495 | 197 | 70 | 29 | 83 | 2 | 12 | 62 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | MAEPT others(490): Show |
chr13 | 44934249 | 44994471 |
| a0002 | 0/1 | 495 | 116 | 12 | 29 | 57 | 2 | 15 | 40 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | MAEPT others(490): Show |
chr13 | 44934249 | 44994471 |
| a0003 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | MAEPT others(490): Show |
chr13 | 44934249 | 44994471 |
| a0004 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | MAEPT others(490): Show |
chr13 | 44934249 | 44994471 |
| a0005 | 0/0 | 495 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | MAEPT others(490): Show |
chr13 | 44934249 | 44994471 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1485 | 153 | 56 | 25 | 60 | 2 | 9 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ATGGC others(1480): Show |
chr13 | 44934249 | 44994471 | ||
| a0001c0003 | 0/0 | 1485 | 41 | 13 | 3 | 23 | 0 | 2 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ATGGC others(1480): Show |
chr13 | 44934249 | 44994471 | ||
| a0001c0006 | 0/0 | 1485 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ATGGC others(1480): Show |
chr13 | 44934249 | 44994471 | ||
| a0001c0007 | 0/0 | 1485 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ATGGC others(1480): Show |
chr13 | 44934249 | 44994471 | ||
| a0001c0008 | 0/0 | 1485 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ATGGC others(1480): Show |
chr13 | 44934249 | 44994471 | ||
| a0002c0002 | 0/1 | 1485 | 113 | 12 | 27 | 56 | 2 | 15 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ATGGC others(1480): Show |
chr13 | 44934249 | 44994471 | ||
| a0002c0010 | 0/0 | 1485 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ATGGC others(1480): Show |
chr13 | 44934249 | 44994471 | ||
| a0002c0011 | 0/0 | 1485 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ATGGC others(1480): Show |
chr13 | 44934249 | 44994471 | ||
| a0002c0012 | 0/0 | 1485 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ATGGC others(1480): Show |
chr13 | 44934249 | 44994471 | ||
| a0003c0004 | 0/0 | 1485 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ATGGC others(1480): Show |
chr13 | 44934249 | 44994471 | ||
| a0004c0009 | 0/0 | 1485 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ATGGC others(1480): Show |
chr13 | 44934249 | 44994471 | ||
| a0005c0005 | 0/0 | 1485 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ATGGC others(1480): Show |
chr13 | 44934249 | 44994471 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3479 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3474): Show |
chr13 | 44934249 | 44994471 |
| a0001c0001t0002 | 1/0 | 3480 | 128 | 36 | 22 | 58 | 2 | 9 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3475): Show |
chr13 | 44934249 | 44994471 |
| a0001c0001t0003 | 0/0 | 3480 | 21 | 18 | 3 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3475): Show |
chr13 | 44934249 | 44994471 |
| a0001c0001t0008 | 0/0 | 3480 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3475): Show |
chr13 | 44934249 | 44994471 |
| a0001c0001t0010 | 0/0 | 3480 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3475): Show |
chr13 | 44934249 | 44994471 |
| a0001c0001t0011 | 0/0 | 3480 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3475): Show |
chr13 | 44934249 | 44994471 |
| a0001c0003t0001 | 0/0 | 3479 | 39 | 12 | 3 | 22 | 0 | 2 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3474): Show |
chr13 | 44934249 | 44994471 |
| a0001c0003t0005 | 0/0 | 3479 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3474): Show |
chr13 | 44934249 | 44994471 |
| a0001c0003t0007 | 0/0 | 3479 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3474): Show |
chr13 | 44934249 | 44994471 |
| a0001c0006t0002 | 0/0 | 3480 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3475): Show |
chr13 | 44934249 | 44994471 |
| a0001c0007t0001 | 0/0 | 3479 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3474): Show |
chr13 | 44934249 | 44994471 |
| a0001c0008t0002 | 0/0 | 3480 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3475): Show |
chr13 | 44934249 | 44994471 |
| a0002c0002t0001 | 0/1 | 3479 | 108 | 11 | 27 | 52 | 2 | 15 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3474): Show |
chr13 | 44934249 | 44994471 |
| a0002c0002t0002 | 0/0 | 3480 | 3 | 1 | 0 | 2 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3475): Show |
chr13 | 44934249 | 44994471 |
| a0002c0002t0006 | 0/0 | 3479 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3474): Show |
chr13 | 44934249 | 44994471 |
| a0002c0002t0009 | 0/0 | 3479 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3474): Show |
chr13 | 44934249 | 44994471 |
| a0002c0010t0001 | 0/0 | 3479 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3474): Show |
chr13 | 44934249 | 44994471 |
| a0002c0011t0001 | 0/0 | 3479 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3474): Show |
chr13 | 44934249 | 44994471 |
| a0002c0012t0001 | 0/0 | 3479 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3474): Show |
chr13 | 44934249 | 44994471 |
| a0003c0004t0003 | 0/0 | 3480 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3475): Show |
chr13 | 44934249 | 44994471 |
| a0004c0009t0004 | 0/0 | 3479 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3474): Show |
chr13 | 44934249 | 44994471 |
| a0005c0005t0002 | 0/0 | 3480 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | ACAGT others(3475): Show |
chr13 | 44934249 | 44994471 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0003 | 0/0 | 7 | 2 | 0 | 0 | 2 | 3 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0006 | 0/0 | 5 | 3 | 1 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0008 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0003g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0003g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0008g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0010g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0001t0011g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0003t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0006t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0007t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0001c0008t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0001 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0004 | 0/0 | 7 | 1 | 3 | 2 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0020 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0002t0009g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0010t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0011t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0002c0012t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0003c0004t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0004c0009t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| a0005c0005t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0159 | EUR | GBR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | CHS | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0028 | EAS | CHS | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00438 | hp1 | a0001 | c0003 | t0001 | g0078 | EAS | CHS | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | CHS | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | CHS | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | CHS | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | CHS | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | CHS | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | CHS | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0057 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0151 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00673 | hp1 | a0001 | c0003 | t0001 | g0064 | EAS | CHS | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | CHS | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0192 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0215 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0182 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0021 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0169 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0054 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0191 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0219 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0171 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0214 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0067 | AMR | CLM | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0152 | AMR | CLM | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0168 | AMR | CLM | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | CLM | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01433 | hp2 | a0002 | c0010 | t0001 | g0181 | AMR | CLM | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | CLM | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01496 | hp2 | a0001 | c0008 | t0002 | g0153 | AMR | CLM | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0183 | EUR | IBS | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0216 | AFR | ACB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0156 | AMR | PEL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PEL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0178 | AMR | PEL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PEL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0180 | AMR | PEL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0196 | AMR | PEL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PEL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0036 | AMR | PEL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02027 | hp1 | a0001 | c0003 | t0005 | g0065 | EAS | KHV | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0211 | EAS | KHV | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02040 | hp1 | a0001 | c0001 | t0011 | g0135 | EAS | KHV | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0056 | AFR | ACB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0107 | AFR | ACB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | KHV | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0063 | EAS | KHV | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02071 | hp1 | a0002 | c0002 | t0009 | g0213 | EAS | KHV | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | KHV | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | KHV | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | KHV | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02129 | hp2 | a0001 | c0003 | t0001 | g0069 | EAS | KHV | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02132 | hp1 | a0002 | c0011 | t0001 | g0223 | EAS | KHV | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02135 | hp1 | a0001 | c0001 | t0008 | g0134 | EAS | KHV | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | ACB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02148 | hp2 | a0002 | c0012 | t0001 | g0224 | AMR | PEL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | CDX | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | ACB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ACB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0155 | AMR | PEL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0179 | AMR | PEL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0189 | AMR | PEL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | ACB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | KHV | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0154 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0202 | SAS | PJL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0052 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0058 | SAS | PJL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0170 | SAS | PJL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0106 | AFR | ESN | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | ESN | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02970 | hp1 | a0001 | c0007 | t0001 | g0076 | AFR | ESN | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0102 | AFR | ESN | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0055 | AFR | ESN | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ESN | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | MSL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0026 | AFR | MSL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0061 | AFR | ESN | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0212 | AFR | ESN | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ESN | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0104 | AFR | MSL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | MSL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | MSL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0074 | SAS | PJL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03453 | hp2 | a0003 | c0004 | t0003 | g0041 | AFR | MSL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0103 | AFR | MSL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0039 | SAS | PJL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0186 | AFR | ESN | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0098 | AFR | ESN | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03579 | hp1 | a0004 | c0009 | t0004 | g0184 | AFR | MSL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | MSL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0187 | SAS | PJL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03654 | hp2 | a0005 | c0005 | t0002 | g0042 | SAS | PJL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | PJL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0037 | SAS | PJL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0039 | SAS | STU | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | STU | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0220 | SAS | PJL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0217 | SAS | BEB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03831 | hp2 | a0001 | c0006 | t0002 | g0092 | SAS | BEB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0162 | SAS | BEB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0116 | SAS | BEB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0210 | SAS | BEB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0087 | SAS | BEB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0160 | SAS | STU | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0201 | SAS | STU | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0200 | SAS | STU | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | YRI | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | YRI | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | YRI | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | YRI | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18940 | hp2 | a0001 | c0003 | t0001 | g0072 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18959 | hp2 | a0002 | c0002 | t0006 | g0195 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18970 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18977 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18978 | hp1 | a0001 | c0003 | t0001 | g0027 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18984 | hp1 | a0001 | c0003 | t0001 | g0066 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18988 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18991 | hp2 | a0001 | c0003 | t0001 | g0028 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18993 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19001 | hp1 | a0001 | c0003 | t0001 | g0070 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19002 | hp2 | a0001 | c0003 | t0001 | g0077 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19006 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19030 | hp1 | a0001 | c0003 | t0007 | g0060 | AFR | LWK | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | LWK | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0221 | AFR | LWK | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | LWK | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19057 | hp1 | a0001 | c0003 | t0001 | g0073 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19062 | hp1 | a0001 | c0003 | t0001 | g0062 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0068 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19077 | hp1 | a0001 | c0003 | t0001 | g0027 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19088 | hp1 | a0001 | c0003 | t0001 | g0071 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | YRI | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | YRI | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | ASW | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | ASW | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0059 | AFR | ACB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0026 | AFR | ACB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0222 | AFR | ACB | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0099 | AFR | MSL | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0100 | AFR | USA | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | USA | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | USA | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | USA | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0161 | REF | REF | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0105 | REF | REF | NUFIP1_chr13_44934249_44994471 | NUFIP1 | chr13 | 44934249 | 44994471 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:44943477 | C | T | 1 | a0005 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.1336G>A | p.Glu446Lys | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/10 | 1371/3480 | 1336/1488 | 446/495 | chr13 | 44943477 | |||
| chr13:44943622 | A | T | 1 | a0004 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.1191T>A | p.Asp397Glu | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/10 | 1226/3480 | 1191/1488 | 397/495 | chr13 | 44943622 | |||
| chr13:44989329 | G | C | 2 | a0002 a0004 |
116 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
missense_variant | MODERATE | c.108C>G | p.Ser36Arg | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/10 | 143/3480 | 108/1488 | 36/495 | chr13 | 44989329 | |||
| chr13:44989397 | A | G | 1 | a0003 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.40T>C | p.Trp14Arg | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/10 | 75/3480 | 40/1488 | 14/495 | chr13 | 44989397 | |||
| chr13:44989400 | C | T | 1 | a0003 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.37G>A | p.Gly13Arg | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/10 | 72/3480 | 37/1488 | 13/495 | chr13 | 44989400 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:44941224 | C | T | 2 | a0001c0006 a0001c0007 |
2 | HG02970.hp1 HG03831.hp2 |
synonymous_variant | LOW | c.1470G>A | p.Ala490Ala | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 10/10 | 1505/3480 | 1470/1488 | 490/495 | chr13 | 44941224 | |||
| chr13:44941254 | T | C | 1 | a0002c0010 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.1440A>G | p.Lys480Lys | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 10/10 | 1475/3480 | 1440/1488 | 480/495 | chr13 | 44941254 | |||
| chr13:44941260 | G | A | 2 | a0001c0003 a0001c0007 |
42 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
synonymous_variant | LOW | c.1434C>T | p.Ile478Ile | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 10/10 | 1469/3480 | 1434/1488 | 478/495 | chr13 | 44941260 | |||
| chr13:44989167 | T | C | 1 | a0001c0008 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.270A>G | p.Gln90Gln | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/10 | 305/3480 | 270/1488 | 90/495 | chr13 | 44989167 | |||
| chr13:44989224 | G | A | 1 | a0002c0011 | 1 | HG02132.hp1 | synonymous_variant | LOW | c.213C>T | p.Ala71Ala | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/10 | 248/3480 | 213/1488 | 71/495 | chr13 | 44989224 | |||
| chr13:44989413 | G | A | 1 | a0002c0012 | 1 | HG02148.hp2 | synonymous_variant | LOW | c.24C>T | p.Phe8Phe | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/10 | 59/3480 | 24/1488 | 8/495 | chr13 | 44989413 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:44939885 | CT | C | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0010 others(12): Show |
179 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*1320delA | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 10/10 | 1320 | chr13 | 44939885 | ||||||
| chr13:44939984 | T | C | 1 | a0002c0002t0006 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1222A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 10/10 | 1222 | chr13 | 44939984 | ||||||
| chr13:44940062 | C | A | 1 | a0001c0003t0007 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1144G>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 10/10 | 1144 | chr13 | 44940062 | ||||||
| chr13:44940187 | A | G | 1 | a0001c0001t0010 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1019T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 10/10 | 1019 | chr13 | 44940187 | ||||||
| chr13:44940566 | T | C | 1 | a0001c0001t0008 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*640A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 10/10 | 640 | chr13 | 44940566 | ||||||
| chr13:44940674 | G | A | 1 | a0002c0002t0009 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*532C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 10/10 | 532 | chr13 | 44940674 | ||||||
| chr13:44940734 | A | C | 1 | a0001c0003t0005 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*472T>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 10/10 | 472 | chr13 | 44940734 | ||||||
| chr13:44940772 | C | T | 1 | a0004c0009t0004 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*434G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 10/10 | 434 | chr13 | 44940772 | ||||||
| chr13:44941122 | G | GA | 3 | a0001c0001t0003 a0001c0001t0010 a0003c0004t0003 |
23 | HG00642.hp1 HG01261.hp1 HG01975.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*83dupT | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 10/10 | 83 | chr13 | 44941122 | ||||||
| chr13:44941153 | G | A | 1 | a0001c0001t0011 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*53C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 10/10 | 53 | chr13 | 44941153 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:44941349 | G | C | 24 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0014 others(21): Show |
37 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.1372-27C>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44941349 | |||||||
| chr13:44941544 | C | T | 1 | a0004c0009t0004g0184 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1372-222G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44941544 | |||||||
| chr13:44941545 | G | A | 2 | a0001c0001t0002g0117 a0002c0002t0001g0162 |
2 | HG02040.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1372-223C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44941545 | |||||||
| chr13:44941752 | A | T | 1 | a0001c0001t0002g0031 | 2 | NA19056.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1372-430T>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44941752 | |||||||
| chr13:44941757 | C | A | 1 | a0002c0002t0001g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1372-435G>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44941757 | |||||||
| chr13:44941765 | G | A | 5 | a0001c0001t0002g0013 a0001c0001t0002g0043 a0001c0001t0002g0075 others(2): Show |
7 | HG00408.hp1 HG02135.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.1372-443C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44941765 | |||||||
| chr13:44941792 | C | T | 1 | a0001c0001t0002g0015 | 3 | HG01074.hp2 HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1372-470G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44941792 | |||||||
| chr13:44941809 | G | A | 112 | a0001c0003t0001g0005 a0001c0003t0001g0010 a0001c0003t0001g0023 others(109): Show |
155 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1372-487C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44941809 | |||||||
| chr13:44941852 | T | C | 2 | a0001c0001t0002g0034 a0001c0001t0002g0141 |
3 | HG02615.hp2 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1372-530A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44941852 | |||||||
| chr13:44941854 | G | C | 24 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0014 others(21): Show |
37 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.1372-532C>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44941854 | |||||||
| chr13:44941914 | C | CT | 25 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0014 others(22): Show |
38 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1372-593dupA | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44941914 | |||||||
| chr13:44941920 | T | C | 1 | a0001c0003t0005g0065 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1372-598A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44941920 | |||||||
| chr13:44942094 | T | G | 1 | a0002c0002t0001g0201 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1372-772A>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44942094 | |||||||
| chr13:44942111 | G | A | 2 | a0002c0002t0001g0154 a0004c0009t0004g0184 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1372-789C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44942111 | |||||||
| chr13:44942205 | C | T | 1 | a0001c0001t0002g0130 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1372-883G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44942205 | |||||||
| chr13:44942263 | G | A | 220 | a0001c0001t0001g0080 a0001c0001t0002g0002 a0001c0001t0002g0003 others(217): Show |
312 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.1372-941C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44942263 | |||||||
| chr13:44942280 | G | C | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | HG00621.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1372-958C>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44942280 | |||||||
| chr13:44942489 | C | A | 1 | a0001c0001t0002g0032 | 2 | HG02071.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.1371+953G>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44942489 | |||||||
| chr13:44942899 | G | A | 1 | a0002c0002t0001g0197 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1371+543C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44942899 | |||||||
| chr13:44942923 | G | A | 1 | a0002c0002t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1371+519C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44942923 | |||||||
| chr13:44942967 | T | TA | 9 | a0001c0001t0002g0014 a0001c0001t0002g0119 a0001c0001t0002g0120 others(6): Show |
11 | HG00609.hp2 HG00621.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.1371+474dupT | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44942967 | |||||||
| chr13:44942967 | TA | T | 16 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0109 others(13): Show |
16 | HG01069.hp2 HG01192.hp1 HG02273.hp2 others(13): Show |
intron_variant | MODIFIER | c.1371+474delT | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44942967 | |||||||
| chr13:44943264 | T | G | 1 | a0002c0002t0001g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1371+178A>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44943264 | |||||||
| chr13:44943351 | A | AAC | 39 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0075 others(36): Show |
53 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.1371+89_1371+90dup others(2): Show |
NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44943351 | |||||||
| chr13:44943351 | AAC | A | 7 | a0002c0002t0001g0157 a0002c0002t0001g0158 a0002c0002t0001g0166 others(4): Show |
7 | HG00408.hp2 HG00544.hp2 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.1371+89_1371+90del others(2): Show |
NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44943351 | |||||||
| chr13:44943376 | A | C | 2 | a0001c0003t0001g0056 a0001c0003t0001g0058 |
2 | HG02055.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1371+66T>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44943376 | |||||||
| chr13:44943378 | C | G | 1 | a0002c0011t0001g0223 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1371+64G>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 9/9 | chr13 | 44943378 | |||||||
| chr13:44943871 | A | G | 1 | a0002c0002t0001g0199 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1139-197T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44943871 | |||||||
| chr13:44943952 | T | C | 1 | a0002c0002t0006g0195 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1139-278A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44943952 | |||||||
| chr13:44944012 | T | C | 80 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0007 others(77): Show |
113 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1139-338A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44944012 | |||||||
| chr13:44944301 | G | A | 1 | a0001c0001t0003g0151 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1139-627C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44944301 | |||||||
| chr13:44944451 | G | A | 50 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0009 others(47): Show |
78 | HG00408.hp1 HG00639.hp2 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.1139-777C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44944451 | |||||||
| chr13:44944506 | T | C | 31 | a0001c0003t0001g0005 a0001c0003t0001g0010 a0001c0003t0001g0023 others(28): Show |
42 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1139-832A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44944506 | |||||||
| chr13:44944651 | T | C | 1 | a0001c0001t0002g0112 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1139-977A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44944651 | |||||||
| chr13:44945550 | A | G | 10 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0185 others(7): Show |
16 | HG00544.hp1 HG00558.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.1139-1876T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44945550 | |||||||
| chr13:44945779 | T | C | 1 | a0001c0003t0007g0060 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1139-2105A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44945779 | |||||||
| chr13:44945883 | C | T | 1 | a0001c0003t0001g0063 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1139-2209G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44945883 | |||||||
| chr13:44945931 | G | C | 1 | a0002c0002t0001g0168 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1139-2257C>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44945931 | |||||||
| chr13:44946754 | T | G | 37 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0009 others(34): Show |
61 | HG00408.hp1 HG00673.hp2 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.1138+2968A>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44946754 | |||||||
| chr13:44946901 | T | C | 1 | a0001c0001t0002g0113 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1138+2821A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44946901 | |||||||
| chr13:44947225 | A | G | 1 | a0001c0003t0001g0010 | 3 | HG02896.hp1 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1138+2497T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44947225 | |||||||
| chr13:44947234 | C | CT | 25 | a0001c0001t0002g0009 a0001c0001t0002g0016 a0001c0001t0002g0018 others(22): Show |
35 | HG00639.hp2 HG00673.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1138+2487dupA | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44947234 | |||||||
| chr13:44947234 | CT | C | 7 | a0001c0001t0002g0046 a0001c0001t0002g0084 a0002c0002t0001g0209 others(4): Show |
7 | HG01168.hp1 HG01943.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1138+2487delA | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44947234 | |||||||
| chr13:44947286 | T | A | 6 | a0001c0001t0003g0029 a0001c0001t0003g0053 a0001c0001t0003g0096 others(3): Show |
7 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1138+2436A>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44947286 | |||||||
| chr13:44947315 | T | C | 1 | a0002c0002t0001g0164 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1138+2407A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44947315 | |||||||
| chr13:44947440 | T | G | 2 | a0002c0002t0001g0203 a0002c0002t0001g0204 |
2 | HG00438.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1138+2282A>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44947440 | |||||||
| chr13:44947469 | C | A | 80 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0007 others(77): Show |
113 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1138+2253G>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44947469 | |||||||
| chr13:44948045 | C | T | 31 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(28): Show |
45 | HG01074.hp2 HG01109.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.1138+1677G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44948045 | |||||||
| chr13:44948095 | C | T | 2 | a0001c0001t0003g0012 a0003c0004t0003g0041 |
4 | HG03195.hp1 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1138+1627G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44948095 | |||||||
| chr13:44948141 | C | CT | 46 | a0001c0001t0001g0080 a0001c0001t0002g0003 a0001c0001t0002g0008 others(43): Show |
63 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1138+1580dupA | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44948141 | |||||||
| chr13:44948141 | C | CTT | 22 | a0001c0001t0002g0006 a0001c0001t0002g0015 a0001c0001t0002g0032 others(19): Show |
29 | HG01074.hp2 HG01109.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.1138+1579_1138+158 others(6): Show |
NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44948141 | |||||||
| chr13:44948141 | C | CTTTT | 9 | a0001c0001t0002g0009 a0001c0001t0002g0016 a0001c0001t0002g0017 others(6): Show |
16 | HG02040.hp1 HG02132.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.1138+1577_1138+158 others(8): Show |
NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44948141 | |||||||
| chr13:44948187 | G | C | 1 | a0001c0001t0002g0088 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1138+1535C>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44948187 | |||||||
| chr13:44948289 | G | A | 2 | a0001c0001t0002g0034 a0001c0001t0002g0141 |
3 | HG02615.hp2 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1138+1433C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44948289 | |||||||
| chr13:44948659 | T | C | 3 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0174 |
3 | HG00544.hp2 NA18979.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1138+1063A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44948659 | |||||||
| chr13:44948829 | G | A | 1 | a0002c0002t0001g0201 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1138+893C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44948829 | |||||||
| chr13:44948835 | C | T | 1 | a0002c0002t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1138+887G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44948835 | |||||||
| chr13:44948890 | C | A | 18 | a0001c0003t0001g0005 a0001c0003t0001g0027 a0001c0003t0001g0028 others(15): Show |
25 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.1138+832G>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44948890 | |||||||
| chr13:44949159 | T | C | 2 | a0001c0003t0001g0052 a0001c0003t0001g0059 |
2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1138+563A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44949159 | |||||||
| chr13:44949199 | A | AT | 147 | a0001c0001t0001g0080 a0001c0001t0002g0003 a0001c0001t0002g0008 others(144): Show |
209 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.1138+522dupA | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44949199 | |||||||
| chr13:44949199 | A | ATT | 38 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(35): Show |
51 | HG00673.hp1 HG01074.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1138+521_1138+522d others(4): Show |
NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44949199 | |||||||
| chr13:44949199 | A | ATTT | 7 | a0001c0001t0002g0016 a0001c0001t0002g0034 a0001c0001t0002g0141 others(4): Show |
10 | HG01192.hp1 HG02615.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1138+520_1138+522d others(5): Show |
NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44949199 | |||||||
| chr13:44949199 | AT | A | 22 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0014 others(19): Show |
35 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1138+522delA | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44949199 | |||||||
| chr13:44949232 | C | G | 1 | a0002c0002t0001g0199 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1138+490G>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44949232 | |||||||
| chr13:44949241 | G | T | 1 | a0002c0002t0001g0199 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1138+481C>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44949241 | |||||||
| chr13:44949243 | C | T | 1 | a0002c0002t0001g0199 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1138+479G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44949243 | |||||||
| chr13:44949350 | C | T | 23 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0014 others(20): Show |
36 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1138+372G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44949350 | |||||||
| chr13:44949447 | C | T | 1 | a0001c0001t0002g0090 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1138+275G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44949447 | |||||||
| chr13:44949448 | G | A | 2 | a0001c0001t0002g0034 a0001c0001t0002g0141 |
3 | HG02615.hp2 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1138+274C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 8/9 | chr13 | 44949448 | |||||||
| chr13:44949948 | A | C | 37 | a0001c0001t0001g0080 a0001c0001t0002g0003 a0001c0001t0002g0008 others(34): Show |
50 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.1022-110T>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44949948 | |||||||
| chr13:44949962 | A | C | 5 | a0001c0001t0002g0008 a0001c0001t0002g0084 a0001c0001t0002g0086 others(2): Show |
8 | HG01081.hp2 HG01167.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.1022-124T>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44949962 | |||||||
| chr13:44950035 | G | C | 1 | a0001c0001t0002g0116 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1022-197C>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44950035 | |||||||
| chr13:44950057 | A | T | 1 | a0001c0001t0002g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1022-219T>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44950057 | |||||||
| chr13:44950257 | T | A | 5 | a0001c0003t0001g0010 a0001c0003t0001g0026 a0001c0003t0001g0054 others(2): Show |
8 | HG01109.hp2 HG02559.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1022-419A>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44950257 | |||||||
| chr13:44950288 | T | C | 37 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(34): Show |
55 | HG00639.hp2 HG01074.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.1022-450A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44950288 | |||||||
| chr13:44950308 | T | A | 23 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0014 others(20): Show |
36 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1022-470A>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44950308 | |||||||
| chr13:44950491 | G | A | 10 | a0001c0003t0001g0010 a0001c0003t0001g0023 a0001c0003t0001g0026 others(7): Show |
14 | HG00639.hp1 HG01109.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1022-653C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44950491 | |||||||
| chr13:44950496 | C | A | 1 | a0002c0002t0009g0213 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1022-658G>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44950496 | |||||||
| chr13:44950535 | T | C | 2 | a0001c0001t0002g0034 a0001c0001t0002g0141 |
3 | HG02615.hp2 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1022-697A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44950535 | |||||||
| chr13:44950840 | A | T | 1 | a0001c0001t0002g0089 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1022-1002T>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44950840 | |||||||
| chr13:44951033 | C | T | 1 | a0001c0003t0001g0052 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1022-1195G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44951033 | |||||||
| chr13:44951429 | T | C | 1 | a0001c0001t0002g0075 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1022-1591A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44951429 | |||||||
| chr13:44951510 | T | C | 1 | a0002c0002t0001g0204 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1022-1672A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44951510 | |||||||
| chr13:44951835 | C | T | 1 | a0001c0001t0002g0049 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1022-1997G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44951835 | |||||||
| chr13:44952361 | G | A | 150 | a0001c0001t0001g0080 a0001c0001t0002g0003 a0001c0001t0002g0008 others(147): Show |
207 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.1022-2523C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44952361 | |||||||
| chr13:44952437 | A | G | 2 | a0002c0002t0001g0040 a0002c0002t0001g0209 |
3 | NA18983.hp2 NA19085.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1022-2599T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44952437 | |||||||
| chr13:44952552 | T | C | 1 | a0001c0001t0002g0091 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1022-2714A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44952552 | |||||||
| chr13:44953589 | C | T | 2 | a0001c0001t0002g0144 a0001c0001t0002g0146 |
2 | HG02647.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1022-3751G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44953589 | |||||||
| chr13:44953774 | T | C | 3 | a0002c0002t0001g0035 a0002c0002t0001g0039 a0002c0002t0001g0186 |
5 | HG03490.hp1 HG03516.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1022-3936A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44953774 | |||||||
| chr13:44953935 | C | T | 36 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(33): Show |
54 | HG00639.hp2 HG01074.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.1022-4097G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44953935 | |||||||
| chr13:44954009 | T | TAAAAAGA others(338): Show |
2 | a0001c0003t0001g0056 a0001c0003t0001g0057 |
2 | HG00639.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1022-4172_1022-417 others(349): Show |
NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44954009 | |||||||
| chr13:44954009 | T | TAAAAAGA others(339): Show |
1 | a0001c0003t0001g0058 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1022-4172_1022-417 others(350): Show |
NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44954009 | |||||||
| chr13:44954193 | T | C | 3 | a0002c0002t0001g0190 a0002c0002t0001g0191 a0002c0002t0001g0192 |
3 | HG00735.hp2 HG01167.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1022-4355A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44954193 | |||||||
| chr13:44954286 | G | A | 1 | a0002c0002t0001g0207 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1022-4448C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44954286 | |||||||
| chr13:44954350 | C | T | 1 | a0001c0001t0002g0024 | 2 | HG00733.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1022-4512G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44954350 | |||||||
| chr13:44954370 | T | C | 20 | a0001c0003t0001g0005 a0001c0003t0001g0027 a0001c0003t0001g0028 others(17): Show |
27 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.1022-4532A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44954370 | |||||||
| chr13:44954520 | C | T | 2 | a0001c0007t0001g0076 a0004c0009t0004g0184 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1022-4682G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44954520 | |||||||
| chr13:44954642 | T | C | 4 | a0001c0001t0002g0083 a0001c0007t0001g0076 a0001c0008t0002g0153 others(1): Show |
4 | HG01496.hp2 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1021+4739A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44954642 | |||||||
| chr13:44955421 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1021+3960C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44955421 | |||||||
| chr13:44955664 | C | G | 5 | a0001c0001t0002g0025 a0001c0001t0002g0044 a0001c0001t0002g0045 others(2): Show |
6 | HG02145.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021+3717G>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44955664 | |||||||
| chr13:44955765 | G | A | 2 | a0002c0002t0001g0154 a0004c0009t0004g0184 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1021+3616C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44955765 | |||||||
| chr13:44955788 | C | A | 1 | a0002c0002t0001g0199 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1021+3593G>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44955788 | |||||||
| chr13:44955823 | T | TA | 24 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0014 others(21): Show |
37 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.1021+3557dupT | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44955823 | |||||||
| chr13:44955823 | TA | T | 112 | a0001c0001t0002g0046 a0001c0001t0002g0050 a0001c0003t0001g0005 others(109): Show |
156 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.1021+3557delT | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44955823 | |||||||
| chr13:44955867 | G | C | 1 | a0002c0002t0001g0167 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1021+3514C>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44955867 | |||||||
| chr13:44955959 | C | T | 30 | a0001c0003t0001g0005 a0001c0003t0001g0010 a0001c0003t0001g0023 others(27): Show |
41 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1021+3422G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44955959 | |||||||
| chr13:44956059 | T | C | 37 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(34): Show |
55 | HG00639.hp2 HG01074.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.1021+3322A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44956059 | |||||||
| chr13:44956059 | T | G | 1 | a0001c0007t0001g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1021+3322A>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44956059 | |||||||
| chr13:44956076 | A | G | 36 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(33): Show |
54 | HG00639.hp2 HG01074.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.1021+3305T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44956076 | |||||||
| chr13:44956136 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1021+3245G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44956136 | |||||||
| chr13:44956141 | C | CA | 36 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(33): Show |
50 | HG00438.hp2 HG01074.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1021+3239dupT | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44956141 | |||||||
| chr13:44956141 | CA | C | 13 | a0001c0001t0002g0011 a0001c0001t0002g0024 a0001c0001t0002g0044 others(10): Show |
16 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1021+3239delT | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44956141 | |||||||
| chr13:44956162 | A | G | 1 | a0002c0002t0001g0169 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1021+3219T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44956162 | |||||||
| chr13:44956281 | C | CAG | 210 | a0001c0001t0001g0080 a0001c0001t0002g0002 a0001c0001t0002g0003 others(207): Show |
298 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.1021+3099_1021+310 others(6): Show |
NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44956281 | |||||||
| chr13:44956437 | G | A | 37 | a0001c0001t0001g0080 a0001c0001t0002g0003 a0001c0001t0002g0008 others(34): Show |
50 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.1021+2944C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44956437 | |||||||
| chr13:44956457 | C | T | 36 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(33): Show |
54 | HG00639.hp2 HG01074.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.1021+2924G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44956457 | |||||||
| chr13:44956675 | G | A | 1 | a0001c0001t0002g0110 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1021+2706C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44956675 | |||||||
| chr13:44956745 | T | C | 113 | a0001c0003t0001g0005 a0001c0003t0001g0010 a0001c0003t0001g0023 others(110): Show |
157 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.1021+2636A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44956745 | |||||||
| chr13:44957433 | A | G | 2 | a0002c0002t0001g0175 a0002c0002t0001g0176 |
2 | NA18981.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1021+1948T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44957433 | |||||||
| chr13:44957666 | G | A | 8 | a0001c0001t0002g0014 a0001c0001t0002g0031 a0001c0001t0002g0119 others(5): Show |
11 | HG00609.hp2 HG00621.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.1021+1715C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44957666 | |||||||
| chr13:44957706 | T | A | 1 | a0001c0001t0002g0114 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1021+1675A>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44957706 | |||||||
| chr13:44957739 | C | T | 2 | a0001c0001t0002g0144 a0001c0001t0002g0146 |
2 | HG02647.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1021+1642G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44957739 | |||||||
| chr13:44958138 | T | C | 2 | a0001c0001t0002g0031 a0001c0001t0002g0123 |
3 | HG00609.hp2 NA19056.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1021+1243A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44958138 | |||||||
| chr13:44958524 | C | T | 2 | a0002c0002t0001g0154 a0004c0009t0004g0184 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1021+857G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44958524 | |||||||
| chr13:44958639 | A | G | 2 | a0001c0001t0002g0128 a0001c0001t0002g0129 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1021+742T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44958639 | |||||||
| chr13:44958774 | G | A | 1 | a0001c0003t0001g0058 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1021+607C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44958774 | |||||||
| chr13:44958884 | G | T | 1 | a0001c0001t0002g0110 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1021+497C>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44958884 | |||||||
| chr13:44959332 | C | T | 1 | a0002c0002t0001g0190 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1021+49G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 7/9 | chr13 | 44959332 | |||||||
| chr13:44959613 | C | T | 1 | a0002c0002t0001g0208 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.828-39G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44959613 | |||||||
| chr13:44959707 | G | A | 1 | a0001c0003t0001g0069 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.828-133C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44959707 | |||||||
| chr13:44959708 | A | G | 1 | a0002c0002t0002g0221 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.828-134T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44959708 | |||||||
| chr13:44959750 | T | C | 4 | a0001c0001t0002g0011 a0001c0001t0002g0024 a0001c0001t0002g0048 others(1): Show |
7 | HG00733.hp2 HG00738.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.828-176A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44959750 | |||||||
| chr13:44959934 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.828-360A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44959934 | |||||||
| chr13:44959953 | A | G | 1 | a0001c0008t0002g0153 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.828-379T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44959953 | |||||||
| chr13:44960207 | G | A | 19 | a0001c0001t0003g0012 a0001c0001t0003g0029 a0001c0001t0003g0030 others(16): Show |
23 | HG00642.hp1 HG01261.hp1 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.828-633C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44960207 | |||||||
| chr13:44960323 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.828-749G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44960323 | |||||||
| chr13:44960324 | A | G | 19 | a0001c0001t0003g0012 a0001c0001t0003g0029 a0001c0001t0003g0030 others(16): Show |
23 | HG00642.hp1 HG01261.hp1 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.828-750T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44960324 | |||||||
| chr13:44960388 | C | A | 1 | a0001c0001t0002g0091 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.828-814G>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44960388 | |||||||
| chr13:44960487 | G | A | 1 | a0002c0002t0001g0192 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.828-913C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44960487 | |||||||
| chr13:44960558 | C | T | 1 | a0001c0003t0001g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.828-984G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44960558 | |||||||
| chr13:44960815 | C | T | 1 | a0004c0009t0004g0184 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.828-1241G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44960815 | |||||||
| chr13:44961052 | G | GA | 13 | a0001c0001t0002g0115 a0001c0001t0002g0125 a0001c0001t0002g0138 others(10): Show |
13 | HG00735.hp2 HG01081.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.828-1479dupT | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44961052 | |||||||
| chr13:44961521 | A | G | 2 | a0001c0001t0003g0096 a0001c0001t0003g0099 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.828-1947T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44961521 | |||||||
| chr13:44961607 | G | A | 1 | a0004c0009t0004g0184 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.828-2033C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44961607 | |||||||
| chr13:44961768 | C | T | 8 | a0001c0001t0002g0014 a0001c0001t0002g0031 a0001c0001t0002g0119 others(5): Show |
11 | HG00609.hp2 HG00621.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.828-2194G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44961768 | |||||||
| chr13:44962083 | T | C | 1 | a0002c0002t0001g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.828-2509A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44962083 | |||||||
| chr13:44962113 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0142 |
6 | HG00639.hp2 HG01243.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.828-2539C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44962113 | |||||||
| chr13:44962443 | G | A | 1 | a0002c0002t0001g0168 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.828-2869C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44962443 | |||||||
| chr13:44962525 | G | C | 1 | a0004c0009t0004g0184 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.828-2951C>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44962525 | |||||||
| chr13:44964250 | G | T | 1 | a0001c0003t0001g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.827+1594C>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44964250 | |||||||
| chr13:44964303 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.827+1541G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44964303 | |||||||
| chr13:44964377 | G | A | 1 | a0002c0002t0001g0214 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.827+1467C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44964377 | |||||||
| chr13:44964498 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.827+1346G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44964498 | |||||||
| chr13:44964719 | G | A | 35 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(32): Show |
53 | HG00639.hp2 HG01074.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.827+1125C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44964719 | |||||||
| chr13:44964760 | T | C | 1 | a0001c0003t0001g0069 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.827+1084A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44964760 | |||||||
| chr13:44964769 | C | T | 1 | a0002c0002t0001g0159 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.827+1075G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44964769 | |||||||
| chr13:44965246 | C | A | 1 | a0001c0003t0001g0066 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.827+598G>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44965246 | |||||||
| chr13:44965275 | C | T | 4 | a0001c0001t0002g0144 a0001c0003t0001g0028 a0001c0003t0001g0073 others(1): Show |
5 | HG00423.hp1 HG00438.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.827+569G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44965275 | |||||||
| chr13:44965367 | A | G | 17 | a0001c0003t0001g0005 a0001c0003t0001g0027 a0001c0003t0001g0028 others(14): Show |
24 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.827+477T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44965367 | |||||||
| chr13:44965555 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.827+289C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44965555 | |||||||
| chr13:44965627 | G | C | 1 | a0001c0003t0001g0023 | 2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.827+217C>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44965627 | |||||||
| chr13:44965744 | A | G | 37 | a0001c0001t0001g0080 a0001c0001t0002g0003 a0001c0001t0002g0008 others(34): Show |
50 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.827+100T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 6/9 | chr13 | 44965744 | |||||||
| chr13:44966001 | G | A | 37 | a0001c0001t0001g0080 a0001c0001t0002g0003 a0001c0001t0002g0008 others(34): Show |
50 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.735-65C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44966001 | |||||||
| chr13:44966245 | C | T | 210 | a0001c0001t0001g0080 a0001c0001t0002g0002 a0001c0001t0002g0003 others(207): Show |
298 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.735-309G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44966245 | |||||||
| chr13:44966264 | A | T | 3 | a0002c0002t0001g0036 a0002c0002t0001g0188 a0002c0002t0001g0189 |
4 | HG00642.hp2 HG02004.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.735-328T>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44966264 | |||||||
| chr13:44966265 | T | A | 1 | a0001c0003t0001g0069 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.735-329A>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44966265 | |||||||
| chr13:44966789 | C | T | 1 | a0001c0001t0003g0103 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.735-853G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44966789 | |||||||
| chr13:44966865 | C | T | 1 | a0002c0002t0001g0160 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.735-929G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44966865 | |||||||
| chr13:44966927 | C | T | 2 | a0001c0001t0003g0097 a0001c0001t0003g0098 |
2 | HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.735-991G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44966927 | |||||||
| chr13:44967066 | A | C | 1 | a0001c0001t0002g0120 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.735-1130T>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44967066 | |||||||
| chr13:44967072 | A | G | 1 | a0001c0007t0001g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.735-1136T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44967072 | |||||||
| chr13:44967304 | T | A | 4 | a0002c0002t0001g0157 a0002c0002t0001g0172 a0002c0002t0001g0173 others(1): Show |
4 | HG00544.hp2 NA18941.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-1368A>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44967304 | |||||||
| chr13:44967326 | A | G | 4 | a0001c0001t0002g0083 a0001c0001t0002g0093 a0001c0001t0002g0094 others(1): Show |
4 | HG02622.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-1390T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44967326 | |||||||
| chr13:44967377 | G | A | 2 | a0002c0002t0001g0203 a0002c0002t0001g0204 |
2 | HG00438.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.735-1441C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44967377 | |||||||
| chr13:44967487 | G | A | 24 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0014 others(21): Show |
37 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.735-1551C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44967487 | |||||||
| chr13:44967572 | C | T | 24 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0014 others(21): Show |
37 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.735-1636G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44967572 | |||||||
| chr13:44967664 | T | C | 2 | a0002c0002t0001g0205 a0002c0002t0001g0207 |
2 | HG02080.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.735-1728A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44967664 | |||||||
| chr13:44967794 | C | T | 5 | a0002c0002t0001g0178 a0002c0002t0001g0179 a0002c0002t0001g0180 others(2): Show |
5 | HG01069.hp2 HG01433.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.735-1858G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44967794 | |||||||
| chr13:44967948 | C | T | 1 | a0001c0008t0002g0153 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.735-2012G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44967948 | |||||||
| chr13:44967959 | CT | C | 3 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0142 |
6 | HG00639.hp2 HG01243.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.735-2024delA | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44967959 | |||||||
| chr13:44967959 | CTT | C | 207 | a0001c0001t0001g0080 a0001c0001t0002g0002 a0001c0001t0002g0003 others(204): Show |
292 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.735-2025_735-2024d others(4): Show |
NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44967959 | |||||||
| chr13:44968068 | G | A | 5 | a0002c0002t0001g0178 a0002c0002t0001g0179 a0002c0002t0001g0180 others(2): Show |
5 | HG01069.hp2 HG01433.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.735-2132C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44968068 | |||||||
| chr13:44968090 | G | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0129 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.735-2154C>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44968090 | |||||||
| chr13:44968406 | GA | G | 109 | a0001c0001t0002g0119 a0001c0001t0002g0149 a0001c0003t0001g0005 others(106): Show |
152 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.735-2471delT | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44968406 | |||||||
| chr13:44968410 | A | G | 1 | a0004c0009t0004g0184 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.735-2474T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44968410 | |||||||
| chr13:44968474 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.735-2538A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44968474 | |||||||
| chr13:44968653 | T | C | 1 | a0002c0002t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.735-2717A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44968653 | |||||||
| chr13:44969411 | T | C | 1 | a0001c0001t0002g0129 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.735-3475A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44969411 | |||||||
| chr13:44969453 | T | C | 4 | a0001c0003t0001g0023 a0001c0003t0001g0056 a0001c0003t0001g0057 others(1): Show |
5 | HG00639.hp1 HG02055.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-3517A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44969453 | |||||||
| chr13:44969550 | T | G | 1 | a0002c0002t0001g0208 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.735-3614A>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44969550 | |||||||
| chr13:44970190 | C | T | 79 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0007 others(76): Show |
112 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.735-4254G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44970190 | |||||||
| chr13:44970376 | A | G | 17 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0081 others(14): Show |
26 | HG00140.hp1 HG00738.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.735-4440T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44970376 | |||||||
| chr13:44970426 | G | A | 17 | a0001c0003t0001g0005 a0001c0003t0001g0027 a0001c0003t0001g0028 others(14): Show |
24 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.735-4490C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44970426 | |||||||
| chr13:44970876 | A | G | 1 | a0002c0002t0001g0218 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.735-4940T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44970876 | |||||||
| chr13:44970939 | G | A | 1 | a0004c0009t0004g0184 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.735-5003C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44970939 | |||||||
| chr13:44970940 | G | T | 215 | a0001c0001t0001g0080 a0001c0001t0002g0002 a0001c0001t0002g0003 others(212): Show |
304 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.735-5004C>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44970940 | |||||||
| chr13:44971011 | G | A | 3 | a0002c0002t0001g0021 a0002c0002t0001g0215 a0002c0002t0001g0216 |
5 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-5075C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44971011 | |||||||
| chr13:44971287 | A | G | 25 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0014 others(22): Show |
38 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.735-5351T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44971287 | |||||||
| chr13:44971345 | C | A | 1 | a0001c0003t0001g0072 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.735-5409G>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44971345 | |||||||
| chr13:44971500 | C | T | 1 | a0002c0002t0001g0159 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.735-5564G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44971500 | |||||||
| chr13:44971793 | A | G | 1 | a0001c0001t0002g0033 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.735-5857T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44971793 | |||||||
| chr13:44971809 | G | C | 4 | a0001c0001t0003g0030 a0001c0001t0003g0102 a0001c0001t0003g0106 others(1): Show |
5 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.735-5873C>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44971809 | |||||||
| chr13:44971911 | AT | A | 80 | a0001c0003t0001g0070 a0002c0002t0001g0001 a0002c0002t0001g0004 others(77): Show |
113 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.735-5976delA | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44971911 | |||||||
| chr13:44971913 | T | C | 2 | a0001c0003t0001g0071 a0001c0003t0001g0072 |
2 | NA18940.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.735-5977A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44971913 | |||||||
| chr13:44972204 | C | T | 1 | a0001c0001t0002g0093 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.735-6268G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44972204 | |||||||
| chr13:44972341 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.735-6405C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44972341 | |||||||
| chr13:44973049 | T | C | 1 | a0001c0006t0002g0092 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.734+6141A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44973049 | |||||||
| chr13:44973122 | C | G | 79 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0007 others(76): Show |
112 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.734+6068G>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44973122 | |||||||
| chr13:44973443 | C | T | 1 | a0001c0007t0001g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.734+5747G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44973443 | |||||||
| chr13:44973488 | T | A | 4 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0142 others(1): Show |
7 | HG00639.hp2 HG01243.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.734+5702A>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44973488 | |||||||
| chr13:44973630 | A | G | 18 | a0001c0003t0001g0005 a0001c0003t0001g0027 a0001c0003t0001g0028 others(15): Show |
25 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.734+5560T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44973630 | |||||||
| chr13:44973757 | G | A | 1 | a0002c0002t0001g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.734+5433C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44973757 | |||||||
| chr13:44973831 | C | T | 9 | a0001c0001t0003g0029 a0001c0001t0003g0053 a0001c0001t0003g0096 others(6): Show |
10 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.734+5359G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44973831 | |||||||
| chr13:44973865 | C | A | 30 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(27): Show |
44 | HG01074.hp2 HG01109.hp1 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.734+5325G>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44973865 | |||||||
| chr13:44974022 | A | G | 4 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0142 others(1): Show |
7 | HG00639.hp2 HG01243.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.734+5168T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44974022 | |||||||
| chr13:44974173 | T | G | 1 | a0001c0001t0003g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.734+5017A>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44974173 | |||||||
| chr13:44974347 | T | C | 1 | a0002c0002t0001g0210 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.734+4843A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44974347 | |||||||
| chr13:44974456 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.734+4734C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44974456 | |||||||
| chr13:44974456 | G | T | 1 | a0001c0001t0002g0082 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.734+4734C>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44974456 | |||||||
| chr13:44974464 | A | G | 1 | a0002c0002t0001g0188 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.734+4726T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44974464 | |||||||
| chr13:44974703 | C | T | 2 | a0001c0001t0002g0109 a0001c0003t0001g0078 |
2 | HG00438.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.734+4487G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44974703 | |||||||
| chr13:44974998 | T | C | 3 | a0001c0001t0002g0093 a0001c0001t0002g0094 a0001c0001t0002g0095 |
3 | HG02622.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.734+4192A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44974998 | |||||||
| chr13:44975707 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.734+3483G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44975707 | |||||||
| chr13:44975745 | T | C | 2 | a0001c0003t0001g0073 a0001c0003t0001g0078 |
2 | HG00438.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.734+3445A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44975745 | |||||||
| chr13:44975910 | A | G | 2 | a0001c0001t0002g0143 a0002c0002t0002g0221 |
2 | HG01243.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.734+3280T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44975910 | |||||||
| chr13:44976124 | A | AG | 37 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(34): Show |
55 | HG00639.hp2 HG01074.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.734+3065dupC | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44976124 | |||||||
| chr13:44976355 | AAGG | A | 4 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0142 others(1): Show |
7 | HG00639.hp2 HG01243.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.734+2832_734+2834d others(5): Show |
NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44976355 | |||||||
| chr13:44976427 | GGAGGAGG others(8): Show |
G | 1 | a0001c0003t0001g0052 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.734+2748_734+2762d others(17): Show |
NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44976427 | |||||||
| chr13:44976439 | G | C | 1 | a0001c0001t0001g0080 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.734+2751C>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44976439 | |||||||
| chr13:44976472 | A | G | 3 | a0002c0002t0001g0190 a0002c0002t0001g0191 a0002c0002t0001g0192 |
3 | HG00735.hp2 HG01167.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.734+2718T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44976472 | |||||||
| chr13:44976473 | TAAC | T | 12 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0043 others(9): Show |
22 | HG00408.hp1 HG00673.hp2 HG02004.hp1 others(19): Show |
intron_variant | MODIFIER | c.734+2714_734+2716d others(5): Show |
NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44976473 | |||||||
| chr13:44976488 | G | C | 1 | a0001c0001t0002g0148 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.734+2702C>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44976488 | |||||||
| chr13:44976614 | T | C | 1 | a0001c0007t0001g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.734+2576A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44976614 | |||||||
| chr13:44976661 | A | G | 23 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0014 others(20): Show |
36 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.734+2529T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44976661 | |||||||
| chr13:44976827 | G | A | 8 | a0002c0002t0001g0157 a0002c0002t0001g0158 a0002c0002t0001g0165 others(5): Show |
8 | HG00408.hp2 HG00544.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.734+2363C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44976827 | |||||||
| chr13:44976922 | C | T | 2 | a0001c0001t0003g0097 a0001c0001t0003g0098 |
2 | HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.734+2268G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44976922 | |||||||
| chr13:44976940 | A | T | 1 | a0001c0003t0001g0061 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.734+2250T>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44976940 | |||||||
| chr13:44977010 | A | T | 2 | a0001c0001t0003g0097 a0001c0001t0003g0098 |
2 | HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.734+2180T>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44977010 | |||||||
| chr13:44977081 | TC | T | 66 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0019 others(63): Show |
93 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.734+2108delG | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44977081 | |||||||
| chr13:44977468 | A | C | 1 | a0001c0001t0002g0081 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.734+1722T>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44977468 | |||||||
| chr13:44977832 | T | C | 1 | a0002c0002t0001g0217 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.734+1358A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44977832 | |||||||
| chr13:44977860 | C | T | 27 | a0001c0003t0001g0005 a0001c0003t0001g0010 a0001c0003t0001g0023 others(24): Show |
38 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.734+1330G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44977860 | |||||||
| chr13:44977867 | G | A | 1 | a0002c0002t0001g0170 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.734+1323C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44977867 | |||||||
| chr13:44977885 | C | A | 1 | a0001c0003t0001g0023 | 2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.734+1305G>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44977885 | |||||||
| chr13:44978262 | G | A | 1 | a0001c0001t0002g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734+928C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44978262 | |||||||
| chr13:44978326 | T | C | 1 | a0004c0009t0004g0184 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.734+864A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44978326 | |||||||
| chr13:44978873 | A | G | 3 | a0002c0002t0001g0036 a0002c0002t0001g0188 a0002c0002t0001g0189 |
4 | HG00642.hp2 HG02004.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.734+317T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44978873 | |||||||
| chr13:44978969 | C | G | 1 | a0001c0001t0003g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.734+221G>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44978969 | |||||||
| chr13:44978986 | A | T | 27 | a0001c0003t0001g0005 a0001c0003t0001g0010 a0001c0003t0001g0023 others(24): Show |
38 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.734+204T>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44978986 | |||||||
| chr13:44979009 | A | T | 1 | a0002c0002t0001g0187 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.734+181T>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44979009 | |||||||
| chr13:44979067 | A | G | 1 | a0001c0003t0001g0066 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.734+123T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44979067 | |||||||
| chr13:44979142 | C | G | 1 | a0002c0002t0001g0158 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.734+48G>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 5/9 | chr13 | 44979142 | |||||||
| chr13:44979492 | C | T | 2 | a0002c0002t0001g0035 a0002c0002t0001g0186 |
3 | HG03516.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.658-226G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 4/9 | chr13 | 44979492 | |||||||
| chr13:44979873 | A | T | 1 | a0002c0002t0001g0157 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.657+17T>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 4/9 | chr13 | 44979873 | |||||||
| chr13:44979878 | A | G | 36 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(33): Show |
54 | HG00639.hp2 HG01074.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.657+12T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 4/9 | chr13 | 44979878 | |||||||
| chr13:44980253 | G | T | 5 | a0001c0001t0002g0025 a0001c0001t0002g0044 a0001c0001t0002g0045 others(2): Show |
6 | HG02145.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.595-301C>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 3/9 | chr13 | 44980253 | |||||||
| chr13:44980388 | T | C | 1 | a0002c0002t0002g0221 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.594+334A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 3/9 | chr13 | 44980388 | |||||||
| chr13:44980425 | C | A | 1 | a0001c0001t0002g0148 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.594+297G>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 3/9 | chr13 | 44980425 | |||||||
| chr13:44980435 | C | T | 1 | a0002c0002t0001g0185 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.594+287G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 3/9 | chr13 | 44980435 | |||||||
| chr13:44980445 | C | G | 1 | a0002c0002t0001g0168 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.594+277G>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 3/9 | chr13 | 44980445 | |||||||
| chr13:44980549 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0142 |
6 | HG00639.hp2 HG01243.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.594+173C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 3/9 | chr13 | 44980549 | |||||||
| chr13:44980927 | C | T | 23 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0014 others(20): Show |
36 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.496-107G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 2/9 | chr13 | 44980927 | |||||||
| chr13:44981144 | T | C | 12 | a0001c0001t0002g0009 a0001c0001t0002g0016 a0001c0001t0002g0017 others(9): Show |
19 | HG02040.hp1 HG02132.hp2 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.496-324A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 2/9 | chr13 | 44981144 | |||||||
| chr13:44981331 | C | A | 1 | a0001c0003t0001g0061 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.496-511G>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 2/9 | chr13 | 44981331 | |||||||
| chr13:44981331 | C | CA | 22 | a0001c0001t0002g0011 a0001c0001t0002g0018 a0001c0001t0002g0024 others(19): Show |
32 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.496-512dupT | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 2/9 | chr13 | 44981331 | |||||||
| chr13:44981331 | C | CAAA | 31 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(28): Show |
45 | HG01074.hp2 HG01109.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.496-514_496-512dup others(3): Show |
NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 2/9 | chr13 | 44981331 | |||||||
| chr13:44981397 | G | A | 4 | a0002c0002t0001g0020 a0002c0002t0001g0168 a0002c0002t0001g0169 others(1): Show |
6 | HG00733.hp1 HG01081.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.496-577C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 2/9 | chr13 | 44981397 | |||||||
| chr13:44981575 | C | T | 23 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0014 others(20): Show |
36 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.495+497G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 2/9 | chr13 | 44981575 | |||||||
| chr13:44981744 | G | A | 1 | a0001c0001t0003g0152 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.495+328C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 2/9 | chr13 | 44981744 | |||||||
| chr13:44981810 | T | TA | 9 | a0001c0001t0002g0014 a0001c0001t0002g0031 a0001c0001t0002g0119 others(6): Show |
12 | HG00609.hp2 HG00621.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.495+261dupT | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 2/9 | chr13 | 44981810 | |||||||
| chr13:44981921 | T | TCATGTTT others(16): Show |
80 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0007 others(77): Show |
113 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.495+150_495+151ins others(23): Show |
NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 2/9 | chr13 | 44981921 | |||||||
| chr13:44981988 | T | C | 37 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(34): Show |
55 | HG00639.hp2 HG01074.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.495+84A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 2/9 | chr13 | 44981988 | |||||||
| chr13:44982386 | C | T | 1 | a0002c0002t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.413-232G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44982386 | |||||||
| chr13:44982476 | T | C | 1 | a0001c0001t0002g0139 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.413-322A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44982476 | |||||||
| chr13:44982667 | CA | C | 5 | a0001c0003t0001g0027 a0001c0003t0001g0063 a0001c0003t0001g0064 others(2): Show |
6 | HG00673.hp1 HG02027.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.413-514delT | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44982667 | |||||||
| chr13:44982732 | C | T | 17 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0081 others(14): Show |
26 | HG00140.hp1 HG00738.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.413-578G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44982732 | |||||||
| chr13:44982939 | T | C | 1 | a0002c0002t0002g0221 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.413-785A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44982939 | |||||||
| chr13:44982970 | T | C | 1 | a0001c0001t0002g0140 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.413-816A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44982970 | |||||||
| chr13:44983123 | G | A | 1 | a0001c0008t0002g0153 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.413-969C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44983123 | |||||||
| chr13:44983133 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.413-979G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44983133 | |||||||
| chr13:44983489 | TA | T | 9 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 others(6): Show |
9 | HG01516.hp2 HG01975.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.413-1336delT | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44983489 | |||||||
| chr13:44983589 | G | C | 31 | a0001c0003t0001g0005 a0001c0003t0001g0010 a0001c0003t0001g0023 others(28): Show |
42 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.413-1435C>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44983589 | |||||||
| chr13:44984193 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.413-2039G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44984193 | |||||||
| chr13:44984439 | G | A | 18 | a0001c0003t0001g0005 a0001c0003t0001g0027 a0001c0003t0001g0028 others(15): Show |
25 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.413-2285C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44984439 | |||||||
| chr13:44984514 | T | C | 2 | a0001c0001t0002g0034 a0001c0001t0002g0150 |
3 | HG02615.hp1 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.413-2360A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44984514 | |||||||
| chr13:44984657 | TAAAATA | T | 2 | a0002c0002t0001g0019 a0002c0002t0001g0156 |
4 | HG00735.hp1 HG00741.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-2509_413-2504d others(8): Show |
NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44984657 | |||||||
| chr13:44984783 | T | C | 1 | a0001c0001t0002g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.413-2629A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44984783 | |||||||
| chr13:44984822 | T | C | 1 | a0001c0003t0001g0074 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.413-2668A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44984822 | |||||||
| chr13:44984831 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.413-2677C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44984831 | |||||||
| chr13:44984868 | C | T | 5 | a0002c0002t0001g0178 a0002c0002t0001g0179 a0002c0002t0001g0180 others(2): Show |
5 | HG01069.hp2 HG01433.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-2714G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44984868 | |||||||
| chr13:44984900 | C | T | 1 | a0002c0002t0001g0155 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.413-2746G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44984900 | |||||||
| chr13:44985239 | T | G | 2 | a0001c0001t0002g0034 a0001c0001t0002g0150 |
3 | HG02615.hp1 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.413-3085A>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44985239 | |||||||
| chr13:44985335 | C | CT | 3 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0142 |
6 | HG00639.hp2 HG01243.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.413-3182dupA | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44985335 | |||||||
| chr13:44985426 | C | T | 1 | a0001c0003t0001g0052 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.413-3272G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44985426 | |||||||
| chr13:44985712 | T | G | 1 | a0001c0008t0002g0153 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.412+3313A>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44985712 | |||||||
| chr13:44986263 | AAGG | A | 23 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0014 others(20): Show |
36 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.412+2759_412+2761d others(5): Show |
NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44986263 | |||||||
| chr13:44986507 | T | G | 1 | a0001c0007t0001g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.412+2518A>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44986507 | |||||||
| chr13:44986608 | C | T | 3 | a0002c0002t0001g0175 a0002c0002t0001g0176 a0002c0002t0001g0177 |
3 | NA18981.hp2 NA19056.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.412+2417G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44986608 | |||||||
| chr13:44986609 | G | A | 12 | a0001c0001t0002g0009 a0001c0001t0002g0016 a0001c0001t0002g0017 others(9): Show |
19 | HG02040.hp1 HG02132.hp2 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.412+2416C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44986609 | |||||||
| chr13:44986641 | A | G | 1 | a0002c0002t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.412+2384T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44986641 | |||||||
| chr13:44986691 | C | CA | 9 | a0001c0001t0002g0025 a0001c0001t0002g0044 a0001c0001t0002g0050 others(6): Show |
11 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.412+2333dupT | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44986691 | |||||||
| chr13:44986912 | C | G | 1 | a0001c0001t0002g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.412+2113G>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44986912 | |||||||
| chr13:44986936 | C | T | 24 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(21): Show |
38 | HG01074.hp2 HG01109.hp1 HG02040.hp1 others(35): Show |
intron_variant | MODIFIER | c.412+2089G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44986936 | |||||||
| chr13:44987018 | C | A | 1 | a0001c0003t0001g0078 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.412+2007G>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44987018 | |||||||
| chr13:44987188 | G | C | 1 | a0002c0002t0001g0220 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.412+1837C>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44987188 | |||||||
| chr13:44987389 | A | T | 116 | a0001c0001t0002g0044 a0001c0001t0002g0075 a0001c0001t0003g0053 others(113): Show |
160 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.412+1636T>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44987389 | |||||||
| chr13:44987413 | T | C | 3 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0174 |
3 | HG00544.hp2 NA18979.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.412+1612A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44987413 | |||||||
| chr13:44987534 | TG | T | 12 | a0001c0001t0002g0011 a0001c0001t0002g0024 a0001c0001t0002g0025 others(9): Show |
16 | HG00733.hp2 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.412+1490delC | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44987534 | |||||||
| chr13:44987898 | G | GTCTT | 1 | a0001c0003t0001g0010 | 3 | HG02896.hp1 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.412+1123_412+1126d others(6): Show |
NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44987898 | |||||||
| chr13:44988121 | T | A | 1 | a0001c0001t0002g0149 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.412+904A>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44988121 | |||||||
| chr13:44988223 | G | A | 1 | a0001c0001t0002g0125 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.412+802C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44988223 | |||||||
| chr13:44988259 | A | G | 23 | a0002c0002t0001g0004 a0002c0002t0001g0019 a0002c0002t0001g0020 others(20): Show |
33 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.412+766T>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44988259 | |||||||
| chr13:44988272 | T | C | 2 | a0001c0001t0002g0034 a0001c0001t0002g0150 |
3 | HG02615.hp1 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.412+753A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44988272 | |||||||
| chr13:44988433 | G | A | 35 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(32): Show |
53 | HG00639.hp2 HG01074.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.412+592C>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44988433 | |||||||
| chr13:44988491 | C | T | 1 | a0001c0001t0002g0043 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.412+534G>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44988491 | |||||||
| chr13:44988504 | T | A | 2 | a0001c0001t0003g0151 a0001c0001t0003g0152 |
2 | HG00642.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.412+521A>T | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44988504 | |||||||
| chr13:44988603 | A | T | 1 | a0001c0003t0001g0023 | 2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.412+422T>A | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44988603 | |||||||
| chr13:44988846 | T | C | 1 | a0002c0002t0001g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.412+179A>G | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44988846 | |||||||
| chr13:44988877 | C | G | 1 | a0002c0002t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.412+148G>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44988877 | |||||||
| chr13:44988926 | C | G | 1 | a0005c0005t0002g0042 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.412+99G>C | NUFIP1 | ENSG00000083635.8 | transcript | ENST00000379161.5 | protein_coding | 1/9 | chr13 | 44988926 |