Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 22927 |
| ensemblid | ENSG00000130956.14 |
| hgncid | 17062 |
| symbol | HABP4 |
| name | hyaluronan binding protein 4 |
| refseq_nuc | NM_014282.4 |
| refseq_prot | NP_055097.2 |
| ensembl_nuc | ENST00000375249.5 |
| ensembl_prot | ENSP00000364398.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 96450169 |
| end | 96491336 |
| strand | + |
| ver | v1.2 |
| region | chr9:96450169-96491336 |
| region5000 | chr9:96445169-96496336 |
| regionname0 | HABP4_chr9_96450169_96491336 |
| regionname5000 | HABP4_chr9_96445169_96496336 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 413 | 305 | 84 | 58 | 110 | 16 | 35 | 82 | HABP4_chr9_96445169_96496336 | HABP4 | MKGAL others(408): Show |
chr9 | 96445169 | 96496336 |
| a0002 | 0/0 | 413 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | MKGAL others(408): Show |
chr9 | 96445169 | 96496336 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1239 | 239 | 42 | 47 | 101 | 15 | 32 | HABP4_chr9_96445169_96496336 | HABP4 | ATGAA others(1234): Show |
chr9 | 96445169 | 96496336 | ||
| a0001c0002 | 0/0 | 1239 | 52 | 28 | 11 | 9 | 1 | 3 | HABP4_chr9_96445169_96496336 | HABP4 | ATGAA others(1234): Show |
chr9 | 96445169 | 96496336 | ||
| a0001c0003 | 0/0 | 1239 | 11 | 11 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | ATGAA others(1234): Show |
chr9 | 96445169 | 96496336 | ||
| a0001c0005 | 0/0 | 1239 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | ATGAA others(1234): Show |
chr9 | 96445169 | 96496336 | ||
| a0001c0006 | 0/0 | 1239 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | ATGAA others(1234): Show |
chr9 | 96445169 | 96496336 | ||
| a0001c0007 | 0/0 | 1239 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | ATGAA others(1234): Show |
chr9 | 96445169 | 96496336 | ||
| a0002c0004 | 0/0 | 1239 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | ATGAA others(1234): Show |
chr9 | 96445169 | 96496336 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2651 | 220 | 34 | 43 | 100 | 12 | 29 | HABP4_chr9_96445169_96496336 | HABP4 | AGGGC others(2646): Show |
chr9 | 96445169 | 96496336 |
| a0001c0001t0003 | 0/0 | 2651 | 9 | 7 | 2 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | AGGGC others(2646): Show |
chr9 | 96445169 | 96496336 |
| a0001c0001t0004 | 0/0 | 2651 | 4 | 0 | 1 | 0 | 2 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | AGGGC others(2646): Show |
chr9 | 96445169 | 96496336 |
| a0001c0001t0007 | 0/0 | 2651 | 1 | 0 | 0 | 0 | 1 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | AGGGC others(2646): Show |
chr9 | 96445169 | 96496336 |
| a0001c0001t0009 | 0/0 | 2651 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | AGGGC others(2646): Show |
chr9 | 96445169 | 96496336 |
| a0001c0001t0010 | 0/0 | 2651 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | AGGGC others(2646): Show |
chr9 | 96445169 | 96496336 |
| a0001c0001t0011 | 0/0 | 2651 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | AGGGC others(2646): Show |
chr9 | 96445169 | 96496336 |
| a0001c0001t0012 | 0/0 | 2651 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | AGGGC others(2646): Show |
chr9 | 96445169 | 96496336 |
| a0001c0001t0013 | 0/0 | 2651 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | AGGGC others(2646): Show |
chr9 | 96445169 | 96496336 |
| a0001c0002t0002 | 0/0 | 2651 | 45 | 22 | 11 | 8 | 1 | 3 | HABP4_chr9_96445169_96496336 | HABP4 | AGGGC others(2646): Show |
chr9 | 96445169 | 96496336 |
| a0001c0002t0003 | 0/0 | 2651 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | AGGGC others(2646): Show |
chr9 | 96445169 | 96496336 |
| a0001c0002t0005 | 0/0 | 2651 | 3 | 3 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | AGGGC others(2646): Show |
chr9 | 96445169 | 96496336 |
| a0001c0002t0006 | 0/0 | 2651 | 2 | 2 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | AGGGC others(2646): Show |
chr9 | 96445169 | 96496336 |
| a0001c0002t0008 | 0/0 | 2651 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | AGGGC others(2646): Show |
chr9 | 96445169 | 96496336 |
| a0001c0003t0003 | 0/0 | 2651 | 11 | 11 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | AGGGC others(2646): Show |
chr9 | 96445169 | 96496336 |
| a0001c0005t0002 | 0/0 | 2651 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | AGGGC others(2646): Show |
chr9 | 96445169 | 96496336 |
| a0001c0006t0002 | 0/0 | 2651 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | AGGGC others(2646): Show |
chr9 | 96445169 | 96496336 |
| a0001c0007t0001 | 0/0 | 2651 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | AGGGC others(2646): Show |
chr9 | 96445169 | 96496336 |
| a0002c0004t0001 | 0/0 | 2651 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | AGGGC others(2646): Show |
chr9 | 96445169 | 96496336 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 2 | 2 | 2 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0012 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0004g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0007g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0009g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0010g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0011g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0012g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0001t0013g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0003 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0002t0008g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0003t0003g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0003t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0003t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0003t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0003t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0003t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0003t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0003t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0003t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0003t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0005t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0006t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0001c0007t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| a0002c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0004 | EUR | GBR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0262 | EUR | GBR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0261 | EUR | FIN | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0002 | EUR | FIN | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00323 | hp1 | a0001 | c0001 | t0007 | g0100 | EUR | FIN | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | FIN | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | CHS | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0113 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0034 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0054 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0027 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0025 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0066 | AMR | PUR | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01257 | hp1 | a0001 | c0001 | t0009 | g0099 | AMR | CLM | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | CLM | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0055 | AMR | CLM | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0046 | AMR | CLM | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0039 | AMR | CLM | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0048 | AMR | CLM | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | IBS | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0041 | EUR | IBS | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | ACB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | ACB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | PEL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CDX | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CDX | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CDX | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02257 | hp2 | a0001 | c0005 | t0002 | g0082 | AFR | ACB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | ACB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02280 | hp1 | a0001 | c0002 | t0005 | g0037 | AFR | ACB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02280 | hp2 | a0001 | c0006 | t0002 | g0223 | AFR | ACB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02451 | hp1 | a0001 | c0003 | t0003 | g0042 | AFR | ACB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0022 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02717 | hp2 | a0001 | c0003 | t0003 | g0044 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0029 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02723 | hp2 | a0001 | c0002 | t0005 | g0040 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0064 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02886 | hp1 | a0001 | c0001 | t0013 | g0216 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0028 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02895 | hp2 | a0001 | c0003 | t0003 | g0051 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02897 | hp2 | a0001 | c0003 | t0003 | g0069 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | ESN | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ESN | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03017 | hp1 | a0001 | c0001 | t0010 | g0131 | SAS | PJL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03041 | hp2 | a0001 | c0002 | t0003 | g0068 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03098 | hp2 | a0001 | c0003 | t0003 | g0062 | AFR | MSL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03139 | hp1 | a0001 | c0003 | t0003 | g0043 | AFR | ESN | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03195 | hp1 | a0001 | c0007 | t0001 | g0127 | AFR | ESN | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03195 | hp2 | a0001 | c0002 | t0005 | g0036 | AFR | ESN | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0035 | AFR | MSL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0065 | AFR | MSL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0073 | AFR | MSL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03490 | hp2 | a0001 | c0001 | t0011 | g0148 | SAS | PJL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0031 | AFR | ESN | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0030 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | MSL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0059 | AFR | MSL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0052 | SAS | BEB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0032 | SAS | BEB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | STU | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | STU | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | STU | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG04204 | hp2 | a0002 | c0004 | t0001 | g0152 | SAS | STU | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0053 | SAS | STU | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | STU | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | YRI | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18985 | hp1 | a0001 | c0002 | t0008 | g0061 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19030 | hp1 | a0001 | c0002 | t0006 | g0081 | AFR | LWK | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0023 | AFR | LWK | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19078 | hp2 | a0001 | c0001 | t0012 | g0104 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0063 | AFR | YRI | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA19240 | hp2 | a0001 | c0003 | t0003 | g0011 | AFR | YRI | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0033 | AFR | ASW | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | ASW | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | TSI | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | GIH | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | GIH | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | ACB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02486 | hp1 | a0001 | c0003 | t0003 | g0011 | AFR | ACB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0021 | AFR | ACB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03471 | hp1 | a0001 | c0003 | t0003 | g0049 | AFR | MSL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG06807 | hp1 | a0001 | c0002 | t0006 | g0083 | AFR | USA | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| HG06807 | hp2 | a0001 | c0003 | t0003 | g0084 | AFR | USA | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA20300 | hp1 | a0001 | c0003 | t0003 | g0050 | AFR | USA | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | USA | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0058 | AFR | LWK | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | LWK | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0103 | REF | REF | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0012 | REF | REF | HABP4_chr9_96445169_96496336 | HABP4 | chr9 | 96445169 | 96496336 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:96450313 | G | C | 1 | a0002 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.34G>C | p.Ala12Pro | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/8 | 145/2651 | 34/1242 | 12/413 | chr9 | 96450313 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:96450627 | G | C | 2 | a0001c0002 a0001c0005 |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
splice_region_variant&synonymous_variant | LOW | c.348G>C | p.Pro116Pro | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/8 | 459/2651 | 348/1242 | 116/413 | chr9 | 96450627 | |||
| chr9:96465367 | G | A | 1 | a0001c0003 | 11 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
synonymous_variant | LOW | c.543G>A | p.Pro181Pro | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 3/8 | 654/2651 | 543/1242 | 181/413 | chr9 | 96465367 | |||
| chr9:96488112 | C | T | 1 | a0001c0007 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.1023C>T | p.Asp341Asp | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 7/8 | 1134/2651 | 1023/1242 | 341/413 | chr9 | 96488112 | |||
| chr9:96488181 | C | T | 2 | a0001c0002 a0001c0006 |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
synonymous_variant | LOW | c.1092C>T | p.Leu364Leu | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 7/8 | 1203/2651 | 1092/1242 | 364/413 | chr9 | 96488181 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:96450204 | A | G | 1 | a0001c0001t0013 | 1 | HG02886.hp1 | 5_prime_UTR_variant | MODIFIER | c.-76A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/8 | 76 | chr9 | 96450204 | ||||||
| chr9:96450234 | G | C | 2 | a0001c0001t0004 a0001c0001t0007 |
5 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-46G>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/8 | 46 | chr9 | 96450234 | ||||||
| chr9:96450242 | G | T | 1 | a0001c0002t0006 | 2 | HG06807.hp1 NA19030.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-38G>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/8 | chr9 | 96450242 | |||||||
| chr9:96450267 | T | G | 1 | a0001c0002t0008 | 1 | NA18985.hp1 | 5_prime_UTR_variant | MODIFIER | c.-13T>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/8 | 13 | chr9 | 96450267 | ||||||
| chr9:96490060 | C | T | 1 | a0001c0002t0005 | 3 | HG02280.hp1 HG02723.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*22C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 8/8 | 22 | chr9 | 96490060 | ||||||
| chr9:96490182 | A | G | 9 | a0001c0001t0003 a0001c0002t0002 a0001c0002t0003 others(6): Show |
74 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*144A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 8/8 | 144 | chr9 | 96490182 | ||||||
| chr9:96490324 | C | T | 1 | a0001c0001t0012 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*286C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 8/8 | 286 | chr9 | 96490324 | ||||||
| chr9:96490455 | G | C | 1 | a0001c0001t0007 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*417G>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 8/8 | 417 | chr9 | 96490455 | ||||||
| chr9:96490800 | C | T | 6 | a0001c0002t0002 a0001c0002t0005 a0001c0002t0006 others(3): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*762C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 8/8 | 762 | chr9 | 96490800 | ||||||
| chr9:96490801 | G | A | 1 | a0001c0001t0009 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*763G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 8/8 | 763 | chr9 | 96490801 | ||||||
| chr9:96491139 | A | G | 1 | a0001c0001t0011 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1101A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 8/8 | 1101 | chr9 | 96491139 | ||||||
| chr9:96491160 | C | T | 1 | a0001c0001t0010 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1122C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 8/8 | 1122 | chr9 | 96491160 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:96450648 | T | G | 71 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(68): Show |
78 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(75): Show |
intron_variant | MODIFIER | c.349+20T>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96450648 | |||||||
| chr9:96450666 | G | T | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 |
3 | HG00741.hp1 HG01106.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.349+38G>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96450666 | |||||||
| chr9:96450709 | G | A | 13 | a0001c0002t0002g0008 a0001c0002t0002g0020 a0001c0002t0002g0021 others(10): Show |
14 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.349+81G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96450709 | |||||||
| chr9:96450767 | G | T | 1 | a0001c0001t0001g0267 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.349+139G>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96450767 | |||||||
| chr9:96450820 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.349+192G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96450820 | |||||||
| chr9:96451088 | G | A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.349+460G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96451088 | |||||||
| chr9:96451381 | G | T | 1 | a0001c0001t0003g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.349+753G>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96451381 | |||||||
| chr9:96451404 | C | G | 2 | a0001c0003t0003g0011 a0001c0003t0003g0084 |
3 | HG02486.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.349+776C>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96451404 | |||||||
| chr9:96451429 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.349+801G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96451429 | |||||||
| chr9:96451617 | C | T | 3 | a0001c0002t0006g0081 a0001c0002t0006g0083 a0001c0005t0002g0082 |
3 | HG02257.hp2 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.349+989C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96451617 | |||||||
| chr9:96451635 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.349+1007G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96451635 | |||||||
| chr9:96451744 | A | T | 1 | a0001c0001t0001g0266 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.349+1116A>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96451744 | |||||||
| chr9:96452134 | G | C | 4 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
4 | HG02451.hp2 HG02572.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+1506G>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96452134 | |||||||
| chr9:96452182 | G | C | 1 | a0001c0002t0002g0032 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.349+1554G>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96452182 | |||||||
| chr9:96452226 | C | CA | 11 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0002t0002g0033 others(8): Show |
11 | HG01069.hp1 HG01109.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.349+1617dupA | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96452226 | ||||||
| chr9:96452226 | CA | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(175): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.349+1617delA | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96452226 | ||||||
| chr9:96452514 | G | A | 74 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(71): Show |
81 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.349+1886G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96452514 | |||||||
| chr9:96452706 | T | C | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | NA18988.hp1 NA18994.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.349+2078T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96452706 | |||||||
| chr9:96452729 | C | G | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | NA18963.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.349+2101C>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96452729 | |||||||
| chr9:96452755 | G | A | 1 | a0001c0002t0002g0041 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.349+2127G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96452755 | |||||||
| chr9:96452770 | T | C | 1 | a0001c0001t0010g0131 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.349+2142T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96452770 | |||||||
| chr9:96452822 | T | C | 59 | a0001c0001t0003g0060 a0001c0001t0003g0085 a0001c0002t0002g0003 others(56): Show |
66 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(63): Show |
intron_variant | MODIFIER | c.349+2194T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96452822 | |||||||
| chr9:96452869 | C | G | 5 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG01106.hp1 HG03704.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+2241C>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96452869 | |||||||
| chr9:96452911 | G | GT | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(112): Show |
132 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.349+2310dupT | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96452911 | ||||||
| chr9:96452911 | G | GTT | 32 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0120 others(29): Show |
32 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.349+2309_349+2310d others(4): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96452911 | ||||||
| chr9:96452911 | GT | G | 36 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0126 others(33): Show |
37 | HG00597.hp1 HG00609.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.349+2310delT | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96452911 | ||||||
| chr9:96452911 | GTT | G | 26 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0125 others(23): Show |
31 | HG01069.hp1 HG01081.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.349+2309_349+2310d others(4): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96452911 | ||||||
| chr9:96452911 | GTTTTTTT others(7): Show |
G | 1 | a0001c0005t0002g0082 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.349+2297_349+2310d others(16): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96452911 | ||||||
| chr9:96453037 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.349+2409C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96453037 | |||||||
| chr9:96453039 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.349+2411G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96453039 | |||||||
| chr9:96453087 | A | AT | 63 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0067 others(60): Show |
75 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.349+2481dupT | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96453087 | ||||||
| chr9:96453087 | A | ATT | 6 | a0001c0001t0001g0119 a0001c0001t0001g0263 a0001c0001t0012g0104 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+2480_349+2481d others(4): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96453087 | ||||||
| chr9:96453127 | C | T | 2 | a0001c0002t0002g0064 a0001c0002t0002g0066 |
2 | HG01243.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.349+2499C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96453127 | |||||||
| chr9:96453143 | T | G | 1 | a0001c0001t0001g0172 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.349+2515T>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96453143 | |||||||
| chr9:96453220 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.349+2592C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96453220 | |||||||
| chr9:96453270 | A | G | 1 | a0001c0001t0001g0258 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.349+2642A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96453270 | |||||||
| chr9:96453326 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0173 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.349+2698G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96453326 | |||||||
| chr9:96453438 | T | TGACCTCA others(18): Show |
1 | a0001c0001t0001g0233 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.349+2812_349+2836d others(27): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96453438 | ||||||
| chr9:96453595 | C | A | 2 | a0001c0002t0002g0063 a0001c0002t0002g0065 |
2 | HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.349+2967C>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96453595 | |||||||
| chr9:96453841 | C | T | 5 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0229 others(2): Show |
5 | HG01928.hp2 HG01978.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.349+3213C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96453841 | |||||||
| chr9:96454417 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.349+3789A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96454417 | |||||||
| chr9:96454448 | C | CT | 14 | a0001c0001t0001g0092 a0001c0001t0001g0096 a0001c0001t0001g0130 others(11): Show |
14 | HG00597.hp1 HG01109.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.349+3840dupT | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96454448 | ||||||
| chr9:96454448 | CT | C | 6 | a0001c0001t0001g0093 a0001c0001t0001g0133 a0001c0001t0001g0134 others(3): Show |
6 | HG01517.hp1 HG02630.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+3840delT | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96454448 | ||||||
| chr9:96454486 | T | C | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0091 others(32): Show |
37 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.349+3858T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96454486 | |||||||
| chr9:96454746 | C | G | 7 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0003g0072 others(4): Show |
7 | HG01081.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.350-3633C>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96454746 | |||||||
| chr9:96454941 | T | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | NA18957.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.350-3438T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96454941 | |||||||
| chr9:96454959 | T | A | 3 | a0001c0002t0006g0081 a0001c0002t0006g0083 a0001c0005t0002g0082 |
3 | HG02257.hp2 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.350-3420T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96454959 | |||||||
| chr9:96455178 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.350-3201C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96455178 | |||||||
| chr9:96455183 | G | T | 1 | a0001c0001t0001g0253 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.350-3196G>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96455183 | |||||||
| chr9:96455216 | C | T | 1 | a0001c0002t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.350-3163C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96455216 | |||||||
| chr9:96455263 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.350-3116C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96455263 | |||||||
| chr9:96455457 | C | CA | 83 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0096 others(80): Show |
89 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.350-2900dupA | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96455457 | ||||||
| chr9:96455457 | C | CAA | 12 | a0001c0001t0001g0077 a0001c0001t0001g0117 a0001c0001t0001g0128 others(9): Show |
12 | HG01261.hp1 HG02109.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.350-2901_350-2900d others(4): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96455457 | ||||||
| chr9:96455457 | CA | C | 20 | a0001c0001t0001g0170 a0001c0001t0003g0071 a0001c0001t0003g0072 others(17): Show |
21 | HG01081.hp1 HG01884.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.350-2900delA | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96455457 | ||||||
| chr9:96455472 | A | G | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0007t0001g0127 |
3 | HG02976.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.350-2907A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96455472 | |||||||
| chr9:96455473 | A | G | 10 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(7): Show |
11 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-2906A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96455473 | |||||||
| chr9:96455506 | G | C | 2 | a0001c0001t0003g0060 a0001c0001t0003g0085 |
2 | HG01952.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.350-2873G>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96455506 | |||||||
| chr9:96455600 | T | C | 71 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(68): Show |
78 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(75): Show |
intron_variant | MODIFIER | c.350-2779T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96455600 | |||||||
| chr9:96455609 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.350-2770C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96455609 | |||||||
| chr9:96455706 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.350-2673C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96455706 | |||||||
| chr9:96455916 | A | ATGG | 14 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0102 others(11): Show |
14 | HG00741.hp1 HG01106.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.350-2459_350-2457d others(5): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96455916 | ||||||
| chr9:96456087 | T | A | 1 | a0001c0002t0003g0068 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.350-2292T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456087 | |||||||
| chr9:96456309 | C | A | 2 | a0001c0001t0003g0060 a0001c0001t0003g0085 |
2 | HG01952.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.350-2070C>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456309 | |||||||
| chr9:96456569 | G | A | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.350-1810G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456569 | |||||||
| chr9:96456623 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.350-1756G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456623 | |||||||
| chr9:96456628 | C | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0266 |
2 | HG02132.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.350-1751C>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456628 | |||||||
| chr9:96456681 | A | G | 1 | a0001c0002t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.350-1698A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456681 | |||||||
| chr9:96456709 | G | A | 5 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG01106.hp1 HG03704.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.350-1670G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456709 | |||||||
| chr9:96456759 | C | CAA | 6 | a0001c0001t0001g0111 a0001c0001t0001g0123 a0001c0001t0001g0146 others(3): Show |
6 | HG03453.hp1 HG03927.hp2 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-1599_350-1598d others(4): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456759 | ||||||
| chr9:96456759 | CAA | C | 13 | a0001c0001t0001g0091 a0001c0001t0001g0164 a0001c0001t0001g0165 others(10): Show |
13 | HG00280.hp1 HG00597.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.350-1599_350-1598d others(4): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456759 | ||||||
| chr9:96456770 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.350-1607_350-1596d others(14): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456770 | ||||||
| chr9:96456770 | AAAAAAAA others(21): Show |
A | 1 | a0001c0001t0001g0126 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.350-1607_350-1580d others(30): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456770 | ||||||
| chr9:96456771 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0014 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.350-1606_350-1596d others(13): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456771 | ||||||
| chr9:96456771 | AAAAAAAA others(6): Show |
A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0247 |
2 | HG01169.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.350-1606_350-1594d others(15): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456771 | ||||||
| chr9:96456772 | A | T | 1 | a0001c0001t0001g0181 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.350-1607A>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456772 | |||||||
| chr9:96456772 | AAAAAAAA others(15): Show |
A | 1 | a0001c0001t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.350-1605_350-1584d others(24): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456772 | ||||||
| chr9:96456773 | AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0001g0248 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.350-1604_350-1592d others(15): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456773 | ||||||
| chr9:96456774 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0168 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.350-1604_350-1603i others(12): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456774 | ||||||
| chr9:96456774 | A | T | 5 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0162 others(2): Show |
5 | HG02572.hp1 HG03225.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-1605A>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456774 | |||||||
| chr9:96456774 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0147 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.350-1603_350-1594d others(12): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456774 | ||||||
| chr9:96456774 | AAAAAAAA others(21): Show |
A | 1 | a0001c0001t0010g0131 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.350-1603_350-1576d others(30): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456774 | ||||||
| chr9:96456776 | A | AAT | 6 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0161 others(3): Show |
6 | HG02109.hp1 HG03239.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-1602_350-1601i others(4): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456776 | ||||||
| chr9:96456776 | A | AATATATA others(3): Show |
2 | a0001c0001t0001g0159 a0001c0001t0001g0260 |
2 | HG02074.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.350-1602_350-1601i others(12): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456776 | ||||||
| chr9:96456776 | A | T | 19 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0091 others(16): Show |
19 | HG01192.hp1 HG01192.hp2 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.350-1603A>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456776 | |||||||
| chr9:96456776 | AAAAAATA others(3): Show |
A | 5 | a0001c0001t0001g0256 a0001c0002t0002g0003 a0001c0002t0002g0033 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-1601_350-1592d others(12): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456776 | ||||||
| chr9:96456776 | AAAAAATA others(5): Show |
A | 1 | a0001c0001t0001g0016 | 2 | HG01358.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.350-1601_350-1590d others(14): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456776 | ||||||
| chr9:96456776 | AAAAAATA others(13): Show |
A | 1 | a0001c0001t0001g0174 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.350-1601_350-1582d others(22): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456776 | ||||||
| chr9:96456777 | AAAAATAT others(12): Show |
A | 4 | a0001c0001t0001g0120 a0001c0001t0001g0178 a0001c0001t0001g0251 others(1): Show |
4 | HG00140.hp2 HG00609.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-1600_350-1582d others(21): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456777 | ||||||
| chr9:96456778 | A | T | 48 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0091 others(45): Show |
49 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.350-1601A>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456778 | |||||||
| chr9:96456778 | AAAATATA others(5): Show |
A | 1 | a0001c0001t0004g0004 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.350-1599_350-1588d others(14): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456778 | ||||||
| chr9:96456779 | AAATATAT others(4): Show |
A | 1 | a0001c0002t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.350-1598_350-1588d others(13): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456779 | ||||||
| chr9:96456779 | AAATATAT others(8): Show |
A | 2 | a0001c0001t0001g0001 a0001c0001t0003g0073 |
2 | HG03453.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.350-1598_350-1584d others(17): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456779 | ||||||
| chr9:96456780 | A | AAAATATA others(3): Show |
1 | a0001c0001t0001g0205 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.350-1598_350-1597i others(12): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456780 | ||||||
| chr9:96456780 | A | AAT | 6 | a0001c0001t0001g0167 a0001c0001t0001g0188 a0001c0001t0001g0217 others(3): Show |
6 | HG00280.hp2 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-1558_350-1557d others(4): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456780 | ||||||
| chr9:96456780 | A | ATAT | 4 | a0001c0001t0001g0135 a0001c0001t0001g0163 a0001c0001t0001g0237 others(1): Show |
4 | HG01074.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-1599_350-1598i others(5): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456780 | |||||||
| chr9:96456780 | A | T | 70 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0015 others(67): Show |
71 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.350-1599A>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456780 | |||||||
| chr9:96456780 | AAT | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0095 a0001c0001t0001g0116 others(5): Show |
8 | HG01258.hp2 HG01981.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.350-1558_350-1557d others(4): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456780 | ||||||
| chr9:96456780 | AATATATA others(1): Show |
A | 6 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0032 others(3): Show |
7 | HG01261.hp1 HG03834.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-1564_350-1557d others(10): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456780 | ||||||
| chr9:96456780 | AATATATA others(3): Show |
A | 9 | a0001c0001t0001g0077 a0001c0002t0002g0008 a0001c0002t0002g0022 others(6): Show |
10 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.350-1566_350-1557d others(12): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456780 | ||||||
| chr9:96456780 | AATATATA others(5): Show |
A | 6 | a0001c0001t0001g0108 a0001c0001t0001g0117 a0001c0001t0001g0227 others(3): Show |
6 | HG02559.hp1 HG02738.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-1568_350-1557d others(14): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456780 | ||||||
| chr9:96456780 | AATATATA others(7): Show |
A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(32): Show |
44 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.350-1570_350-1557d others(16): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456780 | ||||||
| chr9:96456780 | AATATATA others(9): Show |
A | 2 | a0001c0001t0001g0207 a0001c0003t0003g0042 |
2 | HG02451.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.350-1572_350-1557d others(18): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456780 | ||||||
| chr9:96456780 | AATATATA others(13): Show |
A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0109 |
2 | HG02486.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.350-1576_350-1557d others(22): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456780 | ||||||
| chr9:96456780 | AATATATA others(17): Show |
A | 1 | a0001c0001t0004g0113 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.350-1580_350-1557d others(26): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456780 | ||||||
| chr9:96456781 | AT | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0019 others(3): Show |
6 | HG01515.hp1 HG01515.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-1597delT | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456781 | |||||||
| chr9:96456781 | ATAT | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0134 a0001c0001t0001g0166 others(5): Show |
9 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.350-1597_350-1595d others(5): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456781 | |||||||
| chr9:96456781 | ATATATAT others(2): Show |
A | 6 | a0001c0001t0001g0067 a0001c0001t0001g0078 a0001c0001t0001g0079 others(3): Show |
6 | HG01106.hp1 HG03195.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-1597_350-1589d others(11): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456781 | |||||||
| chr9:96456781 | ATATATAT others(4): Show |
A | 2 | a0001c0002t0002g0059 a0001c0002t0002g0063 |
2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.350-1597_350-1587d others(13): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456781 | |||||||
| chr9:96456781 | ATATATAT others(6): Show |
A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0199 others(2): Show |
5 | HG02132.hp1 HG03098.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-1597_350-1585d others(15): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456781 | |||||||
| chr9:96456781 | ATATATAT others(8): Show |
A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0139 others(7): Show |
12 | HG00140.hp1 HG00642.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.350-1597_350-1583d others(17): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456781 | |||||||
| chr9:96456781 | ATATATAT others(24): Show |
A | 1 | a0001c0001t0001g0096 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.350-1597_350-1567d others(33): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456781 | |||||||
| chr9:96456782 | T | A | 12 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0001g0130 others(9): Show |
12 | HG01071.hp1 HG01928.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.350-1597T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456782 | |||||||
| chr9:96456782 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.350-1597T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456782 | |||||||
| chr9:96456784 | T | A | 15 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0115 others(12): Show |
15 | HG01071.hp1 HG01258.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.350-1595T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456784 | |||||||
| chr9:96456786 | T | A | 14 | a0001c0001t0001g0012 a0001c0001t0001g0116 a0001c0001t0001g0119 others(11): Show |
14 | HG00738.hp2 HG01258.hp2 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.350-1593T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456786 | |||||||
| chr9:96456788 | T | A | 7 | a0001c0001t0001g0134 a0001c0001t0001g0145 a0001c0001t0001g0149 others(4): Show |
7 | HG00323.hp2 HG00738.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.350-1591T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456788 | |||||||
| chr9:96456790 | T | A | 6 | a0001c0001t0001g0145 a0001c0001t0001g0149 a0001c0002t0002g0009 others(3): Show |
7 | HG00323.hp2 HG02129.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-1589T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456790 | |||||||
| chr9:96456792 | T | A | 11 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(8): Show |
11 | HG01106.hp1 HG01243.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.350-1587T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456792 | |||||||
| chr9:96456794 | T | A | 14 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(11): Show |
14 | HG01106.hp1 HG01243.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.350-1585T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456794 | |||||||
| chr9:96456796 | T | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(36): Show |
49 | HG00099.hp2 HG00544.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.350-1583T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456796 | |||||||
| chr9:96456798 | T | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0112 others(17): Show |
22 | HG00642.hp1 HG01169.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.350-1581T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456798 | |||||||
| chr9:96456800 | T | A | 1 | a0001c0001t0003g0060 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.350-1579T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456800 | |||||||
| chr9:96456805 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0012g0104 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.350-1573_350-1563d others(13): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456805 | |||||||
| chr9:96456814 | T | A | 5 | a0001c0002t0002g0029 a0001c0002t0002g0035 a0001c0002t0005g0036 others(2): Show |
5 | HG02280.hp1 HG02723.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-1565T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456814 | |||||||
| chr9:96456819 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0193 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.350-1557_350-1556i others(12): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 96456819 | ||||||
| chr9:96456819 | A | C | 3 | a0001c0001t0001g0143 a0001c0001t0001g0165 a0001c0001t0001g0176 |
3 | HG02155.hp1 HG02155.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.350-1560A>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96456819 | |||||||
| chr9:96457056 | A | T | 1 | a0001c0001t0001g0219 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.350-1323A>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96457056 | |||||||
| chr9:96457114 | G | A | 5 | a0001c0002t0002g0003 a0001c0002t0002g0033 a0001c0002t0002g0034 others(2): Show |
8 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.350-1265G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96457114 | |||||||
| chr9:96457133 | C | T | 2 | a0001c0002t0002g0064 a0001c0002t0002g0066 |
2 | HG01243.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.350-1246C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96457133 | |||||||
| chr9:96457192 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.350-1187C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96457192 | |||||||
| chr9:96457497 | C | T | 71 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(68): Show |
78 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(75): Show |
intron_variant | MODIFIER | c.350-882C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96457497 | |||||||
| chr9:96457571 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.350-808A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96457571 | |||||||
| chr9:96457574 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.350-805A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96457574 | |||||||
| chr9:96457665 | C | T | 1 | a0001c0002t0002g0030 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.350-714C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96457665 | |||||||
| chr9:96457858 | C | T | 8 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(5): Show |
9 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.350-521C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96457858 | |||||||
| chr9:96457891 | A | G | 3 | a0001c0001t0001g0163 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG02630.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.350-488A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96457891 | |||||||
| chr9:96458113 | A | G | 66 | a0001c0001t0003g0060 a0001c0001t0003g0070 a0001c0001t0003g0071 others(63): Show |
73 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(70): Show |
intron_variant | MODIFIER | c.350-266A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 1/7 | chr9 | 96458113 | |||||||
| chr9:96458626 | CT | C | 11 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0147 others(8): Show |
11 | HG01099.hp1 HG01884.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.512+101delT | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 96458626 | ||||||
| chr9:96458838 | T | A | 1 | a0001c0001t0001g0194 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.512+297T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96458838 | |||||||
| chr9:96459056 | G | A | 5 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0229 others(2): Show |
5 | HG01928.hp2 HG01978.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.512+515G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96459056 | |||||||
| chr9:96459110 | G | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0007t0001g0127 |
3 | HG02976.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.512+569G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96459110 | |||||||
| chr9:96459484 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(245): Show |
276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.512+943T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96459484 | |||||||
| chr9:96459503 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.512+962A>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96459503 | |||||||
| chr9:96459565 | A | G | 1 | a0001c0001t0013g0216 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.512+1024A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96459565 | |||||||
| chr9:96459938 | C | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0266 |
2 | HG02132.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.512+1397C>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96459938 | |||||||
| chr9:96460042 | A | T | 7 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0003g0072 others(4): Show |
7 | HG01081.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.512+1501A>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96460042 | |||||||
| chr9:96460091 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.512+1550C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96460091 | |||||||
| chr9:96460260 | A | G | 7 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0003g0072 others(4): Show |
7 | HG01081.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.512+1719A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96460260 | |||||||
| chr9:96460289 | C | G | 7 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0003g0072 others(4): Show |
7 | HG01081.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.512+1748C>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96460289 | |||||||
| chr9:96460378 | G | C | 1 | a0001c0001t0004g0113 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.512+1837G>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96460378 | |||||||
| chr9:96460539 | A | G | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0003g0070 others(6): Show |
9 | HG01081.hp1 HG01884.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.512+1998A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96460539 | |||||||
| chr9:96460816 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.512+2275G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96460816 | |||||||
| chr9:96461222 | T | G | 2 | a0001c0002t0006g0081 a0001c0002t0006g0083 |
2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.512+2681T>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96461222 | |||||||
| chr9:96461307 | G | A | 2 | a0001c0001t0003g0060 a0001c0001t0003g0085 |
2 | HG01952.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.512+2766G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96461307 | |||||||
| chr9:96461476 | C | G | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0007t0001g0127 |
3 | HG02976.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.512+2935C>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96461476 | |||||||
| chr9:96461572 | G | A | 1 | a0001c0001t0011g0148 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.512+3031G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96461572 | |||||||
| chr9:96461633 | G | A | 5 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG01106.hp1 HG03704.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.512+3092G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96461633 | |||||||
| chr9:96461745 | T | A | 5 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG01106.hp1 HG03704.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.512+3204T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96461745 | |||||||
| chr9:96461793 | G | A | 2 | a0001c0001t0003g0060 a0001c0001t0003g0085 |
2 | HG01952.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.512+3252G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96461793 | |||||||
| chr9:96461797 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.512+3256C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96461797 | |||||||
| chr9:96461878 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.512+3337C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96461878 | |||||||
| chr9:96461898 | G | A | 1 | a0001c0001t0001g0016 | 2 | HG01358.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.512+3357G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96461898 | |||||||
| chr9:96461986 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.513-3351G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96461986 | |||||||
| chr9:96462157 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.513-3180A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96462157 | |||||||
| chr9:96462464 | A | T | 71 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(68): Show |
78 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(75): Show |
intron_variant | MODIFIER | c.513-2873A>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96462464 | |||||||
| chr9:96462465 | T | C | 1 | a0001c0001t0003g0070 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.513-2872T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96462465 | |||||||
| chr9:96462495 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.513-2842C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96462495 | |||||||
| chr9:96462611 | CA | C | 46 | a0001c0001t0001g0264 a0001c0001t0009g0099 a0001c0002t0002g0003 others(43): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.513-2712delA | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 96462611 | ||||||
| chr9:96462665 | C | A | 1 | a0001c0001t0001g0114 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.513-2672C>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96462665 | |||||||
| chr9:96462680 | C | G | 5 | a0001c0002t0002g0039 a0001c0002t0002g0046 a0001c0002t0002g0048 others(2): Show |
5 | HG01261.hp1 HG01361.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-2657C>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96462680 | |||||||
| chr9:96462724 | G | C | 1 | a0001c0001t0001g0215 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.513-2613G>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96462724 | |||||||
| chr9:96462816 | G | A | 10 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(7): Show |
11 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.513-2521G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96462816 | |||||||
| chr9:96462906 | A | G | 1 | a0001c0001t0001g0257 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.513-2431A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96462906 | |||||||
| chr9:96463415 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.513-1922C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96463415 | |||||||
| chr9:96463455 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.513-1882A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96463455 | |||||||
| chr9:96463584 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.513-1753C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96463584 | |||||||
| chr9:96463688 | TATAAG | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0220 a0001c0001t0001g0267 |
3 | HG04115.hp1 HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.513-1647_513-1643d others(7): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 96463688 | ||||||
| chr9:96463702 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.513-1635A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96463702 | |||||||
| chr9:96463985 | T | G | 7 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0003g0072 others(4): Show |
7 | HG01081.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.513-1352T>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96463985 | |||||||
| chr9:96464171 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.513-1166G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96464171 | |||||||
| chr9:96464326 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.513-1011G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96464326 | |||||||
| chr9:96464399 | G | A | 32 | a0001c0001t0001g0013 a0001c0001t0001g0086 a0001c0001t0001g0087 others(29): Show |
33 | HG00323.hp2 HG00741.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.513-938G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96464399 | |||||||
| chr9:96464491 | C | T | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0213 |
3 | NA18955.hp1 NA18955.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.513-846C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96464491 | |||||||
| chr9:96464655 | A | C | 5 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG01106.hp1 HG03704.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.513-682A>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96464655 | |||||||
| chr9:96464657 | G | A | 12 | a0001c0001t0003g0060 a0001c0001t0003g0085 a0001c0003t0003g0011 others(9): Show |
13 | HG01952.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.513-680G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96464657 | |||||||
| chr9:96464756 | T | G | 1 | a0001c0001t0001g0197 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.513-581T>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96464756 | |||||||
| chr9:96464932 | C | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0241 |
2 | HG00544.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.513-405C>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96464932 | |||||||
| chr9:96465176 | A | G | 1 | a0001c0002t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.513-161A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96465176 | |||||||
| chr9:96465318 | T | C | 7 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0003g0072 others(4): Show |
7 | HG01081.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.513-19T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 2/7 | chr9 | 96465318 | |||||||
| chr9:96465554 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.674+56G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 3/7 | chr9 | 96465554 | |||||||
| chr9:96465688 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.675-22G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 3/7 | chr9 | 96465688 | |||||||
| chr9:96466063 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.743+285G>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96466063 | |||||||
| chr9:96466108 | C | G | 4 | a0001c0001t0001g0120 a0001c0001t0001g0174 a0001c0001t0001g0178 others(1): Show |
4 | HG00609.hp1 NA18941.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+330C>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96466108 | |||||||
| chr9:96466322 | ATG | A | 7 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0003g0072 others(4): Show |
7 | HG01081.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.743+545_743+546del others(2): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96466322 | |||||||
| chr9:96466448 | C | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | NA18953.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.743+670C>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96466448 | |||||||
| chr9:96466626 | A | G | 1 | a0001c0002t0002g0029 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.743+848A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96466626 | |||||||
| chr9:96466716 | T | G | 10 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(7): Show |
11 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.743+938T>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96466716 | |||||||
| chr9:96466750 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0246 |
2 | HG00597.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.743+972C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96466750 | |||||||
| chr9:96466922 | C | CT | 14 | a0001c0001t0001g0095 a0001c0001t0001g0191 a0001c0001t0003g0060 others(11): Show |
15 | HG01952.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.743+1162dupT | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 96466922 | ||||||
| chr9:96467023 | AGTGATTC others(5): Show |
A | 1 | a0001c0001t0001g0179 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.743+1246_743+1257d others(14): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96467023 | |||||||
| chr9:96467321 | AC | A | 10 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(7): Show |
11 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.743+1545delC | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 96467321 | ||||||
| chr9:96467454 | G | A | 1 | a0001c0001t0003g0060 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.743+1676G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96467454 | |||||||
| chr9:96467527 | C | CT | 26 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0160 others(23): Show |
27 | HG01081.hp1 HG01884.hp1 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.743+1765dupT | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 96467527 | ||||||
| chr9:96467549 | G | A | 10 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(7): Show |
11 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.743+1771G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96467549 | |||||||
| chr9:96467671 | G | T | 1 | a0001c0001t0001g0212 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.743+1893G>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96467671 | |||||||
| chr9:96467795 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.743+2017G>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96467795 | |||||||
| chr9:96467949 | C | G | 1 | a0001c0002t0003g0068 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+2171C>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96467949 | |||||||
| chr9:96468062 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.743+2284T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96468062 | |||||||
| chr9:96468084 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0180 |
3 | HG01169.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.743+2306T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96468084 | |||||||
| chr9:96468085 | T | C | 2 | a0001c0002t0002g0064 a0001c0002t0002g0066 |
2 | HG01243.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.743+2307T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96468085 | |||||||
| chr9:96468175 | C | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0007t0001g0127 |
3 | HG02976.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.743+2397C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96468175 | |||||||
| chr9:96468246 | T | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(263): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.743+2468T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96468246 | |||||||
| chr9:96468256 | A | AT | 12 | a0001c0001t0001g0089 a0001c0001t0001g0101 a0001c0001t0001g0107 others(9): Show |
12 | HG01081.hp1 HG01884.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.743+2495dupT | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 96468256 | ||||||
| chr9:96468299 | C | A | 2 | a0001c0001t0001g0117 a0001c0001t0009g0099 |
2 | HG01257.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.743+2521C>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96468299 | |||||||
| chr9:96468539 | G | A | 10 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(7): Show |
11 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.744-2472G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96468539 | |||||||
| chr9:96468767 | A | T | 1 | a0001c0001t0003g0074 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.744-2244A>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96468767 | |||||||
| chr9:96468814 | T | A | 71 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(68): Show |
78 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(75): Show |
intron_variant | MODIFIER | c.744-2197T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96468814 | |||||||
| chr9:96468824 | G | C | 10 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(7): Show |
11 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.744-2187G>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96468824 | |||||||
| chr9:96468850 | G | A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.744-2161G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96468850 | |||||||
| chr9:96468875 | T | G | 1 | a0001c0001t0001g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.744-2136T>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96468875 | |||||||
| chr9:96468906 | T | G | 12 | a0001c0001t0003g0060 a0001c0001t0003g0085 a0001c0003t0003g0011 others(9): Show |
13 | HG01952.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.744-2105T>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96468906 | |||||||
| chr9:96469042 | A | G | 1 | a0002c0004t0001g0152 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.744-1969A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96469042 | |||||||
| chr9:96469148 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.744-1863A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96469148 | |||||||
| chr9:96469228 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.744-1783G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96469228 | |||||||
| chr9:96469273 | C | A | 1 | a0001c0001t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.744-1738C>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96469273 | |||||||
| chr9:96469543 | T | C | 5 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG01106.hp1 HG03704.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.744-1468T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96469543 | |||||||
| chr9:96469550 | T | C | 2 | a0001c0002t0006g0081 a0001c0002t0006g0083 |
2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.744-1461T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96469550 | |||||||
| chr9:96469963 | TAGG | T | 3 | a0001c0002t0005g0036 a0001c0002t0005g0037 a0001c0002t0005g0040 |
3 | HG02280.hp1 HG02723.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.744-1043_744-1041d others(5): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 96469963 | ||||||
| chr9:96470195 | G | A | 2 | a0001c0001t0003g0060 a0001c0001t0003g0085 |
2 | HG01952.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.744-816G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96470195 | |||||||
| chr9:96470233 | C | T | 1 | a0001c0003t0003g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.744-778C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96470233 | |||||||
| chr9:96470436 | C | G | 2 | a0001c0001t0003g0060 a0001c0001t0003g0085 |
2 | HG01952.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.744-575C>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96470436 | |||||||
| chr9:96470597 | A | C | 1 | a0001c0001t0001g0196 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.744-414A>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96470597 | |||||||
| chr9:96470620 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.744-391A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96470620 | |||||||
| chr9:96470770 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0134 a0001c0001t0001g0187 |
4 | HG00738.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.744-241G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | chr9 | 96470770 | |||||||
| chr9:96470894 | C | CA | 18 | a0001c0001t0001g0018 a0001c0001t0001g0108 a0001c0001t0001g0146 others(15): Show |
19 | HG00544.hp2 HG01106.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.744-101dupA | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 96470894 | ||||||
| chr9:96470894 | CA | C | 57 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(54): Show |
64 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.744-101delA | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 96470894 | ||||||
| chr9:96471125 | TGTTG | T | 10 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(7): Show |
11 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.827+35_827+38delGG others(2): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 96471125 | ||||||
| chr9:96471149 | CT | C | 70 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(67): Show |
77 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.827+67delT | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 96471149 | ||||||
| chr9:96471217 | A | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0007t0001g0127 |
3 | HG02976.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.827+123A>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96471217 | |||||||
| chr9:96471299 | C | T | 1 | a0001c0007t0001g0127 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.827+205C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96471299 | |||||||
| chr9:96471301 | C | A | 2 | a0001c0001t0003g0060 a0001c0001t0003g0085 |
2 | HG01952.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.827+207C>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96471301 | |||||||
| chr9:96471316 | C | T | 5 | a0001c0002t0002g0008 a0001c0002t0002g0020 a0001c0002t0002g0023 others(2): Show |
6 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.827+222C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96471316 | |||||||
| chr9:96471355 | C | G | 1 | a0001c0006t0002g0223 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.827+261C>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96471355 | |||||||
| chr9:96471466 | T | A | 5 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG01106.hp1 HG03704.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.827+372T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96471466 | |||||||
| chr9:96471467 | C | A | 5 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG01106.hp1 HG03704.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.827+373C>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96471467 | |||||||
| chr9:96471475 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.827+381G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96471475 | |||||||
| chr9:96471551 | A | G | 4 | a0001c0001t0001g0111 a0001c0001t0001g0121 a0001c0001t0001g0123 others(1): Show |
4 | HG01433.hp1 HG02293.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.827+457A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96471551 | |||||||
| chr9:96471562 | C | T | 10 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(7): Show |
11 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.827+468C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96471562 | |||||||
| chr9:96471689 | T | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0134 a0001c0001t0001g0187 |
4 | HG00738.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.827+595T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96471689 | |||||||
| chr9:96471779 | C | T | 5 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG01106.hp1 HG03704.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.827+685C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96471779 | |||||||
| chr9:96472047 | C | T | 57 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0090 others(54): Show |
59 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.827+953C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96472047 | |||||||
| chr9:96472190 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.827+1096C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96472190 | |||||||
| chr9:96472275 | T | G | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.827+1181T>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96472275 | |||||||
| chr9:96472303 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.827+1209C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96472303 | |||||||
| chr9:96472401 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.827+1307G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96472401 | |||||||
| chr9:96472484 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.827+1390C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96472484 | |||||||
| chr9:96472715 | G | T | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.827+1621G>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96472715 | |||||||
| chr9:96472749 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | NA18953.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.827+1655C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96472749 | |||||||
| chr9:96472753 | C | T | 4 | a0001c0002t0002g0035 a0001c0002t0005g0036 a0001c0002t0005g0037 others(1): Show |
4 | HG02280.hp1 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.827+1659C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96472753 | |||||||
| chr9:96472891 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0255 |
2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.827+1797C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96472891 | |||||||
| chr9:96473044 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.827+1950T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96473044 | |||||||
| chr9:96473336 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.827+2242C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96473336 | |||||||
| chr9:96473372 | C | G | 5 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG01106.hp1 HG03704.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.827+2278C>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96473372 | |||||||
| chr9:96473453 | G | A | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | NA18998.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.827+2359G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96473453 | |||||||
| chr9:96473501 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.827+2407C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96473501 | |||||||
| chr9:96473544 | C | G | 2 | a0001c0001t0003g0060 a0001c0001t0003g0085 |
2 | HG01952.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.827+2450C>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96473544 | |||||||
| chr9:96473618 | C | A | 1 | a0001c0001t0001g0205 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.827+2524C>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96473618 | |||||||
| chr9:96473634 | T | C | 1 | a0001c0001t0001g0208 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.827+2540T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96473634 | |||||||
| chr9:96473810 | G | A | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.827+2716G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96473810 | |||||||
| chr9:96473927 | G | A | 2 | a0001c0001t0003g0060 a0001c0001t0003g0085 |
2 | HG01952.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.827+2833G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96473927 | |||||||
| chr9:96474044 | A | G | 35 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(32): Show |
41 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.827+2950A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96474044 | |||||||
| chr9:96474094 | A | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0134 a0001c0001t0001g0187 |
4 | HG00738.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.827+3000A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96474094 | |||||||
| chr9:96474105 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.827+3011T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96474105 | |||||||
| chr9:96474257 | T | C | 1 | a0001c0002t0002g0056 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.827+3163T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96474257 | |||||||
| chr9:96474418 | T | C | 1 | a0001c0002t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.827+3324T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96474418 | |||||||
| chr9:96474562 | C | A | 12 | a0001c0001t0003g0060 a0001c0001t0003g0085 a0001c0003t0003g0011 others(9): Show |
13 | HG01952.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.827+3468C>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96474562 | |||||||
| chr9:96474691 | C | T | 1 | a0001c0005t0002g0082 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.827+3597C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96474691 | |||||||
| chr9:96474824 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.827+3730G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96474824 | |||||||
| chr9:96474987 | C | A | 1 | a0001c0001t0001g0146 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.827+3893C>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96474987 | |||||||
| chr9:96475192 | C | T | 2 | a0001c0001t0003g0060 a0001c0001t0003g0085 |
2 | HG01952.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.827+4098C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96475192 | |||||||
| chr9:96475199 | A | G | 1 | a0001c0002t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.827+4105A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96475199 | |||||||
| chr9:96475220 | C | G | 1 | a0001c0001t0001g0210 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.827+4126C>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96475220 | |||||||
| chr9:96475269 | A | G | 4 | a0001c0002t0002g0035 a0001c0002t0005g0036 a0001c0002t0005g0037 others(1): Show |
4 | HG02280.hp1 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.827+4175A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96475269 | |||||||
| chr9:96475302 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0243 a0001c0001t0001g0253 |
4 | HG02040.hp1 HG02523.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.827+4208G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96475302 | |||||||
| chr9:96475325 | G | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG02572.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.827+4231G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96475325 | |||||||
| chr9:96475351 | G | A | 10 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(7): Show |
11 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.827+4257G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96475351 | |||||||
| chr9:96475390 | C | CAAAAAA | 37 | a0001c0001t0003g0060 a0001c0001t0003g0085 a0001c0002t0002g0003 others(34): Show |
43 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.827+4308_827+4313d others(8): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 96475390 | ||||||
| chr9:96475390 | C | CAAAAAAA | 8 | a0001c0002t0002g0021 a0001c0002t0002g0025 a0001c0002t0002g0028 others(5): Show |
8 | HG01243.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.827+4307_827+4313d others(9): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 96475390 | ||||||
| chr9:96475390 | C | CAACAAAA | 7 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0003g0072 others(4): Show |
7 | HG01081.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.827+4298_827+4299i others(9): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 96475390 | ||||||
| chr9:96475390 | C | CAACAAAA others(2): Show |
9 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(6): Show |
10 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.827+4298_827+4299i others(11): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 96475390 | ||||||
| chr9:96475390 | CA | C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0077 a0001c0001t0001g0133 others(5): Show |
9 | HG02698.hp2 HG03492.hp1 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.827+4313delA | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 96475390 | ||||||
| chr9:96475405 | A | G | 11 | a0001c0001t0011g0148 a0001c0003t0003g0011 a0001c0003t0003g0042 others(8): Show |
12 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.827+4311A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96475405 | |||||||
| chr9:96475431 | G | C | 10 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(7): Show |
11 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.827+4337G>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96475431 | |||||||
| chr9:96475574 | T | C | 1 | a0001c0002t0002g0032 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.827+4480T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96475574 | |||||||
| chr9:96475634 | G | C | 1 | a0001c0001t0001g0149 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.827+4540G>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96475634 | |||||||
| chr9:96475638 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.827+4544G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96475638 | |||||||
| chr9:96475857 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.827+4763G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96475857 | |||||||
| chr9:96476091 | G | C | 7 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0003g0072 others(4): Show |
7 | HG01081.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.827+4997G>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96476091 | |||||||
| chr9:96476166 | T | C | 2 | a0001c0001t0003g0060 a0001c0001t0003g0085 |
2 | HG01952.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.827+5072T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96476166 | |||||||
| chr9:96476891 | T | C | 74 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(71): Show |
81 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.827+5797T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96476891 | |||||||
| chr9:96477048 | C | G | 12 | a0001c0001t0001g0090 a0001c0001t0001g0147 a0001c0001t0001g0159 others(9): Show |
12 | NA18612.hp2 NA18944.hp2 NA18945.hp2 others(9): Show |
intron_variant | MODIFIER | c.827+5954C>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96477048 | |||||||
| chr9:96477081 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.827+5987G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96477081 | |||||||
| chr9:96477340 | A | G | 1 | a0001c0002t0002g0046 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.827+6246A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96477340 | |||||||
| chr9:96477463 | A | G | 6 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(3): Show |
6 | HG02257.hp1 HG02572.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.827+6369A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96477463 | |||||||
| chr9:96477553 | T | A | 1 | a0001c0001t0001g0240 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.827+6459T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96477553 | |||||||
| chr9:96477559 | A | C | 74 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(71): Show |
81 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.827+6465A>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96477559 | |||||||
| chr9:96477770 | T | C | 4 | a0001c0002t0002g0035 a0001c0002t0005g0036 a0001c0002t0005g0037 others(1): Show |
4 | HG02280.hp1 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.827+6676T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96477770 | |||||||
| chr9:96477931 | A | G | 7 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0003g0072 others(4): Show |
7 | HG01081.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.828-6531A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96477931 | |||||||
| chr9:96477939 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.828-6523A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96477939 | |||||||
| chr9:96478051 | T | C | 5 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG01106.hp1 HG03704.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.828-6411T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96478051 | |||||||
| chr9:96478210 | G | C | 10 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(7): Show |
11 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.828-6252G>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96478210 | |||||||
| chr9:96478211 | C | T | 10 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(7): Show |
11 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.828-6251C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96478211 | |||||||
| chr9:96478218 | C | T | 2 | a0001c0001t0003g0060 a0001c0001t0003g0085 |
2 | HG01952.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.828-6244C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96478218 | |||||||
| chr9:96478321 | C | T | 1 | a0001c0002t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.828-6141C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96478321 | |||||||
| chr9:96478549 | T | C | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0007t0001g0127 |
3 | HG02976.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.828-5913T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96478549 | |||||||
| chr9:96478556 | C | T | 5 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG01106.hp1 HG03704.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.828-5906C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96478556 | |||||||
| chr9:96478590 | G | A | 5 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG01106.hp1 HG03704.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.828-5872G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96478590 | |||||||
| chr9:96478656 | G | T | 2 | a0001c0002t0002g0034 a0001c0002t0002g0054 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.828-5806G>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96478656 | |||||||
| chr9:96478656 | GT | G | 10 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(7): Show |
11 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.828-5793delT | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 96478656 | ||||||
| chr9:96478666 | T | C | 1 | a0001c0001t0001g0208 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.828-5796T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96478666 | |||||||
| chr9:96479244 | C | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(38): Show |
56 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.828-5218C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96479244 | |||||||
| chr9:96479305 | T | G | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.828-5157T>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96479305 | |||||||
| chr9:96479358 | G | GT | 59 | a0001c0001t0003g0060 a0001c0001t0003g0085 a0001c0002t0002g0003 others(56): Show |
66 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(63): Show |
intron_variant | MODIFIER | c.828-5102dupT | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 96479358 | ||||||
| chr9:96479412 | AT | A | 6 | a0001c0002t0002g0035 a0001c0002t0002g0064 a0001c0002t0002g0066 others(3): Show |
6 | HG01243.hp2 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.828-5046delT | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 96479412 | ||||||
| chr9:96479511 | A | AT | 9 | a0001c0001t0001g0132 a0001c0001t0001g0140 a0001c0001t0001g0156 others(6): Show |
9 | HG00609.hp1 HG00609.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.828-4939dupT | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 96479511 | ||||||
| chr9:96479565 | A | G | 7 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0003g0072 others(4): Show |
7 | HG01081.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.828-4897A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96479565 | |||||||
| chr9:96479635 | C | T | 1 | a0001c0002t0002g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.828-4827C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96479635 | |||||||
| chr9:96480008 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.828-4454C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96480008 | |||||||
| chr9:96480137 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.828-4325C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96480137 | |||||||
| chr9:96480278 | T | C | 1 | a0001c0001t0011g0148 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.828-4184T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96480278 | |||||||
| chr9:96480306 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.828-4156A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96480306 | |||||||
| chr9:96480838 | A | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.828-3624A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96480838 | |||||||
| chr9:96480844 | C | A | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.828-3618C>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96480844 | |||||||
| chr9:96481196 | T | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.828-3266T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96481196 | |||||||
| chr9:96481238 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.828-3224C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96481238 | |||||||
| chr9:96481239 | G | A | 1 | a0001c0002t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.828-3223G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96481239 | |||||||
| chr9:96481282 | C | T | 10 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(7): Show |
11 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.828-3180C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96481282 | |||||||
| chr9:96481388 | G | A | 10 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(7): Show |
11 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.828-3074G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96481388 | |||||||
| chr9:96481472 | G | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
65 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.828-2990G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96481472 | |||||||
| chr9:96481938 | C | CT | 21 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0102 others(18): Show |
22 | HG02109.hp1 HG02145.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.828-2509dupT | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 96481938 | ||||||
| chr9:96481938 | CT | C | 49 | a0001c0001t0001g0193 a0001c0001t0001g0199 a0001c0002t0002g0003 others(46): Show |
55 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.828-2509delT | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 96481938 | ||||||
| chr9:96482012 | T | G | 1 | a0001c0001t0001g0207 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.828-2450T>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96482012 | |||||||
| chr9:96482038 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.828-2424C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96482038 | |||||||
| chr9:96482068 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.828-2394T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96482068 | |||||||
| chr9:96482299 | C | A | 35 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(32): Show |
41 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.828-2163C>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96482299 | |||||||
| chr9:96482388 | C | T | 1 | a0001c0001t0007g0100 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.828-2074C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96482388 | |||||||
| chr9:96482516 | G | A | 46 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(43): Show |
52 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.828-1946G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96482516 | |||||||
| chr9:96482783 | A | T | 10 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(7): Show |
11 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.828-1679A>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96482783 | |||||||
| chr9:96482828 | TTGTTTC | T | 10 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(7): Show |
11 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.828-1632_828-1627d others(8): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 96482828 | ||||||
| chr9:96483164 | G | A | 3 | a0001c0002t0006g0081 a0001c0002t0006g0083 a0001c0005t0002g0082 |
3 | HG02257.hp2 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.828-1298G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96483164 | |||||||
| chr9:96483207 | C | A | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.828-1255C>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96483207 | |||||||
| chr9:96483208 | TGTGG | T | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.828-1253_828-1250d others(6): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96483208 | |||||||
| chr9:96483214 | T | A | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.828-1248T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96483214 | |||||||
| chr9:96483215 | T | G | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.828-1247T>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96483215 | |||||||
| chr9:96483216 | T | A | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.828-1246T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96483216 | |||||||
| chr9:96483292 | C | T | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.828-1170C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96483292 | |||||||
| chr9:96483376 | C | CT | 22 | a0001c0001t0001g0089 a0001c0001t0003g0060 a0001c0001t0003g0070 others(19): Show |
23 | HG01081.hp1 HG01884.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.828-1072dupT | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 96483376 | ||||||
| chr9:96483376 | C | CTT | 43 | a0001c0001t0003g0085 a0001c0002t0002g0003 a0001c0002t0002g0008 others(40): Show |
49 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.828-1073_828-1072d others(4): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 96483376 | ||||||
| chr9:96483408 | T | C | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.828-1054T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96483408 | |||||||
| chr9:96483877 | C | T | 71 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(68): Show |
78 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(75): Show |
intron_variant | MODIFIER | c.828-585C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96483877 | |||||||
| chr9:96483887 | G | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(245): Show |
276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.828-575G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96483887 | |||||||
| chr9:96483935 | C | T | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.828-527C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96483935 | |||||||
| chr9:96484098 | G | C | 1 | a0001c0001t0001g0156 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.828-364G>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96484098 | |||||||
| chr9:96484223 | C | A | 2 | a0001c0001t0001g0222 a0001c0001t0001g0226 |
2 | NA18945.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.828-239C>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96484223 | |||||||
| chr9:96484345 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.828-117A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 5/7 | chr9 | 96484345 | |||||||
| chr9:96484730 | G | A | 35 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(32): Show |
41 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.999+97G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96484730 | |||||||
| chr9:96484769 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0173 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.999+136G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96484769 | |||||||
| chr9:96484821 | T | C | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.999+188T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96484821 | |||||||
| chr9:96484884 | T | G | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.999+251T>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96484884 | |||||||
| chr9:96484986 | C | G | 1 | a0001c0001t0001g0254 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.999+353C>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96484986 | |||||||
| chr9:96484992 | C | T | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.999+359C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96484992 | |||||||
| chr9:96485019 | T | A | 74 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(71): Show |
81 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.999+386T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96485019 | |||||||
| chr9:96485034 | A | T | 1 | a0001c0001t0001g0235 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.999+401A>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96485034 | |||||||
| chr9:96485212 | C | T | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.999+579C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96485212 | |||||||
| chr9:96485239 | C | T | 1 | a0001c0001t0003g0076 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.999+606C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96485239 | |||||||
| chr9:96485476 | C | T | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.999+843C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96485476 | |||||||
| chr9:96485545 | C | T | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.999+912C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96485545 | |||||||
| chr9:96485775 | T | G | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.999+1142T>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96485775 | |||||||
| chr9:96485787 | G | A | 46 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(43): Show |
52 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.999+1154G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96485787 | |||||||
| chr9:96485887 | T | C | 1 | a0001c0002t0002g0066 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.999+1254T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96485887 | |||||||
| chr9:96486127 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0228 |
2 | HG02698.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.999+1494G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96486127 | |||||||
| chr9:96486163 | G | T | 2 | a0001c0001t0001g0117 a0001c0001t0009g0099 |
2 | HG01257.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.999+1530G>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96486163 | |||||||
| chr9:96486391 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1000-1698A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96486391 | |||||||
| chr9:96486531 | ATTTGTCC others(729): Show |
A | 1 | a0001c0001t0001g0154 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1000-1556_1000-821 others(3): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 96486531 | ||||||
| chr9:96486692 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1000-1397A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96486692 | |||||||
| chr9:96486793 | C | T | 4 | a0001c0001t0001g0111 a0001c0001t0001g0121 a0001c0001t0001g0123 others(1): Show |
4 | HG01433.hp1 HG02293.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000-1296C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96486793 | |||||||
| chr9:96486903 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1000-1186C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96486903 | |||||||
| chr9:96486917 | C | T | 24 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(21): Show |
25 | HG01081.hp1 HG01106.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1000-1172C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96486917 | |||||||
| chr9:96486922 | C | T | 24 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(21): Show |
25 | HG01081.hp1 HG01106.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1000-1167C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96486922 | |||||||
| chr9:96487129 | G | A | 5 | a0001c0001t0001g0142 a0001c0001t0001g0189 a0001c0001t0001g0205 others(2): Show |
5 | HG02145.hp1 HG02602.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1000-960G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96487129 | |||||||
| chr9:96487255 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1000-834C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96487255 | |||||||
| chr9:96487266 | A | T | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.1000-823A>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96487266 | |||||||
| chr9:96487268 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1000-821T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96487268 | |||||||
| chr9:96487317 | T | G | 1 | a0001c0002t0005g0037 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1000-772T>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96487317 | |||||||
| chr9:96487317 | T | TTG | 3 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0076 |
3 | HG01081.hp1 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1000-755_1000-754d others(4): Show |
HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 96487317 | ||||||
| chr9:96487334 | T | A | 2 | a0001c0001t0001g0091 a0001c0001t0013g0216 |
2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1000-755T>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96487334 | |||||||
| chr9:96487336 | A | G | 2 | a0001c0002t0002g0064 a0001c0002t0002g0066 |
2 | HG01243.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1000-753A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96487336 | |||||||
| chr9:96487350 | G | T | 1 | a0001c0001t0001g0090 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1000-739G>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96487350 | |||||||
| chr9:96487427 | T | C | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.1000-662T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96487427 | |||||||
| chr9:96487573 | T | C | 2 | a0001c0002t0002g0063 a0001c0002t0002g0065 |
2 | HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1000-516T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96487573 | |||||||
| chr9:96487635 | T | G | 10 | a0001c0003t0003g0011 a0001c0003t0003g0042 a0001c0003t0003g0043 others(7): Show |
11 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000-454T>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96487635 | |||||||
| chr9:96487662 | A | G | 5 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG01106.hp1 HG03704.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000-427A>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96487662 | |||||||
| chr9:96487695 | C | CT | 47 | a0001c0002t0002g0003 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
53 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.1000-388dupT | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 96487695 | ||||||
| chr9:96487999 | C | G | 1 | a0001c0002t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1000-90C>G | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96487999 | |||||||
| chr9:96488039 | T | C | 3 | a0001c0001t0001g0192 a0001c0001t0001g0225 a0001c0002t0008g0061 |
3 | NA18985.hp1 NA19011.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1000-50T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 6/7 | chr9 | 96488039 | |||||||
| chr9:96488459 | C | T | 7 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0003g0072 others(4): Show |
7 | HG01081.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1185+185C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 7/7 | chr9 | 96488459 | |||||||
| chr9:96488610 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1185+336C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 7/7 | chr9 | 96488610 | |||||||
| chr9:96488685 | C | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1185+411C>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 7/7 | chr9 | 96488685 | |||||||
| chr9:96488691 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1185+417C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 7/7 | chr9 | 96488691 | |||||||
| chr9:96488894 | G | A | 1 | a0001c0001t0001g0240 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1185+620G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 7/7 | chr9 | 96488894 | |||||||
| chr9:96488899 | C | T | 4 | a0001c0001t0001g0120 a0001c0001t0001g0174 a0001c0001t0001g0178 others(1): Show |
4 | HG00609.hp1 NA18941.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1185+625C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 7/7 | chr9 | 96488899 | |||||||
| chr9:96488933 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1185+659C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 7/7 | chr9 | 96488933 | |||||||
| chr9:96489594 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1186-388G>A | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 7/7 | chr9 | 96489594 | |||||||
| chr9:96489637 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1186-345C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 7/7 | chr9 | 96489637 | |||||||
| chr9:96489682 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1186-300C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 7/7 | chr9 | 96489682 | |||||||
| chr9:96489826 | T | C | 2 | a0001c0002t0002g0064 a0001c0002t0002g0066 |
2 | HG01243.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1186-156T>C | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 7/7 | chr9 | 96489826 | |||||||
| chr9:96489885 | G | T | 1 | a0001c0001t0001g0218 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1186-97G>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 7/7 | chr9 | 96489885 | |||||||
| chr9:96489921 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1186-61C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 7/7 | chr9 | 96489921 | |||||||
| chr9:96489930 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1186-52C>T | HABP4 | ENSG00000130956.14 | transcript | ENST00000375249.5 | protein_coding | 7/7 | chr9 | 96489930 |