Variant report
Variant | rs586224 |
---|---|
Chromosome Location | chr4:119163784-119163785 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:5)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:5 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr4:119162629..119164449-chr4:119200299..119202750,2 | K562 | blood: | |
2 | chr4:119162986..119165560-chr4:119198064..119200853,3 | MCF-7 | breast: | |
3 | chr4:119162210..119165172-chr4:119175600..119178135,2 | MCF-7 | breast: | |
4 | chr4:119159048..119162234-chr4:119163656..119166520,3 | K562 | blood: | |
5 | chr4:119162949..119165228-chr4:119199833..119201799,2 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000269893 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10000812 | 0.88[ASN][1000 genomes] |
rs10008049 | 0.83[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs10014096 | 0.83[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10015232 | 0.89[ASN][1000 genomes] |
rs10016285 | 0.85[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs10020473 | 0.81[ASN][1000 genomes] |
rs10021128 | 0.81[ASN][1000 genomes] |
rs10021781 | 0.89[ASN][1000 genomes] |
rs10023699 | 0.89[ASN][1000 genomes] |
rs10026541 | 0.85[ASN][1000 genomes] |
rs10027893 | 0.81[ASN][1000 genomes] |
rs10033308 | 0.85[ASN][1000 genomes] |
rs10033412 | 0.87[ASN][1000 genomes] |
rs1022287 | 0.92[JPT][hapmap];0.86[ASN][1000 genomes] |
rs1022288 | 0.85[JPT][hapmap];0.87[ASN][1000 genomes] |
rs1040105 | 0.81[ASN][1000 genomes] |
rs10440400 | 0.89[ASN][1000 genomes] |
rs11098422 | 0.81[ASN][1000 genomes] |
rs11098424 | 0.84[ASN][1000 genomes] |
rs11098425 | 0.84[ASN][1000 genomes] |
rs11098427 | 0.83[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs11098428 | 0.85[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1110948 | 0.83[ASN][1000 genomes] |
rs11722962 | 0.81[ASN][1000 genomes] |
rs11728724 | 0.83[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs11730541 | 0.85[ASN][1000 genomes] |
rs11733562 | 0.81[ASN][1000 genomes] |
rs11736688 | 0.85[ASN][1000 genomes] |
rs11937777 | 0.87[ASN][1000 genomes] |
rs11947071 | 0.91[ASN][1000 genomes] |
rs12499751 | 0.81[ASN][1000 genomes] |
rs12505156 | 0.94[ASN][1000 genomes] |
rs12508017 | 0.87[ASN][1000 genomes] |
rs12711064 | 0.89[ASN][1000 genomes] |
rs13104129 | 0.81[ASN][1000 genomes] |
rs13111697 | 0.89[ASN][1000 genomes] |
rs13114621 | 0.87[ASN][1000 genomes] |
rs13114895 | 0.87[ASN][1000 genomes] |
rs13124806 | 0.82[ASN][1000 genomes] |
rs13126882 | 0.85[ASN][1000 genomes] |
rs13127321 | 0.85[ASN][1000 genomes] |
rs13134901 | 0.84[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs13139875 | 0.81[ASN][1000 genomes] |
rs1319938 | 0.87[ASN][1000 genomes] |
rs1514657 | 1.00[CHD][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes] |
rs1514659 | 1.00[CHD][hapmap];0.86[JPT][hapmap];0.86[ASN][1000 genomes] |
rs1994384 | 0.81[ASN][1000 genomes] |
rs2049362 | 0.94[ASN][1000 genomes] |
rs2140475 | 0.92[ASN][1000 genomes] |
rs2389510 | 0.81[ASN][1000 genomes] |
rs2389511 | 0.81[ASN][1000 genomes] |
rs2389512 | 0.81[ASN][1000 genomes] |
rs2389513 | 0.84[ASN][1000 genomes] |
rs2389514 | 0.84[ASN][1000 genomes] |
rs2389515 | 0.84[ASN][1000 genomes] |
rs2389516 | 0.84[ASN][1000 genomes] |
rs2389517 | 0.84[ASN][1000 genomes] |
rs2389518 | 0.85[ASN][1000 genomes] |
rs2389519 | 0.85[ASN][1000 genomes] |
rs2389520 | 0.85[ASN][1000 genomes] |
rs2389521 | 0.84[ASN][1000 genomes] |
rs2389522 | 0.85[ASN][1000 genomes] |
rs2389523 | 0.85[ASN][1000 genomes] |
rs2389524 | 0.85[ASN][1000 genomes] |
rs2389525 | 0.87[ASN][1000 genomes] |
rs2389526 | 0.87[ASN][1000 genomes] |
rs2389527 | 0.87[ASN][1000 genomes] |
rs2389620 | 0.88[ASN][1000 genomes] |
rs2892787 | 0.81[ASN][1000 genomes] |
rs2892788 | 0.85[ASN][1000 genomes] |
rs2892789 | 0.85[ASN][1000 genomes] |
rs2892790 | 0.85[ASN][1000 genomes] |
rs2892791 | 0.87[ASN][1000 genomes] |
rs2892799 | 0.93[ASN][1000 genomes] |
rs4131600 | 0.85[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs4240316 | 0.87[ASN][1000 genomes] |
rs4240317 | 0.87[ASN][1000 genomes] |
rs4240318 | 0.87[ASN][1000 genomes] |
rs4279285 | 0.92[JPT][hapmap];0.88[ASN][1000 genomes] |
rs4280816 | 0.87[ASN][1000 genomes] |
rs4362895 | 0.92[ASN][1000 genomes] |
rs4397073 | 0.83[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs4437319 | 0.81[ASN][1000 genomes] |
rs4452509 | 0.87[ASN][1000 genomes] |
rs4546313 | 0.99[ASN][1000 genomes] |
rs4566725 | 0.87[ASN][1000 genomes] |
rs4569819 | 0.87[ASN][1000 genomes] |
rs4576085 | 0.87[ASN][1000 genomes] |
rs4616829 | 0.87[ASN][1000 genomes] |
rs4833560 | 0.89[ASN][1000 genomes] |
rs4833561 | 0.83[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs4833563 | 0.89[ASN][1000 genomes] |
rs4833566 | 0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes] |
rs4833567 | 0.99[ASN][1000 genomes] |
rs4834656 | 0.81[ASN][1000 genomes] |
rs4834657 | 0.87[ASN][1000 genomes] |
rs4834660 | 0.83[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs4834661 | 0.89[ASN][1000 genomes] |
rs4834664 | 0.85[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs4834665 | 0.85[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs4834666 | 0.85[ASN][1000 genomes] |
rs4834679 | 1.00[CHD][hapmap];0.86[JPT][hapmap];0.88[ASN][1000 genomes] |
rs4834681 | 0.86[ASN][1000 genomes] |
rs581739 | 1.00[ASN][1000 genomes] |
rs582448 | 0.80[CEU][hapmap];0.81[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes] |
rs586073 | 0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs593966 | 1.00[ASN][1000 genomes] |
rs597881 | 1.00[ASN][1000 genomes] |
rs607961 | 0.99[ASN][1000 genomes] |
rs608228 | 0.99[ASN][1000 genomes] |
rs610222 | 0.97[ASN][1000 genomes] |
rs613083 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs613443 | 1.00[ASN][1000 genomes] |
rs615165 | 0.92[ASN][1000 genomes] |
rs615837 | 0.97[ASN][1000 genomes] |
rs617140 | 0.93[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes] |
rs62328865 | 1.00[ASN][1000 genomes] |
rs62328871 | 0.99[ASN][1000 genomes] |
rs625546 | 0.98[ASN][1000 genomes] |
rs627249 | 0.80[CEU][hapmap];0.93[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes] |
rs641962 | 1.00[ASN][1000 genomes] |
rs644797 | 0.94[ASN][1000 genomes] |
rs6534082 | 0.85[ASN][1000 genomes] |
rs662086 | 1.00[ASN][1000 genomes] |
rs674514 | 0.98[ASN][1000 genomes] |
rs678177 | 0.99[ASN][1000 genomes] |
rs6820061 | 0.87[ASN][1000 genomes] |
rs6820108 | 0.85[ASN][1000 genomes] |
rs6823125 | 0.83[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs6823295 | 0.81[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs6825105 | 0.87[ASN][1000 genomes] |
rs6828232 | 0.86[ASN][1000 genomes] |
rs6828552 | 0.89[ASN][1000 genomes] |
rs6837896 | 0.94[ASN][1000 genomes] |
rs6838716 | 0.83[ASN][1000 genomes] |
rs6842393 | 0.87[ASN][1000 genomes] |
rs6848037 | 0.87[ASN][1000 genomes] |
rs6848598 | 0.87[ASN][1000 genomes] |
rs6851494 | 0.88[ASN][1000 genomes] |
rs6857041 | 0.89[ASN][1000 genomes] |
rs6857232 | 0.89[ASN][1000 genomes] |
rs705838 | 0.93[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes] |
rs705841 | 0.91[ASN][1000 genomes] |
rs7435948 | 0.89[ASN][1000 genomes] |
rs7439663 | 0.87[ASN][1000 genomes] |
rs7655439 | 0.85[ASN][1000 genomes] |
rs7655519 | 0.85[ASN][1000 genomes] |
rs7669243 | 0.84[ASN][1000 genomes] |
rs7671232 | 0.87[ASN][1000 genomes] |
rs7671359 | 0.87[ASN][1000 genomes] |
rs7671434 | 0.86[ASN][1000 genomes] |
rs7671515 | 0.87[ASN][1000 genomes] |
rs7671562 | 0.87[ASN][1000 genomes] |
rs7677274 | 0.81[ASN][1000 genomes] |
rs7679658 | 0.87[ASN][1000 genomes] |
rs7681830 | 0.84[ASN][1000 genomes] |
rs7685325 | 0.83[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs7686670 | 0.83[ASN][1000 genomes] |
rs7695706 | 0.87[ASN][1000 genomes] |
rs7699653 | 0.92[ASN][1000 genomes] |
rs788647 | 0.87[CHB][hapmap];0.93[JPT][hapmap];0.93[ASN][1000 genomes] |
rs788650 | 0.93[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes] |
rs788651 | 0.92[JPT][hapmap];0.93[ASN][1000 genomes] |
rs788655 | 0.93[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes] |
rs788656 | 1.00[CHD][hapmap];0.93[JPT][hapmap];0.90[ASN][1000 genomes] |
rs788658 | 0.93[JPT][hapmap];0.91[ASN][1000 genomes] |
rs788661 | 0.99[ASN][1000 genomes] |
rs788662 | 0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs788668 | 0.93[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes] |
rs788669 | 0.86[ASN][1000 genomes] |
rs871769 | 0.81[ASN][1000 genomes] |
rs871770 | 0.81[ASN][1000 genomes] |
rs908152 | 0.81[ASN][1000 genomes] |
rs9307452 | 0.89[ASN][1000 genomes] |
rs9637622 | 0.87[ASN][1000 genomes] |
rs9637623 | 0.87[ASN][1000 genomes] |
rs9790637 | 0.87[ASN][1000 genomes] |
rs9995675 | 0.83[EUR][1000 genomes];0.89[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv519017 | chr4:118828807-119771481 | Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 39 gene(s) | inside rSNPs | diseases |
2 | nsv1009076 | chr4:118949490-119269424 | Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
3 | nsv1001236 | chr4:118949490-119271243 | Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
4 | esv34038 | chr4:119035124-119455391 | Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
5 | nsv1001138 | chr4:119095147-119461837 | Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
6 | nsv537230 | chr4:119095147-119461837 | Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
7 | nsv1002771 | chr4:119125361-119571237 | Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 28 gene(s) | inside rSNPs | diseases |
8 | nsv1003731 | chr4:119138262-119506032 | Active TSS Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:119154800-119165600 | Strong transcription | Dnd41 | blood |