Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:67695892..67697817-chr1:67702175..67704682,3	K562	blood:

Variant related genes	Relation type
ENSG00000203963	Chromatin interaction

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10489628	0.93[CHB][hapmap];0.84[JPT][hapmap];0.92[ASN][1000 genomes]
rs10489629	0.93[CHB][hapmap];0.84[JPT][hapmap]
rs10789228	0.81[ASN][1000 genomes]
rs10889673	0.97[ASN][1000 genomes]
rs10889674	0.97[ASN][1000 genomes]
rs10889676	0.93[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs10889677	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs11465802	0.85[ASN][1000 genomes]
rs12030107	0.99[ASN][1000 genomes]
rs12030948	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12031203	0.99[ASN][1000 genomes]
rs12567232	0.93[ASN][1000 genomes]
rs12743974	0.97[ASN][1000 genomes]
rs2180294	0.96[ASN][1000 genomes]
rs2201841	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs35380856	0.97[ASN][1000 genomes]
rs35427944	0.86[ASN][1000 genomes]
rs4655529	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs6665959	0.82[ASN][1000 genomes]
rs6686950	0.99[ASN][1000 genomes]
rs7518660	0.86[CHB][hapmap]
rs7523955	0.81[ASN][1000 genomes]
rs7543633	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1243	chr1:67700289-67745337	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:67703800-67722000	Weak transcription	K562	blood

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