Variant report

No.	Distal block	Cell Line	Cell type
1	chr1:61532379..61538050-chr1:61538671..61543551,8	K562	blood:
2	chr1:61535095..61537087-chr1:61539736..61541620,2	MCF-7	breast:
3	chr1:61527980..61529698-chr1:61534455..61537045,2	K562	blood:
4	chr1:61536281..61537893-chr1:61555336..61557070,2	K562	blood:

Variant related genes	Relation type
ENSG00000162599	Chromatin interaction

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10789092	0.86[CHD][hapmap];0.84[TSI][hapmap]
rs11207690	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11207691	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11207694	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11207695	0.86[CHD][hapmap];0.82[TSI][hapmap]
rs12126737	0.87[CHD][hapmap];0.84[TSI][hapmap]
rs12130085	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12142294	0.81[CHD][hapmap]
rs12402756	0.82[CEU][hapmap]
rs12403502	0.87[CHD][hapmap];0.84[TSI][hapmap]
rs12404093	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12406426	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12565220	0.82[CEU][hapmap]
rs1573249	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs17121533	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2051153	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4620575	0.84[TSI][hapmap]
rs4915584	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs4915585	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs4915725	0.86[CHB][hapmap];0.81[CHD][hapmap];1.00[JPT][hapmap]
rs4915726	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4915729	0.87[CHD][hapmap];0.82[TSI][hapmap]
rs904271	0.81[CHD][hapmap];1.00[JPT][hapmap]
rs924274	0.86[CHB][hapmap];0.81[CHD][hapmap];1.00[JPT][hapmap]
rs964091	0.84[TSI][hapmap]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:61535000-61537000	Enhancers	K562	blood
2	chr1:61535400-61541200	Weak transcription	HepG2	liver
3	chr1:61536200-61537000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
4	chr1:61536200-61537400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
5	chr1:61536400-61537000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
6	chr1:61536600-61537200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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