Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:166279128..166280930-chr4:166292985..166295203,2	K562	blood:
2	chr4:166279563..166282339-chr4:166287037..166289622,2	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10015275	0.94[EUR][1000 genomes]
rs10021532	0.92[EUR][1000 genomes]
rs10025377	0.94[EUR][1000 genomes]
rs10031858	0.92[EUR][1000 genomes]
rs13106028	0.93[EUR][1000 genomes]
rs13137171	1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes]
rs17046337	0.94[EUR][1000 genomes]
rs17046351	0.96[EUR][1000 genomes]
rs17489067	1.00[CHB][hapmap]
rs17585655	0.94[EUR][1000 genomes]
rs17585739	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs28484900	0.94[EUR][1000 genomes]
rs28735257	0.94[EUR][1000 genomes]
rs4691187	1.00[JPT][hapmap]
rs6536907	1.00[JPT][hapmap]
rs6536909	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6817186	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs6842704	0.98[EUR][1000 genomes]
rs6846664	0.94[EUR][1000 genomes]
rs72701627	0.92[EUR][1000 genomes]
rs72701628	0.94[EUR][1000 genomes]
rs72701629	0.94[EUR][1000 genomes]
rs72701630	0.94[EUR][1000 genomes]
rs72701632	0.96[EUR][1000 genomes]
rs72701634	0.96[EUR][1000 genomes]
rs72701636	0.96[EUR][1000 genomes]
rs72701637	1.00[EUR][1000 genomes]
rs72701639	1.00[EUR][1000 genomes]
rs72701642	1.00[EUR][1000 genomes]
rs72701645	1.00[EUR][1000 genomes]
rs72701652	0.98[EUR][1000 genomes]
rs72701657	1.00[EUR][1000 genomes]
rs72701659	1.00[EUR][1000 genomes]
rs72701664	1.00[EUR][1000 genomes]
rs7656675	1.00[EUR][1000 genomes]
rs7657847	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7671176	0.98[EUR][1000 genomes]
rs7677572	1.00[JPT][hapmap]
rs7679322	0.88[EUR][1000 genomes]
rs7679808	0.94[EUR][1000 genomes]
rs7696111	0.93[EUR][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	esv1847399	chr4:166259587-166284836	Strong transcription Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:166263200-166280400	Weak transcription	Adipose Nuclei	Adipose
2	chr4:166277400-166280400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr4:166277400-166280400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:166277600-166280800	Weak transcription	Fetal Lung	lung
5	chr4:166277600-166285400	Weak transcription	HepG2	liver
6	chr4:166278200-166282800	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr4:166278400-166280400	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr4:166279200-166281800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:166279400-166280200	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr4:166279400-166281200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr4:166279600-166280200	Weak transcription	HSMMtube	muscle
12	chr4:166279800-166280000	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr4:166279800-166281600	Enhancers	HMEC	breast

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