Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:121889359..121891616-chr7:121898116..121900388,2	K562	blood:

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11979786	0.89[EUR][1000 genomes]
rs12706389	0.85[AFR][1000 genomes]
rs12706390	1.00[CEU][hapmap]
rs12706399	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13231553	0.84[EUR][1000 genomes]
rs1663006	0.96[EUR][1000 genomes]
rs1697517	0.96[EUR][1000 genomes]
rs2134057	1.00[ASW][hapmap];0.85[CEU][hapmap];0.94[LWK][hapmap];0.95[MKK][hapmap];0.92[TSI][hapmap]
rs284353	0.89[EUR][1000 genomes]
rs284354	0.89[EUR][1000 genomes]
rs284355	0.89[EUR][1000 genomes]
rs284381	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs284393	0.96[EUR][1000 genomes]
rs284394	0.96[EUR][1000 genomes]
rs505005	0.93[EUR][1000 genomes]
rs627355	1.00[CEU][hapmap];0.83[GIH][hapmap];1.00[TSI][hapmap]
rs627845	1.00[CEU][hapmap]
rs628339	1.00[CEU][hapmap]
rs673757	0.89[EUR][1000 genomes]
rs675027	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034624	chr7:121813180-121899703	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1024868	chr7:121818974-121899703	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1024364	chr7:121843701-121916791	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1020645	chr7:121843701-121929598	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1034945	chr7:121843701-121933166	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:121895600-121900400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:121896000-121900200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr7:121896000-121901400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr7:121896400-121900200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr7:121896400-121900400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr7:121896400-121900400	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr7:121896600-121900200	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr7:121896800-121900200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr7:121896800-121900400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr7:121896800-121900600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr7:121899200-121902800	Enhancers	HUES48 Cell Line	embryonic stem cell

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