Variant report

No.	Distal block	Cell Line	Cell type
1	chr7:27384042..27388224-chr7:27459528..27463800,5	MCF-7	breast:
2	chr7:27459213..27461483-chr7:27463058..27464839,2	MCF-7	breast:
3	chr7:27455758..27458549-chr7:27459040..27460885,2	K562	blood:

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

rs_ID	r²[population]
rs10242634	0.84[EUR][1000 genomes]
rs10252511	0.83[EUR][1000 genomes]
rs10252636	0.83[EUR][1000 genomes]
rs10269160	0.83[EUR][1000 genomes]
rs10272561	0.90[EUR][1000 genomes]
rs10272948	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10276795	0.83[EUR][1000 genomes]
rs1112620	0.83[EUR][1000 genomes]
rs11762257	1.00[ASN][1000 genomes]
rs1476538	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17501766	1.00[CHB][hapmap]
rs2074340	0.83[EUR][1000 genomes]
rs28418930	0.84[EUR][1000 genomes]
rs28668661	1.00[ASN][1000 genomes]
rs3915089	0.83[EUR][1000 genomes]
rs4141138	0.84[EUR][1000 genomes]
rs4719892	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4722698	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4722700	0.87[EUR][1000 genomes]
rs4722706	0.83[EUR][1000 genomes]
rs4722707	0.83[EUR][1000 genomes]
rs62454765	0.89[EUR][1000 genomes]
rs62454789	0.84[EUR][1000 genomes]
rs62454790	0.84[EUR][1000 genomes]
rs62454832	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531024	chr7:27194426-27461954	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
2	nsv830930	chr7:27395838-27587355	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 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	chr7:27458000-27461000	Enhancers	Stomach Mucosa	stomach
2	chr7:27458400-27460000	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr7:27458600-27462600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr7:27458800-27460000	Enhancers	Rectal Mucosa Donor 29	rectum
5	chr7:27458800-27461000	Enhancers	Liver	Liver
6	chr7:27458800-27463200	Weak transcription	Spleen	Spleen
7	chr7:27458800-27464000	Weak transcription	HUVEC	blood vessel
8	chr7:27459000-27460800	Enhancers	Fetal Intestine Small	intestine
9	chr7:27459200-27464600	Weak transcription	Pancreas	Pancrea
10	chr7:27459400-27460400	Weak transcription	Fetal Stomach	stomach
11	chr7:27459400-27460600	Enhancers	Duodenum Smooth Muscle	Duodenum
12	chr7:27459600-27460000	Enhancers	Duodenum Mucosa	Duodenum
13	chr7:27459600-27461800	Weak transcription	Sigmoid Colon	Sigmoid Colon

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