Variant report

Variant	rs7011270
Chromosome Location	chr8:121374194-121374195
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:121371779..121374394-chr8:121390931..121392739,2	K562	blood:
2	chr8:121372776..121375145-chr8:121376209..121379714,3	MCF-7	breast:
3	chr8:121369184..121371852-chr8:121371968..121374570,3	MCF-7	breast:

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs1563391	0.81[CHB][hapmap]
rs1563399	0.87[CHB][hapmap]
rs2034844	0.81[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891420	chr8:121194900-121561369	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv612112	chr8:121234298-121385167	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv891421	chr8:121292407-121653902	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv1033386	chr8:121369943-121501239	Flanking Active TSS Strong transcription Active TSS Enhancers Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:121333800-121383800	Weak transcription	Fetal Intestine Large	intestine
2	chr8:121346400-121377600	Weak transcription	Colon Smooth Muscle	Colon
3	chr8:121360200-121376600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr8:121365200-121380600	Weak transcription	Gastric	stomach
5	chr8:121369600-121377400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr8:121369600-121406200	Weak transcription	Left Ventricle	heart
7	chr8:121370400-121377400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr8:121370800-121376600	Weak transcription	Stomach Smooth Muscle	stomach
9	chr8:121371600-121375400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
10	chr8:121372000-121374400	Strong transcription	Fetal Stomach	stomach
11	chr8:121372000-121375400	Strong transcription	Fetal Lung	lung
12	chr8:121372400-121383000	Weak transcription	Fetal Muscle Trunk	muscle
13	chr8:121373000-121374200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr8:121373200-121383000	Weak transcription	Fetal Muscle Leg	muscle
15	chr8:121373400-121381800	Weak transcription	Fetal Intestine Small	intestine
16	chr8:121373600-121374600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr8:121373600-121374600	Enhancers	Osteobl	bone
18	chr8:121373600-121375000	Enhancers	NHDF-Ad	bronchial
19	chr8:121373600-121375200	Enhancers	Fetal Brain Male	brain
20	chr8:121373800-121374200	Enhancers	Aorta	Aorta
21	chr8:121374000-121376400	Strong transcription	Ovary	ovary
22	chr8:121374000-121381600	Weak transcription	Placenta	Placenta

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