Variant report

Variant	rs10181094
Chromosome Location	chr2:173242043-173242044
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:173241953..173243647-chr2:173245498..173247532,2	MCF-7	breast:
2	chr2:173238115..173240809-chr2:173241863..173243674,2	MCF-7	breast:
3	chr2:173238964..173242268-chr2:173243569..173246875,3	K562	blood:
4	chr2:173240902..173243860-chr2:173291446..173293970,2	MCF-7	breast:
5	chr2:173237258..173239804-chr2:173240383..173243388,3	K562	blood:

Variant related genes	Relation type
ENSG00000226963	Chromatin interaction
ENSG00000091409	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs10202550	1.00[CHB][hapmap]
rs13394924	1.00[CHB][hapmap]
rs13417334	1.00[CHB][hapmap]
rs6752257	1.00[CHB][hapmap]

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	nsv533927	chr2:173161637-173796894	Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:173238400-173243800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:173239200-173260200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:173239800-173242200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr2:173239800-173245400	Weak transcription	Fetal Kidney	kidney
5	chr2:173240000-173242800	Enhancers	Liver	Liver
6	chr2:173240200-173243600	Weak transcription	Fetal Intestine Small	intestine
7	chr2:173240400-173243400	Weak transcription	HepG2	liver
8	chr2:173240400-173245000	Weak transcription	HSMMtube	muscle
9	chr2:173240800-173242200	Weak transcription	Left Ventricle	heart
10	chr2:173240800-173243800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr2:173240800-173244800	Weak transcription	Fetal Intestine Large	intestine
12	chr2:173241000-173245400	Weak transcription	Gastric	stomach
13	chr2:173241200-173242200	Weak transcription	Pancreas	Pancrea
14	chr2:173241200-173244800	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr2:173241400-173242400	Enhancers	HUVEC	blood vessel
16	chr2:173241600-173242800	Enhancers	Fetal Muscle Leg	muscle
17	chr2:173241800-173243400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr2:173242000-173242200	Enhancers	Lung	lung
19	chr2:173242000-173242600	Enhancers	Primary B cells from peripheral blood	blood
20	chr2:173242000-173242600	Enhancers	Adipose Nuclei	Adipose
21	chr2:173242000-173242800	Enhancers	Right Atrium	heart
22	chr2:173242000-173242800	Enhancers	Spleen	Spleen
23	chr2:173242000-173244400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr2:173242000-173245200	Weak transcription	Stomach Mucosa	stomach

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