Variant report

Variant	rs436628
Chromosome Location	chrX:31140296-31140297
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chrX:31135102..31137027-chrX:31138705..31140641,2	K562	blood:
2	chrX:31134552..31137060-chrX:31137454..31140316,3	K562	blood:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs12391957	0.83[CEU][hapmap]
rs12557265	0.83[CEU][hapmap]
rs12557283	0.83[CEU][hapmap]
rs12687954	0.83[CEU][hapmap];0.82[TSI][hapmap]
rs1484854	0.83[CEU][hapmap]
rs1484855	1.00[ASW][hapmap];1.00[CEU][hapmap];0.87[GIH][hapmap];0.87[LWK][hapmap];0.86[MKK][hapmap];0.87[TSI][hapmap]
rs1921383	0.90[CEU][hapmap]
rs1921385	0.81[CEU][hapmap];0.86[JPT][hapmap]
rs1921386	0.83[CEU][hapmap];0.80[JPT][hapmap]
rs1921388	0.81[CEU][hapmap];0.80[JPT][hapmap]
rs1921395	0.83[CEU][hapmap]
rs1921710	0.81[CEU][hapmap]
rs2178538	0.83[CEU][hapmap]
rs2404495	0.83[CEU][hapmap];0.82[TSI][hapmap]
rs2404496	0.83[CEU][hapmap]
rs2404497	0.83[CEU][hapmap]
rs2896876	0.83[CEU][hapmap]
rs3747385	0.83[CEU][hapmap];0.82[TSI][hapmap]
rs3788887	0.86[CHB][hapmap]
rs426228	0.90[CEU][hapmap];0.88[JPT][hapmap]
rs4829210	0.83[CEU][hapmap]
rs5926986	0.90[CEU][hapmap]
rs5926987	0.90[CEU][hapmap]
rs5927688	0.90[ASW][hapmap];0.81[CEU][hapmap];0.87[GIH][hapmap];0.87[LWK][hapmap];1.00[TSI][hapmap]
rs5927689	0.90[CEU][hapmap];1.00[TSI][hapmap]
rs5972322	0.84[CEU][hapmap]
rs5972328	0.83[CEU][hapmap]
rs6527061	0.83[CEU][hapmap];0.87[TSI][hapmap]
rs6527062	0.82[CEU][hapmap]
rs6653848	0.83[CEU][hapmap]
rs7057738	0.83[CEU][hapmap]

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	nsv530449	chrX:30962926-31375215	Strong transcription Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	esv3416705	chrX:31099481-31213379	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:31131000-31144400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chrX:31131000-31149400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chrX:31131200-31144000	Weak transcription	Muscle Satellite Cultured Cells	--
4	chrX:31132800-31143400	Weak transcription	Fetal Muscle Trunk	muscle
5	chrX:31133400-31156200	Weak transcription	Colon Smooth Muscle	Colon
6	chrX:31134000-31141200	Weak transcription	Fetal Heart	heart
7	chrX:31134000-31144000	Weak transcription	Ovary	ovary
8	chrX:31134000-31188200	Weak transcription	Aorta	Aorta
9	chrX:31135400-31143200	Weak transcription	Fetal Muscle Leg	muscle
10	chrX:31135800-31163800	Weak transcription	Rectal Smooth Muscle	rectum
11	chrX:31135800-31182800	Weak transcription	Pancreas	Pancrea
12	chrX:31136000-31144200	Weak transcription	HSMMtube	muscle
13	chrX:31136200-31154000	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chrX:31136200-31156200	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chrX:31136400-31143400	Weak transcription	Left Ventricle	heart
16	chrX:31136600-31150000	Weak transcription	Fetal Intestine Large	intestine
17	chrX:31136800-31155800	Weak transcription	Stomach Smooth Muscle	stomach
18	chrX:31137200-31140400	Weak transcription	Hela-S3	cervix
19	chrX:31137200-31143400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chrX:31137200-31183000	Weak transcription	Gastric	stomach
21	chrX:31137600-31140600	Strong transcription	Liver	Liver
22	chrX:31137800-31144000	Weak transcription	NH-A	brain
23	chrX:31137800-31165200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chrX:31138000-31154200	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chrX:31138400-31156200	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chrX:31139200-31143400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chrX:31140000-31140600	Strong transcription	Skeletal Muscle Female	skeletal muscle
28	chrX:31140200-31227600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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