Variant report

Variant	rs2367178
Chromosome Location	chrX:74618159-74618160
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10047013	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap]
rs1017681	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs1017682	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap]
rs11093538	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12008941	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12009021	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap]
rs12156864	1.00[CHB][hapmap]
rs12861282	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1318846	1.00[CHB][hapmap];0.82[YRI][hapmap]
rs1353592	0.84[ASW][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.82[YRI][hapmap]
rs1874557	1.00[CHB][hapmap];0.82[YRI][hapmap]
rs1936914	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap]
rs1936918	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1936919	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs1936923	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1998492	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs1998493	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1998494	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2146767	0.84[ASW][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.82[YRI][hapmap]
rs2209045	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2209046	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2209052	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs2224753	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs2224754	1.00[ASW][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MKK][hapmap];1.00[YRI][hapmap]
rs2367108	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap]
rs2367165	1.00[CHB][hapmap]
rs2367177	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.98[MKK][hapmap];1.00[YRI][hapmap]
rs3850144	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap]
rs4892404	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs4892579	0.84[ASW][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.82[YRI][hapmap]
rs4892583	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[MKK][hapmap]
rs4892587	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4892588	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs5937370	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs5937392	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap]
rs5938009	1.00[CHB][hapmap]
rs5938014	1.00[CHB][hapmap];1.00[GIH][hapmap]
rs5938015	1.00[CHB][hapmap]
rs5938047	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap]
rs5938053	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs5938054	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs5938065	0.84[ASW][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.82[YRI][hapmap]
rs5938066	0.84[ASW][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.82[YRI][hapmap]
rs5938069	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs5938070	1.00[ASW][hapmap];1.00[CHB][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.94[MKK][hapmap];0.86[YRI][hapmap]
rs5938077	0.84[ASW][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.82[YRI][hapmap]
rs5938079	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap]
rs5938085	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap]
rs5938091	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap]
rs5981343	1.00[CHB][hapmap];0.82[YRI][hapmap]
rs5981358	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap]
rs5981362	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.98[MKK][hapmap]
rs5981831	1.00[CHB][hapmap];1.00[GIH][hapmap];0.84[MKK][hapmap]
rs5981834	1.00[CHB][hapmap];0.82[YRI][hapmap]
rs6647105	0.84[ASW][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.89[LWK][hapmap];1.00[MKK][hapmap]
rs6647123	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6647687	1.00[CHB][hapmap];1.00[GIH][hapmap]
rs6647741	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap]
rs6647747	0.84[ASW][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MKK][hapmap];0.82[YRI][hapmap]
rs7052066	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap]
rs7885952	1.00[CHB][hapmap];0.82[YRI][hapmap]
rs7886499	1.00[CHB][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	esv13841	chrX:74461978-74657064	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv532360	chrX:74462926-74651249	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv916109	chrX:74463757-74651249	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv949041	chrX:74523871-74645058	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	esv3354641	chrX:74603980-74643202	ZNF genes & repeats Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:74615800-74621400	Weak transcription	Fetal Lung	lung
2	chrX:74616600-74619200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chrX:74617200-74631200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chrX:74617400-74619400	Strong transcription	Cortex derived primary cultured neurospheres	brain
5	chrX:74617600-74618800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
6	chrX:74617800-74619600	ZNF genes & repeats	Fetal Stomach	stomach
7	chrX:74618000-74618600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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