Variant report

Variant	rs7060124
Chromosome Location	chrX:109940046-109940047
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10047014	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs10126502	0.94[CEU][hapmap];1.00[CHB][hapmap]
rs12012172	0.95[CEU][hapmap];1.00[CHB][hapmap];0.80[YRI][hapmap]
rs12395955	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs12396834	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs12857107	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs191800	1.00[CHB][hapmap]
rs197023	1.00[CHB][hapmap]
rs197036	1.00[CHB][hapmap]
rs2016878	0.86[CEU][hapmap];1.00[CHB][hapmap]
rs2206971	0.95[CEU][hapmap];1.00[CHB][hapmap];0.80[YRI][hapmap]
rs2223782	0.95[CEU][hapmap];1.00[CHB][hapmap];0.84[LWK][hapmap];0.89[YRI][hapmap]
rs2404177	0.95[CEU][hapmap];1.00[CHB][hapmap];0.84[LWK][hapmap];0.89[YRI][hapmap]
rs5942660	0.95[CEU][hapmap];1.00[CHB][hapmap];0.84[LWK][hapmap];0.89[YRI][hapmap]
rs5942661	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs5942674	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs5942675	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs5942676	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs5942677	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs5942678	0.95[CEU][hapmap];1.00[CHB][hapmap];0.80[YRI][hapmap]
rs5942680	0.95[CEU][hapmap];1.00[CHB][hapmap];0.83[LWK][hapmap]
rs5942681	0.95[CEU][hapmap];1.00[CHB][hapmap];0.94[LWK][hapmap];1.00[YRI][hapmap]
rs5942953	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs5942955	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs5943019	0.95[CEU][hapmap];1.00[CHB][hapmap];0.84[LWK][hapmap];0.89[YRI][hapmap]
rs5943044	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs5943045	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs5943046	0.95[CEU][hapmap];1.00[CHB][hapmap];0.84[LWK][hapmap];0.89[YRI][hapmap]
rs5943047	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs5943048	0.95[CEU][hapmap];1.00[CHB][hapmap];0.83[LWK][hapmap]
rs5943050	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs5943051	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs5943052	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs5943053	0.83[CEU][hapmap];1.00[CHB][hapmap]
rs5943055	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs5943056	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs5943057	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs5985302	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs5985519	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs5985544	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs5985545	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs5985546	0.95[CEU][hapmap];1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817233	chrX:109693720-110244649	Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv7037	chrX:109927893-109972675	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
3	esv3484416	chrX:109938469-109942251	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	inside rSNPs	n/a
4	esv3484417	chrX:109938515-109942228	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	inside rSNPs	n/a
5	esv3484414	chrX:109938519-109942176	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	inside rSNPs	n/a
6	esv3484418	chrX:109938519-109942176	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	inside rSNPs	n/a
7	esv3484415	chrX:109938534-109942212	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	inside rSNPs	n/a
8	esv14139	chrX:109938628-109942201	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	inside rSNPs	n/a
9	nsv442813	chrX:109938680-109940297	Weak transcription Genic enhancers Strong transcription	n/a	n/a	inside rSNPs	n/a
10	nsv515161	chrX:109938728-109941552	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	inside rSNPs	n/a
11	nsv438151	chrX:109939205-109941159	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:109919400-109948800	Weak transcription	Adipose Nuclei	Adipose
2	chrX:109936800-109941000	Weak transcription	Fetal Thymus	thymus
3	chrX:109937000-109940800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chrX:109937200-109941200	Weak transcription	Primary hematopoietic stem cells	blood
5	chrX:109937400-109940800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chrX:109939600-109943400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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