Variant report

Variant	rs210435
Chromosome Location	chrX:104953503-104953504
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1156923	1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap]
rs17343011	1.00[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap]
rs17343018	1.00[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap]
rs210427	1.00[JPT][hapmap]
rs210428	1.00[JPT][hapmap];1.00[YRI][hapmap]
rs210430	1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs210433	0.84[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs210437	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs210544	1.00[JPT][hapmap]
rs210545	1.00[JPT][hapmap]
rs210547	0.84[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap]
rs210548	0.84[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs210549	0.84[CHB][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs210554	1.00[JPT][hapmap];1.00[YRI][hapmap]
rs210556	1.00[JPT][hapmap]
rs210726	1.00[JPT][hapmap];1.00[YRI][hapmap]
rs210729	1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap]
rs210730	1.00[YRI][hapmap]
rs210731	1.00[JPT][hapmap];1.00[YRI][hapmap]
rs210734	1.00[JPT][hapmap];1.00[YRI][hapmap]
rs400761	0.84[CHB][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs440424	1.00[JPT][hapmap]
rs448592	0.84[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap]
rs482764	0.87[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap]
rs5916928	1.00[JPT][hapmap];1.00[YRI][hapmap]
rs5916929	1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6621983	1.00[JPT][hapmap]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:104951200-104955200	Weak transcription	Placenta	Placenta
2	chrX:104953000-104955600	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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