Variant report

Variant	rs11187158
Chromosome Location	chr10:94502429-94502430
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs11187172	1.00[AFR][1000 genomes]
rs61861412	1.00[ASN][1000 genomes]

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	esv3446249	chr10:94374508-94549394	Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:94499400-94505600	Enhancers	Primary B cells from peripheral blood	blood
2	chr10:94500800-94504200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr10:94501000-94503000	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr10:94501000-94503000	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr10:94501200-94506800	Weak transcription	Spleen	Spleen
6	chr10:94502000-94502600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr10:94502000-94502600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr10:94502000-94504600	Enhancers	Primary hematopoietic stem cells	blood
9	chr10:94502200-94502600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr10:94502200-94503200	Flanking Active TSS	GM12878-XiMat	blood
11	chr10:94502200-94507400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr10:94502400-94504600	Enhancers	Primary B cells from cord blood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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