Variant report

Variant	rs536518389
Chromosome Location	chr10:94625647-94625648
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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	nsv1041805	chr10:94624759-94699623	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:94619800-94626800	Weak transcription	K562	blood
2	chr10:94619800-94627000	Weak transcription	A549	lung
3	chr10:94619800-94628800	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr10:94619800-94632800	Weak transcription	Primary B cells from peripheral blood	blood
5	chr10:94620000-94657600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr10:94622400-94632400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr10:94623400-94628000	Weak transcription	Small Intestine	intestine
8	chr10:94624400-94646000	Weak transcription	Fetal Intestine Small	intestine
9	chr10:94624600-94627000	Weak transcription	Primary hematopoietic stem cells	blood
10	chr10:94624600-94627200	Weak transcription	HUVEC	blood vessel
11	chr10:94624600-94628600	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr10:94624600-94632600	Weak transcription	Primary T cells from cord blood	blood
13	chr10:94624600-94632600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr10:94624600-94633000	Weak transcription	Primary B cells from cord blood	blood
15	chr10:94624800-94632600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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