Variant report

Variant	rs149175318
Chromosome Location	chr15:40785337-40785338
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34145	chr15:40549617-40889824	Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	esv3443211	chr15:40783910-40786008	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:40785000-40785400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr15:40785000-40785800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
3	chr15:40785000-40786600	Enhancers	Primary T cells fromperipheralblood	blood
4	chr15:40785000-40786600	Enhancers	Dnd41	blood
5	chr15:40785000-40786800	Enhancers	Primary T helper cells PMA-I stimulated	--
6	chr15:40785200-40785400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
7	chr15:40785200-40785800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
8	chr15:40785200-40785800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
9	chr15:40785200-40785800	Enhancers	K562	blood
10	chr15:40785200-40786000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
11	chr15:40785200-40786000	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr15:40785200-40786200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr15:40785200-40786200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr15:40785200-40786400	Enhancers	NHEK	skin
15	chr15:40785200-40786600	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr15:40785200-40786600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr15:40785200-40786600	Enhancers	HMEC	breast

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Input of quick search could be:

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

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