Variant report

Variant	rs575920347
Chromosome Location	chr9:101153763-101153764
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430085	chr9:100928245-101339645	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv831664	chr9:101024862-101205637	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv3356278	chr9:101153231-101157729	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:101128200-101164200	Weak transcription	Brain Germinal Matrix	brain
2	chr9:101129000-101156000	Weak transcription	Fetal Brain Female	brain
3	chr9:101143200-101156000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr9:101143200-101157000	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr9:101144000-101172000	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr9:101149000-101153800	Weak transcription	Primary B cells from cord blood	blood
7	chr9:101149800-101158600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr9:101150400-101157800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr9:101152000-101156200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr9:101153600-101154200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr9:101153600-101154400	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr9:101153600-101154800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr9:101153600-101155000	Enhancers	Primary B cells from peripheral blood	blood

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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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