Variant report

Variant	rs9851661
Chromosome Location	chr3:42851251-42851252
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:42846800-42856400	Weak transcription	Right Atrium	heart
2	chr3:42847000-42852200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr3:42847000-42852400	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr3:42847200-42852000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr3:42847200-42852200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr3:42847200-42852200	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr3:42847200-42852400	Weak transcription	Pancreas	Pancrea
8	chr3:42847200-42856400	Weak transcription	NHEK	skin
9	chr3:42847400-42852800	Weak transcription	Fetal Heart	heart
10	chr3:42847400-42852800	Weak transcription	Stomach Mucosa	stomach
11	chr3:42847400-42856200	Weak transcription	Colonic Mucosa	Colon
12	chr3:42847600-42852200	Weak transcription	K562	blood
13	chr3:42849000-42852200	Weak transcription	HepG2	liver
14	chr3:42849400-42853000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr3:42849800-42856400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr3:42850200-42852000	Weak transcription	Fetal Intestine Small	intestine
17	chr3:42850800-42851400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr3:42850800-42854200	Active TSS	Placenta	Placenta
19	chr3:42851000-42851800	Active TSS	Placenta Amnion	Placenta Amnion

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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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