Variant report

Variant	rs12072085
Chromosome Location	chr1:47693222-47693223
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47689800-47696600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr1:47690000-47697600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr1:47690200-47696800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
4	chr1:47690400-47693600	Enhancers	Spleen	Spleen
5	chr1:47691000-47694400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
6	chr1:47691600-47694400	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr1:47691600-47694800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
8	chr1:47691800-47695200	Weak transcription	Pancreas	Pancrea
9	chr1:47691800-47695600	Flanking Active TSS	HUVEC	blood vessel
10	chr1:47692000-47693800	Transcr. at gene 5' and 3'	K562	blood
11	chr1:47692200-47693800	Bivalent Enhancer	Left Ventricle	heart
12	chr1:47692200-47694200	Bivalent Enhancer	Adipose Nuclei	Adipose
13	chr1:47692200-47694400	Enhancers	Primary hematopoietic stem cells	blood
14	chr1:47692400-47693400	Enhancers	Right Atrium	heart
15	chr1:47692400-47696600	Weak transcription	Gastric	stomach
16	chr1:47692600-47693800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
17	chr1:47692600-47694200	Weak transcription	Lung	lung

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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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