Variant report

Variant	rs4951537
Chromosome Location	chr1:211797879-211797880
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211790400-211798400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr1:211790400-211803600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:211793400-211803000	Weak transcription	Fetal Intestine Small	intestine
4	chr1:211795200-211798200	Weak transcription	Hela-S3	cervix
5	chr1:211795200-211800000	Weak transcription	Left Ventricle	heart
6	chr1:211795200-211802400	Weak transcription	Right Atrium	heart
7	chr1:211795200-211803400	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr1:211795400-211798200	Weak transcription	HepG2	liver
9	chr1:211795400-211800200	Weak transcription	Fetal Muscle Trunk	muscle
10	chr1:211796400-211798400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr1:211796400-211798600	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr1:211796600-211798400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr1:211796600-211803600	Weak transcription	Spleen	Spleen
14	chr1:211797000-211800000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:211797200-211800400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr1:211797800-211798400	Weak transcription	K562	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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