Variant report

Variant	rs7545586
Chromosome Location	chr1:56610710-56610711
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:56603000-56612000	Weak transcription	Psoas Muscle	Psoas
2	chr1:56604400-56613600	Weak transcription	HUVEC	blood vessel
3	chr1:56605800-56622600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr1:56606400-56611600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr1:56607400-56611200	Enhancers	Fetal Intestine Large	intestine
6	chr1:56607600-56610800	Enhancers	Fetal Intestine Small	intestine
7	chr1:56608000-56611000	Weak transcription	Thymus	Thymus
8	chr1:56610000-56611400	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr1:56610400-56610800	Enhancers	Aorta	Aorta
10	chr1:56610400-56612200	Weak transcription	Fetal Muscle Leg	muscle
11	chr1:56610600-56611000	Weak transcription	Fetal Thymus	thymus
12	chr1:56610600-56612200	Enhancers	Primary T cells from cord 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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