Variant report

Variant	rs4916193
Chromosome Location	chr1:172684613-172684614
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172678400-172685800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr1:172679000-172685400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr1:172679000-172685400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr1:172681000-172685400	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr1:172683000-172684800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:172683400-172685000	Weak transcription	HMEC	breast
7	chr1:172683400-172689200	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr1:172683600-172685000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:172684000-172688000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr1:172684000-172688400	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr1:172684000-172689000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr1:172684000-172692400	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:172684600-172685000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr1:172684600-172686200	Enhancers	NHEK	skin

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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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