Variant report

Variant	rs61806151
Chromosome Location	chr1:172683570-172683571
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	chr1:172678400-172685800	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	chr1:172682800-172684200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr1:172683000-172684000	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr1:172683000-172684000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr1:172683000-172684000	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr1:172683000-172684000	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr1:172683000-172684800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr1:172683200-172683600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr1:172683200-172683600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:172683200-172683600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr1:172683200-172684000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr1:172683200-172684600	Weak transcription	NHEK	skin
16	chr1:172683400-172685000	Weak transcription	HMEC	breast
17	chr1:172683400-172689200	Weak transcription	H1 Cell Line	embryonic stem cell

Quick Search:

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

what's new

Quick links