Variant report

Variant	rs12822701
Chromosome Location	chr12:9934613-9934614
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9927600-9938800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr12:9927800-9935400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:9928000-9935600	Enhancers	Primary T helper cells PMA-I stimulated	--
4	chr12:9928400-9945400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr12:9929800-9935200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr12:9929800-9936000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr12:9930000-9945400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr12:9930200-9945800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr12:9934200-9934800	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr12:9934200-9935200	Enhancers	Primary T cells fromperipheralblood	blood
11	chr12:9934400-9938400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr12:9934600-9937600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr12:9934600-9938200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr12:9934600-9939800	Weak transcription	Primary T cells from cord blood	blood
15	chr12:9934600-9940000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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