Variant report

Variant	rs7977927
Chromosome Location	chr12:106661434-106661435
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:106660000-106662200	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr12:106660600-106661800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
3	chr12:106660600-106662400	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr12:106660800-106662000	Enhancers	Primary T cells fromperipheralblood	blood
5	chr12:106660800-106662000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr12:106660800-106663200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
7	chr12:106661000-106661800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr12:106661000-106662000	Enhancers	Fetal Heart	heart
9	chr12:106661000-106663800	Weak transcription	Left Ventricle	heart
10	chr12:106661200-106664200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr12:106661400-106661600	Enhancers	Psoas Muscle	Psoas
12	chr12:106661400-106662400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr12:106661400-106664000	Enhancers	K562	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