Variant report

Variant	rs7672704
Chromosome Location	chr4:100886082-100886083
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100872600-100886200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr4:100880400-100889600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr4:100882600-100889000	Weak transcription	Osteobl	bone
4	chr4:100882800-100888400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr4:100882800-100892800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr4:100883000-100889000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr4:100883200-100887800	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr4:100885400-100886400	Enhancers	Dnd41	blood
9	chr4:100885400-100886800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr4:100885400-100887400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr4:100885600-100887800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
12	chr4:100885800-100887400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr4:100885800-100887600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr4:100886000-100886800	Enhancers	Primary T cells from cord blood	blood
15	chr4:100886000-100887400	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr4:100886000-100887800	Enhancers	Primary T helper cells PMA-I stimulated	--

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