Variant report

Variant	rs6873878
Chromosome Location	chr5:36492067-36492068
allele	C/T
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	chr5:36488200-36494000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr5:36490200-36492400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr5:36490400-36495800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr5:36490600-36492400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr5:36490600-36493200	Weak transcription	HSMM	muscle
6	chr5:36490800-36492400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr5:36491200-36493400	Weak transcription	HMEC	breast
8	chr5:36491200-36499800	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr5:36491400-36493400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr5:36491600-36492600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr5:36491800-36492200	Weak transcription	Lung	lung
12	chr5:36491800-36492400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:36492000-36492200	Enhancers	Stomach Smooth Muscle	stomach
14	chr5:36492000-36492400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr5:36492000-36492400	Enhancers	Adipose Nuclei	Adipose
16	chr5:36492000-36492400	Flanking Active TSS	Hela-S3	cervix
17	chr5:36492000-36492400	Enhancers	NHEK	skin

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