Variant report

Variant	rs73393994
Chromosome Location	chr8:130522151-130522152
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130519200-130522400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr8:130519400-130522200	Enhancers	NHEK	skin
3	chr8:130519400-130524000	Strong transcription	K562	blood
4	chr8:130519600-130522200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:130519600-130523000	Enhancers	HMEC	breast
6	chr8:130519600-130524400	Weak transcription	Dnd41	blood
7	chr8:130521000-130523000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr8:130521200-130526600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr8:130521400-130526200	Weak transcription	NH-A	brain
10	chr8:130521400-130526400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr8:130521400-130526400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr8:130521400-130526400	Weak transcription	HSMM	muscle
13	chr8:130521400-130526400	Weak transcription	Osteobl	bone
14	chr8:130521400-130526600	Weak transcription	Muscle Satellite Cultured Cells	--

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