Variant report

Variant	rs73711569
Chromosome Location	chr8:130523791-130523792
allele	C/T
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	chr8:130519400-130524000	Strong transcription	K562	blood
2	chr8:130519600-130524400	Weak transcription	Dnd41	blood
3	chr8:130521200-130526600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr8:130521400-130526200	Weak transcription	NH-A	brain
5	chr8:130521400-130526400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr8:130521400-130526400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr8:130521400-130526400	Weak transcription	HSMM	muscle
8	chr8:130521400-130526400	Weak transcription	Osteobl	bone
9	chr8:130521400-130526600	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr8:130522200-130526000	Weak transcription	NHEK	skin
11	chr8:130522200-130526200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr8:130522400-130526200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr8:130523000-130526000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr8:130523000-130526200	Weak transcription	HMEC	breast
15	chr8:130523600-130524200	Enhancers	Fetal Heart	heart

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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

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