Variant report

Variant	rs7071093
Chromosome Location	chr10:93072477-93072478
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93071000-93072600	Enhancers	Fetal Lung	lung
2	chr10:93071000-93073800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr10:93071200-93072800	Enhancers	NHDF-Ad	bronchial
4	chr10:93071200-93073800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr10:93071400-93072600	Enhancers	Fetal Stomach	stomach
6	chr10:93071400-93074000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr10:93071600-93074200	Enhancers	K562	blood
8	chr10:93071800-93073800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr10:93071800-93074600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr10:93072000-93074200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr10:93072400-93072600	Enhancers	NH-A	brain

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

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