Variant report

Variant	rs6484674
Chromosome Location	chr11:33851995-33851996
allele	A/G
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	chr11:33851200-33852400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr11:33851200-33853400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:33851200-33853400	Enhancers	HMEC	breast
4	chr11:33851400-33852400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr11:33851400-33852400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr11:33851400-33852400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr11:33851400-33852400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr11:33851400-33852400	Weak transcription	HUVEC	blood vessel
9	chr11:33851400-33853000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr11:33851600-33852200	Weak transcription	NHEK	skin
11	chr11:33851800-33852800	Weak transcription	A549	lung

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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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