Variant report

Variant	rs999651
Chromosome Location	chr11:26298144-26298145
allele	A/C
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	chr11:26286000-26306200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:26296400-26298200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr11:26296800-26298600	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr11:26297000-26298400	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr11:26297000-26298400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr11:26297000-26298600	Enhancers	NHDF-Ad	bronchial
7	chr11:26297200-26298400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr11:26297200-26305400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr11:26297400-26298200	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr11:26297800-26298400	Enhancers	Hela-S3	cervix
11	chr11:26298000-26298400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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