Variant report

Variant	rs17042486
Chromosome Location	chr2:113606125-113606126
allele	C/T
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	chr2:113605200-113608800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr2:113605400-113606200	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr2:113605400-113607800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:113605600-113607200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr2:113605600-113607200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr2:113605600-113608000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr2:113605600-113610000	Enhancers	H1 Cell Line	embryonic stem cell
8	chr2:113605800-113606200	Enhancers	H9 Cell Line	embryonic stem cell
9	chr2:113605800-113606400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:113605800-113607400	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr2:113605800-113607400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr2:113605800-113607400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr2:113605800-113607600	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr2:113605800-113610000	Enhancers	HUES6 Cell Line	embryonic stem cell

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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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