Variant report

Variant	rs12193514
Chromosome Location	chr6:114006396-114006397
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:113999000-114007000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr6:114004400-114008400	Enhancers	HepG2	liver
3	chr6:114005200-114006600	Enhancers	HMEC	breast
4	chr6:114005400-114006600	Enhancers	NHEK	skin
5	chr6:114005600-114006600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr6:114005600-114006600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr6:114005600-114006600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr6:114006000-114007000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr6:114006000-114011000	Weak transcription	HSMM	muscle
10	chr6:114006000-114014800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr6:114006000-114015600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr6:114006200-114006600	Weak transcription	Stomach Mucosa	stomach

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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