Variant report

Variant	rs6542174
Chromosome Location	chr2:114570255-114570256
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	chr2:114567400-114576000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr2:114568200-114586000	Weak transcription	Primary T cells from cord blood	blood
3	chr2:114568600-114570600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr2:114569800-114570400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr2:114570000-114572600	Weak transcription	Right Ventricle	heart
6	chr2:114570000-114575800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:114570200-114571000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:114570200-114575400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr2:114570200-114575400	Weak transcription	A549	lung
10	chr2:114570200-114575400	Weak transcription	NHDF-Ad	bronchial
11	chr2:114570200-114575600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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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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