Variant report

Variant	rs34966125
Chromosome Location	chr6:15968728-15968729
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15963200-15969000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:15963200-15969000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr6:15963600-15969000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:15966000-15971200	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr6:15968400-15970800	Enhancers	Placenta	Placenta
6	chr6:15968400-15971000	Enhancers	HMEC	breast
7	chr6:15968600-15970600	Enhancers	NHEK	skin
8	chr6:15968600-15971000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:15968600-15971000	Enhancers	K562	blood

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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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