Variant report

Variant	rs1928638
Chromosome Location	chr6:14057157-14057158
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:14052400-14057200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr6:14054400-14059800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr6:14054600-14058600	Weak transcription	NH-A	brain
4	chr6:14054600-14059200	Weak transcription	NHEK	skin
5	chr6:14056200-14059600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr6:14056200-14059800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr6:14056600-14058400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:14057000-14057200	Enhancers	NHDF-Ad	bronchial

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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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