Variant report

Variant	rs17038157
Chromosome Location	chr4:160330905-160330906
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:160323200-160331000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:160323400-160335800	Weak transcription	Left Ventricle	heart
3	chr4:160330000-160331000	Enhancers	HMEC	breast
4	chr4:160330400-160332200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:160330600-160331000	Enhancers	NH-A	brain
6	chr4:160330600-160331400	Enhancers	NHEK	skin
7	chr4:160330600-160332200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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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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