Variant report

Variant	rs28392558
Chromosome Location	chr12:103890884-103890885
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:103890000-103893200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:103890200-103891000	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr12:103890200-103891600	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr12:103890200-103893000	Weak transcription	GM12878-XiMat	blood
5	chr12:103890200-103893200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr12:103890200-103893200	Weak transcription	NHEK	skin
7	chr12:103890200-103894000	Weak transcription	Fetal Brain Female	brain
8	chr12:103890200-103894200	Weak transcription	Brain Germinal Matrix	brain
9	chr12:103890400-103891200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr12:103890400-103891200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr12:103890400-103893200	Weak transcription	HMEC	breast
12	chr12:103890400-103895800	Weak transcription	Thymus	Thymus
13	chr12:103890600-103891000	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr12:103890600-103891000	Weak transcription	A549	lung

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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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