Variant report

Variant	rs10948143
Chromosome Location	chr6:44492647-44492648
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	chr6:44492400-44492800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
2	chr6:44492400-44493000	Enhancers	Thymus	Thymus
3	chr6:44492400-44493200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:44492400-44493200	Enhancers	Dnd41	blood
5	chr6:44492400-44493400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr6:44492400-44496600	Enhancers	Fetal Thymus	thymus
7	chr6:44492400-44509800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr6:44492600-44492800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
9	chr6:44492600-44492800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr6:44492600-44493200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
11	chr6:44492600-44493400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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