Variant report

Variant	rs4869661
Chromosome Location	chr5:36425194-36425195
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	chr5:36419800-36430200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:36422800-36432000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr5:36423800-36425400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr5:36423800-36425600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr5:36424000-36425400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr5:36424000-36425800	Enhancers	Hela-S3	cervix
7	chr5:36424200-36425400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr5:36424400-36425400	Weak transcription	Primary hematopoietic stem cells short term culture	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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