Variant report

Variant	rs491548
Chromosome Location	chr6:44801851-44801852
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	chr6:44791000-44805600	Weak transcription	Ovary	ovary
2	chr6:44792000-44811600	Weak transcription	Pancreas	Pancrea
3	chr6:44798200-44811200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr6:44798400-44822800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr6:44798600-44810600	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr6:44799000-44802600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr6:44799200-44802000	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr6:44799200-44806000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr6:44799800-44803000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr6:44800000-44804800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr6:44800400-44802000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr6:44801400-44802600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr6:44801800-44802600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr6:44801800-44802800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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