Variant report

Variant	rs74090266
Chromosome Location	chr1:71553116-71553117
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71547600-71555200	Weak transcription	Lung	lung
2	chr1:71547600-71555800	Weak transcription	NHLF	lung
3	chr1:71547800-71554600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:71549600-71555200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:71550800-71553400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr1:71551400-71553200	Enhancers	Muscle Satellite Cultured Cells	--
7	chr1:71552000-71554800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr1:71552000-71555200	Weak transcription	NH-A	brain
9	chr1:71552000-71555600	Weak transcription	HSMMtube	muscle
10	chr1:71552400-71554600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:71552400-71554600	Weak transcription	NHDF-Ad	bronchial
12	chr1:71552400-71555200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr1:71552600-71554400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr1:71552600-71556000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr1:71552800-71554800	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr1:71552800-71555600	Weak transcription	HSMM	muscle
17	chr1:71553000-71554200	Enhancers	Rectal Mucosa Donor 29	rectum
18	chr1:71553000-71555000	Weak transcription	Sigmoid Colon	Sigmoid Colon

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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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