Variant report

Variant	rs34995680
Chromosome Location	chr4:81204217-81204218
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	chr4:81190200-81207600	Weak transcription	HSMMtube	muscle
2	chr4:81190600-81223800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:81193000-81206200	Weak transcription	Fetal Heart	heart
4	chr4:81196800-81211400	Strong transcription	NH-A	brain
5	chr4:81198400-81204600	Genic enhancers	Osteobl	bone
6	chr4:81198400-81206600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr4:81200000-81216600	Weak transcription	HMEC	breast
8	chr4:81201200-81206400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr4:81201600-81205800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr4:81201800-81206200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr4:81202200-81226200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:81202600-81205200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr4:81202600-81206200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr4:81202600-81206200	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr4:81203200-81207800	Weak transcription	HSMM	muscle
16	chr4:81203800-81205600	Weak transcription	NHLF	lung
17	chr4:81204200-81204400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr4:81204200-81204800	Enhancers	NHDF-Ad	bronchial

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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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