Variant report

Variant	rs1432770
Chromosome Location	chr5:145302666-145302667
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:145297200-145309200	Weak transcription	Pancreas	Pancrea
2	chr5:145297400-145304600	Weak transcription	Aorta	Aorta
3	chr5:145298000-145303600	Weak transcription	Osteobl	bone
4	chr5:145299200-145304600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr5:145299200-145305200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr5:145299400-145303000	Enhancers	HMEC	breast
7	chr5:145299400-145303800	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr5:145299400-145304400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:145299400-145304400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr5:145299400-145304400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr5:145299600-145306000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr5:145300800-145304200	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr5:145301000-145303600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr5:145301200-145303000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr5:145301200-145304000	Weak transcription	NH-A	brain
16	chr5:145301800-145304200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr5:145302200-145303200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr5:145302600-145303600	Weak transcription	NHEK	skin
19	chr5:145302600-145311800	Weak transcription	Esophagus	oesophagus

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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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