Variant report

Variant	rs6897206
Chromosome Location	chr5:68144143-68144144
allele	A/G
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	chr5:68143400-68144200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr5:68143400-68144600	Enhancers	HSMM	muscle
3	chr5:68143400-68144800	Enhancers	Placenta Amnion	Placenta Amnion
4	chr5:68143400-68145000	Enhancers	HMEC	breast
5	chr5:68143400-68145200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr5:68143400-68145600	Enhancers	HSMMtube	muscle
7	chr5:68143600-68144200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:68143600-68144200	Enhancers	Adipose Nuclei	Adipose
9	chr5:68143600-68144200	Enhancers	Right Atrium	heart
10	chr5:68143600-68146000	Enhancers	NHDF-Ad	bronchial
11	chr5:68143800-68144400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr5:68143800-68145000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr5:68143800-68145000	Enhancers	Left Ventricle	heart
14	chr5:68143800-68146000	Enhancers	Breast Myoepithelial Primary Cells	Breast

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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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