Variant report

Variant	rs10748346
Chromosome Location	chr12:43357064-43357065
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:43351400-43357800	Enhancers	Muscle Satellite Cultured Cells	--
2	chr12:43351400-43357800	Enhancers	HUVEC	blood vessel
3	chr12:43351800-43359600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr12:43354000-43359800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:43354400-43357800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr12:43355400-43357200	Enhancers	A549	lung
7	chr12:43355600-43369000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr12:43356200-43360000	Enhancers	Fetal Lung	lung
9	chr12:43356600-43357400	Weak transcription	HSMM	muscle
10	chr12:43356800-43359200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr12:43357000-43357400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr12:43357000-43359600	Weak transcription	HMEC	breast
13	chr12:43357000-43359600	Weak transcription	NHEK	skin
14	chr12:43357000-43362600	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr12:43357000-43362600	Weak transcription	Hela-S3	cervix

Quick Search:

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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