Variant report

Variant	rs1320344
Chromosome Location	chr12:103887477-103887478
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:103885400-103887800	Enhancers	Thymus	Thymus
2	chr12:103886400-103888200	Enhancers	Fetal Thymus	thymus
3	chr12:103886400-103888800	Enhancers	NHEK	skin
4	chr12:103886400-103889200	Enhancers	HMEC	breast
5	chr12:103886600-103888800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr12:103886800-103887800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr12:103886800-103888000	Enhancers	Dnd41	blood
8	chr12:103887400-103888400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr12:103887400-103889400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	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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