Variant report

Variant	rs3997666
Chromosome Location	chr8:130378681-130378682
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130369400-130383800	Strong transcription	K562	blood
2	chr8:130375400-130379400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:130375600-130379600	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr8:130377400-130383800	Enhancers	Dnd41	blood
5	chr8:130378200-130378800	Enhancers	Thymus	Thymus
6	chr8:130378200-130379800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr8:130378200-130380000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr8:130378200-130380200	Enhancers	NHEK	skin
9	chr8:130378200-130380400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr8:130378200-130381000	Enhancers	HMEC	breast
11	chr8:130378200-130381600	Genic enhancers	Fetal Thymus	thymus
12	chr8:130378600-130379800	Enhancers	Muscle Satellite Cultured Cells	--

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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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