Variant report

Variant	rs12211587
Chromosome Location	chr6:150513642-150513643
allele	C/T
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	chr6:150499600-150519600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr6:150506600-150515600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr6:150508400-150517000	Weak transcription	K562	blood
4	chr6:150510600-150518000	Weak transcription	Psoas Muscle	Psoas
5	chr6:150510800-150514800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:150511000-150513800	Enhancers	NHEK	skin
7	chr6:150511200-150513800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr6:150512000-150514000	Enhancers	HMEC	breast
9	chr6:150512200-150513800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr6:150512400-150514000	Weak transcription	Left Ventricle	heart
11	chr6:150512600-150514600	Weak transcription	Right Atrium	heart
12	chr6:150512800-150514000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr6:150513200-150513800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr6:150513400-150514200	Weak transcription	Fetal Heart	heart
15	chr6:150513600-150517200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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