Variant report

Variant	rs60712953
Chromosome Location	chr6:44756869-44756870
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44755000-44757200	Enhancers	Primary T helper cells fromperipheralblood	blood
2	chr6:44755600-44757200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:44755800-44757400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr6:44756000-44757000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:44756000-44757200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr6:44756000-44757200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr6:44756200-44761600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr6:44756400-44757000	Enhancers	NHLF	lung
9	chr6:44756400-44759200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr6:44756600-44757000	Enhancers	Osteobl	bone

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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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