Variant report

Variant	rs12273170
Chromosome Location	chr11:8001313-8001314
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:7997000-8008200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:7997000-8008800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr11:7999200-8007600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:8000200-8007000	Weak transcription	Osteobl	bone
5	chr11:8000200-8007600	Weak transcription	HMEC	breast
6	chr11:8000400-8002800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr11:8000400-8004800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr11:8000400-8005200	Weak transcription	HSMMtube	muscle
9	chr11:8000400-8006400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr11:8000400-8006600	Weak transcription	HSMM	muscle
11	chr11:8000400-8007000	Weak transcription	NHLF	lung
12	chr11:8000400-8007400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr11:8000400-8007600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr11:8000600-8007000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr11:8000600-8008200	Weak transcription	Lung	lung
16	chr11:8000800-8007600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr11:8001000-8006800	Weak transcription	HUVEC	blood vessel

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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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