Variant report

Variant rs1185985
Chromosome Location chr12:104257772-104257773
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:104250000-104263800 Weak transcription Liver Liver
2 chr12:104253600-104261600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr12:104254000-104258600 Weak transcription HSMMtube muscle
4 chr12:104254400-104257800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr12:104254400-104258000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr12:104254400-104258000 Weak transcription NHEK skin
7 chr12:104254400-104258600 Weak transcription HSMM muscle
8 chr12:104254400-104258800 Weak transcription Muscle Satellite Cultured Cells --
9 chr12:104254800-104278200 Weak transcription Aorta Aorta
10 chr12:104255000-104257800 Weak transcription HMEC breast
11 chr12:104255000-104259200 Weak transcription Osteobl bone
12 chr12:104255200-104257800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr12:104255600-104258000 Enhancers Rectal Smooth Muscle rectum
14 chr12:104255600-104262200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr12:104256200-104257800 Weak transcription Breast Myoepithelial Primary Cells Breast
16 chr12:104256800-104258200 Enhancers Stomach Smooth Muscle stomach
17 chr12:104257000-104258000 Enhancers Pancreas Pancrea
18 chr12:104257000-104259200 Enhancers HepG2 liver
19 chr12:104257200-104259200 Enhancers Placenta Placenta
20 chr12:104257400-104257800 Active TSS Colon Smooth Muscle Colon
21 chr12:104257600-104259200 Enhancers Esophagus oesophagus

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