Variant report

Variant rs2029298
Chromosome Location chr11:47234718-47234719
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:24 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:47226400-47235800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr11:47227200-47235600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr11:47231600-47235200 Weak transcription Fetal Adrenal Gland Adrenal Gland
4 chr11:47232000-47235800 Weak transcription HMEC breast
5 chr11:47232400-47235400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr11:47232400-47235600 Weak transcription NHEK skin
7 chr11:47233000-47235400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr11:47234400-47234800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr11:47234400-47234800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr11:47234400-47235200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr11:47234400-47235400 Enhancers HepG2 liver
12 chr11:47234400-47235600 Enhancers Breast Myoepithelial Primary Cells Breast
13 chr11:47234400-47235800 Enhancers Placenta Placenta
14 chr11:47234600-47234800 Enhancers H1 Cell Line embryonic stem cell
15 chr11:47234600-47234800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr11:47234600-47234800 Enhancers Liver Liver
17 chr11:47234600-47234800 Enhancers Duodenum Mucosa Duodenum
18 chr11:47234600-47234800 Enhancers Gastric stomach
19 chr11:47234600-47235200 Weak transcription Fetal Intestine Small intestine
20 chr11:47234600-47235400 Enhancers Dnd41 blood
21 chr11:47234600-47235600 Enhancers Esophagus oesophagus
22 chr11:47234600-47235600 Weak transcription Osteobl bone
23 chr11:47234600-47235800 Enhancers Spleen Spleen
24 chr11:47234600-47235800 Weak transcription NH-A brain

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