Variant report

Variant rs73276709
Chromosome Location chr8:103653830-103653831
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:103644800-103659600 Weak transcription Spleen Spleen
2 chr8:103645600-103660000 Weak transcription Placenta Amnion Placenta Amnion
3 chr8:103647000-103661600 Weak transcription Fetal Muscle Trunk muscle
4 chr8:103647000-103662000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr8:103647000-103662000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr8:103648200-103661800 Weak transcription H1 Cell Line embryonic stem cell
7 chr8:103649000-103659800 Weak transcription Primary Natural Killer cells fromperipheralblood blood
8 chr8:103649600-103659800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr8:103649800-103662000 Weak transcription Fetal Stomach stomach
10 chr8:103650000-103659600 Weak transcription Placenta Placenta
11 chr8:103650200-103660000 Weak transcription Colon Smooth Muscle Colon
12 chr8:103652200-103654200 Weak transcription HepG2 liver
13 chr8:103652400-103659600 Weak transcription Duodenum Mucosa Duodenum
14 chr8:103652400-103659800 Weak transcription Rectal Mucosa Donor 31 rectum
15 chr8:103652600-103659600 Weak transcription Fetal Intestine Small intestine
16 chr8:103652600-103659800 Weak transcription Fetal Intestine Large intestine
17 chr8:103653200-103654200 Weak transcription Fetal Brain Male brain
18 chr8:103653800-103654000 ZNF genes & repeats Aorta Aorta
19 chr8:103653800-103654000 Enhancers Gastric stomach

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