Variant report

Variant rs4373556
Chromosome Location chr8:11821333-11821334
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:11813800-11823600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr8:11813800-11824600 Weak transcription Pancreas Pancrea
3 chr8:11814200-11821400 Weak transcription Rectal Smooth Muscle rectum
4 chr8:11815200-11823000 Weak transcription Monocytes-CD14+_RO01746 blood
5 chr8:11815400-11821600 Weak transcription Primary monocytes fromperipheralblood blood
6 chr8:11820200-11822400 Enhancers Fetal Stomach stomach
7 chr8:11820600-11821800 Bivalent Enhancer Fetal Muscle Trunk muscle
8 chr8:11820800-11821600 Enhancers Stomach Smooth Muscle stomach
9 chr8:11821000-11821400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
10 chr8:11821000-11822000 Enhancers ES-I3 Cell Line embryonic stem cell
11 chr8:11821200-11821600 Bivalent Enhancer Adipose Nuclei Adipose
12 chr8:11821200-11821800 Enhancers HUES6 Cell Line embryonic stem cell
13 chr8:11821200-11821800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
14 chr8:11821200-11821800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
15 chr8:11821200-11821800 Enhancers Ovary ovary
16 chr8:11821200-11822000 Enhancers Brain Germinal Matrix brain
17 chr8:11821200-11822200 Enhancers ES-WA7 Cell Line embryonic stem cell
18 chr8:11821200-11823800 Enhancers Fetal Adrenal Gland Adrenal Gland

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