Variant report

Variant rs17153139
Chromosome Location chr8:8374037-8374038
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:8364400-8374400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr8:8366200-8374400 Weak transcription Brain Germinal Matrix brain
3 chr8:8367200-8375400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
4 chr8:8370400-8374200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr8:8373000-8374200 Weak transcription Placenta Placenta
6 chr8:8373000-8374200 Weak transcription HMEC breast
7 chr8:8373200-8374400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr8:8373400-8374600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr8:8373600-8375000 Enhancers HSMMtube muscle
10 chr8:8373800-8374800 Enhancers Fetal Kidney kidney
11 chr8:8373800-8375000 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr8:8373800-8376000 Enhancers Breast Myoepithelial Primary Cells Breast
13 chr8:8374000-8374600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
14 chr8:8374000-8374800 Enhancers Fetal Muscle Leg muscle
15 chr8:8374000-8374800 Enhancers Placenta Amnion Placenta Amnion
16 chr8:8374000-8375000 Enhancers Esophagus oesophagus
17 chr8:8374000-8382800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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