Variant report

Variant rs17151239
Chromosome Location chr8:10025901-10025902
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:9996600-10036200 Weak transcription Primary T cells from cord blood blood
2 chr8:10003400-10026600 Weak transcription Liver Liver
3 chr8:10016200-10026000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr8:10021400-10029600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr8:10024000-10026000 Enhancers Brain Germinal Matrix brain
6 chr8:10025000-10029200 Enhancers Primary neutrophils fromperipheralblood blood
7 chr8:10025000-10030000 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
8 chr8:10025200-10031200 Weak transcription Brain Angular Gyrus brain
9 chr8:10025400-10030200 Weak transcription Brain Substantia Nigra brain
10 chr8:10025400-10030800 Weak transcription Brain Cingulate Gyrus brain
11 chr8:10025600-10026600 Weak transcription Fetal Brain Male brain
12 chr8:10025600-10027600 Weak transcription Cortex derived primary cultured neurospheres brain
13 chr8:10025600-10029600 Weak transcription Fetal Brain Female brain
14 chr8:10025600-10030800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
15 chr8:10025800-10026400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
16 chr8:10025800-10026400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
17 chr8:10025800-10026400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr8:10025800-10026600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
19 chr8:10025800-10027000 Enhancers Fetal Intestine Large intestine
20 chr8:10025800-10027000 Enhancers Fetal Intestine Small intestine

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