Variant report

Variant rs13128319
Chromosome Location chr4:76975206-76975207
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:76965000-76977400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr4:76974600-76975600 Enhancers HUES64 Cell Line embryonic stem cell
3 chr4:76974600-76976000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr4:76974800-76975400 Bivalent Enhancer H9 Derived Neuron Cultured Cells ES cell derived
5 chr4:76974800-76975600 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr4:76974800-76975600 Enhancers HUES6 Cell Line embryonic stem cell
7 chr4:76974800-76975600 Enhancers iPS-20b Cell Line embryonic stem cell
8 chr4:76974800-76975600 Enhancers Cortex derived primary cultured neurospheres brain
9 chr4:76974800-76975800 Enhancers iPS-15b Cell Line embryonic stem cell
10 chr4:76975000-76975400 Enhancers ES-WA7 Cell Line embryonic stem cell
11 chr4:76975000-76975400 Enhancers H1 Cell Line embryonic stem cell
12 chr4:76975000-76975400 Flanking Active TSS Ganglion Eminence derived primary cultured neurospheres brain
13 chr4:76975000-76975400 Enhancers HMEC breast
14 chr4:76975000-76975600 Enhancers HUES48 Cell Line embryonic stem cell
15 chr4:76975000-76975600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr4:76975000-76975600 Enhancers Primary monocytes fromperipheralblood blood
17 chr4:76975000-76975800 Weak transcription Fetal Intestine Small intestine
18 chr4:76975000-76976200 Enhancers Fetal Intestine Large intestine
19 chr4:76975200-76975400 Enhancers Brain Cingulate Gyrus brain
20 chr4:76975200-76976400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
21 chr4:76975200-76976400 Weak transcription iPS-18 Cell Line embryonic stem cell

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