Variant report

Variant rs7684996
Chromosome Location chr4:174012452-174012453
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:174000000-174012600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr4:174006000-174012600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr4:174007600-174020400 Weak transcription Stomach Mucosa stomach
4 chr4:174008400-174012600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
5 chr4:174011800-174012600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
6 chr4:174012200-174016800 Enhancers iPS-15b Cell Line embryonic stem cell
7 chr4:174012400-174012800 Enhancers Fetal Brain Male brain
8 chr4:174012400-174013000 Enhancers HUES6 Cell Line embryonic stem cell
9 chr4:174012400-174013000 Enhancers Brain Germinal Matrix brain
10 chr4:174012400-174013400 Enhancers HUES64 Cell Line embryonic stem cell
11 chr4:174012400-174013600 Enhancers Cortex derived primary cultured neurospheres brain
12 chr4:174012400-174013600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
13 chr4:174012400-174014200 Enhancers K562 blood

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