Variant report

Variant rs539139763
Chromosome Location chr7:97502856-97502857
allele -/CAAA
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:97501800-97503000 Weak transcription Esophagus oesophagus
2 chr7:97501800-97503200 Enhancers Spleen Spleen
3 chr7:97502000-97503200 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr7:97502200-97503000 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
5 chr7:97502200-97503200 Enhancers HepG2 liver
6 chr7:97502200-97504400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr7:97502400-97503000 Enhancers H9 Cell Line embryonic stem cell
8 chr7:97502400-97503200 Bivalent Enhancer HUES64 Cell Line embryonic stem cell
9 chr7:97502600-97503000 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
10 chr7:97502800-97503000 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
11 chr7:97502800-97503000 Bivalent Enhancer H1 Cell Line embryonic stem cell
12 chr7:97502800-97503200 Flanking Bivalent TSS/Enh HUES48 Cell Line embryonic stem cell
13 chr7:97502800-97503200 Flanking Bivalent TSS/Enh HUES6 Cell Line embryonic stem cell
14 chr7:97502800-97503200 Flanking Bivalent TSS/Enh iPS-20b Cell Line embryonic stem cell

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