Variant report

Variant rs73080681
Chromosome Location chr4:3809812-3809813
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:3805600-3810000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr4:3807400-3811800 Weak transcription HepG2 liver
3 chr4:3808000-3810800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr4:3808800-3810000 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
5 chr4:3809200-3810200 Enhancers iPS-15b Cell Line embryonic stem cell
6 chr4:3809200-3810600 Enhancers HUES48 Cell Line embryonic stem cell
7 chr4:3809400-3810000 Enhancers HUES6 Cell Line embryonic stem cell
8 chr4:3809400-3810200 Bivalent Enhancer HUES64 Cell Line embryonic stem cell
9 chr4:3809400-3810200 Enhancers Fetal Brain Male brain
10 chr4:3809400-3810600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr4:3809600-3810000 Enhancers H1 Cell Line embryonic stem cell
12 chr4:3809600-3810000 Enhancers Brain Germinal Matrix brain
13 chr4:3809600-3810600 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
14 chr4:3809600-3810600 Bivalent Enhancer iPS-20b Cell Line embryonic stem cell
15 chr4:3809800-3810000 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
16 chr4:3809800-3810000 Flanking Bivalent TSS/Enh iPS-18 Cell Line embryonic stem cell

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