Variant report

Variant rs28698639
Chromosome Location chr4:3805005-3805006
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:3801000-3809400 Weak transcription Right Atrium heart
2 chr4:3802800-3805400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
3 chr4:3803000-3805200 Enhancers iPS-18 Cell Line embryonic stem cell
4 chr4:3803000-3805600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr4:3803400-3805400 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr4:3803400-3809200 Weak transcription iPS-15b Cell Line embryonic stem cell
7 chr4:3803800-3805200 Enhancers ES-WA7 Cell Line embryonic stem cell
8 chr4:3803800-3805200 Enhancers iPS-20b Cell Line embryonic stem cell
9 chr4:3803800-3805600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr4:3804000-3805200 Enhancers HUES6 Cell Line embryonic stem cell
11 chr4:3804000-3805800 Enhancers H1 Cell Line embryonic stem cell
12 chr4:3804000-3806000 Flanking Active TSS HepG2 liver
13 chr4:3804200-3805200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
14 chr4:3804400-3805400 Bivalent Enhancer Fetal Stomach stomach
15 chr4:3804800-3805200 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
16 chr4:3804800-3805600 Bivalent Enhancer Fetal Intestine Small intestine
17 chr4:3805000-3805400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
18 chr4:3805000-3805400 Bivalent Enhancer Placenta Placenta
19 chr4:3805000-3809200 Weak transcription ES-I3 Cell Line embryonic stem cell

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