Variant report

Variant rs13165022
Chromosome Location chr5:180086560-180086561
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:180085800-180086600 Bivalent/Poised TSS ES-I3 Cell Line embryonic stem cell
2 chr5:180085800-180086600 Bivalent/Poised TSS H1 Cell Line embryonic stem cell
3 chr5:180085800-180086600 Bivalent Enhancer H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr5:180085800-180086600 Bivalent/Poised TSS HUES6 Cell Line embryonic stem cell
5 chr5:180085800-180086600 Bivalent/Poised TSS HUES64 Cell Line embryonic stem cell
6 chr5:180085800-180086600 Bivalent/Poised TSS iPS-20b Cell Line embryonic stem cell
7 chr5:180085800-180086600 Bivalent Enhancer Primary T cells fromperipheralblood blood
8 chr5:180086200-180086600 Flanking Active TSS iPS DF 19.11 Cell Line embryonic stem cell
9 chr5:180086200-180086600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
10 chr5:180086200-180086800 Bivalent/Poised TSS iPS-18 Cell Line embryonic stem cell
11 chr5:180086200-180100400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
12 chr5:180086400-180086600 Bivalent Enhancer Cortex derived primary cultured neurospheres brain
13 chr5:180086400-180086600 Bivalent Enhancer Fetal Thymus thymus

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