Variant report

Variant rs568803624
Chromosome Location chr20:14940848-14940849
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:14932200-14947600 Weak transcription H9 Cell Line embryonic stem cell
2 chr20:14933000-14944200 Weak transcription ES-WA7 Cell Line embryonic stem cell
3 chr20:14934000-14943400 Weak transcription HUVEC blood vessel
4 chr20:14936000-14941200 Enhancers Hela-S3 cervix
5 chr20:14936600-14944000 Weak transcription HUES48 Cell Line embryonic stem cell
6 chr20:14937000-14943600 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr20:14937000-14943800 Weak transcription HUES64 Cell Line embryonic stem cell
8 chr20:14937000-14943800 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr20:14938200-14943800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr20:14938200-14944000 Weak transcription iPS-18 Cell Line embryonic stem cell
11 chr20:14938600-14941400 Enhancers HMEC breast
12 chr20:14939000-14941200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr20:14939000-14941200 Enhancers NHEK skin
14 chr20:14939200-14941200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr20:14940000-14941000 Enhancers Esophagus oesophagus
16 chr20:14940200-14941000 Enhancers HepG2 liver
17 chr20:14940400-14941400 Enhancers A549 lung
18 chr20:14940800-14943200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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