Variant report

Variant rs73738236
Chromosome Location chr6:27197110-27197111
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:27183000-27197200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr6:27193200-27198600 Weak transcription GM12878-XiMat blood
3 chr6:27196200-27199800 Active TSS HUES6 Cell Line embryonic stem cell
4 chr6:27196400-27198600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr6:27196800-27197600 Bivalent/Poised TSS HUES64 Cell Line embryonic stem cell
6 chr6:27196800-27199600 Active TSS HUES48 Cell Line embryonic stem cell
7 chr6:27196800-27200200 Active TSS A549 lung
8 chr6:27197000-27197200 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
9 chr6:27197000-27197200 Bivalent Enhancer HepG2 liver
10 chr6:27197000-27197400 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
11 chr6:27197000-27197400 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
12 chr6:27197000-27198600 Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr6:27197000-27199200 Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr6:27197000-27199400 Active TSS H1 Cell Line embryonic stem cell
15 chr6:27197000-27199600 Active TSS ES-I3 Cell Line embryonic stem cell
16 chr6:27197000-27199600 Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
17 chr6:27197000-27200400 Active TSS K562 blood

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