Variant report

Variant rs4713036
Chromosome Location chr6:26756924-26756925
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:26747600-26757400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr6:26756000-26757200 Weak transcription HMEC breast
3 chr6:26756200-26757200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr6:26756400-26758800 Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
5 chr6:26756600-26757200 Enhancers K562 blood
6 chr6:26756600-26758200 Bivalent/Poised TSS H9 Derived Neuron Cultured Cells ES cell derived
7 chr6:26756600-26759000 Bivalent/Poised TSS HUES64 Cell Line embryonic stem cell
8 chr6:26756800-26757200 ZNF genes & repeats H9 Cell Line embryonic stem cell
9 chr6:26756800-26757200 Flanking Bivalent TSS/Enh HUES6 Cell Line embryonic stem cell
10 chr6:26756800-26757200 Flanking Bivalent TSS/Enh iPS-15b Cell Line embryonic stem cell
11 chr6:26756800-26757200 Bivalent/Poised TSS Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr6:26756800-26757600 Bivalent/Poised TSS H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr6:26756800-26757800 Bivalent/Poised TSS ES-I3 Cell Line embryonic stem cell
14 chr6:26756800-26758000 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin01 Skin
15 chr6:26756800-26758200 Bivalent/Poised TSS HUES48 Cell Line embryonic stem cell
16 chr6:26756800-26758600 Bivalent/Poised TSS Fetal Brain Female brain

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