Variant report

Variant rs11080970
Chromosome Location chr18:272535-272536
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:269000-272600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr18:269200-272600 Weak transcription H9 Cell Line embryonic stem cell
3 chr18:269200-275600 Weak transcription Right Atrium heart
4 chr18:269200-276200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr18:269800-273200 Weak transcription Stomach Smooth Muscle stomach
6 chr18:269800-273400 Weak transcription GM12878-XiMat blood
7 chr18:270000-272600 Weak transcription HUES64 Cell Line embryonic stem cell
8 chr18:270000-275000 Weak transcription Primary monocytes fromperipheralblood blood
9 chr18:270200-272600 Weak transcription H1 Cell Line embryonic stem cell
10 chr18:271400-273000 Enhancers K562 blood
11 chr18:271800-272800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr18:271800-273000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr18:272000-272800 Enhancers iPS-20b Cell Line embryonic stem cell
14 chr18:272200-273000 Enhancers ES-I3 Cell Line embryonic stem cell
15 chr18:272200-273000 Enhancers HUES48 Cell Line embryonic stem cell
16 chr18:272400-272600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
17 chr18:272400-273000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr18:272400-273000 Genic enhancers NHEK skin
19 chr18:272400-273200 Enhancers HMEC breast

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