Variant report

Variant rs66600814
Chromosome Location chr2:212232053-212232054
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:212227200-212232400 Weak transcription H1 Cell Line embryonic stem cell
2 chr2:212230200-212232400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
3 chr2:212230400-212232400 Weak transcription iPS-15b Cell Line embryonic stem cell
4 chr2:212231000-212232200 Weak transcription HUES6 Cell Line embryonic stem cell
5 chr2:212231000-212232400 Weak transcription HUES64 Cell Line embryonic stem cell
6 chr2:212231000-212232600 Weak transcription HUES48 Cell Line embryonic stem cell
7 chr2:212231000-212232600 Weak transcription iPS-18 Cell Line embryonic stem cell
8 chr2:212231800-212232200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr2:212231800-212233000 Enhancers NHEK skin
10 chr2:212231800-212233200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr2:212232000-212232200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr2:212232000-212232600 Enhancers HMEC breast
13 chr2:212232000-212232800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr2:212232000-212233200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr2:212232000-212233200 Enhancers H9 Cell Line embryonic stem cell
16 chr2:212232000-212234400 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

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