Variant report

Variant rs3783581
Chromosome Location chr2:113537151-113537152
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:113522800-113541600 Weak transcription ES-WA7 Cell Line embryonic stem cell
2 chr2:113523400-113539200 Weak transcription Hela-S3 cervix
3 chr2:113526800-113537800 Weak transcription NHDF-Ad bronchial
4 chr2:113530200-113541200 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr2:113530400-113538600 Weak transcription K562 blood
6 chr2:113534000-113538800 Weak transcription GM12878-XiMat blood
7 chr2:113534000-113551800 Weak transcription Fetal Heart heart
8 chr2:113534800-113537600 Genic enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr2:113535400-113540200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr2:113535400-113540400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr2:113535400-113540800 Weak transcription Primary hematopoietic stem cells short term culture blood
12 chr2:113535600-113540800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr2:113535600-113541200 Weak transcription HUES6 Cell Line embryonic stem cell
14 chr2:113535800-113538200 Strong transcription HMEC breast
15 chr2:113536600-113538200 Transcr. at gene 5' and 3' NHEK skin
16 chr2:113536600-113541600 Transcr. at gene 5' and 3' Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr2:113537000-113537600 Genic enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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