Variant report

Variant rs2271761
Chromosome Location chr2:180311444-180311445
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:180307400-180312800 Enhancers NHEK skin
2 chr2:180307800-180320800 Weak transcription HepG2 liver
3 chr2:180308200-180332600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr2:180309200-180352200 Weak transcription Skeletal Muscle Male skeletal muscle
5 chr2:180309400-180312200 Weak transcription Fetal Brain Female brain
6 chr2:180310200-180312200 Weak transcription HUES48 Cell Line embryonic stem cell
7 chr2:180310200-180312200 Weak transcription iPS-18 Cell Line embryonic stem cell
8 chr2:180310200-180312400 Weak transcription HUES6 Cell Line embryonic stem cell
9 chr2:180310400-180312200 Weak transcription HUES64 Cell Line embryonic stem cell
10 chr2:180311000-180312600 Enhancers iPS-15b Cell Line embryonic stem cell
11 chr2:180311000-180312600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr2:180311200-180311800 Enhancers Placenta Amnion Placenta Amnion
13 chr2:180311200-180312400 Enhancers Fetal Intestine Small intestine
14 chr2:180311200-180312400 Enhancers HMEC breast
15 chr2:180311200-180312600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
16 chr2:180311200-180312800 Enhancers Cortex derived primary cultured neurospheres brain
17 chr2:180311200-180312800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr2:180311400-180311800 Weak transcription Fetal Intestine Large intestine
19 chr2:180311400-180312400 Weak transcription iPS-20b Cell Line embryonic stem cell
20 chr2:180311400-180312600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
21 chr2:180311400-180319200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
22 chr2:180311400-180322200 Weak transcription Liver Liver

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