Variant report

Variant rs2881754
Chromosome Location chr7:7191181-7191182
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:7188800-7196400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
2 chr7:7188800-7196400 Weak transcription Placenta Amnion Placenta Amnion
3 chr7:7189000-7195800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr7:7189000-7196800 Weak transcription Duodenum Mucosa Duodenum
5 chr7:7189200-7199600 Weak transcription K562 blood
6 chr7:7189400-7191200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr7:7189600-7191800 Weak transcription Placenta Placenta
8 chr7:7189600-7196400 Weak transcription Stomach Mucosa stomach
9 chr7:7190000-7191800 Enhancers Primary T helper memory cells from peripheral blood 1 blood
10 chr7:7190200-7191400 Enhancers HepG2 liver
11 chr7:7190600-7192200 Enhancers Primary T helper cells fromperipheralblood blood
12 chr7:7190800-7193000 Weak transcription Fetal Intestine Large intestine
13 chr7:7190800-7193200 Weak transcription Fetal Intestine Small intestine
14 chr7:7191000-7191600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
15 chr7:7191000-7191800 Enhancers Thymus Thymus
16 chr7:7191000-7192000 Enhancers Primary monocytes fromperipheralblood blood
17 chr7:7191000-7192000 Enhancers Primary T helper cells PMA-I stimulated --
18 chr7:7191000-7192200 Enhancers Primary T cells fromperipheralblood blood
19 chr7:7191000-7192400 Enhancers Primary T helper naive cells fromperipheralblood blood

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