Variant report

Variant rs2541956
Chromosome Location chr22:21388605-21388606
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:21386800-21391600 Weak transcription HMEC breast
2 chr22:21386800-21391600 Weak transcription NHDF-Ad bronchial
3 chr22:21386800-21391800 Weak transcription HSMM muscle
4 chr22:21386800-21399400 Weak transcription Gastric stomach
5 chr22:21387200-21392800 Weak transcription Right Atrium heart
6 chr22:21387200-21397400 Weak transcription Duodenum Mucosa Duodenum
7 chr22:21387200-21398200 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
8 chr22:21387200-21398600 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
9 chr22:21387600-21390800 Enhancers GM12878-XiMat blood
10 chr22:21387600-21391800 Weak transcription HSMMtube muscle
11 chr22:21387600-21392000 Weak transcription Skeletal Muscle Female skeletal muscle
12 chr22:21388000-21391200 Weak transcription NHLF lung
13 chr22:21388000-21391600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr22:21388000-21391800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr22:21388200-21391400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr22:21388200-21391600 Weak transcription Fetal Intestine Large intestine
17 chr22:21388200-21391800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
18 chr22:21388400-21391800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
19 chr22:21388600-21390800 Weak transcription Placenta Placenta
20 chr22:21388600-21391600 Weak transcription Osteobl bone
21 chr22:21388600-21391800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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