Variant report

Variant rs377892
Chromosome Location chr2:33302342-33302343
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:33289600-33308200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr2:33295600-33308800 Weak transcription K562 blood
3 chr2:33295800-33308400 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr2:33296200-33302600 Weak transcription Stomach Mucosa stomach
5 chr2:33296400-33302800 Weak transcription Fetal Stomach stomach
6 chr2:33296400-33310800 Weak transcription Esophagus oesophagus
7 chr2:33296600-33311000 Weak transcription Stomach Smooth Muscle stomach
8 chr2:33296800-33310000 Weak transcription Skeletal Muscle Male skeletal muscle
9 chr2:33297200-33302400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
10 chr2:33297600-33302400 Weak transcription Left Ventricle heart
11 chr2:33297600-33308400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
12 chr2:33298200-33310800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
13 chr2:33298200-33310800 Weak transcription Psoas Muscle Psoas
14 chr2:33298200-33311000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr2:33298400-33303000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr2:33299200-33309400 Weak transcription HUVEC blood vessel
17 chr2:33302000-33303400 Enhancers Aorta Aorta
18 chr2:33302000-33303600 Enhancers Fetal Heart heart
19 chr2:33302000-33312400 Enhancers Primary B cells from cord blood blood
20 chr2:33302200-33303200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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