Variant report

Variant rs2539005
Chromosome Location chr2:211057100-211057101
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:211046800-211059800 Weak transcription Pancreas Pancrea
2 chr2:211051000-211086600 Weak transcription Adipose Nuclei Adipose
3 chr2:211052200-211085600 Weak transcription Aorta Aorta
4 chr2:211052400-211067400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr2:211053600-211059800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr2:211053800-211059800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr2:211053800-211059800 Weak transcription Fetal Thymus thymus
8 chr2:211053800-211059800 Weak transcription Thymus Thymus
9 chr2:211054600-211059800 Weak transcription Fetal Intestine Small intestine
10 chr2:211054600-211059800 Weak transcription Stomach Mucosa stomach
11 chr2:211054800-211059400 Weak transcription Pancreatic Islets Pancreatic Islet
12 chr2:211054800-211059800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
13 chr2:211055000-211059600 Weak transcription Dnd41 blood
14 chr2:211055000-211059800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr2:211055200-211059800 Weak transcription HepG2 liver
16 chr2:211055400-211060000 Weak transcription Fetal Intestine Large intestine
17 chr2:211056000-211058800 Weak transcription Liver Liver

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