Variant report

Variant rs556459874
Chromosome Location chr4:187059992-187059993
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:187039200-187065000 Weak transcription Fetal Brain Female brain
2 chr4:187047200-187063200 Weak transcription Fetal Stomach stomach
3 chr4:187050600-187065000 Weak transcription Gastric stomach
4 chr4:187054200-187065000 Weak transcription Fetal Kidney kidney
5 chr4:187054400-187065000 Weak transcription Fetal Intestine Small intestine
6 chr4:187055000-187065000 Weak transcription Fetal Intestine Large intestine
7 chr4:187058600-187065200 Weak transcription Pancreas Pancrea
8 chr4:187058800-187064800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr4:187058800-187064800 Weak transcription Stomach Smooth Muscle stomach
10 chr4:187058800-187065000 Weak transcription Adipose Nuclei Adipose
11 chr4:187058800-187065000 Weak transcription Liver Liver
12 chr4:187058800-187065200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr4:187058800-187065200 Weak transcription Rectal Mucosa Donor 31 rectum
14 chr4:187059800-187060000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
15 chr4:187059800-187060200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived

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