Variant report

Variant rs7960437
Chromosome Location chr12:31383292-31383293
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31373400-31386400 Enhancers Fetal Muscle Leg muscle
2 chr12:31376800-31384400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr12:31378600-31387600 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
4 chr12:31379200-31383600 Enhancers Adipose Nuclei Adipose
5 chr12:31381000-31384000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr12:31381800-31383600 Enhancers Fetal Intestine Small intestine
7 chr12:31382200-31384600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr12:31382200-31388000 Weak transcription Gastric stomach
9 chr12:31382600-31383400 Enhancers Fetal Muscle Trunk muscle
10 chr12:31382800-31385000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr12:31382800-31386200 Weak transcription Esophagus oesophagus
12 chr12:31382800-31388200 Weak transcription Liver Liver
13 chr12:31383000-31387800 Weak transcription Rectal Mucosa Donor 31 rectum
14 chr12:31383000-31388000 Weak transcription Stomach Mucosa stomach
15 chr12:31383000-31388400 Weak transcription A549 lung
16 chr12:31383200-31384400 Weak transcription Fetal Intestine Large intestine
17 chr12:31383200-31388000 Weak transcription Duodenum Mucosa Duodenum
18 chr12:31383200-31388000 Weak transcription Pancreas Pancrea
19 chr12:31383200-31388400 Weak transcription Psoas Muscle Psoas

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