Variant report

Variant rs73298542
Chromosome Location chr12:31387115-31387116
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31378600-31387600 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
2 chr12:31382200-31388000 Weak transcription Gastric stomach
3 chr12:31382800-31388200 Weak transcription Liver Liver
4 chr12:31383000-31387800 Weak transcription Rectal Mucosa Donor 31 rectum
5 chr12:31383000-31388000 Weak transcription Stomach Mucosa stomach
6 chr12:31383000-31388400 Weak transcription A549 lung
7 chr12:31383200-31388000 Weak transcription Duodenum Mucosa Duodenum
8 chr12:31383200-31388000 Weak transcription Pancreas Pancrea
9 chr12:31383200-31388400 Weak transcription Psoas Muscle Psoas
10 chr12:31385000-31387600 Weak transcription iPS-15b Cell Line embryonic stem cell
11 chr12:31385400-31387200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
12 chr12:31385400-31388400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
13 chr12:31385800-31388800 Enhancers Adipose Nuclei Adipose
14 chr12:31386200-31390200 Bivalent Enhancer Fetal Muscle Trunk muscle
15 chr12:31386400-31387200 Bivalent Enhancer Fetal Muscle Leg muscle
16 chr12:31386400-31387200 Bivalent Enhancer HSMMtube muscle
17 chr12:31386600-31387600 Weak transcription Brain Germinal Matrix brain
18 chr12:31386800-31388000 Weak transcription Esophagus oesophagus
19 chr12:31387000-31387200 Bivalent Enhancer HSMM muscle
20 chr12:31387000-31388000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
21 chr12:31387000-31388800 Enhancers Cortex derived primary cultured neurospheres brain
22 chr12:31387000-31389200 Enhancers Fetal Intestine Large intestine

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