Variant report

Variant rs10843918
Chromosome Location chr12:31386971-31386972
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 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 chr12:31385200-31387000 Weak transcription Fetal Intestine Large intestine
12 chr12:31385400-31387200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
13 chr12:31385400-31388400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr12:31385800-31388800 Enhancers Adipose Nuclei Adipose
15 chr12:31386200-31390200 Bivalent Enhancer Fetal Muscle Trunk muscle
16 chr12:31386400-31387000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr12:31386400-31387200 Bivalent Enhancer Fetal Muscle Leg muscle
18 chr12:31386400-31387200 Bivalent Enhancer HSMMtube muscle
19 chr12:31386600-31387000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
20 chr12:31386600-31387600 Weak transcription Brain Germinal Matrix brain
21 chr12:31386800-31388000 Weak transcription Esophagus oesophagus

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