Variant report

Variant rs7970136
Chromosome Location chr12:38531951-38531952
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:38529400-38532200 Weak transcription Hela-S3 cervix
2 chr12:38530600-38533000 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
3 chr12:38531400-38532200 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
4 chr12:38531600-38532000 Bivalent/Poised TSS ES-I3 Cell Line embryonic stem cell
5 chr12:38531600-38532000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
6 chr12:38531600-38532000 Bivalent Enhancer Stomach Mucosa stomach
7 chr12:38531600-38532200 Enhancers Colon Smooth Muscle Colon
8 chr12:38531600-38532600 Active TSS Gastric stomach
9 chr12:38531600-38533000 Active TSS Thymus Thymus
10 chr12:38531800-38532000 Enhancers Primary hematopoietic stem cells blood
11 chr12:38531800-38532000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
12 chr12:38531800-38532000 Active TSS Brain Germinal Matrix brain
13 chr12:38531800-38532000 Flanking Active TSS A549 lung
14 chr12:38531800-38532200 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
15 chr12:38531800-38532400 Flanking Active TSS Breast Myoepithelial Primary Cells Breast
16 chr12:38531800-38532400 Enhancers Spleen Spleen
17 chr12:38531800-38532600 Flanking Bivalent TSS/Enh Primary hematopoietic stem cells G-CSF-mobilized Male --
18 chr12:38531800-38532600 Flanking Active TSS Pancreas Pancrea
19 chr12:38531800-38533000 Active TSS HUES6 Cell Line embryonic stem cell
20 chr12:38531800-38533200 Active TSS Pancreatic Islets Pancreatic Islet
21 chr12:38531800-38533200 Active TSS HMEC breast

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