Variant report

Variant rs12626231
Chromosome Location chr21:46805159-46805160
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:46787600-46806800 Weak transcription Right Atrium heart
2 chr21:46793400-46806400 Weak transcription Esophagus oesophagus
3 chr21:46798200-46807600 Weak transcription H9 Cell Line embryonic stem cell
4 chr21:46800200-46805200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
5 chr21:46800800-46805800 Weak transcription Pancreas Pancrea
6 chr21:46802800-46808800 Bivalent Enhancer Fetal Muscle Trunk muscle
7 chr21:46803200-46807400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr21:46804000-46805400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr21:46804200-46805400 Bivalent Enhancer Fetal Stomach stomach
10 chr21:46804200-46808400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr21:46804400-46805200 Enhancers Fetal Muscle Leg muscle
12 chr21:46804400-46805400 Enhancers K562 blood
13 chr21:46804400-46808800 Enhancers Ovary ovary
14 chr21:46804600-46805200 Strong transcription iPS DF 19.11 Cell Line embryonic stem cell
15 chr21:46804600-46805200 Flanking Active TSS Foreskin Fibroblast Primary Cells skin02 Skin
16 chr21:46804600-46805200 Enhancers Fetal Lung lung
17 chr21:46804600-46805600 Bivalent Enhancer Placenta Placenta
18 chr21:46804800-46806600 Enhancers NHDF-Ad bronchial
19 chr21:46805000-46805800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
20 chr21:46805000-46806000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung

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