Variant report

Variant rs6556987
Chromosome Location chr5:96880511-96880512
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:96870600-96881200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
2 chr5:96878800-96882800 Weak transcription Fetal Intestine Large intestine
3 chr5:96879600-96880800 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr5:96879600-96882000 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr5:96879800-96880800 Weak transcription Fetal Muscle Leg muscle
6 chr5:96880000-96882000 Enhancers HUES6 Cell Line embryonic stem cell
7 chr5:96880200-96880600 Flanking Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
8 chr5:96880200-96880600 Active TSS NHDF-Ad bronchial
9 chr5:96880200-96880600 Active TSS Osteobl bone
10 chr5:96880200-96882200 Enhancers HUES48 Cell Line embryonic stem cell
11 chr5:96880200-96883000 Weak transcription Duodenum Mucosa Duodenum
12 chr5:96880400-96881000 Enhancers iPS-20b Cell Line embryonic stem cell
13 chr5:96880400-96881200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr5:96880400-96882400 Enhancers HUES64 Cell Line embryonic stem cell
15 chr5:96880400-96886000 Enhancers Fetal Intestine Small intestine

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