Variant report

Variant rs2387671
Chromosome Location chr10:1454993-1454994
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:1443600-1456000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr10:1451200-1455200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr10:1451600-1455400 Enhancers Dnd41 blood
4 chr10:1451800-1461600 Weak transcription Gastric stomach
5 chr10:1453800-1455200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr10:1454000-1455000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr10:1454000-1456000 Enhancers Primary B cells from cord blood blood
8 chr10:1454200-1455200 Enhancers Primary B cells from peripheral blood blood
9 chr10:1454200-1455400 Enhancers Primary hematopoietic stem cells blood
10 chr10:1454400-1455200 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr10:1454800-1455600 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell

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