Variant report

Variant rs2839012
Chromosome Location chr21:47244758-47244759
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:47217800-47260400 Weak transcription Right Atrium heart
2 chr21:47239400-47247200 Weak transcription Primary T cells from cord blood blood
3 chr21:47240600-47256600 Weak transcription Dnd41 blood
4 chr21:47240800-47244800 Weak transcription Thymus Thymus
5 chr21:47241000-47251800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr21:47241000-47255400 Weak transcription ES-WA7 Cell Line embryonic stem cell
7 chr21:47241200-47250200 Weak transcription HUES6 Cell Line embryonic stem cell
8 chr21:47241400-47249600 Weak transcription Primary neutrophils fromperipheralblood blood
9 chr21:47241600-47257400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
10 chr21:47241800-47246200 Weak transcription H1 Cell Line embryonic stem cell
11 chr21:47241800-47246400 Weak transcription Fetal Thymus thymus
12 chr21:47241800-47257600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
13 chr21:47242600-47246800 Weak transcription Spleen Spleen
14 chr21:47244000-47245400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
15 chr21:47244600-47244800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
16 chr21:47244600-47245200 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived

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