Variant report

Variant rs377591614
Chromosome Location chr21:16262501-16262502
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:16249200-16264600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr21:16259400-16262600 Enhancers Fetal Intestine Small intestine
3 chr21:16259600-16262800 Enhancers Fetal Intestine Large intestine
4 chr21:16260000-16264600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr21:16260600-16262600 Enhancers HMEC breast
6 chr21:16261200-16262600 Enhancers Primary hematopoietic stem cells short term culture blood
7 chr21:16261200-16263400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
8 chr21:16261400-16263000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chr21:16261400-16267000 Weak transcription Fetal Muscle Leg muscle
10 chr21:16261800-16265200 Weak transcription Dnd41 blood
11 chr21:16262000-16262800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr21:16262000-16263000 Enhancers HepG2 liver
13 chr21:16262000-16263400 Weak transcription Sigmoid Colon Sigmoid Colon
14 chr21:16262000-16284200 Weak transcription Primary hematopoietic stem cells blood
15 chr21:16262200-16262800 Enhancers Fetal Adrenal Gland Adrenal Gland

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