Variant report

Variant rs668856
Chromosome Location chr3:142699990-142699991
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:142695400-142700200 Weak transcription HUES64 Cell Line embryonic stem cell
2 chr3:142695800-142700200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr3:142695800-142701000 Weak transcription HUES6 Cell Line embryonic stem cell
4 chr3:142695800-142701000 Weak transcription Primary neutrophils fromperipheralblood blood
5 chr3:142695800-142701400 Weak transcription Primary hematopoietic stem cells short term culture blood
6 chr3:142695800-142705800 Weak transcription Left Ventricle heart
7 chr3:142696000-142705800 Weak transcription Right Atrium heart
8 chr3:142696200-142700000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr3:142696400-142700200 Weak transcription ES-I3 Cell Line embryonic stem cell
10 chr3:142698600-142700800 Enhancers K562 blood
11 chr3:142699000-142701600 Enhancers A549 lung
12 chr3:142699200-142700200 Enhancers Fetal Adrenal Gland Adrenal Gland
13 chr3:142699600-142701400 Enhancers iPS-18 Cell Line embryonic stem cell
14 chr3:142699600-142704600 Enhancers HepG2 liver
15 chr3:142699800-142700400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr3:142699800-142700600 Enhancers ES-WA7 Cell Line embryonic stem cell
17 chr3:142699800-142701600 Enhancers iPS-15b Cell Line embryonic stem cell

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