Variant report

Variant rs611386
Chromosome Location chr1:211770318-211770319
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:211757400-211775200 Weak transcription Fetal Intestine Small intestine
2 chr1:211764600-211770600 Weak transcription Primary neutrophils fromperipheralblood blood
3 chr1:211766000-211770400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr1:211766000-211772200 Weak transcription Placenta Placenta
5 chr1:211766200-211770800 Weak transcription NHLF lung
6 chr1:211766400-211770600 Weak transcription NHDF-Ad bronchial
7 chr1:211766800-211771400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr1:211768600-211771800 Enhancers Primary monocytes fromperipheralblood blood
9 chr1:211768600-211772400 Enhancers Primary hematopoietic stem cells short term culture blood
10 chr1:211769000-211770600 Enhancers Liver Liver
11 chr1:211769200-211771200 Enhancers Monocytes-CD14+_RO01746 blood
12 chr1:211769400-211770800 Enhancers HepG2 liver
13 chr1:211769600-211770600 Weak transcription Primary Natural Killer cells fromperipheralblood blood
14 chr1:211769800-211772200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
15 chr1:211770000-211771800 Enhancers Osteobl bone
16 chr1:211770200-211775200 Weak transcription Fetal Intestine Large intestine

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