Variant report

Variant rs10899947
Chromosome Location chr10:44399052-44399053
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:44392400-44402000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr10:44395000-44406200 Weak transcription Esophagus oesophagus
3 chr10:44395200-44400000 Weak transcription Fetal Heart heart
4 chr10:44395200-44400000 Weak transcription Left Ventricle heart
5 chr10:44395200-44400200 Weak transcription Fetal Kidney kidney
6 chr10:44395400-44400400 Weak transcription NHDF-Ad bronchial
7 chr10:44395800-44399800 Weak transcription Adipose Nuclei Adipose
8 chr10:44395800-44401400 Weak transcription Duodenum Smooth Muscle Duodenum
9 chr10:44396000-44399800 Weak transcription Right Atrium heart
10 chr10:44396000-44399800 Weak transcription Spleen Spleen
11 chr10:44396400-44401200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
12 chr10:44396600-44399400 Enhancers HepG2 liver
13 chr10:44397200-44400400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr10:44397200-44400800 Weak transcription Osteobl bone
15 chr10:44397800-44400000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
16 chr10:44397800-44400400 Weak transcription Muscle Satellite Cultured Cells --
17 chr10:44397800-44401000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
18 chr10:44398000-44399200 Enhancers Liver Liver
19 chr10:44398800-44402600 Enhancers Fetal Muscle Leg muscle
20 chr10:44399000-44399200 Enhancers Right Ventricle heart

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