Variant report

Variant rs16822793
Chromosome Location chr1:184263526-184263527
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:184255600-184266400 Weak transcription Spleen Spleen
2 chr1:184256000-184266000 Weak transcription Right Atrium heart
3 chr1:184258600-184267400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr1:184258800-184265200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr1:184259600-184265600 Weak transcription Gastric stomach
6 chr1:184259600-184266400 Weak transcription Pancreas Pancrea
7 chr1:184261400-184265200 Weak transcription NHLF lung
8 chr1:184261600-184264800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr1:184261600-184264800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
10 chr1:184261600-184265200 Weak transcription NHDF-Ad bronchial
11 chr1:184261600-184265600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr1:184261600-184268000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr1:184262600-184265200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
14 chr1:184263000-184263600 Enhancers Psoas Muscle Psoas
15 chr1:184263000-184263800 Enhancers Skeletal Muscle Male skeletal muscle
16 chr1:184263000-184265400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
17 chr1:184263000-184265600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
18 chr1:184263200-184263800 Enhancers Fetal Brain Female brain
19 chr1:184263400-184266200 Enhancers Fetal Heart heart

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