Variant report

Variant rs4076492
Chromosome Location chr8:11825524-11825525
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:11821800-11826200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
2 chr8:11821800-11828200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr8:11821800-11833000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr8:11821800-11834400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr8:11824000-11826200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr8:11824200-11826000 Weak transcription Primary monocytes fromperipheralblood blood
7 chr8:11824200-11827000 Enhancers Fetal Stomach stomach
8 chr8:11824600-11826200 Enhancers Duodenum Smooth Muscle Duodenum
9 chr8:11824600-11826600 Enhancers Rectal Smooth Muscle rectum
10 chr8:11824600-11826800 Enhancers Colon Smooth Muscle Colon
11 chr8:11824600-11826800 Enhancers Stomach Smooth Muscle stomach
12 chr8:11824600-11826800 Enhancers Dnd41 blood
13 chr8:11824800-11826400 Enhancers Fetal Thymus thymus
14 chr8:11825200-11826600 Enhancers Primary T killer naive cells fromperipheralblood blood
15 chr8:11825200-11826600 Enhancers Pancreas Pancrea

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