Variant report

Variant rs17149606
Chromosome Location chr7:87072505-87072506
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:86980000-87085600 Weak transcription Right Ventricle heart
2 chr7:87019800-87079400 Strong transcription Liver Liver
3 chr7:87024800-87093200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr7:87040800-87085600 Weak transcription Psoas Muscle Psoas
5 chr7:87047000-87078000 Strong transcription Primary B cells from cord blood blood
6 chr7:87051200-87085600 Weak transcription Fetal Heart heart
7 chr7:87055800-87075000 Weak transcription GM12878-XiMat blood
8 chr7:87056200-87075200 Strong transcription Primary B cells from peripheral blood blood
9 chr7:87064600-87077800 Weak transcription Spleen Spleen
10 chr7:87065000-87077800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr7:87066800-87085600 Weak transcription Left Ventricle heart
12 chr7:87070400-87072800 Strong transcription Skeletal Muscle Male skeletal muscle
13 chr7:87071800-87072800 Strong transcription Skeletal Muscle Female skeletal muscle
14 chr7:87071800-87073200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
15 chr7:87072000-87073800 Strong transcription HepG2 liver
16 chr7:87072400-87072800 Genic enhancers Aorta Aorta

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