Variant report

Variant rs4719491
Chromosome Location chr7:17171738-17171739
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17169400-17172600 Enhancers Fetal Intestine Large intestine
2 chr7:17169600-17172800 Enhancers Fetal Intestine Small intestine
3 chr7:17170200-17172600 Enhancers Fetal Kidney kidney
4 chr7:17170600-17174000 Weak transcription Primary T helper cells PMA-I stimulated --
5 chr7:17170800-17171800 Enhancers HepG2 liver
6 chr7:17170800-17172000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr7:17170800-17172200 Enhancers Liver Liver
8 chr7:17170800-17172400 Enhancers A549 lung
9 chr7:17170800-17172600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
10 chr7:17170800-17177400 Weak transcription Dnd41 blood
11 chr7:17171000-17172000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr7:17171000-17172000 Weak transcription NHDF-Ad bronchial
13 chr7:17171000-17172000 Weak transcription NHLF lung
14 chr7:17171000-17172400 Weak transcription Osteobl bone
15 chr7:17171000-17176600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
16 chr7:17171000-17182400 Weak transcription Stomach Mucosa stomach
17 chr7:17171200-17172400 Weak transcription Fetal Lung lung
18 chr7:17171200-17182200 Weak transcription Rectal Smooth Muscle rectum

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