Variant report

Variant rs291432
Chromosome Location chr2:191200381-191200382
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:191191600-191208000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr2:191197800-191200800 Enhancers Fetal Intestine Small intestine
3 chr2:191198200-191200800 Enhancers Hela-S3 cervix
4 chr2:191198400-191207400 Weak transcription Spleen Spleen
5 chr2:191198400-191207600 Weak transcription NHLF lung
6 chr2:191198600-191208000 Weak transcription Aorta Aorta
7 chr2:191198800-191208000 Weak transcription Ovary ovary
8 chr2:191199400-191200800 Enhancers Stomach Mucosa stomach
9 chr2:191199600-191205000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr2:191199600-191207600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr2:191199600-191208000 Weak transcription HMEC breast
12 chr2:191200000-191200800 Enhancers Fetal Adrenal Gland Adrenal Gland
13 chr2:191200000-191200800 Enhancers Fetal Intestine Large intestine
14 chr2:191200200-191200800 Flanking Active TSS Liver Liver
15 chr2:191200200-191200800 Enhancers Pancreas Pancrea
16 chr2:191200200-191200800 Flanking Active TSS HepG2 liver
17 chr2:191200200-191200800 Enhancers K562 blood
18 chr2:191200200-191204400 Weak transcription A549 lung

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