Variant report

Variant rs11171640
Chromosome Location chr12:56045395-56045396
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:56040400-56048400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr12:56040800-56046000 Weak transcription Primary T helper cells PMA-I stimulated --
3 chr12:56040800-56046800 Weak transcription Stomach Mucosa stomach
4 chr12:56041200-56048400 Weak transcription Lung lung
5 chr12:56042600-56046000 ZNF genes & repeats Primary monocytes fromperipheralblood blood
6 chr12:56043200-56047000 Enhancers Fetal Intestine Large intestine
7 chr12:56043800-56045400 Enhancers Primary neutrophils fromperipheralblood blood
8 chr12:56043800-56045800 Enhancers HepG2 liver
9 chr12:56044400-56045800 ZNF genes & repeats Primary B cells from peripheral blood blood
10 chr12:56044800-56045400 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
11 chr12:56044800-56045400 Enhancers Fetal Adrenal Gland Adrenal Gland
12 chr12:56045000-56045600 ZNF genes & repeats Monocytes-CD14+_RO01746 blood
13 chr12:56045000-56045800 Flanking Active TSS Duodenum Mucosa Duodenum
14 chr12:56045000-56047000 Enhancers Fetal Intestine Small intestine
15 chr12:56045200-56045400 Enhancers Fetal Muscle Trunk muscle
16 chr12:56045200-56045600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell

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