Variant report

Variant rs3734248
Chromosome Location chr6:167763298-167763299
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167762200-167764200 Enhancers Liver Liver
2 chr6:167762200-167764600 Enhancers HepG2 liver
3 chr6:167762600-167764400 Enhancers Placenta Amnion Placenta Amnion
4 chr6:167762800-167763400 Enhancers Thymus Thymus
5 chr6:167762800-167764000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr6:167762800-167764000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr6:167762800-167764200 Enhancers Fetal Brain Male brain
8 chr6:167763000-167764200 Weak transcription Gastric stomach
9 chr6:167763200-167763600 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
10 chr6:167763200-167763600 Bivalent/Poised TSS Duodenum Mucosa Duodenum
11 chr6:167763200-167763600 Bivalent Enhancer Fetal Kidney kidney
12 chr6:167763200-167763600 Enhancers Rectal Smooth Muscle rectum
13 chr6:167763200-167763800 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
14 chr6:167763200-167763800 Flanking Active TSS Fetal Intestine Small intestine
15 chr6:167763200-167764200 Bivalent Enhancer H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr6:167763200-167764200 Flanking Active TSS Fetal Intestine Large intestine

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