Variant report

Variant rs7784759
Chromosome Location chr7:100130674-100130675
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:100091800-100136200 Weak transcription Right Atrium heart
2 chr7:100125800-100136000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr7:100129800-100136000 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
4 chr7:100130000-100131200 Enhancers Colonic Mucosa Colon
5 chr7:100130000-100131200 Enhancers Rectal Mucosa Donor 31 rectum
6 chr7:100130000-100132200 Enhancers Duodenum Mucosa Duodenum
7 chr7:100130000-100133000 Enhancers Fetal Intestine Small intestine
8 chr7:100130200-100131200 Enhancers Rectal Mucosa Donor 29 rectum
9 chr7:100130200-100131400 Enhancers Fetal Intestine Large intestine
10 chr7:100130200-100131400 Enhancers Stomach Mucosa stomach
11 chr7:100130400-100131400 Flanking Active TSS K562 blood
12 chr7:100130600-100132400 Enhancers HepG2 liver

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