Variant report

Variant rs10464490
Chromosome Location chr7:97715319-97715320
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:97709400-97715600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr7:97712800-97716400 Enhancers Rectal Mucosa Donor 31 rectum
3 chr7:97713000-97715600 Enhancers Duodenum Mucosa Duodenum
4 chr7:97713400-97715400 Weak transcription Colonic Mucosa Colon
5 chr7:97714000-97715400 Weak transcription Fetal Intestine Large intestine
6 chr7:97714000-97715400 Enhancers Sigmoid Colon Sigmoid Colon
7 chr7:97714000-97715600 Enhancers Fetal Intestine Small intestine
8 chr7:97714000-97716000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr7:97714000-97716000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr7:97714000-97716000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr7:97714200-97715400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
12 chr7:97714800-97715800 Enhancers HepG2 liver
13 chr7:97714800-97716400 Enhancers NHEK skin
14 chr7:97715000-97716600 Enhancers HMEC breast
15 chr7:97715200-97715600 Enhancers Esophagus oesophagus
16 chr7:97715200-97715600 Flanking Active TSS Rectal Mucosa Donor 29 rectum
17 chr7:97715200-97716000 Enhancers Stomach Mucosa stomach

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