Variant report

Variant rs12291861
Chromosome Location chr11:67402393-67402394
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:67398600-67403200 Enhancers Fetal Intestine Large intestine
2 chr11:67398600-67403200 Enhancers Fetal Intestine Small intestine
3 chr11:67398800-67402800 Enhancers Rectal Mucosa Donor 29 rectum
4 chr11:67398800-67404400 Weak transcription GM12878-XiMat blood
5 chr11:67398800-67418600 Weak transcription Right Atrium heart
6 chr11:67399600-67407200 Weak transcription Spleen Spleen
7 chr11:67399800-67407000 Weak transcription K562 blood
8 chr11:67400400-67402800 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr11:67401200-67403000 Enhancers Rectal Mucosa Donor 31 rectum
10 chr11:67401400-67402400 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
11 chr11:67401400-67402800 Enhancers HepG2 liver
12 chr11:67401600-67402400 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
13 chr11:67401800-67407600 Weak transcription Gastric stomach
14 chr11:67402000-67402400 Flanking Active TSS Duodenum Mucosa Duodenum
15 chr11:67402000-67402600 Enhancers Placenta Placenta
16 chr11:67402000-67405400 Weak transcription Stomach Mucosa stomach
17 chr11:67402200-67402400 Bivalent Enhancer Stomach Smooth Muscle stomach
18 chr11:67402200-67402600 Enhancers H1 Cell Line embryonic stem cell

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