Variant report

Variant rs5744312
Chromosome Location chr1:86937235-86937236
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:86933000-86937800 Weak transcription Primary hematopoietic stem cells short term culture blood
2 chr1:86933000-86938000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr1:86933000-86942800 Weak transcription K562 blood
4 chr1:86934200-86938000 Active TSS Rectal Mucosa Donor 31 rectum
5 chr1:86934600-86938200 Active TSS Fetal Intestine Large intestine
6 chr1:86934600-86938800 Active TSS Rectal Mucosa Donor 29 rectum
7 chr1:86935400-86942800 Weak transcription Rectal Smooth Muscle rectum
8 chr1:86936000-86938000 Enhancers NHDF-Ad bronchial
9 chr1:86936200-86939400 Weak transcription Pancreatic Islets Pancreatic Islet
10 chr1:86936600-86938200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
11 chr1:86936800-86937800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
12 chr1:86936800-86938200 Active TSS Fetal Intestine Small intestine
13 chr1:86936800-86938200 Enhancers Osteobl bone
14 chr1:86937000-86937400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr1:86937000-86938800 Enhancers GM12878-XiMat blood
16 chr1:86937200-86937400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain

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