Variant report

Variant rs1410252
Chromosome Location chr1:70449089-70449090
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:70440600-70456600 Weak transcription Brain Cingulate Gyrus brain
2 chr1:70446200-70455400 Weak transcription Brain Germinal Matrix brain
3 chr1:70447800-70449600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr1:70447800-70450600 Enhancers Hela-S3 cervix
5 chr1:70448000-70449600 Enhancers NHDF-Ad bronchial
6 chr1:70448000-70449800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr1:70448200-70449600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr1:70448200-70449600 Enhancers Muscle Satellite Cultured Cells --
9 chr1:70448400-70449200 Enhancers Placenta Amnion Placenta Amnion
10 chr1:70448400-70449400 Enhancers NH-A brain
11 chr1:70448400-70449400 Enhancers Osteobl bone
12 chr1:70448400-70449600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr1:70448400-70449600 Enhancers HSMM muscle
14 chr1:70448600-70449200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr1:70448600-70449200 Enhancers HUVEC blood vessel
16 chr1:70448600-70456600 Weak transcription Brain Inferior Temporal Lobe brain
17 chr1:70448800-70449400 Enhancers NHLF lung
18 chr1:70449000-70449400 Strong transcription Fetal Brain Female brain

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