Variant report

Variant rs191399941
Chromosome Location chr1:103318820-103318821
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:103311200-103319200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr1:103316400-103319400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
3 chr1:103316600-103319400 Enhancers Fetal Muscle Leg muscle
4 chr1:103317800-103319200 Enhancers Cortex derived primary cultured neurospheres brain
5 chr1:103317800-103319400 Enhancers Brain Germinal Matrix brain
6 chr1:103317800-103321800 Weak transcription NHDF-Ad bronchial
7 chr1:103318000-103319000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
8 chr1:103318000-103319200 Enhancers Fetal Stomach stomach
9 chr1:103318200-103319200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
10 chr1:103318200-103319200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr1:103318200-103320800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
12 chr1:103318400-103324000 Weak transcription Osteobl bone
13 chr1:103318400-103324600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr1:103318800-103319000 Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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