Variant report

Variant rs112082899
Chromosome Location chr1:69593696-69593697
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:69586400-69596800 Weak transcription HUES48 Cell Line embryonic stem cell
2 chr1:69592000-69594800 Enhancers Fetal Brain Male brain
3 chr1:69592400-69595600 Enhancers iPS-15b Cell Line embryonic stem cell
4 chr1:69593000-69593800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr1:69593200-69595000 Enhancers Fetal Heart heart
6 chr1:69593200-69595200 Weak transcription H1 Cell Line embryonic stem cell
7 chr1:69593400-69593800 Enhancers Stomach Smooth Muscle stomach
8 chr1:69593400-69594600 Enhancers Fetal Brain Female brain
9 chr1:69593600-69593800 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
10 chr1:69593600-69594000 Enhancers Colon Smooth Muscle Colon
11 chr1:69593600-69594600 Enhancers Rectal Smooth Muscle rectum
12 chr1:69593600-69595600 Enhancers ES-I3 Cell Line embryonic stem cell
13 chr1:69593600-69595600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived

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