Variant report

Variant rs537987719
Chromosome Location chr1:69593938-69593939
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 chr1:69593200-69595000 Enhancers Fetal Heart heart
5 chr1:69593200-69595200 Weak transcription H1 Cell Line embryonic stem cell
6 chr1:69593400-69594600 Enhancers Fetal Brain Female brain
7 chr1:69593600-69594000 Enhancers Colon Smooth Muscle Colon
8 chr1:69593600-69594600 Enhancers Rectal Smooth Muscle rectum
9 chr1:69593600-69595600 Enhancers ES-I3 Cell Line embryonic stem cell
10 chr1:69593600-69595600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr1:69593800-69594000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr1:69593800-69594200 Active TSS Stomach Smooth Muscle stomach
13 chr1:69593800-69595800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived

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