| Tag | Content |
|---|
EnhancerAtlas ID | HS139-30015 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr2:127892680-127893450 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr2:127892877-127892898 | GGTGGAGGGAGAGGCGAAGGG | + | 6.79 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_03883 | chr2:127892867-127895357 | Brain_Anterior_Caudate | | SE_04777 | chr2:127891531-127896949 | Brain_Cingulate_Gyrus | | SE_05775 | chr2:127890293-127896626 | Brain_Hippocampus_Middle | | SE_06689 | chr2:127890066-127895918 | Brain_Hippocampus_Middle_150 | | SE_07740 | chr2:127891582-127895664 | Brain_Inferior_Temporal_Lobe | | SE_29563 | chr2:127892140-127894110 | Fetal_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I127132 | chr2 | 127890067 | 127896949 |
|
Enhancer Sequence | GAGCCCCACT AAGATGACTT CTTTTATTCC CTATGCATAG CCAGTGACTT ACGCTGACTT 60
TTCTGGAAAC TGGGACTTTA AATAGGAGTT TTTAAAAAGG AAAGAAATCT CTGTTCTGCT 120
TCTTAAAAAC ACCCTTTTCC CCTTTTTACT TTCAGAAGAA GGAACCAGAG AAGACTAGAA 180
ACAGGATGGA ACGGGAAGGT GGAGGGAGAG GCGAAGGGGA AGTCTCGATG CTGACTACAA 240
GGCCCCCTCA TCCTCCGGCC TCCGGCTTGC AGGGACTGCC CCTGCCTTGG GAGAGTCCTC 300
ACAGGCCACA CCTGCCACTG GGCCAGGCCC AGAGCAGACA CTCACGACAG ATGATAAGAA 360
TGACAGCTGC CTGCGTTTGA GCAGGCACTC TAGGTGACTG TTGTACACAG TGCTTTTCAA 420
GCATAATCTA CCCTAACCTT CACACCAGCC CTGTGGGGTA GGTGAATCTC ACCCCATCTT 480
ACAGAGGAGG AAACAGGGGT TTGGAGTGGT TGAGTGACTT GCTGTCAGAC AAGTCTAAAT 540
CTGACAGCAA CGCCTGTGTT TGGATCCCAT GCCAGAGACT GCGAGCTAGC CCCAGGCTGG 600
TTCCAGGCTG TACACAGGTT TCACTTGATT CACACACATG GGGCCTCCTC AGAGTTTTAA 660
ATTTTATTTG TTGTCAACAT TTAGCAATCA GAAGAGTTAA CATTAAATCT CACATTTCTG 720
AATTCTCTAG AAAAATTAGG ACATCAGGCT CCACTGGGCT TATGTTTCCT 770
|
