Tag | Content |
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EnhancerAtlas ID | HS177-21345 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr7:90032860-90033640 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2C | MA0497.1 | chr7:90033121-90033136 | TGCTATTTTTGAATA | - | 6.02 | ZNF263 | MA0528.1 | chr7:90033329-90033350 | GGAGGAGAGGAGGCGGAGGGG | + | 6.23 | ZNF263 | MA0528.1 | chr7:90033337-90033358 | GGAGGCGGAGGGGGGAGGAGG | + | 7.19 | ZNF263 | MA0528.1 | chr7:90033334-90033355 | AGAGGAGGCGGAGGGGGGAGG | + | 7.46 | ZNF263 | MA0528.1 | chr7:90033350-90033371 | GGAGGAGGGGGGCGGAGGGGG | + | 7.61 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | CAGGTAGGTG TGGTCAAGAT GTTCCGATTT CTGGGTCTTT TGCATAAGTA ACTGAGGATT 60 TTATGTAAAA TGGCTAAATC CAGGAGAATC AGGAGCGTTG GAAAACGCTG ACCACATCTG 120 TGGATGTGAA AATTGAGTAG GTATTTGGTA AGGCTTTAAA AAATTATTTT GTACACAGGA 180 GTATGGAAAT GTCGAGGTGT GTTGCCGGAG CCGCCAAGGA CTGGGAGCTT TGCTGGCGCG 240 GGTTTGTGGG GGAGCCCAAG CTGCTATTTT TGAATAACCA GCTGATGCTG GTTGCGTAAT 300 GATGACCTGC TTGCGGTTCA AACCCACTCA GTGTTGCAGG GATGGGCTAG CTCTGAGAGC 360 GTTAACAGTC ACTGTTGCGG TCTCTCTCCA TTGGCTCTAA CTAGTAGGGC GTTTTCTTCC 420 TTCTGCCAGG TCTGGGTCTA CCACACACAG GGCTCTTCGA AAAGAGGGAG GAGGAGAGGA 480 GGCGGAGGGG GGAGGAGGGG GGCGGAGGGG GATGCGGATT GCTCTGGAAG CTTGGTTTGC 540 TTTCCTGTAA GTTCTGTGCA CCCGGCCTTG TAAGGGGCCC ATAGCCACGT TAGGGAAAGG 600 TCAGACTTGG TGACCTCACT TAAAATGATT GCTCAAGGAT TCTATTGTGC GTTATTAATT 660 GTAAAACGAT TTCCTCTGAC TTTGGAGTGT GCAATTATGA TTGATACCAA CCCAAGAAAC 720 ACATTTGGGG CGGGGGAGGG GTTGGGGGGG ACTTGACTGA AATCTCCGAG CAGCCAGTTG 780
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