Tag | Content |
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EnhancerAtlas ID | HS098-26866 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr19:4296290-4297080 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HEY2 | MA0649.1 | chr19:4296701-4296711 | GGCACGTGTC | - | 6.02 | LBX2 | MA0699.1 | chr19:4296624-4296634 | GCTAATTGGC | - | 6.02 | Npas2 | MA0626.1 | chr19:4296701-4296711 | GGCACGTGTC | + | 6.02 |
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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 | CAGCAGAGGG AACTGGCACA GAGAGGTCAA GTCACTTGCT CAAGGTCACA CAGCAAGTAA 60 ATGAAACAGA GGATTGAATC CAGGTTGTAT AATTTACAGG AACCCCAGCT AAAGGCTGTG 120 AATGCCGCAA TTAAGATAAG GTCCAGCACC CCAACCCCCT TCTTTTGCAG CCTCTGAGGT 180 TGGCAGGGGA TCCCTGGGGA CTGCCAAGCT GCTGTTCAGG ATTGGTGGGG TGTGGGGAAG 240 CCAGCTGTGT GGGGTTGGAC CCGCGCCCAC TCCCTGCTCT CTCACAGCTG CCAACGCACA 300 GCCTGGCGCC TCCACCACCC CGCCTCCTCT AATTGCTAAT TGGCCCCTTT GACATCAGAG 360 GGGTGGGAAG AGGTGGGTAA CACAGCCATA ACACACCCCT CCCTTGAGGC AGGCACGTGT 420 CCCCCGCCAG CAGGCTGGTC CTACCAGCTG GAGAGGAACA GGCATCTCTA GGGGCTGAGA 480 GCTGGGTGCT TCATTCTGCC AGAGGGGGCT GGACAGAGGC CCGGGGCCCA CAGGCACCTC 540 TCACAGAGCA GGAGGCAAAG CCTGCATCCC CTTGGGTTTC CCGATTCTGC CCAGGATGGG 600 TCCATAAGTG GGGGACATGG CAAAGGGGAC AGTGCATAGG GTGCACCCCT GCCTGGTGCA 660 TAACGCTAGA TATGTCTTGG CCCTCTCTGG TTCACCTGGC TCATCTGTAA AGTGAGGCAG 720 CTGGCGTTGC TGACCTGGAA AGCTATCTGG AGGGTTTCTT CCAACTTTGA GAGTCTGTGG 780 CTTTTTTTTT 790
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