Tag | Content |
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EnhancerAtlas ID | HS007-07948 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr19:4295900-4297110 | 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 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGCATTGTTT TGTTGTTGTT GTTTGTTTTT CTGGAGACAG GGTCGCTCTG TGTCACCCAG 60 GCTGGAGTGC AGTGGCGTGA TCGTAGCTCA CTGCAGTCTC CAACTCCTGG GCTCAAGTGA 120 TCCTCCCGCC TCAACCTCTC AAGTAGCTGG GACTATGGGT ATATGCCACC ATGCCTGGCT 180 AATTTTAGAA TTTCTTGTAG AGATGAGGTC TTGCTGTGTT GGCCAAGCTG GTCTCGACCT 240 CCTGGCCTCA AACAATCCTC CCACCTTGGC CTCCCAAAGT GCTGGGATAT CAGGCGTGAG 300 CCACTGCACT TGGATTATAG CAAGCACTTT GGCTATAACT GCTCTAAAGT CACCCGACCT 360 GATGAGGAAA AACTATTCAC TGTATTTTGA CAGCAGAGGG AACTGGCACA GAGAGGTCAA 420 GTCACTTGCT CAAGGTCACA CAGCAAGTAA ATGAAACAGA GGATTGAATC CAGGTTGTAT 480 AATTTACAGG AACCCCAGCT AAAGGCTGTG AATGCCGCAA TTAAGATAAG GTCCAGCACC 540 CCAACCCCCT TCTTTTGCAG CCTCTGAGGT TGGCAGGGGA TCCCTGGGGA CTGCCAAGCT 600 GCTGTTCAGG ATTGGTGGGG TGTGGGGAAG CCAGCTGTGT GGGGTTGGAC CCGCGCCCAC 660 TCCCTGCTCT CTCACAGCTG CCAACGCACA GCCTGGCGCC TCCACCACCC CGCCTCCTCT 720 AATTGCTAAT TGGCCCCTTT GACATCAGAG GGGTGGGAAG AGGTGGGTAA CACAGCCATA 780 ACACACCCCT CCCTTGAGGC AGGCACGTGT CCCCCGCCAG CAGGCTGGTC CTACCAGCTG 840 GAGAGGAACA GGCATCTCTA GGGGCTGAGA GCTGGGTGCT TCATTCTGCC AGAGGGGGCT 900 GGACAGAGGC CCGGGGCCCA CAGGCACCTC TCACAGAGCA GGAGGCAAAG CCTGCATCCC 960 CTTGGGTTTC CCGATTCTGC CCAGGATGGG TCCATAAGTG GGGGACATGG CAAAGGGGAC 1020 AGTGCATAGG GTGCACCCCT GCCTGGTGCA TAACGCTAGA TATGTCTTGG CCCTCTCTGG 1080 TTCACCTGGC TCATCTGTAA AGTGAGGCAG CTGGCGTTGC TGACCTGGAA AGCTATCTGG 1140 AGGGTTTCTT CCAACTTTGA GAGTCTGTGG CTTTTTTTTT TTTTTTTTTT TGAGACAGAG 1200 TCTTGCTCTG 1210
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