Tag | Content |
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EnhancerAtlas ID | HS080-00243 | Organism | Homo sapiens | Tissue/cell | H9 | Coordinate | chr1:11371850-11373120 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr1:11372332-11372343 | AGCCAATCAGA | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 11372075 | 11372447 | chr1 | 11372253 | 11372842 |
| Enhancer Sequence | TAAAGGATGG CTTAAAGTCC TGGTGTCCCA CTGTGTCCCA GCGTGGCCAG TGCTGAGGGG 60 CAGGAGAGCT GCCTTGCTTG CCTGTCTTCT GAGAGGATGG TTGTGGACAC CTGAGGTCAG 120 AGACAGATCA CCTGTGGACT CCAGTCCTGC TGCTGGCTGC TCCTGTTTAT TGAGAGCTTT 180 GCAGGCCCAG AGAAACCCAG TCATTTATCT ACAGTCCCAC AGCAGGAAGC TGCAGGGCTG 240 AGATTTGCTC CCAGTCCTGT CTGACCTCAA AATCCCCTGC TCTTGATCGT GAGGCCACAC 300 TCCCTCAGCC TGGTGAGCCT GTGGGCCCAG CTGCTCTAGG GGTAACGCAC CACCTCCCAG 360 CCCCTAGTTC ACCCAGGGGC CTTATAAGAT GCAGCAGGAC TGAGCCAGAA GCCGAAGGGA 420 ATGACAGCCT GGGGCTGAGG TTCCTGGGTC CCTGACACTC ACAAACTGCT CCAGCTCTCA 480 GAAGCCAATC AGAGACTCCG TAGTTTCCTG CTCGGCTGAA TTCTCCTCTC TGGAGGCAGA 540 GAAAGGAGGT GCTTTGCCAT CTCTGGTTGT GGGGCTTTAT CTCTGGAAAC TCTGCAGTGC 600 GTGTGAAAAC CTGTGGACCA AAGAACGAGG AAGAAAGATT AAAGAGGGAA AGGATTAAGA 660 TCTACAGGGC TTCCCATGCT CTGCACAGCC GCTCTCAGAA GCTGCTCTGC GATCTCTCTA 720 TTAGATGACC GACAGCTGCC AGCTCTGGAG GTGAGAAGGG CTGAGCCCCT CACCCCAGCC 780 AGGAGCCACT GAGAAAGCAG CATAGTCAGG ACAAAAAGAC AGGAAGGGCG GGGGCGGGGG 840 TGTCGGGGTG TTGGGAGGTG GCAGAACACA GAAGTGGATT TCACTGGAAT AAAAGGGCAG 900 ATGGGAGGGC AGAGCCGTGG ATGTGTTCCA TGAGTGCCAT GCTGCAGGGT GAAGGGACCC 960 TGGCCCTCCC ATCTGTCTCC CTTCCCACCT GGATTAGTGA GCTACCCCAA ACTTAGCAGC 1020 TTAAGACAAC AATAAACATC TCTATATTCC AGTTTCTGTG GGTCAGGAAC CTGTGGGCAG 1080 CTGAGTTCAG GGTCTCTCCT GAGGTCACCG TCGTCAGGGG TCTTGCTGGG GCTGGAGGAC 1140 CCACCTCCAA GATAGAACTC ACATGGTGCT AGGCTCCTTC AGCACAGGCC TCCCCACGTG 1200 TTGGCACTCC CCAGAGTGGG TGATACAGAA GAGAAAGAAC CAGGCCAAAG CCGCCATGGT 1260 TGTTTTTTTT 1270
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