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EnhancerAtlas ID | HS007-09498 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr2:191670040-191671390 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:191670089-191670107 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr2:191670097-191670115 | GGAAGGAAGGGAAGGAAG | + | 6.1 | EWSR1-FLI1 | MA0149.1 | chr2:191670098-191670116 | GAAGGAAGGGAAGGAAGG | + | 6.33 | EWSR1-FLI1 | MA0149.1 | chr2:191670102-191670120 | GAAGGGAAGGAAGGAAGA | + | 7.39 | EWSR1-FLI1 | MA0149.1 | chr2:191670106-191670124 | GGAAGGAAGGAAGAAAAC | + | 7.54 | EWSR1-FLI1 | MA0149.1 | chr2:191670061-191670079 | GGGAGGAAAGAAGGAAGG | + | 7.87 | EWSR1-FLI1 | MA0149.1 | chr2:191670093-191670111 | GGAAGGAAGGAAGGGAAG | + | 8.57 | EWSR1-FLI1 | MA0149.1 | chr2:191670069-191670087 | AGAAGGAAGGAAGGAAGG | + | 9.09 | EWSR1-FLI1 | MA0149.1 | chr2:191670077-191670095 | GGAAGGAAGGACGGAAGG | + | 9.09 | EWSR1-FLI1 | MA0149.1 | chr2:191670085-191670103 | GGACGGAAGGAAGGAAGG | + | 9.17 | EWSR1-FLI1 | MA0149.1 | chr2:191670073-191670091 | GGAAGGAAGGAAGGACGG | + | 9.35 | EWSR1-FLI1 | MA0149.1 | chr2:191670081-191670099 | GGAAGGACGGAAGGAAGG | + | 9.35 | EWSR1-FLI1 | MA0149.1 | chr2:191670065-191670083 | GGAAAGAAGGAAGGAAGG | + | 9.47 | ZNF263 | MA0528.1 | chr2:191670059-191670080 | AGGGGAGGAAAGAAGGAAGGA | + | 6.15 | ZNF263 | MA0528.1 | chr2:191670094-191670115 | GAAGGAAGGAAGGGAAGGAAG | + | 6.24 | ZNF263 | MA0528.1 | chr2:191670090-191670111 | GAAGGAAGGAAGGAAGGGAAG | + | 6.31 | ZNF263 | MA0528.1 | chr2:191670062-191670083 | GGAGGAAAGAAGGAAGGAAGG | + | 6.35 | ZNF263 | MA0528.1 | chr2:191670078-191670099 | GAAGGAAGGACGGAAGGAAGG | + | 6.39 | ZNF263 | MA0528.1 | chr2:191670098-191670119 | GAAGGAAGGGAAGGAAGGAAG | + | 6.39 | ZNF263 | MA0528.1 | chr2:191670082-191670103 | GAAGGACGGAAGGAAGGAAGG | + | 6.62 | ZNF263 | MA0528.1 | chr2:191670048-191670069 | GAGGGAGGGAGAGGGGAGGAA | + | 7.03 | ZNF263 | MA0528.1 | chr2:191670044-191670065 | GAGGGAGGGAGGGAGAGGGGA | + | 7.29 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAGAGAGGGA GGGAGGGAGA GGGGAGGAAA GAAGGAAGGA AGGAAGGACG GAAGGAAGGA 60 AGGAAGGGAA GGAAGGAAGA AAACAAGAAA ACCTTAATGA TGAAGTGAAA CATCCCAGCT 120 GAGTAACTTT CTGTAAGTAA AATTGTACAT TTTTTTAAGT AAAATCTATA CTCAGTGCCC 180 AGAGTCAGTT CCTTGTGCTG GGAGAGGACA CTTGTCAACT GGTTCCTACC TAAGATAAGC 240 AACAGAAAGG AAGAGCACAT TAATGCCAAA GCTCAAACTG TGGCGTCTCT GGCCCCCAAC 300 CATGCTAAGG AACTCACATC TTGAGGCCCT CAAATCACCC TGGCGATGTG TGGGGCATCC 360 GTGGTGGTCT CATGGATGGC TGGCAACAGG TTCATTTGTG TTTTCACTAT GGCCTCCTGT 420 ATCACAGAGA TGTGATACAG TGATCTACAT TGGGCCTGGG AATCTGCATT AAAATAAGCA 480 CTCTAGGAGA TTCTGATAGG AATGAATGAC GAAAGGCATA TAAGGGTTGC ACAATGTAGG 540 AAAAATCATG CGTTGAGAGA CCCAGCAAAG ATTAGTTTTT CTGCTCCAGC TTGCTGCACT 600 TATTGGAATG GAGTCAAGTA GTACATCTAT ACTCAGTGGG AACTCTGATT GAATATCAGT 660 TATGATTGCC AGGAGACACT CTGATTCAAG CTAAGTGTGC CCTTAGGGTT CTGGTGTTGC 720 AAACTCGGTG GTTTATTGGC CATTGCTGCA GTAAAAGACC ATTATGAGGG TGAACTAATT 780 CTGCCTTCTT ATCTGCTGCC CACCATGAAT CAAATCAGGT TGTTTAAGCT AGCCCAGGGT 840 CCAGCACAGA GTGTTGCACA AAGAAGGTAT TCAGTAAATA TATATTGAAC AGAATCCTTG 900 TGGCACCACG ATACCAGTTA CATCAAAGGT TGGAGTTTAA TTGAAAGATA TATTTACTGG 960 GCCCTGTATT GAGGACCAAG CAGCCCTTCC AAGCACTGGA TGCCCATCTG CTGTAGCTTT 1020 TCTCCAGGTA ACTCAGGAGT AGGAGTTTTA GGAAGTTTGA GTCCTAATGT GCCCCCCAAA 1080 AAACTAGCTG CATTTTCAGA TTATAACTCT GGCTTACCAC CATTTACTTA TGGCAGCTTG 1140 TGAAAAATCA CATTCTATTG ATATTCTTAA AGTAGAGCTA CACTGGCACT TGGGCAAGGT 1200 TGGGGTGAAG AGCAAAAAAA ATTAGGATTC AATATATTGG ATAATTATAT GGGGATTAAG 1260 CAGGTTCTGT CATTGATGGT CATTAGTTTA GTGGCCAGGC GTTAAAGAAT GGTGTTAGAT 1320 CTCTCTCTCT CTCCTTTTTT TTTTTTTTTA 1350
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