Tag | Content |
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EnhancerAtlas ID | HS051-25611 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chr7:140104020-140104940 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELK1 | MA0028.2 | chr7:140104219-140104229 | ACCGGAAGTG | + | 6.02 | ELK4 | MA0076.2 | chr7:140104219-140104230 | ACCGGAAGTGG | - | 6.32 | ERG | MA0474.2 | chr7:140104219-140104229 | ACCGGAAGTG | + | 6.02 | ETS1 | MA0098.3 | chr7:140104219-140104229 | ACCGGAAGTG | + | 6.02 | FEV | MA0156.2 | chr7:140104219-140104229 | ACCGGAAGTG | + | 6.02 | FLI1 | MA0475.2 | chr7:140104219-140104229 | ACCGGAAGTG | + | 6.02 | Gabpa | MA0062.2 | chr7:140104220-140104231 | CCGGAAGTGGA | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGCGACAGGT GAACCAGGAA GGCGAAGGCT GCGGGATGCC GGCGGGAGGA CATCATCGGG 60 GTGGACGCTG CCTGTGCCTC CCAGCAAGGC TTGTAGGCTC AATGAAAGGG GGCTTTAGTG 120 GAAACCCTGA GGACTCCTGA GGGTGGGGGG AGACATGGAA GTAAAGTCTC AGCTCAAGTT 180 ACAGTGATAA GACCAAGACA CCGGAAGTGG AATGGCTGTC TTTAGTTGAA AAGTCAGACA 240 GGAAAAAAGT GGTTTGATTG TGTCTGTTGT CTGCTGGATC ATCTACCCAT ATGTGATTTC 300 AGAGAGGTCC AAGAGAGGTA TGGGATCCTT CTTCATCGCC TTAAAGCCCT GGGTTTTTGC 360 ATGCAGATTG GACATTTGAG TGCATTTTAC CTTGTGTGAT GAGACAGAGT GTCCTTGTCT 420 ATGACTTTAG AGAAAACCAA AGTAAAACGG AGAGGTGAAG AAGGATGTCA CAAGGCAGGG 480 GCAATTTGCA GCACATCAAA TGTAATCATT AAGTGGGATC AGGTTTCAGT TACTTTTAGA 540 GCAATTGGAT GAGGAGTCCG AACACACTCT CAGGAAGAAC AGTTAAAGAG GATGGGGATA 600 TTCTCCTTGG GGGAATATTC TTGCTGCTTC AAATATCTGA TGGGCTGTCA TGTGGAACAG 660 GAATGTGATG TGTCTTGGCA GAGTAAGGAT AGCACGGAGC TAGACAGATG GAAACCTCAT 720 GGAGGGAGGT GTCAATCCCA CAGAAGTGAG AGCTGCCCAG TGCAAAATGG AAATTTTTCA 780 GGAGGTAGTC AGTTCCTTGT GATCAGAGAT ATTTAAGCAT AGGTGGACAT TTAAGCCAGG 840 GATGCTGATG GTGGGAGTAA GTTTCAGGTA GGTGACTTGG TCGATTGGTG TTTTCCAAAC 900 CTGGCTCATC ATCAGAATCA 920
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