Tag | Content |
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EnhancerAtlas ID | HS107-00299 |
Organism | Homo sapiens |
Tissue/cell | Jurkat |
Coordinate | chr1:25421500-25422940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELK1 | MA0028.2 | chr1:25421716-25421726 | ACCGGAAGTG | + | 6.02 | ERG | MA0474.2 | chr1:25421716-25421726 | ACCGGAAGTG | + | 6.02 | ETS1 | MA0098.3 | chr1:25421716-25421726 | ACCGGAAGTG | + | 6.02 | FEV | MA0156.2 | chr1:25421716-25421726 | ACCGGAAGTG | + | 6.02 | FLI1 | MA0475.2 | chr1:25421716-25421726 | ACCGGAAGTG | + | 6.02 | HSF1 | MA0486.2 | chr1:25421973-25421986 | TTCTAGAATGTTC | + | 7.34 | RREB1 | MA0073.1 | chr1:25422079-25422099 | CCCCCCACCACCTCCCCACT | + | 6.27 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 25421873 | 25422200 | chr1 | 25422200 | 25422400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I025095 | chr1 | 25421721 | 25422579 |
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Enhancer Sequence | ACAGACACTC GAGCTCACAG TTGGATGGCC ATGGAACAAA CCCTTGGCAG GGTGCTGAAT 60 CTGAACACGG GAGGAAGGAG GACGTGCAGG CAGTGGGAGC CTCCCTGGAG GAGTGAAGTT 120 TCAGCTGAGT CTGGAGGCGC GAGGAGTCAG CTAGGAAATG AGTGTGGGGA AGAGCATTCC 180 AGGCAGAAGG AACAACAGGA AGGAAGGCCC AGAGTCACCG GAAGTGAGAG GAATAAGAGA 240 GTACTCAGGG AACTAAAACA AACGGGGGTA TGGCAGCGCT TCAGGACCTA GGAAGAGAGG 300 AGCTCGAGGC GAGGACCTAC CCACTGGGCA TAATCTTTAG GAAGGTTGTT CAATCAGCAA 360 TGCTCCACCT GTTCTTGCCA ACACCTAGCC TGGGCATTGT ATCAAAAAGA CAATGGAGTT 420 AGTTCGGCAA GACTTTATTC CCAGGAGTCA TCACTTTCAG TTGTTTTTCA CTCTTCTAGA 480 ATGTTCCAGT AGTGCAAGGC TATGCCTCGT GGTTGGTCAG TAATTGCTCA GAATCTGAAT 540 ATTCCTCTTT TTTGAAAATG ATACAAGGCC CAGCACCACC CCCCCACCAC CTCCCCACTC 600 TCGCCAGCCT TCTAATGCCA CGCTGGTTTT CATTCCTTAG GGATGGACAT TATGGGGTCA 660 CTTCAGAGGT TCTTGCAGGG CTTGAAGATC TGAAGTCATG TAAAGGACCC TAGTATTCTC 720 CTGTGGTGTT CTCACCTATC TTGGGCTGCC ATTTATTTTT AACCATATTT GGTCTGCAAG 780 TTGCCAAGAA ACCATGTAGA GAAAACCAGT GTGGTTTGGG TTAAGCCCCA ACAGGGTGCA 840 GACAGCAGCC AAACTATTTC CTTCTTCCTC TAAGATTTCT TCTGCCGTCT TAGCCCAGAG 900 CAGACCTGAA GAAAGCTCTC TCTGCAACCC TCTACTGCAC CAGCTCCCCC AAGCTCTCCA 960 GAGAGCCCAG CCCCAGCCCT CACCTGGAAC CACTCCCTGA CACTGGGGCG TGGGTTCTTC 1020 CGGTGGGAAA TTGGCCAAGC ACTGACCATA GAGACTATAA GGACGAAGGG AGGAATAGAG 1080 AGGCCTCCTC AGAAAGGCAG CAAGAAACAG CTCCGTGGAA CATGGGGGGA AATGGATCAG 1140 GGAGATCATG GAGAGCACAC ACACTGAGCC TCACAGAGGG CAAGTGGAGC CCCCATCTCT 1200 TCCATCTTGG AAGGCTGATC ATATTAAAAA GTGGGAGGAA ATACTGACAC AAAGTGCAAA 1260 TATCAAGATC TATTTCAAAT ATTCACATGT AGCTAATTTA ACACCCTAAA GATTACAGGG 1320 CAATTTAGTT GTGATATTCT CAAGATTGCT CCAGGACTGA TGCTAACGCA TGTAAATTTG 1380 TAGTGTCCTC CACAGTGAGG GGAAGTAATG GAACAGATTC TTCTCTCAGC TGAGTGGAAG 1440
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