Tag | Content |
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EnhancerAtlas ID | HS196-00833 |
Organism | Homo sapiens |
Tissue/cell | ZR75-1 |
Coordinate | chr1:46022550-46023890 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr1:46022589-46022600 | AGTGACTCATG | + | 6.14 | Nr2f6(var.2) | MA0728.1 | chr1:46022645-46022660 | GAGGTCAGGAGTTCA | + | 6.22 | RARA | MA0729.1 | chr1:46023287-46023305 | GAGGCCAACAGGTCATTG | + | 6.63 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I045556 | chr1 | 46022501 | 46022650 | GH01I045557 | chr1 | 46022945 | 46023870 |
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Enhancer Sequence | AACAAAATAA ATAAATAAAG TAAAAGATAG GCTGGGCACA GTGACTCATG CCTGTAATCC 60 CAGCACTTTG AAAAGCTGAG ACTGGTGGAT CACCTGAGGT CAGGAGTTCA AGACCAGCCT 120 GGCCAACATG GTGAAACCCT GTCTCTACTA ATAATACAAA AATTAGCTGG GCGTGGTGGC 180 ACATGCCTGT AATCCCAGCT ACTGGGGAGG CTGAGGCAGG AGAATCGCTT GAACCCAGGA 240 GGTGGAGGTT GCAGTGAGCC AAGATCGCGC CATTGCACCC CAGCCTGGGT GACAAGAATG 300 AAACTCTATC TCAAAAAAAT AAAAATAAAA AAGATAACAT GAGGGTTTCT GAATGCTGCC 360 AAAGGTCCAG ATAGGCAGTT CCTGACAAGC TCAGAGTCTG GAATCTGTTC ACGCACAGCT 420 AGGCTGGAAA GCAGTTGTAT CAAGCAGAAG ATGAGGAAGT CAAGAGCTGG CCGAGGATGA 480 TTTTCTGTCC TAGAGAAAAA CATCTATGTG GCACCTTCAT TCTTCCCTAG GGAGCTCTTG 540 TTCTTTGCAG ATCTCCTCCA TCTTTCATCC CTGTTCCCCA AGCCTCAGCC TTTTCGGTGT 600 TCAGTTTCAC CAGCAAAAGA AAGGGAGAAG CAAGATTCAG GTTTCTTCTT CCTTTTCCCC 660 TTAAGCCAGG GTGTTGTTCA AGCTCTCACC CCAGGTGTAA TTTCAGAGCC TTCTCATGCG 720 TGCTGGGTAA TCTGCGAGAG GCCAACAGGT CATTGGGCAT TAAGCCCAGG AAACCTGCCT 780 TAGACCCTGG TGGCAGCAGG CCACCAGGTT CCTCTTGTCA AGTCCAGACT TGCTTGCTTG 840 ATCCCTTGGA AATTTGATTA TAAAGAGCAT TGCCCTGGTA GCTTGTGGTT TGACACTCAG 900 ATTGAAGTTT TGATTTTGTT TTAGCAGAAA AGAGTGGTTT CCAAAACCAA CTTAAACTAG 960 ACTATAAAAT TCTTCCTGGG TCAGAAGTAT TAGGAAAGAC AGTGTTGGTG TACTGGCTTT 1020 ACTCACAACT TGTCTTTTTT TTTTTTTTTG AGATGGAGCC TCACTCTGTA TCCCAGGCTG 1080 GAGTGCAGTG GCATGATCTC AGCTCACTGC AACCTCTGCC TCCTGGGTTC AAGCGATTCT 1140 CCTGCCTCAG CCACCCGAGT AGCTGGGATT AAGGTGTGCA CCACCATGTC CAGCTAATTT 1200 TTGTATTTTT AGTAGAGAGG GGGTTTCGCC TTGTTGGCCA GGCTGGTCTC GAACTCCTGA 1260 CCTCAAGTCT TAAGTGATCT GCCTGCCTCG GCCTCCCAAA GTGCTGGGGT TACAGACGTT 1320 AGCCACTGTA CCCAGCCTCA 1340
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