Tag | Content |
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EnhancerAtlas ID | HS051-22593 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr5:169784660-169786160 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr5:169785726-169785744 | CCTTCCTTGCCTCTTTCT | - | 6.02 | Nr5a2 | MA0505.1 | chr5:169785455-169785470 | ACTGACCTTGGACCC | - | 6 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 169784990 | 169785480 | chr5 | 169785140 | 169785479 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I170357 | chr5 | 169784605 | 169786203 |
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Enhancer Sequence | ATAGCTGAGA CCACACATGT GCACCACCAC AACCAGCTAA TTTTGACTGT TTATAGAGAC 60 AGGGTCTCAC TATGTTGCCC AGGTTGATGT CAAACTCCTG GCTCAAGAGA CCCTCCTGCC 120 TTGGGCTCCC AAAGTGCTGG GATTACAGGC ATGAGCCACC ACGTCCAGCC ACTGGATGAC 180 TTTAGACCAC TGCTTCCCCT CTGCTCAACT TGTTTTCTTA AGGGCCTACC CAGAGCCATC 240 TCCCTCACCT GATTCCTTAT TAGGAGTTAA AAGCCTGACT CCCAGAGCCA GGTCCTCGCC 300 TGCTGTTTAA CCTAGGAGAA GCCCAGCTCC TGGCTCGGAT GCTTGGTGAA ATCAGGGGTC 360 TGGGGAACCT GCGTCTTCCT CTTTCTGCAC AGTCAGCTCC CCTCCACCCG CCTCACAGAC 420 TTCCTGGGGG CCGCTGGCAG GAACCAGAAG TTGTGCAGGC TCCATTCTGG CTGGGGAGGT 480 TTAAACTCAT CTCCTTCTGC ACTGGGAACA AATGTTACCC CAGGCACAGA TGACAGAGCC 540 AAAGTGAGCA GAAGGGAGGA ATCCAATCCA GGAGAGCTTC TAGTGTCCTC CAGGCCACCC 600 ATGAGGCTGC GGGGGTGGGG AAAAGGGGTG TGGGAAGATG AGATCTATCT CAAGGACAAG 660 GCCCTGGAGC CGTAACTCTC CCCTCCCGCC CAGGCCCAGG CTGTTCCTCT TTTTTCGAGG 720 CAAAACCTCA GCTGCCCCAT CAGTGACACA CTGTTCCTCT TGCCTCCTCC CACTGCTGTT 780 CAAGATCCTC AAGAGACTGA CCTTGGACCC GGGCATGGAC TCTGCCTTCA AGCAGGCCAG 840 GCTGGAGTAC CAACTCTGCC TCTTACCAGC TGTGTGAAGT TGTGTCATTT GAACACCACC 900 CCAAGCCAAG GCTCCCCACT TTTAATTGGA GATAATAATA ATATCAATGG CACAAGGCTG 960 TTTTTTAATG TAATGATGAT ATGAGTAAGA GATATCAGCT CACAGGCAAA TCCCAACTCT 1020 GCTCTTGCAG GGCACCCGCC CCCGCTTACA TTTTGTGCCC TAGGCACCTT CCTTGCCTCT 1080 TTCTAGTCTT GATCCTGGAG GTAGGGATTG CAATCACCAT TTCAGCAGGT AAGGAAACTG 1140 GGGTTTAGCT AAGTGTCGTG GCTCCCCTGG TGAGTGGCAG AGCTGGGATT AGAACCCAGG 1200 TCTTGCTGCA GCCAAGACAA GGTACATTCC TCTGCACTCC TAGGGCTGGA GAAGTCACGC 1260 CTGCCTGCAC TACTCCCCAC CTTGCCACCA GCAGAGAGTC CCCCAGCGTC CCACTAATTC 1320 TGTTGGTGGG TTTTTCCCTG CTGGGTCTGA TCAGAGCAGC CACCTGTCAT GCAAAGGGTT 1380 GTGACAAATT CCATAAAGTG TCATCACCTG GGTTATGGGG AAAGGGAACA CTCCAGAGGC 1440 CAAGATCAGC AGGACAGCCA TACCCATGCT CTCTCAGTAT CCCTATCACC TCTCAGGCAG 1500
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