Tag | Content |
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EnhancerAtlas ID | HS139-42461 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr4:170266020-170267450 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr4:170266663-170266674 | CATGAGTCACT | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr4 | 170266400 | 170266800 | chr4 | 170266800 | 170266979 | chr4 | 170266348 | 170267006 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I169345 | chr4 | 170266219 | 170267320 |
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Enhancer Sequence | TAGAATATAT TTCACATATT TTTGTAAATA TAAGTAAAAT ATATTTCACA TATTATTTTT 60 GTAAATATAA GTAATATGTG TTTTATATAT TAGAACATAC AGTAACAAAG TAGATTAAAA 120 AAAAACCTCC ACCACTATTT ACCAATTTGG TGTATTTTCT TTCAATCTTT TTTTATTTGC 180 TGAGAGAGAG AGAAATGGGA GGGGTGAGAA CTAGTATTTA TTACCTACAT ATTTATGTAT 240 CTATCAGATA TATTTTTGTT ACATTCTGGA AATCAATAAC ATCAGTGAAA AGGAGAGAGA 300 ATTCTTACCC CCTGTTCCTT TAACCTTTAC CGAAGAAAGG CAATGGGTGG GGCAGCACGT 360 TTTATGGGCA GTTTGTCAGA TCTCCAAGAC TCTAAGGAAT TACAGTGACC CCACACAGCA 420 GGCACAGGGA CTGTCCAGCC ACAGGTGGAT GGCCAGGGAT ATCCGCAGGG GCTGAAAGAG 480 AAGCACTCCC ACCAGCTTCT GGGTTTGGTC AGCAACTGGT GAGAGACTGG ACAGCTGAAG 540 AATGTGCCCC CAGTGGAACA TTTTCAATAA CCATTAGGCT TCCAATAAAA AGAAGTTAGA 600 AGCAACAGTG TGAAAGATGT GACTGTTTCC TCAGAGGTCA AAGCATGAGT CACTGTGAAT 660 TAGGCAGTCA AGGGATGGCC CTTTTTTGTG CACTCACCCC CCTGTCATCA ACCAGAGTCA 720 TTGTTCTTCT GAATAACCCC CCCGTTTCAA TGCCAGGGGG TTCACATCTG GTGGTGACAG 780 GAGAGTTTTG CCAACAGGAT TCCAAATGTC AGCAGGCTGA CTGGTCAATG CTTACTCAGG 840 CAAGCCTTCC CAGTGAAGCC ATAATTACCT CCCGCTCTCA GAATAGGATT AACAAATGCA 900 GTTATTTGTG TATGATCCTT TTACATACAA CCTCATGCAT TTTACTCATG CCAGTTAATA 960 TTTCCCATTA GAAAAATCCT CTTATATGAA TGCCATGATA AATAAATTAT TGGCATTTTA 1020 AAAAAACCTT GTTAACCAGA AATGGCCGCA AGGGTGAAAG TGTTTATACC TTCATACAAT 1080 AATGCATTTC TCTTTTTATT TTAAGACTGT TTCCTTTCAT TCAGTTTATG AGTAAGGCTG 1140 GGAATCAATT AAGTTTTAAG TGCAAAGACA AGGGATATGA TTCCTAAAAA TAAAAGAAGA 1200 TAATTTAGGT GTACTTTAGA GGTAATTATA GCAGGATTTT GTTCAAAAGT TTCCCAATAT 1260 AACTATGTGA CTTGTGAAAA CCTATCTCAA CACTAGTTTC ATCACCTATA AACTGGAGGT 1320 AATTCACGCC AACCTCACAG AGATGTTTTG ATTCAGTAAT GAGTCTTGTC TTTTGTGGCA 1380 GTTCTAGAAG CTCCAAGGAC AGGTGCTGCC AACTGTCCCA ATTTAGCCTG 1430
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