Tag | Content |
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EnhancerAtlas ID | HS098-41552 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr4:3203280-3204800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr4:3203939-3203950 | CTGAGTCACCC | - | 6.02 | JUNB | MA0490.1 | chr4:3203939-3203950 | CTGAGTCACCC | - | 6.02 | RREB1 | MA0073.1 | chr4:3203880-3203900 | CGCTTGTGGGTGTGTTGTGG | - | 6.28 |
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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: 1 | ID | Chromosome | Start | End |
GH04I003200 | chr4 | 3202481 | 3206731 |
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Enhancer Sequence | TTAATGGATC AATGGATTTT TAACCTAATA ATTAAATTTC AAAAAATATC GTTCTTTAAT 60 GGTAATGTAA AGGTAAAATT AAGATAATAT GTAACAAGCA TGTGAGTGTC TAAGGTGTCC 120 CCGTGGTGGA AGGAAAAAAT AAATCCCCAT AAGTGTCCAA GATGCCCATA GAGAGCAGAG 180 CTGTTCTGGT TTAAACCCCT GCTCTTAGCA CTGTGTTTTT CCAGCTGTGG GTGGTGGGGG 240 ATGAGTATCT TTTTATTTCC ATGAGATGAG AAAAATGAAT TACTAGAAGT GTGAAATACA 300 AAACACAGCT GCTCTTTTTT TAGCCATAGA CTCAGCAGCC ATAAAATTGC TGTATCCAGT 360 TGCAGAAATT CCTGCTGCTT ACTCTTGACC CTCTCTCGGT TTGTGTGCAT CTCCTCTCAG 420 GCTGGCTCCC AGATGGGAGC TGGCTCCAGG CGACACTGGG TGCTCTGCTC CAGGAGGTCC 480 TTATGTGGGT CCTGCCCTAG CCTAGCCCCT CTCTTATGGA CTCTGTCACT GTGGGTTTAT 540 GATTCACTCT CAATCTGTCT TACCTCTTGG TGAACTGTTA GAGTCCTGCC TATACTTTGG 600 CGCTTGTGGG TGTGTTGTGG TACACATGAT GTGTTGGTCA CTTCCCAGCT CATCTTGTTC 660 TGAGTCACCC TAGATTTGGG ACATTCATTC GCCACCAGTA CCGGGCGGTG TATGGCCTGA 720 GATTTGGGGG GGCTTGTGCT GCTACAAATT GGGGCTGAAT TTGAGTTGAC AGTGGACCTT 780 CTTTATGTCT ACTGCTCATA TTTGAATTGC AAATACTGCC TCTTCTCTTT CAGAGGCTCA 840 TTACCCTATA GCTGTATTAT TGCAAAGTGC ACAATTACAG CTTGAGTGTA AGTCACACTG 900 CGCTGGCAGG ACGGCCCACT GAGAAAGGGC ACGTTTCCTG TTCGTTAGTT TTCACATTGA 960 CACATAATTT ACAATACAGT AAAATGTACT TTTCTATCAA CTGTAGTCAG TAACAGCCCC 1020 CCTCCCCCAA CCACATCAAG ATATAGAGGA GTGCTGTCAC TTCAAACAGT TCCCTCTTCC 1080 TCTGCCACAT CCTGCCCCTC CCCAGGTCTA ACCACCAATC CGTGCTCTGT CCCTCTGTTC 1140 AGCCCATTGC AGAAGGCCAT AGAAATAGAA TCTATAGGCT AGGTGTGGTG GCTCATGCCT 1200 GTAATCCCAG TATTTTGAGA GGCTGAAGTG GGAGGATGAC TTGAGGCTGG GAGTTCAAGA 1260 CTAGCCTGGG CTGCCTAGCA AGACCCCATC TCCAGAAAAA AAAAATTTAA AAATTACAAT 1320 CACGTCCCTG TAGTTCAGCT GCTTGGGAGG CTGAGGCAGG AGGATCACTT GAGCTCAGGA 1380 GTTAGAGGTT ACAGTGAGCT ATGATCGTGC CACTGTGCTC CAGCCTAGGT GACACAGCAA 1440 GACGTTGTCT CTGGGGAAAA AAGAAAGAAA CGGAACCACG CGGTGTGCAG CCTTCTGAGT 1500 CTGGCCCCTT TCGGTGAGCA 1520
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