Tag | Content |
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EnhancerAtlas ID | HS073-10881 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr4:3203580-3204960 |
Target genes | |
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 | AAACACAGCT GCTCTTTTTT TAGCCATAGA CTCAGCAGCC ATAAAATTGC TGTATCCAGT 60 TGCAGAAATT CCTGCTGCTT ACTCTTGACC CTCTCTCGGT TTGTGTGCAT CTCCTCTCAG 120 GCTGGCTCCC AGATGGGAGC TGGCTCCAGG CGACACTGGG TGCTCTGCTC CAGGAGGTCC 180 TTATGTGGGT CCTGCCCTAG CCTAGCCCCT CTCTTATGGA CTCTGTCACT GTGGGTTTAT 240 GATTCACTCT CAATCTGTCT TACCTCTTGG TGAACTGTTA GAGTCCTGCC TATACTTTGG 300 CGCTTGTGGG TGTGTTGTGG TACACATGAT GTGTTGGTCA CTTCCCAGCT CATCTTGTTC 360 TGAGTCACCC TAGATTTGGG ACATTCATTC GCCACCAGTA CCGGGCGGTG TATGGCCTGA 420 GATTTGGGGG GGCTTGTGCT GCTACAAATT GGGGCTGAAT TTGAGTTGAC AGTGGACCTT 480 CTTTATGTCT ACTGCTCATA TTTGAATTGC AAATACTGCC TCTTCTCTTT CAGAGGCTCA 540 TTACCCTATA GCTGTATTAT TGCAAAGTGC ACAATTACAG CTTGAGTGTA AGTCACACTG 600 CGCTGGCAGG ACGGCCCACT GAGAAAGGGC ACGTTTCCTG TTCGTTAGTT TTCACATTGA 660 CACATAATTT ACAATACAGT AAAATGTACT TTTCTATCAA CTGTAGTCAG TAACAGCCCC 720 CCTCCCCCAA CCACATCAAG ATATAGAGGA GTGCTGTCAC TTCAAACAGT TCCCTCTTCC 780 TCTGCCACAT CCTGCCCCTC CCCAGGTCTA ACCACCAATC CGTGCTCTGT CCCTCTGTTC 840 AGCCCATTGC AGAAGGCCAT AGAAATAGAA TCTATAGGCT AGGTGTGGTG GCTCATGCCT 900 GTAATCCCAG TATTTTGAGA GGCTGAAGTG GGAGGATGAC TTGAGGCTGG GAGTTCAAGA 960 CTAGCCTGGG CTGCCTAGCA AGACCCCATC TCCAGAAAAA AAAAATTTAA AAATTACAAT 1020 CACGTCCCTG TAGTTCAGCT GCTTGGGAGG CTGAGGCAGG AGGATCACTT GAGCTCAGGA 1080 GTTAGAGGTT ACAGTGAGCT ATGATCGTGC CACTGTGCTC CAGCCTAGGT GACACAGCAA 1140 GACGTTGTCT CTGGGGAAAA AAGAAAGAAA CGGAACCACG CGGTGTGCAG CCTTCTGAGT 1200 CTGGCCCCTT TCGGTGAGCA GTGTCTAAAG TTCTGTCGCG TGTTGCCCAC GCGTCGGTGG 1260 CTCGCTCCTT GCAACTGCTG AGCATTGTAT GGCTAGGCTG TAGTTTGTTT TCACTTCACC 1320 AGTTGGGAAA CAGAGAAAAG GCACTTTTTA AAAAGTTTAA ATCTGTAGAA TTTTGGTTTT 1380
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