Tag | Content |
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EnhancerAtlas ID | HS105-38766 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr19:8488270-8489380 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr19:8488997-8489008 | AGTGACTCATG | + | 6.14 | IRF1 | MA0050.2 | chr19:8488876-8488897 | AAAAAAAAAAAGAAAGAAAAA | - | 6.59 | KLF14 | MA0740.1 | chr19:8489023-8489037 | GGCCACGCCCCCTG | + | 6.69 | KLF16 | MA0741.1 | chr19:8489024-8489035 | GCCACGCCCCC | + | 6.62 | SP1 | MA0079.4 | chr19:8489021-8489036 | TGGGCCACGCCCCCT | + | 6.12 | SP3 | MA0746.2 | chr19:8489023-8489036 | GGCCACGCCCCCT | + | 6.82 | SP4 | MA0685.1 | chr19:8489021-8489038 | TGGGCCACGCCCCCTGC | + | 6.03 | SP8 | MA0747.1 | chr19:8489024-8489036 | GCCACGCCCCCT | + | 6.92 | Zfx | MA0146.2 | chr19:8489311-8489325 | GAGGCCGAGGCGGG | - | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 8488334 | 8488459 | chr19 | 8488784 | 8489136 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I008422 | chr19 | 8487743 | 8490043 |
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Enhancer Sequence | TTTTCACAGT TTCCCAGAAC AAGCTCCAAA CTGACATGAT TCTTCCTCAA GATTCTCGTC 60 ACTTCTGTTT CCCTGGGTTG GTTTCCGGAC AAAGGGTTCC TTTTTTGTTA ACTTTGTTTG 120 TGTGTGTACT TGGGGGAGGG TGGGATCGGG GTATGGGTTC AGAAAGGAGG CAGGCAGGCA 180 TGCCCTTTTG CCATTGCAGG AGGAAATAGC AGTCCAGGGA CAGGACTGTT GAGAAAGCAG 240 CCATGAGCAG CCTGTTGGGC TCTTTTTAAA GCCGCCCAAC TCCACCCCGC AGCATGAGAA 300 TCTGAGAAAA GGATAGAAAA CAGTCATTTC CAGGCAGGCG TGGTCGCTCA TGCCTGTAGT 360 CCCAGCACTT TGGAAGTCCA AGGCTGAAGG ATCGCTTGAG CCCAGAAGCT CAAGACCAGC 420 CTGGTCAACA TAGTGAGACC CCCCTCTCTA GAAAAAGTTA AAAAATATTA GCTGTGTGGC 480 GTGGTGCCAC CTGTAGTCCC AGCTACTCGG GAGACTGAGG CAGGAGGATC GCTCGAGCTA 540 GGGAGTCCGA GGCTGCAGTG AGCTGTGATT GCACCACTGC ACTCCAGCCT GGGTGACTCA 600 AAAAAAAAAA AAAAAAAGAA AGAAAAAAAA ATACAGTCTC TCTGAGAGGA AATTGGCGTT 660 GTCTGGAAAA TAGCTCTTCT TTGTGTGACC TCACAGTCTG CCTTCTGGCC AGAAATGTTT 720 GGGAAACAGT GACTCATGGC TGTTTGGCCT CTGGGCCACG CCCCCTGCCT CCTGAGCTGC 780 CCTGGGAAGG ACCCGGCATC CCCAGAGACT GGGCCAGGGC TGGAGACTTT TCCGAGGCAG 840 CTTTCTGCAG ATGCTTTTTA TTTCTATTTC CCCCTCACAA GGGCAGAGGA GCAGGTGAGC 900 ACTTCTCTCT GGATGCACAG GTTTCTCAGG TAGCACGGGC TTCAGGTGTG ATTAGATCCA 960 GGGGCCCGCA AAGATGTCCT TAAGAATCTA CCTTTCCCAG GCCTTGCGCA GTGGCTCACG 1020 CCTGTAATCC CAGCACTTTG GGAGGCCGAG GCGGGTGGAT CACGAGGTCA GGAGATCGAG 1080 ACCATCCTGG CTAACACGGT GAAACCCCGT 1110
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