Tag | Content |
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EnhancerAtlas ID | HS088-49655 | Organism | Homo sapiens | Tissue/cell | HeLa-S3 | Coordinate | chr7:149807040-149808340 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr7:149807827-149807846 | GAGCCAGCAGGGGGCGGGG | + | 6.25 | INSM1 | MA0155.1 | chr7:149807783-149807795 | TGGCAGGGGGCG | + | 6.07 | KLF16 | MA0741.1 | chr7:149807836-149807847 | GGGGGCGGGGC | - | 6.02 | KLF16 | MA0741.1 | chr7:149807963-149807974 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr7:149807837-149807847 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr7:149807964-149807974 | GGGGCGGGGC | - | 6.02 | SP1 | MA0079.4 | chr7:149807835-149807850 | AGGGGGCGGGGCTTG | - | 6.98 | SP2 | MA0516.2 | chr7:149807547-149807564 | AAGAGGGTGGGGCTTAC | - | 6.11 | SP2 | MA0516.2 | chr7:149807616-149807633 | AAGAGGGTGGGGCTTAC | - | 6.11 | SP2 | MA0516.2 | chr7:149807685-149807702 | AAGAGGGTGGGGCTTAC | - | 6.11 | SP2 | MA0516.2 | chr7:149807834-149807851 | CAGGGGGCGGGGCTTGC | - | 7.28 | SP4 | MA0685.1 | chr7:149807833-149807850 | GCAGGGGGCGGGGCTTG | - | 6.98 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AACACCATAG GCAATACCTG GGGACAGTCA TGGAGGGAGG GGTCCCACTG CCATGAAGGC 60 CACCATTAAA ACAAGAGCAA TGCACCTGCC TGTGAGGCAC GGCGGCCCTT GGACAGGGGG 120 CTCCAGGGCA GGCGAGGGCC AAGACCTGTT CTCGGAAGCT ACCTCGTGTT TTCCAAACAA 180 TAGGAACTGG TACTAAAAGG CAAAAGCAAG CCTGAGCCCT CTCCCTTGAC ACCCACATCC 240 ACGCTGAATG CCTCTCATTT TATTAACTGT GTATTGAAAC TGATTGCAAT TCCCTGGGCA 300 AAGCAAAAAC AGTAAGAAAG AGTTGTCTTT TTGAGCATTT AAATTGTTCT CTCTGCTCTC 360 CTGGCTGTTC TAGGGCAGAA GGATGTCTCG GAGGCATTGG GGTCACCCTG GTAGTCAGGG 420 GCAAGACCCA GGAACCCATG TGGGTGGCAG GGGCGGGACT GCTCAGCAAG GCTGGAAGCA 480 GGTGGGGCTG CCTGAGGGTG GGGCTGGAAG AGGGTGGGGC TTACTAAGAG ATTCACTCTG 540 GCTGGAGGAG GTGGGGCTGC CTGAGGGTGG GGCTGGAAGA GGGTGGGGCT TACTAAGAGA 600 TTCACTCTGG CTGGAGCAGG TGGGGCTGCC TGAGGGTGGG GCTGGAAGAG GGTGGGGCTT 660 ACTAAGAGAT TCACTCTGGC TGGAGGAGGT GGGGCTGGCA AGGGGCAAAA CTGTCTGAGG 720 GCGGGGATGA TCAGTGGTGG GGCTGGCAGG GGGCGGGACT GCCTGAGGGT GGGGCTTAGA 780 AGGGCCAGAG CCAGCAGGGG GCGGGGCTTG CTGGGGGACT GGCTCTGGCT GGCAGAGGCA 840 AGGCCGGCAG GGGGCAGGAC TGAGGGCAAG GCTGGCAGGG GGGTGGGCTG TTGGGGGTGT 900 GGCTCTTAGG GGTGGGGCTT GCTGGGGGCG GGGCTGGCCA CTGCGAGGCT GGCAGGTGGC 960 AGGACTGTCA GGTCAGGGGA CATTGGAGAG AGGGCCCCCT TGCATCTTGC AGGTGGGCAG 1020 AGCCCTGTGT AATTGGACAT GCTGTCCCTA TCCTGGCCTA AAACAGTGGT CCACGCTCTC 1080 TCATCCAGGG ATAACACGTG GCAAACCTCG CACCAGTACC TCACAGGTAC CCACATCCTC 1140 CTACCTCTGC ACCACACCAA GCATCCCCAG TGTTCTCCAT CCCCAGACTC TCTCAAGCTC 1200 ATTCTGGGGC AAGTCACTGC CTGTGGGCTC CAGGGACTCG CTCCAGCTGT GAGCACCCCC 1260 CTTTTCCTCC CTGGACCGCA GCTGGGGTCC TGCTTCCCGC 1300
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