Tag | Content |
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EnhancerAtlas ID | HS102-22929 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr9:100476330-100477830 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr9:100476883-100476903 | TGGGGTTTTGTGGTTTGGGT | - | 6.49 | Zfx | MA0146.2 | chr9:100477458-100477472 | CCCGCCTCGGCCTC | + | 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 |
chr9 | 100476461 | 100477800 | chr9 | 100476679 | 100477155 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I097713 | chr9 | 100476036 | 100477716 |
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Enhancer Sequence | TCAACATAAA AATATGTTTA TTGGCCTTTG TGCTGCTTCT CCCACACAAA ATCATTTTCT 60 TTGTTTCTAC ATTTATTGGC AAAAGTCAAT GCATATTCTT GACTTTTGCC AACTTTTAAT 120 GGCCCATATA TATTTAAATT TGTATGTAAG CACTCTTCCT GTGTTATGGA TATGAACCAT 180 CTCTGTGAAA TGTTACAATT GTTTTCATTT GTCATTAGCT TTGCCATTTT GTGGTCTTTA 240 GAAAGAATTG ATGCCCTGTG TTCAGTGCGA TGACAAAGAT TGGCTAAATA AGTGATAAAG 300 GGAATAGTGA AGGTTGTTTT ATCCTTACAG CAGTCCTGGA GGTTAGACAG GTCCTAGGGC 360 TCATTATCCC CATTTTACAG AGGAAAAGCA GAGCCCCAAG AGGGTAAATG CTGAAATCAT 420 AAGGCTAGGA CGTGTTAGAG TTGCATCTCA ACAGTCCTTA ACTCCTGACT CAAAGCCTTG 480 AAAAACCCCT GCTCACCAGG GAAAGGAAGT CAAAGGTCCA GGGTGTGTAC ACAGACAGCC 540 CTTGAAAGGA ATGTGGGGTT TTGTGGTTTG GGTTTTTCCT CCCCTTTCTA AGCACGCTTC 600 GCATGCCAGC AAAGGGTGTG CATTTGTGTA TTGGGGGGCA GGAGGGAGGT GCAGGGTTGC 660 ATGTCATTCC TCAGCCTTTT CATAAAGGAG GTCAAAGCAT GGAGCTTGTG ATGAAGCTCA 720 AAAGTCCCTT CAGGCTTCTG GTGGTGTGCA CCTGTAGAAC TCCTGCCAGG AATGACTTGA 780 ATGAGACTCA CCCCAACAAT GAGAACTAGG CTTTGGGTCC ATGTAATATG ACTCATTAAA 840 TGGTTTATTG TGACCCATAC ATGAGCTTCA AATTTATAAA ATACCCCCTT TGTTATTTAT 900 TTATTTATTT TGAGATGGAG TTCCACTCTT TTTGCCCAGG CTGGAGTGCA ATGGCACGAT 960 CTCAGCTCAC TGCAACCTCT GTCTCCAGGG TTCAGATGAT TCTCCTGCCT CAGCTTCCCA 1020 AGTAGCTGGG ATTATAGGTG CCTGGCTAAT TTTTTTGTAT TTTTAGTAGA GACAGGGTTT 1080 TACCATGTTG GCCAGGCTGG TCTTGAACTC CTCACCTCAG GTGATCCTCC CGCCTCGGCC 1140 TCCCAAAGAG CTGGGATTAC AGGCATGAGC CACTGCACTC AGCAAAATAC CCCCTTTGTG 1200 ACAACAGAGA TAGACAAACT CTGCTTCATG GCCTCAAAAC TAAAATTGAA AAGATTTTTT 1260 AAAGGCTTTA CATGCCTATG ACACTGCATA TCCCAATGAG AAGTCTTCTT TGTGGAAGAT 1320 CTCTATTTCA TTTTATTTTA TTTCATTTCA TTTTTGAGGC AAGGTCTTGG TCTGTCACCC 1380 AGGCTGGAGT CCAGTGGGGG TGATCTTAGC TCACTGCATC CTCAGACTCC TAGGCTCAAG 1440 TGATCCTCCC ACCTCGGCCT CCCAAGTAGC TGGGACTACA GGCCTGCATG AGCCACCACA 1500
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