| Tag | Content |
|---|
EnhancerAtlas ID | HS027-00569 | Organism | Homo sapiens | Tissue/cell | Colo320 | Coordinate | chr18:10121640-10123870 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr18:10121788-10121808 | GGTGTGTGTTTGGCTTGGGG | - | 6.21 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH18I010121 | chr18 | 10121674 | 10123843 |
| Enhancer Sequence | ATGTTGAAAA CTTCCCCTAA ACATTTTCAA TCAAAAACTT GCACATAAAA TTTCCCAGGT 60
TCATGTGTAA ACATGCACCA TTGCTACATG TGTGTCACAG AAGGGTCCAC TGATGGAAGA 120
GTCTGTGTTA CTGTACTCTC AGTGACTGGG TGTGTGTTTG GCTTGGGGTT TATTTTGTAT 180
CACCCCCTCA CTCCACTCAA GGGCATATAA GAGGTCGCAG GATTAACTTC TGGGTGTGGA 240
TGGAGGCCAA CGTAAAGGCT GCTCTACCTA TACATCAGGG GACTGCAGGG CTTTATTAGG 300
TTTACCCAGA CCTCTTTCAG AGAGATGATG TGTTCACACA TGTGGAGCAG ACACTGAGTG 360
CCAAAAATAC TTCCAGAGTG CTTTGCAACT TTGCTATCTC CTAAATAATT GTAGACATCT 420
ATGCATTCTT CAGTAAACTG TGTTTATGTA CTGTTCCATG GCAGTGAAAT CTCTTTCAAT 480
ATCTTGGTAG CCTCAGCACC CTCTGTCCCA TGTGCTTCTC GTGTGACCCC GGCTGTGGTC 540
TGCAGAGCTG AGCCCGTGGT ATTTGGGTCA CATAACTGTT TCTGTGCCAA CGCACGTTTT 600
CTTTCACATT GCTATTAACT GTGCAGTAAA GAAGGGAGAT TGGCTGGTGA AAGTGTCCTG 660
GGTCCTTCAA GGATTACTCA GATTTCACAG TGCCTGTAAT CTGAGCTCCC TACACTGAGT 720
GGTTTAGTGG TTATGGTCAG ATGTCTGCTT TATCCTAACC TGTCAGCTGA ACAATCATGT 780
TTGGGTGTGT GTGTTTGAAC AGTGCTATAA TTGGTACGAG GGGTTCAGAA ACGCCCTGGG 840
GATGCCCTGA CATCGGATGG GCACGTGCAG CCGGTATCAC AGCCTGCCAT GCCATCAGCT 900
CCGTACTTGA CATTCAGGCC TGGTGATCAC CCCTGATCCC CCAGCTTGAG TCCCCACCAC 960
TCAGTTTACC CACAGGAGGA AACTGAGAGC TACAGCTTAG GTGAGAAGCT GCCACTTTCT 1020
TGTCTGACAC AGCCATAGCT ATCATAGGAT GGTGAAAAAT TGGTGTTCAC ATTAACAAGA 1080
GAGGCCTGAT AGAAGAGGCA GAGTTGTTTT GAAGTTGAGG GTCGCAGCTC TTTTACCCCT 1140
TAGGCCAGGG AGCTAGGGAG GGACCAGAGA GTGGTATTTG TAAGGCCTCC AATTCCTTTT 1200
ATTTAAGAAG TGTGTGCACA CACACTTTTG CTGTAGCGAT TTATAAGCAC ACTTACGTCT 1260
CAGTCAGTCA CCGTGCTTAT TAAAGACATA AATATTTTAC CTCTTAGCAA AGACGAAAAT 1320
AGTTTTCACA GATTTCCTGG CAGGCAACAA CACAACCTAG CCAACCCTTT TCATCTGTAG 1380
ATTTCAACCT AATAAAGTAT TGATCTAGGG AACAGAACTT GTTTCTACGT CCCATTCCTG 1440
AAAAGTAGAA AACCAGATTG ACCAGGGCTA GGGGGAGGGT TTGCCTCTAC CTGAGGATAT 1500
TCTGAATTTT ATGGATGCTT TGTTGAGCAA TGTTGAAACT GAAAGCGCTG ATGGAATAAA 1560
AGACGTCAAA CTCTCTAAGG CTTGAGGATG CATTATAGAA AAGAAAACCG CCTTTCTTGC 1620
AGGTTTCCTG ATTACTCATC TTAATTAGGT ATTGCCCTGA ATGACAAAAC TTCCTCTGGC 1680
TCCTACGCCC CTTAACCATT TTAATTCTAC AACCAAACCC ACAATCACAG CTCTCCTTGC 1740
ATGGCAGAGG CCTTAGGCTC GGGGTGGGAA TCTGGCCACG TCTGAATGCA GACTGTAGAG 1800
GTGCAGATAC GGCCCTACTG AAGGAGCAAG GCTGGGCACA GAGGTTAGGG GAGGCCGACT 1860
TGTCCCTGGG CACGTTAAGA AAGACAGTTC CTCAGTCATC TGGGACTTGG TAGAAAAGGG 1920
AGAAAGGAAA GGAGACTTTT TCAAAGAACA AGATAATAAT CATGGTCAGC CACTGTGTTA 1980
GCACTTCTTA TATGTTTTCT CCTTAATTCC AGCCATGCCT GTGCAGTGGT CGCTTCTTTC 2040
TTTTGCTGTG TGACTGCGGC CTGGTAGGCT CACAGAGGCT TGGCCATCTG CTTGTCCATC 2100
GCCCCCTGCC CAGCTTGCTG GCCTGCGGCT CCTCTCACTC CACAGCCACC AACGCTCCAC 2160
CATCCTGCAC GGACAGGATT CTCTTTCTCT ACCCTTCGCT GGGAGGCCGT TGCTTCATCT 2220
CCTCTCTGGC 2230
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