Tag | Content |
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EnhancerAtlas ID | HS101-02902 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:156520500-156521490 |
Target genes | Number: 30 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:156521368-156521388 | ACCCCCCTCACCCCCACCCA | + | 6.58 |
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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 |
GH01I156551 | chr1 | 156520877 | 156524211 |
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Enhancer Sequence | TGGAGGCTCC AACTACCTGC CCCCACGCCC CACTCCCCTA TGCCTCATTG CACACCTTCT 60 CAGGCCAATC CTGACCCTGA CCCTTACCTT CTCTTTCCTT TTCTTGCTCC ACACTCCTCT 120 ACCCGACAAG GTAGTGGGAA GATTACATGA GCCCACAGGT CAAGTAAGCC TATGCCTGCC 180 ACACTGTCAG ACTGATAAAG GCTTGAACCC TTCCTTGCCT CACACAACCC CAGATTCTAC 240 TCCTTCCCAA CTCTCCTCAA TAATAATAGA CTTTGTAAAC TAACATTTTA TTGAGTACTG 300 ACTATGTGCC AGGCAGTATT CTAAAGCACT TTCTTATGCA TTAATACTTG TAAAGCACAT 360 AAAATGATGC TTGGCACAGA GTAAGGACTC AATAAATGTT AGCCAGTACT ACTGTCATAT 420 TATCTCACTT ACACCCCATA ACTATGAGAT ACACTCTTTA CTGCCACAAG CTTCTAGGTG 480 ATGAAACAGA GGCACAGAGA GGTTAAGTAA CACGTGCAGG GTCAGGCCGC CAGGATGTAG 540 GCTCCAGTAG TCTGGCCCAG GAGTCTGAGC TCTCAACCAC TCTCTACTGC AACATACTCA 600 GGGTGTTTCA GGTTCAGAAC CCTGCCCCAT TTGTCAATTC ATTTGATTTT CACCCTCATT 660 CTGGGAGCTG GGTAGGACCA GCGTAGGCAG TACTTTACAG ATGAGTAAAT AGAGCTCAGA 720 GATATCAAGG GATTTGCTCA AGGTCACATG GTCACTAAGG GTCAGAGTGG GAAATCCAGC 780 CTGTTTCTCT GGCTCCCAGG CCTGTGCTTT TCCCATGGAC TGCCCACTGC CCTGGCAACA 840 GGGCCATCCT TCTTTACCAG ATTGGAACAC CCCCCTCACC CCCACCCAGA AGCCATTGTG 900 TCCATCAGAA TAGAGCTCTG CCAGACTGGG TACAGTGCAA CCCACAGAGA ATGTTCTTCC 960 TGCTCTGATG ACCAACCCAA CCAGCCCTAA 990
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