| Tag | Content |
|---|
EnhancerAtlas ID | HS101-02758 | Organism | Homo sapiens | Tissue/cell | HT29 | Coordinate | chr1:152926040-152927660 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:152926214-152926235 | CTTTCCCTCATGCCCTCCTCC | - | 6.23 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 152926285 | 152927322 | | chr1 | 152926955 | 152927187 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I152953 | chr1 | 152925757 | 152927718 |
| Enhancer Sequence | GAAAGAGAGT ACCTACACAT CTTGGAGTGT GACAGACCTG GGCTCAAATC TCCTCTTCCT 60
TACTTTTGTA TTAATCTTGG CCAACTTAAC CTTTCTAAGC TAAAAAATGA GAATAACTTG 120
AACTTCAAGT CCTAAATTTG AAGCTCAGAG TTTCTGACAG CAGTGGTGTT CTATCTTTCC 180
CTCATGCCCT CCTCCACAAG CCCCAGGGAA AGGGAACCCC ACTGCTAGAT GCACATCCTG 240
CTGTGTATGC CCAGGTTGTG GGGAGCAGGG GGACCCTAGC TGGTAATGGA TTTCTGCAAT 300
GAAGCTTCAG CACTCGGCAG TCAGTCATCC TTTGAAGGAA GCCCTGCCTG TGGGTGCGGC 360
CAGCTTCAGT GTGCTCCACC ATCTCCTGCA GGTTTGTACG TGTGCCCTGG CAATCTGACA 420
TTCCTGGGAG AATCACAGAT GCCTGGCACT GAAGACGCCC TGGGCGTGGC TTATACCCAC 480
CTATGCTGAA ACTCCTCCCA GTCACTTTGG GGCTATCAGT TCGGCATGCC ATGTTTAAGT 540
GTGTTATTGT TGTCTGGGGG TCTTGTTCAT ACGCAGAGAA CAGTCATTGT TTTACCCCAG 600
ACTCCTGACC CTTGATATTT GGTCCTCTGT CTTCTGGAAT TTTTATGTCA ACTCTCAGGA 660
ATTAGACTAT GCAGCTTCCA TCTCACTCTT AAATAAAATA AAAAGGGAAC CATTTTCCCT 720
GTCCTGGGCT CTCCAGGCAG CCCTTTGGCT CAAGTCTCCT CTGCCACCAA GGGCCGATGA 780
TGTGTGTGAC ATGAATGCTC ATCTTCGGTG GACTTAGGAG ACACTGGAGC TCTGAATTAG 840
GAGCACTGGA CAGAGTATAT GAGAGCTGAG TATTGTCTTA GTTATTCTGC TGTTCTTCTG 900
CGGGACCCAG GACAAGTCAT TCCCTTTTCC CAGTGTCCTC ACCTGTACAT GACAATGTTG 960
GACTTCCTGA ACTATTTCTA AGCTTCTTTC AGTTCTGACT CTGTATGAGG TGACTCACGC 1020
TAATCTTTGT GTTTAATCTC TTCGCCTAAT GATTCATCAT CATGGAAAAC CCTAAAAGAG 1080
GTAAGTCTGG GGTTGAAGGC CACCAGATGC TTCTGCATGG AGGCGTAGAG AAAGCTTAGC 1140
TAAAACATGC ATCTGTATTT GAAGAGCACT CGGGCTTAGG ACTAACTTTC CTCCCTCCAG 1200
GGAACCAACA CATCCACCTT CCGGGGCCAG GTGTGTGTGT GTGTGTGTAT GTGTGTTTAA 1260
GCAGCAATTT ACTACTATAA GCAAGACACT ATACTGGGAT CTTAATACTT ATCTTATATA 1320
ATATACATTA CTACCATATA AGTAAAAAAT TTAATTTTGC AAATGAGGAA AGCAAGAACC 1380
AAAGAGGTTA TAAACTTTGC CAGCTGAAAG AGCTGAGAGT CAAATATAGA TCATTCTTGG 1440
CACAGAAAGA CAAATACCAC ATGATCTACT TATGTGTGGG ATCTAGAAAG TCAAACTCAT 1500
GGAAGCAGAA AGTAGAAGGG TGGTTACCAG AGGCTGGGCA TTGGGGAAGG ACTGGGGAGA 1560
TATTGGTCAA AGCAATATAA AATTTCAGTT TGATAGGAGG AATAAGTTCA AGAGATCTAT 1620
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