| Tag | Content |
|---|
EnhancerAtlas ID | HS012-09935 | Organism | Homo sapiens | Tissue/cell | Caco-2 | Coordinate | chr12:65099890-65101350 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr12:65100729-65100750 | GGAGGAGGAAGGGAGAAGTGA | + | 6.75 |
| | | 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 |
| GH12I064706 | chr12 | 65099924 | 65101628 |
| Enhancer Sequence | TTGTTTAGTG CCTTGCCTTG TGCTCCCTAA AAATACAGTC ACAAAGTGTT CTTTCTTCCT 60
TGACAAGATA GAGTCCAAAT GCTCAGAGCA GCTGAGACTG GGGATGCCCA GGTTTTCATA 120
TCAACATAAG GCACAGAGTG GTGTTGCATG ATCCAAACCA GACGGCTGTG TGTCGGTGCA 180
GTCGGGGGCC TTGACCTTTG TTTCTAGTCC ATGTTTTTAT GCATGTAAAT TCTCCCCTAG 240
ATAGTAATCT CCTTGGAGAC TGGACCATAT CTTCAGTTCA CTTTGCATCT CTCCTAGCTG 300
CAGGGCACAG CATTTGTGGG ACTAAACATT TCATAGACAT GTCTGGAAAC AGCTAGTTGG 360
GCAGCTTTGA GACAGGAAGG TAGCCCTCTA CAGAGAGACC CGGAGCTGCA GCTTCCTGCT 420
GCTCCTCATC CAGCCAGTGT TCACCTTTGG CTGAACTCTT AAACAGGACC TTCGTTGGCA 480
TTACAGGAAG AAGGAGAGGG GCCAGGATGA TTGCAGGCCA GAGTGTTGTT ATCCCCTGCT 540
GTGCAGAGGA CCAGACGTGG CATCATGGGC TTCATCCTCT GTGGGAGCAT TGATGGGCAT 600
TGAGCTTTAG GCTGAAGCCT GCCCTGATAG ATGACAAAGT GAATAGTCAC TTGCACCAGA 660
CTGCTGGAAA GAACCCGAGT TGTCATGTTG ATCTCAGGCC TAATTAGTGT GCTGCTCACT 720
TAATCTGGGA GACGCTGGGT AAAAGGGACT GGGAGAAAAT GTACACGAAG CAGCCCCTTT 780
CTTAGGGACT TAAGTGGGAA CAGAATCAAT TGTGCATCTG AGCTACTTTC CCATCGTTGG 840
GAGGAGGAAG GGAGAAGTGA CTGATGGTCT TGATTTGGAC AACAGGTGCC TCGGAAACCC 900
AGCCAGAATC TTGGCGTGCT GCAGCTGCTG AGGGGCCACT CTCCCAAGCT GCAACTCTCC 960
CTCGCACCAG CTTTTGGAAG TTACAGAGAC CCACTAGAGA GAAGACTTTG GACTCATGAC 1020
TGGAGCCTTC CAGCCAAGAG TCCATTAAAA TATTTTCCAA CATGTGCTGA GAACATTTTA 1080
GCAACCATTC CAACAAAGAA GCTTCCATTT GGTTTTAGTA ACAATAGCTA GGAACCAGTG 1140
CTTATTTCTA TTATTTCAGT ATGTAATGTA CATATTTTCC CCCACTTTGG AGACAATCTG 1200
AGCCTCTACC GCTGGACAGC TCTGCTCTAC CCTGTAGTAA AAAGGGCTCA CTGCTCGATG 1260
CACCGGAAGC TGATACCACG ACACTGGGTT TTTTGTTGTT TTTGAGAAAA GCTTTATATT 1320
ATATATAAGT CGACTCACAA GGAGATAGGA GTGTCAAGCT CAAATATTTC TCCCTGTGCT 1380
GTCTTTAAGG CAGGCAGTAA TTTTATTAGA AAAGATTAGA CAGGCATGCT GGAGCATGCC 1440
TGTAGCATGC CTGTAGTCCC 1460
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