| Tag | Content |
|---|
EnhancerAtlas ID | HS012-10020 | Organism | Homo sapiens | Tissue/cell | Caco-2 | Coordinate | chr12:66512860-66514230 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr12:66513239-66513254 | TGACCTTTGACCTGA | - | 6 | | NR2C2 | MA0504.1 | chr12:66513239-66513254 | TGACCTTTGACCTGA | - | 6.87 | | Nr2f6 | MA0677.1 | chr12:66513239-66513253 | TGACCTTTGACCTG | - | 7.73 | | Rxra | MA0512.2 | chr12:66513239-66513253 | TGACCTTTGACCTG | - | 7.58 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 66513087 | 66513276 | | chr12 | 66513334 | 66513671 |
| Enhancer Sequence | CTATACTCTG GGACAGGCGG CTTGCTCACT ACTTAGCAGT TGCATGACTT TGGGTAAATT 60
TAGTTAACCT TTCAAACTGT TTTCTCATCT GAAAATAGGG ATAATTAAAG TATTGATCCC 120
ACAGTGTTTT AAAGATTAAA TAATATACAT AAAGCATTTA AGAGAGTACG CATTCTCTAA 180
ATGTTGGCTG TTGGGTTATT TTTACTGCTT GCCTACCAAA TTAAGCTTAT TTGGCAACAC 240
ATTGTATTTT CTCCCCTGCT CTAAAATAAC TGCAAAAGAC TCTTGGCATT CAACTGCGTA 300
AAATTTAGGG TTTTGTAAGC AGGCCCAAAA GTGGCCCTGG GCCTCCTGGC TACCTGACAG 360
TCCTCTGGAA ACAGCAGAGT GACCTTTGAC CTGATGTAAG TATTTAACAG TCCCACCTCA 420
CCCCTAAACA TTTCCTTGTA AAATTGGTAT GTGTCTACTG CAACAGTGTT TTTATTAATA 480
CATGCAGGCA AATAGAGGGA AAAAGACATA TATTTTGTGT TTAGCACAAA TTTGAATCAC 540
TCTGCCAGAT GGCATCAGAA GTTAGTCACT TAACTAGTAA GATTAGCCAA CAGCTTAGCA 600
TCTGCATTTC TATTGTAGTA TTTATAAATT TGGCAATGCC TTAGATTCCT CCCAATTTTA 660
TGTTGTGGTC AGCACTTCCC TAAATTACAC ATTGCTGCCC CTCACCATCA CCACCAGTCC 720
ATTTCAGATA TTTGATTCAA GTCATTTATA GCTATTTTTC TTCTCCAACT CTTAAGCCAT 780
ATTCCAGAAA CACGGATCCA AATTTTGAAA ATATCTGAAT TTCCTAATAA GCAAATATAT 840
ACTGCTGCAT CCTTATTTGA TGTAGCATGT GAATTACATA GTGGGAAGAG ATATCTACAC 900
TAATGTGACA GTAGAAAATA GGATGTGGTC AAAACCACTA CTTGATTCTA CCTTAGAGCT 960
TCAACTGCAG TTTGCATTTC TTCTCTGATT AGTACCTTGG GCAACTACTG ATCATGGCCT 1020
ACACCTTCCC CTTTTGGATT GGTCAGCCCA TTCCTAATGA AGTGTCACCT GAGGAAATCC 1080
AGTCTGCCTT AGGCCTAGAG ATTTGAGGAG GGTTCTGTAC ATCATTATTC TACTTAAACC 1140
TGCTCTTTAT CTGATCCTGA GCCCACATGA ACCCAATCTA TCACAGGTTG ACCCAAAAAT 1200
AGGTATTCTA TCCTAAAATC ACCTTTCTCT CTTAGCAAGA GTTTGCACAT CCTTGAGAGG 1260
CAGAATGGCA TTGTAAGAGT ATAGGCTCTA GAGCCACACT GCCTAAATTT GAATCCCAGA 1320
TTTCAGTTTT AGTTGTATGG CCTGTGTGCC TCAGTTTCCC CATGTGTAAA 1370
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