| Tag | Content |
|---|
EnhancerAtlas ID | HS012-04605 | Organism | Homo sapiens | Tissue/cell | Caco-2 | Coordinate | chr11:77010100-77011530 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TBX21 | MA0690.1 | chr11:77010866-77010876 | AAGGTGTGAA | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 77010566 | 77010927 | | chr11 | 77011147 | 77011316 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH11I077298 | chr11 | 77010023 | 77011577 |
| Enhancer Sequence | TCCTCACACT GGCCTCATAT GAAAACCAGG TAATCCCTCT CACCCAGAGT ATCACACATT 60
CCCATCCTGG ACCCTCTTTA TGAGACAGGG GCCGGAGGTA GCAGTTGCTA GGCAACACCA 120
ACCACCCCAC AGCTTCTCAC CAGCCCCATA GAATACCATC AGCATCCCGA TTATAAGAAT 180
TAGGTATTCT GTCCCATTAA TTTGCCCAAA GATGGAAGAA ATCCTAAATG ACTATCTCAC 240
CCTCAAAAGT AGTAGTTACC TCACTTCCTT CAATTCCTTG CTCAAATGTC ACCTTCTCAA 300
CAAGGTCAAC CCTAACCACT TTATTTAATA CTGCAATCTG CTCCCTCCTT CTAACTCCTC 360
TATTGCACTC TACTTTTTTT CTATAGAAAA TAAAACATTA TATAATGTAT TTATTTAGGA 420
AGTTTACTGT TTATTGTCTG TCTTTACCTC CTAGAGCGTA TGTTCCACAT TTAACAGTAA 480
GAGTTTATTG CTCACACATC TGAGCTAATG GGCTATCTGT TCTGCTGATC TGTTCTGCCT 540
CAGCTAGAAT GACTGGGATG ACTTGGCTTT CCTTCATGTG TCACTCAACC AGGTTGGCCT 600
GGGTATGTTC TCATGGTGTT GGAAGTTGTC CAAGAGAGTA AGTCCCAAAT GCAAGCCCAT 660
TTCAAGCCTC TGCCTCACCG GATGTCTGTT CATATGGTTG AGCCCAAAGT CAACAATCAG 720
CGCAGGTCAC CTCATGGTGG TTGGTCACAG TAAAGTTACA CAGAAAAAGG TGTGAACACA 780
AAGAATGTAA CTAAGGGAAG GGTGAACAGT TGGAGTCAAA TAATACAATC TACCTCTCTA 840
TATGACAAGC AAAGTAAACT ATGAGGCATA AAAGCAATAC TAGAGACAAA GAGGGACATT 900
TCATAATGTG AAAAAACAAA AATTTTAATT TGCAATTTGT AAGTACTATT AGATATGAGT 960
TCTAAATTTC TCTTCAAAGA ATCAATATGT CAGTATGTTC AATTCTTTGC CTTCTACTTT 1020
TAAACTTCCT CGTAAAGCAA CCTTTTTTGA TCACCTGCTC CATCCTGACT CATTCTGATT 1080
ACCAGCTCTG CCCTGACTCA TCCTGATCAC CTGCTCCACC CTCACTCCCG CCAAACCACT 1140
CACCCCGTCA CTCTCTCTAA ATTAGCCAAT TGGAATTAGT TTAGCCTGTG CGGTCTAACA 1200
CTAGCCAATA GGGGAACGAC ACAGCAGCAG GGGCCACGTG TGTCAGGAAT AAGAACCCCT 1260
TCCCCTCCCT TGTCCAAGTG TGTGCTCACC ATTGCTCCAT ATGTAAGGGT GCACCCTTCT 1320
ATAGAAGTAT ATTGCCTTGC TAAGAATTAA AAAGAAAATT TTATATTTGA GTGCTATTTC 1380
TTTTGCGGCA CCGAAACTAT AACAGTACCC AATCACCTAG TCTCTAAGGG 1430
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