| Tag | Content |
|---|
EnhancerAtlas ID | HS012-19258 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr4:99700700-99702160 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLI2 | MA0734.2 | chr4:99701016-99701031 | AGGCCACCCACCAAG | + | 6.2 | | Myog | MA0500.1 | chr4:99701058-99701069 | AACAGCTGCAG | + | 6.02 | | Tcf12 | MA0521.1 | chr4:99701058-99701069 | AACAGCTGCAG | + | 6.62 |
|
| | 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 |
| GH04I098779 | chr4 | 99700176 | 99702165 |
|
Enhancer Sequence | GGGAAGCGAG TTTGGGCTGT ATCCTTAAGA GTCTTGGTCT GGGGAGAGAT GTGCTGAGAG 60
CTGGGCTGCA GACATTGATC TAGCTAGTCC TACTCAGACC AGTGAGGCAG ACAGGGCTGC 120
ATCTGGGAAG AACATGCCAG CACTCAGCAA AGGCATTTTA TTGTCAGCTT CTCCCTCCCC 180
TTAGCCATAG CTTGGGGGGC CTTTCCTTAG TCCCTCCTCC CCTCCATTTG TGCAGCTCCT 240
TTTTCCATGC AGGTCACTGC CTTGACAGAG GTGGGCATGC CTACAGTGCC CAGGCCTCTG 300
AGGAATGCCC TAGTATAGGC CACCCACCAA GAGTAACACT GATGCCTCCA AGATATGGAA 360
CAGCTGCAGC CTGGGTTATG GCTGTGAGCC CTGCCAAAGT GCACATGGAG GGAAGCTTGT 420
GTGTCCCTCT GTGCCAGTCC AACAACTCCA CTCACATGCC GTGCATCGAA GAATCTTCCT 480
GGTGAGTATG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTATGTG TTTTCATGAT 540
GTCTTTTTTT GGGTTGGAAG AGAGACGCCT TGCTCTCTCT CAGAAATTCT GTGAATGGTC 600
ATTTTACTCA GAATTTCCAG CATGTAAGAT AGAAGCTCTC CAGGGTTATC TCTGGTCAGG 660
GATCAAACAG CTGCTCTCCA CTGTCTCAGC AGAATAAAAT GCTTCTACCA AAGCAAAGCT 720
GACGCAGACA TACAAAACAG ATAAGCGTGA GATCTGGGCT GTGGGAGGCA TGGTTATCTG 780
GAACACTTTT CCTTACCCAG GAGAGAAGCA TTTGTCTGAG GAGTACTGTA ACCATGTACT 840
TTCAGATAAC AAAATTTCCT AGGGAATCCC TCATATCAGC AGTGACTGTA TCCCTTGGAC 900
TTACTCTTAA AATCCAGTAC ATATTTCTTT GCCTTATATG GCTAAGACGA AGTGTATGAG 960
TGTCGGGGAA GGGGAGGATT TGAGAAGAGC TTCTTCAAAT GTATGTCCTA GCCTCTGCCC 1020
TTAGCAAAGA AAAAGGAAGA GCTACAAAAG TTGTGGAAGG GAATAAATTA CCTTGCAGTG 1080
GGTGGGAATA AATTACCTTG CAGTGGGTAG GCATAGTCGA GGTATAACTT GATGGCCTAA 1140
AAGGCCACTT CCCTGCCTTC CTCCAAAAGG AACCCCTTCC TCAGTAGTAT TGCCTTTGAT 1200
TCCCTCATTA ATGACTCCTT GAGGCCAACG CAGTAGTTTT CAATCTGGGA CACGTGGAAT 1260
TCCAGGGGTC TGGGGCAAGC CAGGGTGGGC ATGGAGGGTG TTCTACCCCT TCTCCCCATC 1320
CTTTAAATGG GGGTGCTCTC ACCTTCTCCA TGGTACATAT CACACTTCCC TTTGAGATTT 1380
CTTCTGCAAG TTTTCTTCTT CTTAGTAGGT GTGATGGTTA ATTGTATGTG TCAGGTTGGT 1440
GAGGCCACGG TACCCAGATA 1460
|
