| Tag | Content |
|---|
EnhancerAtlas ID | HS012-16229 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr2:73418480-73419380 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr2:73418665-73418677 | TAAATCACTGCA | + | 6.92 | | IRF1 | MA0050.2 | chr2:73419335-73419356 | AGAGAGAAAGAGAAAGGAAGG | - | 6.44 | | ZNF263 | MA0528.1 | chr2:73419073-73419094 | GGTGCAGGGGAAGCAGGAGGG | + | 6.25 | | ZNF263 | MA0528.1 | chr2:73419082-73419103 | GAAGCAGGAGGGGCAGGGGAG | + | 7.07 |
|
| | 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 |
| GH02I073191 | chr2 | 73418261 | 73419727 |
|
Enhancer Sequence | GTTCAAGCAA TTCTCCTGCC TCAGCCTCCT GAGTGGCTGG GATTACAGGC ATGCACCACC 60
ATGCCTGGCT AATTTTGTAT TTTTAGTAGA GACAGGGTTT CACTATGTTG GCCAGGCTGG 120
TCTTGAACTC CAGACCTCAG GTGATCTGCC TGCCTCGGCC TCCCAAAGTG TGGGGATTAC 180
AGGCATAAAT CACTGCACCT GGCCTATGAA GTTATTACTA ATCTCTCCAT CCTTTGTACT 240
CCCATAGAAT CCATCCCTTT GGTTTGGCAG TTGCATTAGC TAGTTGTGGA TGAGTCTCTC 300
TGTCCCCTCC CTCCACCCTC ACCGTAAGAC TCTGAGCTCC CATTGGGCAG GAATTGTATA 360
TTTCATTGCA CTTTGTACCC CTCATAAAAC CCAACACAGA ATAGGCCTCA AACAAGTAAA 420
TGTTTGTCGA CTTCAGTCTA ATTGAAGGGC ATAGAATTTC AGAGAAAATC TTAAAGGCAG 480
CATACATAAG AAAAAGTTAG GAAACACTAG GTAACTGCAA AGTGCAATGT GTTAGCTGTG 540
CATTCCAGGG AGGGAGGAAC AAACAACCAA CCTTGTTTGC TCTTGGCCTG TCAGGTGCAG 600
GGGAAGCAGG AGGGGCAGGG GAGGGGAGAG CAGGTGTGGG CTGGAGCTGA GACAGCCCAG 660
GCAGGGGGTA GGGGGAGGTG GTATGGGGCC TCCCCAAGGC AGCTCTGGGG CCCTCTGACC 720
CTGCAAGCTG GGCTTGACTT AGGGCACGTT GCATGGCAGC CCTCCATCCA GGTCCAACAA 780
ACTCCATCAT CACCATTTAG CACCTTTCTT CTGCATGAAA AAGCTTCCCT TTGGAAAGAC 840
AAGGAAGAAG AAAAGAGAGA GAAAGAGAAA GGAAGGAATA GAGGGAAGGA CAAAGAGAGG 900
|
