| Tag | Content |
|---|
EnhancerAtlas ID | HS012-12091 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr12:121901980-121903130 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr12:121903013-121903025 | GTTTGTTTGTTT | + | 6.32 |
|
| | 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 |
| GH12I121465 | chr12 | 121903004 | 121906704 |
|
Enhancer Sequence | AGTTATAATC ATATCACTGT ACTCCAGCCT GCGTGACAGA GCAGGACCCT GACTCAAAAC 60
AAAAAACAAG ATGGAACAAG AATTCTTCTA AAAGCCCTCC TTTAGGAGAC ACCTCTTCAA 120
CTTGGAAAGC AAGCTGAAGA ATTTTCTGAC ACATTTTGTA CTAGAGAAGC AAATGAAGTC 180
TGTGGGAGAA GTTCCCGCCA AGGGTGCACA CCGGCAAAGA GCACACAAGG GGTCTCCCGC 240
CAACATGGCT CGCTCACCGC GGGCCCATCC CCTGTCTCCT GTCCCACAGG CTGTGACACT 300
TGGGGAAACC CAGGCTGCTG AGGGAAGGCA TGGGGCAGAC AGGCCAGCGC AGCACGACAG 360
GTCTCAGGTG GGGATGAGAA GTACACAGGC TCGGAAGGTG GAGCAGCCAA AACTCTGATG 420
GGGTGGGCGT GAGGGCTACA CCAACTACAG AGATGGACGG GGCAGCAGCA GCCTCCCACC 480
AGGGCCTCCC TCCGACGGGT CCTTTCATCC AGCAGGTGGG CAAGTCTACT TGTTCATCCA 540
CACTCCAGGA CTTGGCAACC TCTCCTCATG AAGGATCTTC TCCTTTGGTG CCAAACCCAT 600
TCAGCAGGGT GGGACAGAGG TACAGAGAAA CTTCGAGAAG AGCTGGGTCT GGAGCCTGCA 660
AGCTGGAGAC TCCAGAGACC CTCGCTGTGC TTTGGAAGAT GCAAATGCTT TCGAGGTCCT 720
CAGAGGAAGC CACTCTTCTC AGGCTCAGGC TGAGAAAACT GTTGAGGAAA GCATGCAGGG 780
AGGCAAGGAG AGTGTCCCCC AACTACGGGG TACCTTAGCT GACAAACACC TTCTCTGTTG 840
GGACTACGAG ACAAGCCTGC CCCCCACTGC CCTGGCTTAG ATGTCGTCTC CCTCAGTGCA 900
CTGAGTGGGA AAAAAAAATC ATCTTAAAGT TAACAATACA ACCTCAAGTC GTTGCTAAGG 960
ACTCCACAAG TGCCACAATC GGCTTGACCA ATGTGAGAAG GAGGAAGAAA AAATTTGGCT 1020
ACAGTGAATA CAGGTTTGTT TGTTTTTGTT TTTGTTTTTG TTTTTTTGAG ACAGAGTCTC 1080
ACTCTCGTCG CTCAGGCTGG AGTGCAGTGG CACGATCTCG GCTCATTGCA ACCGCAACCT 1140
CCGCCTCCTG 1150
|
