| Tag | Content |
|---|
EnhancerAtlas ID | HS012-18062 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr3:41309120-41310110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr3:41309723-41309738 | CATGCTGAGTCACGC | - | 6.27 | | Nfe2l2 | MA0150.2 | chr3:41309725-41309740 | TGCTGAGTCACGCTG | - | 7.95 |
|
| | 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 |
| GH03I041267 | chr3 | 41309096 | 41310997 |
|
Enhancer Sequence | CTAAAAAGGT GACAGTTCTA AATGCCCTAC CACTATAAAT TCTGCATGAC TCTTAGAGCC 60
TAATTTGACA TCAGCCACAG TGAAAAGTCC TTAACATGCA CTCCTCCTGT CCACACCAGA 120
TCAATGAGTC CTGCTGCTAC TCTCGTTTAC AGATGAGGAA ACTGTCACCT CAGGAGGCAA 180
AGTGACTAGC CATGGTCTTC CTGACTTCGA ATCCTTGATC TCAACCATCA AAGGACACTG 240
AGAAAGAATG AAGGAGTCAG CAGTTGTAGC TGAGATGTCT ACCAGATTGA GAGAGCCCGT 300
GAAATAGGAG TCCAACTGTA GCTGTGTTTG ATTCAGTGGC TTCATGGCAC AGCCGACTAC 360
TTCACATTCA TATTCCTCAA CTGGGGGTGA TTTTGACCCC CAGGAGACAT TTGGCAATGT 420
CTGGAAACAC TTTTGGTGGT CACAACTGGG GATAAGGGGA GGTGGACTGG CATCTAATGG 480
GTAGAGCCAG AAATGCTGCT ATACACTCCA TATTGCACAG GACAGTCCCC ATGATAAAGA 540
ATTATCTGAC TCACAATGTC AATAGTGCCG AGGTTGAGAA ACCATAGGCT AGACCATCTG 600
ATCCATGCTG AGTCACGCTG TGTTGCCTTC TCATGTTACA TCAGGATGCC TTTCTTTGAA 660
AGGTTACTAA CCACCCTCCC CACTGGACTA CAAACCCTTC TTTTCCTCTC TCCTGAGGTT 720
GAAGTCTTGG ACCAGCCTTT CTTCCAACAC ATAATACTCT TACTTCTGCG GTACTTGGGT 780
CAGTGGCTAT CACTTGGTTA TATCCTGTCC CAGGGTGAAC TTGTGCTTCA AGGTCCTTCT 840
GGGCTGCCCA AGGCAGAGAG GTTCTGGCAG ACTACCCTTA AATGCCTCAC ACTCGGCAGG 900
GCATGGTGGC TTATGCCTGT AATCCCAGCA CTTTGGGAGA CCGAGGCGGG CAGATCATTT 960
GTGGTCAGGA GTTCGAGACC AGTCTGGCCA 990
|
