| Tag | Content |
|---|
EnhancerAtlas ID | HS012-01211 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr1:246872840-246873990 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYB | MA0502.1 | chr1:246873963-246873978 | AAACGCACCAATCAG | + | 6.73 | | ZNF263 | MA0528.1 | chr1:246873459-246873480 | GGATGAGGGAAGAGGGAAGGG | + | 6.39 | | ZNF263 | MA0528.1 | chr1:246873456-246873477 | GGAGGATGAGGGAAGAGGGAA | + | 6.92 |
|
| | 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 |
| GH01I246709 | chr1 | 246872517 | 246873810 |
|
Enhancer Sequence | CTCTACAAAT AATTTGAAAT TTAACCAGGC ATGATGGTGT GCACCTGAGG TTTCAGCTAC 60
TCGGGAGGCA GAGGTGGAGG ATCACTTGAG CCCTGATGTT GAGGCTGCAG TGAGCTGTGA 120
CAGTGCCACT GCACTCCAGC TTGGGTGACA GAGTGAGACT CTGTCTCAAA AAATAATGGT 180
AATAATAAAA TAAAATGTGG CAGTACATGA TGGAATTTCT GAATTGGATT AGCTACTTTC 240
CTTGCTTTTT GTTTCTTTCT CTTATCTACT AGAGATCAGC AAATAATTCA GGTAATCAAA 300
AGTTGCAAAA AAAAAAAAAA ACCATGATTT TTCATAGATG ACTCCCCATG ACTTCTTCCC 360
TTCACATTTA GCCACAGCTG CCATACCACT TCCTAAGTGT GGCAAGTTCA GCTTCCTTCT 420
CACTTTCAGC TTCAAATGGA CTTTTGGACT ACCTGGGCGT TCCTTTATTT GTCTCTTTCT 480
GATTTCCTAT GTCAAAGATA AACAAGGTGG AAGGACAGAT TTTAATCAGT AATATACTAT 540
TGCAAAGTGA AAACGAGTCT AGCATGAGCT GAACTCAACT TCTGAACCCA GTCAGAGGTG 600
ACTAGGCATT TTAAAGGGAG GATGAGGGAA GAGGGAAGGG TAAGTGAGGG CTCAGGAGAG 660
TCAGGGAAAT GAAAAATTAC AAAAAGTAGA AGGGGGGTGG TAAATTAGTC CATTCTGTGT 720
TGCTATAAAG GAATACCTGA GACCAGGTAA TTTATCAAGA AAAGAGGTTT ATTTGACTCA 780
TGGTTGATGA GGACCTCGGG AAGTTTACCC TCATGGTAGA AGGTGAAGAG GGGGCAGGCA 840
TGTCACATGG CGGGAAGCTT ACCATCATGG TGGAAGGCAA AGAGGGAGCA GGCACATCAC 900
ATGGTGAGAG TGGGGGCAAG AGAGAGAGGA GGCAATACTT GGCTGTCTTA AACAAGTAGC 960
TCCCACATGA ACTAATAGAG TGAGAGCTCA CTTATTACTA TGGGGATGTC ACCAGGCCAT 1020
TCGTGAAGGA TCCACTTCCA TGACCCAACT GAGAGGTGAA GCCAGCTGGG CTTCTGTGTC 1080
AGGCGGGGAC CTGGAGAACT TTTCTGTCTA GCTAAAGGAT TGTAAACGCA CCAATCAGTG 1140
CTCTGTGTCT 1150
|
