| Tag | Content |
|---|
EnhancerAtlas ID | HS101-04449 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:246872510-246874020 |
Target genes | |
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 | AAAAAAATAG AAGTAGCTGC TTAATTGACA ATAAAAGCAC TTAGTTTCTG CTGCATACCT 60
AAAAGGTCAG CCTGGACTAA CTCCTTTTCG CTGTGCCATT CCAGCATGAT GCGCAGAGCT 120
TGGTAGAAGG ACCAGGTATT GGGAGGTAGG CCTGTGTTGT ACTATTGTGC AACTTTCAGT 180
ATGCTGAGAC AAAAACATGT TCTAAAATGG GGCAGCTGGC CAAGCATGGT GGCTCACACC 240
TGTAATCCCA GCAGTTTGGG AGGCTGAGGT AGGCATATCA TTTGGGGCCA AGAGGTCGAG 300
ACCAGCCTGG GCAACATAGT GAGGCCTCGT CTCTACAAAT AATTTGAAAT TTAACCAGGC 360
ATGATGGTGT GCACCTGAGG TTTCAGCTAC TCGGGAGGCA GAGGTGGAGG ATCACTTGAG 420
CCCTGATGTT GAGGCTGCAG TGAGCTGTGA CAGTGCCACT GCACTCCAGC TTGGGTGACA 480
GAGTGAGACT CTGTCTCAAA AAATAATGGT AATAATAAAA TAAAATGTGG CAGTACATGA 540
TGGAATTTCT GAATTGGATT AGCTACTTTC CTTGCTTTTT GTTTCTTTCT CTTATCTACT 600
AGAGATCAGC AAATAATTCA GGTAATCAAA AGTTGCAAAA AAAAAAAAAA ACCATGATTT 660
TTCATAGATG ACTCCCCATG ACTTCTTCCC TTCACATTTA GCCACAGCTG CCATACCACT 720
TCCTAAGTGT GGCAAGTTCA GCTTCCTTCT CACTTTCAGC TTCAAATGGA CTTTTGGACT 780
ACCTGGGCGT TCCTTTATTT GTCTCTTTCT GATTTCCTAT GTCAAAGATA AACAAGGTGG 840
AAGGACAGAT TTTAATCAGT AATATACTAT TGCAAAGTGA AAACGAGTCT AGCATGAGCT 900
GAACTCAACT TCTGAACCCA GTCAGAGGTG ACTAGGCATT TTAAAGGGAG GATGAGGGAA 960
GAGGGAAGGG TAAGTGAGGG CTCAGGAGAG TCAGGGAAAT GAAAAATTAC AAAAAGTAGA 1020
AGGGGGGTGG TAAATTAGTC CATTCTGTGT TGCTATAAAG GAATACCTGA GACCAGGTAA 1080
TTTATCAAGA AAAGAGGTTT ATTTGACTCA TGGTTGATGA GGACCTCGGG AAGTTTACCC 1140
TCATGGTAGA AGGTGAAGAG GGGGCAGGCA TGTCACATGG CGGGAAGCTT ACCATCATGG 1200
TGGAAGGCAA AGAGGGAGCA GGCACATCAC ATGGTGAGAG TGGGGGCAAG AGAGAGAGGA 1260
GGCAATACTT GGCTGTCTTA AACAAGTAGC TCCCACATGA ACTAATAGAG TGAGAGCTCA 1320
CTTATTACTA TGGGGATGTC ACCAGGCCAT TCGTGAAGGA TCCACTTCCA TGACCCAACT 1380
GAGAGGTGAA GCCAGCTGGG CTTCTGTGTC AGGCGGGGAC CTGGAGAACT TTTCTGTCTA 1440
GCTAAAGGAT TGTAAACGCA CCAATCAGTG CTCTGTGTCT AGCTAAAGGT TTATAAACAC 1500
ACCAATCAGC 1510
|
