| Tag | Content |
|---|
EnhancerAtlas ID | HS101-37233 | Organism | Homo sapiens | Tissue/cell | HT29 | Coordinate | chr6:33228120-33229250 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr6:33228504-33228515 | AGTGACTCATG | + | 6.14 | | HES2 | MA0616.2 | chr6:33228643-33228653 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr6:33228643-33228653 | GGCACGTGCC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCATGCCTGG CTTTTTTTTT TTTCTTTTTT GCCTTGCTGT TTTCTTGCCT TGTCTCATCA 60
GTGTTTATAT CATTAAAAAA TAAAACAACC CAGTGCAGTG GCTGTTTTGT TTTTTAATGA 120
TATAAACACT CACAAACACA CCACACAATC CAAGTAGCAG CAGCTTGGCA AAAGTCACCA 180
TCAAACTATG AAATCCTACT GAAACCATCC CTGTGCTTCT CGTGCACAGG TACTCGTTGA 240
TCTAAATGTT GCATTTATTG TGTTCTTGCT TTTTTCCCCC TTTTTTTGTG TGTGTTCTTG 300
CTTTTAAAAG TAAAGCTATA TATATGCCAA AACAAAAATT CGTTGTTTTC CAGTGTCATT 360
AAAAACAGAA TCTAGGCCGG GTGCAGTGAC TCATGCCTAT AATCCCAGCA CTTTGGGAGG 420
CTGAGGCGGG TGAATCACCT GAGGTCAGGA GTTTTAAGAC CAGCTGGGCC AACATGGTGA 480
AACCCCATCT CTACTAAAAA TACAAAAATT AGCTGGACAT GGTGGCACGT GCCTGCAGTC 540
CCAGCTACTC AGAGGCTGAG GCAGGAGAAT CACTTAACCT GGGAGGCGGA CGTTGCAGTG 600
AGCTGACATC GTATCGCTGC ACTCCAGTGT GGGAGTCAGA GTGAGACTCC GTCTTTAAAA 660
AAAAAAAAGA ATCATAAGAT TTTTCACTTG AGGGCAGTAA TTCAAGACCA GCCCAGGCAA 720
CAGTTGTCTT TTGTAAAGAC AACTGTCTTT ACAAAATTAA AAAATTAGCT GGCACACACC 780
TACAGTAAAC TCATTTTTGG TAAAAGTGCC AAGAACATAC ACTGGGGAAA AGATAGTCTC 840
TTGGTCAGGC ACGGTAGCTC ACGCCTGTAA TCCCAGCACT TGGGAGGCCC AGGTGGGAGG 900
ATCACTTGAA GTCAGGAGTT CAAGACAAGC CTGGCTAACA TGGTGAAATC CCGTCTCTAC 960
TAAAAACACA AAAACTAGCC CGGCGTGGTG GCAGGCATCA GTAATCCCAA CTATTCAGGA 1020
GGCTGAGGCA GGAGAATCAC TTGAACCAAG GAGGCAGAGG TTGCAGTGAG CCAATACTGC 1080
ACCACTGCAC TCCAGCCTAG GTGACAGAGC AAGACTCCGT CTGAAAAAAA 1130
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