| Tag | Content |
|---|
EnhancerAtlas ID | HS101-11979 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr13:27785800-27787220 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EN2 | MA0642.1 | chr13:27786616-27786626 | GCTAATTGGG | - | 6.02 | | NFYB | MA0502.1 | chr13:27786716-27786731 | AAACAGACCAATCAG | + | 6.36 | | NFYB | MA0502.1 | chr13:27786692-27786707 | AAACGGACCAATCAG | + | 8.25 | | NFYB | MA0502.1 | chr13:27786764-27786779 | AAATGAACCAATCAG | + | 8.73 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ATAAAAGTAG TATGTCCATA TAATGGAATA TTATTCAGCC ATAACAAGAG TTAAAATTCA 60
GCTGGGTGCA GTGTCTCATG TCTGTAATCC TGGAAGGCTG AGGCAGGTAG ATCACTTGAG 120
CCCAGGAGTT CGAGACCAGC CTGGGCAACA TGGCGAAACC CTGTCTCTAC AAAAATATAC 180
AAAAATTAGC CAGGCCTGGT GGTGCATATC TGTAGTCCCA GCTACTCGGG AAGCTGATGT 240
GGAAGGATTG CTTGAACCTG GGAGGCAGAG GCTGCAGTGA GTCAGAAGCT GCAGTGAGTC 300
AGAAGCTGCA GTGAGCTGAG ATTGCACTGA GAGGTGACAA CGTGCTGGCA GCCCTTGCTC 360
ACTCTTGGCA CCTCCTTGGC CTCGGCGTCC GCTCTGGCCA CGCTTGAGGA GCCCATCAGC 420
CCACCGCTGC ACTGTGAGGG CCCCCCTTGG AGTCTGGCCA AAGCCAGAGC TGGCTCCCTC 480
TGCTCCTGGG GAGATTTCAG GGAGAGGCGT GGGTGGGAGC CAGGGCTGCA GGCGCAGGTT 540
CTGGGTGGGC ATGGGCTTGG CGGGCCCTGC ACTCCTAGTG GCCGGCACCT ACTGGGCTTC 600
ATCTGGGACG AGCTCCCTCT GGGCTGCCGG AATGCCTGGG CTAGGTGCCG CAAAGTCCCA 660
TGGGAAGTGC CACTGAGAGG TGAACCCGGC TGGGCTTCTG GGTTGGGTGG GGACCTGGAG 720
AACTTTTCTG TCTAGCTAAA GGTTTGTAAA AACACACCAA TCAGCACTGT GTCTAGCTAA 780
AGGTTTGTAA ATGCACCACT CAGCACTCTG CGTCTAGCTA ATTGGGTAGG GGACTTGGAG 840
AACTTTTGTG TCTAGCTAAA GGTTTGTAAA TGCAGCAATC AGCCTTCTGT CAAAACGGAC 900
CAATCAGCTC TCTGTAAAAC AGACCAATCA GCTCTCTGTA AAATGGACCA GTCAGCTCTC 960
TGTAAAATGA ACCAATCAGT AGGATGTGGG TGGGACCAGA TAAGGGAATA AAAAGCAGGC 1020
TACCCAAGCC AGCAGCGGCA AGCCGCTTGG GTCCCCTTCC ATGTTGTGGA AGCTTTGTTC 1080
TTTCACTCTT CACAATAAAT CTTGCTGCTG CTCACTCTTT GGCTCTGCAC CACCTTTATG 1140
AGCTATAACA CTCACCACGA AGGTCTGCAG CTTCACTCCT GAGGCCAGCA AGACCACAAA 1200
CTCACCGGAA GGAACAAACA ACCCCAAACG CACCGCCTTT AAGAGCTGTA ACACTCACCG 1260
CAAAGGTCTG CAGCTTAATT CCTGAAGTCA GCGAGACCAC GAACCCACCA GAAGGAAGAA 1320
ACTCTGGACA CATCTGAACA TATGAAGGAA CAAACTCTGG ACACACCATC TTTAAGAACT 1380
GTAACACTCA CTGCGAGGGT CCACGGCTTC ATTCTTGAAG 1420
|
