Tag | Content |
---|
EnhancerAtlas ID | HS180-04450 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:212015950-212016880 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CUX1 | MA0754.1 | chr1:212016809-212016819 | TTATCGATTA | - | 6.02 | CUX2 | MA0755.1 | chr1:212016809-212016819 | TTATCGATTA | - | 6.02 | IRF1 | MA0050.2 | chr1:212016667-212016688 | TCTTCCTTTCACTTTCACTTA | + | 7.86 | PRDM1 | MA0508.2 | chr1:212016675-212016685 | TCACTTTCAC | + | 6.02 | RAX | MA0718.1 | chr1:212016701-212016711 | GTTAATTGGC | - | 6.02 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 212016062 | 212016200 | chr1 | 212016200 | 212016763 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I211843 | chr1 | 212016343 | 212016742 |
|
Enhancer Sequence | AGCACAGAAA GAGTCAATTT AGTGTAATTC TTAAGGGCTA GAATTTTCAG AATGGTAAAT 60 GAGCATTGGC TTCTGCCCAG TCATCAGTTA CATTAGTCCC TAACAAGAGC CTTAGTCATC 120 CTTTGAAGCT TTGAAGTCAG GCATTGACTT CTCTCTAGCT GTGAAAGTTC TAGATGGCAT 180 CTCCTCCCAA TATAAATCTA TTCTGTCGAC ATTGAAAATC TAGGGTGTAG TGTAGCCCCC 240 TTCATCAATC ATCTTAGCTA GATCTTCTGG ATAACTTGCT ACAGTTTCTA CATCAGCACT 300 TGCTGCTTCA CTTTGCACTT TATGTTATGG AAATGGCTTC TTTCCTTAAA CCTCATGAAC 360 CAACCTCTGC TAGCTTTCAA CTTTTCTTTT GCAGCTTCCT CACCTGTCTC AGCCTTCATC 420 AAATTAAAGA GTTAGGGCCT TGCTCTGGAT TAGACTTTAG CTTAAGTAAA TGTTGTGGCT 480 GATTTGATCT ATCTAGACCA CAAACTTTCT CCCTATCTGC AGTAAGCCTG TTTTGCTTTC 540 TTATTCATGT GTTTACTACA GTAGCACTTT TAATTTCCTT CAATAACTTT TTCTTTGCAG 600 TCACAACCTG GGTAACTGGT GAAAAAGGCC TAGTTTTTGG CCTGTCTTGG CTTTCAACCT 660 GCCTTCCTCA CTAAGCTTCA TTATGTCCAG CTTTTGATTT AAAGTGAAAA ATGCAACTCT 720 TCCTTTCACT TTCACTTAGA GGCCATTGTA GGTTAATTGG CCTAATTTCA ATTTTGTTGT 780 GCCTCAAGGA ATAGGGAGGC TCAAGGAGAG GAAGAAAGAT GGGAATGGCC AGTTGGTGGA 840 AAGAACAGAA CACACACATT TATCGATTAA GTTCACCCAC CTTCTATGAG CAAGGTTCTT 900 GGAACTCCAA AACAATTACA ATAGTAACAT 930
|