| Tag | Content |
|---|
EnhancerAtlas ID | HS076-46874 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr5:176114780-176115700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYB | MA0502.1 | chr5:176115087-176115102 | CTGATTGGTCCACGG | - | 6.14 | | RREB1 | MA0073.1 | chr5:176115379-176115399 | AGTTTGGGGGTGGGGGGTGG | - | 6.46 |
|
| | 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 |
| GH05I176688 | chr5 | 176115041 | 176115190 |
|
Enhancer Sequence | ATAGCTCTTT TAGCTCCACC ATTTGGCGGT CCCGAGTTCT TCTCCTGCAG CCAGAAAGAA 60
TGAGGTATGC AAACAAGTGC AGGGTGAGCA AGATGAAGAA GAGCTTACTG AGCAACAGAA 120
CAACTCACAG GAGACCTACA GGGGGTAGCT CCTTTCTGCA GCCAGGGTGT CCCAATGAGT 180
GTTCAGCTCC TAGCAGAGAG GAGACCCTGG AGTGTGAAGC TCCTCTCTGC TGCTAGTCAT 240
CCCACTGTCT GCTCAGCTCT GGCTGAGCCC AGGGCTTTTA TGGGCCTCAG AGGCGGGGAC 300
GTGCATGCTG ATTGGTCCAC GGGCGGCCAT GGGCAGACCC AGAAAAGACA CTTGGGTCAG 360
TGGGACTGGA AGCCTGGCCC CCAGCTTTCA GGCTCTCCCT GGCCTGAAGA TGGAGCCTCA 420
CTGGGGACTG CCGCCTTCTG CCCAGGAATT TGTCTGCCTC CTGCTGCAGT TCATGGCACT 480
GGGCTCAGCC CTGATAGCAA GGAGAAGCCA GGCAAGGGGA GCAGGCACTT CCAAGCCTGC 540
AAGGGCAGGG GGACTTCCCA AGCCTCCAAG AGTGCAGGGA TGCCTGAGCC TGCAGCAGCA 600
GTTTGGGGGT GGGGGGTGGG GGCAGGGCTC CTGTCTGCTC CTGGAGTGGG AAGCCCAGGT 660
CTGCAGCCTT GGTTTGGGCG GTTGCAGCTG CACCCAGGAG GGCAGGGTTC CTGTCTGTTC 720
CTGGCCCCAC AAGAGCACAG GGAGACTCGG ATCCGCAGCC AGGACTTGGG TGGCTGCAAT 780
GTCACCTGGG GAGCTCCTAC CCCAGCTTGG AAAGGGTGGG ACTCCTGTCT GTCCCCACCT 840
GTGCAGCCCT GGCTGTGACT CCCTGCTGCA GCCGGCATGA TGGAGCCACT GCTGCCATCA 900
GTAAGAAAAC AAAAAACCCA 920
|
