| Tag | Content |
|---|
EnhancerAtlas ID | HS028-01446 |
Organism | Homo sapiens |
Tissue/cell | Colo829 |
Coordinate | chr17:15393700-15394750 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SREBF2 | MA0596.1 | chr17:15394465-15394475 | ATCACCCCAT | - | 6.02 | | Stat6 | MA0520.1 | chr17:15394201-15394216 | GCTTCTCAGGAAATC | - | 6.69 |
|
| | 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 |
| GH17I015490 | chr17 | 15393439 | 15395762 |
|
Enhancer Sequence | TTTGAGAGGT TTGTAGTAAG TTTGTAGAAT ACTGGTGAGT CGGTCAGGGA CAGCTTGAGT 60
ATGATTCGCA ACCCCCAAAA CCACCTCCCT ATGGGCAAAC CGTATCCACA GAGCACATTC 120
ATAAGCCTGA TTTAAAATAC TCGCTCCTTG TGCCTCAGCC ATTACTCTCT TTCTGTCCAG 180
GTCTCTTATT CTGACTTAGT GGAAAATAAG GTTGTTACAG CAATGGCTCC ATTCGTCCTG 240
TGGGCAAGAA ACTCATGGAG AGAATTAGTC AATTCTTCCT GGACATTCGG GAGCTTCTGG 300
GTGGAGGGAA GACTGCGAAG CAGAAACAAA CAGAAATCCT AGAGAGGCAG TCATCTGAGC 360
ATTCGTCACA GGGGCACTCC TAGGATCCAC CCTCAGAAGC CGTGAAAGGC CCATTGATCT 420
GGCTGGGGCA GGGAGTGGCC CTGAGCTGGT GACATCTCAG GCGAGGAAAG GCACAGATGT 480
CTGTGCTGGC TGTGATAAGA GGCTTCTCAG GAAATCTGAG TCACCTCGGG CCGGCTCTTC 540
GAAGCATAGA GGCCCAGCAA GCACCACAGC CTGGAGGCAA AGCTTCCTGC TAGCCCTGGG 600
ACCCTGGGAC TTTGCATTTC CTGTTGGTGT CCTTTGACTT GGGCAGCCAC CACCCCTGGG 660
AAGTTTTCCA ACACCCTCAC TCATGCATTT TGAACCTGGT GTTCACAGCT CTTTGTCTCT 720
GCTCATCTCG CTTTTGTTTC CTCTGGAATG TTCCAAGCCC CCTGCATCAC CCCATGCCAG 780
GAATCTGACA TCCCAGAGTG GAAGCCGGCT TCATGTTACT CACCCCACCC TGTGATTTCC 840
TGATGGAGGA TCCGGAGACC TGAACTCTGG TCCAGGTTTA CAGACAACTC ATAATCATGG 900
TTGAGGCCCC TTTCTAGGCC TTACTGTTCT CATACTTTTA ACTGGGGATG GGGGCAGGAT 960
GGGAAACTTT TGGAAAAACA GACTTTTTAA AACTGGAATG ATGCTAGACA TTTATTTGCT 1020
ACTACCTGCT GGCTGCTGCC TGTCATTTCA 1050
|
