| Tag | Content |
|---|
EnhancerAtlas ID | HS108-17714 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:72902160-72903040 |
Target genes | | Number: 22 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYB | MA0502.1 | chr17:72902991-72903006 | CTGATTGGTGCATCT | - | 6.14 | | NFYB | MA0502.1 | chr17:72902513-72902528 | CTGATTGGTCTGTTT | - | 6.36 | | NFYB | MA0502.1 | chr17:72902919-72902934 | CTGATTGGTGCATTC | - | 6.64 | | NFYB | MA0502.1 | chr17:72902640-72902655 | CTGATTGGTGCATTT | - | 7.1 | | NFYB | MA0502.1 | chr17:72902537-72902552 | CTGATTGGTCCGTTT | - | 8.25 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTGGTGGGTT TGTGGTCTCA TTGGCTTCAG GAGTGAAGCT GCAGACCTTC GCAGTGAGTG 60
TTACAGCTCT TAAGGTGGCA TGTCCGGAAT TGTTCATTCC TCCCGGTGGG TTCATGGTCT 120
CACTGGCCTC AGGAGAGAAG CTACAGACCT TTGCGGTGAG TGTTACAGCT CATAAAGGCA 180
GTGCGGACCC AAAGAGTGAG AAGCAGCAAG ATTTATTGCA AAGGGCAAAA GAAGAAAGCT 240
TCCACAGTGT GGAAGGGGAC CCGAATGGGT TGACACTGCT GGCTTGGCAG CCTGCTTTTA 300
TTCCTTTATC TGGCCCCACC CACATCCTGC TGCTTGTTCC ATTTTACAGA AAGCTGATTG 360
GTCTGTTTTA CAGAGAGCTG ATTGGTCCGT TTTGACAGGG TGCTGATGGG TGCATTTACA 420
ATCCCTGAGC TAGACACAAA AGTTCTCCAA GTCCCCACTA GATTAGCTAG ACACAGAGCA 480
CTGATTGGTG CATTTACAAA CCTCGAGCTA GACACAGGGT GCTGATTGGT GTATTTACAA 540
ACCTTGAGCT AGACACAGAG TGCTGATTGG TATATTTACA ATCCCTTAGC TAGACATAAA 600
GATTCTCCAA GTCCCCACTA GATTAGCCAG ATACAGAGTG CCGATTGGTG TGTTTACAAA 660
CCTTGAGCTA GACACAGAGT GCTGATTGGT GTATCCACAA TCCCTTAGCT AGACATAAAG 720
GTTCTCCAAG TCCCCACCAG ATTAGCCAGA TACAGAGTTC TGATTGGTGC ATTCACAAAC 780
TTTGAGTTAG TTTATGTTTG CATTTACAAA CCTCTAGCTA GACACAGAGT GCTGATTGGT 840
GCATCTACAA TCCCTTAGCT AGACATAAAG TTTCTCCAAG 880
|
