| Tag | Content |
|---|
EnhancerAtlas ID | HS086-05558 | Organism | Homo sapiens | Tissue/cell | HEK293 | Coordinate | chr17:53315270-53316350 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NRF1 | MA0506.1 | chr17:53315795-53315806 | TGCGCATGCGC | - | 6.32 |
| | | 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 |
| GH17I055237 | chr17 | 53314453 | 53316761 |
| Enhancer Sequence | GTCTAGAGAG CAGAGTCTAT TTGTTTTTAA GAGCTGCAGA CAACTTCAAG TGTGGCCCAA 60
CCATAATTTA CGTTTCTATG AATTTAACCG GTGTTATCGT TGGACATTTT GACTGTTTCT 120
GGCCGTTTGT GATGTCCAAC AATGATGTAA TGATTATCCT TGCAGGGACT TCACTTCGCA 180
GGAGCAGAAG CCCATTTGCA GGATAAATTC TGAGTTGCGG AACTAGTGAT TTACAGGGCA 240
GAGGTGCAGT CTTTGTCTTA ATTTCTGAAT TCACGAATGT TGAATGTGAT GAATTCGTGG 300
GAAGCCCCGC AGGGAGCCTA AGCAGCTCTC CAGAGGCTGT GGTTGTCACG GATGATGATT 360
GCGGGACCCG CAGACTGAGT CTCCAAGCGC TCCGCCCCGC CGCGCCCCTC TCCGCGGGTC 420
CCACCGCGGA CCCGCCCCTG CGCGCCCCGG GCCAGGAGCC CCTAGCTGCA GGACCAGGCA 480
CGTGCGATTC CACGTGAGCC TCCCGGCCGG AGCGCAGATG GGAAGTGCGC ATGCGCCTAC 540
CGCCTGGAAA GTAGGTCAGA CTCCTCCTCT CACGTGACCT GCTCCCCTTA GCTACCCTCG 600
GCGCCTCCCC GCCGGGGCGC AGCCGGGATG CGCTCGGCAG CCAACGTGAC GGGGCTGGGC 660
GCGGGCGGCT CCGCGAGCGC CCAGCGCCCG CGAGGATTTG CCGGTTCTCC TCACACCCGA 720
GCGCTCCGCT CAGAAGTCGG GCGGGCAAAA GGGAGCGCCT CGGGAAGTAT CTGGGAGCCG 780
GGCTGGAAAT GAATGGGGCC CGGAAGCGAG CTCAAATCGC TGACACCTGG CACCGGGCTG 840
CGTCCACTTT CATGCTTCCT AAGGCAGTTC TGCCTGCAAG AAGGGAACGC GCATCGCCTT 900
TCAGTAGATC ACACCGATCG TTTGCACGTT TGCATTCTCA ATTTCTGCAC TATATAGGGC 960
AACTCAGACA TGAAAACAAT CTTTGTAAGA AGAAGTGGAA TGCTAATGGT TCCTGGAGTT 1020
TTGCAGGAAT ATTCCACCGG CCCCATTTCT AATCTCCCAC TCACTCCCTC CCCAAAGACA 1080
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