| Tag | Content |
|---|
EnhancerAtlas ID | HS129-15993 | Organism | Homo sapiens | Tissue/cell | MCF10A | Coordinate | chr17:53315330-53316500 | 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 | CCATAATTTA CGTTTCTATG AATTTAACCG GTGTTATCGT TGGACATTTT GACTGTTTCT 60
GGCCGTTTGT GATGTCCAAC AATGATGTAA TGATTATCCT TGCAGGGACT TCACTTCGCA 120
GGAGCAGAAG CCCATTTGCA GGATAAATTC TGAGTTGCGG AACTAGTGAT TTACAGGGCA 180
GAGGTGCAGT CTTTGTCTTA ATTTCTGAAT TCACGAATGT TGAATGTGAT GAATTCGTGG 240
GAAGCCCCGC AGGGAGCCTA AGCAGCTCTC CAGAGGCTGT GGTTGTCACG GATGATGATT 300
GCGGGACCCG CAGACTGAGT CTCCAAGCGC TCCGCCCCGC CGCGCCCCTC TCCGCGGGTC 360
CCACCGCGGA CCCGCCCCTG CGCGCCCCGG GCCAGGAGCC CCTAGCTGCA GGACCAGGCA 420
CGTGCGATTC CACGTGAGCC TCCCGGCCGG AGCGCAGATG GGAAGTGCGC ATGCGCCTAC 480
CGCCTGGAAA GTAGGTCAGA CTCCTCCTCT CACGTGACCT GCTCCCCTTA GCTACCCTCG 540
GCGCCTCCCC GCCGGGGCGC AGCCGGGATG CGCTCGGCAG CCAACGTGAC GGGGCTGGGC 600
GCGGGCGGCT CCGCGAGCGC CCAGCGCCCG CGAGGATTTG CCGGTTCTCC TCACACCCGA 660
GCGCTCCGCT CAGAAGTCGG GCGGGCAAAA GGGAGCGCCT CGGGAAGTAT CTGGGAGCCG 720
GGCTGGAAAT GAATGGGGCC CGGAAGCGAG CTCAAATCGC TGACACCTGG CACCGGGCTG 780
CGTCCACTTT CATGCTTCCT AAGGCAGTTC TGCCTGCAAG AAGGGAACGC GCATCGCCTT 840
TCAGTAGATC ACACCGATCG TTTGCACGTT TGCATTCTCA ATTTCTGCAC TATATAGGGC 900
AACTCAGACA TGAAAACAAT CTTTGTAAGA AGAAGTGGAA TGCTAATGGT TCCTGGAGTT 960
TTGCAGGAAT ATTCCACCGG CCCCATTTCT AATCTCCCAC TCACTCCCTC CCCAAAGACA 1020
CTCCTACTAG AAAGCTTATC GGTAGATTTC TCACCTTCCA CAAGAGACTT CAGGGGCGCT 1080
GCTGCTGCTG CTGCTGCTGC TGCTGCTGCT GGAGGCTGGA GGGGGTTGGG AGCAGGGAAC 1140
GAAGGCAGGT CTGAATTAGC TGAAGCTAAA 1170
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