| Tag | Content |
|---|
EnhancerAtlas ID | HS147-37611 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr7:4821390-4822940 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr7:4822479-4822491 | CGGCACGTGGCC | - | 6.52 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 4822384 | 4822539 | | chr7 | 4822544 | 4822598 |
| Enhancer Sequence | GCAGCAGTCA CCACCCCAGT TGGCACCGGA TGGCTGCTTC CCAAGGAACA GGGGAGACAG 60
GAAGCAGGGG CGCCAGAGCC GGCAGGTGGC TGCTTGTTGT AGACGCATCT CGGTGCTGAG 120
TGCCTGGCAC ACTTGAGGCT GGGGCATGCC CTGTTGACTG GAACGGGGTC CCATGCCCAG 180
CAGGCCCACG TGGTATGTTG GTGCTCAGGA GAGGTGGTGG AGTTTGGTTT CTCAGACAGA 240
GCCTTGAGAC AGCGAGTCAG TGGAGGCTGG GCCTCCAGAC CTTCTTTTTG GGGTTTTTGT 300
TTTGTTTTTT AGAAACAGGG TCTCACTCTG CTGTCCAGTG TAGAGTGCCA TGGAGTGATC 360
AATGCTCACT GCAGCCTCGA CCTCCCTGGC TCAAGCAATC CTCCCATCTC AGCCTCCTGA 420
GTAGCTGGGA TTACAGGCAT GCATCACCAC ACCCAGTTAA TGTTTGTATT TTTTTGTAGG 480
GACCTGGGGT CTCACTATGT TGCCCAGGCT GGTCTCAAAC TTCTGGGCTC AAGCAATCCA 540
CCCTCCTTGG CCAGGAGTTT TTGCCAAGTC CATGTCCTCC CTCCCTCTGT GTCGGGAGCA 600
GGCCTGGGCA CTCAGCGTGG GGATCCAGGG GTTCACAGGC TGCCTTTGTG TGAGAGAAGC 660
TGCTATCTCT GCTCATGGGT TGCCCAGGGG TGCAGAGTCT GCAGGAAGGT TGCGATGGAG 720
CTGGGCTTTT CCCTCCGTTC CCAGCCTGCA GCGTCATGAG TTGCCTCCTG TGCTGGGGTG 780
CAGCCTGCGG TTGCTTTAGT TCTGTGTGGG CGAGAGCTTG TGGGCCCCGG CGTACTCAGG 840
GCGTTGTACT TCATCACTGG GGTCATCCTG GTTGGTGCCC AGCCCCCTCA CCTCACAGAC 900
CTCCTGCAGG CCACCTCCAG GCCTCCGAGA TGACCCCGGT AATGCTGTGG TAGCTCCTGG 960
CCTTTGGAAC AAGATGACTC CGGCTCTTCT TGTTTGTTTC ACCCGCCCTT CTCCTCAAGC 1020
AACTCATTTT TTTCAGTGGA AGATGATCTT GCAGAACTGC TGCCAGGCGC CAGCGGTGCA 1080
CCCCCCGCCC GGCACGTGGC CTCCCAGCCA CCCAGCCGCC CTCCTCCCTG CCCTGACGGC 1140
CCTGCCCCTG TGCTGGGTGT CTCTGGTGCT GCTCAGATGT TTCAGCACCT GGGTGTGCAG 1200
AGTGAGGTGG GTGGTTTAAA GACTGGGATC CACACTGGAG GCCCCGCAGG ACGGGGTGTC 1260
CTGTGTCTGC GGCCAGGGCC ATGGTGGCCG CCAGTGTGTT TTTAGCATTG AATCAGCCGT 1320
GCCCTCACCC AGGCCCCCTC CAGCCTCAGC GATGCAGCTC CCAGGGAGAG AGGCTGGAGG 1380
CGGAGCAGGC ACCTTGTGGC CCGGGGTGGG CCTGCGCGGG ACATCCTCCC TGCCACCTGC 1440
TAGGCCGGGG TCTCAGCGAC CGACGCTTCT CAGGAGTGTC ACACAGACTT CCGAAATGGG 1500
GGAGCTGGTC TCTGGCACAG GCCAGTACCC CAGCGTTTGC CCTGTTTGAT 1550
|
| |
|
|
|
