Tag | Content |
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EnhancerAtlas ID | HS147-41466 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr8:140962480-140963680 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr8:140962936-140962956 | CAACAAACCAACCCCCAAAC | + | 6.47 |
| | 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 |
GH08I139950 | chr8 | 140963181 | 140963350 |
| Enhancer Sequence | GTCCAGGTTC TGCTTAGTCC TCGTCTATGG AATGAAGGCA ACTTTCATCC TCAATGAGTT 60 CTCATGAGGA TTCAAAGTAA CAATATGCAC AAATACTTTT TACTTGGCAA ACCGCGGAGC 120 TCAGGCTTTT TATCGCTTGC CTACGAAATG GAAGGTGAAC CTGTCAGCAG ATGATGCCTG 180 TCAATTAACA ATGGTTCTCG CGAATTCAAG GCTGAGGGAA TTGAAGTTCA GGGTGGTTGG 240 GGAACTTGTC CAGAGTGGTA TTGCTGATTT CACAATGAGT AAACCAGGGC TCAAGTCAAA 300 TCTGCTGTTG AACAGACAGC ATTAAGCAAG ATAACCAGTT GGCCGAGTTG TGACTTTCAA 360 CAGGATGAAT GCTTAAGTTG CCGCTGTGAG GCATAACAGA CATCATGTTG ACAAGGCTGC 420 ACCAGCCAAG GGCCTTCCAA GAACTGGTGA TAAAAGCAAC AAACCAACCC CCAAACCTTA 480 GAATGCTACA GGTATGAATC AGACCTTTCC CAAATCACCA TGGGTTTCTT GATATAGTCC 540 CAGAAATCAA CAACTTAAAC ACTGGTGAAA ACATTCAGCA ACTGACAATT CAATTAGGCT 600 ACAAGAGCAG AAAAAACGGA CTGATGTAGT GGTTGCACAC CAACCAGTAA GTGAACACCG 660 GCTCCGAAGG CCTCTTTGGT ATGCACCAAA ACACATGGCA TGCGGCAAGA GGAGGCGCGG 720 CAGGGAGGGA GCCGCACCCG CCTTACAGCC AAACAAATGA ACTATAAAAG GGTGAGGTGA 780 GTCAACCGAG GACAATGCCC TGCCAAACAG AGTGCCTCAC CTGCTCACGG CTTGGAGTCA 840 GCCAGACCCA GGCGCGCACA TCCCCACCGC CACCTCCCCA CCTGTGACAC AGGCCTGGTT 900 ACGCCACCTC TCTGAGCTCC ATTTCTTCCT CCTAAGAAGT TGGAGAATCA CCCTGACACC 960 TCACAGAATT GGTATGGGAA GGAACAAAGC CTCTGCCAAC GCTCCTCACA CAAAGCCCTA 1020 CTCCTATAGG GGCTTGATGC CTGCAGGCCC CACCGTTCTC TTCGAAGTGG TCACAGCTGG 1080 GTGTCCCAGT GGTTAGCACA CGAGTCAGGC CAGTTGGAGC TACTCATTTT TTTCTGTCGC 1140 CTTCCTATTC AAACCACTGA ACAAAAACTG TGCCATGAGG GTTCAAGATG AGAAGAAATG 1200
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