| Tag | Content |
|---|
EnhancerAtlas ID | HS177-04245 | Organism | Homo sapiens | Tissue/cell | SK-N-SH_RA | Coordinate | chr11:68924380-68925370 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EN2 | MA0642.1 | chr11:68924768-68924778 | GCTAATTGGG | - | 6.02 |
| | | 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 |
| GH11I069155 | chr11 | 68922878 | 68926322 |
| Enhancer Sequence | GCCTGTGCGC CCCAGCTTAG GGCTACAGGT CCCACCTAAG GCTTCTTGAT GGAGGTTGGA 60
GGGGCGAGCT GGAGGGAGGT GCTGCTGGGG GTCCACCGGT CCCCTTCCTG GGGGATGAAG 120
CCGGTTTCCC GCGCTGACCC CCTTGCCATC AGAGGCCCAG AGCGCGGTCC TTGTGCTGCT 180
GAGCTGTGTT TGGGGCCGCC TGTGGGCTGT GGCCGCCTGT CCTCATCTTC TCCCCTTTTC 240
TCCTTGGCTT TTCATCCTCA GGCTCCGTCC TTCTTCCCCG TGGTGGCCCC AGCCTCCCTG 300
CCAAGCTTCC CGGCCCCCGC CCCATCCCGG GCCTGCTGCT GCGGAGACCG TGGGCCGGCG 360
CTGGACGGCG CGGCCTCCAG AAGTGATAGC TAATTGGGGA GAGAAAGGGC CCAATTGTCT 420
GGCGGGGCCG GAAGAGCCGC GTGGGCTGCT GAAAGCGTCG GGAGGAGGTG GCCGCTTCGC 480
CCAGCAGCTG CCGCCGGGGA TGTTTGCAGA TTACGTCAGC GCTGGCGAGC AGGGGGCGCG 540
GGGACAGCGA GGGGGGCGGG CTCCCGGCGG CCTCCCGCCC CCCAGGCCCC TGGACAATGC 600
TGTCATTGTC AGCACGGAGA GTGGTTAATT CTGGATGAAT GGTACACGGG CCTCTTGACC 660
AAGGAGGCTG CTCGTCGTCC CCAGTCTGTC CTCTCACATG CCAGGGAGGC CCCGGGCTGG 720
AGTCTGGCGG GCAGATCTGG CCTGCTTGGT GGCACCAGAG AGAACAGGGC GGTCCCTTGG 780
GGGCGCCGGC TGCAGAGGCC CCAGGCTGGA CGGAGCTTCC TGTCCTGGGT CTGCACAGCA 840
GCCACTTGGC AGTGCCGGGC TAGGGTGGCA GGGCCCCACT GCATCTCGGT TCCAGGGCAG 900
AGGCTGCTGC TGCCCTTTGG GGCTGACTTC AGGCATGACC TCCTGGCCAG GTGGCAGCTT 960
TGGCCCTGAC CCGCTCCTGG CCCTGCTGGT 990
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