| Tag | Content |
|---|
EnhancerAtlas ID | HS154-04041 | Organism | Homo sapiens | Tissue/cell | Osteoblast | Coordinate | chr11:68924140-68925590 | 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 | CTTTCTGAAG GCATCCACTG AGAGGCAGGG GCCAGGATCT CTGTGCCCAG GCGCTGGGCG 60
TGGCCCCTGA GAAGTGCTCT CTCCCCTAAT CCTTCAAAGC AGGAGGTATT TGCTTCACTT 120
TCTAAGGCAG GATCTGCGGC TCTGAGAGGT TGCACAACTT GCCCGAGGTC ACTCAGCTAG 180
TAGAAGGCAG GACTGGCCTC CGGTCCAGGG TGACTGTGAG GATGTCAGGG GACCCTGCAG 240
GCCTGTGCGC CCCAGCTTAG GGCTACAGGT CCCACCTAAG GCTTCTTGAT GGAGGTTGGA 300
GGGGCGAGCT GGAGGGAGGT GCTGCTGGGG GTCCACCGGT CCCCTTCCTG GGGGATGAAG 360
CCGGTTTCCC GCGCTGACCC CCTTGCCATC AGAGGCCCAG AGCGCGGTCC TTGTGCTGCT 420
GAGCTGTGTT TGGGGCCGCC TGTGGGCTGT GGCCGCCTGT CCTCATCTTC TCCCCTTTTC 480
TCCTTGGCTT TTCATCCTCA GGCTCCGTCC TTCTTCCCCG TGGTGGCCCC AGCCTCCCTG 540
CCAAGCTTCC CGGCCCCCGC CCCATCCCGG GCCTGCTGCT GCGGAGACCG TGGGCCGGCG 600
CTGGACGGCG CGGCCTCCAG AAGTGATAGC TAATTGGGGA GAGAAAGGGC CCAATTGTCT 660
GGCGGGGCCG GAAGAGCCGC GTGGGCTGCT GAAAGCGTCG GGAGGAGGTG GCCGCTTCGC 720
CCAGCAGCTG CCGCCGGGGA TGTTTGCAGA TTACGTCAGC GCTGGCGAGC AGGGGGCGCG 780
GGGACAGCGA GGGGGGCGGG CTCCCGGCGG CCTCCCGCCC CCCAGGCCCC TGGACAATGC 840
TGTCATTGTC AGCACGGAGA GTGGTTAATT CTGGATGAAT GGTACACGGG CCTCTTGACC 900
AAGGAGGCTG CTCGTCGTCC CCAGTCTGTC CTCTCACATG CCAGGGAGGC CCCGGGCTGG 960
AGTCTGGCGG GCAGATCTGG CCTGCTTGGT GGCACCAGAG AGAACAGGGC GGTCCCTTGG 1020
GGGCGCCGGC TGCAGAGGCC CCAGGCTGGA CGGAGCTTCC TGTCCTGGGT CTGCACAGCA 1080
GCCACTTGGC AGTGCCGGGC TAGGGTGGCA GGGCCCCACT GCATCTCGGT TCCAGGGCAG 1140
AGGCTGCTGC TGCCCTTTGG GGCTGACTTC AGGCATGACC TCCTGGCCAG GTGGCAGCTT 1200
TGGCCCTGAC CCGCTCCTGG CCCTGCTGGT GGTGATCCTG CTAGCACGCC TCATCCTGTG 1260
GTCCTGCCTC GGGACCTACA TCGACTACAG ACTGGCCCAG CGGCGGCCCC AGAAACCCAA 1320
GCAGGACTAA GCCTCTGCAG GCTGCGGCCT CCACGCGCCC TGTCCCGAGA CTCAGCCGGC 1380
CCTTCCAGTG GTGGTGGGAG GGAGGGGAGC AGGGCAGGCG CATGATCCCC ATGTCCCACC 1440
CCTGGGGCAG 1450
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