| Tag | Content |
|---|
EnhancerAtlas ID | HS095-13299 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr17:77733540-77734420 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr17:77733567-77733588 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | | NR2C2 | MA0504.1 | chr17:77734103-77734118 | CGAGGGCAGAGGGCA | + | 6.6 | | Nr2f6(var.2) | MA0728.1 | chr17:77733792-77733807 | TGAACTCCTGACCTT | - | 6.04 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCCACCAGCT TCAGGGCTGG AGACATTTCT TTCTTTCTTT TTTTTTTTTT AAGATGGAGT 60
CTCGCTCTTG TTGCCCAGGC TGGGGTACAA TGACGTAATC TCAGCTCGCT GCAACCTCCG 120
CCTCCAGGGT TCAAGCGATT CTCCTGACTC AGCCTCCCGA GTAGCTGGGA TTACAGGTGC 180
GTGCCACCAC GTCCAGCTAA TTTTTGTATT TTTAGTAGAG ACGGGGTTTC ACCATGTTGG 240
CCAGGTTGGT CTTGAACTCC TGACCTTAGG TGATCCACCC ACCTCAGCCT CCCAAAGTGC 300
TGGGATTACA GGCATGAGCC ACCACACCCA GTCAGGGCTG AAGACATTTC TAAATGCTTG 360
CACTTGAGAA ATGGTGAGCT CAAAAGGAAC TCCTGCTTGC CTGGCTGAAG GCCTTGTCCA 420
GGAGCAGGCC TTGTCCTGGC TGTAACTGCG TCTGGGTTCA CACAGCTTTG CATTGACAAA 480
GACGGGAGAA AGGGGCTCTG GGGAGCCCTG GGCAGCTTCC AGTAGTCAGG GGAGGTTTCC 540
TGCCACGACT ACAGTGGGGC GACCGAGGGC AGAGGGCAAG TTCAGGCAAG CCTTGAAGAG 600
ACCCAGCTGT GTCAGCACAA AACGCAACCG TCTTTCCAGC TGTTGACCTC ATAGCTGCCA 660
AGTCAGTGCC CAAGGGGCTG GAGACAACAG GGCACCCACA GCTGTGCTCC GGGGCGGACA 720
CCTCAGCCCC CCAGGCAGCA GTGTGGATAA CCCACGTGGC CTGGATGTGG TGGGTAAAGT 780
GCTGGCATGC ACCTTTGTTC GGGTGGACTT TGGGTCTTGT TGGTCAGATG GTCGTGGCTC 840
CGCTGCTTTG ATCCAGGGAG AAACAGGAAA GCAGAAGAGA 880
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