| Tag | Content |
|---|
EnhancerAtlas ID | HS087-09429 | Organism | Homo sapiens | Tissue/cell | HEK293T | Coordinate | chr17:65774240-65775820 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:65775272-65775291 | TAGCGCCCCCTGCTGCCTG | - | 6.44 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 65775203 | 65775744 | | chr17 | 65775257 | 65775783 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH17I067779 | chr17 | 65775116 | 65775877 |
| Enhancer Sequence | ACCACAACAC TTTACTAAAG GCCTATTTGC TAGGATTCTT TACGCATTAG ACTGTGAAAC 60
AAAATTCTTA GCTGAGGCTG GGTGCAGTGG CTCATGCCTA TAATCCCAGC ACTTTGGGAG 120
GTCAAGGGAG GTGGATCACT TGAGGTCTGG AGTTCAAGAC CAGCCTGGCC AACATGGCGA 180
AACCCCATCT CTACTAAAAA TACAAAAGTG GCCGGGTGCG GTGGCTCATG CCTGTAATCC 240
CAGCACTTTG GAAGGCCGAA GCGGGTGGAT CACCTGAGGT CGGGAGTTCG AGACCAGCCT 300
GACCAACATG GAGAAATCCC ATCTCTACTA AAAATACAAA ATTAGCTGAG CGTAGTGGCA 360
CATGCCTGTA ATCCCAGCTA CCCAGGAGGC TGAGGCAGGA GAATCGCTTG AACCCGGAAG 420
GCAGAGGTTG CGGTGAGCCG AGATTGCACC ATTGCACTCC AGCCTGGGCA ACAAGAGCAA 480
AACTCCGTCT CCAAAAAAAA ACAAAATACA AAAATAGCCG GGTGTGGTGG GGCACACCTG 540
TAATCCCAGC TACTTGGGAG GCTGAGGCAG GAGAAATGCT TGAACCCAGG AGGCAGAGGT 600
TGCAGTGAGC CAAGATGGCG CTACTATACT CCAGCCTGGG CAGCAGAGTG AGACTCTGTC 660
TTAAAAAAAA AAAAAAAAAG GGGGGGCCGG GTGCGGTGGC TCACGCCTGT AATCCCAGCA 720
CTTTGGGAGA CCGAGGCGGG CAGATCACGA GGTCAGGAGA TCGGGACCAT CCCAGCTAAA 780
ACGGTGAAAC CCCGTCTCTA CTAAAAATAC AAAAAATTAG CCGGGCGTAG TGGCGGGCGC 840
CTGTAGTCCC AGCTACTTGG GAGGCTGAGG CAGGAGAATG GCGTGAACCC GGGAGGCGGA 900
GCCTGCAGTG AGCCGAGATC CCGCCACTGC ACTCCAGCCT GGGCGACAGA GCGAGACTCC 960
GTCTCAAAAA AAATAAAATA AAATAAATGC TTTTCTGTGA CTTTGCCACC TTTCCCTCTC 1020
CGGAAGAGCC ATTAGCGCCC CCTGCTGCCT GAGCCGGCGC ACTCCACTCT GCCCTAGTGG 1080
AGAGGGGCCG GGTGATGGGG GCGGCAATAA TGGGAGCGGC CCCCTGGGCT AGAGCGGTGC 1140
CTCCAACCCC TGATCCTCCT CATCACAACC CATTTGTCAG GGCCAGGGCC AGGGACTCGG 1200
CCAGATACAG GGAGACAACC CCACAGGAAC ATCAGGGAAG GTGATGCAGT CGAGACTTGC 1260
TGGTGTCCTG TCCCAGACCA TGATGACGTC CATCTGTGCT GCTGCCAAGT TAAACCAGAG 1320
TGTTCTGGTT AACCTGGATT TGACCTTGGA GTTCTGGCCT CTGATTTGCC TTCCCTAGGA 1380
CTCCATGTGC TCACTCTGCG TACAGATATT CTTGATGCAT TTGCTAGTCT GATTTTGGAC 1440
TTCAAATGTC TTGGTGTTTT TTGTTTGCTT TTTTCTTTTT TCCAGACAGA TTCTCATTCT 1500
GTCGCCCAGG CTGGAGTACA GAGGTGTGAT CTTAGCTCAC TGCAACCTCT GCCTCCCCGG 1560
TTCAAGCAAT TATCCTGCCT 1580
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