| Tag | Content |
|---|
EnhancerAtlas ID | HS080-14965 | Organism | Homo sapiens | Tissue/cell | H9 | Coordinate | chr17:48663140-48664570 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr17:48663575-48663593 | ATCTCCTTCCTCCCTTCC | - | 6.45 | | EWSR1-FLI1 | MA0149.1 | chr17:48663579-48663597 | CCTTCCTCCCTTCCCACC | - | 6.88 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr17 | 48663826 | 48664311 | | chr17 | 48663779 | 48664374 | | chr17 | 48664384 | 48664498 |
| Enhancer Sequence | GAAGACTTGC CTCCCACTGA CCCAGTGACC CTCACTGCCT CACTGCAGCC TGTCTGTGCC 60
CCTGTCCTGG GTGGGTGGGA GCAGCAGGCA GGCCCATCAG AAGCAGAGGT GAGGTGAGCT 120
GAGGAGTCTG AACAGAAGAG CAGAGATTTC AGGGTCAGTG GAGCAGGTGG AAGCTGGGGC 180
GATGGCAGCT GGCTGGGGTC GGGCTTGGGC AGAGCACGAG TGACTGGTCC AAGCCTCTGC 240
TCAGCTCTGA CGAGGCCTGT CCAGCCCCTC ATGCCCTCTC TGCAAGAGGC ACATCACTGT 300
CTGCCAGAGC TGGCTCTCAG GCCTCCTGCC TGGACTGCTG CAGTATCCTA ATTGGTTTCT 360
GTCTCTACCC TCCAAGCCGT CCACACGCTG CCACCACTGC AGCCAGATTA ATCTTCTTCA 420
TACACTGCTT TGTACATCTC CTTCCTCCCT TCCCACCCGC CCCCAGGGCC TCAGTGGCAG 480
CGTGGTAGGC AGAGACTTGT CCAGAGGGAG CAGAGGAAGG CTGTTCCACC TGGCCCTGCC 540
GACCTTGTAG CCTTCTCTCC CACCAGCCCC TCTCACCCTC TGATCTGGGC AGACAACTTG 600
ATTCTTGGTT CTGCACTGTG CCCTGCACAC CCCTTCCCTT GCTGTCCCCA GCTGGGGACA 660
CCCTCCATGG ACATCCTCCC AGGCTGTCCT CCCCACTGGC CCACTGACCT CAGCCGGGAT 720
TGAGCTCCCG TGGCTCCTGG GTTTTGCCCC CAGTGTGGTG TTTAGTTGCA GCCTTGCAGA 780
TATCGGTCCT GCCTTCTGTG AGCTTGGCCC TGGGGCTGGG GTTTCTCACA GCCTTTCACT 840
CCTTTGTTCT GTAGAGCAGC CTCCCAGGAG GTAGTGTTAC CCTGTTTAAC AGAAGAGGCC 900
ACTGGGGATC TGAGAGGCAA AGGGAATTGC CCAAGGTCAC ATAGGAAGAA AGTCTCAGAG 960
TTGGTGGCAC CTTTCTAACA CCAGTGTTTG GCACACAGAA GGCACTTTTA GGGCTAGTTG 1020
ATGGAGCAGC TATGAGGCTT GGGGAGCCCC GGTGCTGGGA AGTACTGAGC AGCTTAACGC 1080
TGCTGCAAGG TGACAGCCGG AGGGGAGGGG AGTGGAGGTG TTAGGAAATG GGAGATGGAG 1140
ATTTACAGTC AACATCAGCA CAGACAAGAG ACCTGGGACC TCTGGGTGGG ATAAGCTCAG 1200
GCTGCCTGGC CTCATTTCAC CGAAACCTCC ACTGGGCCTT GACATCTGTG AACAGCAGGA 1260
AGGATGCAGG CTAGACCTGG GAAGGGACTT CCACAGCTGG GGGTGGCCAG TGAGGGGTGG 1320
CTGGCTCCAG CCTGATGAGT TTGTGTGCTC TCTGTGTGAG CTCTGTCTGG GTATATGGTG 1380
GGGGCGATGT TGTGGAAAAG GTCTTGAGGG CAGAGATGTA GAGGGAGGCA 1430
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