| Tag | Content |
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EnhancerAtlas ID | HS127-12863 | Organism | Homo sapiens | Tissue/cell | Macrophage | Coordinate | chr17:17991400-17992870 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr17:17991422-17991440 | CCTTCCTTTCTGCCTGCC | - | 6.5 | | Foxd3 | MA0041.1 | chr17:17992460-17992472 | GTTTGTTTGTTT | + | 6.32 | | HES2 | MA0616.2 | chr17:17992593-17992603 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr17:17992593-17992603 | GGCACGTGCC | - | 6.02 | | JUN(var.2) | MA0489.1 | chr17:17992431-17992445 | ATGACTCATTCCTT | - | 6.8 | | Zfx | MA0146.2 | chr17:17992697-17992711 | CCCGCCTCGGCCTC | + | 6.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGTGAGGGCC GGCCGGGCGG GGCCTTCCTT TCTGCCTGCC TCAGTTTTCC TGTCTGTAAA 60
ATGGGGGAAC AACTCCAGCA GTAATGCTGG GGCAAGATCC GAGGCCGCGG AGAAGTTGCC 120
AGACAAGTGC CGAGGCCGCC CTGCGCGCCC AAGGCAGGGC CAGGCGGGAG CGGGTCTCAC 180
GCCCAGGTCT GACTGCAAAC GTACCCCAAG AGATCTGGTC AGTCCCAGAC CGTGTGCCCG 240
AGTAGAGTAG TCCCAGCTCA CAGAGCAAGC ATCTGACCCA GAGAGAGGCG GAGCTGGGGT 300
TCAAACCTCA GTCTCCTGAT GGCTGGGCCT GGGGCCTGGG TCTACTCTGT TGTTTTGGGA 360
AGTGCAAGAG GAGACCTCTC AGGAACAGCC TCACCCAGCA GCTGAGAGCC CATTGGAGCA 420
AGGGAATCAG GACTCTGGAG TCTGGAAGGC CTGGGTTTGA GCCCCAGGTC CACCACGTAC 480
CTTCTGTAAA ACATTGGAAA GTCACTTCAT TTCTTGGAGT CTCAGTGTCC TCATCTGTAA 540
ATGGGGTAAT ACTCCCCTGC TCCATCTTAG TACACAGCTG AGTTAAATTA GATGGCCTTT 600
ACAAAGCACT GGGCACATGG TGAGCACTCA GTATTTAAAG TAAACACCCC AACATAGATA 660
ATACATAATG AAGCCTCAAA TCTGGACTTT AGAATGTAAG GGCTGGAGGA GCTCACAGAA 720
GAGAGGTGAG GAGAGAACGA TGACACCAGG ACAAAGTGGG ACTTGAGCTG GTTGTTGGAA 780
GGGTATCCCA GGTGGGGGCC ACTGCTGAGA CAAAGACATG GGAGTGAGCA TGGTATGTTC 840
ATGGGACAGT GAGAACAATC TAGATCAGAA GGGGGTTATG GAAGAGTAAT GGGAGATGCA 900
ATTGGCCAGG CTAGTGGCTA GCCATTCAGG CTTGTGGGAG CAGGAAGCAA GCAACACTAG 960
ATAGCTGGTC CCAGTGTCTG CCCTCCCTTG GTTCCATTTA GGTTTGAAGG CCAAGGAGTT 1020
GAGGGCCCTC TATGACTCAT TCCTTCTGTA AATCTTTTTT GTTTGTTTGT TTGAGACAGT 1080
CTTGTTCTGT CACCCAGGCT AGAGTGCAGT GGTGCCATCT GGGCTCACTG CAACCTCTGC 1140
CTCCCAGGTT CAAGCGATTC TCCTGCCTCA GCCTCCAAAT AGCTGGGATT ACAGGCACGT 1200
GCCACCACAC CCGGCTAATT TTTGTATTTT TTTAGTAGAG AGGGGGTTTT GCCATGTCGT 1260
CCAGGCTGGT CTCAAACTCC TGACCTCAGG TGATCCACCC GCCTCGGCCT CCCAAAGTGC 1320
TGGGATTACA GGCATGAGCC ACCGTGCCTG GCCGATCTTT CCTGAGCCTT TACTATGTGC 1380
TAGGCACTGT GGTTAAAGCA GTGAACACAG CAGGCATATC CCAGCCCTTG GATCTGATCT 1440
TCTAGTTGAC GGTCTGAAAA CTAGAAATCA 1470
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