| Tag | Content |
|---|
EnhancerAtlas ID | HS052-16460 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr17:58219530-58220940 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:58220409-58220428 | GGGACAGCAGAGGGCGCCA | + | 6.28 | | EWSR1-FLI1 | MA0149.1 | chr17:58220339-58220357 | GGAAAGGAGACAGGAAGG | + | 6.15 | | IRF1 | MA0050.2 | chr17:58219752-58219773 | AAAAAGAAAGAAAAAGAAAAG | - | 6.5 | | SPIB | MA0081.2 | chr17:58219927-58219939 | CACTTCCCCATT | - | 6.18 |
|
| | 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 |
| GH17I060141 | chr17 | 58218762 | 58220961 |
|
Enhancer Sequence | TGCACTCCAG CCTGGACGGC AGAGAGACAC TCTGTCTCAA AAAAAAAAAA AAAAAAAAAA 60
AAAAATTAGC TGGGCGTGGT GGCTTGTGCC TGTAATCCCA GGGAGGCTGA GGTAGGAGGA 120
GCACTTGAGC CAGGGAGGTG GAGTTTGCAG TGAGCCAAAA TCACGTCACT GCATTCCAGC 180
CTGGGCAACA GATTGAGACT CTGTCTCAAG AAAAGAAAGG AAAAAAAGAA AGAAAAAGAA 240
AAGAAAAAAG AAAATGTGAA GCTCTTCTAA GTGCAGCTGC TCTGCAACTA TGCAAGCCCC 300
TGCCCCATGA AGCCAGGCCT GCCCCTAATC CTTTACCACA CAAGGCTCAT TAAACTTCGG 360
AAATCTCGGA GTTACTTGCT AGGAAAAAGC CATTCCCCAC TTCCCCATTT GCATAATAAA 420
CGGAGGGGCA GGGAAGACCC ATCTAACCAC CCCACGTGTA CCCATGTGTC ACCCTTATCA 480
GATGCAGGAG GTGAGCTGAG CTGCCAAATG CTTGGCTTCT TTCTGGGGCT GTAATACAGC 540
CATCCCTCCC CAGGGCCACA CCTGGAGAAG GGAGTGGCTA GGACAGGGTC TTCAGGGAAA 600
CTGCTGCCTT ATTCTCAACT GCTTGTCTCA GTCCCCATCC CCCCAACCCC CAACTCAATA 660
TCTAAGAGAG AGAGAGAGTA GTTCCAATAG GGAAGTCTCC TGAAGGAGGC TAAAGTTCTG 720
GGTACTGGGT TTGGGGTGGA CCTAAAGAGT TTTTTTTCAA TTCTCTGAAT GCTATTTCAT 780
TGCTGTTAAA TGATACTCTT CCCCTAAATG GAAAGGAGAC AGGAAGGACA GACTGGTCTA 840
CAGTTACACA GAAAGAACTT CCAAAGTATT AGACGAGCAG GGACAGCAGA GGGCGCCAAT 900
GTGGTGCAAG GGCACTCAGG GAGGAGTCGC CCACAAGCAC ATTTTTTTCT CACACGCTGC 960
AAATCTATTC AGAACCACCT CACCCCCAAC CTCACACATA TTTCCCATCT CACAGGCACA 1020
TCAGAGGTCA GAGTGAGGAC TCCAGGCTCT GATTCTCCCA CTGGCCGCCA AGGGACCTTC 1080
ACCAGCCCCC ACCGCACTCC TCAACTATTT TCATGAACTT AGTTAGGGCA GCTCCCCTCA 1140
GTAGGGAGCT GGGTAGAGGA GCTGAGACTC CCAGGTTCCC TGCCCATCCA GCGGCCCTGT 1200
CCATCTAGCG GGAAGGCGTT TGCTGCAATG TTCTTTATAA TGGGGAGTGA GCTGATGATA 1260
CAACCTGGGT GTACTGTGGA GCCACAAAAT GAAAGTTGCA AAGGCTGCCC AGTAACACGG 1320
ACTCAGGTTT ACACTGAAAT GTGGACATTA AAAAGCAGGA CCCTCCATTG TTCACTATGT 1380
CAATAGCGCG CTTGCATATA GATAAAGGCT 1410
|
