| Tag | Content |
|---|
EnhancerAtlas ID | HS024-03171 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr11:117381320-117383160 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELK1 | MA0028.2 | chr11:117382852-117382862 | CACTTCCGGT | - | 6.02 | | ERG | MA0474.2 | chr11:117382852-117382862 | CACTTCCGGT | - | 6.02 | | ETS1 | MA0098.3 | chr11:117382852-117382862 | CACTTCCGGT | - | 6.02 | | FEV | MA0156.2 | chr11:117382852-117382862 | CACTTCCGGT | - | 6.02 | | FLI1 | MA0475.2 | chr11:117382852-117382862 | CACTTCCGGT | - | 6.02 | | RAX | MA0718.1 | chr11:117382577-117382587 | GTTAATTGGC | - | 6.02 | | TP53 | MA0106.3 | chr11:117382650-117382668 | CACATGTGCAGGCATGTT | - | 6.48 | | TP53 | MA0106.3 | chr11:117382650-117382668 | CACATGTGCAGGCATGTT | + | 6.4 | | ZNF263 | MA0528.1 | chr11:117382375-117382396 | CTCTCTCCTCTCTGCTCCTCC | - | 6.78 |
|
| | 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 |
| GH11I117510 | chr11 | 117381527 | 117384259 |
|
Enhancer Sequence | ACATCTCTGG GGTATTTACC GTAGGATCCC TTTCCTCACT AAAATGTAAA CTCCCTGATG 60
GCAGGGATTT TTGTCTATTT TGAGCATAGC TGTATTCATA GAACCTAAAA TAGTGCCTGG 120
AATCTAGTGG AGGCACAGTA GATGTCACTG AATGAATGAC ATTCGTGGTC ATTATCCTCA 180
TCACCACTAC CATCGTCATG AGCCCTGTCT GTCCCACGGG AGTTTGCTTC CTCCTTTGTT 240
ACTGGCTCCC TTGGCTGAGG AAGTAAGGTT GTTGGCAGTG GCTTCCTTGG TGTTCCTCCC 300
CCAAATGGCA TGCAGGCCAT CTCCTCCTAG GGAGCCTGCT GTGCCCCTTT CCTGTGGATC 360
CCAGTGAGGT TCCTCCCAAA TCTCCACCTT CACCAGTAGC AGGCACTTGG CCAGGTGGCT 420
GACTCTCCCT TAAGCTTATC ATCATAGAAA CCCCCAACCT ACTCGTTAGG GTGGGAGAGG 480
GTCTCTGGCA CATGCTCCCA GGCATACGGC AGAGGCTGGG TGGAGCAGTG CTGAAGCTCA 540
GCATTGAACA GCTAGGGAAA AATTAGGGAG GGAGGAGGGA ACATGGGCAT TTGGGAGAGA 600
GGGTGTTTGT GTGTGGGTGA GTATGTCCCT CTTCCACTTG TCCTCCACAG AAGCCTGGCA 660
CCACCTCCCT GTCCTGGTCC TGCTGAGCAT GGGCAGAAAG CACCTCTTGG CCTTGTTTTG 720
GCTCAAGAAG CCCTCGGAAG CTCAGATGTA GGAATGGAGA TGTTTCTTCA CGGAGCCAAT 780
GCAAAGGGGC CCCAGTTGCA GCCCTGCCTT CCTAGTTAAT TAAACATTCA GCCTGCATGC 840
CCAGAGATGC TTTTGTGCTA CATTATTTTT CAGCTACAGG TGGCCCTAAA GTCACCAAAT 900
CTAGGTTTGA TCTGTGTGCT CTCCTCTTAG CATCCTGCCA AGGATTTCTC CGGATGACCA 960
GAGACAAATA CCAGCCATCC CTGCAGCCTG GCTCTCCACT GCCAGCCAGT GTCACATATG 1020
CCAAGGCACA CACAGCCTTC AAAGCACCCT CCACCCTCTC TCCTCTCTGC TCCTCCCACT 1080
TTACTGGAAC ACAGCAGGCT CCCTTGGGCA ATATTTCATA TGGTCCCACC TGCAGCCACT 1140
TTTTGGGCTC AGGAATGTTG CCTTACGGGA GGGCCCTGGT GGACAACACA CTTGCGTATG 1200
TGTAACTGCT GGCATGCATG TTTACGTATG TGTGCTCAAG TGTGAATGGG CTAATGTGTT 1260
AATTGGCTGC ACGTGCATGC AATACGTACC AGGGTGCACA CGCACGAGTG CTCACACACA 1320
GGTCTCTGCA CACATGTGCA GGCATGTTGG GCGTGTGCTG CTGTTCGCAG CTTAGTGTTA 1380
GAAAAATTCG TTAGAAGACA AGCAGTCCCA GAAGGAATGG AGTCAGCAGT TGTTTTTCCG 1440
GCTCATGGAG CAGCATGGGT TTCAGCCCCA CCCTGCCCAC TGACCCTTGG CCCCACAGAG 1500
AGCTGGGGTG GGAGACTTCC AGTTTTATCT CACACTTCCG GTGCTCTGTC CCCACCATCC 1560
CTGCCCCCGC AACTTGCCCT TTTCTACTTT CTAGCTCTCT GCTCTGAACC TTGAGTGGGA 1620
TGCACTTCCT AGTCGGGCAG CAGCAGTGGG GTCTGGAGAG CTGCCCCCAG GCCCACACCC 1680
TTCTCCCCCT CCAAGTCAGG GCCCCCGCCA TGCCCACGGG CACCTCCTCC ACCCCCCTCC 1740
TTGGGTAGTT CTTGGAACAG CGCATCCGCT AATCAAGCAG CGTGATCATA ATCAGCTCTG 1800
ATGGTTCTTC TGCAAAAGCG CATTCTAATG AGGTGGGAGA 1840
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