Tag | Content |
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EnhancerAtlas ID | HS182-01293 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:117420850-117422510 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr1:117421083-117421093 | TCTAATTAAA | + | 6.02 | EWSR1-FLI1 | MA0149.1 | chr1:117421685-117421703 | CCTCCCTTCCCCCTTTCC | - | 6.04 | RFX1 | MA0509.2 | chr1:117420967-117420983 | TGTCTCCATGGCAACC | - | 6.09 | RFX1 | MA0509.2 | chr1:117420967-117420983 | TGTCTCCATGGCAACC | + | 6.1 | RFX2 | MA0600.2 | chr1:117420967-117420983 | TGTCTCCATGGCAACC | + | 6.24 | RFX2 | MA0600.2 | chr1:117420967-117420983 | TGTCTCCATGGCAACC | - | 6.46 | RFX5 | MA0510.2 | chr1:117420967-117420983 | TGTCTCCATGGCAACC | - | 6.03 | TP53 | MA0106.3 | chr1:117421931-117421949 | GACAGGTCTGGACTTGTC | - | 6.05 | ZNF263 | MA0528.1 | chr1:117422054-117422075 | GAAGAAGGAAGAGCATGAAGA | + | 6.18 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I116877 | chr1 | 117419783 | 117422875 |
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Enhancer Sequence | AGTGAATTGT TTTGCTGAAA TCTGACACTA AAAATAGGGC ACCGGATCCT TCCCCTGCTG 60 GAAAAAGAAA AAAAAGAAAG ACATTAAAAT GAGTGTGTGT CTGTATGTCT GGGAATATGT 120 CTCCATGGCA ACCATTGTCC CACCTCCCCT ATCAACAGCA TTACCCCTCT CCACGGAAAG 180 AGGGCATATG AACGCCTTTC CCAGCACCCC TCTCAATCCC TTACTCCATG AAATCTAATT 240 AAAGAGTGAA ATGAATTTTA GCGCTGGTTC CAGAGGCTGG GAGAAGTCCA CGACTTGGGG 300 GCAGGGTAAA GAGAGGAGCG CTGGGGGAGG GACAGGGAGA CCTGCCCTTC CACACTGGAG 360 CAGCAGCACG CGACTCTGTT CTCATTTTTA AAAAGAGCCA CAGCTCCCAC GCTGAGGAGC 420 TGGAAGGGAG TGATAAACCT GCCATGCAAC GATGTTATTA CTTTAATGGA TACAGGACCG 480 GTTGAGCACT TTATTTCCAC CAGGGCTTTT TACTTTGCAT CTTCCCTTTC CACAACATCC 540 AGTTTTCCTC AGACACTCCC CCCTTTACTA ATGAACGTTG TCCCCATTTC TAATCCCGCT 600 CAGGTGAGGG AGAAAGCAAG CATTATTTGA GATAATAGGT CTGCCTCTGG GGTGAGGCGT 660 ATGAGTCAAT CACACTGGTG AACAACCCCA CCCCCCAACC TCAAAAATCC TTTTCTGTAT 720 AGATTAGAAG CCAGAGAAGA ATAGGGGGAC ATGGAGTGGT GAGGAAGACA CTCTGGGGAG 780 GTTGAAGCTG ATTTGGGCAA ATGAGCTTCA GGGTTTTTTT AGCATCTGCC AGGGACCTCC 840 CTTCCCCCTT TCCAGCAGCT GCCTGCCCTC CCTCCTCCTT CCCCCACCTT TAGTGTCCAG 900 TCAGCAGCAG CTCAGGCGCC TCCCTCTCCC TCCTTTTTGG CCATCCCTGC CCTTAGCTAT 960 CTGGGCATCT GTTCCTCATT CCTGCATCCA AACATTTTCT CCAGGTTGGC TGTCAGTCCG 1020 GCATTGTGCT GCAGGGGTCT CAGCTGGAGC AGAATTGCCT TCACATGAGC ATGAGCATTC 1080 GGACAGGTCT GGACTTGTCC CTCTGACAAG GAGGAAGCGG TGGCAGGAAG CCTGTGGGCC 1140 CTCCTGGGAG AGAGGGGAGA GTTAGTTTTA CACGGGCTCC AACTGTGTGA TGTTTCAGCG 1200 ACAAGAAGAA GGAAGAGCAT GAAGAGTAAA TCGGAGCCTG TCACTCAGAC TTGTGTCTTC 1260 TGTCCTGGTG GACTGAGTGT GGCGGGCTGC AAGCACAAGG AAAGTCAAAG ATGTGCTTTT 1320 TTACCCACAA CAGGGTGGCA GGGTCGAGAG TCGATTGGCA CAGGGCAGCC AGCGTGTGAC 1380 TGTGGGCACC AGCAGGAGAC AGCACCAGCT GTGGCATCTG CAGTAGCCGC CACCTTGACT 1440 GCCAGCCCTG CCGCTTCAGC AGCAGGCACC TCCATGTCCT TGGAAGGGAT AACCAGCCTC 1500 TCCACCTGGA CAGTGGGCCT TAAGCGAGCC TTCCCTTCTT GCAGCCAACT GAGGCAGCCG 1560 GCACCCTTGC TTGCCAGATA CCCTGAAGCG TTCTGGAAAA AGTCAGGGAA GACCCACAAG 1620 CATGGGTCAC TGTCAAACCA GAGAAATTCC TCTGACTTTA 1660
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