Tag | Content |
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EnhancerAtlas ID | HS182-13713 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr20:23635980-23637450 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFF | MA0495.3 | chr20:23637234-23637249 | GTGCTGAGTCAGCTC | - | 6.55 | MAFF | MA0495.3 | chr20:23637234-23637249 | GTGCTGAGTCAGCTC | + | 6.63 | MAFG | MA0659.1 | chr20:23637231-23637252 | CTGGTGCTGAGTCAGCTCTTC | + | 6.02 | MAFK | MA0496.2 | chr20:23637232-23637251 | TGGTGCTGAGTCAGCTCTT | - | 6.31 | MAFK | MA0496.2 | chr20:23637232-23637251 | TGGTGCTGAGTCAGCTCTT | + | 6.68 |
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| 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 |
GH20I023655 | chr20 | 23636038 | 23637437 |
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Enhancer Sequence | CAGAATCCTT TGGGGATTCT GAAGCAAATT TCTTAAGCAG TCTGAATTCT CAAAATTTAG 60 TCCAACATTC TTCATTAACA GGCCTGGGTA AATGCAAGCT TCATCTCTTC CAGAATTTAA 120 ATTTCTCCTT ATGAGAACAG AAGAGGGTAG AATAAAGGAG TTTATTGTCA GCCCACACTC 180 TCGTACTTAA AACTCAGGGC AGAAATCTCA GGCTGGCACC ATTGCCACTT CACTTGGATG 240 GAGAGCAGCA TCTGGAATAT GTTAGAAAAG GCCTTGCTGT GCTGCAGAAA CCGGAACATG 300 GGGCTTGGTC CAGGACTCAG CCCGGAATTG GCTAAATACA CAACACTTTT GTAAAACGGC 360 ATTGACATAG GCTTTTGTTT CTCCTCTGCT TCGAACCCCA CGCACGCCCA TTTGGTGCCC 420 AGCCTGACAC CCACCCCCGC ACCCCCACAT AGGTGATCCG GACTTGGCTG CTGGGGCTGC 480 AGGGATGCCA GCCCGTCAGG CAGGGCTCCC CCTGAGGACT GGAGGGGTTC CCTCAGCCCC 540 CTCGCTTCCT GGGCTGCATT GAGAGGGCCG GTGTTGCCTT CTTTTCACTT CCTCACTGAG 600 AGACTGGAAA AGGGCCAGAC CTCTCCCACC CCTCGGGAGG AAGTTCAGTT CTTTTCCTTC 660 CCTCTTTCAC TTCCCCCTGC CAAGCCTGGA GCACGCGAAG GACCGGCCGA GGGTGGGCAG 720 GCCCTGCCCT GTGCTCACCA GCGGCTGGGC AGTCTGGGCG GAGGAGGGCA CCAGCAGGAG 780 AGAGGTCCTA CAACTCGGAG TTCGGAGTTC GGCAGAAAGG CCTCCCCGGG AGGGGCTGGG 840 AGCTCCCCAA GCAAGGGCAG GCACTTCCCC TCCCTTTGGC CACTTGGCCC TGGAGGGCTT 900 CTTTGGAGAT AAATCCCACA GAAGGGGAGG GGAAATTATG TAACTCAGGG AAAAACGCTA 960 TGTGGAGTCC CATGTACTCA CAATCTCTCT GGAGGAAACC AGGCTTCACC GTCGCCAGGT 1020 GACAACGAAA TGCCCTAACC CCGGGCTGCC AGCAGCACAG GGCCATGGAA TCCAGGGAGA 1080 AACAAGCTCT GAGCTGAGGG GTGTGTAAAA TGGAGGTTCT GATTCGGTAG CTCCGGGGCG 1140 GGCCTGAGCT CTGCATTTCT GATGCTCCCA GGGATGCTGA TGTTGCTGGT CTGGGGACCG 1200 CTCTGAGGTC AGGGCTGTGG AGGGCAGGCA CCAGGCTGAG CAGCGGCACT GCTGGTGCTG 1260 AGTCAGCTCT TCCCTCAGCC CCTGAGGTCT GGAGTGCTTC CCGTTGGGAG ATTTACTAGT 1320 TTTCTTGCTT GGCTACCCGG CATTAACAGG TACGGTAAAT GGGAATACAT GGCTACAGTT 1380 GAGTTCTAGT GGGCGAAATG TCCAGTTACA TGTTAGCTGC AACCCTTAAC AAGCAGAAGT 1440 GAATAATCTA TTCGGCTACT CCACAACACA 1470
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