Tag | Content |
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EnhancerAtlas ID | HS188-08688 | Organism | Homo sapiens | Tissue/cell | Th2 | Coordinate | chr22:41983910-41985720 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SPDEF | MA0686.1 | chr22:41985107-41985118 | CACATCCGGGT | - | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAAAGGCACT AAGCACAGAG GCTGGCCCGT AGACAAATTA ATAGGCTGTT CTTATTCAGG 60 TTGTTATGTT TGTGGAGCAA AAGGTCAGAG GGAGGAGTCA GAACTGTGCC TAGGCCCTGC 120 CACTTTTGTT CCAGTTCTTT TATTCATTTA TTTGTTTGTT TGAGACGGAG TTTCACTCTT 180 GTTGCCCAGG CTGGAGTGCA ATGGCACAAT CTTGGCTCAC TGCAACCTCC ACCTCCTGGG 240 TTCAATCGAT TCTCCTGCCT CTGCCTCCCC AGTAGCTGGG ACTACAGGCA CACGACACCA 300 CGCCCATCTA CTTTTTGTTT TGTTTTGTTT TGAGACTGAG TCTCCCTCTG TCGCCCAGGC 360 TGTAGTGCAA TGGCACATTC TCGGCTCACT GCAACTTCTG CCTCTCGGGT TCAAGTGATT 420 CTCCTGCCTC AGCCTCCCGA CTAGCTAGGA TTACAGGTGC ATGCCACCAC GCCTGGCTAA 480 TTTTTTGTAT TTTTAGTAGA GATAGGGTTT CACGATATTG GTCAGGCTGG TCTTAAACTC 540 CTGACATCGT GATCTGTCTG CCTCGGCCTC CCAAAGTGCT GGGATTACAG GCGTGAGCCA 600 CTGAACCCAG CCTAATTTTT GTATTTTTAG TAGAGACGGG GTTTCACCAT GTTAGCCAGA 660 CTGATCTAGA ATTCCTGACC TCAGGTGATC TGCCCACCAT GGCCTCCCAA AGTGCTGGGA 720 TTACAGGCGT GACCCACAAG CAAATGGCCC ACCTTTGCTC CAGTCCTGCT ATCTTCCTCC 780 CGGATCCACC CCTGCAGGAA GGCCTCCAGG GCCCAAGCCA GGGCAACTTC ACCACAGAGG 840 ATGGGGAGGG GCATTCGGGA CCTAAGAGAG GAGGCTAAGA CCTGGGTTCC CATCAGCCAC 900 TGCCCAGTAA AGCCCATCCC ACTGCTCCCC CACGCTAGGA GACCTGTTGG TTGGTCCTTG 960 AGGCCCCCAG ACTGGAGGGT GGGTTACCCA CAGGGAGGGC ATGAATGAAG CCTGCTTACT 1020 GATGCATCCA GCTGGTGAGG GGGCTTTTGG GGACTCACTC ACAATGAGAC CCAATGGGAG 1080 AAAAACTGAG CAGAGGTAAG AGGCTCAACA CAGCGAGAGT CTTTAGAAGA AAACTAGACT 1140 CTTACCCTCA CTATTCCTCA GTGTCCTCAC AGCAAACAGG CTAGGCCTGG AGCCTCTCAC 1200 ATCCGGGTGG GTAGAGCTCA TAAACGAATT TGAAAAGAAG CCCTCTCTGC TCCACGACTG 1260 GGGGTGGAAG GTAAAGTGGG TGATGGGGCT TCAGAAACTA GACCCAGTCC CAGGCCTGCA 1320 AAGGTCGGGG TGGGAAGACT CCGAGACGCC CTGTCTCCCA CCAGATGATG ACTGACGCTT 1380 GGCTGTGTGC TTGTGTGCCT GGAACCCCGG TTCAGAAGCC AGCTCCGACC ACTGGTGTGT 1440 CGTAGGGCTG AACTAGGGTG GGATCCCCAG CTCAGGAGGC GGGGGCGTCC GTGAGCCAGG 1500 CCTTAGCGGC GTGTGACAGC CTCCGGGGAG GGAGGGAGCT AGGCCCCTGC TCGCAGCCTC 1560 CTCCCTCCAG TACTGGATCC AACCCCAGCA CTCCCAAGCA GAACACAGGC AAGGACGCTG 1620 CGGGGTCAGT GACGTGAGGG CCAGGTCCCC TCACTCCCGG TGGGTGGCCC CGGATGTCAG 1680 GGGGCCGGGT ACCGCCGCAT CCCACACTCG GTCCCCGGGT GTCCACGGTC ACGCTGCTGC 1740 AGACCCCACA CTCAGCCTCG GGGGTGTCCG CGTGACACTC CCGGTGGGAG CTTCCAATCT 1800 TCAGGGTCCT 1810
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