| Tag | Content |
|---|
EnhancerAtlas ID | HS041-14274 | Organism | Homo sapiens | Tissue/cell | EWS502 | Coordinate | chr22:41984040-41985250 | 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 | CCAGTTCTTT TATTCATTTA TTTGTTTGTT TGAGACGGAG TTTCACTCTT GTTGCCCAGG 60
CTGGAGTGCA ATGGCACAAT CTTGGCTCAC TGCAACCTCC ACCTCCTGGG TTCAATCGAT 120
TCTCCTGCCT CTGCCTCCCC AGTAGCTGGG ACTACAGGCA CACGACACCA CGCCCATCTA 180
CTTTTTGTTT TGTTTTGTTT TGAGACTGAG TCTCCCTCTG TCGCCCAGGC TGTAGTGCAA 240
TGGCACATTC TCGGCTCACT GCAACTTCTG CCTCTCGGGT TCAAGTGATT CTCCTGCCTC 300
AGCCTCCCGA CTAGCTAGGA TTACAGGTGC ATGCCACCAC GCCTGGCTAA TTTTTTGTAT 360
TTTTAGTAGA GATAGGGTTT CACGATATTG GTCAGGCTGG TCTTAAACTC CTGACATCGT 420
GATCTGTCTG CCTCGGCCTC CCAAAGTGCT GGGATTACAG GCGTGAGCCA CTGAACCCAG 480
CCTAATTTTT GTATTTTTAG TAGAGACGGG GTTTCACCAT GTTAGCCAGA CTGATCTAGA 540
ATTCCTGACC TCAGGTGATC TGCCCACCAT GGCCTCCCAA AGTGCTGGGA TTACAGGCGT 600
GACCCACAAG CAAATGGCCC ACCTTTGCTC CAGTCCTGCT ATCTTCCTCC CGGATCCACC 660
CCTGCAGGAA GGCCTCCAGG GCCCAAGCCA GGGCAACTTC ACCACAGAGG ATGGGGAGGG 720
GCATTCGGGA CCTAAGAGAG GAGGCTAAGA CCTGGGTTCC CATCAGCCAC TGCCCAGTAA 780
AGCCCATCCC ACTGCTCCCC CACGCTAGGA GACCTGTTGG TTGGTCCTTG AGGCCCCCAG 840
ACTGGAGGGT GGGTTACCCA CAGGGAGGGC ATGAATGAAG CCTGCTTACT GATGCATCCA 900
GCTGGTGAGG GGGCTTTTGG GGACTCACTC ACAATGAGAC CCAATGGGAG AAAAACTGAG 960
CAGAGGTAAG AGGCTCAACA CAGCGAGAGT CTTTAGAAGA AAACTAGACT CTTACCCTCA 1020
CTATTCCTCA GTGTCCTCAC AGCAAACAGG CTAGGCCTGG AGCCTCTCAC ATCCGGGTGG 1080
GTAGAGCTCA TAAACGAATT TGAAAAGAAG CCCTCTCTGC TCCACGACTG GGGGTGGAAG 1140
GTAAAGTGGG TGATGGGGCT TCAGAAACTA GACCCAGTCC CAGGCCTGCA AAGGTCGGGG 1200
TGGGAAGACT 1210
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