| Tag | Content |
|---|
EnhancerAtlas ID | HS007-10639 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr22:20122550-20124060 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr22:20123452-20123462 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr22:20123452-20123462 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr22:20123452-20123462 | ATTTTCCATT | + | 6.02 | | ZIC4 | MA0751.1 | chr22:20123202-20123217 | GCCCCCCTGCTGGGA | + | 6.05 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 20122875 | 20123311 | | chr22 | 20123476 | 20123745 |
| Enhancer Sequence | CGCAAGTGAT CATCCCACCT CAGCCTCCTG AGTACCTGGG ATGACAGGTG GGCACCCTCA 60
CACCTGGCTA ATTTATTTAT TTTTTGTTTT TTTGTTTTTT TTTAGTAGAG ATGGGGTCTC 120
GCTATGTTGC CCAGGCTATT CTCCTGAGCT CAGGTGATCT GCCAGCCTTA GCCTCCCAAA 180
GTGCTGGGAT TACATGTGTG ATCACTGCTC CCGGCCCCTT CCTATGTTTC TGGGGGTTTT 240
GTATCCCCCT GGGCTTCAGA AGCCCTTTAT ACCATGGTAT AATGCTAGGC TGGGTCAGCT 300
GCTGGCAGAG GGTTCGAAGA CCCCTAGGCC AGGCTCCCGA CCCTGCCCTG ACTTCACTCC 360
AGAGCCACAT TGCAGAATGA CAGGGACCCT GTGAATGTCC GAGGGCTGGG GCTGCCTGGC 420
AGGCTGCCAG TGCCTGGGGC TGAGCCAGGC TGGCTTATCT CTGTCTGGGG CATCTGGGAT 480
GGTGTGGCTG GTCCCTAGAT CGTCCTGAGC CCTCTCCTTG CCTGGAGGCC CAGCTCAGGA 540
CAGCAGTCAG AACAGGCCCT GGGCCAGACT AGCCTTGGTG GGCCAGGAGG GACTGAACTG 600
CTGACTGGGA CCTCATGAGT CTGGGGAACC TGGGAGTGAA AACTCAGTGT GAGCCCCCCT 660
GCTGGGACCC ACCGCATGTG GCCTGGGGTA TTCCTGGCCC CCGAGCCTCA GTTTCCCCAT 720
CTGTCCAGGT GTCTATAGGG ATTGGACAGG TAGGTGCAGG TACTTCGAGG CCCAAAGGCC 780
TGGCCTGACA AGGGCGCAGC AGCTTCTGCC CCGCCGGTCC CGAGCGCCCC ACGGGCGAGT 840
GCCACTCATA CACAAACAGT GCTAATGAAG AACCTGATTT AAATGAAAAC GTCTGAGTTA 900
AAATTTTCCA TTCCACATTT AGCTGTGGCG GACATTCTGC CCCTAAGCCA CCCCTCTTGC 960
TCGGCGGTAT CTCCCTGCCA GCCCAGGCGG GACTTGGGGC CTCAGCCCGG GTGGGGCCTA 1020
TGGTGGTGGT GCATGTCCCT GCCTGTGGCC CTGGAGGAGG GATTGGAACC TCGGGGCTGG 1080
GCCCCCTGGA CCTGCCCTCC ACCCGTAGCT TGGCTGGAGC CAGCCAGGAG GGGCTCAGAG 1140
GGACATGGCG GGCCAGACAC TCCACCTCCA GCCCAGGCCC AGAGCCTGTC TTTGCCTGGC 1200
CCTCCGGCAG GCGAGCCTGG TGTGCACCAT CAGGTCTGGG TGGGAGTGGA GCCTCCCCGA 1260
GCCTGGACCC AGACTACTGC CTGCTAGGCC CTGCCTGTGG GAATGCGTGT CTTTGAGTGT 1320
CCCTGAGCAT CCACACATGG CCTCCCCTGT CCCCATGTGT CCTCATGCAT CCTTGCATGT 1380
CCTTGTGTGT CCTCCCGTGT TCTTGCGCAC CCTGAGAGTG CTTGTGTGTC CTCACACTTG 1440
CCCTATCCAC AGAGGGGCAA AGGGAAGCCC AGAGAGTGGG AGGGCCGTGT CTGAGGCCCA 1500
GAGTGAGGGG 1510
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