| Tag | Content |
|---|
EnhancerAtlas ID | HS197-22120 | Organism | Homo sapiens | Tissue/cell | ZR75-30 | Coordinate | chr9:129987500-129988800 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Znf423 | MA0116.1 | chr9:129988732-129988747 | TCACCCCTGGGTGCC | - | 6.86 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGGACGTGGG CTGCGGCGCG CGAGCCGAGC GGCCGGCCGA GGCCCGAGCC CACCCGAGTG 60
CGCCCGAGCC CGCGGCCCCC GCCCGGGGCG ATGGAACCGG AGCCCGGCGG GGTGGCCGCT 120
GCGCTCCTGC GGCAGAAGAG GGCGGCGCTG CGGCGCAGGG GGTGCAGCTT CGAGAGCCCA 180
AGGTACTGCG GACGGGGAGG GGTGCGGCCG GGCGGGGTGC CGGCCACGTG GGGGGATGGC 240
GATGTGAAGG GACAGCGGGG CGAGGCCGTG GCGTGGGAAG GGTCTGCGGA GGTTCTCAGG 300
AGACCGGGCG CGGAGCCCGG GCTGAACGGC CGTGGGCTGT GGGAGGGGCC GGGCCGTCGC 360
GCGGGAGGTG CAGGGACGGG TGTCGGGCGT CCAGAAGCGT CGGTCCAGTG GCAGGCCCCG 420
CACGCCCGCG GCTTCGGCGG GGCATGGGCT GAGGAGAATG TGCCCTGCCC ACCTCTGGTA 480
AACCCTCAAG GGCAAGGTCG GGAGCTCACC CCTCCGTCCA CTGGAGGCTT CCTTCCGGCG 540
CCCGCGTGCC CTGGCAGCCG CACACCTGCT GCCTCCGCGG CCCCCGCGCC CCTCGCGCCC 600
CTTGCGCCCC TCGCGCCCCT TGCGCCCCTC TCCCTCGCGA CGCCGGCCTC TGCCCGGGCC 660
GCCGGCGCCC CTAGGCTGCT CTTCCCCCGG GGCCTCTCAC GGGACTACAG CCGCCCGGGC 720
GCGTGCCCTC CCTCAGCTTC CCTGGCAGTC CCTGAACTTG GAACGGATTC TCCTGCTTCG 780
ACGTCGCTCA AGTCGGCCCT ACCATTTTCT CAGGTCTTGG AGATGACTCC AACGTCCTCT 840
CAGCCACACT TCCCATCTCT GTTCTGACAC CTCTGAAATC CACACCCCAG CCGGCCGCGA 900
AAGAGGTCTT CCTAAAGCCG TGACTGTGCC CTTCGCGGCC AACACCCCTT GAGGAGCTCC 960
CCATCACCCG CAGCAGTGGT AGGGACCAGA GTGGGGGACA GAGAGAGAGA AGGATGTGGA 1020
CTCCGACCCG CACTGAGGCC AATAAGAGGG TTCCATTGCT AGGATAAAAA GCAAACTAAC 1080
CAGGATCCTT AAGATGAAGT GCGGGGCCCT TGACTTGGCC TTTTCCCTCC ATCCTCAGTT 1140
CTTGGCATTC CCTGCCTCAC CCTTGGCGCT CCAGCAGTAC TGGTGAGCCT GGCATATAAG 1200
CATCGCGGGG GCAGAGAACA GAGCTGTCCT GGTCACCCCT GGGTGCCCAG AGCTGGCTCA 1260
GGCCTGGCCC ATGGGACATC ATCTGTGTGT TGTATGAGTC 1300
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