| Tag | Content |
|---|
EnhancerAtlas ID | HS121-34120 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr7:97853030-97854110 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| INSM1 | MA0155.1 | chr7:97853345-97853357 | TGTCAGGGGTCA | + | 6.18 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTGCAAGGAG GAAGAAGATG AAATCAGGGC CACTTCGTGG AAGTTTCTGG AAAGGGACCG 60
TGCATGTAAA CATTCTTGTT CTACCCGTTA CAGGGCATGG GGACTGGGTG GAAGCCATGG 120
ATGGGGTTCA GAGAAGGAGG TGTCACCACG CGCGGCTCTC AGGAGGCGCT TCCTGGCTGC 180
CCCGGCAGGA TCAGGGTTGA GTGCAGCCCT GGGGACCTGC AGGGAGGGCC TCCTGGGGGT 240
TGGGGCCTCC CAGGGGCAGG GGTCTCCCTG GGGAAGGGGG TCGGGCCTCC CTGGGGCTGG 300
AGCGGAGCAG TCACTTGTCA GGGGTCAGGC TAAGGGGACT CAGCCCTCCC CTCCCCAGGC 360
CCCATCAGAG CCCTTTTGGG GAGCAAGAGC CCTCGGTCAG GATGAGGCCC GAGGCTGAGC 420
GGAGGGTGGT CCAGGAGGCC TGGCTGTGGC CGAGGGGACG GTCCTGGTCT GCTCAGAAGC 480
CACCTGGCTC TGGGCCCCAG CTCAGGCTGT CCTGGCTCCA TCTTCCAACA GGCTGAGACT 540
GTGCCGTGAA GGGCCTGCCC ACGCCGTGCA CCTGCACCGC CAGGGTCCAG GGCCTCGTGA 600
CAGCCACTGC ATCTCTCCGA GGGGCTCACA CTGCCCCTTC ACCTAACATC TCGTGTTGGG 660
TCCCTCAACA CTAAGGGCCT GGCTCAAAGC CCCCCAGAGC TCACCCTGCT AAGGCTGTAG 720
AGGCCACTCG CCCTCCTCAA GCCCCTCAGT CTGGTGCCCT GGGTGCCACC ATCTGACCCT 780
CCCAGAGCCC GTGCCTGGCA CAGCAGGGAT GAACGTGGCG TGGGGGAGCC ATGGTGCTCC 840
TACCCGTGCC ACACATGGAG GCCAGGGGTG CCACGTGTGC AGGGAGCACT CCCCTGGGCC 900
CCTCCTGGCC TCTCTGCTGG CTCCTCCCCC TCCAGTAGCA GGGCTGGCAC CAGGGGTCTG 960
CTCCTTGGCC AGGCCTAGGG GGCAGGGTTC AGCCTGGAAG AGCAGTGAGG CCAGAGGCCA 1020
CACACTCCAG GGCCCTGACA TTCAGGACCC AGCCCGAAGG CCCTGTGCAG GGAGAGGCTT 1080
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