| Tag | Content |
|---|
EnhancerAtlas ID | HS121-34571 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr7:128520580-128521670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr7:128520686-128520697 | CAGCAGCTGTC | - | 6.14 | | Tcf12 | MA0521.1 | chr7:128520686-128520697 | CAGCAGCTGTC | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I128879 | chr7 | 128519434 | 128520918 |
|
Enhancer Sequence | AGCTGAAGGG ATAGGAGCTG GGAGGGTCAG CTGCTCCTCC CACATGCCCA GAAGGTCTGG 60
CTTACCCCTC CCCCATCACC CTGGCTGCGC ACCTTGGCAT CGCTCACAGC AGCTGTCAGC 120
CTGGGGCACC TTCGCCCAGC CATGGGGGCA GGAGAGGGCC TGGCACTCCT CGAGGTGGCA 180
CTCCACATGG CCCCGCTGAG GACAGACATC ATTGTTCTGG GGTTTTCTGC AGGGCCGGAG 240
TCCCCAGCCT CATGCTTCTG GGGGCCTCTG GGCATGGACT TCTGCCTGCC CCTCCCACAA 300
TACATTCTTC ACAGTTCAAG AGGGGAATGA AATCCAGCCT TCGGCTCCAT GCCCCGGTGC 360
AGGGATGCCC CTGACCCTTA AAGACCCCAT ATCTGCTGGT GGAGTGTTGG ACACTCCTCC 420
CTTTATCCAT CTGCGAGATC CTCCACCCTC CCAGGCCCAC CCCAGCTCAC ATGGCAGGTG 480
CAGGCGATGC ACGCATTGCT GGGGTCCCGC CAGCTCTCTC CATCTGCCAC TCTCCGGCCC 540
TCGGCCTCCA CCACACATTC TGAGGGGGGA GACATGGGAT GGGCAGGCAC TGTCCCTCCT 600
GCTGTATCCT CCCTCCTTGG AGCTTACCCA GCATTTCACG GCAGGAAAGC ACCCACTCCG 660
TGTCCCTACC ACCCTGATGG TGTTGATTTC TTCAGCCAAT ATCCACAGGG CCTATTAGAC 720
ATCAGGCCTC ACATCAGAGC TCAGGATGTC TCTAGGGTCC TAGGAGCCCA AAGGGCCAGA 780
GGCTGGAACC CCACTCTGGG CCAGCTGCCC GCTCAGCAGT GCAATGCCCT CTTCATGGGC 840
CTGGGGATCC TGAGCCCCCT GACAGGCATC AGGCCAGACC TTGAGAATCT AGGCTTCATC 900
CCAGCTTCCC CCTGCCTCAT GGGTCTCTTC TCCACCTCAA GAACAGCCCC CCTCCATTTC 960
TAGAAAAGAA TGAACCCTGC ATTCTGTTCT AGAAACCGAG TACAAACCCT GGGCTGCCCG 1020
CTTGGCCCAT GAATGCCTCC CCTTCCTGTG TTCCCCCTGG GCTCCTCTCT GAGGGTGGAG 1080
GCCAAGGCTG 1090
|
