| Tag | Content |
|---|
EnhancerAtlas ID | HS121-13267 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr16:1545620-1547030 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Znf423 | MA0116.1 | chr16:1546254-1546269 | GGCACCCTGGGGTCC | + | 6.03 | | Znf423 | MA0116.1 | chr16:1546254-1546269 | GGCACCCTGGGGTCC | - | 6.57 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr16 | 1546159 | 1546209 | | chr16 | 1546387 | 1546477 | | chr16 | 1546722 | 1546794 |
| Enhancer Sequence | CAAGGTGAGG CCCTGCCTCG GGGACCCCCT TTGCCACCCG TCTTCTTGGG TCCTCGTCCC 60
CTGCCACCCT CTGGTGCCTC ACGGCCTCTG GAGACTTTGG AGTCTCTGGT TGATGCCGTC 120
AGGCAGGTGG GGATGTCCCT GTCCCGCACA GTAGTGACCG GCAGGGCTCA TCCGCTGTGG 180
GCTGAAGTCC GCTGCCCTCC ACGCGGGCTT CTCTTGTCCC TGCAGTCCCT TGGGTTTCCA 240
GGGCCCAACT GTGCTGTGGT GGCCAGGTGG GGGATCTCGA GGTTCTCAGG TCTGGAGGCA 300
GACGCTGGCG GTGCCCTGGA GAGGGGGTGC TGTGGGAACG GCCTTGCCCG CTGCTGGGCT 360
GCAGGGCCCC GTGAGCGCCC ATGCTCGCTC TGTTTTCCCT GGGGCGCCAG ATGGCGGCTG 420
CCGCGAGTGT GCGTTTCACT AGCGAGAAGG AGGCTGGGCC GGGGGCCTGC ACAGCACCCG 480
GAGCGTCTGC CTCTCCCTGC AGGGTGACCC CTTCCTTCTC TTGCCTTTCC CGAGCTCCAG 540
GCGACAGCTC AGACGCAGGT CGAGCACCTG GGTCCGGACT CCACCCTCCA CATGCTGCCC 600
CGACCTCGTT CTGAAACTCC CTCCCTCGCT CAGGGGCACC CTGGGGTCCT GGAGCAGCTC 660
GGCGCCCCCT CAGAGCCCAG GAGGAAGCCG GGCCCCTCGA GTCCCTGCGT GGGGCCTGTG 720
TGGCCCAAGC CCCCTCGCCT CACCTGGGGG TTCCTGCAGC AACCTCCTGA GCCCCTCCTG 780
TCTTTTCCGA ACGTAGCCCT AGGCTTGCAG CTGCTGCTGT GCATGGGCCC ATGTATTAAG 840
GAGGCTTTGG GAACATCTCG GACACATGTG GAATGCGGCT TTTTCACGTG TTCGGGGTTG 900
GCTGGGGCCG TCCTGGTCCC CACGCGGCTC TGTGCTTTCC GCTGCCCCGC GTCCCAGCTC 960
TTCTGTGGGG CTGGTACAGC CCGGCCCCTC CCGGTTCCCC ACGTTCCCTG GAGTGCGCTC 1020
CTTCCCTGTG GGCGGCCGTG GTGGTGGTGC TGCTCCAGGG TCTCATGCCC GGCTCAGGGC 1080
CCAGGCCTAC CCTGCGTGGC TGACCCAACT TGGCCGGGCC CTATCGATGC TTTCTCTCCT 1140
TCCTCGGCAA CATCATACCG GTCCCGACCT CCTACACCAT CGTGACGATT AAGTGGGCTA 1200
AGATGGGTGA AGGTTTGAAA GGATTGTGAT TTGCTTGTCA GGTTCCACGC ACTCCTGTTC 1260
AGATTTGCTG GGTAGGCTGA TGGGCACCAG CCGTTGTTTT GAGTGAGTTT TGCTGTCGGT 1320
TGGAGTCCGC CTGACCGAGA GCAGCTCTCC CCACACCTAG ATGTTCTTTT GTGCCTTCCC 1380
GCCGGCTTCC TCATCAGGCC TCCCTTTCTG 1410
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