| Tag | Content |
|---|
EnhancerAtlas ID | HS120-01473 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr12:53931610-53933080 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXF2 | MA0030.1 | chr12:53931907-53931921 | CAATGGTAAACAAA | + | 6.23 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 53932591 | 53932896 | | chr12 | 53932003 | 53932800 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I053537 | chr12 | 53931322 | 53933398 |
|
Enhancer Sequence | CTCAGCCTCC CAAGTAGCTG GGATTATAGG CATGTGCCAC CACGCCCAGC TAATTTTTTA 60
TTTTTAATAG AGATGGGGTT TCTCCATGTT GGTCAGGCTG ATCTCGAACT CCCGACCTCA 120
GGTGATTCAC CTGCCTCAGC CTCCCAAAGT GTTGGGATTA CAGGAATGAG CCACTGCATC 180
CGGCCAAGAA ATATGGGCCC CTTATGTTTT ATGTACAATT CTGGCCAAAT CATTTTGTCG 240
GTAATTCTCA GGGCTTCTGT TTCCCCAACT ATAAGATGAA GATAATACCT GCTTCACCAA 300
TGGTAAACAA ATATTTATAA AGACCTGAAA AAAAAGATGC CATTTAAATC CATGCAAATA 360
TTATGATAAT ATTTTTCAGG AAATCAAAAT AATTCCTGAA TCTGCTGGCC ACTGGAGAGC 420
TGTGAACACT TTCTCTGCCA ACAAGGATTA CCCAATTACC AAAAGCAAAC AAAGACAAAC 480
TGGCTATTCA AGTACTGCAA ACCAGATAGG AAAGGTATTT TCTGGGGAAC TCACCATGCT 540
TGATGGTGAT CTCACCCCAA AATATGGTGC TGGATGTATC AGGTAGACAA GGGGTTTGGG 600
GTAACAGAAA AGAAAGGCTG ATCATCTGAT TGGTGAAATA AATGACAACT TGGTCTTAGG 660
AGCAAGACTG GAGAAAACCA GAAAGGAAAG AGAGCACTTT CCTGGCAGTG ATGCAATCAC 720
CTCACAGAAC TGTGGAGCTG TAAACGGCCT TGCAGGGAAC AATAAACCAT CTGAGATAAT 780
GGCCTTGACA CTGAACCAGG ATAGGAGGGT TGGCATTGCA GTTCAGTTTC ATAACAAAGT 840
GGATCCTTTG TTCTATCTAT CCTGTATCCC AGGCTTCTTG GTGAAGCAAC TGCTTGTTTC 900
AAGATCTTCC CTTGCTACCC TAACCCTTAG AAACCTTCTT GATAGCTAGC TGAGTAAATT 960
AAAGATAATG TGATATCTAC TACATTAGAG AAGGTAGTAG TGGTTCATTT TCCCCAATCT 1020
GAGGAGGGTG AGCAACAGCA AAAGTAGCTT CATTTCTGCC TCATTTTTTC TACATAGCTA 1080
AGATGTCAGG TCCAATTTAG CTAATTCTGA GATCTCTTAA GTCAGAGACT AGTGGGAAGG 1140
AGAAGCCTCT AAGTAAATAC AACCATAGAT TTGAAATCCT CTAGGGCATC TCCTAGCAAA 1200
GCTGCGGTTC AGCAAAGTTC CACACTCATT AAACACTTCT GGAGACTCTT CCACTGAGCC 1260
TGTACTTCTC ATTAAGGGGA AGTAAAGACC ACTCCTGTAC AGGCAGGAGG ATACACCAAG 1320
GAATGCCCAG TGAGGAAAGG GCTGACTATA AACTAGTCTC CCAGAAGTGT CAACTGAGCT 1380
AAAATGGCAA TGAAAAAGAC TTGAAGCTTT TTATGGGAAG CTAATTTTCT TGAATTTGCC 1440
TATAATAAAT TGGGTATAAA ATCCCTCATA 1470
|
