Tag | Content |
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EnhancerAtlas ID | HS161-04942 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr14:102494480-102495870 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr14:102494576-102494587 | AGTGACTCATG | + | 6.14 | Klf1 | MA0493.1 | chr14:102495229-102495240 | TGGGTGTGGCT | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I102026 | chr14 | 102493039 | 102497208 |
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Enhancer Sequence | GGGTTCAGTT TTGAGATCAA CAGATAAACC ACAAAACTAA CCATCATGCT AATATAAAAC 60 TAAATTGCTA TAAAAATAGA CCTTAAGGCC AGGTGCAGTG ACTCATGCCT GTAATCCCAG 120 CACTTTGGGA GGCCAAGGCG GGAGGATCAC TTGAACCCAG GAGTTCAAGA CCAGCCTGGG 180 CAACATGGCG AGACCCCATC TCTACAAAAA ATACAAAGAA AATTAGCCGG GCATGGTGGT 240 GGGCACCTAT AGTCCCAGCT ACTCAGGAAG CTGAGGTGGG AGGATCACTT AAGCCCAGGA 300 GGCAGAGGTT ATATTGAGCT GAGATCACGG CACTGCAATC CAGCCTGGGC AACAGAGCAA 360 GACCCAGACT CAAAACAACA TAAATAGACC TTAGGGCACT TCATGTTTGA CATTGTACTG 420 TTATTTGTAA AGGAAATACT TGTTTCTTAC CTCTTACCTC TTTAGTAACA TCTCATTCTT 480 GTCACTGGGC TGTAAATTCT GGAGCCGTCT AACACTTTAG TGCCCCCACT GACTCTGCCT 540 CTGATAAAAT GATCTCCTTT GCCTTTGTCT CCCACTGCTG CTGTATGTTC AGGCCCTTAC 600 TCTTTCCTCT AGATCAGGAA TCAGCACGCT TTCTCTTTAA AGAGCCAGAT CATAAATGTT 660 TTAACCTTTA CAGGTGGAGT AGTCTCGGGC ACAGCTACTC AGTGCTGCCA TTGTAGGGCA 720 AAAGCCTCCA GAGACCATAT ATAAATGAAT GGGTGTGGCT GTGGCCAGTA AAACCTCATT 780 ACTGAAAAAT GCAAGGCTTG GCCTGCTAAC CATGTTTTGC TAATCCTTGC TGTAGATTCT 840 GTGTGATAGA AGAATTCAGT CTACTCCTCC CTCCCAGAAG AGCTTTGTGA AATCCACTCT 900 GAGCTTGTAG GTGTCCTGCT GCCCAGCCCC TGCAGGCCAT CTCCATTGCC CTTGGAATGT 960 CGTCCAGCCC TGGCTTCCCC TGGTAGTCTG ATCATCTTGC TGTGCTTCAG AAATCAAGGG 1020 ACCAGAGCAG TTTCTCACAT CAGGCCTGCC TTGCCCCTTT CTTGTCATTT CTTACTAATA 1080 AAAGGTGGAA GCAGGCTAGC TAACCTTTCT ATAGTAACTG ACATTTGTGA TGCCTTTTCA 1140 CATAAGTACA CCTCTAAAGT TGGTGTAATC ACCATCCTCA GTTTAGAGAA GTTAAAGGGC 1200 TTAGAGAGGT TTGGAAGTGT AAGGGGTATC TCGAAAGCTC TAAGTGGCTA AGCTGAGGCC 1260 CGACTCGAGT GTTCTGGCCC CGAGGGCCAG GCTCCTTCTA TCATGTCACA CCCATCTGCC 1320 AAGGCCAAAA TTGTTTTCTG AGGTTAAGTC ACAGAGTTTC CTGAAGAGTG AGAAGATGTA 1380 ACTATTTTCT 1390
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