Tag | Content |
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EnhancerAtlas ID | HS119-00363 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-1F5 |
Coordinate | chr2:3473600-3474550 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Ar | MA0007.3 | chr2:3474048-3474065 | AAGAACACCCTGTTCCA | + | 6.14 | Ar | MA0007.3 | chr2:3474048-3474065 | AAGAACACCCTGTTCCA | - | 6.44 | NFAT5 | MA0606.1 | chr2:3474538-3474548 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr2:3474538-3474548 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr2:3474538-3474548 | ATTTTCCATT | + | 6.02 | NR3C1 | MA0113.3 | chr2:3474048-3474065 | AAGAACACCCTGTTCCA | - | 6.01 | NR3C2 | MA0727.1 | chr2:3474048-3474065 | AAGAACACCCTGTTCCA | - | 6.01 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_01750 | chr2:3467163-3477139 | Aorta | SE_41159 | chr2:3468278-3477371 | Left_Ventricle | SE_49115 | chr2:3468345-3477656 | Right_Atrium |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 3473716 | 3473801 | chr2 | 3473893 | 3474499 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I003469 | chr2 | 3473020 | 3475997 |
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Enhancer Sequence | AGCAGCAGTC ATGAGCATCC CTTACAAATC ACATTGTAAC ATCTGAAGTC ATGTAACACA 60 AAGCTAAACG CGCGTGGAAT AAGATTGATT TCGTTTCTCT GAGATTAGTT TCTACTCTTA 120 TGTGCATGGA GATACAAGGG AGGCTCGGCA TTTTCTACAA TCTTGAATGT TATCTCCAGA 180 CCAGGGAGGA TTTGGGTTTC ATCAGCATTG AAGGTGGGAG ATGAGGTGGG CATCGCGTCG 240 ATGCTGAGTC TCGGGGAGAA AGCTAGGAAA TGTCCCCAGC AGGTAGGGAA ACGCTTGGCA 300 AAGCACAAAG GCAGAGGGAC CCACATAGCT GGGCCCATTC TGCTCACGCC CTGGCACTAC 360 TGCAAGAACT GTGGTTTTCC GGGTCAACCC TAGCGAGGAG GGAGCACAAG CAGAGCTTCT 420 CTGCGGAGAA GGCAGATTTC CAGCTCCTAA GAACACCCTG TTCCACAAGG AAGCTGACGT 480 GCCCCTCCCC AGGGACCCAC GCCAAAAGGC CATTCTTCCA GGCCAGCGTC CCAGGGCGCT 540 GCTGTGCGTG GTTCGCAGCC CCGGCAAACG ATGGCCTGCA CTGCGTGCTG TCCGCCCTGT 600 TCCTGCTGGA CTCTCTGCAC TGTGTCCTGA TCACCCTCTC AGCTGATAGT GGGCACTGCA 660 GTGTGAATCT TCTCATGGAC AACAGACCAA TCCTGCCTCC ACCAGTGCCG TCGCCAAATC 720 AGTAACACAG AGCAACCTCA AACATTTCTG AATGTTTAGG TCATCTAATA CTTGGCAAAA 780 GAGTGGGCCG AACACCTCCA CCCTCAGCTT TCTCTTCTGT TTGTGTGTGA GTGTGTGTAG 840 CAGAGTCTGA GAAAGATACA TACAGCCACC TTCCTTTTCT GAGCTTGGGA AAATTTGAAC 900 AAGAGCACTG AAATGCAAAC ACTAATCAAA AAGGAAGTAT TTTCCATTTT 950
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