Tag | Content |
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EnhancerAtlas ID | HS092-01985 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:64648800-64650310 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr1:64649649-64649660 | TCAAGGTCAAT | + | 6.02 | Nkx2-5(var.2) | MA0503.1 | chr1:64649643-64649654 | AAGCACTCAAG | + | 6.02 |
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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 |
GH01I064183 | chr1 | 64648897 | 64650390 |
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Enhancer Sequence | CCTTTATTCC CCTTTAAAGA AAATCAAGTT TTACTGTAAA ATTCAGCACT AAAAGCTGTT 60 TGTGTTAGCC ATTTGACAAT TAGCTATATT TTTTGAAGTT GTTCCCTTGG ATAGAAAACT 120 GACAACATGT AGTCTTTGTC AAGAAGATAT TCCTCATCCA GTTCACCTGA GACCTAAATT 180 CTTGGATAGT GGCCAAATGC TTTTTCCTTC ATATGGACAA ACTCAAAGAA GTTGGTCTCT 240 TAGTACGCGT TTTTTTGACC CATGAACTGA TGATTGACAA AACAAAACAA AACAAAAATC 300 CCTTCTATGT TGCAACTTAA CAAAGATAAG GTCAAGGATA GGCTGGTCTT TGGGAGGAGG 360 GATAGGCTCA GCCCTAGTAA GCATCAAGCA GGAAGCTGCT GCAGGGGCTC CCCTCCCTCC 420 CTTGCACTTC CTGTGATGCC CTGACCCAGC TGGCTGGATG CAGACACCTG TGGCTTGTTC 480 TGCTGTTTTC CTTGGCCAGC TGGAATCCAT CATCAGTCCC TGGCTGGCCA TGAGTGCTCT 540 TCTGCCCGGA CTTTGCTCTC CTCTGCCTTT AAAGGGCTGA AAGCTCTGAG GAAGGACAGA 600 AAGAGGGATC CAAGGGAGGT TCTGGGGTGC AGTTCATACT CTTCTTAATT TATACGCATT 660 TTTTTCAGCC AATAGCTCTA ATGCTAAAGA GGAAGTGCCA GATTAGCGGA GAAAGAACAA 720 GGGAGCACAC ACAAGAAAGG GTTTTTGCAG CCAAAATATG ACTGCATTGA AGTTTGTTAC 780 CGTAAATGCC AATGGTAATA GGACGCTGTT AGCTCAAGAA AAGGAGAGTC TTACAAACCA 840 TCAAAGCACT CAAGGTCAAT GTAATCCTCT GGGAAATTAG GCTGGGAAGG CTTAAAAATA 900 TAGACATATA GAGGGAGAAG GTCTGCTGAC ATATTTATGA CTAGTTGAAT CTTAAGCACG 960 TATGAATTGC TTACTCACAA ATGAGTACCA TAACATTTGC TGACCGGGAT TGGCAAGATA 1020 CCTTACCAAA TGACTATGTT AGTAAATACA GTCATGCATT ACTTAACGAA GGGGATACAT 1080 TCTGAGAAAT GTCCTTAGGT GATTTCGTCA CGGTGCAAAC ATTATGGTGT ACAATTACAC 1140 ACACAGTACA GACTGCTACA AACCTAGGCT ACATAGAGTA TGGCATACTG CTCCCAAGCT 1200 ACAAACCTGT ACAGCATGTT ACAGTACTGA ATACTGTAGG CAACTGTAAT ACAATGGCAA 1260 GTATTTGTGA ATCTAAGCAC TTATCATGAA TGGAGCTTGT AAAACTGGAA GTTGCTCTGG 1320 GTGAGTCAGT GAGTGAGTGG TGGGTATTGT ACACTACTGT AGACTTTATA AACACTGTAC 1380 ACTTAAACTA CACTAAATTT ATTTAAAAAT TCTTCAATCA TAAATTAACC TTTTGATTTA 1440 TGAACTTTTT ATTTTAACTT TTTGACTCTT GTAATAACAC TTAGCTTCAA ACATGTACAG 1500 CTGCACAAAA 1510
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