Tag | Content |
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EnhancerAtlas ID | HS106-00014 |
Organism | Homo sapiens |
Tissue/cell | iPSC |
Coordinate | chr1:8051550-8052520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2F1 | MA0017.2 | chr1:8052246-8052259 | CAAAGGTCACAGG | + | 6.44 | Nr2f6(var.2) | MA0728.1 | chr1:8051816-8051831 | TGAACTCCTGACCTC | - | 6.22 | TEAD1 | MA0090.2 | chr1:8051920-8051930 | ATGGAATGTG | - | 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 |
GH01I007991 | chr1 | 8051285 | 8053003 |
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Enhancer Sequence | TCCAGAAGAG AATAAGATTT CACAAAGTAT ACTGAAGAGA AAGTTATGTT TCCTTTTTTT 60 CTTTGAGATA GAGTTTCACT CTTGTCGCCC AGGCTGGAGT GCAATGGTGC GGTCTCCGCT 120 CACTGCAACC TCCGCCTCTC GGGTTCAAAG GATTCTCCTG CCTCAGCCTC TCAAGTAGCT 180 GGGATTACAG GCGCCCACCA CCACACCCGG CTAATTTTTA TATTTTTAGT AGAGATGGGA 240 TTTCACTATG TTGGCCAGGC TGGTCTTGAA CTCCTGACCT CAGGTGATCC ACCCACCTCG 300 GCCTCCCAAA GTGCTGGGAT TACAGGAGTG AGCCGCTGCT CCAGGCTGTT TCCTTGTTTT 360 TTAGACCTAG ATGGAATGTG GCCTGGCGAC AGTCCCGTAT TCACCTGGTC CTGAAAATTC 420 CTCCCTCCAG CCCTCCGTAT CTGTTGTGCG GCGGTCTTAG GCCCTGCCTG CCTGGCGCCT 480 GGGGCCCTAC TGTGCTATGT GGTCAGTCTT ACAAAATGCA GAATTCTCTC TATTTGCATT 540 GCTGAGTGAC TAGCTGAGGC AGGTAGGGTG ACTGGGAGGA AGCTTTGTTA CAGATAACTT 600 GACAGCCGGG GGCAAGTTAA AGGATGATGG TAATAAAAGG ATGGTCAGGC CTCAAATTTG 660 GGCTTCAGCA GTAAATCAGT GCAAGAATAA AACTTACAAA GGTCACAGGC AAGAGTGAGA 720 TCATCCTCTT TTCTAATACT TGCTTATGCT TCTACATCCC TTATTGAGGA ATGCCAGCCA 780 CTCAGCACAC TTATGAAAGA GTAAATTATC TCCGGATGGT GGATAATACC ATGTCATTAG 840 TCCATGAGGC ATCTAGCTCA GCGCCACCTG GGTCTTAAAG CACTTAAAAA TGTAATTATA 900 CAACAAATAC ACCAATACCT GTTCATTGGG AAAGACTCAA ATGATACATG AATACATAAA 960 GCAAGACTTG 970
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