Tag | Content |
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EnhancerAtlas ID | HS104-03663 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:150185800-150186840 |
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) |
NRF1 | MA0506.1 | chr1:150185928-150185939 | CGCGCATGCGC | - | 6.02 | NRF1 | MA0506.1 | chr1:150185929-150185940 | GCGCATGCGCA | + | 6.32 | SPI1 | MA0080.4 | chr1:150185878-150185892 | GCAAAGCGGAAGTA | + | 6.04 | SPIB | MA0081.2 | chr1:150185880-150185892 | AAAGCGGAAGTA | + | 6.37 | SPIC | MA0687.1 | chr1:150185878-150185892 | GCAAAGCGGAAGTA | + | 6.11 | USF2 | MA0526.2 | chr1:150186010-150186026 | GGACCACGTGACTGGG | - | 6.06 |
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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 |
GH01I150213 | chr1 | 150185372 | 150186896 |
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Enhancer Sequence | AGACAGTAAA GAAAAGGAAG GTCCTAAGAA TCTGACCCAC GAGTTTCAGT CCAAGTAACC 60 TGGACCTGCC CAGAGGAAGC AAAGCGGAAG TAGGATCCAA AACGCTTTCA GCAGGCCGCC 120 TGCGCCCCCG CGCATGCGCA GGTCTCTGAC TTTGACCGTT TTGGCGGGTG CGCGCCAGCC 180 CTAGTTTATC TAGAGGGGAA GGGCGGTGCG GGACCACGTG ACTGGGGTTG CGGCATTTCT 240 GGCCCAATCC GAGACGGTTT CGTAGAGCGC CCTGTAGAGC AATTCGGGTT GCCCGGGTCC 300 TTTCCGAGTC TTGACCTCCT CTTTTGCTTC TGGCTTTTCG ACTCTGCTCT CGAATCTAAA 360 AATTTGCCTT GGCAGAAGTT TTTCCCTGTG TTCCAGGAAT TACATTAGGG ACACACTCTA 420 AAGTGATCAG CACTTTTTAT TTTTTTCCTT CATCAACTAA AATAACATTG CTGTCTCCCC 480 AAGACGCTCG AATTCTGTTC TATTGCTTGA GATTCCAGAA TCGCTGGAGG GCGCCCTGTT 540 GTAAAAATAG CACTCCCCAC AAAAAGAGAG AGAAAGTTTT ATCTATATCA GGGGGTTGAG 600 GATTGGAGAA ATAAAGATGA AAAATTTAAA GAAGCAAGTG TCCCCTAGGA CTATGACAGA 660 TACGTACCTC AACACGTACC CCCAAAGGTC ACTTTGTCAG TTTAAGCATT TAAAATCTCC 720 CAATCTGTCT ATTCAAGCCT ATCAAAAATC TGAAGTAGTG ATGCTGAGAT AATATGTGGT 780 TGGTCCAACC CAGTGGAGTG TGACGGGGAA ACAGGGCTTA GAGAAATTTA ATCTTAAAAC 840 TGGAGTACTT TCCTCATTTC CCTGAAATAA AGGGAATTGG GGGAAAAGCA AAATGGATGA 900 GGCTGAGTTC TAGAGCTCTA ATCCTTCACG TACTGACTGC TACAGCCCAG GAAGCTTAGC 960 AGTGGTTCAT GTCACATACC CCAATATACA TGGCTTGGTA AAAATACGTG TTGACAGGCC 1020 GGGCGCAGTG GCTCACCCCT 1040
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