Tag | Content |
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EnhancerAtlas ID | HS048-02290 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:150185340-150186800 |
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: 2 | Chromosome | Start | End |
chr1 | 150185878 | 150186128 | chr1 | 150185600 | 150185848 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I150213 | chr1 | 150185372 | 150186896 |
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Enhancer Sequence | AGCCCCTGGG GACAAGAAGA GAAATTCACT TAAGCAAAGG TCACCTAAGT GCAAACTTGA 60 ACCAGACTGT GCACAAACAA GTGACAGAAG CGAAAGTGGC CTCAGCTGCA AACGCAGCAC 120 TTGATAAACC ACACTCATGA TCAGCCCTCA TTTCCACCTT AGAGAGATTG AAAACATACC 180 TAACTCCACC ATTTATAGCT GCTGAGCAGG TGGATGACAT TCGTCAACGT GGGGTTTAGA 240 ATAATGCAAT GTTTGAAATA AAATTAGAAA GAAAATAAGG CCAGGCACGG TGGCTCACGC 300 CTCGAACCCC AGCATTTTGG GAGGCCGAGG CAGGAGGATC GCTTGAGCCC AAGAATTCGA 360 GACCAACCTG GGCAACAGGA CAAGACTCCA TGTGTATTAA AAAAAAAAAA TTAAGAAAAC 420 AAAAGCTTTG TTAATCGTTA AGTAAGGATT GCAAAATGGA AGACAGTAAA GAAAAGGAAG 480 GTCCTAAGAA TCTGACCCAC GAGTTTCAGT CCAAGTAACC TGGACCTGCC CAGAGGAAGC 540 AAAGCGGAAG TAGGATCCAA AACGCTTTCA GCAGGCCGCC TGCGCCCCCG CGCATGCGCA 600 GGTCTCTGAC TTTGACCGTT TTGGCGGGTG CGCGCCAGCC CTAGTTTATC TAGAGGGGAA 660 GGGCGGTGCG GGACCACGTG ACTGGGGTTG CGGCATTTCT GGCCCAATCC GAGACGGTTT 720 CGTAGAGCGC CCTGTAGAGC AATTCGGGTT GCCCGGGTCC TTTCCGAGTC TTGACCTCCT 780 CTTTTGCTTC TGGCTTTTCG ACTCTGCTCT CGAATCTAAA AATTTGCCTT GGCAGAAGTT 840 TTTCCCTGTG TTCCAGGAAT TACATTAGGG ACACACTCTA AAGTGATCAG CACTTTTTAT 900 TTTTTTCCTT CATCAACTAA AATAACATTG CTGTCTCCCC AAGACGCTCG AATTCTGTTC 960 TATTGCTTGA GATTCCAGAA TCGCTGGAGG GCGCCCTGTT GTAAAAATAG CACTCCCCAC 1020 AAAAAGAGAG AGAAAGTTTT ATCTATATCA GGGGGTTGAG GATTGGAGAA ATAAAGATGA 1080 AAAATTTAAA GAAGCAAGTG TCCCCTAGGA CTATGACAGA TACGTACCTC AACACGTACC 1140 CCCAAAGGTC ACTTTGTCAG TTTAAGCATT TAAAATCTCC CAATCTGTCT ATTCAAGCCT 1200 ATCAAAAATC TGAAGTAGTG ATGCTGAGAT AATATGTGGT TGGTCCAACC CAGTGGAGTG 1260 TGACGGGGAA ACAGGGCTTA GAGAAATTTA ATCTTAAAAC TGGAGTACTT TCCTCATTTC 1320 CCTGAAATAA AGGGAATTGG GGGAAAAGCA AAATGGATGA GGCTGAGTTC TAGAGCTCTA 1380 ATCCTTCACG TACTGACTGC TACAGCCCAG GAAGCTTAGC AGTGGTTCAT GTCACATACC 1440 CCAATATACA TGGCTTGGTA 1460
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