Tag | Content |
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EnhancerAtlas ID | HS048-19797 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:16233260-16235920 |
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) |
CEBPA | MA0102.3 | chr2:16233605-16233616 | ATTGCATAATA | + | 6.02 | PAX6 | MA0069.1 | chr2:16235138-16235152 | TTCACGCTTGAGCT | + | 6.55 | POU2F2 | MA0507.1 | chr2:16234612-16234625 | TGCATTTGCATGT | + | 6.37 | STAT3 | MA0144.2 | chr2:16233309-16233320 | CTTCTGGGAAA | + | 6.62 | ZNF263 | MA0528.1 | chr2:16233417-16233438 | TTTTCCACCTCTGCCTCCCTC | - | 6.14 |
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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 |
GH02I016093 | chr2 | 16233591 | 16238433 |
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Enhancer Sequence | TTGGAGAAAT CTCTAAATTC ATGTGGCAAA AACTAGTTTT CTCAGGGTGC TTCTGGGAAA 60 TGCGGCACGT TCTTTCTGGT TCCAATTTCC ACACACACAT ACCAAACAGG TTCTATCTCT 120 TTGGGAGAGT TATGGTGCGC CTATGAGTCC CTTGCCATTT TCCACCTCTG CCTCCCTCAG 180 GGGCTGGACT CCACTCAGCC AGAATGCTAG AAGCCAGCTG GGCTCTGATC TGAGGCACCT 240 GCACCCTGGA GAGACAGAGC AAGACCTCGG GGCCTTTGCA CAGCCTTCCA AACCGAGCAC 300 CCACAAGATG AATGGATCTT TCATTTCTAA TATTTATCCC CTCTCATTGC ATAATACCTA 360 TGCCAACGAA TTTTTGTTCT ATTTTACCGA AGACTTCCCA GTGAACCCAA GGGCTCTGGG 420 GTAGGGGTGG GTAGTCCCAC GGCACGGGTA CCAGGCAATT ACATTACAGC ATGATAAATA 480 CAGATATCTC TGGGCTCTTG GGAGAAACAG AGCCCTGTGT TTCCAGGTAG GTAGGCTTCC 540 TGGAGGAGTT GACACTTTAA CAGAGATTTA AAGGATTGGC ACAAGCTATA TGGAAGAGGA 600 GGTGTGGGGT TGCATTTGAG GCCTGGATGG AACAAATGGT CAGAATTGGC TCTGGGTAGA 660 ACAAATGGTG GGGCAGAGGG TGAGGCTGGG GAGCAGGAGG AAGCCAGCCC CGCAGGAGGC 720 AGCATGAGCT TCCTGGCCAG GGTCCTGAGG AAAGGCATCA AGGGACCTCC GGGGAGCATG 780 GCAGGGCTTT CCTGTTAGAG CCTCCTGATG ATGATGGACT GTGGTGTAGA AGGATGCATG 840 CCAGCCGTGG GCTGAGGCTG TGATCCACAG AGACGAGAAC CCACCCAGGG CAGCAGCTTT 900 GGGGCTCATG GCAGAGCCTC CGCCCTCGGC TCCAGTGGGA TAATAGGGCG ACATGACAAG 960 CTCTTCGTGC TCCCTGGAGG CTTGGTGCTC CCCCTGGCTG GATGTCAGAA CAAATTAAGG 1020 GCACTTGTCT CACAAGCCCC ACCTGGCCGG CAGCGTCGTG GGGCCGGCTG GCAGGGGAAA 1080 TGTGTCACCA GCAGCATCTT GGACCTTGGC CATTGGCCTC AGAGCAAGAA AAGCTCTCTC 1140 TGCCCTGCCT GTTTAGTGAA CAATGTACAG GAGTACAAGA GACTCTATGG CAACCAAAGA 1200 CCTGTGTCAG GGTCATGGTT CGAGGTTTTC TGTGCTCACT AATGTGGAAA ACAGAAGCCT 1260 CATGCTACAT CAGCATCGCG GCTGGTTTAC ATAAGCAGTC GGAGGCTGCA CAGAGCCAGA 1320 GCTGGAGCTG GGGCCGGGGC AGCTCCACAT CTTGCATTTG CATGTTGCTA AGTGTGCATG 1380 TGTACATGAT CTCCTTTGAC TTCACAATAC CCTGTAACTC TGGGATTCCT TGTTATCCCC 1440 ATTTTACAGA CAAGGAAACC CTGTAGGTTC CAGGGAGGGG CAAGGACTTA CCCAAAGTCT 1500 GATTCTAACT TCAGTGCTCT CTTGAATTGA CTAGATGTGG AGGCGTCTCA GAGCTTGGTG 1560 TAACGTGAGC TGGTGGGCAG AGTCCCCTTC CCCACCAGTG TCTCCCTGAG TCCTGATGCC 1620 AGGAGGGCAG GGCCCCCTAA GGTAGGGCAC CTTGAATGCA TCCTGGGCTG ATTCTGGGGT 1680 CTGAGGACCA AATGGCTGGG AATGAAACAG GGACAATGAG TTGGATGTTT TCATCCAGTG 1740 CTTGGAAGCC GTCCTGGAGT TACCACTAAC AGTGCTGAAG AGTGGAGAGC CTCTGGGTTC 1800 TGGAGAAACA CCTGGGCCCA TGCTGTCCCT TCTTCCTGAA AGCTCCTCTT CTCCTGTCCC 1860 TGCATGAGGC TTCGCCCCTT CACGCTTGAG CTAGCATATC CTGTTATCTG CAAAGTGTCT 1920 TGAATCTCTC ATCTGGGCTG GGTGCCTCCA CTCTGTCTGC TCACTGCTCT TGGGACACCC 1980 CTCCCACAGC GCTTATGCCA CTCTCAGGTC ACGGCTTCAT TTGTGCTTTT CATTGCACGA 2040 AGACAGAGAC CTCCCATGGG CCCTCAGATG TGTCCCTAGC ACCTAGTATT GTGCCTGGCA 2100 CACAGAAGGC TCAACGAATA TTTGATGAAT GAGCAAAGGA AGAAATGAAC AAATGAAAGA 2160 TTTCCAATGG TAGAAAAACA GACATTAGGG CTCAGGAAAG CTTGCTCCAT GGCTGGGGCA 2220 GCTGGGCTGG TGGTTCTAAT TATGGGTAAA TCTGAGCACT GGATCCCCTG AGCTCAACTG 2280 AGGTGTGCAG TGGCTCCTGG CATCTGCCTG CCAGTAGAAG CTTGTCAGGG TTCTAAGGCA 2340 AACAGTTATT TTGTTGAATT ATGCAAAGAG TCAGATTGTT GGAATTCCAT GTAGATCTCA 2400 GCCAAAGCCT GGTGATGCTT TGAGAAGATG GAAATACAAA TGGAATTCAG AAACAACTAT 2460 TTTTTTAAAG TAATATGTGT TTGCTATAGA AATTTTAGAA ATGCGGGTAT ACACAAAGGA 2520 TCAAATAAAT AGGCTGGGCA CAGTGGCTCA CACCTGTAGT CCCAGCACTT TGGGAGGCTG 2580 AGGCAGGCAG ATTACTTGAG GCCAAGGAGG TTGAGACCAG CCTGGCTAAC ATGGTGAAAC 2640 CCCATCTCTA CTAAAAATAC 2660
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