Tag | Content |
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EnhancerAtlas ID | HS180-01385 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:41509660-41512070 |
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) |
EWSR1-FLI1 | MA0149.1 | chr1:41510119-41510137 | GGAAGGCAGGCAGGCAAG | + | 6.45 | EWSR1-FLI1 | MA0149.1 | chr1:41510115-41510133 | GGCAGGAAGGCAGGCAGG | + | 7.44 | MEF2C | MA0497.1 | chr1:41509676-41509691 | TTCTATTTTTGTAAC | - | 6.42 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 41510928 | 41510993 | chr1 | 41511399 | 41511832 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I041044 | chr1 | 41509803 | 41512830 |
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Enhancer Sequence | TCATGGTTGC TTATTGTTCT ATTTTTGTAA CTTTTCTGTA GGTTTGAAAT TTTTAAAATA 60 AAACATTGGA GAAAAAAGTA GTAGTCTCAA CTTAGGTAGG AAAGCTTAAT GGGATATGAA 120 ATCTCCCTGA GCTTTGGGTG ACTACCTGCT ATATCGGAAG TGCATGGTCA GTTGGGCCAG 180 GACTCTAAGT GGTAGGGTAG TGTGGAGACA AGGATATAGG AAAGGGGGAG GGCCAGTAAG 240 CACCCAGATA ACAGAGGTGG TACCTATGTA TGTCTAGCAG AAGCGTGTAG CCAGGCAGAA 300 GGGCAGGAGT CATAAATACC AGATCCAAAG GGCAAAGCAA AAGACAGCTC TTGTACAGAT 360 CGAGCTCTTT GGCAGAGGTT TAGGTAAGTA ATCAGAAAAA CACAGGAAAT GATAATATCA 420 GAGGTGGGGC AAAGGGTCAG TAAGGCAGGC AAGCAGGCAG GAAGGCAGGC AGGCAAGCAG 480 GCAGAAAGGA TACACTAAGA AGCACAGAGG AATTAGAAGT TTAGGCAAGG CTCTGGCTTG 540 TCTGGGCATA GTTAAAGGCT AATTTCAGGG AAGCAAATAG AAACTAGAGT GAGAGCAGAC 600 AAGTTGCTGA GCACCCACGA TGAGAAACAG CTTAAGAGCA GAGGAGGACA CAAAAAGTGG 660 GCTCAATCTG TCTGAAAATG GGGAAGGGAG AGGTAGCAGC TAATGGCAGA ATGTGATACC 720 TTGGTCTTTG TTTCTCTTAG TTGGTGAGGC AAGAAGAGTC TGGCTAAAGT TTGCTTCCTC 780 TTATCTAGTG GCTGAATCAG AGAGATGTAA ATTGGGGCAG AATTCCCAGG AAAGGTCATG 840 CCCCGGTCCC AAACCACTTT TGGGACTGCA GGCCCATGAG GTACATCCTT ACCAGTCTCT 900 GAATGCTGCT ACCAGTATGT TTCTCTCACT TCTTAATGAT GGCATTCCAT TTAAGAATTC 960 GGAGTTCCTA TTTCTTTGAG AAATCTCTTT TTAAACTAGC AGCTACATTC ATGGATGTGC 1020 TAACCCCCAT TCATGCATCC ATTCTTTCAG AATCCCAGGT AGGCCTAACT TTCACGTCTG 1080 AAATGTAGAT CAGAGTTCCT GAATGCCTAA CTGGAGGTAT TTAAAACTTG CCTTTGTCTG 1140 GACCAGCTCT ACCATGCCCA GTCCAGACTC CCAGTGCAAC ATTCTAACTG CAAGTCAGAA 1200 TGCCTTTTTC TTTTCTCAGA GACTCTGGTA CTGAAAGAAA GCAATCTAGC ATGGGTTAGG 1260 TGAGGAGAAG TTCCCTCCAT AGAAAAGGAT CAGCCAGGGG ATCATAGAAA TGGCTGCAGG 1320 GATCAGATGG TCTGGCCCCC ACAGAGTATT TAAAATTCAG GTATCTTTTT GACCTGCTTG 1380 CAAGTCACAT AAGCAATACG GATTTGGGTA CAGAAGTATC TATGAGGGAA AGGGGGAAGG 1440 AGAATGGGGG AACAGTCACT TCCCTGGGCA CATTCTCTAG AAGCAGTGCT TTTATCGGAG 1500 GTGATTCTGT TAAGACTATG ATGAAAAGAC ACCAGGGAAG GCAGTGTGGG AACAAGACTT 1560 GTTTGTGTAG AGGAAGGTCG GAAAAGACAC CTTTCAGACC TGTGCCCTCC CATCAACAGA 1620 CAGCACAGCA CTCACACTGG CAGCACCCCT CCCTATTTCT CTGCTCAGGA CACAATCTGC 1680 AGGGCTTTTT TAAGGGCCTT TCCTCCCTCT CAGTAATGAC CTACCTTGCT ATGTTTAAGG 1740 CTGAGCTTTT CTTCCCTCCC TTGTTCTGTG TCCTGGGTTC CAGATGAGAG ACGCAGAGTT 1800 CCATTGAATC TTTAATCTCT CTCGGAAGTA CTTAGTCACT GATTTGGCCA CGTGGCATCT 1860 GCTTTCCCAT TGTGGGTCTG GTATGTTAAC TAAGAAAGTT ATTTTCCAGC CGAGTTAGAA 1920 ATAGCAGGAA CTTGAATTGA CTTGCTAGAC TGGCAGTGCT GGAAGTTAGG GCCATGTGCC 1980 AAAGGAAAGA ATAGATGGCC AATCACCAGG GAGCAAATTT CTCAATCTGT AGCCTGAGAC 2040 TAAACCTTCC TGCTGGCAAG GGAGATGTGT GTTAGGCCTT TGCTGCCAGG TTCACACTGG 2100 GAGACGTTCT GTGACTTCTT GGTGGCTCCA CATGCAGTCT GAAACTCAGA AGGGGAATTG 2160 CGAACCACCT TTTATCTAGG GATAAGGATC TAGAAGAAAT AGGGGTGATC CTAGAGACAG 2220 AAAACAAAAT CCTGAAGAAA AAGTAAAGAT GAGAGGAGGC TGAGAAGTCT CAGATATGGC 2280 AAAGGTAAGG GACAGAAAAG CAGACCTCTA GATAGTAGGT GCCAGGCCAG TAGTTCTGAA 2340 GGCTGACCCT GGGCCCCTGC AGGTGCTGCT GCTAGCCCTG TCCCCCACTC TCAGCCCAGG 2400 CCCCATCCCA 2410
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