Tag | Content |
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EnhancerAtlas ID | HS101-08318 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr11:70247820-70249640 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr11:70249066-70249077 | TGCTGAGATTT | - | 6.32 | NFE2L1 | MA0089.2 | chr11:70248957-70248972 | GTTGCTGAGTCATAC | - | 6.8 | Nfe2l2 | MA0150.2 | chr11:70248959-70248974 | TGCTGAGTCATACAG | - | 6.93 | STAT1 | MA0137.3 | chr11:70248668-70248679 | TTTCCTAGAAA | - | 6.14 | Stat4 | MA0518.1 | chr11:70248665-70248679 | ACATTTCCTAGAAA | - | 6 | Zfx | MA0146.2 | chr11:70249536-70249550 | CCCGCCTCGGCCTC | + | 6.01 |
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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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Enhancer Sequence | TCCTAGCTAC TCGGGAGGCT GAGGTGGGAG GATCACCTGA ACCTGGGACA CAGAGGTTGC 60 AGTGAGCTGA GATTGTGCCT CTGCACTCTA GCCTGGGCCA CAGTGCAAGA CCCTGTCTCA 120 GAAAAAAAAA AGAAAAAAAA GGCTGGTGGG GGGCTTTTAG GCGCGGTGGT TCGTGCCTGT 180 AATCCCAGCA CTTTGAGAGG CTGAGGCTGG CAAATCACTT GAGGCCAGGA GTTGGAGATC 240 AGCCTGGACC AACATAATGA AACCCCATCT CTACTAAAAA TACAAAAAAT TAGCTGGGTG 300 TGATGGCGCA TGCCTGTAAT CCCAGCTACT CGGGAAGCTG AGGCAGGAAA ATCACTTGAA 360 CCTGGGAGAC AGAGGTTGCA GTGAGCCGAG ATCGCGCTGT TGCACTCCAA CCTAGGCAAC 420 AGAGCAAGAC TGTCTGAAAA AGAAAAAAAA AGTTATTGTG TAGAGGAATT TTTCACTCTG 480 TCTAGACAGC AAGATTACTT CACGTTTGTG CAATCTTGAT TTGTACACTG ACGTTTGCAA 540 GGAAGGTTTA ATGTTGAGGA TGGACAGAGT CATTATCTTC TTTTGAACCG TATTGTAACA 600 GCTTTATCGA GATATAATTC ACATACCATA CAATACGCCT GTGTAGTGTG TACTCTCCAC 660 TGGTTTTTAG TATCTTCATG CAGTTGTACA ACTGTCACCA CAGTCAATTT CAGAATAATT 720 TTATCACCTC AAAAAGAAGC CCTTGTACCT TTTAGCCATG ACCTCCCTAT CCTCACCACC 780 ACCATCCGCC CAGCCCTGGG CAACCAGCAA TGTATCTTTT GTCTCTGTAG ATTTGTGAAC 840 TCCAGACATT TCCTAGAAAT TGAATCGTAT AATATGTGGT CTTTTGTGCG TGGTTTTCCT 900 TTGCGCAATG GATTTGAGGT CCCTCCACGC TGTAGCAGGT GTCACTGCTG GATCCTCTTT 960 GTGGCAGAAT AAAATGCCTT TGTGTTAGGT AGACCACATG TTATGTATCT ATCAGTTGAT 1020 GGACATTTGG AGTGTTTCTG TTTTTTGGCT GCTATGAATA GTGCTGTTCT GAACACTCAC 1080 GCACAAGTTT TTGTGTGCTT ATACTTTATT TCTCTTGGGC ATAGACCTAG GAGTGGAGTT 1140 GCTGAGTCAT ACAGTACCTG AGTTTAACCT TCTGAGGAAC TGCCAGACCT TTTCCATTTA 1200 ACATCCCTGT CAGCAGTCTA TGAGGCTTCC AGTTTTTCAA CACTGTTGCT GAGATTTGTC 1260 ATTGGCTGTT TTATTTTAGT CATCCTAGTG GGTATGAGGT GGGTTCTCAT TGCAGTTTTG 1320 ATTTGCATTT CCTTGGTGGT TAATGACATT GAACAAACTT TTCCTGAGCT TGTTGGCCAT 1380 TTGTATATCT CCTCTGAAGA AATGTCTCTT CAGATCCTTC AATCATTTTT AAATGGGGTT 1440 ATTCGTCCTT TTTATTGAAT TATAAGAGTT CCTTTTTTTT TTTTTTTTTT TTTGAGATGG 1500 AGTCTCACTC TGTCGCCAGG CTGCAGTATA GTGGCGCAAT CTCGGCTCAC TACAGCCTCT 1560 GTCTCCCGGG TTCAAGCAGT TCTCCTGCTT CAGCCTCCCA AGTAGCTGGG ACTACAGGCA 1620 TGCGTCACCA CGCCCTGTTA ATTTTTGTAT TTTTCGTAGA GACGGGGTTT CACCATGTTG 1680 GCCAGGATGG TCTCGATCTC TTGACCTAGT AATCCGCCCG CCTCGGCCTC CGAAAGTGCT 1740 GGGATTACAG GCGTGAGCCA CCTCACCTGG CCAAGAGTTC TTTATATATT CTGGATCTAC 1800 AGTTCAAAAT ACTTTTCTCT 1820
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