Tag | Content |
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EnhancerAtlas ID | HS040-00928 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:23157300-23159580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr1:23159451-23159464 | GAATGTTCTGGAA | - | 6.62 | IRF1 | MA0050.2 | chr1:23157853-23157874 | TAGCAGAAAGTGAAAGCATTT | - | 6.19 | IRF2 | MA0051.1 | chr1:23157857-23157875 | AGAAAGTGAAAGCATTTT | + | 6.29 | SREBF2 | MA0596.1 | chr1:23157402-23157412 | ATCACCCCAT | - | 6.02 | TBX21 | MA0690.1 | chr1:23158262-23158272 | AAGGTGTGAA | + | 6.02 | TBX2 | MA0688.1 | chr1:23158262-23158273 | AAGGTGTGAAA | + | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 23157740 | 23157851 | chr1 | 23158530 | 23159269 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I022824 | chr1 | 23151232 | 23159621 |
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Enhancer Sequence | GCCTCCCAAA GTCCTAGAAT TACAGGCATG AGCCACCGCA CCCTGCCTCA TATTCATTTC 60 TTTATGCCAA CGGTCTTAGA TCAACAAGAA GCATTTAGTC CAATCACCCC ATTTTACAGG 120 TAGGAAAACA GAGGCTCCAA GAACGACAGC AGACATTTCA AATGTAGAAT GGCCAAGTGT 180 GTGGGTGTCA GGAAGAGGAA GCTAGATGAA GGAAGAGGGG TAATGCTCCA CGTTGACTAC 240 CAGAGTCTGA AAGTCTGAAC CTGGGATGCC AGGCAGGCAG TAAACCCAGG GGCTCCCCAG 300 ATCAACCCAG CAGTACTGAC TGCATCTTTG CAGGTCCACA CTGGCAGCCT GTACACTTTG 360 AAGAACAGCA GGTCCACTGG GGATGAAGGG CGGCTGCAGG GATGGTGATG GGCATTGAGT 420 GAGGTGATTT ATATAGGGCA ACTTACAGAG TGTCTTGCAC ATAGAAGGTG TTCAGGTCCT 480 GGGAGGTAAG TGAGCACCAG ATACAAACCC AGAACTGGGA TGGGGAGTGG CTGCCCCTTG 540 CTACCTCCCC CCTTAGCAGA AAGTGAAAGC ATTTTGCACA AAAACTCAGC TGTAGGCATT 600 GTGTAATAGC ATTGATCTAT CCAAAAATAT TGAGTGCCTA CTGTGTGCCA GGCAGCCTGT 660 GAAGCCTTTT GCGTGAATCC TCTCATTTCA ACCCAGGAAC CCTTACAAGT CAGTCTACTA 720 TTATTTCCAT TTTATGGATG AAGAAACTGA GGCTCAAGGA GCCTGAGTGG TTTGCCTAAG 780 GTCAAGCAGA GCAGGGCAGG AATCCAGGGC TTTCCAAATT CAGAGCCTTA ACACCATGCC 840 ACACTGTGCT GGCAGAGATA GCAAGAGTTG TTGGAGATGA TTATAAGGGG AGGGCCAAAA 900 TGATCGTGGG AATCCAATCC CCGTGGCAGT AGGTGGGAGA TGCTGACCTG GGCTTCCTCA 960 GAAAGGTGTG AAATGTTGAC ACCCTCCCCT TGGGCTCTTC AAGGGCTCAA GAGGGGCTGT 1020 GTTAGGCTGG GCTGGAAACA GAGGGCTGAC CATCATGGGT TCCAGAGGGA GCTATCCACC 1080 CCCCTACCTA GCCAGAGGCA GCCAGGATTC CATTAACCTG ATTCTCTGCC CCACATAAAC 1140 CTGCAAAGGG AGCCCCTGGA GGGAGGGGTA CTGGGGAGAG GAAGAATTGG GCTTCCCCAG 1200 GCCCCAAATG GAGCAGCCAG TGGTGCTAGT TTCCTCTCTT GCAGTCCAGG AGGACCTTCG 1260 AGGCCCCTGG CTGTTTGAGC GGGGAATAGG GAGAGCGATG GAGAGCCAGA AAGTAGGGAC 1320 AAGAGACTCC AGGCTGGGGT GCAACAGCAG GAATAGCAGG AACAGGGTGC ACGTCATCAG 1380 AACAATGGGT CCTGAGTCAC TCTGTGCCTG CCCAGCCCTG CATGGCCCTG GGTGAGTCAT 1440 GTCACTTCTC TGAGCTGTGG GTTCTTCCTC AATAGTAAGG GCAAACCAAT GCCACCTCTC 1500 AGTGTTGCTG GGCTGATTCA CAATACCGGG CCTCAAGAAA TGGTGGCTGT TGCCAATGCT 1560 ATAATTTTAC AATCTTGACC CCATGTATCC CTTCTCAGCT TGCAAGCCAC ATTCATCCTT 1620 TTTCTCCTTG GAGCCTCACA ATACTTCTGC AAGGTGTCCA GGATTCTTAC CAGAGAGGTT 1680 AAGGGACTTG TTCAGAATCA CACAGCTTCT AACCCTTGGC CTGGGATGCA CCCCTAGTGA 1740 TTGTCATGGA GTGGGCCATC CCAGCCAGGC TACGCCACTC TTCTTCAGTC TGGGTGGTTG 1800 CTATTCCTCT GCCATGATTC ACGTCAGATG CCTCTTCCTC CAGGAATCCC TCCCTGACCA 1860 CACAAGAGCC TGGTTAGTAC AACTCTCTGC TTTCCCACAA CCTTTGAGAC ATTTATCAGA 1920 GTGTTTATCA GCAGTCATCA CAACCGTTAG GTGCTCCCAC CTAAGACTTT GAGGGTTCAG 1980 CCAATACTTT ATAATAGAAG AAGAGGGGGT ACAATAAATA TTTTGTTAAT GACTACAGCA 2040 CCTGTACAAA GGGACAGATA GGTGTCCACA GACTCACATG TATAAGTAAC AGTCATGCAT 2100 GCACAGCCAT GCACATGTGG CTTAGTGAAT ACACATGTAT ACAGACAGGG AGAATGTTCT 2160 GGAACATGAA TTGTGCTCAT GTGGATGCCC CATCCCCCCA CCCCCATATA AACACATAAA 2220 AATACTAGAG ATGATATTGA TACAACCTGG TAAGAGAGAA AGGAAAATCC TTGGGTGACT 2280
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