Tag | Content |
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EnhancerAtlas ID | HS017-00449 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr1:23157340-23159610 |
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 | CCCTGCCTCA TATTCATTTC TTTATGCCAA CGGTCTTAGA TCAACAAGAA GCATTTAGTC 60 CAATCACCCC ATTTTACAGG TAGGAAAACA GAGGCTCCAA GAACGACAGC AGACATTTCA 120 AATGTAGAAT GGCCAAGTGT GTGGGTGTCA GGAAGAGGAA GCTAGATGAA GGAAGAGGGG 180 TAATGCTCCA CGTTGACTAC CAGAGTCTGA AAGTCTGAAC CTGGGATGCC AGGCAGGCAG 240 TAAACCCAGG GGCTCCCCAG ATCAACCCAG CAGTACTGAC TGCATCTTTG CAGGTCCACA 300 CTGGCAGCCT GTACACTTTG AAGAACAGCA GGTCCACTGG GGATGAAGGG CGGCTGCAGG 360 GATGGTGATG GGCATTGAGT GAGGTGATTT ATATAGGGCA ACTTACAGAG TGTCTTGCAC 420 ATAGAAGGTG TTCAGGTCCT GGGAGGTAAG TGAGCACCAG ATACAAACCC AGAACTGGGA 480 TGGGGAGTGG CTGCCCCTTG CTACCTCCCC CCTTAGCAGA AAGTGAAAGC ATTTTGCACA 540 AAAACTCAGC TGTAGGCATT GTGTAATAGC ATTGATCTAT CCAAAAATAT TGAGTGCCTA 600 CTGTGTGCCA GGCAGCCTGT GAAGCCTTTT GCGTGAATCC TCTCATTTCA ACCCAGGAAC 660 CCTTACAAGT CAGTCTACTA TTATTTCCAT TTTATGGATG AAGAAACTGA GGCTCAAGGA 720 GCCTGAGTGG TTTGCCTAAG GTCAAGCAGA GCAGGGCAGG AATCCAGGGC TTTCCAAATT 780 CAGAGCCTTA ACACCATGCC ACACTGTGCT GGCAGAGATA GCAAGAGTTG TTGGAGATGA 840 TTATAAGGGG AGGGCCAAAA TGATCGTGGG AATCCAATCC CCGTGGCAGT AGGTGGGAGA 900 TGCTGACCTG GGCTTCCTCA GAAAGGTGTG AAATGTTGAC ACCCTCCCCT TGGGCTCTTC 960 AAGGGCTCAA GAGGGGCTGT GTTAGGCTGG GCTGGAAACA GAGGGCTGAC CATCATGGGT 1020 TCCAGAGGGA GCTATCCACC CCCCTACCTA GCCAGAGGCA GCCAGGATTC CATTAACCTG 1080 ATTCTCTGCC CCACATAAAC CTGCAAAGGG AGCCCCTGGA GGGAGGGGTA CTGGGGAGAG 1140 GAAGAATTGG GCTTCCCCAG GCCCCAAATG GAGCAGCCAG TGGTGCTAGT TTCCTCTCTT 1200 GCAGTCCAGG AGGACCTTCG AGGCCCCTGG CTGTTTGAGC GGGGAATAGG GAGAGCGATG 1260 GAGAGCCAGA AAGTAGGGAC AAGAGACTCC AGGCTGGGGT GCAACAGCAG GAATAGCAGG 1320 AACAGGGTGC ACGTCATCAG AACAATGGGT CCTGAGTCAC TCTGTGCCTG CCCAGCCCTG 1380 CATGGCCCTG GGTGAGTCAT GTCACTTCTC TGAGCTGTGG GTTCTTCCTC AATAGTAAGG 1440 GCAAACCAAT GCCACCTCTC AGTGTTGCTG GGCTGATTCA CAATACCGGG CCTCAAGAAA 1500 TGGTGGCTGT TGCCAATGCT ATAATTTTAC AATCTTGACC CCATGTATCC CTTCTCAGCT 1560 TGCAAGCCAC ATTCATCCTT TTTCTCCTTG GAGCCTCACA ATACTTCTGC AAGGTGTCCA 1620 GGATTCTTAC CAGAGAGGTT AAGGGACTTG TTCAGAATCA CACAGCTTCT AACCCTTGGC 1680 CTGGGATGCA CCCCTAGTGA TTGTCATGGA GTGGGCCATC CCAGCCAGGC TACGCCACTC 1740 TTCTTCAGTC TGGGTGGTTG CTATTCCTCT GCCATGATTC ACGTCAGATG CCTCTTCCTC 1800 CAGGAATCCC TCCCTGACCA CACAAGAGCC TGGTTAGTAC AACTCTCTGC TTTCCCACAA 1860 CCTTTGAGAC ATTTATCAGA GTGTTTATCA GCAGTCATCA CAACCGTTAG GTGCTCCCAC 1920 CTAAGACTTT GAGGGTTCAG CCAATACTTT ATAATAGAAG AAGAGGGGGT ACAATAAATA 1980 TTTTGTTAAT GACTACAGCA CCTGTACAAA GGGACAGATA GGTGTCCACA GACTCACATG 2040 TATAAGTAAC AGTCATGCAT GCACAGCCAT GCACATGTGG CTTAGTGAAT ACACATGTAT 2100 ACAGACAGGG AGAATGTTCT GGAACATGAA TTGTGCTCAT GTGGATGCCC CATCCCCCCA 2160 CCCCCATATA AACACATAAA AATACTAGAG ATGATATTGA TACAACCTGG TAAGAGAGAA 2220 AGGAAAATCC TTGGGTGACT TGGTTTTTCA TTTAAGGGAT TTTTTTTTCT 2270
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