Tag | Content |
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EnhancerAtlas ID | HS187-18313 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr4:9994950-9996880 |
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) |
IRF1 | MA0050.2 | chr4:9995941-9995962 | GGTAGCTTTCTTTTTCAATTT | + | 6.11 | IRF1 | MA0050.2 | chr4:9996165-9996186 | TTTCTCTTTTGCTTTCCTTTT | + | 6.47 | IRF1 | MA0050.2 | chr4:9996171-9996192 | TTTTGCTTTCCTTTTCCTTTT | + | 6.75 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_53020 | chr4:9996030-9996905 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I009993 | chr4 | 9995466 | 9999128 |
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Enhancer Sequence | TGACTCTGTC AAGTGATGGA ATGACCCGTC TCAAATAAAG CCAATGAGGT TGGTGATGGT 60 GAAGATGATG ATGATGTTGA TGATGATGAC ACTAGTGAAC AAAGGCTGGG CGAAGAGTCT 120 GGGTCAATTG TAGGGATGAA CACTTCACAT CCACCATTTC ATTTAATCTT CACAACAACC 180 CTCTGACATG GCCATTCTTT ATCTTCATGT CATCGTGAAC TAAGTAAAGA TGAAAGAGTT 240 TAAGAAACAC ATAGCTGTGT GTATCGGAGC CCAGACTTGA AGCTGGGCCC GTAGCTAGTG 300 TTTGTACACC AAACATAGTC ACTGTCCTGT CTCATGAGGG AAGGAGGGTC CTGTCACTAT 360 GGTCATGCAA GCAGAGGACA GAGGATGCTA AATGGGTCAC TGAGCTTCAA CCAGAATTCT 420 TGATCGCTGA GAATTCCCTC AGCCAGAGAC TCCAAGAGGT GAGGAACCTG CATCTGTGTG 480 AGGCCCAGGT CATGTGGTAT GGCCCATCTC CAGAGACTCT TCCTGGCCCC CTTTGCTTCC 540 CTGCCCTCCT TTGTCACCGA AATCACAAAC GAGCTCAACA TTCCCTAGCT AGGAACAGCC 600 CCACTGCTGG AGCAGCCAGT GACCAGCCCC ATCGGAACTC TTCCCCACTT CCCTGGAATG 660 TCTCCCCCAG CTATACCTTT GAGCACCTTC CACTGGGCCT CCCAGGCTGC CATTGCAGTT 720 TCCTCTCCCT CCCTGAGAAT CCCCATGGGA GAGGAATAAC AGAGCATCAG GAAGGCGTTT 780 CAAATAGCAT CATGTCACAG GAAGAGTGTT GGCCTGTGGT CAAACACATG CAGATCTGAA 840 CTTCAGTTCA ACTCCATTTT GAAACCTTGG TCCAATTGAC CACTGGGTCT TGGACTCATC 900 ATTTGAAAAG TGCAGGTAAT GATGCAAACA TGGAGTTTTA AGAAGTAAAT GATATATGGG 960 ATGTCAAGGA CAAGGCAGGA GGTCAATAGA TGGTAGCTTT CTTTTTCAAT TTTTGCTCCT 1020 TTTCTCCCCA GCAGAGTTGC TCTTCAAGCT GAAACTTCAG CCCAAATCAA CTTTTACTCT 1080 CATAATGATG AAAAGGAAAC TGGCAGCTGC TTGGGGCATA ACAACCAACA CATCCTTTGA 1140 TCTGATCTTT TTCTGCATCC TCACTTCTTT ATGACTCCTC CATTACTTAG AGATTGAAGG 1200 TATTTTCAAA GTTGTTTTCT CTTTTGCTTT CCTTTTCCTT TTTTTTTTTT TTTTTTGTTG 1260 CCATGCCAGT GAGGGTAGTA AAGCTACTTT CATTGCCCTC ATTTTATAGG TAAGAATAAT 1320 GCTGGCTGAG AAGTGAGGTG TCAAAGTCCC TTGTAACACA CCTGATACAC AGCAGAGTCA 1380 GGACTTGCTG AGCCACGGCA TTCTGACCCG ATTCTAGTGT TCCTTTTCCT ATTCCATCTG 1440 CATGGGTTCA GAGCCTCCTT GAGGAGCAGC CTTGGGGTAT AAATGCCACG GTCAGGTATA 1500 AAGCAAGGAG ACATCACAGG CCAGATCCTG GGGCATGGGG AGTGACTCCA TCCCACTAGG 1560 ACAAGCAAGA GGACCATGGG CAGGGTCTGG CTTGGGCAGG AGGCTTAGTG ACCATGCCTC 1620 AGGGACCCTG GCCAGTGATG CCAATCTGAG TGCCAGCCTG TTGTCAAACA GTCATGGTTT 1680 TACAGTACAT TCCCAGCATT GGGAATTGGC CCCTAACTAA GATCTGCTTG GCATAGTGGA 1740 AAGATCATGA TTCCAGCCTA AGCTCAGCCA CAGTGCAAGC TAGCTAAGCT TGTGCAGATG 1800 CCCTCACCTC TCTAACCTCC CATTCCCCAT CTACAGACCC CACAGCAGAT AGAAAATTAA 1860 ACAAGAGAAT GTGTGAGTGG CTGGAACCTT GAAGGACCTC AGACAATGGC ATCTCTCACT 1920 ACATCATGCA 1930
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