Tag | Content |
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EnhancerAtlas ID | HS073-13741 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr8:22329920-22332460 |
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 | chr8:22331780-22331801 | CTTTTCTTTCATTTTCTTTAA | + | 6.41 | Nr2f6(var.2) | MA0728.1 | chr8:22331626-22331641 | TGAACTCCTGACCTC | - | 6.22 | TFAP2A | MA0003.3 | chr8:22330075-22330086 | TGCCTGAGGCT | - | 6.32 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_11137 | chr8:22329689-22333774 | CD20 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I022472 | chr8 | 22329690 | 22333774 |
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Enhancer Sequence | TGAGCCTAGG TCTACACAGG GTCAGGATCA TGAATATCCC TGGCTTGCCC CCCTACATCT 60 TTATCCACTG GCACACCTTC AGGAGCAGTA ACAGGCATGG AGCTGTTATC TCCTAGGATA 120 ACAATACCTT CTTCTGGAAG TCCTCCTGAA GGACCTGCCT GAGGCTCTTG AGGAGATGTC 180 ACTCTTTTCA GAAATTTGCC CATGGTGTTT TGCTTGGTTT ATTTCTATTT TTCATTGTAG 240 ATTTGTTTGT AAGCAGTTAA TGCAGCATGA ACATTCCTGT GTATTAATGA AAACCTTTCT 300 GTTTTTGGGG GTCCATGTTT TCACACTTCC TAAGGAGTTT GTTGAGGTGT GCAAAAGCTT 360 CTCCCAAACC CTTCACTGTG AGTTTTGTTG GGGGTTCTTT TTCTTTCTCC AGCAAACTTC 420 CTTCTCTCTT GCTGCTTCTT CAGCTTTGCA TTCCTATTCC AGTTCCCACT CATTAGTCAA 480 TTCCTGCGAT GTTATTGTGG CTATAACGTT ACTAGATGAC AGGAGTTTTT CAGCTCCATT 540 TAACTACAGT CCATTGTTGA CCAAAACATC ATTTTGTGGC ACACAACTGT ATTTAGCTAT 600 TTTAGTGGTT GGGTAGCTGC TATCGTTTTT TCAGTGAAAT TTGAGTAGTT AAAATGAGTC 660 AAGTAGTAGC TGAAAGCATG ACGAAACTTA TAATAGGACT TTCTTTACTT GTAAATGATA 720 CAATATGGTA TGGCTAGATT AAGTCTTTTA AAAATACTCA TAGATTTCAA CTTGGTTCCA 780 TAAAGCTGGA AGTGGAAACA TTGGACATAT ATCAGAAATT CAATTGAACG CCTCCTTTTA 840 AATTTATGGT TTACAGACTT GTGGCTCTTA GATCCCAGGG GATCTAAAGT AGACTGTGTT 900 ATAAAGTAGG CACATAACAA GACAACAGCC AATTTAAAAA TATTAAATGA ACTTGCTAAT 960 TCTCCATGAT ATTATATATA TAAACTTTGT ACCTAATGTA AACTGAAGGT AGTTATTAGC 1020 ATTTCCAGGT TAGAAAACAT AACTGGACTT CCCTTATCCA CTTTTTTTTT TTTTGAAACG 1080 GAGTCTTGCT CTGTCGCCCA GGCTGAAGTG CAGTGTCACA ATCTCGGCTC ACTGCAACCT 1140 CCATCTCCCA GATTCAAGCA ATTCTTCTGC CTCAGCCTCC CAGGTAGCTG GGATTACAGG 1200 TGTGTGCCAT CACACCCGGC TAATTTTTGT ATTTTTAGTA AAGACAGGGT TTCACCATGT 1260 TGGCCAGGCT GGTTTTGAAC TCCCGACCTC AGGTGATCCA CCTACCTTGG CCTCCCAAGG 1320 TGCTGGGATT ACAAGCGTGA GCCACACCAC ACCCGGCCCC TTATCCATTC TTTTATGCTC 1380 TGTTACTACA GCAAATTATT CTCAGACATA GCTCCATCTT GGTAGTAGTG TTCTTGTTAT 1440 TATCAGTAAC AAAGTACATT AAGCTACTGC CTTTTGTTTT ATTCTGTTTT GTTTTGTTTT 1500 ATTTTGAGAC AGTGTCTTGC TCTGTTGCCC AGGCTGGAGT TCAGTGGCGC GATCTCAGCT 1560 CACTGCAACC TCTGCCTCCC ACGTTCAAGC GATTCTTCTG CCTCAGCTTC CCGAGTAGCT 1620 GGGATTATGG GCACTTGTCA CTACACCTGG CTAATTTTTG TATTTTTAGT AGAGGTGGAG 1680 TTTTGCCATG TTGCCCAGGC TGGTCTTGAA CTCCTGACCT CAAGTGATCT GCCTGCCTCA 1740 GCCTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCATGGTG CCCGGCCGAG ACTTCTAAAA 1800 CATAGGTGTC ATTAGGACAG TTCTATAGGA GAAATAAATG CCATTTTAGT ATTATGACTA 1860 CTTTTCTTTC ATTTTCTTTA ACCATAGTTT CATTTTTAAC ACCTGTTCTA TAGATAGAAA 1920 AACAAAGATA CTCATGTCAT CTAGTGTCTT GTCTCATTTA TAACTTGTTC CCTGAATCAG 1980 CTTCAAGTCT TTCATGTTTA TGTGTAAAAC ATAGGGCTGG GCGCAGTGGC TCACTCCTGT 2040 AATCCCAGCA CTTTGGGAGG CCGAGGCAGG TGGATCACCT GAGGTCAGGA GTTCGAGAGC 2100 AGGCTGGCCA ACATGGTGAA ACCCTGTGTC TACTAAAAAT GCAAAAATTA GCCAGGTGTG 2160 GTGGCATGCT TCTGTAATCC CAGCTACTCA GAAGGCTGAG ACAGAAGAAT CGCTTGAACT 2220 CAGGAGGCGG AGGTTGCAGT GAGCTGAGAT CGTGTCACTG CATTCCAGCC TGGGTTGACA 2280 GAGCAAGCCT CCATCTCAAA AAAACAAACA ACAAAAACCA TTATAATTTA TGCACACACA 2340 AATATTTAAA ATGACTGTCA CCTTTTTATA CTTAGAATTG ATCATTTATG ATACATAGTA 2400 TCTTAGAATT TTTTCCCCAC GTACTGGTGC TGTGGATGTG AAATCATGGT GATTTATTAG 2460 GTTTAATTTG TCATGTAAAA GAATTGTGTT CTGTTTGTTC TCTATACATT TAAATATTTT 2520 AAATTATTAT TATTATTTTT 2540
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