Tag | Content |
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EnhancerAtlas ID | HS081-20633 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr9:93939590-93941650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr9:93940526-93940537 | TTCTGTGGTTT | + | 6.32 | STAT3 | MA0144.2 | chr9:93940313-93940324 | TTTCCCAGAAG | - | 6.62 | Stat4 | MA0518.1 | chr9:93940310-93940324 | CTGTTTCCCAGAAG | - | 6.01 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_20662 | chr9:93939420-93940686 | CD56 | SE_25080 | chr9:93939736-93941207 | Colon_Crypt_3 | SE_27567 | chr9:93939295-93941541 | Esophagus | SE_39461 | chr9:93939246-93940576 | Jurkat | SE_39461 | chr9:93940602-93941251 | Jurkat | SE_44449 | chr9:93941179-93943074 | NHDF-Ad | SE_44911 | chr9:93940201-93941027 | NHLF | SE_44911 | chr9:93941368-93942000 | NHLF | SE_66540 | chr9:93939246-93940576 | Jurkat | SE_66540 | chr9:93940602-93941251 | Jurkat |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I091177 | chr9 | 93939622 | 93943446 |
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Enhancer Sequence | TAATCCATGT CCTCTGTGTT TTACAAAAGC ACTGGCCCAA GACAGATTGG GGAAAAACTA 60 CAAAAAATTG CTCCTTCCCT ACAGGCTGTT CCAGGACAGC AGCTCTGGAG TGTGGCTTGG 120 CGGTCATTTC TGGGGGAAGC TGCAGACAAT TAGCCACAGA TGATACTTAG GGTCTCAGAC 180 CCCACAGTTG ATGCTTAAAA TAGATGTTAA TGACTTCAGA GATGTCCCTA AGCTTATCTG 240 ATTCATACCC TCTCATTTCC AATGTGTTTT CTGAGGGAAA AAGAAGGGTT TTCGGTCAGT 300 GTGCCAGGAG ATCCAAAATC CAGGGCATCC CTGGGTAGCC TGACCTGCTG GGACAATGAA 360 AAGGTGGAGA GAGGACTCCC AGGGACGGCA ATGAGGAAAC AGGGCTGCCA CGGCCCACAG 420 GCCTGGGTGT GATCTTGCTG CAGAGCCAGG AAGCTCCTTG CAGCGGTGAA TGTGGTGGCG 480 GTGCTGGCCG GGCACCGTGG CTGTGCCTGG CAGGCCTGCT GAGGGCACAG GGATTCATCG 540 CGCTTGGCTC AGAAGCTTCG TTTTTCTGAG ACAGCTCCCA GCTTCACTCA AACGTGGTTA 600 CCTACAGATG CAAACTGGAA ACGATGCACT GTTTGTTCCC TTGCAATCTC TACGGTGAGC 660 AGGCAGGAGC CCCAGCCAGA GTCCTGTGGT CACACACCCA CTGGTGGTCA GGTAAATTTT 720 CTGTTTCCCA GAAGGTTTTA TTTTACAGAG TTAACAGACT GTGGCCTGCT TCCATTGCTC 780 TGAAACACGC CAACTCCAGT TTCCCCACCT TTGTGAGGAC GATCAAAAAC CCAGAGAACG 840 GCAGTGTTAA GATTTGATTT CATGATAAGC CCATCTTGTG GCAAGTTGAG TCTGGCTCTG 900 GAAGGTGTGT TTGCCAGGAA ACAAGCTGTG TATTATTTCT GTGGTTTGGC AAGGGAAACT 960 CTGAGCTGGA TGGATTTGGG AACCAGGGGA AACATAGCTC AGGCCATGAG AAGTCTGGAT 1020 GAACAGGAAA ACAGAGGAGG GGTCCCAGGT ATTGCACAGC TCAGAGAGAC AACGCCCCAG 1080 CGCCAGAACT CAGCAGCCAG CAGGGGTGTG GGCAGCACTG GGGTGTGGCT GGAAACTTCG 1140 GACACCACCC ACACGGCCCA CAGTGCCAAG CCCTGCTGCC TGGCCCTGCC CACAGAACCC 1200 CCCCATCCTT CTCAGCTGTG GGCTAAACAC CCCCAGGATG GAAATGGCTG GGCTGTCCAG 1260 GGTGTGGAGT GAGCAGAGGC GCACAGGCAG CCTGCCTATG TGGGCCTGTG TTGGTGGGGC 1320 CCCACGTGTG GACATGCCCC GCCTGACACC AGGACTTGCC CGTGAGCCTC CCTCATCCCC 1380 AGCAGGCCTT GCTGGGACTC CTGTCTGGGG CTCAGTCCCG CTCTGGGGAC ATTTTAGGAG 1440 AGGCAGGTGA GTTCCTGCTG CTCCCAGGGG CCAGTCCCAG GGGACCTCAT CTGTGACAGA 1500 GGATACCTCA TTTATGACAG AAGACGAATT GTTGGGCACA GCCCAAGGCC TACGGAGAGC 1560 AAGGTAGGGT TGTGTCAGAG TTGCCCTGAA ACCAACATCT TGTAGGTAAA GTTACTGAGG 1620 TTTGTCAAGT TGCACAGCAT GGAGTAAGCC GCAGAGTGGA GGACAGGAGG TCACTCTGTG 1680 GTTCCCGGGC ATCTCATACC ACCTGGTGCC ATCTGGAAAC AAGTGTATTC ACCTGCAGTG 1740 GGGAGACCCC GCCTCCCCTG CCTCAGAGCA GCCAGCCCCT TTGTCTGCCA CCTGGAGGTG 1800 TCACAGGCCT TCAGAGGAGA GGGCTGTGGG GCTGCAGGGA GTCATCAGGG TGGACAAAGA 1860 GGTGCACTTG TGCAGATGTG GGCCTCATGG AGCCGAGAAG GGAAAGACTT CCCTGCAGAT 1920 GACCATACAA TGAGCAGGCA AGAAAGAGGA CCGGAAGGCG TGAGCTGAAC CCGCAGCTGG 1980 CTGAGGAGCC AACACACACG TTTCCGAGGG ATCCAGGCTT AGGCTGGTGG CTCTTACGAT 2040 CCCAACATCG GCTCCATTCG 2060
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