Tag | Content |
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EnhancerAtlas ID | HS091-33098 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr22:38131450-38133550 |
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) |
CEBPA | MA0102.3 | chr22:38132690-38132701 | ATTGCACAATC | + | 6.32 | Gata1 | MA0035.3 | chr22:38131735-38131746 | ACAGATAAGGA | - | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_31741 | chr22:38126902-38131826 | Gastric |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I037733 | chr22 | 38129912 | 38131607 |
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Enhancer Sequence | TAAGGAGGTT TCCACCCTCC CAAGGGTAGC CAGAAAGTCA GCCCCACTCA GCCAAGTCTC 60 CTTGGAAAAG CCTCCCCTTG GAGTAGCCTA AGCTCCTGCA TCCCCCTCCA GGCTCAGACC 120 TCAGCCTCCC TGCTGACCAC AACCCATCCC GATCACCAAA CTGGCCCAAC AATGATGATG 180 AGCAACACAG TTTTAAGCGT TTATGGGCCA AGCCCTGATC TGAATGTTTG ACGTGTGCTT 240 TTCCCATTTA GTCTCCTTAG CAACCAGGTG AGAAATACAC TATTTACAGA TAAGGAAACT 300 GATGCGCAGG GTGAAGCCAC TTGCTGGTGG GGCATGGGCA AAACCCAGGT CTGCTCAGTG 360 CAGACCACAC TGAGGCCTCA AGCAAGATGC TCTGGCCAGG GCCTATTCCC CTCCTGGCTC 420 CACCATACCT GGTTTATGTT GTGTCTGGTG GCACACACCT GACCCCACCT GGGACTGTAG 480 CCAGTGTGGG CATGCCCCTT CCCCTGGTGG TACTCAGGTA CCTGAGTCCA GGACAGCCTC 540 GCTTACCCTC TCTGGCCCCT ACAGCTCCTC TCAGACACAG AGAAGAGGGT GCATCAATGC 600 TCACTGGGTT CAGCTAGCTG CCAAGACAGG CTGCTTAAAT GAGGGTCGTG TGCAAAGTGG 660 GCCCAGCGCC GGGCACACAG TAGGTGCTCG CCCTTCCCCT GCTTCACTGG TGCTTTGGTG 720 CTGCCTTGAA GCCCAGAACA TTCTTCATCT GAAGATGGTG GGCAGGGAGG GTCTTGGAGG 780 CCAGAATCCT GCACCCTGGC AATAGCTCAT TGGGAGGACG GCATGTGGTT TTGAACACCA 840 GCCTCTCTCT CTCTCTGTAA GATGGACCAA CCACTTCTCT GACGGGCAGC GCTGGGGTGC 900 CGTGGGGGTT CCTGCTTGTT TCTCCAAAGC CTCCTCATCT CCTAGATGCA AAGTCCAACG 960 CCACCTGCCC CAGGATGAGC AGGGCTTCCA GGCATCAGGG TGCACCCCGT GCTGGGCCCA 1020 GGGCCTTGCC ATATGTGCCT CAAGTGGATA GGAGGCAGCT GCCACTTGAC AGATGGGGAA 1080 ACTGAGGCTC AGACTCCTTA GGCATTTGCT GGGGGTCACA CATGCATAGG TCGTGAGAAA 1140 TGAGATCAAA GCATCCACTC CAAAGTTTGT GCTTTTATTT TTATTTATTT ATTTACTTAT 1200 TGAGACGGAG TTTCGCTCTT GTTGCCCAGA CTGGAGTGCA ATTGCACAAT CTCAGCTCAC 1260 TGCAACCTCC GCCCCCCAGG TTCAAGCTAT TCTCCTGCCT CAGCCTCCCG AGTAGCTGGG 1320 ATTACAGGCA TGTGCCACCA TGCCCGGCTA ATTTTGTGTT TTTAGTAGAG ATGGGGTTTC 1380 TCCATGTTGG TCAGGCTGGT CTTGGACTCC TGACTTCAGG TGATGCATCC ACCTTGGCCT 1440 CCCAAAGTGC CGGGATTACA GGTGCGAGCC ACCATGCCCG GCCTAAGTCT GTGCTTTTAG 1500 CCACCACGTC ACAAAGCTCC TGAGCCCATG GGAGGACTGG AGAACCCTCT CCCCTGTATT 1560 TCCCTGTGGC TTTGATGAGT TGACCCTCCA ATCAACTCAA TGCGTGGACA TCAGAGAAGC 1620 AGGGATAAGT CAGCTCGTCC TGCCCTCAGA TTGCTGTCAG GCTTGTTAGG AAGGCACACA 1680 GACAGCTCAA GGAGGACACG GTGCTGTGTC CCGGGGCATG CTGGGTGCCA CAGGCCGGCC 1740 AGGTCAAGAA GGAAGTTAGA AAGATTCTTC AGTTTCATGG TGAAGCTCAG GGTTCTCAGG 1800 AGGCTAGGAG ATGGTGGCTG GGAAGGGATG GGAGCACCAT GTACTGAAAG GAATTTCACA 1860 GATGACAAAA CGAGTAACCA CCAGGTCCTG CTGGGGCTCC AGCTGCTCCT CTCTATGAAA 1920 ATCCTTGGCT TGGCACAGCT GGGTGCAGTG GCTCACATCT GTAATCCCAG CACTTTGGGA 1980 GGCTGAGGCA GGCAAATCAC GAGCTCAGGA GATCGACACC AGCCTGGCTA ACACGGTGGA 2040 ACCCCGTCTC TACTAAAAAT ACAAAAAATT AGCCGGGCGT GGTGGCGGGT GCCTGTAGTC 2100
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