Tag | Content |
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EnhancerAtlas ID | HS003-24845 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr2:20777340-20780110 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr2:20779461-20779475 | AGTCCCACGGGAAT | - | 6.01 | NFE2L1 | MA0089.2 | chr2:20779231-20779246 | GCATGACTCATCAGT | + | 6.26 | TFAP2C | MA0524.2 | chr2:20777681-20777693 | TGCCTCAGGGCA | + | 6.18 | Zfx | MA0146.2 | chr2:20780038-20780052 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
SE_00252 | chr2:20777587-20781075 | Adipose_Nuclei | SE_00875 | chr2:20777193-20780159 | Adrenal_Gland | SE_01560 | chr2:20777104-20780268 | Aorta | SE_03248 | chr2:20778851-20780021 | Brain_Angular_Gyrus | SE_03957 | chr2:20777502-20780166 | Brain_Anterior_Caudate | SE_05080 | chr2:20777321-20780424 | Brain_Cingulate_Gyrus | SE_05880 | chr2:20776875-20781185 | Brain_Hippocampus_Middle | SE_07306 | chr2:20778329-20780235 | Brain_Hippocampus_Middle_150 | SE_07924 | chr2:20777875-20781156 | Brain_Inferior_Temporal_Lobe | SE_26682 | chr2:20777960-20780158 | Esophagus | SE_27973 | chr2:20778080-20780172 | Fetal_Intestine | SE_29010 | chr2:20775624-20777732 | Fetal_Intestine_Large | SE_29010 | chr2:20778147-20780228 | Fetal_Intestine_Large | SE_30023 | chr2:20777612-20780174 | Fetal_Muscle | SE_31621 | chr2:20775912-20777626 | Gastric | SE_31621 | chr2:20777799-20780192 | Gastric | SE_33420 | chr2:20778091-20780181 | H2171 | SE_35251 | chr2:20776665-20781321 | HeLa | SE_37942 | chr2:20765354-20785913 | HUVEC | SE_40480 | chr2:20777911-20780167 | K562 | SE_40670 | chr2:20766731-20780277 | Left_Ventricle | SE_42169 | chr2:20775741-20780279 | Lung | SE_46601 | chr2:20777664-20780171 | Osteoblasts | SE_46720 | chr2:20778380-20778703 | Ovary | SE_46720 | chr2:20778705-20779635 | Ovary | SE_46720 | chr2:20779741-20780036 | Ovary | SE_47850 | chr2:20778895-20779597 | Pancreas | SE_48588 | chr2:20776905-20780113 | Right_Atrium | SE_50417 | chr2:20775896-20780176 | Sigmoid_Colon | SE_52547 | chr2:20777559-20780186 | Small_Intestine | SE_53551 | chr2:20777658-20780109 | Spleen | SE_54496 | chr2:20778077-20780207 | Stomach_Smooth_Muscle | SE_65409 | chr2:20777658-20779864 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I020566 | chr2 | 20766626 | 20781108 |
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Enhancer Sequence | AGGCCCAAGG TGAGGGGCAC CTCCCAGCAC CGCCATCTGG GAGCGTAAGA GTGCCTGTCT 60 GTGGCTGCAG CCTGGGAGGG AGAGAGGGTC CAGAGATGGA GGCAAGCAGA GGCCAGACCA 120 ACTCAGGCCG GGTGCATGAG CTGGAATTGC CAGGCCTCTG AACCTCAGGC TAGGTCGCAT 180 TCTTGGAGCA GCAGATTAAA GTATGAGGGG GTATTGTCTA AGCTACACTC CCCGGCACTG 240 GGGCTGGATG GGGATTGGGC TTCCAGGGTT CTGTTATACT GATCAGATCA ATGATTCATA 300 TGCTGATGTA TCAGAACCAC CTGCAAACAC ATTTCCAGGC CTGCCTCAGG GCACTCGTTC 360 CTCAAGCCTG TCCAGTGTGA CTTCAACCCC CTTCACAGCT GAGTAGGTTG TGGCCAGGGG 420 CCATGGATCT GCAAAGACTG AGTAACGTGC CTGATGTCTC ATCATGATCC AGCCGGCTGG 480 GGACCTCTGG CATGGAACAC TCCAAGCTGC ATCATGTCCC CTCAGGCAAC TTGCTGATCC 540 CTGGCAAGGG GTGCAGGAAG CAGGCTCACG TGGCTGTGCC CTTGAATCAG GGCTCGGGAG 600 AGTGGCACAG GGTGGGGGTG GGAACAGCCT CTCTTGACCA GTGCCTAGCG TCCTACCTGT 660 GGCTCCTAAG TGGCTCCAGG GCTGCCCTCA GAGGCGGGAT GGGATGCAGT CTTCATAGGA 720 GGGGACTTGG TCTCCATGGT TTTCAGGGCA GAGCCCCACA CCTATTACCT GGGCCCTGAG 780 GCTCTACCCT AGCATGTCTC TCTGGGCTGT CCTCTGAAAA GTTGCTCACC ATGGTAACCA 840 ACCAGAAGTA GAGCCCCAGC TGAGGGCAGT GATGACACCA TCTTTGGCCC TTGGACAACC 900 GGGGCAGTTC TTGCCCGGAG GCTCTCGCAG GCAGCCCCAC ACACCACCTA TATCCCGAGG 960 AAAGATGGGC ATTCCCAAGG AACATGTTCA GGCCAGACCC TCTGGGAGGT GAATAAGAAT 1020 AGATGCCCAG CCAAGAACCT CTTCAAAGCT CAAGAGGAAT GAAGAGAAGA GAGAGGACCA 1080 CCATTCACTG AGGGCTGGCC ATGGGTGAGG CACTGGGCGT AGGCAATCTC CTACATGCTC 1140 ATGACAGCCC TGGGAGCAGT ACTGCCACCT GCACTGGACA GGGGAGGAAA CTGAGGCTCA 1200 GAATGGGAAA GTAATTTGCT CAAGGCCAGA GTCCCTGGGT GTGTAGCTGT GACTCTGGAG 1260 CCATGCTCTG TATCAACCAG TGGGGTGTAC ATGAAACATC AACAGTAACA GCAATGTCCA 1320 GGTTCAAAAC ATTAAAAATA GCCTCAGTAC TACAAGGCTT TCTGTTTCTG AAACCTCTGT 1380 TGAAGGCAGC CAAGTGGAAA GTCAGGCGGT GTCCCCTCCC AAGCCTCACA GGCTGAGCCA 1440 GGTTTGGTGG CCACTGAAGC CCTTGACTTC CTTCCGGTCT CAGGTCAGTC CTCCCTGGGG 1500 CACTCCTAAT ATGCTCATCT GGAGGCTTCT GTTAAGTCCA GGAAACTCTA CAGGACACAG 1560 CTGAGGCTGG GCGGCCACCA GACACGTGCT GTGTCCAGAG AGAACAAAGC GGGGGTTTCC 1620 CTGGGTTCCA TGAGCACAGG AGCCTTTTCC TCCAGGCTGG CTCCATCCGA GCTGGCTGAG 1680 GGTTGGCGGC AGCTGCCCAG CATCTATAGG GTGCCTCCGG GAACTGTCTC AAGGCCAGAG 1740 CATCCAGCCT CCTGGCTGTT AGTGGGCCGT GAGCCTACCG GGACTTCGAG AGACAGGGCT 1800 TCCCCAGATC CAGCCTGATG AGATCATCTG CCATTTCAGG CTGGGCTGAA AGATCCTCCG 1860 GCACAACAAA GCTGGGCCCA GGAGATATCC TGCATGACTC ATCAGTTGGC CATGCATTGG 1920 AGACTTCCGG CCCTCAGAGA AACCAGACAC AGAGAGCCAT TGTTTGCCTT GGAAGCCCCC 1980 CGGCATACCA GGCTCAATGG GGTCATTTGT GTTTTCTCCC TAGTCCTCCA TAACCCATAC 2040 TCTTTCTGGG AGGTGGGGGC CCACTGAGCT GCCTGGGACC CTGTGACAAG AGGAAAACCA 2100 ATACCAAGTC ACCTACCCAC AAGTCCCACG GGAATACCCT CCCTCCAGGA CCAGGGCCTG 2160 GCTGGGAAGC AGAAAACCTG GGTTCTGAGC CATGGTTTAA GTCTCCAAGA CTCACTGATT 2220 CTTCTGTCTT CATTTTTCAA ATGGAGAAAA TCATTCAAAA AAGACAAAGC TATTGTGAGG 2280 ATGACCTAAC GTAAGGCACA TAAAGTTCCA GGCTCAGGCC TTGCACCTAC AAAGGTTCTG 2340 CATGTGATCT TTCCTTCCCA CTTCTCTCTT CCTCCTGCCT TTAAAATGTA AGTGAAAATG 2400 TTTTGTTTGT GGATCTGTTT CTATCCTAAT CTACATACCC TTATCTAGGG CAGAAACTCC 2460 CTGAACTCAT ACCCACAGTC TACCCACAAT TTGGCCCACA CCCAGGGACA CAGCCCCAAG 2520 GGGGCAAGGA CTGGAGCAGA GGGCACACAG CCTAGTGGCT AAGCTGGGCA GAGATGCAAG 2580 AATAAGCAAG GCAAGGCTGA GGGCCTGCCC CTGGGTTTCA AACAAGCTGG AGGCCTTTAG 2640 AAACTTCCAA GGGGGAAGCT GAGTGTGGTG GCTCATGCCT GTAATCCTAG CACTTTGGGA 2700 GGCCGAGGCG GGTGGATTGC CTCAGCTCAG AAGTTCGAGA CCAGCCTGGG CGACACAGTG 2760 AAACCTCGTC 2770
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