Tag | Content |
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EnhancerAtlas ID | HS105-42047 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:20777240-20780090 |
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: 34 | 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 | chr2:20775677-20777611 | Fetal_Intestine | 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 | GACCATGCAA TCTTCCTGTC TCCCTGCATT TCCTGTGACA TGTTAGCGGC TTGGAGGTGT 60 CCCCCCAGCT CCACCAGGGG CATAGGAAGA AAGAGCCTCC AGGCCCAAGG TGAGGGGCAC 120 CTCCCAGCAC CGCCATCTGG GAGCGTAAGA GTGCCTGTCT GTGGCTGCAG CCTGGGAGGG 180 AGAGAGGGTC CAGAGATGGA GGCAAGCAGA GGCCAGACCA ACTCAGGCCG GGTGCATGAG 240 CTGGAATTGC CAGGCCTCTG AACCTCAGGC TAGGTCGCAT TCTTGGAGCA GCAGATTAAA 300 GTATGAGGGG GTATTGTCTA AGCTACACTC CCCGGCACTG GGGCTGGATG GGGATTGGGC 360 TTCCAGGGTT CTGTTATACT GATCAGATCA ATGATTCATA TGCTGATGTA TCAGAACCAC 420 CTGCAAACAC ATTTCCAGGC CTGCCTCAGG GCACTCGTTC CTCAAGCCTG TCCAGTGTGA 480 CTTCAACCCC CTTCACAGCT GAGTAGGTTG TGGCCAGGGG CCATGGATCT GCAAAGACTG 540 AGTAACGTGC CTGATGTCTC ATCATGATCC AGCCGGCTGG GGACCTCTGG CATGGAACAC 600 TCCAAGCTGC ATCATGTCCC CTCAGGCAAC TTGCTGATCC CTGGCAAGGG GTGCAGGAAG 660 CAGGCTCACG TGGCTGTGCC CTTGAATCAG GGCTCGGGAG AGTGGCACAG GGTGGGGGTG 720 GGAACAGCCT CTCTTGACCA GTGCCTAGCG TCCTACCTGT GGCTCCTAAG TGGCTCCAGG 780 GCTGCCCTCA GAGGCGGGAT GGGATGCAGT CTTCATAGGA GGGGACTTGG TCTCCATGGT 840 TTTCAGGGCA GAGCCCCACA CCTATTACCT GGGCCCTGAG GCTCTACCCT AGCATGTCTC 900 TCTGGGCTGT CCTCTGAAAA GTTGCTCACC ATGGTAACCA ACCAGAAGTA GAGCCCCAGC 960 TGAGGGCAGT GATGACACCA TCTTTGGCCC TTGGACAACC GGGGCAGTTC TTGCCCGGAG 1020 GCTCTCGCAG GCAGCCCCAC ACACCACCTA TATCCCGAGG AAAGATGGGC ATTCCCAAGG 1080 AACATGTTCA GGCCAGACCC TCTGGGAGGT GAATAAGAAT AGATGCCCAG CCAAGAACCT 1140 CTTCAAAGCT CAAGAGGAAT GAAGAGAAGA GAGAGGACCA CCATTCACTG AGGGCTGGCC 1200 ATGGGTGAGG CACTGGGCGT AGGCAATCTC CTACATGCTC ATGACAGCCC TGGGAGCAGT 1260 ACTGCCACCT GCACTGGACA GGGGAGGAAA CTGAGGCTCA GAATGGGAAA GTAATTTGCT 1320 CAAGGCCAGA GTCCCTGGGT GTGTAGCTGT GACTCTGGAG CCATGCTCTG TATCAACCAG 1380 TGGGGTGTAC ATGAAACATC AACAGTAACA GCAATGTCCA GGTTCAAAAC ATTAAAAATA 1440 GCCTCAGTAC TACAAGGCTT TCTGTTTCTG AAACCTCTGT TGAAGGCAGC CAAGTGGAAA 1500 GTCAGGCGGT GTCCCCTCCC AAGCCTCACA GGCTGAGCCA GGTTTGGTGG CCACTGAAGC 1560 CCTTGACTTC CTTCCGGTCT CAGGTCAGTC CTCCCTGGGG CACTCCTAAT ATGCTCATCT 1620 GGAGGCTTCT GTTAAGTCCA GGAAACTCTA CAGGACACAG CTGAGGCTGG GCGGCCACCA 1680 GACACGTGCT GTGTCCAGAG AGAACAAAGC GGGGGTTTCC CTGGGTTCCA TGAGCACAGG 1740 AGCCTTTTCC TCCAGGCTGG CTCCATCCGA GCTGGCTGAG GGTTGGCGGC AGCTGCCCAG 1800 CATCTATAGG GTGCCTCCGG GAACTGTCTC AAGGCCAGAG CATCCAGCCT CCTGGCTGTT 1860 AGTGGGCCGT GAGCCTACCG GGACTTCGAG AGACAGGGCT TCCCCAGATC CAGCCTGATG 1920 AGATCATCTG CCATTTCAGG CTGGGCTGAA AGATCCTCCG GCACAACAAA GCTGGGCCCA 1980 GGAGATATCC TGCATGACTC ATCAGTTGGC CATGCATTGG AGACTTCCGG CCCTCAGAGA 2040 AACCAGACAC AGAGAGCCAT TGTTTGCCTT GGAAGCCCCC CGGCATACCA GGCTCAATGG 2100 GGTCATTTGT GTTTTCTCCC TAGTCCTCCA TAACCCATAC TCTTTCTGGG AGGTGGGGGC 2160 CCACTGAGCT GCCTGGGACC CTGTGACAAG AGGAAAACCA ATACCAAGTC ACCTACCCAC 2220 AAGTCCCACG GGAATACCCT CCCTCCAGGA CCAGGGCCTG GCTGGGAAGC AGAAAACCTG 2280 GGTTCTGAGC CATGGTTTAA GTCTCCAAGA CTCACTGATT CTTCTGTCTT CATTTTTCAA 2340 ATGGAGAAAA TCATTCAAAA AAGACAAAGC TATTGTGAGG ATGACCTAAC GTAAGGCACA 2400 TAAAGTTCCA GGCTCAGGCC TTGCACCTAC AAAGGTTCTG CATGTGATCT TTCCTTCCCA 2460 CTTCTCTCTT CCTCCTGCCT TTAAAATGTA AGTGAAAATG TTTTGTTTGT GGATCTGTTT 2520 CTATCCTAAT CTACATACCC TTATCTAGGG CAGAAACTCC CTGAACTCAT ACCCACAGTC 2580 TACCCACAAT TTGGCCCACA CCCAGGGACA CAGCCCCAAG GGGGCAAGGA CTGGAGCAGA 2640 GGGCACACAG CCTAGTGGCT AAGCTGGGCA GAGATGCAAG AATAAGCAAG GCAAGGCTGA 2700 GGGCCTGCCC CTGGGTTTCA AACAAGCTGG AGGCCTTTAG AAACTTCCAA GGGGGAAGCT 2760 GAGTGTGGTG GCTCATGCCT GTAATCCTAG CACTTTGGGA GGCCGAGGCG GGTGGATTGC 2820 CTCAGCTCAG AAGTTCGAGA CCAGCCTGGG 2850
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