Tag | Content |
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EnhancerAtlas ID | HS108-21655 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr2:20777190-20780170 |
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 | chr2:20775677-20777611 | 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_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 | CCAGGGCTTC CTTTGAAACA AGTGCAGCGA TCTCCCAGAG AGAAGTTCTA GACCATGCAA 60 TCTTCCTGTC TCCCTGCATT TCCTGTGACA TGTTAGCGGC TTGGAGGTGT CCCCCCAGCT 120 CCACCAGGGG CATAGGAAGA AAGAGCCTCC AGGCCCAAGG TGAGGGGCAC CTCCCAGCAC 180 CGCCATCTGG GAGCGTAAGA GTGCCTGTCT GTGGCTGCAG CCTGGGAGGG AGAGAGGGTC 240 CAGAGATGGA GGCAAGCAGA GGCCAGACCA ACTCAGGCCG GGTGCATGAG CTGGAATTGC 300 CAGGCCTCTG AACCTCAGGC TAGGTCGCAT TCTTGGAGCA GCAGATTAAA GTATGAGGGG 360 GTATTGTCTA AGCTACACTC CCCGGCACTG GGGCTGGATG GGGATTGGGC TTCCAGGGTT 420 CTGTTATACT GATCAGATCA ATGATTCATA TGCTGATGTA TCAGAACCAC CTGCAAACAC 480 ATTTCCAGGC CTGCCTCAGG GCACTCGTTC CTCAAGCCTG TCCAGTGTGA CTTCAACCCC 540 CTTCACAGCT GAGTAGGTTG TGGCCAGGGG CCATGGATCT GCAAAGACTG AGTAACGTGC 600 CTGATGTCTC ATCATGATCC AGCCGGCTGG GGACCTCTGG CATGGAACAC TCCAAGCTGC 660 ATCATGTCCC CTCAGGCAAC TTGCTGATCC CTGGCAAGGG GTGCAGGAAG CAGGCTCACG 720 TGGCTGTGCC CTTGAATCAG GGCTCGGGAG AGTGGCACAG GGTGGGGGTG GGAACAGCCT 780 CTCTTGACCA GTGCCTAGCG TCCTACCTGT GGCTCCTAAG TGGCTCCAGG GCTGCCCTCA 840 GAGGCGGGAT GGGATGCAGT CTTCATAGGA GGGGACTTGG TCTCCATGGT TTTCAGGGCA 900 GAGCCCCACA CCTATTACCT GGGCCCTGAG GCTCTACCCT AGCATGTCTC TCTGGGCTGT 960 CCTCTGAAAA GTTGCTCACC ATGGTAACCA ACCAGAAGTA GAGCCCCAGC TGAGGGCAGT 1020 GATGACACCA TCTTTGGCCC TTGGACAACC GGGGCAGTTC TTGCCCGGAG GCTCTCGCAG 1080 GCAGCCCCAC ACACCACCTA TATCCCGAGG AAAGATGGGC ATTCCCAAGG AACATGTTCA 1140 GGCCAGACCC TCTGGGAGGT GAATAAGAAT AGATGCCCAG CCAAGAACCT CTTCAAAGCT 1200 CAAGAGGAAT GAAGAGAAGA GAGAGGACCA CCATTCACTG AGGGCTGGCC ATGGGTGAGG 1260 CACTGGGCGT AGGCAATCTC CTACATGCTC ATGACAGCCC TGGGAGCAGT ACTGCCACCT 1320 GCACTGGACA GGGGAGGAAA CTGAGGCTCA GAATGGGAAA GTAATTTGCT CAAGGCCAGA 1380 GTCCCTGGGT GTGTAGCTGT GACTCTGGAG CCATGCTCTG TATCAACCAG TGGGGTGTAC 1440 ATGAAACATC AACAGTAACA GCAATGTCCA GGTTCAAAAC ATTAAAAATA GCCTCAGTAC 1500 TACAAGGCTT TCTGTTTCTG AAACCTCTGT TGAAGGCAGC CAAGTGGAAA GTCAGGCGGT 1560 GTCCCCTCCC AAGCCTCACA GGCTGAGCCA GGTTTGGTGG CCACTGAAGC CCTTGACTTC 1620 CTTCCGGTCT CAGGTCAGTC CTCCCTGGGG CACTCCTAAT ATGCTCATCT GGAGGCTTCT 1680 GTTAAGTCCA GGAAACTCTA CAGGACACAG CTGAGGCTGG GCGGCCACCA GACACGTGCT 1740 GTGTCCAGAG AGAACAAAGC GGGGGTTTCC CTGGGTTCCA TGAGCACAGG AGCCTTTTCC 1800 TCCAGGCTGG CTCCATCCGA GCTGGCTGAG GGTTGGCGGC AGCTGCCCAG CATCTATAGG 1860 GTGCCTCCGG GAACTGTCTC AAGGCCAGAG CATCCAGCCT CCTGGCTGTT AGTGGGCCGT 1920 GAGCCTACCG GGACTTCGAG AGACAGGGCT TCCCCAGATC CAGCCTGATG AGATCATCTG 1980 CCATTTCAGG CTGGGCTGAA AGATCCTCCG GCACAACAAA GCTGGGCCCA GGAGATATCC 2040 TGCATGACTC ATCAGTTGGC CATGCATTGG AGACTTCCGG CCCTCAGAGA AACCAGACAC 2100 AGAGAGCCAT TGTTTGCCTT GGAAGCCCCC CGGCATACCA GGCTCAATGG GGTCATTTGT 2160 GTTTTCTCCC TAGTCCTCCA TAACCCATAC TCTTTCTGGG AGGTGGGGGC CCACTGAGCT 2220 GCCTGGGACC CTGTGACAAG AGGAAAACCA ATACCAAGTC ACCTACCCAC AAGTCCCACG 2280 GGAATACCCT CCCTCCAGGA CCAGGGCCTG GCTGGGAAGC AGAAAACCTG GGTTCTGAGC 2340 CATGGTTTAA GTCTCCAAGA CTCACTGATT CTTCTGTCTT CATTTTTCAA ATGGAGAAAA 2400 TCATTCAAAA AAGACAAAGC TATTGTGAGG ATGACCTAAC GTAAGGCACA TAAAGTTCCA 2460 GGCTCAGGCC TTGCACCTAC AAAGGTTCTG CATGTGATCT TTCCTTCCCA CTTCTCTCTT 2520 CCTCCTGCCT TTAAAATGTA AGTGAAAATG TTTTGTTTGT GGATCTGTTT CTATCCTAAT 2580 CTACATACCC TTATCTAGGG CAGAAACTCC CTGAACTCAT ACCCACAGTC TACCCACAAT 2640 TTGGCCCACA CCCAGGGACA CAGCCCCAAG GGGGCAAGGA CTGGAGCAGA GGGCACACAG 2700 CCTAGTGGCT AAGCTGGGCA GAGATGCAAG AATAAGCAAG GCAAGGCTGA GGGCCTGCCC 2760 CTGGGTTTCA AACAAGCTGG AGGCCTTTAG AAACTTCCAA GGGGGAAGCT GAGTGTGGTG 2820 GCTCATGCCT GTAATCCTAG CACTTTGGGA GGCCGAGGCG GGTGGATTGC CTCAGCTCAG 2880 AAGTTCGAGA CCAGCCTGGG CGACACAGTG AAACCTCGTC TCTACTAAAA TACAAAAAAT 2940 TAGCCAGGCG TATCAGTGTG CACCTGTAAT CCCAGCTATT 2980
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