Tag | Content |
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EnhancerAtlas ID | HS049-04373 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr2:20777170-20780190 |
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 | TTTTACCCCA AGGGCCTTGT CCAGGGCTTC CTTTGAAACA AGTGCAGCGA TCTCCCAGAG 60 AGAAGTTCTA GACCATGCAA TCTTCCTGTC TCCCTGCATT TCCTGTGACA TGTTAGCGGC 120 TTGGAGGTGT CCCCCCAGCT CCACCAGGGG CATAGGAAGA AAGAGCCTCC AGGCCCAAGG 180 TGAGGGGCAC CTCCCAGCAC CGCCATCTGG GAGCGTAAGA GTGCCTGTCT GTGGCTGCAG 240 CCTGGGAGGG AGAGAGGGTC CAGAGATGGA GGCAAGCAGA GGCCAGACCA ACTCAGGCCG 300 GGTGCATGAG CTGGAATTGC CAGGCCTCTG AACCTCAGGC TAGGTCGCAT TCTTGGAGCA 360 GCAGATTAAA GTATGAGGGG GTATTGTCTA AGCTACACTC CCCGGCACTG GGGCTGGATG 420 GGGATTGGGC TTCCAGGGTT CTGTTATACT GATCAGATCA ATGATTCATA TGCTGATGTA 480 TCAGAACCAC CTGCAAACAC ATTTCCAGGC CTGCCTCAGG GCACTCGTTC CTCAAGCCTG 540 TCCAGTGTGA CTTCAACCCC CTTCACAGCT GAGTAGGTTG TGGCCAGGGG CCATGGATCT 600 GCAAAGACTG AGTAACGTGC CTGATGTCTC ATCATGATCC AGCCGGCTGG GGACCTCTGG 660 CATGGAACAC TCCAAGCTGC ATCATGTCCC CTCAGGCAAC TTGCTGATCC CTGGCAAGGG 720 GTGCAGGAAG CAGGCTCACG TGGCTGTGCC CTTGAATCAG GGCTCGGGAG AGTGGCACAG 780 GGTGGGGGTG GGAACAGCCT CTCTTGACCA GTGCCTAGCG TCCTACCTGT GGCTCCTAAG 840 TGGCTCCAGG GCTGCCCTCA GAGGCGGGAT GGGATGCAGT CTTCATAGGA GGGGACTTGG 900 TCTCCATGGT TTTCAGGGCA GAGCCCCACA CCTATTACCT GGGCCCTGAG GCTCTACCCT 960 AGCATGTCTC TCTGGGCTGT CCTCTGAAAA GTTGCTCACC ATGGTAACCA ACCAGAAGTA 1020 GAGCCCCAGC TGAGGGCAGT GATGACACCA TCTTTGGCCC TTGGACAACC GGGGCAGTTC 1080 TTGCCCGGAG GCTCTCGCAG GCAGCCCCAC ACACCACCTA TATCCCGAGG AAAGATGGGC 1140 ATTCCCAAGG AACATGTTCA GGCCAGACCC TCTGGGAGGT GAATAAGAAT AGATGCCCAG 1200 CCAAGAACCT CTTCAAAGCT CAAGAGGAAT GAAGAGAAGA GAGAGGACCA CCATTCACTG 1260 AGGGCTGGCC ATGGGTGAGG CACTGGGCGT AGGCAATCTC CTACATGCTC ATGACAGCCC 1320 TGGGAGCAGT ACTGCCACCT GCACTGGACA GGGGAGGAAA CTGAGGCTCA GAATGGGAAA 1380 GTAATTTGCT CAAGGCCAGA GTCCCTGGGT GTGTAGCTGT GACTCTGGAG CCATGCTCTG 1440 TATCAACCAG TGGGGTGTAC ATGAAACATC AACAGTAACA GCAATGTCCA GGTTCAAAAC 1500 ATTAAAAATA GCCTCAGTAC TACAAGGCTT TCTGTTTCTG AAACCTCTGT TGAAGGCAGC 1560 CAAGTGGAAA GTCAGGCGGT GTCCCCTCCC AAGCCTCACA GGCTGAGCCA GGTTTGGTGG 1620 CCACTGAAGC CCTTGACTTC CTTCCGGTCT CAGGTCAGTC CTCCCTGGGG CACTCCTAAT 1680 ATGCTCATCT GGAGGCTTCT GTTAAGTCCA GGAAACTCTA CAGGACACAG CTGAGGCTGG 1740 GCGGCCACCA GACACGTGCT GTGTCCAGAG AGAACAAAGC GGGGGTTTCC CTGGGTTCCA 1800 TGAGCACAGG AGCCTTTTCC TCCAGGCTGG CTCCATCCGA GCTGGCTGAG GGTTGGCGGC 1860 AGCTGCCCAG CATCTATAGG GTGCCTCCGG GAACTGTCTC AAGGCCAGAG CATCCAGCCT 1920 CCTGGCTGTT AGTGGGCCGT GAGCCTACCG GGACTTCGAG AGACAGGGCT TCCCCAGATC 1980 CAGCCTGATG AGATCATCTG CCATTTCAGG CTGGGCTGAA AGATCCTCCG GCACAACAAA 2040 GCTGGGCCCA GGAGATATCC TGCATGACTC ATCAGTTGGC CATGCATTGG AGACTTCCGG 2100 CCCTCAGAGA AACCAGACAC AGAGAGCCAT TGTTTGCCTT GGAAGCCCCC CGGCATACCA 2160 GGCTCAATGG GGTCATTTGT GTTTTCTCCC TAGTCCTCCA TAACCCATAC TCTTTCTGGG 2220 AGGTGGGGGC CCACTGAGCT GCCTGGGACC CTGTGACAAG AGGAAAACCA ATACCAAGTC 2280 ACCTACCCAC AAGTCCCACG GGAATACCCT CCCTCCAGGA CCAGGGCCTG GCTGGGAAGC 2340 AGAAAACCTG GGTTCTGAGC CATGGTTTAA GTCTCCAAGA CTCACTGATT CTTCTGTCTT 2400 CATTTTTCAA ATGGAGAAAA TCATTCAAAA AAGACAAAGC TATTGTGAGG ATGACCTAAC 2460 GTAAGGCACA TAAAGTTCCA GGCTCAGGCC TTGCACCTAC AAAGGTTCTG CATGTGATCT 2520 TTCCTTCCCA CTTCTCTCTT CCTCCTGCCT TTAAAATGTA AGTGAAAATG TTTTGTTTGT 2580 GGATCTGTTT CTATCCTAAT CTACATACCC TTATCTAGGG CAGAAACTCC CTGAACTCAT 2640 ACCCACAGTC TACCCACAAT TTGGCCCACA CCCAGGGACA CAGCCCCAAG GGGGCAAGGA 2700 CTGGAGCAGA GGGCACACAG CCTAGTGGCT AAGCTGGGCA GAGATGCAAG AATAAGCAAG 2760 GCAAGGCTGA GGGCCTGCCC CTGGGTTTCA AACAAGCTGG AGGCCTTTAG AAACTTCCAA 2820 GGGGGAAGCT GAGTGTGGTG GCTCATGCCT GTAATCCTAG CACTTTGGGA GGCCGAGGCG 2880 GGTGGATTGC CTCAGCTCAG AAGTTCGAGA CCAGCCTGGG CGACACAGTG AAACCTCGTC 2940 TCTACTAAAA TACAAAAAAT TAGCCAGGCG TATCAGTGTG CACCTGTAAT CCCAGCTATT 3000 CAGGAGGTTG AGGCAGGAGA 3020
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