Tag | Content |
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EnhancerAtlas ID | HS091-01501 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:44046800-44049180 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TP53 | MA0106.3 | chr1:44048046-44048064 | AGCAGGCCCAGGCATGCT | - | 6.03 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_05962 | chr1:44045982-44048063 | Brain_Hippocampus_Middle | SE_23829 | chr1:44046994-44048030 | Colon_Crypt_2 | SE_23829 | chr1:44048164-44048638 | Colon_Crypt_2 | SE_26649 | chr1:44045820-44048922 | Esophagus | SE_27645 | chr1:44047195-44049958 | Fetal_Intestine | SE_28595 | chr1:44047280-44048969 | Fetal_Intestine_Large | SE_33537 | chr1:44045757-44056755 | H2171 | SE_52524 | chr1:44047044-44048792 | Small_Intestine | SE_65452 | chr1:44047303-44047936 | Pancreatic_islets | SE_65452 | chr1:44048025-44048999 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 44047816 | 44048271 | chr1 | 44047550 | 44048400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I043581 | chr1 | 44046992 | 44049104 |
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Enhancer Sequence | GAGCATCCCT GTCTGTGGGG CTCCCTGTTT ACACATGGTA GACTCAGGCA GGGCCCTGAC 60 TGGCTCTTGC CATGGCCCAA CCCCTAACTC TACCAGCTCT TCTTGAATCT ACCCTTCTGG 120 CTCCATCCCC ACATGCCTTT TGGTAGGAAA TACGGGGGTT CCTTTAGTTC CAGCCCCACT 180 TGCCAGGGAC TCCAAAACAG CCAAACCTGA CTTCTGTTGT CTCTCTCACA CACACATACG 240 ACGTTCCTCT AGGCCCTGAT GTCTCAGGAC CGTTTCTAAG CTCTGTCCCC AGGACCTGCC 300 TCATGTAGAC CCTAATTGAA TCTACACCAC CCTGCTTTGC CAAGAGCAAC CTGCCCCATA 360 GGCCCTACTG TCCTACTGAC AGGACTTAGG CACACCTGAA AGGCCCTGCT CCCTGGGTGC 420 CTTGCCTCTG GTGCCCCCAC TGCTCGTCAT CTCATGGTTG GCAAAACCCC TGCCTTCTGC 480 CCTCAGCAGT ACTAGGGGCC CTTCAGCCCC AGCGCCTGGG GACAGCCTGT ACTGGGCTGA 540 CCACCAGCTC TGCATCCTGA GCCCTGCTTG TGGGTGGATG GCCGTGGAGG AGTCCCCAGT 600 GCCAGCCTGC TTTCTGGCCT GCACCCCGTC CCATCTCCCA GCAGAGAGGC TTCGAGGTTT 660 CCTCCCACAG CAGGCTCCTG AGCCTCAGAC GGCTTGATGT GGGCTCTAGC CCTGAACTTC 720 TCAGCCGCAG CACTGTTGAC ATTTTGGGCT GGACGATTCT TAGTTGTGAG GGGCCATCCT 780 GTGCATTGGA GGGTGTTTAG CAGCATCTCT AGCTCACTAG ATGCCAGTGG CACCCCTCAG 840 TCAAAACAAA CGTTGCAACG TGTCACCTGG GGGAAATTAC TGATGGCTTC CCACTGCCAT 900 TGTCTCCACC CATCTGACTC TCTTCACCTG TGTCCACTGG CCGCAAGGCT TCGTCTCCTC 960 ATCAGACTTG GCTTCGGTGT CTACCTCACA TCTCCCTTCT GTCCCCCAAA TTCTCAGGGC 1020 TCCCAGTGTC GCTCTCTGAG GCCACGCGAC TGCTACATTT AATGGGACAG TACACGTGAA 1080 GCACCAGGCA CATTGCCAGG CACACAGGAA GCACTTGCTA GTCAGTAGCC TCTGCAGCTA 1140 GCACTCGGCT ACTAGTCAGT AGCCTCTCGG ATAGCACTGT GGGGGGATGT GTCATCCAGT 1200 TACATCTGAC TTTGTTCACA GTTGCCTGCA GCTCCACCCA CAGTCTAGCA GGCCCAGGCA 1260 TGCTGGGTGG GCCAGAGCCT TTCTCCTTCA CCACCTGACT CTCCCTGAGT GACTCATTCT 1320 CTCCTTCCAT CTACAGCTCT CTGGGTGTAC AGCTGCTGGG GCCAGGGTGG AGCCCTGCCC 1380 TCCTCAGAGC CTGGCCTACC TGTGCCAGGA CTACCAGCCT TCCCCCTTTC TCTAGGGACC 1440 TGGCTGCGGG CCACAGCTGT CTAAAACAGG GACAGTGCCT TTTTCCCCAC AGGTGCCCAG 1500 ACATGCTCCT TACACCGGTG GTGTGTGTGG GGGTGGCTTC TAGTGGCTCC TGTACCTTGG 1560 CAGGTTTGTG GGCTGGGTGG GCCTTGACCC CAGAGCCCGG TCCACAGGGT CTGTCTGAGC 1620 TGTGGGGTGC GTGTGAGGCA TGGGGGCCTG CCTGTGCCCC ATTTTCACCT GCCCCGGCCC 1680 CACCCTCGGC CTCCCTGGCG CCTGCTGGCG GGCCTCAGCC CTGTCCACCA TGTCCTCCAT 1740 GAGTCCTGAG TCTTTTGTGA GTGATGTGGT TCGTGTGCAC CTGTGTGCAT GTGTGTGTGC 1800 GAGGGGGCAC AGGAGTCTCG TCTCGTCTCC GTGCTGTGTG GGCAGATGAA GGTTGGCCTG 1860 TTTTTACTCT CTCTGTGTTT CTCCTTGTCT TTTTTTTATT CCCTCCTCAT CTTCATCGCA 1920 CTCTGCCATC AACCCAAACT CTCATCTCTC AGATCAGCGA GAAGGTTGGT CCTTTTCACT 1980 TCTTATCCAT CTACAGTTCG CCCATCGATG GGACACGCCT GTCAGTAGGG CCCAGCGGGC 2040 TCGGTCAGCT CCCTCAGGCT CACTGCGCCG TGCCTGCCTG CCAGTCTCTG TTGTTTGGGC 2100 CGGCGGGCAG GCAGGACCAG GGATGGGTGG GCAGACCCCT GACCTGCATG TTCCTGCTGC 2160 TTGGGTCCCT GGTGCACCAC GTGTCTGCAT GTCCCCTTAG CCTGGTTCCC CTGCAAGGGT 2220 GGTGGGGTGG GCATGCTGCA TGGCATGAAA CTGTACCCCA CCTTTGCACC CAGGCCGGGC 2280 CAGCTGTCTG ATCCAGGCGG TGCTCAGGAA TGGTTGTGGG GGGCTGTGGT CAGAGAGAGG 2340 TGTAAGACCT GTAGCGCTTT GTGTGCACCT GTGGGACCTT 2380
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