Tag | Content |
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EnhancerAtlas ID | HS077-00442 |
Organism | Homo sapiens |
Tissue/cell | H128 |
Coordinate | chr1:44047350-44048700 |
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 | TGCATCCTGA GCCCTGCTTG TGGGTGGATG GCCGTGGAGG AGTCCCCAGT GCCAGCCTGC 60 TTTCTGGCCT GCACCCCGTC CCATCTCCCA GCAGAGAGGC TTCGAGGTTT CCTCCCACAG 120 CAGGCTCCTG AGCCTCAGAC GGCTTGATGT GGGCTCTAGC CCTGAACTTC TCAGCCGCAG 180 CACTGTTGAC ATTTTGGGCT GGACGATTCT TAGTTGTGAG GGGCCATCCT GTGCATTGGA 240 GGGTGTTTAG CAGCATCTCT AGCTCACTAG ATGCCAGTGG CACCCCTCAG TCAAAACAAA 300 CGTTGCAACG TGTCACCTGG GGGAAATTAC TGATGGCTTC CCACTGCCAT TGTCTCCACC 360 CATCTGACTC TCTTCACCTG TGTCCACTGG CCGCAAGGCT TCGTCTCCTC ATCAGACTTG 420 GCTTCGGTGT CTACCTCACA TCTCCCTTCT GTCCCCCAAA TTCTCAGGGC TCCCAGTGTC 480 GCTCTCTGAG GCCACGCGAC TGCTACATTT AATGGGACAG TACACGTGAA GCACCAGGCA 540 CATTGCCAGG CACACAGGAA GCACTTGCTA GTCAGTAGCC TCTGCAGCTA GCACTCGGCT 600 ACTAGTCAGT AGCCTCTCGG ATAGCACTGT GGGGGGATGT GTCATCCAGT TACATCTGAC 660 TTTGTTCACA GTTGCCTGCA GCTCCACCCA CAGTCTAGCA GGCCCAGGCA TGCTGGGTGG 720 GCCAGAGCCT TTCTCCTTCA CCACCTGACT CTCCCTGAGT GACTCATTCT CTCCTTCCAT 780 CTACAGCTCT CTGGGTGTAC AGCTGCTGGG GCCAGGGTGG AGCCCTGCCC TCCTCAGAGC 840 CTGGCCTACC TGTGCCAGGA CTACCAGCCT TCCCCCTTTC TCTAGGGACC TGGCTGCGGG 900 CCACAGCTGT CTAAAACAGG GACAGTGCCT TTTTCCCCAC AGGTGCCCAG ACATGCTCCT 960 TACACCGGTG GTGTGTGTGG GGGTGGCTTC TAGTGGCTCC TGTACCTTGG CAGGTTTGTG 1020 GGCTGGGTGG GCCTTGACCC CAGAGCCCGG TCCACAGGGT CTGTCTGAGC TGTGGGGTGC 1080 GTGTGAGGCA TGGGGGCCTG CCTGTGCCCC ATTTTCACCT GCCCCGGCCC CACCCTCGGC 1140 CTCCCTGGCG CCTGCTGGCG GGCCTCAGCC CTGTCCACCA TGTCCTCCAT GAGTCCTGAG 1200 TCTTTTGTGA GTGATGTGGT TCGTGTGCAC CTGTGTGCAT GTGTGTGTGC GAGGGGGCAC 1260 AGGAGTCTCG TCTCGTCTCC GTGCTGTGTG GGCAGATGAA GGTTGGCCTG TTTTTACTCT 1320 CTCTGTGTTT CTCCTTGTCT TTTTTTTATT 1350
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