Tag | Content |
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EnhancerAtlas ID | HS061-00853 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr1:44047670-44048690 |
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: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I043581 | chr1 | 44046992 | 44049104 |
|
Enhancer Sequence | GGGAAATTAC TGATGGCTTC CCACTGCCAT TGTCTCCACC CATCTGACTC TCTTCACCTG 60 TGTCCACTGG CCGCAAGGCT TCGTCTCCTC ATCAGACTTG GCTTCGGTGT CTACCTCACA 120 TCTCCCTTCT GTCCCCCAAA TTCTCAGGGC TCCCAGTGTC GCTCTCTGAG GCCACGCGAC 180 TGCTACATTT AATGGGACAG TACACGTGAA GCACCAGGCA CATTGCCAGG CACACAGGAA 240 GCACTTGCTA GTCAGTAGCC TCTGCAGCTA GCACTCGGCT ACTAGTCAGT AGCCTCTCGG 300 ATAGCACTGT GGGGGGATGT GTCATCCAGT TACATCTGAC TTTGTTCACA GTTGCCTGCA 360 GCTCCACCCA CAGTCTAGCA GGCCCAGGCA TGCTGGGTGG GCCAGAGCCT TTCTCCTTCA 420 CCACCTGACT CTCCCTGAGT GACTCATTCT CTCCTTCCAT CTACAGCTCT CTGGGTGTAC 480 AGCTGCTGGG GCCAGGGTGG AGCCCTGCCC TCCTCAGAGC CTGGCCTACC TGTGCCAGGA 540 CTACCAGCCT TCCCCCTTTC TCTAGGGACC TGGCTGCGGG CCACAGCTGT CTAAAACAGG 600 GACAGTGCCT TTTTCCCCAC AGGTGCCCAG ACATGCTCCT TACACCGGTG GTGTGTGTGG 660 GGGTGGCTTC TAGTGGCTCC TGTACCTTGG CAGGTTTGTG GGCTGGGTGG GCCTTGACCC 720 CAGAGCCCGG TCCACAGGGT CTGTCTGAGC TGTGGGGTGC GTGTGAGGCA TGGGGGCCTG 780 CCTGTGCCCC ATTTTCACCT GCCCCGGCCC CACCCTCGGC CTCCCTGGCG CCTGCTGGCG 840 GGCCTCAGCC CTGTCCACCA TGTCCTCCAT GAGTCCTGAG TCTTTTGTGA GTGATGTGGT 900 TCGTGTGCAC CTGTGTGCAT GTGTGTGTGC GAGGGGGCAC AGGAGTCTCG TCTCGTCTCC 960 GTGCTGTGTG GGCAGATGAA GGTTGGCCTG TTTTTACTCT CTCTGTGTTT CTCCTTGTCT 1020
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