Tag | Content |
---|
EnhancerAtlas ID | HS082-00805 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr1:44047100-44048880 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TP53 | MA0106.3 | chr1:44048046-44048064 | AGCAGGCCCAGGCATGCT | - | 6.03 |
|
| 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 |
|
| 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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I043581 | chr1 | 44046992 | 44049104 |
|
Enhancer Sequence | TCATGTAGAC CCTAATTGAA TCTACACCAC CCTGCTTTGC CAAGAGCAAC CTGCCCCATA 60 GGCCCTACTG TCCTACTGAC AGGACTTAGG CACACCTGAA AGGCCCTGCT CCCTGGGTGC 120 CTTGCCTCTG GTGCCCCCAC TGCTCGTCAT CTCATGGTTG GCAAAACCCC TGCCTTCTGC 180 CCTCAGCAGT ACTAGGGGCC CTTCAGCCCC AGCGCCTGGG GACAGCCTGT ACTGGGCTGA 240 CCACCAGCTC TGCATCCTGA GCCCTGCTTG TGGGTGGATG GCCGTGGAGG AGTCCCCAGT 300 GCCAGCCTGC TTTCTGGCCT GCACCCCGTC CCATCTCCCA GCAGAGAGGC TTCGAGGTTT 360 CCTCCCACAG CAGGCTCCTG AGCCTCAGAC GGCTTGATGT GGGCTCTAGC CCTGAACTTC 420 TCAGCCGCAG CACTGTTGAC ATTTTGGGCT GGACGATTCT TAGTTGTGAG GGGCCATCCT 480 GTGCATTGGA GGGTGTTTAG CAGCATCTCT AGCTCACTAG ATGCCAGTGG CACCCCTCAG 540 TCAAAACAAA CGTTGCAACG TGTCACCTGG GGGAAATTAC TGATGGCTTC CCACTGCCAT 600 TGTCTCCACC CATCTGACTC TCTTCACCTG TGTCCACTGG CCGCAAGGCT TCGTCTCCTC 660 ATCAGACTTG GCTTCGGTGT CTACCTCACA TCTCCCTTCT GTCCCCCAAA TTCTCAGGGC 720 TCCCAGTGTC GCTCTCTGAG GCCACGCGAC TGCTACATTT AATGGGACAG TACACGTGAA 780 GCACCAGGCA CATTGCCAGG CACACAGGAA GCACTTGCTA GTCAGTAGCC TCTGCAGCTA 840 GCACTCGGCT ACTAGTCAGT AGCCTCTCGG ATAGCACTGT GGGGGGATGT GTCATCCAGT 900 TACATCTGAC TTTGTTCACA GTTGCCTGCA GCTCCACCCA CAGTCTAGCA GGCCCAGGCA 960 TGCTGGGTGG GCCAGAGCCT TTCTCCTTCA CCACCTGACT CTCCCTGAGT GACTCATTCT 1020 CTCCTTCCAT CTACAGCTCT CTGGGTGTAC AGCTGCTGGG GCCAGGGTGG AGCCCTGCCC 1080 TCCTCAGAGC CTGGCCTACC TGTGCCAGGA CTACCAGCCT TCCCCCTTTC TCTAGGGACC 1140 TGGCTGCGGG CCACAGCTGT CTAAAACAGG GACAGTGCCT TTTTCCCCAC AGGTGCCCAG 1200 ACATGCTCCT TACACCGGTG GTGTGTGTGG GGGTGGCTTC TAGTGGCTCC TGTACCTTGG 1260 CAGGTTTGTG GGCTGGGTGG GCCTTGACCC CAGAGCCCGG TCCACAGGGT CTGTCTGAGC 1320 TGTGGGGTGC GTGTGAGGCA TGGGGGCCTG CCTGTGCCCC ATTTTCACCT GCCCCGGCCC 1380 CACCCTCGGC CTCCCTGGCG CCTGCTGGCG GGCCTCAGCC CTGTCCACCA TGTCCTCCAT 1440 GAGTCCTGAG TCTTTTGTGA GTGATGTGGT TCGTGTGCAC CTGTGTGCAT GTGTGTGTGC 1500 GAGGGGGCAC AGGAGTCTCG TCTCGTCTCC GTGCTGTGTG GGCAGATGAA GGTTGGCCTG 1560 TTTTTACTCT CTCTGTGTTT CTCCTTGTCT TTTTTTTATT CCCTCCTCAT CTTCATCGCA 1620 CTCTGCCATC AACCCAAACT CTCATCTCTC AGATCAGCGA GAAGGTTGGT CCTTTTCACT 1680 TCTTATCCAT CTACAGTTCG CCCATCGATG GGACACGCCT GTCAGTAGGG CCCAGCGGGC 1740 TCGGTCAGCT CCCTCAGGCT CACTGCGCCG TGCCTGCCTG 1780
|