| Tag | Content |
|---|
EnhancerAtlas ID | HS099-00753 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr1:44047650-44048590 |
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: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I043581 | chr1 | 44046992 | 44049104 |
|
Enhancer Sequence | CGTTGCAACG TGTCACCTGG GGGAAATTAC TGATGGCTTC CCACTGCCAT TGTCTCCACC 60
CATCTGACTC TCTTCACCTG TGTCCACTGG CCGCAAGGCT TCGTCTCCTC ATCAGACTTG 120
GCTTCGGTGT CTACCTCACA TCTCCCTTCT GTCCCCCAAA TTCTCAGGGC TCCCAGTGTC 180
GCTCTCTGAG GCCACGCGAC TGCTACATTT AATGGGACAG TACACGTGAA GCACCAGGCA 240
CATTGCCAGG CACACAGGAA GCACTTGCTA GTCAGTAGCC TCTGCAGCTA GCACTCGGCT 300
ACTAGTCAGT AGCCTCTCGG ATAGCACTGT GGGGGGATGT GTCATCCAGT TACATCTGAC 360
TTTGTTCACA GTTGCCTGCA GCTCCACCCA CAGTCTAGCA GGCCCAGGCA TGCTGGGTGG 420
GCCAGAGCCT TTCTCCTTCA CCACCTGACT CTCCCTGAGT GACTCATTCT CTCCTTCCAT 480
CTACAGCTCT CTGGGTGTAC AGCTGCTGGG GCCAGGGTGG AGCCCTGCCC TCCTCAGAGC 540
CTGGCCTACC TGTGCCAGGA CTACCAGCCT TCCCCCTTTC TCTAGGGACC TGGCTGCGGG 600
CCACAGCTGT CTAAAACAGG GACAGTGCCT TTTTCCCCAC AGGTGCCCAG ACATGCTCCT 660
TACACCGGTG GTGTGTGTGG GGGTGGCTTC TAGTGGCTCC TGTACCTTGG CAGGTTTGTG 720
GGCTGGGTGG GCCTTGACCC CAGAGCCCGG TCCACAGGGT CTGTCTGAGC TGTGGGGTGC 780
GTGTGAGGCA TGGGGGCCTG CCTGTGCCCC ATTTTCACCT GCCCCGGCCC CACCCTCGGC 840
CTCCCTGGCG CCTGCTGGCG GGCCTCAGCC CTGTCCACCA TGTCCTCCAT GAGTCCTGAG 900
TCTTTTGTGA GTGATGTGGT TCGTGTGCAC CTGTGTGCAT 940
|
