| Tag | Content |
|---|
EnhancerAtlas ID | HS040-01546 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:44046970-44048660 |
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 | CAGCCCCACT TGCCAGGGAC TCCAAAACAG CCAAACCTGA CTTCTGTTGT CTCTCTCACA 60
CACACATACG ACGTTCCTCT AGGCCCTGAT GTCTCAGGAC CGTTTCTAAG CTCTGTCCCC 120
AGGACCTGCC TCATGTAGAC CCTAATTGAA TCTACACCAC CCTGCTTTGC CAAGAGCAAC 180
CTGCCCCATA GGCCCTACTG TCCTACTGAC AGGACTTAGG CACACCTGAA AGGCCCTGCT 240
CCCTGGGTGC CTTGCCTCTG GTGCCCCCAC TGCTCGTCAT CTCATGGTTG GCAAAACCCC 300
TGCCTTCTGC CCTCAGCAGT ACTAGGGGCC CTTCAGCCCC AGCGCCTGGG GACAGCCTGT 360
ACTGGGCTGA CCACCAGCTC TGCATCCTGA GCCCTGCTTG TGGGTGGATG GCCGTGGAGG 420
AGTCCCCAGT GCCAGCCTGC TTTCTGGCCT GCACCCCGTC CCATCTCCCA GCAGAGAGGC 480
TTCGAGGTTT CCTCCCACAG CAGGCTCCTG AGCCTCAGAC GGCTTGATGT GGGCTCTAGC 540
CCTGAACTTC TCAGCCGCAG CACTGTTGAC ATTTTGGGCT GGACGATTCT TAGTTGTGAG 600
GGGCCATCCT GTGCATTGGA GGGTGTTTAG CAGCATCTCT AGCTCACTAG ATGCCAGTGG 660
CACCCCTCAG TCAAAACAAA CGTTGCAACG TGTCACCTGG GGGAAATTAC TGATGGCTTC 720
CCACTGCCAT TGTCTCCACC CATCTGACTC TCTTCACCTG TGTCCACTGG CCGCAAGGCT 780
TCGTCTCCTC ATCAGACTTG GCTTCGGTGT CTACCTCACA TCTCCCTTCT GTCCCCCAAA 840
TTCTCAGGGC TCCCAGTGTC GCTCTCTGAG GCCACGCGAC TGCTACATTT AATGGGACAG 900
TACACGTGAA GCACCAGGCA CATTGCCAGG CACACAGGAA GCACTTGCTA GTCAGTAGCC 960
TCTGCAGCTA GCACTCGGCT ACTAGTCAGT AGCCTCTCGG ATAGCACTGT GGGGGGATGT 1020
GTCATCCAGT TACATCTGAC TTTGTTCACA GTTGCCTGCA GCTCCACCCA CAGTCTAGCA 1080
GGCCCAGGCA TGCTGGGTGG GCCAGAGCCT TTCTCCTTCA CCACCTGACT CTCCCTGAGT 1140
GACTCATTCT CTCCTTCCAT CTACAGCTCT CTGGGTGTAC AGCTGCTGGG GCCAGGGTGG 1200
AGCCCTGCCC TCCTCAGAGC CTGGCCTACC TGTGCCAGGA CTACCAGCCT TCCCCCTTTC 1260
TCTAGGGACC TGGCTGCGGG CCACAGCTGT CTAAAACAGG GACAGTGCCT TTTTCCCCAC 1320
AGGTGCCCAG ACATGCTCCT TACACCGGTG GTGTGTGTGG GGGTGGCTTC TAGTGGCTCC 1380
TGTACCTTGG CAGGTTTGTG GGCTGGGTGG GCCTTGACCC CAGAGCCCGG TCCACAGGGT 1440
CTGTCTGAGC TGTGGGGTGC GTGTGAGGCA TGGGGGCCTG CCTGTGCCCC ATTTTCACCT 1500
GCCCCGGCCC CACCCTCGGC CTCCCTGGCG CCTGCTGGCG GGCCTCAGCC CTGTCCACCA 1560
TGTCCTCCAT GAGTCCTGAG TCTTTTGTGA GTGATGTGGT TCGTGTGCAC CTGTGTGCAT 1620
GTGTGTGTGC GAGGGGGCAC AGGAGTCTCG TCTCGTCTCC GTGCTGTGTG GGCAGATGAA 1680
GGTTGGCCTG 1690
|
