| Tag | Content |
|---|
EnhancerAtlas ID | HS050-02041 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:44046990-44049030 |
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 | TCCAAAACAG CCAAACCTGA CTTCTGTTGT CTCTCTCACA CACACATACG ACGTTCCTCT 60
AGGCCCTGAT GTCTCAGGAC CGTTTCTAAG CTCTGTCCCC AGGACCTGCC TCATGTAGAC 120
CCTAATTGAA TCTACACCAC CCTGCTTTGC CAAGAGCAAC CTGCCCCATA GGCCCTACTG 180
TCCTACTGAC AGGACTTAGG CACACCTGAA AGGCCCTGCT CCCTGGGTGC CTTGCCTCTG 240
GTGCCCCCAC TGCTCGTCAT CTCATGGTTG GCAAAACCCC TGCCTTCTGC CCTCAGCAGT 300
ACTAGGGGCC CTTCAGCCCC AGCGCCTGGG GACAGCCTGT ACTGGGCTGA CCACCAGCTC 360
TGCATCCTGA GCCCTGCTTG TGGGTGGATG GCCGTGGAGG AGTCCCCAGT GCCAGCCTGC 420
TTTCTGGCCT GCACCCCGTC CCATCTCCCA GCAGAGAGGC TTCGAGGTTT CCTCCCACAG 480
CAGGCTCCTG AGCCTCAGAC GGCTTGATGT GGGCTCTAGC CCTGAACTTC TCAGCCGCAG 540
CACTGTTGAC ATTTTGGGCT GGACGATTCT TAGTTGTGAG GGGCCATCCT GTGCATTGGA 600
GGGTGTTTAG CAGCATCTCT AGCTCACTAG ATGCCAGTGG CACCCCTCAG TCAAAACAAA 660
CGTTGCAACG TGTCACCTGG GGGAAATTAC TGATGGCTTC CCACTGCCAT TGTCTCCACC 720
CATCTGACTC TCTTCACCTG TGTCCACTGG CCGCAAGGCT TCGTCTCCTC ATCAGACTTG 780
GCTTCGGTGT CTACCTCACA TCTCCCTTCT GTCCCCCAAA TTCTCAGGGC TCCCAGTGTC 840
GCTCTCTGAG GCCACGCGAC TGCTACATTT AATGGGACAG TACACGTGAA GCACCAGGCA 900
CATTGCCAGG CACACAGGAA GCACTTGCTA GTCAGTAGCC TCTGCAGCTA GCACTCGGCT 960
ACTAGTCAGT AGCCTCTCGG ATAGCACTGT GGGGGGATGT GTCATCCAGT TACATCTGAC 1020
TTTGTTCACA GTTGCCTGCA GCTCCACCCA CAGTCTAGCA GGCCCAGGCA TGCTGGGTGG 1080
GCCAGAGCCT TTCTCCTTCA CCACCTGACT CTCCCTGAGT GACTCATTCT CTCCTTCCAT 1140
CTACAGCTCT CTGGGTGTAC AGCTGCTGGG GCCAGGGTGG AGCCCTGCCC TCCTCAGAGC 1200
CTGGCCTACC TGTGCCAGGA CTACCAGCCT TCCCCCTTTC TCTAGGGACC TGGCTGCGGG 1260
CCACAGCTGT CTAAAACAGG GACAGTGCCT TTTTCCCCAC AGGTGCCCAG ACATGCTCCT 1320
TACACCGGTG GTGTGTGTGG GGGTGGCTTC TAGTGGCTCC TGTACCTTGG CAGGTTTGTG 1380
GGCTGGGTGG GCCTTGACCC CAGAGCCCGG TCCACAGGGT CTGTCTGAGC TGTGGGGTGC 1440
GTGTGAGGCA TGGGGGCCTG CCTGTGCCCC ATTTTCACCT GCCCCGGCCC CACCCTCGGC 1500
CTCCCTGGCG CCTGCTGGCG GGCCTCAGCC CTGTCCACCA TGTCCTCCAT GAGTCCTGAG 1560
TCTTTTGTGA GTGATGTGGT TCGTGTGCAC CTGTGTGCAT GTGTGTGTGC GAGGGGGCAC 1620
AGGAGTCTCG TCTCGTCTCC GTGCTGTGTG GGCAGATGAA GGTTGGCCTG TTTTTACTCT 1680
CTCTGTGTTT CTCCTTGTCT TTTTTTTATT CCCTCCTCAT CTTCATCGCA CTCTGCCATC 1740
AACCCAAACT CTCATCTCTC AGATCAGCGA GAAGGTTGGT CCTTTTCACT TCTTATCCAT 1800
CTACAGTTCG CCCATCGATG GGACACGCCT GTCAGTAGGG CCCAGCGGGC TCGGTCAGCT 1860
CCCTCAGGCT CACTGCGCCG TGCCTGCCTG CCAGTCTCTG TTGTTTGGGC CGGCGGGCAG 1920
GCAGGACCAG GGATGGGTGG GCAGACCCCT GACCTGCATG TTCCTGCTGC TTGGGTCCCT 1980
GGTGCACCAC GTGTCTGCAT GTCCCCTTAG CCTGGTTCCC CTGCAAGGGT GGTGGGGTGG 2040
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