| Tag | Content |
|---|
EnhancerAtlas ID | HS180-01477 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:44046920-44048710 |
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 | CTCCATCCCC ACATGCCTTT TGGTAGGAAA TACGGGGGTT CCTTTAGTTC CAGCCCCACT 60
TGCCAGGGAC TCCAAAACAG CCAAACCTGA CTTCTGTTGT CTCTCTCACA CACACATACG 120
ACGTTCCTCT AGGCCCTGAT GTCTCAGGAC CGTTTCTAAG CTCTGTCCCC AGGACCTGCC 180
TCATGTAGAC CCTAATTGAA TCTACACCAC CCTGCTTTGC CAAGAGCAAC CTGCCCCATA 240
GGCCCTACTG TCCTACTGAC AGGACTTAGG CACACCTGAA AGGCCCTGCT CCCTGGGTGC 300
CTTGCCTCTG GTGCCCCCAC TGCTCGTCAT CTCATGGTTG GCAAAACCCC TGCCTTCTGC 360
CCTCAGCAGT ACTAGGGGCC CTTCAGCCCC AGCGCCTGGG GACAGCCTGT ACTGGGCTGA 420
CCACCAGCTC TGCATCCTGA GCCCTGCTTG TGGGTGGATG GCCGTGGAGG AGTCCCCAGT 480
GCCAGCCTGC TTTCTGGCCT GCACCCCGTC CCATCTCCCA GCAGAGAGGC TTCGAGGTTT 540
CCTCCCACAG CAGGCTCCTG AGCCTCAGAC GGCTTGATGT GGGCTCTAGC CCTGAACTTC 600
TCAGCCGCAG CACTGTTGAC ATTTTGGGCT GGACGATTCT TAGTTGTGAG GGGCCATCCT 660
GTGCATTGGA GGGTGTTTAG CAGCATCTCT AGCTCACTAG ATGCCAGTGG CACCCCTCAG 720
TCAAAACAAA CGTTGCAACG TGTCACCTGG GGGAAATTAC TGATGGCTTC CCACTGCCAT 780
TGTCTCCACC CATCTGACTC TCTTCACCTG TGTCCACTGG CCGCAAGGCT TCGTCTCCTC 840
ATCAGACTTG GCTTCGGTGT CTACCTCACA TCTCCCTTCT GTCCCCCAAA TTCTCAGGGC 900
TCCCAGTGTC GCTCTCTGAG GCCACGCGAC TGCTACATTT AATGGGACAG TACACGTGAA 960
GCACCAGGCA CATTGCCAGG CACACAGGAA GCACTTGCTA GTCAGTAGCC TCTGCAGCTA 1020
GCACTCGGCT ACTAGTCAGT AGCCTCTCGG ATAGCACTGT GGGGGGATGT GTCATCCAGT 1080
TACATCTGAC TTTGTTCACA GTTGCCTGCA GCTCCACCCA CAGTCTAGCA GGCCCAGGCA 1140
TGCTGGGTGG GCCAGAGCCT TTCTCCTTCA CCACCTGACT CTCCCTGAGT GACTCATTCT 1200
CTCCTTCCAT CTACAGCTCT CTGGGTGTAC AGCTGCTGGG GCCAGGGTGG AGCCCTGCCC 1260
TCCTCAGAGC CTGGCCTACC TGTGCCAGGA CTACCAGCCT TCCCCCTTTC TCTAGGGACC 1320
TGGCTGCGGG CCACAGCTGT CTAAAACAGG GACAGTGCCT TTTTCCCCAC AGGTGCCCAG 1380
ACATGCTCCT TACACCGGTG GTGTGTGTGG GGGTGGCTTC TAGTGGCTCC TGTACCTTGG 1440
CAGGTTTGTG GGCTGGGTGG GCCTTGACCC CAGAGCCCGG TCCACAGGGT CTGTCTGAGC 1500
TGTGGGGTGC GTGTGAGGCA TGGGGGCCTG CCTGTGCCCC ATTTTCACCT GCCCCGGCCC 1560
CACCCTCGGC CTCCCTGGCG CCTGCTGGCG GGCCTCAGCC CTGTCCACCA TGTCCTCCAT 1620
GAGTCCTGAG TCTTTTGTGA GTGATGTGGT TCGTGTGCAC CTGTGTGCAT GTGTGTGTGC 1680
GAGGGGGCAC AGGAGTCTCG TCTCGTCTCC GTGCTGTGTG GGCAGATGAA GGTTGGCCTG 1740
TTTTTACTCT CTCTGTGTTT CTCCTTGTCT TTTTTTTATT CCCTCCTCAT 1790
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