| Tag | Content |
|---|
EnhancerAtlas ID | HS095-00974 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:44047010-44048990 |
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 | CTTCTGTTGT CTCTCTCACA CACACATACG ACGTTCCTCT AGGCCCTGAT GTCTCAGGAC 60
CGTTTCTAAG CTCTGTCCCC AGGACCTGCC TCATGTAGAC CCTAATTGAA TCTACACCAC 120
CCTGCTTTGC CAAGAGCAAC CTGCCCCATA GGCCCTACTG TCCTACTGAC AGGACTTAGG 180
CACACCTGAA AGGCCCTGCT CCCTGGGTGC CTTGCCTCTG GTGCCCCCAC TGCTCGTCAT 240
CTCATGGTTG GCAAAACCCC TGCCTTCTGC CCTCAGCAGT ACTAGGGGCC CTTCAGCCCC 300
AGCGCCTGGG GACAGCCTGT ACTGGGCTGA CCACCAGCTC TGCATCCTGA GCCCTGCTTG 360
TGGGTGGATG GCCGTGGAGG AGTCCCCAGT GCCAGCCTGC TTTCTGGCCT GCACCCCGTC 420
CCATCTCCCA GCAGAGAGGC TTCGAGGTTT CCTCCCACAG CAGGCTCCTG AGCCTCAGAC 480
GGCTTGATGT GGGCTCTAGC CCTGAACTTC TCAGCCGCAG CACTGTTGAC ATTTTGGGCT 540
GGACGATTCT TAGTTGTGAG GGGCCATCCT GTGCATTGGA GGGTGTTTAG CAGCATCTCT 600
AGCTCACTAG ATGCCAGTGG CACCCCTCAG TCAAAACAAA CGTTGCAACG TGTCACCTGG 660
GGGAAATTAC TGATGGCTTC CCACTGCCAT TGTCTCCACC CATCTGACTC TCTTCACCTG 720
TGTCCACTGG CCGCAAGGCT TCGTCTCCTC ATCAGACTTG GCTTCGGTGT CTACCTCACA 780
TCTCCCTTCT GTCCCCCAAA TTCTCAGGGC TCCCAGTGTC GCTCTCTGAG GCCACGCGAC 840
TGCTACATTT AATGGGACAG TACACGTGAA GCACCAGGCA CATTGCCAGG CACACAGGAA 900
GCACTTGCTA GTCAGTAGCC TCTGCAGCTA GCACTCGGCT ACTAGTCAGT AGCCTCTCGG 960
ATAGCACTGT GGGGGGATGT GTCATCCAGT TACATCTGAC TTTGTTCACA GTTGCCTGCA 1020
GCTCCACCCA CAGTCTAGCA GGCCCAGGCA TGCTGGGTGG GCCAGAGCCT TTCTCCTTCA 1080
CCACCTGACT CTCCCTGAGT GACTCATTCT CTCCTTCCAT CTACAGCTCT CTGGGTGTAC 1140
AGCTGCTGGG GCCAGGGTGG AGCCCTGCCC TCCTCAGAGC CTGGCCTACC TGTGCCAGGA 1200
CTACCAGCCT TCCCCCTTTC TCTAGGGACC TGGCTGCGGG CCACAGCTGT CTAAAACAGG 1260
GACAGTGCCT TTTTCCCCAC AGGTGCCCAG ACATGCTCCT TACACCGGTG GTGTGTGTGG 1320
GGGTGGCTTC TAGTGGCTCC TGTACCTTGG CAGGTTTGTG GGCTGGGTGG GCCTTGACCC 1380
CAGAGCCCGG TCCACAGGGT CTGTCTGAGC TGTGGGGTGC GTGTGAGGCA TGGGGGCCTG 1440
CCTGTGCCCC ATTTTCACCT GCCCCGGCCC CACCCTCGGC CTCCCTGGCG CCTGCTGGCG 1500
GGCCTCAGCC CTGTCCACCA TGTCCTCCAT GAGTCCTGAG TCTTTTGTGA GTGATGTGGT 1560
TCGTGTGCAC CTGTGTGCAT GTGTGTGTGC GAGGGGGCAC AGGAGTCTCG TCTCGTCTCC 1620
GTGCTGTGTG GGCAGATGAA GGTTGGCCTG TTTTTACTCT CTCTGTGTTT CTCCTTGTCT 1680
TTTTTTTATT CCCTCCTCAT CTTCATCGCA CTCTGCCATC AACCCAAACT CTCATCTCTC 1740
AGATCAGCGA GAAGGTTGGT CCTTTTCACT TCTTATCCAT CTACAGTTCG CCCATCGATG 1800
GGACACGCCT GTCAGTAGGG CCCAGCGGGC TCGGTCAGCT CCCTCAGGCT CACTGCGCCG 1860
TGCCTGCCTG CCAGTCTCTG TTGTTTGGGC CGGCGGGCAG GCAGGACCAG GGATGGGTGG 1920
GCAGACCCCT GACCTGCATG TTCCTGCTGC TTGGGTCCCT GGTGCACCAC GTGTCTGCAT 1980
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