| Tag | Content |
|---|
EnhancerAtlas ID | HS059-01483 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:44047120-44048680 |
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 | TCTACACCAC CCTGCTTTGC CAAGAGCAAC CTGCCCCATA GGCCCTACTG TCCTACTGAC 60
AGGACTTAGG CACACCTGAA AGGCCCTGCT CCCTGGGTGC CTTGCCTCTG GTGCCCCCAC 120
TGCTCGTCAT CTCATGGTTG GCAAAACCCC TGCCTTCTGC CCTCAGCAGT ACTAGGGGCC 180
CTTCAGCCCC AGCGCCTGGG GACAGCCTGT ACTGGGCTGA CCACCAGCTC TGCATCCTGA 240
GCCCTGCTTG TGGGTGGATG GCCGTGGAGG AGTCCCCAGT GCCAGCCTGC TTTCTGGCCT 300
GCACCCCGTC CCATCTCCCA GCAGAGAGGC TTCGAGGTTT CCTCCCACAG CAGGCTCCTG 360
AGCCTCAGAC GGCTTGATGT GGGCTCTAGC CCTGAACTTC TCAGCCGCAG CACTGTTGAC 420
ATTTTGGGCT GGACGATTCT TAGTTGTGAG GGGCCATCCT GTGCATTGGA GGGTGTTTAG 480
CAGCATCTCT AGCTCACTAG ATGCCAGTGG CACCCCTCAG TCAAAACAAA CGTTGCAACG 540
TGTCACCTGG GGGAAATTAC TGATGGCTTC CCACTGCCAT TGTCTCCACC CATCTGACTC 600
TCTTCACCTG TGTCCACTGG CCGCAAGGCT TCGTCTCCTC ATCAGACTTG GCTTCGGTGT 660
CTACCTCACA TCTCCCTTCT GTCCCCCAAA TTCTCAGGGC TCCCAGTGTC GCTCTCTGAG 720
GCCACGCGAC TGCTACATTT AATGGGACAG TACACGTGAA GCACCAGGCA CATTGCCAGG 780
CACACAGGAA GCACTTGCTA GTCAGTAGCC TCTGCAGCTA GCACTCGGCT ACTAGTCAGT 840
AGCCTCTCGG ATAGCACTGT GGGGGGATGT GTCATCCAGT TACATCTGAC TTTGTTCACA 900
GTTGCCTGCA GCTCCACCCA CAGTCTAGCA GGCCCAGGCA TGCTGGGTGG GCCAGAGCCT 960
TTCTCCTTCA CCACCTGACT CTCCCTGAGT GACTCATTCT CTCCTTCCAT CTACAGCTCT 1020
CTGGGTGTAC AGCTGCTGGG GCCAGGGTGG AGCCCTGCCC TCCTCAGAGC CTGGCCTACC 1080
TGTGCCAGGA CTACCAGCCT TCCCCCTTTC TCTAGGGACC TGGCTGCGGG CCACAGCTGT 1140
CTAAAACAGG GACAGTGCCT TTTTCCCCAC AGGTGCCCAG ACATGCTCCT TACACCGGTG 1200
GTGTGTGTGG GGGTGGCTTC TAGTGGCTCC TGTACCTTGG CAGGTTTGTG GGCTGGGTGG 1260
GCCTTGACCC CAGAGCCCGG TCCACAGGGT CTGTCTGAGC TGTGGGGTGC GTGTGAGGCA 1320
TGGGGGCCTG CCTGTGCCCC ATTTTCACCT GCCCCGGCCC CACCCTCGGC CTCCCTGGCG 1380
CCTGCTGGCG GGCCTCAGCC CTGTCCACCA TGTCCTCCAT GAGTCCTGAG TCTTTTGTGA 1440
GTGATGTGGT TCGTGTGCAC CTGTGTGCAT GTGTGTGTGC GAGGGGGCAC AGGAGTCTCG 1500
TCTCGTCTCC GTGCTGTGTG GGCAGATGAA GGTTGGCCTG TTTTTACTCT CTCTGTGTTT 1560
|
