| Tag | Content |
|---|
EnhancerAtlas ID | HS077-00442 |
Organism | Homo sapiens |
Tissue/cell | H128 |
Coordinate | chr1:44047350-44048700 |
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 | TGCATCCTGA GCCCTGCTTG TGGGTGGATG GCCGTGGAGG AGTCCCCAGT GCCAGCCTGC 60
TTTCTGGCCT GCACCCCGTC CCATCTCCCA GCAGAGAGGC TTCGAGGTTT CCTCCCACAG 120
CAGGCTCCTG AGCCTCAGAC GGCTTGATGT GGGCTCTAGC CCTGAACTTC TCAGCCGCAG 180
CACTGTTGAC ATTTTGGGCT GGACGATTCT TAGTTGTGAG GGGCCATCCT GTGCATTGGA 240
GGGTGTTTAG CAGCATCTCT AGCTCACTAG ATGCCAGTGG CACCCCTCAG TCAAAACAAA 300
CGTTGCAACG TGTCACCTGG GGGAAATTAC TGATGGCTTC CCACTGCCAT TGTCTCCACC 360
CATCTGACTC TCTTCACCTG TGTCCACTGG CCGCAAGGCT TCGTCTCCTC ATCAGACTTG 420
GCTTCGGTGT CTACCTCACA TCTCCCTTCT GTCCCCCAAA TTCTCAGGGC TCCCAGTGTC 480
GCTCTCTGAG GCCACGCGAC TGCTACATTT AATGGGACAG TACACGTGAA GCACCAGGCA 540
CATTGCCAGG CACACAGGAA GCACTTGCTA GTCAGTAGCC TCTGCAGCTA GCACTCGGCT 600
ACTAGTCAGT AGCCTCTCGG ATAGCACTGT GGGGGGATGT GTCATCCAGT TACATCTGAC 660
TTTGTTCACA GTTGCCTGCA GCTCCACCCA CAGTCTAGCA GGCCCAGGCA TGCTGGGTGG 720
GCCAGAGCCT TTCTCCTTCA CCACCTGACT CTCCCTGAGT GACTCATTCT CTCCTTCCAT 780
CTACAGCTCT CTGGGTGTAC AGCTGCTGGG GCCAGGGTGG AGCCCTGCCC TCCTCAGAGC 840
CTGGCCTACC TGTGCCAGGA CTACCAGCCT TCCCCCTTTC TCTAGGGACC TGGCTGCGGG 900
CCACAGCTGT CTAAAACAGG GACAGTGCCT TTTTCCCCAC AGGTGCCCAG ACATGCTCCT 960
TACACCGGTG GTGTGTGTGG GGGTGGCTTC TAGTGGCTCC TGTACCTTGG CAGGTTTGTG 1020
GGCTGGGTGG GCCTTGACCC CAGAGCCCGG TCCACAGGGT CTGTCTGAGC TGTGGGGTGC 1080
GTGTGAGGCA TGGGGGCCTG CCTGTGCCCC ATTTTCACCT GCCCCGGCCC CACCCTCGGC 1140
CTCCCTGGCG CCTGCTGGCG GGCCTCAGCC CTGTCCACCA TGTCCTCCAT GAGTCCTGAG 1200
TCTTTTGTGA GTGATGTGGT TCGTGTGCAC CTGTGTGCAT GTGTGTGTGC GAGGGGGCAC 1260
AGGAGTCTCG TCTCGTCTCC GTGCTGTGTG GGCAGATGAA GGTTGGCCTG TTTTTACTCT 1320
CTCTGTGTTT CTCCTTGTCT TTTTTTTATT 1350
|
