| Tag | Content |
|---|
EnhancerAtlas ID | HS145-00771 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr1:44047500-44048460 |
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 | GGGCTCTAGC CCTGAACTTC TCAGCCGCAG CACTGTTGAC ATTTTGGGCT GGACGATTCT 60
TAGTTGTGAG GGGCCATCCT GTGCATTGGA GGGTGTTTAG CAGCATCTCT AGCTCACTAG 120
ATGCCAGTGG CACCCCTCAG TCAAAACAAA CGTTGCAACG TGTCACCTGG GGGAAATTAC 180
TGATGGCTTC CCACTGCCAT TGTCTCCACC CATCTGACTC TCTTCACCTG TGTCCACTGG 240
CCGCAAGGCT TCGTCTCCTC ATCAGACTTG GCTTCGGTGT CTACCTCACA TCTCCCTTCT 300
GTCCCCCAAA TTCTCAGGGC TCCCAGTGTC GCTCTCTGAG GCCACGCGAC TGCTACATTT 360
AATGGGACAG TACACGTGAA GCACCAGGCA CATTGCCAGG CACACAGGAA GCACTTGCTA 420
GTCAGTAGCC TCTGCAGCTA GCACTCGGCT ACTAGTCAGT AGCCTCTCGG ATAGCACTGT 480
GGGGGGATGT GTCATCCAGT TACATCTGAC TTTGTTCACA GTTGCCTGCA GCTCCACCCA 540
CAGTCTAGCA GGCCCAGGCA TGCTGGGTGG GCCAGAGCCT TTCTCCTTCA CCACCTGACT 600
CTCCCTGAGT GACTCATTCT CTCCTTCCAT CTACAGCTCT CTGGGTGTAC AGCTGCTGGG 660
GCCAGGGTGG AGCCCTGCCC TCCTCAGAGC CTGGCCTACC TGTGCCAGGA CTACCAGCCT 720
TCCCCCTTTC TCTAGGGACC TGGCTGCGGG CCACAGCTGT CTAAAACAGG GACAGTGCCT 780
TTTTCCCCAC AGGTGCCCAG ACATGCTCCT TACACCGGTG GTGTGTGTGG GGGTGGCTTC 840
TAGTGGCTCC TGTACCTTGG CAGGTTTGTG GGCTGGGTGG GCCTTGACCC CAGAGCCCGG 900
TCCACAGGGT CTGTCTGAGC TGTGGGGTGC GTGTGAGGCA TGGGGGCCTG CCTGTGCCCC 960
|
