| Tag | Content |
|---|
EnhancerAtlas ID | HS138-00887 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:44047530-44048490 |
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 | CACTGTTGAC ATTTTGGGCT GGACGATTCT TAGTTGTGAG GGGCCATCCT GTGCATTGGA 60
GGGTGTTTAG CAGCATCTCT AGCTCACTAG ATGCCAGTGG CACCCCTCAG TCAAAACAAA 120
CGTTGCAACG TGTCACCTGG GGGAAATTAC TGATGGCTTC CCACTGCCAT TGTCTCCACC 180
CATCTGACTC TCTTCACCTG TGTCCACTGG CCGCAAGGCT TCGTCTCCTC ATCAGACTTG 240
GCTTCGGTGT CTACCTCACA TCTCCCTTCT GTCCCCCAAA TTCTCAGGGC TCCCAGTGTC 300
GCTCTCTGAG GCCACGCGAC TGCTACATTT AATGGGACAG TACACGTGAA GCACCAGGCA 360
CATTGCCAGG CACACAGGAA GCACTTGCTA GTCAGTAGCC TCTGCAGCTA GCACTCGGCT 420
ACTAGTCAGT AGCCTCTCGG ATAGCACTGT GGGGGGATGT GTCATCCAGT TACATCTGAC 480
TTTGTTCACA GTTGCCTGCA GCTCCACCCA CAGTCTAGCA GGCCCAGGCA TGCTGGGTGG 540
GCCAGAGCCT TTCTCCTTCA CCACCTGACT CTCCCTGAGT GACTCATTCT CTCCTTCCAT 600
CTACAGCTCT CTGGGTGTAC AGCTGCTGGG GCCAGGGTGG AGCCCTGCCC TCCTCAGAGC 660
CTGGCCTACC TGTGCCAGGA CTACCAGCCT TCCCCCTTTC TCTAGGGACC TGGCTGCGGG 720
CCACAGCTGT CTAAAACAGG GACAGTGCCT TTTTCCCCAC AGGTGCCCAG ACATGCTCCT 780
TACACCGGTG GTGTGTGTGG GGGTGGCTTC TAGTGGCTCC TGTACCTTGG CAGGTTTGTG 840
GGCTGGGTGG GCCTTGACCC CAGAGCCCGG TCCACAGGGT CTGTCTGAGC TGTGGGGTGC 900
GTGTGAGGCA TGGGGGCCTG CCTGTGCCCC ATTTTCACCT GCCCCGGCCC CACCCTCGGC 960
|
