| Tag | Content |
|---|
EnhancerAtlas ID | HS054-00196 |
Organism | Homo sapiens |
Tissue/cell | FT246 |
Coordinate | chr1:44047200-44048600 |
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 | AGGCCCTGCT CCCTGGGTGC CTTGCCTCTG GTGCCCCCAC TGCTCGTCAT CTCATGGTTG 60
GCAAAACCCC TGCCTTCTGC CCTCAGCAGT ACTAGGGGCC CTTCAGCCCC AGCGCCTGGG 120
GACAGCCTGT ACTGGGCTGA CCACCAGCTC TGCATCCTGA GCCCTGCTTG TGGGTGGATG 180
GCCGTGGAGG AGTCCCCAGT GCCAGCCTGC TTTCTGGCCT GCACCCCGTC CCATCTCCCA 240
GCAGAGAGGC TTCGAGGTTT CCTCCCACAG CAGGCTCCTG AGCCTCAGAC GGCTTGATGT 300
GGGCTCTAGC CCTGAACTTC TCAGCCGCAG CACTGTTGAC ATTTTGGGCT GGACGATTCT 360
TAGTTGTGAG GGGCCATCCT GTGCATTGGA GGGTGTTTAG CAGCATCTCT AGCTCACTAG 420
ATGCCAGTGG CACCCCTCAG TCAAAACAAA CGTTGCAACG TGTCACCTGG GGGAAATTAC 480
TGATGGCTTC CCACTGCCAT TGTCTCCACC CATCTGACTC TCTTCACCTG TGTCCACTGG 540
CCGCAAGGCT TCGTCTCCTC ATCAGACTTG GCTTCGGTGT CTACCTCACA TCTCCCTTCT 600
GTCCCCCAAA TTCTCAGGGC TCCCAGTGTC GCTCTCTGAG GCCACGCGAC TGCTACATTT 660
AATGGGACAG TACACGTGAA GCACCAGGCA CATTGCCAGG CACACAGGAA GCACTTGCTA 720
GTCAGTAGCC TCTGCAGCTA GCACTCGGCT ACTAGTCAGT AGCCTCTCGG ATAGCACTGT 780
GGGGGGATGT GTCATCCAGT TACATCTGAC TTTGTTCACA GTTGCCTGCA GCTCCACCCA 840
CAGTCTAGCA GGCCCAGGCA TGCTGGGTGG GCCAGAGCCT TTCTCCTTCA CCACCTGACT 900
CTCCCTGAGT GACTCATTCT CTCCTTCCAT CTACAGCTCT CTGGGTGTAC AGCTGCTGGG 960
GCCAGGGTGG AGCCCTGCCC TCCTCAGAGC CTGGCCTACC TGTGCCAGGA CTACCAGCCT 1020
TCCCCCTTTC TCTAGGGACC TGGCTGCGGG CCACAGCTGT CTAAAACAGG GACAGTGCCT 1080
TTTTCCCCAC AGGTGCCCAG ACATGCTCCT TACACCGGTG GTGTGTGTGG GGGTGGCTTC 1140
TAGTGGCTCC TGTACCTTGG CAGGTTTGTG GGCTGGGTGG GCCTTGACCC CAGAGCCCGG 1200
TCCACAGGGT CTGTCTGAGC TGTGGGGTGC GTGTGAGGCA TGGGGGCCTG CCTGTGCCCC 1260
ATTTTCACCT GCCCCGGCCC CACCCTCGGC CTCCCTGGCG CCTGCTGGCG GGCCTCAGCC 1320
CTGTCCACCA TGTCCTCCAT GAGTCCTGAG TCTTTTGTGA GTGATGTGGT TCGTGTGCAC 1380
CTGTGTGCAT GTGTGTGTGC 1400
|
