| Tag | Content |
|---|
EnhancerAtlas ID | HS078-00781 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr1:40425610-40426970 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr1:40426047-40426067 | CCCCCACCCACCCCAATCCT | + | 6.6 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_34178 | chr1:40425200-40426993 | HCC1954 | | SE_64654 | chr1:40425188-40426196 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 40426773 | 40426921 | | chr1 | 40426208 | 40426621 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I039959 | chr1 | 40425449 | 40427071 |
|
Enhancer Sequence | CATGTGGGAC CCTCCAACAG CACAGTGATA AATAATTTGG CACCCCTTCA GGGTGGCTCC 60
TGGCAGAGCA GGGGATGGGG TAATACCCGG AATGGGGTAG CAAACCCATA ACCTTTGGCA 120
CCTTGGATGA CGTAAATTAC CTTCTCCCTT GGTACAAAGC CTGTGCTACT CAGCTTCAGG 180
GGCAAAGTAG GCGGAGGTGG TGCCACGGAT CGGATCAGAC GGCAGGGGAG ACGCACAGGA 240
TAGGCTGTCA GGCGGGGGCT CTGGTTCCCT CCAGGACATC CTGCTTCAGG GTGTGGGGGG 300
GCATACCCCT TTCATCTCCA GCCCATCCAG GCTTAAGTGG GCGCCTTCCT GCCCCAGGGG 360
CGCCCATACC TGGCCTCCGG CCTTCAAAGC TCTTCCCGCA ACCCCTTCCC CCACTACAGC 420
TTCCTTTCCC ACGAGGCCCC CCACCCACCC CAATCCTGCC AGCCCCTGGC TAAGGCCCAG 480
GTTGGAGCCT TTGATCCAGT CTTCAGGGCC GGGGGCAGGA CAGCCTGCCT TACCTGTGCA 540
GGCTGCTCAG GGCTCCCCCG GCGCCAGCCC GTGAGACTTG GCCCTGTGCC CGCCTCCCTG 600
GCAGCCAGTA GAAGGGGAGG CTCTGCTGCC ACGTCGCCTC ATGAGGCCCA GCCAATGGGA 660
GGCAGCCGCT CCCAGGGATG GTGGCTGCAG GCCGGGTTAC TCCCAGTTAC ACTGGGTTCC 720
TCAGCAGCAG CTGCTCAGCT GCTTATGAGC AGAGGATGGA GTGTTTGACA AAGGCTGATG 780
AGGAGCTCTT GTTCCCTGAG GAGACAGAGT CAAGAGAGGT GGAGGTGGGC AGGCCTTCCC 840
TGTGGCATGT AGGAACTGAG CAACTTCCTG GGCAGGCGTG GCAGCCAGTT TGGGGAAGTT 900
GCTGGGGGCC CTTCAGGCTG GTTTCTGATC TAGCAGGTGC CTGTGTGCAC ATGCTTCTGT 960
GGCTGGTGGT GCCTGTGTAT GCCTGCACGC GGGATGGCTC GTGGGCTGAA GGCTGGTGTG 1020
CATATGACCT CCCTGTCCAA ACTTTTTTTC CTTTTTGTGG TGAATGGGGT CTGGCTATGT 1080
TGCTCAGGCT GGTCTCAAAC TCCTGGGCTG GAGCTATTCT CCTGCCTCTG CCTCCCTAAG 1140
TGCTGGGATT AAAGGCATGA ACATCACCAT GCCTGGCCAG ACCTCTCCAT CCATACCACC 1200
TGACCCCTCC TCAGGCCAGG CCTGGAGACC TGGAACCCCC TTTCCTTTCA GTGTAGGAAG 1260
AAACTGGGTC TGTCAGGGTT TGTGAACCCT GTAGCTCTCT CTCCTCCTGG GCCTCAGGGC 1320
AACCCCTGCT TTAAGCCTAC ATTTAAATCC TCTTCTTGAA 1360
|
