| Tag | Content |
|---|
EnhancerAtlas ID | HS141-00493 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:40425630-40426980 |
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 | CACAGTGATA AATAATTTGG CACCCCTTCA GGGTGGCTCC TGGCAGAGCA GGGGATGGGG 60
TAATACCCGG AATGGGGTAG CAAACCCATA ACCTTTGGCA CCTTGGATGA CGTAAATTAC 120
CTTCTCCCTT GGTACAAAGC CTGTGCTACT CAGCTTCAGG GGCAAAGTAG GCGGAGGTGG 180
TGCCACGGAT CGGATCAGAC GGCAGGGGAG ACGCACAGGA TAGGCTGTCA GGCGGGGGCT 240
CTGGTTCCCT CCAGGACATC CTGCTTCAGG GTGTGGGGGG GCATACCCCT TTCATCTCCA 300
GCCCATCCAG GCTTAAGTGG GCGCCTTCCT GCCCCAGGGG CGCCCATACC TGGCCTCCGG 360
CCTTCAAAGC TCTTCCCGCA ACCCCTTCCC CCACTACAGC TTCCTTTCCC ACGAGGCCCC 420
CCACCCACCC CAATCCTGCC AGCCCCTGGC TAAGGCCCAG GTTGGAGCCT TTGATCCAGT 480
CTTCAGGGCC GGGGGCAGGA CAGCCTGCCT TACCTGTGCA GGCTGCTCAG GGCTCCCCCG 540
GCGCCAGCCC GTGAGACTTG GCCCTGTGCC CGCCTCCCTG GCAGCCAGTA GAAGGGGAGG 600
CTCTGCTGCC ACGTCGCCTC ATGAGGCCCA GCCAATGGGA GGCAGCCGCT CCCAGGGATG 660
GTGGCTGCAG GCCGGGTTAC TCCCAGTTAC ACTGGGTTCC TCAGCAGCAG CTGCTCAGCT 720
GCTTATGAGC AGAGGATGGA GTGTTTGACA AAGGCTGATG AGGAGCTCTT GTTCCCTGAG 780
GAGACAGAGT CAAGAGAGGT GGAGGTGGGC AGGCCTTCCC TGTGGCATGT AGGAACTGAG 840
CAACTTCCTG GGCAGGCGTG GCAGCCAGTT TGGGGAAGTT GCTGGGGGCC CTTCAGGCTG 900
GTTTCTGATC TAGCAGGTGC CTGTGTGCAC ATGCTTCTGT GGCTGGTGGT GCCTGTGTAT 960
GCCTGCACGC GGGATGGCTC GTGGGCTGAA GGCTGGTGTG CATATGACCT CCCTGTCCAA 1020
ACTTTTTTTC CTTTTTGTGG TGAATGGGGT CTGGCTATGT TGCTCAGGCT GGTCTCAAAC 1080
TCCTGGGCTG GAGCTATTCT CCTGCCTCTG CCTCCCTAAG TGCTGGGATT AAAGGCATGA 1140
ACATCACCAT GCCTGGCCAG ACCTCTCCAT CCATACCACC TGACCCCTCC TCAGGCCAGG 1200
CCTGGAGACC TGGAACCCCC TTTCCTTTCA GTGTAGGAAG AAACTGGGTC TGTCAGGGTT 1260
TGTGAACCCT GTAGCTCTCT CTCCTCCTGG GCCTCAGGGC AACCCCTGCT TTAAGCCTAC 1320
ATTTAAATCC TCTTCTTGAA ACCAGGAAGA 1350
|
