| Tag | Content |
|---|
EnhancerAtlas ID | HS187-00676 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:40425540-40426980 |
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 | ACACCAGGGG AACTGCAGAA TCCTGGGCTG GGAATTAGAC TTCAGGCCCA GCCTGCTGCA 60
TCTCTACCTC CATGTGGGAC CCTCCAACAG CACAGTGATA AATAATTTGG CACCCCTTCA 120
GGGTGGCTCC TGGCAGAGCA GGGGATGGGG TAATACCCGG AATGGGGTAG CAAACCCATA 180
ACCTTTGGCA CCTTGGATGA CGTAAATTAC CTTCTCCCTT GGTACAAAGC CTGTGCTACT 240
CAGCTTCAGG GGCAAAGTAG GCGGAGGTGG TGCCACGGAT CGGATCAGAC GGCAGGGGAG 300
ACGCACAGGA TAGGCTGTCA GGCGGGGGCT CTGGTTCCCT CCAGGACATC CTGCTTCAGG 360
GTGTGGGGGG GCATACCCCT TTCATCTCCA GCCCATCCAG GCTTAAGTGG GCGCCTTCCT 420
GCCCCAGGGG CGCCCATACC TGGCCTCCGG CCTTCAAAGC TCTTCCCGCA ACCCCTTCCC 480
CCACTACAGC TTCCTTTCCC ACGAGGCCCC CCACCCACCC CAATCCTGCC AGCCCCTGGC 540
TAAGGCCCAG GTTGGAGCCT TTGATCCAGT CTTCAGGGCC GGGGGCAGGA CAGCCTGCCT 600
TACCTGTGCA GGCTGCTCAG GGCTCCCCCG GCGCCAGCCC GTGAGACTTG GCCCTGTGCC 660
CGCCTCCCTG GCAGCCAGTA GAAGGGGAGG CTCTGCTGCC ACGTCGCCTC ATGAGGCCCA 720
GCCAATGGGA GGCAGCCGCT CCCAGGGATG GTGGCTGCAG GCCGGGTTAC TCCCAGTTAC 780
ACTGGGTTCC TCAGCAGCAG CTGCTCAGCT GCTTATGAGC AGAGGATGGA GTGTTTGACA 840
AAGGCTGATG AGGAGCTCTT GTTCCCTGAG GAGACAGAGT CAAGAGAGGT GGAGGTGGGC 900
AGGCCTTCCC TGTGGCATGT AGGAACTGAG CAACTTCCTG GGCAGGCGTG GCAGCCAGTT 960
TGGGGAAGTT GCTGGGGGCC CTTCAGGCTG GTTTCTGATC TAGCAGGTGC CTGTGTGCAC 1020
ATGCTTCTGT GGCTGGTGGT GCCTGTGTAT GCCTGCACGC GGGATGGCTC GTGGGCTGAA 1080
GGCTGGTGTG CATATGACCT CCCTGTCCAA ACTTTTTTTC CTTTTTGTGG TGAATGGGGT 1140
CTGGCTATGT TGCTCAGGCT GGTCTCAAAC TCCTGGGCTG GAGCTATTCT CCTGCCTCTG 1200
CCTCCCTAAG TGCTGGGATT AAAGGCATGA ACATCACCAT GCCTGGCCAG ACCTCTCCAT 1260
CCATACCACC TGACCCCTCC TCAGGCCAGG CCTGGAGACC TGGAACCCCC TTTCCTTTCA 1320
GTGTAGGAAG AAACTGGGTC TGTCAGGGTT TGTGAACCCT GTAGCTCTCT CTCCTCCTGG 1380
GCCTCAGGGC AACCCCTGCT TTAAGCCTAC ATTTAAATCC TCTTCTTGAA ACCAGGAAGA 1440
|
