| Tag | Content |
|---|
EnhancerAtlas ID | HS091-03012 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:155151320-155152100 |
Target genes | | Number: 36 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr1:155151535-155151550 | TGACCCTTGCCCTCT | - | 6.39 | | Nr2f6(var.2) | MA0728.1 | chr1:155151519-155151534 | TGACCTTTTGTCCTT | - | 6.82 | | SPI1 | MA0080.4 | chr1:155151825-155151839 | AGAAAGGGGAAGTG | + | 6.22 | | SPIB | MA0081.2 | chr1:155151827-155151839 | AAAGGGGAAGTG | + | 6.07 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_25271 | chr1:155151846-155152505 | Colon_Crypt_3 | | SE_41836 | chr1:155145054-155151547 | LNCaP |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 155151396 | 155151574 | | chr1 | 155151423 | 155151800 |
|
Enhancer Sequence | AGGCAAGTCA GCGGCCCTGC CCCGGGGGCC CTGCCCGCCG CCGGGCCCCC TTCCCACCCC 60
GCTGCTCCCA CGCATCTCAG CCAACCACTC ATTGCTTCCT TCTCTTTCCT GCCTTGCCCC 120
GACCTCGTGG TCCTCCCACT GGACCAATGC CCTGTCTCCC TTCTGCCTTC TTCAGGCGCT 180
TGCGTAATCC TGGCCCTTCT GACCTTTTGT CCTTGTGACC CTTGCCCTCT GGCCTTGCAC 240
TTCCTTTCCC TTGACCTCCA ACCCCTGCCC TCAGCTTTTG CTGTCCCTCT GTTGTCCCCA 300
CTTTCCACCT CGCTGCCTCC TAAATCTCTC TTCTGAGCCT GGTCCCCTTC CTTCCTGCTC 360
AGCGCCCTCT TGCCTGTGGG CTCCAGTGGC CTTTGCCTGC CCCTCCCTGG GGCTCCTCTT 420
AATTCATAGA ATAACTGAGC TGCAAGGGCC CCCAGAACTT ACCTGATCTG ATACCCTCAT 480
TTGACAGGGG AGGAAACTGA GGCCCAGAAA GGGGAAGTGA CTTATTCCAG GCCAGAGTGA 540
GGTAGCAGCA GCCCAGAACT AGCACACAGG TGTCCTGACC CCCAGCCCAG CGCTTTCCTG 600
CCTCGTTCTC TCTTGGGCCC TGCCCTACCC CTCCTGTGCC CAGTTCCCAG ATGAGCCCTT 660
CCCCAGCTCC CTCTCACCCA CACTCACCCC CCCGGCTCCC GCTGCTTTCC CTTTTCCTGC 720
CTGCCCCTGC CCTCCATGCC AGGCCAGTGG CCAGGCCCTG ACTGACACCC GCTGTCTCTT 780
|
