| Tag | Content |
|---|
EnhancerAtlas ID | HS091-33343 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr22:45131040-45132650 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr22:45131897-45131916 | GCCCGCCACCTGGTGGCCA | - | 7.51 | | Myod1 | MA0499.1 | chr22:45132545-45132558 | TGCAGCTGCCCCT | + | 6.22 | | RARA(var.2) | MA0730.1 | chr22:45132375-45132392 | AGGTCAAACAGAGGTCG | + | 6.57 | | REST | MA0138.2 | chr22:45131247-45131268 | GGCAACACCTTGGAGAGCTCC | + | 6.97 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 45131285 | 45131498 | | chr22 | 45131593 | 45131600 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I044735 | chr22 | 45131474 | 45132490 |
|
Enhancer Sequence | GGGTAGGGGT CCGCCTGGGC CTTGGGCTGG GGCAGGGGTG ACCACGGGCC CCATCCATTG 60
TGAACAAATG GGCAAGCCGA GGCCCCACGA CAGAACCAGG ATCTGACTCC AGACTGGTTC 120
TCAGCCGGGC AGCAGCCCCC AGCCTGCCAT ATGCTGGCCT GGACGTGGGG ATCCGTGAGA 180
GTGGGCACAC ACCCTGAGCG GTGATGTGGC AACACCTTGG AGAGCTCCAC CAGACCTCCG 240
TGTTCCCCAG GAGGCCACAT TCATGTGCAG TCTTGAAAGT CAGAAGTGGG CCAGGCGGAG 300
TGCTCGGAAC ATGCAAATGC CGAAGCTTGA GGACTCCTGG CTCAGTTAGG GGACCCAGGC 360
TGGGAGGGAC TCGGCCTGGG GGTGGGCAGG CTGAGCCCTG TGGGCAGCAT CCCGGGACTG 420
CTTGGCGCGT CCAGCACAGC TGGCCACGTT GCTCCCTTGA CGGAGGGCCT CTGGGTTCCT 480
TCAGCAATGT CCCTTGAGTA CCTGTTGTGC CCCATCCCGA GCCCACGCCC TTCCCCTCCC 540
GCGGGGGAGG CCGACCAGTG AGTCTCCTCC ACGACCCACC ATTAGCTGGA AGCTGGGAGC 600
ATCCCAGGCA GAGGGGACAG AGCTGGGGCA AGGCCCGCTT GGGACTATGC CCTCCTCATC 660
CAGAGGGGCT CCCCGTCCCC ACCTGCTGGT GTAAAACCTG CCCACTGGTG TGTCTCAGCT 720
CAGGCAGTGC CCTGGCTGCT GGAGAACTTT GAGCCACCCA GGCTTGGTGT AGCCCTGGAT 780
GGCAGGACCC CAGCCCCTGC CTGATGGGAC CCGCATCCTC TGGTCTGGGA AAGGCCCCTG 840
AGCCGCTCGT GTGTGTCGCC CGCCACCTGG TGGCCACTCT TGGGATTGCA GGGTCCTGCA 900
TGGGAACCTG AACCCTGCCC CCCAACCAGC CTTGGCCACC TGTGCCACTG CCTCCCGCCC 960
AGATGAACCA AGGGGCCTCC TCCCTGGGTC CCCACGTCTA CCCTCAGCCC CCACAGTCTA 1020
TTACTCTCCA CGCAGCGGCC AGCGAGGCCC ATTTACAACT GCCTGGCTAC AGGCTCCCCG 1080
CATCCCCAGG ATGGAATCCC CGCCTTGACC TTACATGGAG GGCCTGTCCC CATCTGCTCC 1140
CATCACAGCC CCACAACCTG GCCCCATGGC TCGCCTCTTT GGGCTTCTTG GCCCTCCCAC 1200
CATCCCCTTG GACACCAGCT CCAGTGGGGC AGGGGCTGCG CCTGCCTGGG AAAGTACAGG 1260
TGTCCAGCAG GTGCCAAAGT CCATACACTT CCACAAGTGG GGAAACTGAG GCACGGGGGT 1320
GAGGTAACTT ACCTAAGGTC AAACAGAGGT CGCTGGCGGG GTGCAGGTTC AAACCCAGGC 1380
ATTTGACTTG AGGTCCTGTG TGACCAGGCT GGGCCTAGGC TGGAGAAGAG AGACTGGAAC 1440
CTGAGCTGGT GTCAGGGCTT GTGGCGGTGG GACCTGCTGA GCCGGGCCCC GGGTCGGGCC 1500
TTCCCTGCAG CTGCCCCTGC ACAGGGACCC AGTGTGCAGT GAGCAGCAGG TGCCAAGGCG 1560
GGCGGGGACC CAGGTGGCCT CTGGTGTGAC AGTGCCCGTG TCTCTCCCCA 1610
|
