| Tag | Content |
|---|
EnhancerAtlas ID | HS062-09385 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr2:131554920-131556090 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr2:131555179-131555198 | CTGCCAGCAGGGGGCGCGC | + | 7.01 | | KLF5 | MA0599.1 | chr2:131555097-131555107 | GGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr2:131555667-131555677 | GGGGCGGGGC | - | 6.02 | | Zfx | MA0146.2 | chr2:131555096-131555110 | CGGGGCGGGGCCTG | + | 6.18 | | Zfx | MA0146.2 | chr2:131555556-131555570 | CAGGCCGAGGCGGC | - | 6.62 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_35158 | chr2:131554897-131556123 | HeLa | | SE_60027 | chr2:131554825-131595595 | Ly4 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 131555592 | 131555820 | | chr2 | 131555325 | 131555417 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I130797 | chr2 | 131554621 | 131556434 |
|
Enhancer Sequence | AAAGTGCTTG GATTACGGGC TTGAGCCACC GCGCGGGGCC TCTTTGGGGG CTTTTCATAA 60
GGGTGTGTAG AATGTCAGTA AGAGGCTGCT TCTTCAGAGC CCTCTTCGTG CTACATAAGC 120
CGGGCAGGGT GGATAGAAGT GGGTCTCTTG CTGCCTGTGG CCCTGAAACC CAGCCACGGG 180
GCGGGGCCTG ACTTCTTAGC GCAGTCCCCC TGCCGCGTGG AGGACCCTGC TCTCCGGCCC 240
AGCATAGAGC GACTCCCTCC TGCCAGCAGG GGGCGCGCGG AGCTGTCTCT CCGGAGGCTC 300
CCGGCGGCTC AGTCTCGGAA CCCGCAGCCG GGAGCGCAGG GCGGGCCACA CAGGGCGCCA 360
GCACCTCCCA CGAGCTCCGC GGGCCTCGCA TCCGGAAGAC GCCCCGGCTG ACCGCGCGAA 420
TGGCTCGCGC TGCCGCGGAC ACCCGCCTGC CAGGGACGGG GCCTCTCTCC TGGGCCGTTT 480
CATCTCACCG AGAGCGAGAT CCGCTTTCCT AGAGGCTGGG AGGACCAGGC CCGGGCACAG 540
GACTGGCTTC GCACCACTGG CCCCGCAGTC GGGTCCCCGG GGACGCGCCA CGGGTCACTG 600
CTGCCTGCTA AAGCGACACA AGGCGCCTTC ATTCCTCAGG CCGAGGCGGC CGAACGCCTT 660
GGCTCTGGCC GACAGTGAGC ACCCACTGCG AGTCCGCACA CACTGCAGCG CCCCCGGGCA 720
CGCCCCGCAG TCCGCCCAGC GTCCCCCGGG GCGGGGCACA GCCAGAGGAC GGCCCGAGAG 780
CCCTGCTGTC CCCGTCAGCG CCGCAGGAGG GCGCGACTTC CCCGCTGGGC CGAGGCCTTT 840
GCCGGGCCCT CTACTGTACG CCGGTCCTAG GGCTGGGACC GCCGTCCTGG ACCGACCTCA 900
GCCCACTGTT CTGCGGAGGC CGCGTGTTGG GCGACAGCAG CCACCCAGCC CGGAAGCAGC 960
CGTTCCGAGC GCAGGGGCGC CAAGAGCCCC GCGCCCCGCC TGTGCGCCGG CCCTGAGACT 1020
TGGAACGATG GTGCAGGCAG GAGGGGTCAC CGGTAGGGAT GCCACTGGAG GGACTGGGCC 1080
GTCCACACGG ACCAGCTGAC ACACTAAGTG CTGGGTACAC AGCAGGACAA TGGCAAGGGC 1140
TGCTCAGACT GCGTTTTTAA AATCGCCTCA 1170
|
