| Tag | Content |
|---|
EnhancerAtlas ID | HS002-07251 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr4:1748460-1749670 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr4:1748655-1748666 | ACAGGGTGTGG | - | 6.14 | | REST | MA0138.2 | chr4:1749291-1749312 | GGAGCTGTCCTGGGGGCTGCC | - | 6.53 | | Zfx | MA0146.2 | chr4:1748756-1748770 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_25282 | chr4:1747966-1748618 | Colon_Crypt_3 | | SE_25282 | chr4:1748689-1749125 | Colon_Crypt_3 | | SE_47504 | chr4:1748386-1749508 | Pancreas | | SE_69102 | chr4:1747149-1748683 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr4 | 1748791 | 1749189 | | chr4 | 1749368 | 1749530 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I001745 | chr4 | 1747241 | 1752336 |
|
Enhancer Sequence | TCCTGACTGG CTTCCCAGGA CCATCGCGCC CCTCCCTCCC GTGGGCAGCA ACCCCCATCT 60
CAGCCCCGAG CCTGGGTAAC AATAGGGTGT AATCCCTGGC TGAGGGGCCT CTGAGAGCCT 120
TCCGTGGCCC ACTTCACAGA CGAGAAACCG AGGCCCACAG ACCAGTGGCC ATTGGCCGGG 180
GGAGACGGGC CAAGCACAGG GTGTGGGCCC CCTCTCCTGC TTGGGGTTGA GGATATGGGG 240
GAGAAGAAGG GCCCTCGAGC CTCCAGAGCT CACCAGCTGC CCTATGGGCA GCACGGCCCG 300
CCTCGGCCTC CCCGCTGCCC ACAGGCATGT CCGGCCGCAG GACTCCCACC TCTCTTTGCC 360
GGGTCAGCTC TGCTCTGACA AGGTCTCAGG ACACAAGGCG GCTGCCAGGT CCTCCTCCTC 420
ACTCAGCCCT GCCGGTCTGG CCTTCTGGCT CCTCTGACAG CTGCCCAGGG CCCTGTCCCC 480
TGCTGGGGCC TCTCTGAGCC AAGCCGGGAG CCTGCCCGGA GAAGGCCGTG CAGGGCGGCT 540
GAACGTGTCA GGGCACCTGG CCGGGCCTGG GGCCGCGCCG AGGACACCGG CCACCAGGCA 600
GCGTCCTGGG CCGGGAGCCT CTCTCCCAGG ACAAAGGGGC CTTGTGTGGC TGAATGGGTG 660
TTTATCCTGG AGCCTGAGTT AACTCAGGGC TGCGAGGCCG GGCGGGGGCC CTGGCACTGG 720
CCTGCCTGGT AAACATGACC TGAGCTGGGC ACGCAGCCGT GGCCTGGACT TCCGCAGCCC 780
CGGACCCCCT GCACATCCAC GCAGTCGCCT TGTGGGGGGC TCAAGGAAAC AGGAGCTGTC 840
CTGGGGGCTG CCTCCGTGGG AGTCCTCATA CACAGTCATG GAGGCAGCGC TCGGCTCTGC 900
CCTTCCCACA GCTCAGGGCA GGGCTCAGAA ACACCCCCCC GACGTGCCCC ATTGGAAGGA 960
GGGGTGAGGG TTAGACGAGG TCGTGAGGGT GAGGCCCTGG TCTGCTGGGA TTAGTGTCCT 1020
TGCGGGAAGG CAGCAGGCCG GGAGAGCACT TTGGAGGAAC TGACCCGCCA GCACCCTGAT 1080
GGCGGACTTG GCGCCTCCAG AACCCAGAGA AACACGTGTC TGTGGTGCAA GCCATCTGGT 1140
CCCAGGCAGG ATGAGACCCC GCCGTCCGAG GGGCTGTCCA GCCTGGTGCC CACCCACTGC 1200
CCAGCTCCCC 1210
|
