| Tag | Content |
|---|
EnhancerAtlas ID | HS064-00524 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr1:51769170-51770540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr1:51769961-51769972 | CATGAGTCACT | - | 6.14 | | GLIS1 | MA0735.1 | chr1:51769309-51769325 | AGACCCCCCACCTTGT | + | 6.23 | | IRF1 | MA0050.2 | chr1:51769569-51769590 | GAAACAAAACTGAAAGAGACC | - | 6.28 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65473 | chr1:51767666-51773031 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I051303 | chr1 | 51769074 | 51770233 |
|
Enhancer Sequence | TGAGGGCCCA AGGTCTGGTT GGGAGCAGGA GAGACACGGA GGTGGATGAT CCCAGCCATG 60
GGCTCAGGGC ATAGGTGGGG CCTGGGAAGG CTTCCTGGGG GAGAAGCCTC CAGAGCCTGG 120
CTGGGGAGGG GCTGGGGGCA GACCCCCCAC CTTGTTTCCC TGCCTGCAGT CTCTGCCCCT 180
CTGTCTGTCC TCCAGAGCAT TCTTGTTCTT TCTAAAACAC AAATCTGACC TGCCTCACTC 240
CTGCCTCAAA CCCTCCATGG CTCCCCTGCC TTCGAGATAA AGAGGAAGCC CAGGCTGGCA 300
CAGTAGGTCC CGCAACCCTC CTGGCCAGGC CACACTGCCT CACCTCTGGG TCCTCCCTTC 360
ATCCTGAAAT CCTACTCATG ACCCATGCGC TTTCTTAAGG AAACAAAACT GAAAGAGACC 420
TTCACAGCCT CTAGCCAATG TTTTCCAAAG CTCGGGCAGC AGATAGCAGC TAAGATTTCA 480
GGGGTCCATG GGCAGATGCC AGGAAACACT GAGTCACGGT GAGGGTTTTC CCTTCTGTTA 540
TCTTTCTATC CTTTGGTGGT GCCCAGGAGA AATCCCCAGT CCTTTGCTCG TGGGGTTTGA 600
ACTCTCTCAC CCTAAGCCCG CTTTCTCAGA AAGAGGAAGC CTGGCTGAGC CTGGGCTACA 660
CAGTCTAGCT GGGCTTTCCA AAAGATGGCT GGGCCCTCGT GGTATTTATT TTTATGATTA 720
TGTTCTTATC ATGCCAAATA ATATGGAGGT TTGTGTAGAG ATGTTTCCTT TAAATCAATT 780
TCAGTAAAAG TCATGAGTCA CTTTTGAGAA AAGTAATATA TAAATTATAA TAGAGAGGTC 840
CGTGGGTGTG GCAAATATCA GTAAGGGCCA GTGCACGTTT GAGAAACATT TATCTGGTCC 900
ATTAACAAGG CCCTTATTTT ACTAAAAAGA GGCTCAAAGA AGAGAGGGAC TTGCTCAGAG 960
TCACAGAGAA AAGGGGATGA GGCTGGACTG ACCCAGAGCT CCTAACTTCC AGGCCAGTGC 1020
TCCTTCTACC ACACTAGGCC TCCTCCACCA GAAAGCCCTC CCTGATCTGC TGCCTTCAAC 1080
CTGGGGTTGG TACTCAGGTT CTTGCCCTCA GTAAAGTCTT TGGGTGCTTG AGTTCTCTGG 1140
TTCCTCCTCA AGGTCTGATG CCCAGTAGGG CTTCCCTCAG GCATCTGCTG GATGAAGTGG 1200
TAGCACCAGA AAATGGTCCT TGGGGGAAGG ACTTACTCAA AGTCTTAAAG TGAGGCAGTA 1260
TCTAGGGAGA GAGGGACCAG CCCCTGACAC CTGTCAGGCT CAGAGAATGT GTGATCCTGG 1320
GCCACTGATG GAGCTGCCCT TCACACCCAC ACCCACCCAG AGCCTCTGCA 1370
|
