| Tag | Content |
|---|
EnhancerAtlas ID | HS034-03007 | Organism | Homo sapiens | Tissue/cell | ECC-1 | Coordinate | chr10:830370-831440 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr10:830865-830876 | CTGAGTCATCC | - | 6.32 | | JUNB | MA0490.1 | chr10:830865-830876 | CTGAGTCATCC | - | 6.14 |
| | | 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 |
| GH10I000783 | chr10 | 829643 | 831697 |
| Enhancer Sequence | ACCTCCCAGG CCGGCCAGCA CCTGGTGACG GGGGTAATTG AGAGGCCCCG TCCCTCTGTC 60
CACCTCCCAG ACCAGCCAGC ACCTGGTGAC AGGGCCAAGG CGGCAGCCGG GGCAGGATTT 120
GCAATGCCTC CTGCAGGCGA CAAACTGTCT CCCAAGGCCA GACGCAGACA GAGCTGTCAC 180
CGCTCCCACG CCCGGCGTTC CGGGAGCCTC CCTCCCATCC CCAGCAGCAG ACGCCACCTG 240
CCCCCCACCT CCCGCCCCGG GGTCTGAACT CCCAGCCAAG CCCGGCCTCT GCACACAGCA 300
GTGAGAAGCC AGGACCTACG CACACCCCTG GCCGGCTCCC CGCTGGCCCC TCTGCGCGTG 360
GGAGCTTCCA GCCTCCCGGG TCTAGGGGAC TGGGGGATGC GTCTTCCTCC CGCCCCCGCA 420
GCGCCCGGGG CAGGAGTGGC ATCGGCGTCC CCGGCGTCCC CGCATCGGGC TTCTCTGGTC 480
CTTTGTGAAT CGGGCCTGAG TCATCCCCGG CTCACGGCTG CGCCACGTAC CCACTGGGCG 540
CTTTCCTCCG AGCGCTGACG ACAGCGACTC CACCGGCAGC TGCTTCCCAG CGTCTCACGG 600
CGGGCCCTTG GCTCCCCTCT CTGCTGTTTA ATCCGCTGAG GAGCCCTGGT GAGCACGAGA 660
GGGGCTCGTG GCTGATCAAT GCGGGCCGAG GCTGCTGGCA CCTTTCTCCA GGAAACACAC 720
CTGGCGTCCT GCAGGGGCCG GACCGGAGAA GCCCTGTGTG CCCCATACAG CGTGTGCTGC 780
GGGGCAGCCT TTGTGCCCTC GAAGCCGGCC AGGGCCTCCG AGGACTGTTC CAGGAAGGCT 840
CCAGAGAGCA ACGTCCCCAG TTCACTCACA GCTGGCCGCC CCCAGCCCCC TGCCCGCAGC 900
ACCCGCCGTG TCTCCTGCTG GGAAGAGTGG CTGCTGTAGC TTCCTCCCCC TGCCCCTCCT 960
GCCCGCTCTC CTGCCCCATC AGCATCTCAG GGCCGCATGG AAAGCTGCGG GGTGTCAGCA 1020
CAGGCCAGGG TGGGCTGTGG AACAGACACC CCAAGGCAGG GCGTTGGCAG 1070
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