| Tag | Content |
|---|
EnhancerAtlas ID | HS098-05849 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr10:830400-831560 | 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 | GGGGTAATTG AGAGGCCCCG TCCCTCTGTC CACCTCCCAG ACCAGCCAGC ACCTGGTGAC 60
AGGGCCAAGG CGGCAGCCGG GGCAGGATTT GCAATGCCTC CTGCAGGCGA CAAACTGTCT 120
CCCAAGGCCA GACGCAGACA GAGCTGTCAC CGCTCCCACG CCCGGCGTTC CGGGAGCCTC 180
CCTCCCATCC CCAGCAGCAG ACGCCACCTG CCCCCCACCT CCCGCCCCGG GGTCTGAACT 240
CCCAGCCAAG CCCGGCCTCT GCACACAGCA GTGAGAAGCC AGGACCTACG CACACCCCTG 300
GCCGGCTCCC CGCTGGCCCC TCTGCGCGTG GGAGCTTCCA GCCTCCCGGG TCTAGGGGAC 360
TGGGGGATGC GTCTTCCTCC CGCCCCCGCA GCGCCCGGGG CAGGAGTGGC ATCGGCGTCC 420
CCGGCGTCCC CGCATCGGGC TTCTCTGGTC CTTTGTGAAT CGGGCCTGAG TCATCCCCGG 480
CTCACGGCTG CGCCACGTAC CCACTGGGCG CTTTCCTCCG AGCGCTGACG ACAGCGACTC 540
CACCGGCAGC TGCTTCCCAG CGTCTCACGG CGGGCCCTTG GCTCCCCTCT CTGCTGTTTA 600
ATCCGCTGAG GAGCCCTGGT GAGCACGAGA GGGGCTCGTG GCTGATCAAT GCGGGCCGAG 660
GCTGCTGGCA CCTTTCTCCA GGAAACACAC CTGGCGTCCT GCAGGGGCCG GACCGGAGAA 720
GCCCTGTGTG CCCCATACAG CGTGTGCTGC GGGGCAGCCT TTGTGCCCTC GAAGCCGGCC 780
AGGGCCTCCG AGGACTGTTC CAGGAAGGCT CCAGAGAGCA ACGTCCCCAG TTCACTCACA 840
GCTGGCCGCC CCCAGCCCCC TGCCCGCAGC ACCCGCCGTG TCTCCTGCTG GGAAGAGTGG 900
CTGCTGTAGC TTCCTCCCCC TGCCCCTCCT GCCCGCTCTC CTGCCCCATC AGCATCTCAG 960
GGCCGCATGG AAAGCTGCGG GGTGTCAGCA CAGGCCAGGG TGGGCTGTGG AACAGACACC 1020
CCAAGGCAGG GCGTTGGCAG GCGAAAGCTC CTGCCTCCCT GGCGTGCTGG CTGGAGGGGT 1080
CCATCGGCCC CCAGGACACT GCCCTCCTTC ATGTCCCCGC GCAGCCCTGG GAGGAGCCTG 1140
GAGGGTCAGT GCCGACTCTG 1160
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