| Tag | Content |
|---|
EnhancerAtlas ID | HS082-03642 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr10:830180-831610 |
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: 2 | Chromosome | Start | End |
| chr10 | 830904 | 831008 | | chr10 | 830317 | 831561 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I000783 | chr10 | 829643 | 831697 |
|
Enhancer Sequence | TCCGTCCACC TCCCAGGCCG GCCAGCACCT GCTGACGGGG GTGACCGAGA GGCCCCGTCC 60
CTCCGTCCAC CTCCCAGGCC GGCCAGCACC TGCTGACGGG GGTGACCGAG AGGCCCCGTC 120
CCTCTGTCCA CCTCCCAGGC CGGCCAGCAC CTGCTGACGG GGGTGACCGA GAGGCCCCGT 180
CCCTCTGTCC ACCTCCCAGG CCGGCCAGCA CCTGGTGACG GGGGTAATTG AGAGGCCCCG 240
TCCCTCTGTC CACCTCCCAG ACCAGCCAGC ACCTGGTGAC AGGGCCAAGG CGGCAGCCGG 300
GGCAGGATTT GCAATGCCTC CTGCAGGCGA CAAACTGTCT CCCAAGGCCA GACGCAGACA 360
GAGCTGTCAC CGCTCCCACG CCCGGCGTTC CGGGAGCCTC CCTCCCATCC CCAGCAGCAG 420
ACGCCACCTG CCCCCCACCT CCCGCCCCGG GGTCTGAACT CCCAGCCAAG CCCGGCCTCT 480
GCACACAGCA GTGAGAAGCC AGGACCTACG CACACCCCTG GCCGGCTCCC CGCTGGCCCC 540
TCTGCGCGTG GGAGCTTCCA GCCTCCCGGG TCTAGGGGAC TGGGGGATGC GTCTTCCTCC 600
CGCCCCCGCA GCGCCCGGGG CAGGAGTGGC ATCGGCGTCC CCGGCGTCCC CGCATCGGGC 660
TTCTCTGGTC CTTTGTGAAT CGGGCCTGAG TCATCCCCGG CTCACGGCTG CGCCACGTAC 720
CCACTGGGCG CTTTCCTCCG AGCGCTGACG ACAGCGACTC CACCGGCAGC TGCTTCCCAG 780
CGTCTCACGG CGGGCCCTTG GCTCCCCTCT CTGCTGTTTA ATCCGCTGAG GAGCCCTGGT 840
GAGCACGAGA GGGGCTCGTG GCTGATCAAT GCGGGCCGAG GCTGCTGGCA CCTTTCTCCA 900
GGAAACACAC CTGGCGTCCT GCAGGGGCCG GACCGGAGAA GCCCTGTGTG CCCCATACAG 960
CGTGTGCTGC GGGGCAGCCT TTGTGCCCTC GAAGCCGGCC AGGGCCTCCG AGGACTGTTC 1020
CAGGAAGGCT CCAGAGAGCA ACGTCCCCAG TTCACTCACA GCTGGCCGCC CCCAGCCCCC 1080
TGCCCGCAGC ACCCGCCGTG TCTCCTGCTG GGAAGAGTGG CTGCTGTAGC TTCCTCCCCC 1140
TGCCCCTCCT GCCCGCTCTC CTGCCCCATC AGCATCTCAG GGCCGCATGG AAAGCTGCGG 1200
GGTGTCAGCA CAGGCCAGGG TGGGCTGTGG AACAGACACC CCAAGGCAGG GCGTTGGCAG 1260
GCGAAAGCTC CTGCCTCCCT GGCGTGCTGG CTGGAGGGGT CCATCGGCCC CCAGGACACT 1320
GCCCTCCTTC ATGTCCCCGC GCAGCCCTGG GAGGAGCCTG GAGGGTCAGT GCCGACTCTG 1380
ACGTGCCCCC ACAGGTGACA GTCATTTCTG CCCAATTTTA TTGTTCAAAG 1430
|
