| Tag | Content |
|---|
EnhancerAtlas ID | HS138-10491 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr12:112740440-112741600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr12:112741322-112741333 | AAAACAAAGGA | + | 6.32 | | Sox3 | MA0514.1 | chr12:112741322-112741332 | AAAACAAAGG | - | 6.02 |
|
| | 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 |
| GH12I112302 | chr12 | 112740036 | 112741949 |
|
Enhancer Sequence | CTTCTTCCCC TTGGCCTTCT TTCCTTTCAG CGTCTTGGGC AGTGGGAGGC CAGTTAGCTG 60
TTTTTTAACT TTTTCTCATT TTTAATCTTC ATATTAGAAG CTTTCCTCAC TTTTCTAATG 120
ATCCTTGGTA GTCTGCTCTT TTTGTTTAAT TTTAAAACTT TTTATTAGGG AAAATTTTCA 180
ACACACACAA AAGAAAAAAG AATAGAACAA TGAGCTTCCT ATGTGCTGAA CCCCTGGCTT 240
CAATCATTAG CACTATTTTT TTAACCCATT TGCCTCCCCT CCATACACAT ACCTCTCCAA 300
AGTTTGGAAT TTTGTTTGTT TGGGTTTTTA TTTTGTCTGC TCTTTTTTTT TTTTTTTTTT 360
TTTAACAGTT CAGCACTAAT CAGGAATTCT GTGGACAGGG TTGAGTCTTG CTTGCTGGAA 420
GACATCACTT GTGGGTGATT CACCAGGGAG GCAAGTCTTT TTCCTAGATG ACCCCAACAT 480
CAGTATGAGA GGTCTTTTTT CCAGGGTCAT TCAGTTTCTT CAGAAAATAA CTAAGTCTTG 540
GGCCTGGACA GCCAGCATCT GAATGCAAAT GTGTGAACAG GAAGGGGGCC TGCAGGCCCT 600
TATGTAAACT CACGGTCTAC CACCTTGTCT CACAATGGCT GTGTACCACA TCTGATGTCC 660
CAGTTGCTAA CATGCTCTAA GGCTGGTGGG GTGAGTCATC TCTCTTCCTC TGGGTATTCC 720
CCTAAACGTA TACTTGGCTT TCTCCACACG GAAGTATGAG AAAGGATACT ACACTCTCCA 780
TCTTATCTTC TAAAAGTAGG GGGATAAGAG ATACTGCCTA GAGTTCATAA AGAAGAAATA 840
AAGGTTTAAC TGTAAATTAC AAAGATAACT AAAAGAAAAA CTAAAACAAA GGAAATCAAT 900
ATGCTAGGCG GAATCAGAAA AGAAAGAGGG AGGCCAGGTG TGGTGGCTCA GGCCTGTTAT 960
CCTAGCACTT TGGGAGGCTG AGGCATGCTG ATCACTTGAG CTCAGGAGTT CGAAGCCAGC 1020
CCAAGCAACA TGGTGAAACC CTGTCTCTAC AAAAAAACAC AAAAATTAGC TGGGTGTGGT 1080
CATGCACGCC TAAGTCCCAG CTACTTGGGA GGCTGAGGTG GGAGGATCAC CTGAGCCCAG 1140
GAGGTTGAGG CCACAATGAG 1160
|
