| Tag | Content |
|---|
EnhancerAtlas ID | HS098-38646 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:50552860-50554700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MSC | MA0665.1 | chr3:50553528-50553538 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr3:50553528-50553538 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr3:50553528-50553538 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr3:50553528-50553538 | AACAGCTGTT | - | 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 |
| GH03I050514 | chr3 | 50552257 | 50555213 |
|
Enhancer Sequence | CTGCAGAACG GGAGCTCTTG GTACCCCGGC CCAGCTTGCC CCTCAGTTGC CAGAACAACT 60
GTGGGGGCAG AGAGCCCTCT CTCTCAGGCT GCCCCACTTC ATGGAGAGGG GGGCAGGTAT 120
TTATTCATCC TCCCTAAGAA CTGAGGTCTT GGCGAACTCA TCTGCCTCCC AGCTCAGCTA 180
ATTGGAATCA GTTCCCCATT TCTCCTCTGC CTCTCAGTAA ATTATGCGAA TTCCCCCAGT 240
CAGAGGCCTG GGTGATGGAC AGCCCTGTCA CAGCAGCCTA AGTGTTTAGA GAGCAATTGT 300
TCTGGGGAAG GCTGCCATTC CTCAAGCGTG TGCTGTGCGG GGGGCCACGA GGAGAGCCAG 360
CCCGGCCCTG CTGCTGCCCC TGTCCCTGCC CCTGTCCTTG CTCCTCTGCC CGCCCCTTTC 420
CCCACCGCTG CCCCTGCCCA GCCACCAGAG CCTGCTCCGC CCAGCCAGCC AAGCATGGGC 480
TTCCGGTACG TTATCCTTGT CATAACAATC AGAGCAGCCG AGAGGTATTG CTCTTAAACC 540
CTCAACACAC ATTTTTATAA CCTTTCTGTT TAATAAGAAA GAGACAGCTC CAATTAGCTG 600
GGAATATTCT GCCGAAATGG GATTATTTTA AAAGCTCTGG CAATATTACA AAATAGCTTC 660
AGTAAGTGAA CAGCTGTTGC CGGGCCCCGC CTGCCCTGCG CACTGCGCCT CCCGCACCCT 720
CCCATCAGGG CCGGGCCCCT TGCCCCTCCC CAGGGGCTTC AGAGTCCCTG AGAACTGTGC 780
TCTGGCCAGC AGCCAGGGGC CCCTCTTCAG GCAGCAGGAT GTAAGTTGTG GGTGTGGAGC 840
ACAGAGTCTC CATGGCCCGG ACTGGAGGGG AGGGACAGTT CACACCGTGC CCTGAGGCTG 900
GACTATGGCC TTGCTGGGGT CCTGCTTGTC CCAGAAAAAG TCATGTGGGG ACCCCAGCGT 960
CATCTCTAAA GGGCCTGCAG CCTGCTCTGC TGCCCCTGTA GCCTGGACAT GTTCCCTACT 1020
TTTAGCAGGA CTCCCGTCTG CTGCCCAGGC CTTCGCAGGC TCTCTGGCTC TCCAGTCAGG 1080
GGGGCAGGGC AGGGCTGCTT GTGAATCCAT TTCTCCAGAT TGTGAGTTCT GAGTCCACTC 1140
CCCAGGCCCA CCCCTGGGCC AGGTAAGGAT GCTACCTAAG GGGTCCCTCC CTCTCCTTCT 1200
TGGGGCCAAT GCTCATTTCC TCTTTGGCTC CTCTTCCACT CTCCGCAGGG CCCTCTGCAT 1260
TCCTTCTCTC CAGGAGGGGC TGTCTTTGTT TCCTTGCCCA TTGCAGCTGG TAGTGTTATC 1320
AGTAACTGTG TCTAAGTCCC CAGGGCTGAG GGGCAGGGGC CTGGAAGTCC TGGCCTTCCC 1380
CCTTTTCCCA TGCCTGCTGG CAAAGCTCTG CAGAAAGGAG GCCTCCGCTC CCACCTCCTA 1440
AAGCCCTGGG GCTGGATCTT ACCCACAGAC TCAGCATTGG CAGCTGCTTC ACCTGGGCCA 1500
TCTGAGGCAG CAGACTGATG CCAGCTCCTC CAGGAGCCAG CTCAGCCTCT GTGGGGAAAG 1560
CTGGGGCTGG GGCCTTGTAG GAGGCCCTGG GTCTTTTTTG GCCTGCTGCT TCTTGCCCAC 1620
TCTGTCCACT TGCCACTTGG CCCACAGCTG TGGTGCCCCC ATGGTGCTGG GTCCCCCAGA 1680
AGGCTCAGGC TGAAGAGTTG ATGATGTTTG AACAACTTTC AGGGAAGGAT ACAGTTGAAA 1740
AGGACCTCAG AGTCTGGCCC ATGGAACAGG TCACTGTATA GTTGGGGAAA CTAAATCCAA 1800
GTGAGAGGAA GCTCTGAGGC TATATTCTAA GACAGGATGG 1840
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