Tag | Content |
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EnhancerAtlas ID | HS062-04374 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr12:132638140-132639650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr12:132638570-132638589 | CGGCCACCAGAGGCCGCTG | + | 6.36 | HNF4G | MA0484.1 | chr12:132639223-132639238 | TGGCCTTTGGCCTCC | - | 6.67 | ZNF263 | MA0528.1 | chr12:132638501-132638522 | CCCCCCTCCCCGCCCTCCTTG | - | 6.58 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 132638746 | 132639325 | chr12 | 132638362 | 132639503 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I132153 | chr12 | 132637844 | 132639324 |
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Enhancer Sequence | GGCAGAGTGA TGGTGGAGAT GTTGCCTCTG CTCCCAGCAT CCCCCTGGCT GCTTCCCTCT 60 GCCCCAGCGG GCTCCTCAAG TGAACTGGCT CCTGCCCCAG GGCCTTTGCA CCAGCCACAG 120 CTGTGGCCTC TGCCGCTTTT CCCTGTGTTG CCCTGGTTTG AACGTCCCGT CCCCGTCCCC 180 CCGGGAGGCC TTCCCTGGTA CCCCGTGCGT GGTAGTCCTG CACAGGCGCC CCTCCTTCCC 240 CACTCTTCAT GCTGTCCCGC CCGAGCCCTC TCAGCACTCC CGCTGCAGCA GGGCAGACAG 300 GGCCCGTCCT CTTGCTGTGT CCCAGGCAGC CTGTCACACC GGGTACGCTC CAGAGCCCTG 360 GCCCCCCTCC CCGCCCTCCT TGGGCTCCTG GGGCAGGGCT GGGCCTAGGT GCTGGCATCC 420 TGAGCTCATG CGGCCACCAG AGGCCGCTGC AGCCTTGCCC AGGCCTGCAG CGCCCGAGCT 480 GCCCTGCTAG GTTTCACCTC GCCGGGGTCT GCAGTATTTC CTGCTCGGAT TCAGCCAGGG 540 CCTCCCTCCT GACATCACGG AGGGTTTGTG CTGGGCTGTT AGGCGGATCT CGGATGATGG 600 GCGAGGCCAG GAGGAGAGTG AAAGCGCCTC CGAGTCAGCC AGGCTTGGAT TCTGTCGTCA 660 GAGGGGCTCT GTGTCTAGCA ACCTCCACGT AACCGTGTTC GGTCCTCTGC TCCCTGTGTT 720 CCCCGCATGA GCCGGGCATG AACAGGGACC TCCTTCACCG CCTGAGGTCC CCTCTCCCTG 780 GCTGGTGACC CCCATCTCTG AGAGCACGGG GACGTCCCCT GTGCTGTGGA GGAGCGTGTG 840 CTCTCCGAGA TCCAGGTGCT GCCCCCGAGG AGCGCATGCC CTCTGAAATA CAGGTGTTGC 900 CGCCATCCCC GAGAGCACGG GGACGTCCCC TGTGCTGTGG AGGAGCGCCT GCCCTCCCAG 960 ATCCAGGTGC TGCCCACCAG GCGGTGTTAG GAGTGCCTCG TCCGCAAGGG CGCCATCCTT 1020 GTTAATGGGA TTCAGGCCTT TGTAAAAGTG GATTCTTCAC GTGGTGCTGA GCCGGCTGCT 1080 CTCTGGCCTT TGGCCTCCTG TCAGGTTGGG CGCAGCCAGG AGGCCCTCGC TAGAGGCTGG 1140 TGCCTTCATC CTGGACTTCC CGGCCTGCGG AACTGGAGAG AAGACAGTGT CACTTTTTAG 1200 AAGTTACCTG CTCTCAGGTA ACCTGTAACA GTGGTGCAGA CGGACTGAGA CACCGTCAGT 1260 TCCAGAATCT TAGAGAAATT CCAGGGGCCC CTTCAATCAC CTATGAGGCC AATACCCAGC 1320 CGGCACCTGC GTGTACCCGG CGGTGTCCTC ACTGCACACG GAGAACAGCG CCGCACCAGT 1380 GGGGCCTCTC TCCCCCTGTG CTTCCCCCGC TCCCTCTCTG TCTTGTCTCT CCCTCTCCTC 1440 CCGTCCCCCG ATTCCGGGTC TCCCTTCAGG AAATGAACGC GGCTGCCGGA CAGTGAAGTC 1500 ACAGCTACAT 1510
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