Tag | Content |
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EnhancerAtlas ID | HS101-16442 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr16:11472600-11474090 |
Target genes | Number: 10 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr16:11473822-11473834 | TCTATTTTTAGA | - | 7.22 | Nr2f6(var.2) | MA0728.1 | chr16:11472904-11472919 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 11473365 | 11473722 | chr16 | 11473379 | 11473565 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I011379 | chr16 | 11473379 | 11473658 |
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Enhancer Sequence | CAGTTTTCCT TCTAGTATGA TTTCAGTCAT TTCAAATGTA TTAAATCTTG CTTTGAAGCC 60 TAACATACAA TCTTTCCTGG AGAACATTCC ACGTGTACTT TTGAAGAATG TGTATTCTGC 120 TGTTGGGTGA AGTTGTCTGT GTGGTAGGTC CAACTGGTCT ATAGTATTGT TCAAGTACTT 180 TGTTTCCTTC TTGATCTTCT GTCTGGGTGT TGTATCCATT ATTGAAAGTG AGGTATTGGG 240 CCGGGTGCAG TGGCTCAGGC CTGTAACCCC AGCACTTTAG GAGGCCAAGA TGGGTGGATC 300 ACCTGAGGTC AGGAGTTCAA GAGCAGCCTG GACAACATGG TGAAACCCTG TCTCTACTGA 360 AAATAGCTGG TCGTGGTGGC ATACGCCTGT AATCCCAGCT ACTCTGAGGC CTAAGAATCA 420 CTTGAACCCA GGAGGTGGAG GTTGCAGTGA GCCGTTATCA TGCCACTGCA CTCCAGCCTG 480 GGCAACAGAG TGAGATTCCA TCTCAAAAAA ATAAAAAAAG TGAGGTGAAG TCTCCTACCA 540 TTATCGTAGA CCTATCTGTT TCTCCTTTCA TTCTACAGTG TTTGCTTAAT ATATTTAGGA 600 GCTCTGAGGT GTGTTGCATG TACATTTATA ACTGTTACAT CTTTTTGGTG AATTGACTGT 660 TATCATTATC TCTTATAACA GCTTTTGACC TTAGGTCGAT TTTGTCTGAT ATTAGTATAG 720 CTACTCCTTC TCTATCTTAT TTCATCCTTT CACTTTCAAC CTGTGTAAGT CTCTCAGTCT 780 TCTGATGGTG GAATTCATTT GTATTTTTAA AGATTATCAT TCTGATGCAA CTGACTAACC 840 TGGTGACTGT GTCATGAGGC CCACAGCCAA GGACTGCGGT GACCAGTTGC TGTGGGGAGA 900 CTCCAGCACA TTACTGACGG GACTTCCCGA TGGGGAAGGA CTTCCTGGTG CCACGCTGTT 960 GATTGTTTTC TGCATGGCTT ATGGTTTGCT TTCTCTGTCA TTTCGTCCCT TTGTGTTTAA 1020 TTGATGTTTT TATTGTGACA CACTTAGGAT CTCATTTGCT TTTGTGTACG TTCTGTAGAT 1080 ATGTTGTCAT TACCATGGGG ATTACACGAA ACATCCTGAA GTTAGAGCAA TCCATTTTAA 1140 ACTGGTAAGT TCAATCACAT ACAAATACCC CACTCTTTGA CAGCTCTGTC CCCCTCCTAT 1200 GTTGTTGATA TCACAAAGTA TATCTATTTT TAGAGACAGG GTCTCACTCT GTCACCCAGG 1260 CTGGAGTGCA GTGGCATTAT CACAGCTCAA TGTAACCTCA AGCCCCTGGA CTCAAGTGAT 1320 CCTTCGGAGT AGCTGAGACT ACAAGTGCAT GCCACCACCA TGCCTACTTT TTTTCACAAA 1380 TTATATGTTT AACGTAGATG TATAGTTATA CATCTTTTAA ATCCAATAAA ATAATTACAG 1440 AGATGAATGA AAATTACAAT ACAGGTCTTT ATATGTGGCC TCAAACTTCC 1490
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