Tag | Content |
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EnhancerAtlas ID | HS187-21331 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:51928340-51929300 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELK1 | MA0028.2 | chr6:51928521-51928531 | CACTTCCGGT | - | 6.02 | ELK4 | MA0076.2 | chr6:51928520-51928531 | CCACTTCCGGT | + | 6.32 | ERG | MA0474.2 | chr6:51928521-51928531 | CACTTCCGGT | - | 6.02 | ETS1 | MA0098.3 | chr6:51928521-51928531 | CACTTCCGGT | - | 6.02 | FEV | MA0156.2 | chr6:51928521-51928531 | CACTTCCGGT | - | 6.02 | FLI1 | MA0475.2 | chr6:51928521-51928531 | CACTTCCGGT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I052063 | chr6 | 51927941 | 51929154 |
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Enhancer Sequence | ATAAACAGAA AAGTAAGAGC ATATTTTGAA AATATTACTT TAAACCAGGG TTTCTCCACC 60 CCAGCACTAT TGATATTTTA GGCTGGGTAA CTGTTGTGAG GGGGTGTCCT ATGCATTGCA 120 CAATGTCTAG CAGCCTTCCC AGCCTCAGCC CACTAGATGT CAGTATCATC ACCACCACCA 180 CCACTTCCGG TCTAACAGCC AAACATGTTT CTACACATTG CTACGTGTCC CCCGAGGGGC 240 AACATTGCCC CTGGTTGAGA ACAATTGGTT TCCATAGTAA TTCGCCCAGC TTCTGTGGAA 300 GAAACTTCAA AAGCCCTTCA TAAAGGACAA CACTAACTGT CAAACCAGCT GCATTCAGGA 360 AATTATCCTA CCACTACCCA AGTAGCTAAA GCAGGAAATA CTGAAAAAGG GAGCAGACTC 420 TCTATTTCCT GACAGGAAAC ACACATTATC TTGATTACTT GTTTCAGTAG TTTTGTTTCC 480 TTGGATGGAA GCTTTCCCTG AGTAAAAACT GCAGATCTGG GAGCTGGAGA ATTCTCAAGC 540 CAAAACTTTG CATGCATTTT CACACCTGAA TGCCCTTTCT TTAGAAAGGT TTCTTCCCCT 600 GCTGGGCAAC TTTCCTTGTA GGTGCTGTGC CTCTAGAGTT GACTCTCGCT GCCTGTAGTT 660 TAACCATTAA GTCAGGCCCT TGGGCACAGA TGTGCAGCCT GTGGTTCTTG GCTGAGTAAC 720 ATACCAACTG CCCTTCATCC CTGACTACAC TTGAGCCTTC AGTTCTAATG CTCAGCAGAA 780 AAGTGCTCCA GTATTGTGCT CTTAATTTGC TGCTGTAGGG TGGATGCTTT AAACAGAGAA 840 GGACAGCTGG AAGCTCCCTT GCCTCCTCCA TTTCTGCCCA CTTCAGGCAT AACCTGGTGG 900 CAACATCACA ATATATCCCT GTTTCTCAAA GCAGCAGACA GATGCCCACA AGAGAGAAAA 960
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