Tag | Content |
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EnhancerAtlas ID | HS105-67832 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr6:11814980-11816410 |
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) |
YY1 | MA0095.2 | chr6:11815281-11815293 | TCAGCCATCTTG | - | 6.04 |
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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 |
GH06I011813 | chr6 | 11814033 | 11816296 |
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Enhancer Sequence | ATGCAGGGTT AGAGTTAGTG TGAGAGCTAT GAGAGATGGC TAGGGTAAAG GTCAAACAAA 60 AAACACATTC CCTTGAATAA TCATGAAACT TCTGAAGCAA ATGCATATGA AGCCCCTATG 120 ATGTTCTGTA ATGTTTCTCT AAATCCCTTT TTGCTTTGGT TTTCTGCCAG AAATGGATGC 180 AGATGCATCA GCTACCTCAC AAGGAAAACC TGTTCTCACA AGTTTTATCG CACCACTTGG 240 CAGAGAAAAA GGCTTGGGTA GAGGCTGAGA ACTTTCACAT ATAACCAGAA AGCTCGGGAA 300 TTCAGCCATC TTGACTTACC ACCCACCGCT GAAAAGAAAC TTTCGCAAAC TCTCAGAGCC 360 AGGATCTAAG AGTCCCCTCC TAATCAGAAA AGGAGGAAAC TCTACAAGGT CCAACTTTCT 420 CTTTAAAGGA AATTCTGTAG ATGGCTACAA AGCCAGGTCA TTTTAGAATT TCTCACGGTA 480 ATGAGGAGCT CAAAGACTGG TTGGCATGGT TCTCTTACCT CTATCCTTTT CGTCTCTTTC 540 CTCCCAGCCT CCATTGGCCC AAGGCAAGTT CCCTCAGAAG ACTGCACTCC CAGGAAAATG 600 CCAAGCTGGA GCTGGGAGGG ATGAGGGCTG GTATAAAAAA AGGAGCAGGA AGAGCAGTTC 660 TTTCTATTTG GGCCATTCTA TGTATTTGGA AGTCCATGAG AAATATAAGA AGGGCTCACT 720 CTAAAGAGTA AACAATGTAG ATGGCAGGAT ATGTGACTGG GAATCTGCTG AGAATGTCTT 780 CACATTACTC ACAAGTTAAT AATTTCCCTA AGAGTGGGAG TTTCTTGAGG ATGTTTAGGA 840 TTTATTTTTA AGCCTTTTAG AGCTTTGGAA TAACACTCAC AGTTTCTTTT TTACTATTTT 900 CATGGTGTTC AGAGATTTCA AGCCCACATT TTAGAACCCA CCCACCTTCA ACAGATGTAG 960 ACAAATTAGA AATACGCAGG GACCTCTCAA ACTCATTACA GAGCTTATTT GGAACATGTG 1020 AATTATATAT GCATTTTCTA CCTCATTATC TTCATGGGAC ACTGTATATT GATTTCATTG 1080 TAAATCTGCA ATGGTAGCAT CTCACTGTAT ATAACCTGCA ACTGTGTCCC CAAGCTATTA 1140 TCATTTGTGC TAATGACAAT GCTACCTCCT TTTCACAATT AGTGCTGTGG AGTATATAAG 1200 TCAAGAGGCA TTTGCTACGA ACCTACTAGG TAGATACCAA TGCACTAGGG CCTGGGAGGG 1260 AAATATGCCC TCAGAAGATT TGCCCCTCCC TGCCTGGTAA AAGAGGCTTC TGAAAAATTA 1320 TAAAGGGAGG AAAAAACCAG TGAGGAATCT GCATTTCAAT CAGATCTGCC CGTGTTTCCA 1380 GGTTACCTGA TGGGAAAACA AACCATCGAG CTTGCTTACC ATTTGTTGAT 1430
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