Tag | Content |
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EnhancerAtlas ID | HS095-25551 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr6:11814930-11816310 |
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 | AGCTTATAAT TCATCCAAAT GAAAGTGGCT TCCCTGGGTC TTGGATGGTT ATGCAGGGTT 60 AGAGTTAGTG TGAGAGCTAT GAGAGATGGC TAGGGTAAAG GTCAAACAAA AAACACATTC 120 CCTTGAATAA TCATGAAACT TCTGAAGCAA ATGCATATGA AGCCCCTATG ATGTTCTGTA 180 ATGTTTCTCT AAATCCCTTT TTGCTTTGGT TTTCTGCCAG AAATGGATGC AGATGCATCA 240 GCTACCTCAC AAGGAAAACC TGTTCTCACA AGTTTTATCG CACCACTTGG CAGAGAAAAA 300 GGCTTGGGTA GAGGCTGAGA ACTTTCACAT ATAACCAGAA AGCTCGGGAA TTCAGCCATC 360 TTGACTTACC ACCCACCGCT GAAAAGAAAC TTTCGCAAAC TCTCAGAGCC AGGATCTAAG 420 AGTCCCCTCC TAATCAGAAA AGGAGGAAAC TCTACAAGGT CCAACTTTCT CTTTAAAGGA 480 AATTCTGTAG ATGGCTACAA AGCCAGGTCA TTTTAGAATT TCTCACGGTA ATGAGGAGCT 540 CAAAGACTGG TTGGCATGGT TCTCTTACCT CTATCCTTTT CGTCTCTTTC CTCCCAGCCT 600 CCATTGGCCC AAGGCAAGTT CCCTCAGAAG ACTGCACTCC CAGGAAAATG CCAAGCTGGA 660 GCTGGGAGGG ATGAGGGCTG GTATAAAAAA AGGAGCAGGA AGAGCAGTTC TTTCTATTTG 720 GGCCATTCTA TGTATTTGGA AGTCCATGAG AAATATAAGA AGGGCTCACT CTAAAGAGTA 780 AACAATGTAG ATGGCAGGAT ATGTGACTGG GAATCTGCTG AGAATGTCTT CACATTACTC 840 ACAAGTTAAT AATTTCCCTA AGAGTGGGAG TTTCTTGAGG ATGTTTAGGA TTTATTTTTA 900 AGCCTTTTAG AGCTTTGGAA TAACACTCAC AGTTTCTTTT TTACTATTTT CATGGTGTTC 960 AGAGATTTCA AGCCCACATT TTAGAACCCA CCCACCTTCA ACAGATGTAG ACAAATTAGA 1020 AATACGCAGG GACCTCTCAA ACTCATTACA GAGCTTATTT GGAACATGTG AATTATATAT 1080 GCATTTTCTA CCTCATTATC TTCATGGGAC ACTGTATATT GATTTCATTG TAAATCTGCA 1140 ATGGTAGCAT CTCACTGTAT ATAACCTGCA ACTGTGTCCC CAAGCTATTA TCATTTGTGC 1200 TAATGACAAT GCTACCTCCT TTTCACAATT AGTGCTGTGG AGTATATAAG TCAAGAGGCA 1260 TTTGCTACGA ACCTACTAGG TAGATACCAA TGCACTAGGG CCTGGGAGGG AAATATGCCC 1320 TCAGAAGATT TGCCCCTCCC TGCCTGGTAA AAGAGGCTTC TGAAAAATTA TAAAGGGAGG 1380
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