Tag | Content |
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EnhancerAtlas ID | HS039-01571 |
Organism | Homo sapiens |
Tissue/cell | ESC_NPC |
Coordinate | chr11:116573550-116574870 |
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) |
RFX1 | MA0509.2 | chr11:116574306-116574322 | GGTTTCCATGGTAACC | + | 6.82 | RFX1 | MA0509.2 | chr11:116574306-116574322 | GGTTTCCATGGTAACC | - | 6.8 | RFX2 | MA0600.2 | chr11:116574306-116574322 | GGTTTCCATGGTAACC | + | 7.25 | RFX2 | MA0600.2 | chr11:116574306-116574322 | GGTTTCCATGGTAACC | - | 7.28 | RFX5 | MA0510.2 | chr11:116574306-116574322 | GGTTTCCATGGTAACC | - | 7.24 | RFX5 | MA0510.2 | chr11:116574306-116574322 | GGTTTCCATGGTAACC | + | 7.27 |
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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 |
GH11I116703 | chr11 | 116574241 | 116574410 |
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Enhancer Sequence | GTCACCTATC TGTGTCTCCA CCACCTGGTT AAGACATGCA GTGTTACTGG TGCCTGGGAA 60 GCTCCCGGTG TGCCCTTGCT CCCCCGCTGT GCCCCTCCTG CATTGCCCTG GAGTTAACCA 120 CTCTGCTAAC TTTTGTGTGA ATCATTCCCT TGCTTTGCTT TATGGCTGTG CCACTTTTAT 180 GTGTCTCCCT AACAATGTAT CACCTTTTGC TTACACAGCT AGGTTTGTGC TTGCTATTCT 240 GTTTTTCAAA ACCACACAGG ATCTGTGATC GCTGCAGTGC TTAACACTGT TACGTTTAAG 300 TCTTCCCAGT GCAGTGAACT CTGAGCAGAT GCCTGTTATA AAACCAGGCC ACAAACACAT 360 GTACAGAGTC CTCCCATCAG ATCTCACGCG CTCTCTCCTA AAAGCCACTT TATTTTAGGC 420 ACTGAATTAA TGATATACAA ATGACATGCA CAGTGATGTG GAATTAGCAT ATGTCTTGGA 480 TTTTTTTTCA GGAAGAGATT TTGTATGTGT GTGGAAAAGT CAACTGCTCA GGCCCTTTCC 540 AAACGGTTTG TTTTGATCCC AGTTGTCTGA CAACGGGGAC CTGCCCTTGT GTTTGGAGGC 600 AGAAAAGAGC CCCCAGGAGC GTGTGAGGAG AAGCAGGCTC AGAGGGTCCC CCAGGCCCCT 660 CTTCCCTTCC CCCACAGCCA GCTTTCACCA CGGTGGCTTT GGCCCACAGC TGCCCTAGCC 720 CAGGGACCCG ATGGCAGGCA GAAGCAGACC TACTTTGGTT TCCATGGTAA CCGCGGGAGT 780 GCGCCGCAGC CAACAAGGCA GCTGGTTTGA AGGGTGTTGA TCTCTCTGCA GACCAGCAAG 840 GCAGAACCAC TAGGGACCAG AGGTGGCAAC CGAGCCAGAA GGAGCCACAG GAGCTGGGTA 900 TGCAAAGTTC ACGGGGACCT GTCTGAAGAG CCCAACCGCT CTTCCCCAAC CCTCTGCCAC 960 CCATCCACCC AAACAGAGGC ACTCGCTGAG CAGAGCACAT CCAGGCTCCA CTGTGAACAC 1020 AACTCAGACC CGCATTCACA CCAAATACAT CCCAGCTTCA CATCTGTGGA CCCATTTTCA 1080 CCAAGGAGAC ACATGAAAGT GGCACAGCCA TAACACAAAG GAGGGGAATG ATTCACACAA 1140 AAGTTAGGAG AGTGGTTAAC TCAGGGGCAA TGAAGGAAGG GTCATAGTTG GGGGTTGGGG 1200 TGGCACAGGG AGCTTCCAAG GCACTAACAA CATTCGATGA CAAAAATACA GACCCCTGGG 1260 GCTGGGTGCG GTGGCTCATG CCTGTAATCC CAGCAATTTG GGAGGCAGAG GTGGGGGCAT 1320
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