Tag | Content |
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EnhancerAtlas ID | HS026-02911 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr1:207807590-207809840 |
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) |
HNF1A | MA0046.2 | chr1:207808329-207808344 | AGTTAATCATTAATC | + | 6.17 | HNF1A | MA0046.2 | chr1:207808329-207808344 | AGTTAATCATTAATC | - | 7.85 | HNF1B | MA0153.2 | chr1:207808330-207808343 | GTTAATCATTAAT | - | 6.05 | HNF1B | MA0153.2 | chr1:207808330-207808343 | GTTAATCATTAAT | + | 7.22 | ZNF263 | MA0528.1 | chr1:207807917-207807938 | GAAGGAGAACGAAGATGAGGA | + | 6.58 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 207808022 | 207808210 | chr1 | 207808716 | 207809614 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I207632 | chr1 | 207806171 | 207809630 |
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Enhancer Sequence | CTCTTACATC AAAGTACACC TCAAATTGTG TACACTGACT ACTGATCACT TTTCGGTAGG 60 TATAAAGTCC TTAAAAATTT TGTTTCAACT TTCCCTTTTA AGATTAGAAT TTTGACCACA 120 GTGTTCCATG GGAACAAAGT GAATCATCTG TGGCAAAATA TGCTAGTCAA GAAGTGAGTT 180 AGAATCTGTG CCAAGCGTTA AGACCTTGTG CACCCAGGTT CTGGGGCGGA GTAAAGAGGC 240 AGGCTCCAAA GACATAGCTG TGTGTTGGAC ATGAGAGTAT TTGGAGGAAT ACAGGTAACA 300 GGTGATGCTG GGAAGTCCTG TGAAATGGAA GGAGAACGAA GATGAGGAAT CTGGTGGCAG 360 TAATAACCGG GGAACAGATG AGCTGGAGGC CTCATCAGGA GGGGTGTCCC TTGGTGGAAG 420 GACACCATTC CCGGCCTTAA AAGGAGACGC TTCAGCACGG CTGGGGAAGC ACGTGGATAC 480 CTTGTACTAA ATCCACTACT GCAGCTCATT CTTAACTGTA AGTAGAAGAG GAGGACATGC 540 TTTCTGAAGC TGACCCCTCC AAGATGACCA GTTCCTATTT CTGTCCCCTG CTACCACCAT 600 GGTGTAGAAC AACAGAATCA AAAAAACATT TTTTCTGTTA TGGGTGACCT GTACGTTTTC 660 TAGAATGGAA GGAGGCTGTT TAGTAGCTCA ACTCTGAGAA CACTTTTTCT TTGGACAAAA 720 TTAAAAAAGG AAAAGGTCAA GTTAATCATT AATCTCTCTG TTTTCTACTA ATGTCTCCAT 780 TTTCGCCATA CTTTCTATGT CCTACATAGC AGCCATCACA GAGGGCAATA AACACTTCTA 840 ATGACCGTGT AATTTATATG GAATGCTGAA GGGGTGGGTT GGCCCTCCAC ACCTGTGGAT 900 GTTTCTCATT AGGTGGAACT AGAGACTTGG AAAAGAAAGA GACACAGAGA CAAAGTATAG 960 AGAAAGAAAA AAGGGGGCCC AGGGGACCGG TGTTCAGCAT ACGGAGGATC CACCGGCCTC 1020 TGAGTTCCCT TAGTATTTAT TGATCATTAA TGGGTGTTTC TCGGAGAGGG GGATGTGGCA 1080 GGGTCATAGG ATAATAGTGG AGAGAAGTTC AGCAGGTAAA CACGTGAACA AAGGTCTCGG 1140 CATCATAAAC AAGGTAAAGA ATTAACTGCT GTGCTTTAGA TATGTATACA CATAAATATC 1200 TCAATGCCTT AAAGAGCAGT ATTGCTGCCT GCATGTCCCA CCTCCAGCCC TAAGGCGGTT 1260 TTCCCCTAAC TCAGTAGATG GAATATACAA TCGGGTTTTA CACCGAGACA TTCCATTGCC 1320 CAGGGATGAG CAGGAGACAG ATGCCTTCCT CTTGTCTCAA CAGCAACGAG GCGTTCCTTC 1380 CTCTTTTACT AATCTTCCTC AGCGCAGACC CTTTACGGGT GTCAGGCTGG GGGAAGGTCA 1440 GGTCTTTCCC TTCCCATGAG GCCATATCTC AGGCTATCAC ATGGGGAAAA ACCTTGGACA 1500 ATACCTGGAT TTCCTAGACA GAGGTCCCTG CTGCCTTCTG CAGTGTTTTG TGTCCCTGGG 1560 TACTTGAGAT TAGGGAGTGG TGATGACTCT TAACAAGCAT GCTGCCTTCA AGCATTTGTT 1620 TAACAAAGCA CATCTGCACA GCCCTTAATC CATTTAACCC TGAGTTGACA CAGCACATGT 1680 TTCAGGAAGC ACAGGGTTGG GGGTAGGGTT ACAGATCAAC AGCATCTCAA GGCAGAAGAA 1740 TTTTTCTTAG TACAGAACAA AATGGAGTCT CCTATGTCTA CTTCTTTCTA CACAGACACA 1800 GTAACAATCT GATCTTTCTT TTCCCCACAT TTCCCCCTTT TCGACAAAAC CGCCATCATC 1860 ATCATGGCTG TTTCTCGATG GTTGCTGTCT CTTTGGAGCT GTTGGGTACA CCTGCAGACT 1920 AACAACAGAC AAAACAGGCA CACAAGGATT AATATGAAAT TTATAATCGT AGTACTTCCG 1980 ATGGTCTTAA CCCAAGTGAC AGGGTTAAGA TTTGCGAGGC CATCAGCAAC TCCTGCGATT 2040 GCCTCAGTTC CTGGCACCAA ATTTAAATGG GCTTTTGATG TTTCAAAAAT TTGTTCCTTT 2100 AATTTGGAAA TGTCTAAAGT GAGATTATCT TCTGTTCCCT GTAGATGGCA TCTGACCATG 2160 TCCCAGTGAT GCTCAGACTC ATTATAAACT TGGGGTGTAA TACAAAAATC TGAGATATTC 2220 CAGTCACACT GTAACTGGAA ACGATGGTCT 2250
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