Tag | Content |
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EnhancerAtlas ID | HS108-04002 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:207807800-207809860 |
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 | CACCCAGGTT CTGGGGCGGA GTAAAGAGGC AGGCTCCAAA GACATAGCTG TGTGTTGGAC 60 ATGAGAGTAT TTGGAGGAAT ACAGGTAACA GGTGATGCTG GGAAGTCCTG TGAAATGGAA 120 GGAGAACGAA GATGAGGAAT CTGGTGGCAG TAATAACCGG GGAACAGATG AGCTGGAGGC 180 CTCATCAGGA GGGGTGTCCC TTGGTGGAAG GACACCATTC CCGGCCTTAA AAGGAGACGC 240 TTCAGCACGG CTGGGGAAGC ACGTGGATAC CTTGTACTAA ATCCACTACT GCAGCTCATT 300 CTTAACTGTA AGTAGAAGAG GAGGACATGC TTTCTGAAGC TGACCCCTCC AAGATGACCA 360 GTTCCTATTT CTGTCCCCTG CTACCACCAT GGTGTAGAAC AACAGAATCA AAAAAACATT 420 TTTTCTGTTA TGGGTGACCT GTACGTTTTC TAGAATGGAA GGAGGCTGTT TAGTAGCTCA 480 ACTCTGAGAA CACTTTTTCT TTGGACAAAA TTAAAAAAGG AAAAGGTCAA GTTAATCATT 540 AATCTCTCTG TTTTCTACTA ATGTCTCCAT TTTCGCCATA CTTTCTATGT CCTACATAGC 600 AGCCATCACA GAGGGCAATA AACACTTCTA ATGACCGTGT AATTTATATG GAATGCTGAA 660 GGGGTGGGTT GGCCCTCCAC ACCTGTGGAT GTTTCTCATT AGGTGGAACT AGAGACTTGG 720 AAAAGAAAGA GACACAGAGA CAAAGTATAG AGAAAGAAAA AAGGGGGCCC AGGGGACCGG 780 TGTTCAGCAT ACGGAGGATC CACCGGCCTC TGAGTTCCCT TAGTATTTAT TGATCATTAA 840 TGGGTGTTTC TCGGAGAGGG GGATGTGGCA GGGTCATAGG ATAATAGTGG AGAGAAGTTC 900 AGCAGGTAAA CACGTGAACA AAGGTCTCGG CATCATAAAC AAGGTAAAGA ATTAACTGCT 960 GTGCTTTAGA TATGTATACA CATAAATATC TCAATGCCTT AAAGAGCAGT ATTGCTGCCT 1020 GCATGTCCCA CCTCCAGCCC TAAGGCGGTT TTCCCCTAAC TCAGTAGATG GAATATACAA 1080 TCGGGTTTTA CACCGAGACA TTCCATTGCC CAGGGATGAG CAGGAGACAG ATGCCTTCCT 1140 CTTGTCTCAA CAGCAACGAG GCGTTCCTTC CTCTTTTACT AATCTTCCTC AGCGCAGACC 1200 CTTTACGGGT GTCAGGCTGG GGGAAGGTCA GGTCTTTCCC TTCCCATGAG GCCATATCTC 1260 AGGCTATCAC ATGGGGAAAA ACCTTGGACA ATACCTGGAT TTCCTAGACA GAGGTCCCTG 1320 CTGCCTTCTG CAGTGTTTTG TGTCCCTGGG TACTTGAGAT TAGGGAGTGG TGATGACTCT 1380 TAACAAGCAT GCTGCCTTCA AGCATTTGTT TAACAAAGCA CATCTGCACA GCCCTTAATC 1440 CATTTAACCC TGAGTTGACA CAGCACATGT TTCAGGAAGC ACAGGGTTGG GGGTAGGGTT 1500 ACAGATCAAC AGCATCTCAA GGCAGAAGAA TTTTTCTTAG TACAGAACAA AATGGAGTCT 1560 CCTATGTCTA CTTCTTTCTA CACAGACACA GTAACAATCT GATCTTTCTT TTCCCCACAT 1620 TTCCCCCTTT TCGACAAAAC CGCCATCATC ATCATGGCTG TTTCTCGATG GTTGCTGTCT 1680 CTTTGGAGCT GTTGGGTACA CCTGCAGACT AACAACAGAC AAAACAGGCA CACAAGGATT 1740 AATATGAAAT TTATAATCGT AGTACTTCCG ATGGTCTTAA CCCAAGTGAC AGGGTTAAGA 1800 TTTGCGAGGC CATCAGCAAC TCCTGCGATT GCCTCAGTTC CTGGCACCAA ATTTAAATGG 1860 GCTTTTGATG TTTCAAAAAT TTGTTCCTTT AATTTGGAAA TGTCTAAAGT GAGATTATCT 1920 TCTGTTCCCT GTAGATGGCA TCTGACCATG TCCCAGTGAT GCTCAGACTC ATTATAAACT 1980 TGGGGTGTAA TACAAAAATC TGAGATATTC CAGTCACACT GTAACTGGAA ACGATGGTCT 2040 AAGTTCATAA GCCTGTCTCC 2060
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