Tag | Content |
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EnhancerAtlas ID | HS108-19478 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr19:8481690-8483420 |
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) |
FOSL1 | MA0477.1 | chr19:8482926-8482937 | CATGAGTCACC | - | 6.62 | Foxd3 | MA0041.1 | chr19:8483382-8483394 | GTTTGTTTGTTT | + | 6.32 | JUND | MA0491.1 | chr19:8482926-8482937 | CATGAGTCACC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr19:8482866-8482881 | TGAACTCCTGACCTC | - | 6.22 | Zfx | MA0146.2 | chr19:8482565-8482579 | CCCGCCTCGGCCTC | + | 6.01 | Zfx | MA0146.2 | chr19:8482087-8482101 | GAGGCCGAGGCGGG | - | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 8481803 | 8481889 | chr19 | 8482904 | 8483391 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I008417 | chr19 | 8482085 | 8483943 |
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Enhancer Sequence | TCCTCCCACC TCAGCCCCCA AAGTGTTGGG ATTACAGGCA TGAGCCAATG CGCCAGGCCC 60 CAGACAGCAT TGTCGAGAAG GCTTCTCCAG GAAGGTGACC TTTGAAGGAG ACACTTATAA 120 CAACTGTTTC GAGTTCAGTG AGATGATGAC TATGTATGGA GATTGCTTGG CATAGTGTCT 180 GGTTCTTAAT AGATAGAAGC TGCTAGTATA ATTTTGGTGG TTTGCAGGCC TTGCATTAAG 240 AGATTTACCT GTGGTTTTTT TTTTTTCTCC CTGATAGAAG AAATATTAGA ACACCACATG 300 CAGGAGCTGG GATAGTTCCT GTAATATCCA GTTATTTGCA GAAATGTAAA GACCAGGCCA 360 GGGGTGGTGG CTCAAGCCTG TAATCCCAGC ACTTTGGGAG GCCGAGGCGG GCAGATCACT 420 TGAGATCAGC AGTTGGAGAC CAGCCTGGCC AACGTGGTGA AACCCTGTCT CTACTAAAAA 480 TACAAAAACG AGCTGGGTGT GGTGAAACAC AGCTGTAGTC CCAGCTACTC GACAGGCTGA 540 AGCAGGAGAA TTGCTTGAAC CCAGGAGCCT GAGGTTGCAG TAAGCTGAGA TCACACCACT 600 GCATTTCAGC CTGGGTAACA GAGTGAGACC CTGTCTTTTT TTTTGGGCGG GGGGATGAAG 660 TCTTGCTGTC ACCCAGGCTG GAGTGCAGTG GCGTGATCTC AGCTCACTGC AAACTCCATC 720 TCTCAGGTTT AAGCGATTCT CCTGCCTCAG CTTCCCAAGT AGCTGGGATT ACAGTTGCCC 780 GCCACCATGC CCAAGTAATT TTTGTGCTTC TAGTAGAGAT GGGGTTTTGC CATGTTGGCC 840 AGGCTGGTCT CGAACTCCTG ACTTCAGGTG ATCCGCCCGC CTCGGCCTCC CAAAGTGCTG 900 GGATTACAGG CATGAGCCAC TACGCCCGGC CAATACCCTG TCTTTTTTTT TTTTTTTTTT 960 TTTTTTTTTT TTTGAGAAAG AATTTCACTC TTGTTGCCCA GGCTGGAGTG CAATGGTGCG 1020 ATCTCGGCTC ACTGCAACCT CTGCCTCCCA GGTTCAAGTG ATTCTCCTGT CTCAGCCTCC 1080 CGAGTAGCTG GGATTACAGG CATGCGCCAA CATGCCTGGC TAATTTTTTT GTATTTTTAG 1140 TAGACACGGG GTTTCTCCAT GTGGTCAGGC TCGTCTTGAA CTCCTGACCT CAGGTGATCT 1200 GCCCACCTCG GCCTCCCAAA GTGCTGGGAT TACATGCATG AGTCACCACG CCCGGCCAAG 1260 ACCCTGTCTT AAAAAAAAAG AAATGTAAAG ACCTAGCCTC AGAAGGGCTG GGCTGGAGGA 1320 AAGGACTCGC CTCTGCCTGC CTTCCCGTAA AGAGCCCAGC CGCTTCCCCT TTGGCCTCTG 1380 AGCTTAAGGT TCTGGTTGCA GGGACTTGGG AGGGAGAGCA GCAGGCACCC TGTGTCAGGC 1440 CCGGCCACTG CCCTGTGGGT GTTATCTCAG GCCTGCAGTC TTCCTCTTGG GTCCCTGCCT 1500 TTGGGCAATA CTTGCTTATC TGGCCTGCAG AGGCCTGACT ATGATGCTCA GAAGAACATG 1560 TGAGGCCAGG AAGGCTGCTG GCTGAGCTGT TTAGAGGGCA TTTATCCAGC AGTGAACCGT 1620 CCTAGCGCAA GAGTTAGTAA TTGCTCCCCT GTTCCTTCAC CTCCCCACTT TGGAGCTCAG 1680 ATTTGTTTTT TTGTTTGTTT GTTTGCTTGC TTTCTTTTGT TCTGTTTTAG 1730
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