Tag | Content |
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EnhancerAtlas ID | HS108-20681 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr19:46312620-46313860 |
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) |
CEBPA | MA0102.3 | chr19:46313751-46313762 | GATTGTGCAAT | - | 6.32 | Foxo1 | MA0480.1 | chr19:46312943-46312954 | AGTAAACAGGA | - | 6.32 | JUN(var.2) | MA0489.1 | chr19:46313197-46313211 | ATGAGTCATTTCCT | - | 8.12 | Stat4 | MA0518.1 | chr19:46313202-46313216 | TCATTTCCTAGAAG | - | 6.69 |
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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 |
GH19I045809 | chr19 | 46312606 | 46314232 |
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Enhancer Sequence | GGTGCGACCT CCCCTCACTG CAATGTCCAC CTCCCAGTTT CACGCCATTC TCCTGCCTCA 60 GCCTCCCTAG TAGCTGGGAC TACAGGTGCC CGCCACCATG CCCGGCTAAT TTTTTGTATT 120 CTTAGTAGAG ACAGGGTTTC ACTTAGCCAG GATGGTCTTG ATCTCCTGAC CTCGTGAACC 180 ACCCGCCTCA GCCTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCACCGTG CCCGGCTAGT 240 CAAAACTTTT CAAAACAGAG GTTCAGTGAT GGGGAGAATT ATGCTACCAA AACAGCAACA 300 CCTGCCGTGC AGCTGCTGTC AGCAGTAAAC AGGAGAGTCC TAGAGCAGGA AGCCATCCAC 360 AGAGCAAAGG CCGGGAGCAG AGACTCCTGC AGGACCCTGT GTGGGGAGCA GATGGTGCAG 420 GTGGCATTTC AAAGCAGTGG GGGGGCAGGA AGGAATGGTT TATTGCATAA ATGCCATTCA 480 AGGTCCTGGC TAGCCGTCTG GAAGACAGAA AACGAGAGAA ATAAGAGCCT TGCCTTGACA 540 GAAAAAGAAA CACAAAATGC TGAATCATGC ATTTTTTATG AGTCATTTCC TAGAAGCATG 600 TACAGGCCAC AAAAGCCCCC AGTTTTGCCC TTCCACAGAC CCCACATTAA GAACTCCAGC 660 TCTTGGCTGG GAGTGGTGGC TCACGCCTGT AATCCTAATA CTTTGGGAGG CCGAGGCAGG 720 AGGATGGCTT GAGGCCAAGA GTTCAAGACC AACCCGGCCA ACATAGCAAG ACCCCCATCT 780 CAATTATTTT TATTTATTTA TTTATTTTTA TTTATTTATT TTTTTGAGAC AGAGTCTCGC 840 TCTGTTGCCC AGGCTGGAGT GCAGTGGTGT GATCTCGGCT CACTGCCAAG CTCCGCCTCC 900 TGGGTTCATG CCATTCTCCT GCCTCAGCCT CCGGAGTAGC TGGGACTGCA TGTGCCTGCT 960 GCCACGCTTG GCTAATTTCT TATATTTTTA GTAGAGACGG GGTTTCATCA TGTTAGCAAA 1020 GATGGTCTTG ATCTCCTGAC CTCGTGATCT GCCCACCTCG GCCTCCCAAA GTGCTGAGGT 1080 TACAGATGTA AGCCACCCCA TCCTGCCAAG ACTGAAGTTG TTTTGTGACT GGATTGTGCA 1140 ATGCTGTCTT TCGCCTCCAG GCCTTGGCAC AGGCTGTGCC CTAAGTATGC TTGGGCCCCC 1200 ACTGACCCTG ATGCCCACCT CTCCTGACTG GCTCACTCAC 1240
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