Tag | Content |
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EnhancerAtlas ID | HS108-19071 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr19:1787900-1788890 |
Target genes | Number: 19 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr19:1788057-1788078 | AAAATAAAACAGAAACCAATA | - | 6.78 | TFAP2C | MA0524.2 | chr19:1788200-1788212 | TGCCCTGGGGCT | - | 6.11 |
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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 |
GH19I001788 | chr19 | 1788731 | 1791231 |
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Enhancer Sequence | CATGGTGGCA GGTGTCTGTA ATCTCAGCCA CTAGAGGGGC TGAGGCAGGA GGATCACTTG 60 AACCCGGGAG GCAGAGGTTG CAGTGAGCCA AGATCATGCC ACTGCACGAC AGCCTGGGCA 120 ACAGAGTGAG ACTCTGTCTC AAAAGGTAAT AATAATAAAA ATAAAACAGA AACCAATATA 180 TACTTACTAA GGGGTTTCTG TAAAGCTCCC TCTCAAATGC CCAGGTATTA GTGATGGGAG 240 CTCATTCCTT CTCCAAGGCA CCTGCTTCCC AGCAGTTTCC CTACACGCAG GGAATAGCAC 300 TGCCCTGGGG CTCCTCTAGT CCTTGTCAGG ATACCGCTCA GAGTCTGGAC CAGAGCCCCA 360 GCTCCCACAA TCGGATCTTC TCTGGGGTTC AAGGTCTTGT TCACTCAACT CTCCCCAGAA 420 GAGGAGGTCC ATGTGCAGTG CCTGCCCTTG CTTGAAAGCT CTGAGTGTGC CGGGCACGGT 480 GGCTCACGCT GTAATCCCAG CACTTTGGGA GGCCAAAGTG AGCAGGTCAC CTGAGGTCAG 540 GAGTTCGAGA CCAGCCTGGC CAACATGGTG AAACCCTGTC TCTGCTAAAA ATACAAAAAT 600 TAGCCAGGCG TGATGGTACA CGCCTGTAAT CCCAGCTACT TGGGAGGTGG AGGCAAGAGA 660 ATCACTTGAA CCCGGGAGGC GGAGGCTGCA GTGAGCCGAG ATCGTGCCAT TGCACTCCAG 720 CCTGGGTGAC AGAGTGAGAC TCTGTCTCAA AACAAAACAA AACGAAACAA ATATCCTGGA 780 AGGTGTTGGG CACAGAGCTA GACAGGGACC GTCACCTCCC TTCACCTGGA CTCTAGGCCT 840 CCACTAACGC AGCCTTGCCA TGTGGCCTCA GGCAAGCCCT GTCCACCGAG GATCCCAGGG 900 TTCTCAGTGC GTCCAGGGCT GCTCCTGGCA GCTATGGGAG GGGCAGGGCA TCCCCAGAGG 960 CCCTGGTCAT GGGGCAGCCA GGGTGGGGGA 990
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