Tag | Content |
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EnhancerAtlas ID | HS034-14196 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr19:987920-989760 |
Target genes | Number: 34 | Name | Ensembl ID |
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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) |
FOXH1 | MA0479.1 | chr19:989007-989018 | TCGAATCCACA | + | 6.14 | RUNX1 | MA0002.2 | chr19:988438-988449 | CTCTGTGGTTT | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 988183 | 988340 | chr19 | 989107 | 989177 |
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Enhancer Sequence | GGCTCCCAGG TTCAAGCGAT TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG AGGCGCCCGC 60 CACCATGCCT GGCTAATTTT TGTATTTTTA TTAGAGACGG AGTTTTGCCA GGTTGGCCAG 120 GCTGGTTTCG AACTCCTGGT CTCAGGTGAT CCGCCCTTCT CAGCCTCCCA AAGTGCTGGG 180 ATGACAGGCG TGAGCCACTG CAGCTGGCCC TCCTGGAGAG TTTCTGACCC GTGAGCTGTG 240 ACCATGAAGG GGTGTCCCAC ATAGCCAGAG CTCAGGCCGG GACTGCCTCC ACTGTACCCC 300 CCTGCCACGG TCGAAATCCT CCTCCTGTTC TCTGTGTAGG CGACGGGTGT GTGAGCGGTG 360 AGTCAGGAGT GGGCTGGAAA CCTGAGAGCC AGGGCTGTGG GGCGGGAGCT GGTCCGCCCC 420 TCCCACGCCA CAGGGACAGG GACCTCCCGG GAGGCACTGA TGTTCTGAAG CTGCCCGGTC 480 TGTCCCGGCC CTGGGCAGTG GTGGTCACCA GAGCTGCCCT CTGTGGTTTG GGGCTGACCT 540 GGATCCTGCT TCCTCTGGTG CCATTTAACC CTCCCCAGCC ACCCTGGGTT TTGCATGCGA 600 GGAAAGCGAG GCCCAGAGAG GGCATGGCTG TCAGATCTGG GCCCAGCAGG CTCTGCCTGC 660 CCCAACAAAG CACGACGCAC AGGGACTTTC GACAACAGAA ACTCGGCCCC CATCCTTGAG 720 GCCAGACGTC CTAAATCAAG ATGTCTGTGG GGCCACGCTG CCCCTGGAGG CCCTGGGAGG 780 AGCCTTCCCA CCTCTCCGGT GGTGGCCGGC ACCCCTTGGC ACCCTTGGCT TGTGGGTGAC 840 TGTCCCCTGC CTCTGCTGCC ACCACTGCCG CGTGGAGCCC CTGTGTGTTT GCACTTCTCT 900 CAGCTTACAA CAACCGGGAC ACATGGATGG ATGCCCCCGC TCCAGAACCA CCTCATCTTA 960 ACTTATGATA TGTGCAGAGA CACTGCGTCT AAATGAGGCC ATTCACAGGT CCCAGGTCGG 1020 GACTTTTAAC ATGCTTTTGG GGGGAAACAC GATTCAATCC ACAACCCCCA CCAGAGCATC 1080 TCAGCTCTCG AATCCACAAC CCCCCACAGA GCATCTCAGG CCTCGAACCC ACAACCCCCA 1140 CCAGAGCTTC TCAGCCCTCG AACCCACAAC CCCCCAGAGC ATCTCAGCCC TCGAACCCAC 1200 AAACCCCCCC AAGAGCATCT CAGTCCTCGA ACCCACAACC CCCTCCAGAG CATCTCAGTC 1260 CTCGAACCCA CAACCCCCCC CAGAGCATCT CAGCCCTCGA ACCCACAACC CCCACCAGAG 1320 CATCTCAGCC CTCCCCAGGT GTCCTGGAAG GGGCTCCCTG TCCTCTTCCT CAGATGGAGC 1380 TGCCTGGCTT CCTGCCGGAG CTTAAGCTGC CACCACCCTG GGTCAGGCCA CCACAGCCTG 1440 CCCAGAAGCG ACTTCCTGTT GAATGGTGGG AGCCGCCTGC AGGTCCTGAG TGCAGCCGTT 1500 CCTACGGGGC CCACACAGGA CGCCTGGGGT CAGGCTCACA GGGGACCAGC ACCTCCCTGA 1560 GGCAGCAGGG AAGGGCAGGA AACTTGCCCC TTCCTGGGCC ATCATGCAGG TGGGGACGAG 1620 GCGGGAACAG GTGCCCACCC AGCCCAGGCA GGGGCGCGAC GAGGCCCCGC TGTACCTGCT 1680 GGCCGCTGCC CTGACAGGGT CACCCCGCAG TCCTGGGGCA GGGCAGGCAG GGGGCGACAG 1740 TGTGGCCATG GCCGTGCAGT GGTGGGTTCC TGGGGCTGCA GCCCCCCTTT CCTCCCCTGG 1800 GGCTTTCCTC CCCTGACCTG GATACCCTCT GCCCCTCACA 1840
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