Tag | Content |
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EnhancerAtlas ID | HS017-30792 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr7:105449100-105450540 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata4 | MA0482.1 | chr7:105449126-105449137 | AGGAGATAAGA | - | 6.14 | Sox3 | MA0514.1 | chr7:105449652-105449662 | AAAACAAAGG | - | 6.02 |
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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 |
GH07I105805 | chr7 | 105445559 | 105450934 |
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Enhancer Sequence | TGCCCAAGCA TATTTATAAA GGGAGGAGGA GATAAGAATT AATTGGGACA GGAGCTTCTA 60 CCTAAGTGAC ATAAAAGACA CAATTATTTT TGCTGCTTTT ACAGATCAAG TGCCCCTTCC 120 AGGTGGGGAT AGAGCCCTGG CACCACCCAC CATTTTGAAA AATGACTTTT AGTCTTCCGT 180 AGTTCTAACT AAGCTTGAAA TTAAGATGGT TCTTTTGTTT ACTCCCCCTG TTGGGGAAGC 240 TCTAACCACC TATCAAAAAC ACCAATGTCT GGATTATTTA TTTCTCATTG TCCAACCTAC 300 GGGGCATAGA AGAGTTTTAT GAAGCCAACA TGTGAGGCGT TTCTCCCAAA GAAGCGTGGA 360 TGCACCTCCC CATATTGCAG AGCCCTTTTA TACTATGGTC CTTTGATAAT CTGGATTTTG 420 ACAGACAGAA CTAATGCCTG ACTTGGAGCA GGACAAAGAG CCCTGGAAGT CAGAGGCTTC 480 ATTCTTGTCA CCCTCTTTCC TTTATAAGCT GCGAGCACTT GGGTAAGTCC CTTAACCTTG 540 AGAAAATTCA ATAAAACAAA GGGTTAGTGA CTAATATATT ACATCCTTTT TAAAAAACAA 600 GTTGTGGTTT AAAAAGCCCC ATATAACATG AGATCTACTG TCTTAACACA TCTGTGAGTG 660 TATAGTACAG TATTGTTAAC CATAAGCACA CTGTTGTAAA GCAGATCTCT AGAACTGACT 720 CAGCTTGCAC TACTGAAACT CCACGCCCAC TGAGCAGCAA CCTCACTTCC TCCTTCCTCC 780 GGCCCCTGGC ACTCAACCAT TCTATGTTCT GCTTCTACGA GTCAACTGCC TTAGATACCT 840 CATATCAGTG GAATCAGGCA GTATTGGTCC TTTATGACTG GCTTATTTCA TTTAGCATAG 900 TGTCCTCAAG GTTCAAATAT ATATCCTTAC AATGATACTG ACATGGTACT CACTGTTTCC 960 ATGGTAAGTG GTTACATATA TTAACGTATT TAGCCCTCAC AGAAACCCTT CAAGGTAAGG 1020 TGGCATGATT ATCTCCTTTT GATAGATGAG GAAACTGAGG CAAAGGGAGG TGAAGTGAGG 1080 TGCCTATGCT TACCTGCTGT GTAAGTGGCT CCAGACTCCT TTTTTTTTTT TTCCAAGACA 1140 GGGTCTCACT CTGTTGCCCA GGCTAGAGCA TAGTTATGCT ATCATAGCTC ACTGTAGCTT 1200 TGACCTCCTG GGCTCAAGTG ATCCTCCCAA CTCAGCCTCC CAAGTAGCTG GGACGAAAGG 1260 CACATGCCAC CACATCCACC TAATTTTTTA AATTTTTTGT AGAGACGAGG TCTCACTATG 1320 TTGCCCAGGC TGGCCTCGAA TTCCAGGACT CAAATGATCC TCCAGCCTTG GCCTCCCAAA 1380 GTGTTGAGAC TACAGGTGTG AGCCACCACA CCCAGCCCAG ACTCCATTCT CTTGAACATA 1440
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