Tag | Content |
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EnhancerAtlas ID | HS177-17014 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr4:125863880-125865200 |
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) |
Gata1 | MA0035.3 | chr4:125864961-125864972 | AGAGATAAGGA | - | 6.02 | NFAT5 | MA0606.1 | chr4:125864626-125864636 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr4:125864626-125864636 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr4:125864626-125864636 | ATTTTCCATT | + | 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 |
GH04I124942 | chr4 | 125863817 | 125865291 |
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Enhancer Sequence | TTTTTTGGTG GTTCTGTGGT AGAATTGCAC TTCTCCAATT TGAAATTGTG CATGACAAAT 60 ATGACTTTCT TTGAGTAATA ATATATGAGC AGAGGTCTTA CAAGCCAGTG GGAAAGGTGC 120 CATAATCTTT CCCCCTGCCA CGTAGGTATG GATGGAAACT TTACATTCTA GATCCCAGAG 180 TGACAAGACA TAAACCAGGG TTACAGTCAA TTATTTAAGA GAGATTCATG TATTGAGTAC 240 ATATAGTAGT CATCCCTTAT CTGTAGGAGA TGCATTTGAA GACCCCTAGT GGATTCCTGA 300 AACTGGGGAT AGTACCAAAG CCTACATATA CTACGCACAA TTTTTTTTTC CTTCTTCACA 360 ATTTCGTGGA GATTCGTTCT TATTGTAGAT CTTAGCAACC TGAGCATATG ATTTTTTTTT 420 TTATTAGAGA ACTTTTACCC TTTCACTTAA AGGAAGCACT TTATTATTTC TCTTTGGCAT 480 ATCTGAATTA TCAACATCAT TACTCTTGAA CATTAGGTCC ATTATTAAGT AAAATAAAGG 540 GTTACTTCAG TACAAGCAAT GCTATACCTT GACAGTTGAT CTGATAACCT AGAGGGCTAT 600 TAAGTGACTA ACGGGTGGTT AGTGCGTATA CAGCATGGAT ACACCGGACG AGAGATGATT 660 CACGTCCTGG GTGGACTGTC TTAAGATTTC ATCACACTAC TCAAAGGGGT GTGCAACGTA 720 AAAGTTATGA TTTTTAAATT TCTGGTATTT TCCATTTAAT ATTTTTAGAC CATTGTTGCC 780 TGCAAGTAAC TGAAACCACG AAAAGTGAAA CCGTGGATAA GGGGGGGCTA TTGCGCTACA 840 TGCCAAAAGT TATTTATATG GAGGGGATAT AGGAGAGATC CGAATAGTAA ATTTCTTGAT 900 GACATGATGT TAGGTACTAG TTAAGGTGGA AGAAAGAGAA ACTAAATACA TAGGTATGTA 960 GTATGCCAGT GGGCAACATG ACACAGAAGA ATAAAATAGG CTAAGTGGTC AGAATGAGAG 1020 TGAGCCATGG TTCTTCCACA GCACGGTTAG AGAAGGCATT CTAAGATGGT AACACTTGAG 1080 CAGAGATAAG GATATGAGGG AGAAGGTTAT TTAATATTTG GAAAAATAGT TATTTAATAT 1140 TTGAAAAAAG ATGGAATTCC AGTTGCAATG GCTCTCAGTC AGGAGCGTGC TTGGCTTGGA 1200 GCAGCAGGGG AGGTCGGTGT GGCTAGGTCA GGAAAGCACT GCTGGGCTGG TCTGAGTGGC 1260 CCAGTAGAAG AGTAGTCAAA GACCAGATCG TAAAGAGACT TATGGGCCAT GATAAGGTTT 1320
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