Tag | Content |
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EnhancerAtlas ID | HS108-36392 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr7:6519390-6520780 |
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) |
EWSR1-FLI1 | MA0149.1 | chr7:6519730-6519748 | GGAAGGAGGGAAGGAGAC | + | 6.46 | GLI2 | MA0734.2 | chr7:6519468-6519483 | CATAGTGGGTGGTCA | - | 6.17 | TEAD1 | MA0090.2 | chr7:6520044-6520054 | CACATTCCAT | + | 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 |
GH07I006479 | chr7 | 6519369 | 6520277 |
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Enhancer Sequence | AGCCACCACG CCCAGCCAAG AACAAAAACT TTTAATAGCT ACAAGCTGCT GCTCTGAATT 60 GTGTGCCAGT GCCTTGCACA TAGTGGGTGG TCAATAAATG AGAGTAATGA TTACTCAGAG 120 ACTGGCACTC AAAAGAGCAC AGGCCAAACA GCTACAGAGG GAGCTGCATA TGTGAAGCAA 180 AAGCTTCTTG GAGTACTCCA CATCTTACCC ACTATATTAC TCCAAAAATA TCAACTGTCC 240 CATATCTGAA ATGTATGGAC ACCATAAGAT CCAGTATGGG GTTTGGTAGG ATGAAAAGTT 300 TACAACCTAC ATAACAGCTA ACAACAATCT AAGCAACAGG GGAAGGAGGG AAGGAGACAG 360 ACTAGAGGGG GAAGGCCCGG GGTCGTGGAT CTCAGAAAGA CTCCTCTAGC TACAGTAGAT 420 ACACACTACT GATAACTAGC TACAGTAATA CACACTACTA ATAGACACAG CACTACAGTA 480 GATACAGCAC TAATAACCAT TGGCCTACAG GAAAATTTGA ATAGGAAGCC CTTCATCTAA 540 AACCACCGCT TGTTCTTCCG AGGTTATGTA GGTCAGTGTT TAGGACAAAA ATAAAGTGAC 600 AACTTGAGCA TACCGTGGAT CGAGCTGCAA TGATAATTCA GAATAGGAGA AACTCACATT 660 CCATGTTGAC ACCCTTCTGT AATGACAACA GCAGATACAG CCACAAGAGA ATGCAGCCTC 720 AAACATGATC AACTCACTGC CCCCACTTTA AAACGGTCCT TAAAGGCAGC TGTTCTGGAA 780 TCTGCCTATG AGGAACACAG AATCTCCAGC TTCCACACGA GTCAGCCTCA TCCCTGATCC 840 TTATGGGGTA AAAAGCACCA TGGTTCCGAG ACTAAAACAG CATTTTCAAA ATCAGTGCTA 900 AAATCCTAAA AATGAACCTT GGTATGAGTA TTTTCAAAAT GAGAAACACA ATCTGGATGC 960 ACGTTTCTCC TATTCCAGTC ATTTGAGAAA CTCATATCAA ATTCTTACTC TTTCAAAAGA 1020 CTCTAAACAA CTTTTATAAT TTAGTATGGA AAAATAAAGC AGCTTGTCAA AGTTAGCATT 1080 TAATTCTGAA TAAATGATCT GGGTGATTTA CTTAAAATCA GGAAAACACA CAAACCAGGA 1140 CAGAAATCAT CCTAAGTCTG AGAACAAGAA CAATTTAATA ATGTCCCGGG AATACTTGGC 1200 AAACACACAC ACACGAAGTT AACTCATCTA TTTCACTTCC TTCGTTAGCA TTTTAGCTGA 1260 AGTATTTCAT ATTTTCCTTA TATGCTCCTG AATCTCTCAA ATGAAAACAG TGAATAGTAA 1320 AAAACAAACG GCCAGGCGCA GTGGCTTACG CCTGTAATCC CAGCACTTTG TGAGGCCGAA 1380 GCGGGCGGAT 1390
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