Tag | Content |
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EnhancerAtlas ID | HS108-16541 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:28163430-28165080 |
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) |
FOXA1 | MA0148.4 | chr17:28164752-28164768 | GTTTGTTTGCACAGGG | - | 6.03 | NFE2L1 | MA0089.2 | chr17:28163810-28163825 | GAGTGACTCAGCAGA | + | 6.62 | Nfe2l2 | MA0150.2 | chr17:28163808-28163823 | AGGAGTGACTCAGCA | + | 6.61 | Nr2f6(var.2) | MA0728.1 | chr17:28164058-28164073 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr17 | 28163748 | 28164008 | chr17 | 28164662 | 28164874 | chr17 | 28164244 | 28164334 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I029835 | chr17 | 28162400 | 28164410 |
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Enhancer Sequence | GCTTTGTTCA TCACTGAATA CCCATTGCCT AGTGCTCTGT GCCTGCCACA GAGTAGACTT 60 AAATAATTGT GGAATAAATA AGCTCAGTTT TCTCAAAACT CAGAAAACAA GAATATCTCT 120 TCTAGAACAG GGATAAATAC TACTGACATC AGAAATGTAA TGTGAAATAA CGTACGTACT 180 AACATTTGTT TTTACTAACC AGGCACATGG TAGTGCTCAA GAAATGTTAG CCATCTTTTC 240 AGTTATTTGT GGTTTTAACA GCAAGTCATG GCCTTTGTAA CTCTACTTTT CTAATTATAA 300 AGTGAGAGGA AAAATTACTA CCGCTTTTCT ACTGCCAAAG CACACTGTTG AGATTACAGA 360 AAATATACAA AAGGCATTAG GAGTGACTCA GCAGACAGGA TCCACTGAGA TTAAGAATTT 420 GTTAAATTTA CAACTCTCAT GACATTTGTC TTAACCGGGG TCATCCATTG CTCTCTACAA 480 GGTTAACACT TCTTGCCTAA TAGCTTTGAA ATTACAGCTT CACCAGGACT TTACATTCAG 540 CACTAAGAAA ATAGACATCT TAGGCTGGGC GTGGTGGCTC ATGCCTATAA TCTCAGCACT 600 TTGGGAGGCC GAGGAGGGCG GATCACTTGA GGTCAGGAGT TCAAGACCAG CCTGGCCAAC 660 ATAGTGAAAC CCATTCTCTA CTAAAAATAC AAAAATTAGC CAGGTGTGGT GGCAAGCACC 720 TGTAGTCCCA GCTACTTGGG AGGCTGAGGC AGGAGAATCA CTTGAACCTG GGAGGCAGAG 780 GTTGCAGTGA GCCAAGATCA TGCCACTGCA CTCCAGCCTA GGTGACGCAA CAGAGTGAGA 840 CTCTGTCTCA AAAAAAAAAA AAAAGTAAGA AAATAGACAT CTTAGATAGC AAACTAGGGT 900 TGAGAAAGAT TGTGCTTGAG TACAATAGTG GCAGCACTCT AGAAATTCAC GGAAAGAAAG 960 GAAAAAATTA ATCTGGCTAT AAAACACCCC AGTAATATCC AATTTCCAGT GATAGATACC 1020 ATCTTACTGG TGGCAGCAGT GGGCTATCCA TTGTAGCTGC CAGCTGTAGT GGGGAGGCAT 1080 GGGTGGTGGC AGCAGGAGCA GCTATGGGAG CAGCAGTGGT GGCGGTGGGA CCCCTGTGGC 1140 CCATGTCCCC GAGGCAGCCA ACTGCACCAC CCCCACCCTC GCACGGCTGG TCAGGACCCA 1200 CTCTCCCAGG CCCAGAGCCT CTGCTGTGGC CTCAATCTTG CTCCCTGCCA CATCCCAGGA 1260 GCCTGTGAGA ACCCAGCCAA AGACACAGCC AAGACTTGCA GGGCTGGTCC CAGGAGCATC 1320 AGGTTTGTTT GCACAGGGTT GGCTGGGGCC ACTGTGCCAC CTGCATCTTG CCCGCTGCCA 1380 CTGTGAGGGA AACGCAAAGA GGAGGCATGG CCAGGGCTGC GCACTCCATG GAGCTGGGGG 1440 GAGCTGGGGA AAAGCAGAAG CCCTGCCCCT TGCAAGCTGG CAGGGTGGGA GCTCCCCAGG 1500 CACAACTGCA GCTGCACAAG CTCTGGCTGC AACCTGGGCA CCCCTGTGCT CTTGGGAGCC 1560 TGGAGCAGGC GGGAGCCCTG CCCTCCCAGG CATAGCTGCA GCTGCCCAAA CCTCGGCTGC 1620 AGACCCAGGC ATCTCTATAC TTTTGAGGGC 1650
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