Tag | Content |
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EnhancerAtlas ID | HS060-13942 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr17:3992440-3994010 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Stat6 | MA0520.1 | chr17:3993769-3993784 | CCCTTCCTGAGAAGC | + | 6.05 | TFAP2A | MA0003.3 | chr17:3992957-3992968 | AGCCTGAGGCG | - | 6.14 | TFAP2A | MA0003.3 | chr17:3993023-3993034 | AGCCTGAGGCG | - | 6.14 | TFAP2A | MA0003.3 | chr17:3993558-3993569 | AGCCTGAGGCG | - | 6.14 |
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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 |
GH17I004090 | chr17 | 3993941 | 3994842 |
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Enhancer Sequence | GGAGGCAAAA ACCAGAATAG AGGATGAAGA AAAGTACATT TGCTCTGTGG CAGTCATTTT 60 GAAACAGAAA TCAGATATAA GACGAAAACA GTCAATGCCC TCCACCTCAA AGCCCCCAAG 120 TGATATAGGC AACCCCTAAG CTAGAAACCC AGGAAAACAG TCCTGTCTAC TCAAATCTAG 180 GGCCATTTTC CAAACCCAAC TTTCATGCAA ACTACCTGCT TCTTATGGTG AGCGCTCTTT 240 GTTAAGGGCC TTTCAGAATA CACTACTCAA CTGCGTAAAT ATTTACCGAG CACCTACTAT 300 TACGTGCCCT TAAGAGAGTT CCTAATTACT TATTTAAGCC TGAGATTTAC ATCCAAGGTT 360 TAGCAAAAAA TTAAGCAGCC AAATAATGAT TGGTCCTTTC TATGGAAAGA CACCTCTCTT 420 GAGTTGATGC CTGTGTTCTC ACTATTCTCT CAGCCTGAGG TGCCCTCCTC CACACACTGT 480 AGCATGGCTA AGGATGCTGT GTTCTCACTA TTCTCTCAGC CTGAGGCGCC CTCCTCCACA 540 CACTGTAGCC TGGCTAAGGA TGCTGTGTTC TCACTATTCT CTCAGCCTGA GGCGCCCTCC 600 TCCACACACT GTAGCCTGGC TAAGGATGCT GTGTTCTCAA CTATTCTCTC AGCCTGAGAC 660 GCCCTCCTCC ACACACTGCA GCCTGGCTAA GGATGCTGTG TTCTCAACTA TTCTCTCAGC 720 CTGAGACGCC CTCCTCCACA CACTGCAGCC TGGCTAAGGA TGCTGTGTTC TCAACTATTC 780 TCTCAGCCTG AGACGCCCTC CTCCACACAC TGCAGCCTGG CTAAGGATGC TGTGTTCTCA 840 ACTATTCTCT CAGCCTGAGA CGCCCTCCTC CACACACTGC AGCCTGGCTA AGGATGCTGT 900 GTTCTCAACT ATTCTCTCAG CCTGAGACGC CCTCCTCCAC ACACTGCAGC CTGGCTAAGG 960 ATGCTGTGTT CTCAACTATT CTGTCAGCCT GAGACGCCCT CCTCCACACA CTGTAGCCTG 1020 GCTAAGGATG CTGTGTTCTC AACTATTCTC TCAGCCTGAG ACGCCCTCCT CCACACACTG 1080 CAGCCTGGCT AAGGATGCTG TGTTCTCACT ATTCTCTCAG CCTGAGGCGC CCTCCTCCAC 1140 ACACTGTAGC CTGGCTAAGG ATGCTGTGTT CTCACTATTC TCTCAGCCTG AGGTGCCCTC 1200 CTCCACACAC TGTAGCCTGG CTAAGGATGC TGTGTTCTCA ACTATTCTCT CAGCCTGAGA 1260 CGCCCTCCTC CACACACTGT AGCCTGGCTA AGGATGACAA CTTAATCTTC AACATTTGAC 1320 ATCACACCAC CCTTCCTGAG AAGCTTTCGA GTTACATATT TTTCCCCTGG TTGCCAACAG 1380 CTCTCTGTCT CTCCTTTTAT CACAGCTCGT ATCACACTGT CTTACACATC TGTCTCTCCC 1440 ACAGAGTATG AACTCCCTGA AGGTAGATTC GCCTCTGGGG TTGTAGCATT GGCACAGGGC 1500 TGATACACAA TCACTACTCA AAAAACACAG AATAAAAGGA GGGGAGTGGG CAAACGACGC 1560 ACTAATGCTT 1570
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