Tag | Content |
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EnhancerAtlas ID | HS052-30764 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr5:113585490-113586920 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr5:113586744-113586754 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr5:113586744-113586754 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr5:113586744-113586754 | AATGGAAAAT | - | 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 |
GH05I114249 | chr5 | 113584898 | 113586900 |
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Enhancer Sequence | AAGAGGTATG CAAGGCTGAT TTCTTGCAAA AATATCATCG ATCTGAATAT GAAGAGAAGA 60 AGACTTGCAG GTAAGGATAA ATATGCTGAA ATTTAGTACC CCATGTTATG TTTAGTTACA 120 TGTTATGAGA GTGGCTTAGT ATCTTGGCAA CATATGATAC GTATAACATT CTTTTTATGA 180 GAGCTTTTAA AATTACTCAC ATATGCTTGC CTAGATTGTC TGGTTCCTTA TGGTTTCCAT 240 TGTGCTATAT AAACAAAGTT AAGGATGTGC ATTCCTAGTA AGAGCCTGCT AAGAGCCTAG 300 GAAAATGGGA AGAAATCTTT TAATGATAGT GTGTATTTTC ATTTTTCTGT AGCCTTATAA 360 AGAACCAGGA AATACCATGT CTAGCATGAG CAGTTTGGAT AAGCCTTTTA AAAAAAGGAA 420 TGTTATATTA TAAACAAGCT ACATTGTTCC TTAACTGATG TGTATCCCCA AAGTCAGCAT 480 GATTCTCTGT TATCTTAACA GGTTTGGGTC TAGAACTGGG GAACTTGACA GAGCTTCTTC 540 ATTATAATGG GAATCTGAGT GAGTTTCTAA GCCCACTCAG ATAGGGTCTC TGGAGAATTG 600 GAAGTGTCCC TTTTATTGAG GAGTAGAGAG TGCTCGCCTA GTGTTGAGCT CATTTTCAAA 660 GGTTCTCTGA GACCAGAGGT TTAGAAATGA AAGGCTGCTG TATCTGCTTT GATGTGTCAG 720 AACAACATTA GAGACATTTC CAGTAGTTGG ATGGAAATGT CAGCTGATAA TATGAAAAGG 780 TAGAGTGCAC AGGGCACATC TCAGGAAGTT TGATAAAAAT GGCATTCAGG AGATAGCTCG 840 TAATTGGGTC CTATAAGTGA TGTAATGAAG TCTATGGCCC CTGAAGGAAT GCAGGCAAGA 900 GTCTGTGAAA TGCACAAGCA AGATTCAGAG TGAGCCGTCT ATGGTCTATT TTGGGCCACA 960 CTTAGAGCCA CATTGGTCTC ACTGAGTTGT CTCTACTGCC TGATTCTGAG CCTCTTACTA 1020 ATGGAAAGGA ATTTAATATT TCTCTCCGGC CATCCATAGA CCATTCATTG CCCACCCATA 1080 GTGATGAGTA GATTGTGCCT CCATAACCAG CAGGCTGACT CTGGTGTTTT AAGAACATAT 1140 CTAGGACAGA TGATGTTTAG GATGCTTATG TGGTTTGATT GGCAAGCTGT ATTTATACCA 1200 ATATATAAAA ACAGAATATT TCCATGAAGA TATGGATTTC TAATTTCTCC AAATAATGGA 1260 AAATTCCTCT AATAACAGAT CCTGGTAATG CGGTACATTG CATCCTGGTA ACAGTCAGGT 1320 GGAGCTGAGT ATCATGGGCC CTTTGTAAAG GGGTGCAAGT GTTTTCCGGT TGGCCACAGG 1380 CCTTTTGCCA GTGCTGAATT GTGTTGCCTA TTGCAATTAC AACCAGCCTG 1430
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