Tag | Content |
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EnhancerAtlas ID | HS007-13027 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr5:10670990-10672600 |
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) |
NFAT5 | MA0606.1 | chr5:10671967-10671977 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr5:10671967-10671977 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr5:10671967-10671977 | ATTTTCCATT | + | 6.02 | TEAD1 | MA0090.2 | chr5:10672302-10672312 | 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 |
GH05I010671 | chr5 | 10671513 | 10671712 |
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Enhancer Sequence | ATTTCCTTAG TATGCATGAT GGAAATGATT CATAATTACC CCAAATACCA TTTCTTAGGT 60 ATTGTTTTTA TGCATGTATT AATTATGGCT GTGGTTGTTT TTGTTTAGAG ATGCTTTGTA 120 CTCCAGTTTG TCTTCTTAGG CACAGCCTTG CCTGTGATGG GGCAAGTCTC AGGATGTGGG 180 TTTCTTGCAT TGGCCACTGG TCCCACTGGG TGAGGATGGA GGTGTCATTG GTATAGAAGG 240 TAGGGAATTT GTGATGAAAC TTGCATCTTT TGAAAAGTTT TGTTTTGTAC AGTGCTCTGA 300 AATTTGTCTT TTATATATGC GTGACGCAAT CTAGTTGCAC ATGTTGCAGC TAAAAGCGGA 360 ACCAACTAAT TGAACATTTT CAGAGTCTGA CGGAAATGGT GGGTGCCAGC ATTCCTAGTC 420 TATCATCCAG TTAGTTTGGA GGCTTGGGTA AGTGCCAGGT ACGGTAAGAA ATGACCACTT 480 TCTCCCAGAA CTCACATCTA GCCTTCACTC CTGTAATAGA AACAGGGATT TGTTGAGCGG 540 CTGCGATAGG TAGGAATTCT GCTAGCAGAC AGGGACACAG GACAAGGGCA AAGTCCCTGC 600 CCTGAAGGAG ATCTTTACCT ACATGAGTTT CTTTTCATGC TGCTTTTCTG CAGACACACA 660 CATTTTCCTC TCAGCTATTT ATCCCTTTGC CATGCACACT GATATCTGGG AGGTTAATCA 720 ACTTGAGGGA CACATGGTTC ATTTTGGAAA GCAGCTGCAA TTCTTTGCAA AGAGGTTTCT 780 AGACCTGTTT TTGAGAATAT TTAAATCGCT GAGCCAAAAG CCAGTGTGAC TGTCCTTCCT 840 GCCCTAGGTG AGTGTGCTGG GAAGCCACCG AGGACATTGA TCTTGGCTCT TCTTTGTATC 900 AGTGATTGAG AAAACAAACA CTATGCTGGA GAGCCACTGA ACGCTCTCCC TGAAGGCAAA 960 GATTTGCTTT ATCTAAAATT TTCCATTGCG TCCAGGAGCA AATCTGCATC ACAGCAATTT 1020 ACTATTTTCT GCTCCAGGAA CTGGAAAACA CAAGCTTGAG CTACGTTAGC TGCTTCCACG 1080 AAACGTGCTG TCATCACTGA AACACATGTA TTTTTTTTTT TTCAGGATTC CAGGTTGAGG 1140 GAAATTTGCT TTTGATTGTT TAATTGCATT ATTATAGATT TTTAGTGGCA TCTCTGGCCT 1200 CCATCTACTA GCAACCTCCA GACAGTGTCA AATGTTCCCT GGGGGGGCAA CATCACCCCC 1260 AGGTGAAAAT CATTGCCCTA GAAATAATGA AGATCATTAT TAGTCCTCTA AGCACATTCC 1320 ATGTTCTCAG TACATCCCTA TTTAAAGACT AACACAAGTG GGTTTCTGGT GACTTGCACA 1380 GGAAACTGAG TCCTTATGCT GCAAAATGTT GGAGTCTTTC TTTTAAGTGA CCCTTGGCAG 1440 TGCAGAATGC TGATGTCAAA ATATAATCAA AAGCTCATTC CGGGCTTCTG GGTAGAGTTC 1500 CAAATCCTCC AGATTATATT AGTTCATTAT AGCAGACCAT GCTGGGGCTT TTCCAGTTGA 1560 CAAATTAGAT TTTTTTGAAA GCATGGCAGT TGGATTTATG AAAATATTTA 1610
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