Tag | Content |
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EnhancerAtlas ID | HS112-11437 |
Organism | Homo sapiens |
Tissue/cell | KELLY |
Coordinate | chr5:10671040-10672620 |
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 | TTTCTTAGGT ATTGTTTTTA TGCATGTATT AATTATGGCT GTGGTTGTTT TTGTTTAGAG 60 ATGCTTTGTA CTCCAGTTTG TCTTCTTAGG CACAGCCTTG CCTGTGATGG GGCAAGTCTC 120 AGGATGTGGG TTTCTTGCAT TGGCCACTGG TCCCACTGGG TGAGGATGGA GGTGTCATTG 180 GTATAGAAGG TAGGGAATTT GTGATGAAAC TTGCATCTTT TGAAAAGTTT TGTTTTGTAC 240 AGTGCTCTGA AATTTGTCTT TTATATATGC GTGACGCAAT CTAGTTGCAC ATGTTGCAGC 300 TAAAAGCGGA ACCAACTAAT TGAACATTTT CAGAGTCTGA CGGAAATGGT GGGTGCCAGC 360 ATTCCTAGTC TATCATCCAG TTAGTTTGGA GGCTTGGGTA AGTGCCAGGT ACGGTAAGAA 420 ATGACCACTT TCTCCCAGAA CTCACATCTA GCCTTCACTC CTGTAATAGA AACAGGGATT 480 TGTTGAGCGG CTGCGATAGG TAGGAATTCT GCTAGCAGAC AGGGACACAG GACAAGGGCA 540 AAGTCCCTGC CCTGAAGGAG ATCTTTACCT ACATGAGTTT CTTTTCATGC TGCTTTTCTG 600 CAGACACACA CATTTTCCTC TCAGCTATTT ATCCCTTTGC CATGCACACT GATATCTGGG 660 AGGTTAATCA ACTTGAGGGA CACATGGTTC ATTTTGGAAA GCAGCTGCAA TTCTTTGCAA 720 AGAGGTTTCT AGACCTGTTT TTGAGAATAT TTAAATCGCT GAGCCAAAAG CCAGTGTGAC 780 TGTCCTTCCT GCCCTAGGTG AGTGTGCTGG GAAGCCACCG AGGACATTGA TCTTGGCTCT 840 TCTTTGTATC AGTGATTGAG AAAACAAACA CTATGCTGGA GAGCCACTGA ACGCTCTCCC 900 TGAAGGCAAA GATTTGCTTT ATCTAAAATT TTCCATTGCG TCCAGGAGCA AATCTGCATC 960 ACAGCAATTT ACTATTTTCT GCTCCAGGAA CTGGAAAACA CAAGCTTGAG CTACGTTAGC 1020 TGCTTCCACG AAACGTGCTG TCATCACTGA AACACATGTA TTTTTTTTTT TTCAGGATTC 1080 CAGGTTGAGG GAAATTTGCT TTTGATTGTT TAATTGCATT ATTATAGATT TTTAGTGGCA 1140 TCTCTGGCCT CCATCTACTA GCAACCTCCA GACAGTGTCA AATGTTCCCT GGGGGGGCAA 1200 CATCACCCCC AGGTGAAAAT CATTGCCCTA GAAATAATGA AGATCATTAT TAGTCCTCTA 1260 AGCACATTCC ATGTTCTCAG TACATCCCTA TTTAAAGACT AACACAAGTG GGTTTCTGGT 1320 GACTTGCACA GGAAACTGAG TCCTTATGCT GCAAAATGTT GGAGTCTTTC TTTTAAGTGA 1380 CCCTTGGCAG TGCAGAATGC TGATGTCAAA ATATAATCAA AAGCTCATTC CGGGCTTCTG 1440 GGTAGAGTTC CAAATCCTCC AGATTATATT AGTTCATTAT AGCAGACCAT GCTGGGGCTT 1500 TTCCAGTTGA CAAATTAGAT TTTTTTGAAA GCATGGCAGT TGGATTTATG AAAATATTTA 1560 GGATTAAAGG GGAGGATGAG 1580
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