Tag | Content |
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EnhancerAtlas ID | HS187-09669 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr16:74471830-74473190 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr16:74472060-74472070 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr16:74472060-74472070 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr16:74472060-74472070 | AATGGAAAAT | - | 6.02 | ZNF263 | MA0528.1 | chr16:74472372-74472393 | TTTTCTTCCTCTCCTTCCCCT | - | 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 |
GH16I074438 | chr16 | 74472332 | 74473139 |
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Enhancer Sequence | AGTGAGCCTC TGGCCTTGGC TTCCCAAAGT GCTGGGATTA CAGGCATGAG CCACTACACC 60 CAGCCTAGAG ATCAGTCTTA TTTATAGCTT TGTTTTTTGG TAAAACGTAC TAATAATGAA 120 AAGCACAAGT GAATCATTTC TCTTTTTACG TGATTTTTTG GGAACATAGT GATGCATATG 180 TGTGCTTTGC TCCATAAGGC AATACTTCTC TTAAAGTCCA CCTAACTAAA AATGGAAAAT 240 TCTTATGCCT GTAATCCCAG CACTTTGGGA GGCTAAGCGG GGTGTGGATC ACGAGGTCAG 300 GAGTTCGAGA CTAGCCTGGT CAACATAGTG AAACCCCATC TCTACTAAGA AAAATACAAA 360 AAATTAGCCG GGCATGGTGG CGCACGCCTG TAATCCCAAC TACTCAGGAG GTTGAGGCAG 420 AAGGATCTCT TGACCTCAGG AAGCGGAGGT TGCAGTGAGC CAACATTGAA CCACTGCACT 480 CCAGCCTGGG CGACAGAGCT AGACTTTGTC TCAAAAAAAA AAAAAAAAAA GAAAATTCTT 540 GCTTTTCTTC CTCTCCTTCC CCTTGGGGTT TGGTTTTAGG CTCTCTGATG ATAGCCTATG 600 ATCACAATGC TTATGTAAAA CCACTCTGGC TTTATCTGCT GATTGATCAG TTCCAACAGC 660 CCCATAGAGC TGTGGGTTTC CTGTTTCATA TCTGACAGTG GTCATTCTCA GAATAGTCTT 720 TTCCTATCAA CATGTAATTA AATCCTTTTA CTGCTGCTCT TGTGAACACT TTTGAACACT 780 GACAGTTACA CTGATATGTA ACTGAGCAAA CTTCGCTTTG CCTTTATTTT AAAGTTGCCT 840 GTGCTCATCA GGCGATCTGA TACTCCACAT CGAGAAGCTC CAACCTCAGG GTTGTGGGAG 900 TGTTTTTAAT TGTTTCCTGC GTTTCCTACC AGGCATTGCC AAGTGACTAG ACTTAACCTT 960 CTCAGGAAGA CTCGAATGCT TTCCCCTCTC TTACCCTACC CCGTCATTAA GGCATAGCAG 1020 ATCCTCGAGT TGACCTTTCA TACTACTGAC TCTCACGTCA GTCTGCCCGT TGGTCAGTTT 1080 ATGCTTAGTG ACTTGTCCTT CAGTTAGGAG ACTTATGTTT TCTTGTTTGT TTTTTTGAGA 1140 CAAAGTCTCA CTCAGTCACC CAAGCTGAGT GCAGTGGTGC AATCACGGTC ACTGCAGTCT 1200 TGACCTGCTG GCTCAAGCGA TCTTCCCACC TCAGCCTCCT GAGTAGCTGG GACTACAGGC 1260 GTGCACCACC ACATCCAGAT AAATTTTTTT AAGAGATGGG GTCTCACTAT GTTGCCCAGG 1320 CTGATCTCAA ACTCCTGGCC TCAAGTCATC CTCCCACCTC 1360
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