Tag | Content |
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EnhancerAtlas ID | HS147-30289 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr3:196843650-196844680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr3:196844177-196844192 | ATATGACTCAGCAAT | + | 7.68 | Nfe2l2 | MA0150.2 | chr3:196844175-196844190 | CCATATGACTCAGCA | + | 6.37 | RFX5 | MA0510.2 | chr3:196843670-196843686 | GGTTGCTATACCAACC | - | 6.02 | RFX5 | MA0510.2 | chr3:196843670-196843686 | GGTTGCTATACCAACC | + | 6.04 |
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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 |
GH03I197117 | chr3 | 196844121 | 196844270 |
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Enhancer Sequence | CGAAGACACC ACAGGCCTAA GGTTGCTATA CCAACCTTGG AAATGCCCAT CTTCAGGCTT 60 TTTATATGAA ATAATTAAAA CCTATCTGCA GGGGCACAGG TAGGTTTTAT CATATTAGTG 120 ATGTTTTATT TCCTAAATTA GATGGTGAAT TCCGGATTTA CTGTTCCCAT TATGCTTTAA 180 AATATGTATG AATTAGAATT TTATATTAGG AAATTATACT TGATTAAAAA ATACTCAGCT 240 GAAATTCAAC AGTATTTCCA GGGGAAAATA CACTCTGATT TTCAAATAAT GTAAGCACAT 300 GAAAAGGTGC TCAACATCAT CAGTCACTAG GGAAAGAGAT ATAAAAATAA TGAGATACTT 360 CAGGTCTACT AGGATGGCTA TTAAAAAAAC CACAAAACAA AAAGTAACAA GTGTTGATGA 420 GGATGTAAAG AAATTGCAAC TCACACATTA CTGATGAGAA TATAAAACGG TGCAGGCACT 480 ACGAAAACCA GTTTGGTGGT TCCTCAGAAA GCTAACATAG AATTACCATA TGACTCAGCA 540 ATTCCACCCT TAGGTATATA TCCCAAGTAA CTGAAAGCAG TGATTTGGAC AGATACTTGC 600 ATGCCAGTGT TTATTATAGA ATTACTCACA ATAACCAAAA GGTGAAAATA ACTCAAGTGC 660 CCATCATTAG ATGAATAAAC AAAATGTGGC ATATATGTAT AATTGAACAG TATTGTCATA 720 AAAACAAATG AAATTCTGAT ACATGCTAAC AAATGAGTGT ATCTTGACAA CATAAGTGAA 780 ATAGGCCAGT CACAAAAGGA CAAATATTAT ACAGTTCCAC TTTTATAAAC TATCCAGAAT 840 AGGCAAATTC ATAGAGACAA AAAGTAGATT AAAGGTTACC AGGGGCTGGG AAGACAGTGG 900 AAGGGAGAAT TACTGCTTAA TGGTCACAGA GTTTGTCTGA AGTAATGAAA AGGTTTTGGA 960 AATAGTGAAG GGTTCCGAAA ATTGTGAATG CAATTAACAC TACTGAATTG TACACTTAAA 1020 AATAGTTAAA 1030
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