Tag | Content |
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EnhancerAtlas ID | HS147-05147 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:244898090-244899460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr1:244898105-244898120 | TGAACTCCTGACCTC | - | 6.22 | POU2F2 | MA0507.1 | chr1:244899060-244899073 | ATATGCAAATGAG | - | 7.52 | Pou2f3 | MA0627.1 | chr1:244899058-244899074 | CCATATGCAAATGAGA | + | 6.49 | TP53 | MA0106.3 | chr1:244898917-244898935 | GACTTGCCCAGACATGCC | + | 6.95 | TP53 | MA0106.3 | chr1:244898917-244898935 | GACTTGCCCAGACATGCC | - | 7.03 |
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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 |
GH01I244734 | chr1 | 244897975 | 244900245 |
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Enhancer Sequence | TGGCCAGGCT GGTCTTGAAC TCCTGACCTC AGGTGATCCG CCTGCCTTGG CCTCCCAAAG 60 TGCTAGGATT ACAGGCATGA GCCACGGCAC CCAGCCAACT GTAGTGCAAA TTCTTGGTAA 120 CAATTTAGGA ACTGCCTCTT CTTTCCCTTT ATTTTTTATT CTTTCTGTTG AGACAGTCTT 180 GCTCTGTCGC CTAGGCTGGA GTACAGTGGC GTGACCTTGG CTCACTGCAA CCTCTGCCTC 240 CTGGGCTCAA GCCATTCTCC TGCCTCAGCC TCCCAAGTAG GTGGGAATAC AGGCGCCCGC 300 CACCACACTT GGCTAATTTT TGTATTTTTA GTAGAGGCAG TTTTCACCAT GGAGCCCAAA 360 CTGGTGGCCA TGGAGGCCTG ACCTCAAATG ATCCACCCAC CTCGGCCTCC CAAAGTGTTA 420 AGATTACAGG TGTGAGCCAC TGCGTCTGGC CTTCTTTCCA TTTAAAAACC CACTTGCAAC 480 TGCTGCTAAT TGGAGCGTAT CTTCAGGGCA ACTTGAATCT ATGCTCACAG ATTGCAGTTC 540 TCAAGCTTGG GCCCAAATCA GCTCTCTACT TATATTAGTT TTGCCTCTGC TTTTTCCTTT 600 TAAGTTGACA TATCCAGTGT AGTTGGCAGG ATTCAGAGTG ACTGTCCCCC TACCTCATCC 660 CCACTGAGAA AGGAGAAAGG AAAAAATCCG GTCAGGCAGG CAGTTAGGGT GGGTCCTCAG 720 TTGAATCCTT TCAAAGAACA GCCTGAAGGC ACAGATAAGG GAACTTGCAC AGCGGGGCTT 780 GTCTAAGACA TGCCCACAGC TGCACAGACA AGAAAGCCTA CACGGGTGAC TTGCCCAGAC 840 ATGCCCGCAA TGGAAATTTC CATCCCCTGA CACATGTGCA GTAAGGGGAA CAAAGCAATA 900 TGGATGAACT CAAGCTAAGG GCCCACATTC ACATTATGAG GATGGGGCGA AGCTACCAGA 960 AATTGGCACC ATATGCAAAT GAGATGCCCA GCCCTCATCG GTTTCCTATA AAAGCCTTTG 1020 CATTCAACTG TAAAAACAGC AGCCCTCCTC TGGTTCCCAT CTCTGCAGTG GAGAGCTTTC 1080 TTCCACTTAT TAAACATTTG CTCCAACCTC ACCCTTTCCT TTGTATCCAC ACTCCTTAAT 1140 TTCTTGGTCC TGAGACAAAG AACTCCAAGT GATACCTCAC AACAAGAGAC TGCTACATTG 1200 TGGTGCATTG GCGAGACTAA CACCACCACT GTTTCTGAAA ATGGCCTTGA TACTAGCATG 1260 AACTCTCTGT CTTCAGGAGT CCTATTGTAA ATGCCCAGTG GGTTCACCTT GCCTGCTGCC 1320 TAGACAGAAC CGATTTATCA AATCAGGGGA ATTACAATAG GGAAAGAGTT 1370
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