Tag | Content |
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EnhancerAtlas ID | HS147-08931 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr11:63569630-63570920 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PHOX2A | MA0713.1 | chr11:63570671-63570682 | TAATCTAATTA | + | 6.32 | PROP1 | MA0715.1 | chr11:63570671-63570682 | TAATCTAATTA | + | 6.14 | Phox2b | MA0681.1 | chr11:63570671-63570682 | TAATCTAATTA | + | 6.32 | SP2 | MA0516.2 | chr11:63570184-63570201 | AAGGGGGCGGGGGGGAT | - | 6.01 |
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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 |
GH11I063801 | chr11 | 63569407 | 63572303 |
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Enhancer Sequence | TCCTGGGTTC AAGCAGTGAC TCTCCTACCT CAGCCTCCTG AGTAGCTGGG ATTACAGGTG 60 CCCGCCACCA TGCCCAGCTG ATTTTTTTTA CTTTTAGTAA AGACAGGGTT TCACCATGTT 120 CAACACGCTG GTCTCGACCT CCTGACCTCA GGTGATCCGC CCACCTCGGT CTCCCAAAGT 180 GCTGGGATTA CGGGCATGAG CCACCACGCC AGGCCCATAC CTTTTTTTTT TTTTTTTTTT 240 TTGAGACGGA GTCTCACTCT ATCACCCAAG CTGGAGTGCA GTGGTGTGAT CTCAGCTCAC 300 TGCAACCTCT GCCTTCAGGG TTTTAAGCAT TTCTCTCTGC CTCAGCCACC CGAGTAGCTG 360 GGATTACAGG TGCTCACCAC CACGCCCGGC TAATTTTTGT ATTTTTAGTA AAGACAGGGT 420 TTCACCATGT TGGCCAGGCT GGTCTTAAAC TCCTGACCTC AGGTGATCCA CCCACCTAGG 480 CCTCCCAAAG TGCTGGGATT CCAGGTGTGA GCCACTGCAC CCGGCCTGCC AGGCCCATAA 540 AATTAAAAAA AAAAAAGGGG GCGGGGGGGA TTTGGGGAGA GAATGCAGTG TCTGGAGTAT 600 TAGTCAGCTT TTTGTTGTGG CAATGTTGTG TAACCAACAA CCCTGGAACT TAGTCATTTA 660 CGGCAGCAAA CATTTCTTTC TTATAGGTCT GTAGGTCAAC TGTGGCTGCA CTAGGCTAGC 720 TGGGCTCAAC TGTACTTGGC CCAGCTGTAC TGTGAGTTAG GTTCCAGTCT ACTCCAGGTG 780 TCTCTCATTC CAGGACCCAA GCTGAAGAAG CAGCATATCC CTAGGGCATG CTCTTCTCAG 840 ATGGATGGCA CACGCAATAG AAACCAAGCA CACACCATAC AATTACTACA ACGCCTCAGC 900 TAAGATTACT GCTTACTTCA TGTCTGTTCA CGCCCCATTG GCCAAGGCAA GTCACATGGT 960 CACGTCCACA GTCACAAGGG TGGGGAAACA TTCACTGTCT CATTTGAGGC ACTGAAAAGC 1020 AAGGTAATGG GGCTGGACAT ATAATCTAAT TATAGGAGGG GGTGGGATAG CTGGAAACAA 1080 TAAGCCAACC AACTCAGAAC AAATGCTTGC CATTCTTGCT CTACGAGACC TTTAGGGAGC 1140 AGGTCAAGAA GGATTCATCA GGCCAGGCAT GGTGACTCAC GCTTGTAATC CTAGCACTTT 1200 GGGAAGCCGA GGTGGGAGGA TCACTTGAGC TCAGCAGTTC AAGTGGCAGA ACATGGCAGA 1260 ACCCTGCCTC TACCAAAAAA ATATAAAAAT 1290
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