Tag | Content |
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EnhancerAtlas ID | HS073-05260 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr16:29712740-29714320 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr16:29713162-29713177 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr16 | 29713855 | 29714040 | chr16 | 29714168 | 29714307 | chr16 | 29713768 | 29713912 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I029700 | chr16 | 29711421 | 29715069 |
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Enhancer Sequence | CTTTCTGTGC AGTAAGCAAT GGGACCTAGA CTGAATCCCT GGCGTTTCGG TAATACACCC 60 ATCCATCCTG TCCACCCCCA CCCATCCTGT CCACCCCCAT CTATCCTGTC CACCCCCGAC 120 CCATCCTGTC CACCCCCGAC CCATCCTATC CACCCCCTTG TGCTTCCATC CACTCATCAC 180 TCTTCCCACC CCTCCGCCCA CCCACCATCC GATGCTACAG AAGCCCAGAA CTGGGGCACT 240 CAATCTAGAG GTCAAAGATG GCAAGAGGTC AAACCAGATT GACAGTGAGT CACCTCAGTG 300 GATATGAGTT TTAGTGTGCT GAGGCCGTGA AAGGTAAAAG CATTTAAAAA CAGCAAGGCC 360 AGGCACGGTG GCTCACGCCT GTAATCCCAG CACTCTGGGA GGCCAAGGCA GGTGGATCAC 420 CTGAGGTCAG GAGTTCAAAG CTAGCCTGAC CAACATGGGG AAATCCCTTC TCTACTAAAA 480 ATACAAACTT AGCTGGGCGT GGTGGCATGT GCCTGTAGTA CCAGCTACTG CTACTTGGGA 540 GGCTGAGGCA GGAGAATCGC TGAACCCGGG AGGCGGAGGT TTCCATGAGC CGAGATCACA 600 CCACTGCACT CCACCCCGGG GAACAAGATC GAAACTCTGT CTCAAAAAAC AAAAACAAAA 660 AACCCACAAA AATTAGCCAG GCGTAGTGGC GGGTGCCTGT AACCCAGCTA CGCAGGAAGC 720 TGAGGCACAA GAATCACTTG AACCTCAAAG GCAGAGGTTG CAGTGAGCCG AGATCATGCC 780 ACTGCACTCC AGCCTGGGCG ACAGAGTGAG ACTCTGTCCC AAAAAAAACC CAGAGCAAAC 840 AAACAAAAAA CACAACGGCG AGACATTCTT AGCAAACCAA CTATCTGCAA ACAATTCAAC 900 GTCGGATCTT TAAAAAAATC CCGCTGTGGC ATTATGCTGC GGACACATAC ATTAATTTAT 960 GGCTAGCCCT TCAAGACAAC CAGGTGGGTA AAATTATGTA AATGTTCACC GCCTCTATAC 1020 TTTGTTCCAA TGACTTCCTG AGTAATTGAT TGTTTTGCCA ATTACTCAGC AACATTTAAG 1080 ACCTGCTTCC GGAGGCCCTA AGTAGCTCAG CATTCTAAGA CCGAAGTACT GAAGAAAATC 1140 TGCCTGTGTG GCTGTGAATA ACATCTCCAT CCGTCACTGT GCACATCAGA TTTAGGCCAG 1200 ATAACGCAGG CTTTATTTAT TTCAGGTACG CCTTGCGCTT CAGATCATGG GACTCTAGTA 1260 TAGCACCCCC AGAAAATTAT CAAGGGCAAA AAAATCATAA TACATACCTC TAGTTCAGTG 1320 GGTCCTTGGA TAACCTCTTT CCTCTCTCCT AGTTCTTCAG CTAAAAGATT CAGGAGCCTT 1380 AGCAACAAGA AGGAGCTATC CCACAAGTTG CATTATTCTA GATATTCGGA CACTTTTTTT 1440 TTTTTTTAAG CAGGAGTCTT GCTATGTTGC ACAGGCTGGT CCTGAACTCC TGTCCTTAAG 1500 TGATTCTCTT GCCTTGGCCT TCCAAGTAAC TGGGATTACA GCGGTGAGCC ACCGTGCCAG 1560 GGTTTTGGAT GCTTTTTTTT 1580
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