Tag | Content |
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EnhancerAtlas ID | HS060-10865 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr14:103277410-103278830 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-5 | MA0063.2 | chr14:103278330-103278340 | CTCAAGTGGT | - | 6.02 | ZNF263 | MA0528.1 | chr14:103278476-103278497 | TCCCCATTTTTCCCATCCTCC | - | 6.45 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_11188 | chr14:103268895-103279300 | CD20 | SE_32528 | chr14:103278204-103279124 | GM12878 | SE_62609 | chr14:103230342-103288105 | Tonsil |
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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: 3 | ID | Chromosome | Start | End |
GH14I102811 | chr14 | 103277661 | 103277810 | GH14I102814 | chr14 | 103277821 | 103277970 | GH14I102812 | chr14 | 103278205 | 103279124 |
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Enhancer Sequence | TATAGTCTTT GCATCTTTTT TCAGTATGTA TGCACTTAGA TCATCTTGTA GGACGCCAGT 60 CCCATGCATT ATACACTTTG TATCTCACAG TGGAGTGGAG GACAGCCTGA TCCTTAAGGG 120 GATGCCGAAT TGCTGCATCC CCATGATTTT TGCTGCTTTG ATTCTTCTCA TGAGCCCCGT 180 TGCTGCTGTC TGTATTAGCG TCCTTCTGAG CAAACAATGG GTACCTTTTT TTTTTTTTTT 240 CTTAAGAGAG AGTCTTGCTA TGTTGCCTCA GGCGGGAGTG CAGTGGCTAT TCACAGGTGC 300 TGTCGTACTG CCCTGGATGA TAGTACACTG CAGCCATGAA GTCCTGGGCT TAAGCAGTTT 360 TCGCCTCAGC CTCCTGAGTA GCTGGGACAT TAGGCCCGTG CCGCCATGCC TGGCTCTTGA 420 CCATTCCCAC AAGCCACACC TACAAGGAGC TCAAGGAGCT GTTTGCGCTG TAGGCGGTTT 480 TTTTTTTTTT TTTTTTTTTT TGGTTTTTGT TTGTTTTTGT GCAGAGGTCA GATCTCTTGT 540 CTCATAGTGC AAAGGCGATG AAGGCCTTCA TTACAGTCTC TCAATTTGAC TCTCAGTTTG 600 ATCGGAAGTT GCTAAGATGG GCTGACATTG TGAGGAGGAT ACTGCTACAG CAGTAGTGTG 660 TGTGTGTGTG TGTGTGTGTG TGTGTGTGTT TGTACAGACT GTCTCACTCT GCCACCCAGG 720 CTGGAGTGCA GTGGTGCAGT CATAACTTAC TGTAACCTTG AACTCGTGGG CTCAAGTGAT 780 CCTCCTGCCT CAGCCTCCCG AGTAGCTAGG ACTGTAGGCT TGTGCCACCA TGCCTGGCCC 840 TTTTTTTTTT TTTTTTTTTT TTTTTTTTTT GTACAGACAG GGTCTTGCTG TGTTGCTAAG 900 GCTGGTCTCA AACTCCTGGC CTCAAGTGGT CTTCCTGCTT CAGCCTCCCA AAACACTGGT 960 ATTACAGGAG TGAGCCAGAG CACCTGGCCT GAAGCTATAT ATTATTGTTA ACTGCAGTCA 1020 TCCGACAGTG CTATAGAACA CTAGACTCTG TTCCTGTCTA GCTCTCTCCC CATTTTTCCC 1080 ATCCTCCTAC CCTTCCTAAC CTCTAGTATC CTGTGTTTAC TTTTGACTTC TGTGAGATCA 1140 ACTTTTTTTA GCTTCCACAT GTATTAGTGA GAACATGTGG TGTTTAACTT TCTGTTTTTG 1200 GCTTATCTCA CTTAATATAG TGTCCTCCAC TTCTATCCAT GTTGCTGTGA ACGACAGGAT 1260 TTCATTCATT TTTATGGCTA AATAGTAGTC CATTTTGTAT AGATACCACA TTTTCTTCAT 1320 CTGTTGTTGG ACACCTAGAT TGATTCCCTG TTTGGCTATT GTGAATAGTG CTACGGTAAA 1380 TATGGGGTAT AGATGTCTCT TTGATGTCAT GATTTCCTTT 1420
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