Tag | Content |
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EnhancerAtlas ID | HS172-10301 |
Organism | Homo sapiens |
Tissue/cell | SGBS_adipocyte |
Coordinate | chr8:27194360-27195770 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROG2 | MA0669.1 | chr8:27195365-27195375 | GACATATGTT | - | 6.02 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_09156 | chr8:27181374-27208460 | CD14 | SE_10868 | chr8:27181046-27285079 | CD20 | SE_53591 | chr8:27194567-27195731 | Spleen | SE_62276 | chr8:27181124-27271753 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH08I027337 | chr8 | 27194523 | 27195917 |
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Enhancer Sequence | TTTTATTTTT GAGACGGAGT CTCTCTCTGT CACCCAGGCT GGAGTGCAGT GGCACAATCT 60 CGGCTCACTG CACCCTCTGC CTTCTGGATT CAAGCGATTC TCCTGCCTCA GCCCCACGTC 120 CCCACCACCC GTCCCCCCTC CCCCCGCCAC TGCCAGTTTT TTAATAACCG CTAATTAATA 180 CTTATTGATG AATAGTAGTT TTTTGAGATA CAATTCACAT ACCGTAAAAT TCACCTTTTA 240 AAAATGTGCA ATTCAATGAG TTTTAGTACG TTCACAGAGT TGTGCAACCA TCACCGCTTT 300 TTTTCTTTTT TTGACAAGAG TCTTGTTCTG TTGCCCAGGC TGGAGTGAAT GGCATGGTAT 360 CAGCTCACTG CAACCTCTCC CTCCTGGGTT CAAGTGATTC TCCTGCCTCA GCCTCCCAAG 420 TAGCTGGAAT TACAGGCACC TGCCATCATG CCTGGCTAGT TTTTGTATTT TTTAGTAGAG 480 ATGGGGTTTC ACCATGTCGG CCAGGCTAGT CTTGAACTCC TAGCTCAAGT GATCCACCCG 540 CGTTGGCCTC CTAAAGTACT GAGATTACAG GCGTGAGCTA CTGCGCCTGG CCCTCCATCA 600 CTGCTATCTA ATTGCAGAAT ATTCTCGTCA CTCCAAAAAG AAACCCCCGT ACCATAAGCA 660 GTCACACCGT GTTCTCCACT CCCCCGTCCC CTGGCAAGAC TAATCTACTT TCTATTTTTA 720 TGGATCTGCC TTTTCTGGTC ATTCCATATA AGTGGAATTG TACAACACTG TGGCCTTTCG 780 CGACGGCTGC TTTCACTTAG CACAATGTTT TGAAACTTCC TCCATGTTGT AACATCTATT 840 AGTACTTCGT TTCGTTTTGA TTGATATTTA TTGATGAGTA ACATTTTGTT GTGTGGATAT 900 GCCATATTTT GTTTATCTCT TCATTAGTAA ACATTTGGAT TGTTTCCACT TTTTGACCAT 960 TGTAAGTACT GCTGCTATAA ACATTCACAT ACAAGTTTTT TTGTGGACAT ATGTTTTCAT 1020 TTCTCTGAGC TATAGACTTA AGAGTGGAGT TGCCGGGTCC TGTGATAACT CTGTTTAACA 1080 TTTTGAGGAA CTGTTGAATG GTTTTTCACA GCAGCTGCCT CATTTTTTAT TCCCATCAGC 1140 AGTACTTCTT GGTTCTAATA CCTCCACGTT CTCGCCAACA CTTGTTGTTG TCTGTAATTT 1200 CGTTGTTAGC CATCCCAGTG GGGATGAAGT AGTATCTTAC TGTGGTTTTC AGTTGCGTTT 1260 CCCTGATAAT TAATGATGGT GAACATCTTT TCATGTTCTT GTTGGCCATT TGTATGTCTT 1320 CTTGGGAAAA AAAATGTCTG TTCAAATCCT TTACAAAGTA TTTATTTTTT ATGTCAACAA 1380 TATAACCACT CAGTACACTG CTTTTTAGAC 1410
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