Tag | Content |
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EnhancerAtlas ID | HS182-20500 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr8:8685490-8686940 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr8:8686812-8686833 | CTCAGCACCCTGGACATCATC | + | 6.72 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_58469 | chr8:8677423-8751805 | Ly1 |
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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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Enhancer Sequence | TTTTTTTCTA ACAGCTCTTC AGCTGTCCTA AACCACATTT ATTGATGAAT TTACTTCCCC 60 CGGTGATTAG GAATGCCACC TTTTCCCAAT CTGGAGGCAC AGTGTGAAGC AGCCTACATC 120 TGCCAGGACT CTGACATATG CCCTACCTTC GAGAATGTTT CAGTGAATGA TGCTGATGCA 180 AATATACAAG GGAACTCGTC AATCATTTGT GTCGCTTACA ACCAAGAGAA TAAATTAACA 240 GGATGAAACC AGAGATTAAA AAACATCTCA AAAGCATGGA GCAACAGGAA CTGTTTAACA 300 AGATAATGTC TAATAGGATA TAGTTTGAAC TTACACTTAG GTGCGGTGAA ATCAAAGCCA 360 TCAAATACAG AAGAGAAATA GTGGGGAGGC AGAACACATG CCAAGGCCTC CTTGGGACAC 420 TGCCAGTAGC TCTGACCTAG GGCAGTCTGA AGCTGCAGTG TTCTCAGATG GCCTTCAAAG 480 ACGCAGGGCC ATACTGTATC TTAGGCCGTC TTCACAGAAA GAAGGTAACA GCCCGGGCCC 540 TAGTCCACAT TGCTCACACC ATTACCTAGA GCCTGCAATT CAGTTTCAGA CACGACCAGT 600 TAAGGGGAAT ATCAACTAGA CCACTCCACG GAGGAAAAAC GCAAAAGCTA AGGGCATTTA 660 AAACAATATC ACATGAAGAA GGAATAACTG GAGATGCCCA CTGCCCACTA AGCAGTGACA 720 CTCTGTAATG CGGGCAAGGC CCACGCCACC TTTATCTGTG CAGTCCTCAC GGCGTGCATA 780 GCCTGGAAAG AGCTGGCCCC TAATGAATAA GCATTGAGCA AAAGTGGAGA ACTGAGGGGA 840 CAGGATTTGC TGCTTTAGAT TTATGAGGTA GATTCCTTAG AGACTAGTGG CCGAGCTCTT 900 ATCCCGCCCC TAGCTCAGTC CTTCATGTCT TTCCTTTAGA TCAGGCTCTG TCAATCTGCT 960 AAGAGCACCC CTGCCTCCCT CTTCCGGCCC GTTACTGCAG CCAGCAGCCT TCTTCCTACA 1020 ATGCAAATCT ATTCTCCCCA GCCTCTCACA TTCAAGTGAA CTCCTTGGAC ACTGCAGAAT 1080 GGGCCCTTTG TGATCCAGCC CCCTGCCCAC TTTCCCAGCT CCTTGCTACT TTAACATAAG 1140 GAAATCAAAC TTTTCAGGGA CCCCAATACG TCACCTCTCA TGCCTCTGCT AAGCTCTTCT 1200 CTGGGTGCGG AGCGCCCTCC CAGAACCCCT TCCCCATCCT GAGTCTGGCA GATTCCAACT 1260 CAGTATGTGT ACCGGGCTGC ACCCCCACCT GGAGGTCCTC TCCAGCACCC TTCTCCGTGC 1320 AGCTCAGCAC CCTGGACATC ATCTTCTTCA CTGCCTTTCT CACACTGTGC TCTAGTTCAT 1380 TCATGGACAT CTCTATTTCT ATATCAGATC GTGAGATCTG TCCAGCGCCA TGGCCCATGC 1440 CTGTAATCAG 1450
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