Tag | Content |
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EnhancerAtlas ID | HS182-18827 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr6:39306190-39308520 |
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) |
MYC | MA0147.3 | chr6:39306550-39306562 | GGGCACGTGGCT | - | 6.18 | RREB1 | MA0073.1 | chr6:39306715-39306735 | TGACAGGGGGTGGGTGGGGT | - | 6.3 | RREB1 | MA0073.1 | chr6:39306719-39306739 | AGGGGGTGGGTGGGGTGGGG | - | 7.62 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65542 | chr6:39305871-39311798 | Pancreatic_islets |
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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 | AATTCTGTGT GCAAGACCTC TGGCAGGCCT TGCTGTTTAA TTAAACAAAT ATGGTCCTTA 60 TTTTTAAGAC ATTCTGATCT GTCTGAATTG AATTCTAGAA CGGGAAGTAA GAAGACAAGT 120 ACACCGAGCC TATGATGGTC ATGTGTTCCT GTCACTCTGG ACTTGTGGTT CCCAGCTCTG 180 CTACACAACG GAAATCTCTG GAGAATCTCT AGACATCCTG GTGCCCAGAC CACAGCCCAG 240 AACCATTCAG TCAGGATCAC TGGGGTGGGT CCAGGTGATT CTGAGGCATG GCCATGGCTG 300 AAACTCACTG CTTTTGTCTC TCTAGTACAA GGACTGGCAG GGCAAGAGCT GGGGGCCCGT 360 GGGCACGTGG CTGCTGATGA GATCTGGGCT CTGATGTTTC TGCTGCACTG TTGAAATGCA 420 GCCTGGGCCA GGATTGTGAA CGCTGCCGGT GGTAGGGAGC ATGGAGTCTG AGCCATCTCC 480 CACCCAGGAT GGTCTCTGAG CCCCTCACAC ACTTGCATGC AGTAATGACA GGGGGTGGGT 540 GGGGTGGGGC CTGGGAAGAA ATGCTACAGA ATAGGGGGGA GAGCACGCTC TGCCCCAAGA 600 CATAGCTCCT TACATGCACA GACCTCAACA CAAAAGGCAC CATTTCAAAC TCATTCACTT 660 TATGGGCCCC AGTTAAGTGA TGAAGCTCTG TCTGTATTGG GGTTTTGATT ACCGTGGGCT 720 CCCAGAAAGG AGGGCACACT ACAGATGTAC CATTAAGAAA AAGCAAAATC ACACCTCATG 780 GTGTTGGGCC AGCTCTCACC ACAGAGGCCA CTTCCCTGTT AATAATTCCT TGGTGCTTGG 840 GAGTTGATAA GGGACTTTAA TGGAGATTAT CTGGGAAAGG ATCAGAGCCT GGGCAAGGGT 900 GGAATCTGTA CATGACAGAC AGTGAGAGGG AGGCTTGGGG AGGTGACCTG CCCAGTGTCA 960 CGCAGAGCAG AGATGGCCTT GGAATTTCCG CCTTTTCCCT CCCAGCTCGG GGCTCTTTCT 1020 CTTTCCCTGG GAGGGTTTCT GAACACAGAA GAGAGCTGGA GGGTTTCTCT GAGTGGGGCT 1080 GGAGGGCTGG GAGAGGCAGG ACCTCTTCCT AACACCTCTT GGAGAAGACA GACTTGTGGT 1140 TATGGGGGTC GCACCATGGT TCCTTTCCAG ATGGGAATAC TTCCAAACTC AGGGATTAAG 1200 CAAGATTAAA AACAAAAAGG CCCTCTAGAA AGGGGTTAAC CTCATTTCCT CAGACATAAA 1260 AACTGTCCTT GGCAGTTGGA AACAGCAGAG TTGACTCCAC GGATGACTGA TGCCCCTTAC 1320 GGGTGTTATA TACCTGTCCA CGCCTGCCCC TGGCAGGGAT TTAAACATTC CATGCTGTTC 1380 CATGAATCCT AAATCAAATA GATTCATCCT GGCCCTTGGT GAAGCCTAAG AGCTGGCGAG 1440 GCTTATGTTA AATTGCCCTC TCTGGGCTCC TGCTCCTGAG CTGACAGTCA CAAATTCCCC 1500 TTAATGAGCA CTCCTGAAGT AACCAAGGCA GCGCTGTGAG CTAAATTAAG ATTCGAGAGC 1560 CCAGGCAGGG AGAGGGAGGT GTTTGCTTTG GCTGAGAAGG TGCCTGGGCC CCGGCCTGTG 1620 TGTTTGCCTG GGTGCCCTGA TAAGTGGGCT GCATATTAAG TGCCACATGG TGGGACCAGA 1680 ACCATCTGCT GTATGTCTGA GAGGTCACGC CTGCTGGCCC TTTGGGACCT GGTGGCAGAG 1740 GGACCCCGTG TCAACCTGTC TTTGGCTTCC TTTGTGGCCC CGTGGTCACT GAAAAGCCAG 1800 AATGAATATT CTTCCTTTCG GAATAAAAAT TGAGCTGTGG AAGTTTTGTT TGCTTTGATG 1860 AATTACTTCC AGGCTGCTGT TTATTTGGAG AGCAAAGCTC CCCAGCTGCA GGGTGGGTAG 1920 AGGCTGCGGT CACTCCCCTC GTCAATGCTG GTTCCTGTTC CTGAGGCCGA GAGAACTCCT 1980 GACAGCAGAG TGGGCATATC TTGGTAGTTG CAGCTTTTCA AGACAGTGTG GCCCAGTGGG 2040 GAGAGAGCAG AAAACCTGGG TTATGCTGGC TCTGCCATTT ATCAGCTGTG TAACCTTGGG 2100 CAAGTGATAC AACCTCTGTG TGCCTCAGTT TCCTTTCCTC ACCTGTCCAC AGGGGATCAT 2160 AATCTTGGCC CTGCATGCCT TACAGGAGCG TTAAGAGCAT CAAATGAAAC AATAAAAATG 2220 AAAACATTTA TAAATGGTAG TTTGCCATAC ATATTTTAAT AAAAGTGCCT GCCCTTCAAT 2280 CCAGCTCTCT GCACTGCCTG GGGACAGTGT TAGCAGGAGG ACACCACTCT 2330
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