Tag | Content |
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EnhancerAtlas ID | HS105-76438 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr8:11330480-11333190 |
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) |
IRF1 | MA0050.2 | chr8:11331352-11331373 | TGTTTGTTTCTTTTTCTTTTT | + | 6.57 | ONECUT1 | MA0679.1 | chr8:11332082-11332096 | GAAAAATCAATACA | + | 6.15 | ONECUT2 | MA0756.1 | chr8:11332082-11332096 | GAAAAATCAATACA | + | 6.23 | ONECUT3 | MA0757.1 | chr8:11332082-11332096 | GAAAAATCAATACA | + | 6.59 | ZNF263 | MA0528.1 | chr8:11332342-11332363 | AGATGAGGAGGCAGAGGGGGA | + | 6.15 | ZNF263 | MA0528.1 | chr8:11332360-11332381 | GGAGGGGGAGGAAGAAGAAGA | + | 6.23 | ZNF263 | MA0528.1 | chr8:11332354-11332375 | AGAGGGGGAGGGGGAGGAAGA | + | 6.31 | ZNF263 | MA0528.1 | chr8:11332303-11332324 | GAAGGAGAAAGGGAGAGGAAA | + | 6.41 | ZNF263 | MA0528.1 | chr8:11332424-11332445 | AGGGGAGAGGGAGAAGGGAGG | + | 6.41 | ZNF263 | MA0528.1 | chr8:11332333-11332354 | TAAGGAGGAAGATGAGGAGGC | + | 6.49 | ZNF263 | MA0528.1 | chr8:11332412-11332433 | GAAGGAGAGGGGAGGGGAGAG | + | 7.27 | ZNF263 | MA0528.1 | chr8:11332348-11332369 | GGAGGCAGAGGGGGAGGGGGA | + | 7.29 | ZNF263 | MA0528.1 | chr8:11332345-11332366 | TGAGGAGGCAGAGGGGGAGGG | + | 7.52 | ZNF263 | MA0528.1 | chr8:11332357-11332378 | GGGGGAGGGGGAGGAAGAAGA | + | 8.78 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_32248 | chr8:11329569-11331557 | Gastric | SE_32248 | chr8:11331592-11333712 | Gastric | SE_45800 | chr8:11330727-11333787 | Osteoblasts | SE_55688 | chr8:11330676-11333828 | u87 | SE_58515 | chr8:11271776-11367112 | Ly1 | SE_62362 | chr8:11308990-11367697 | Tonsil | SE_65314 | chr8:11330998-11333022 | Pancreatic_islets | SE_67671 | chr8:11330676-11333828 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr8 | 11331132 | 11331186 | chr8 | 11332896 | 11332982 | chr8 | 11330762 | 11330815 | chr8 | 11331684 | 11332387 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I011472 | chr8 | 11330386 | 11335496 |
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Enhancer Sequence | GGTTTTGAGG CTGGGATGAG AGCCAGCCCA GGATGTTCAG GAACAAGGCG GCACCCCCAT 60 CCTGGGGAAG AGCCTGCTTG AACTCAGGGT GAGGTGGCCC TTGACCTGCA GGCAAGACCA 120 GGACCTGCAG TAGAGCTCTG CCCCTTATGG AAGCCAGGAC AGGGAAGCCC AATGTCTTCT 180 CCAACTCAAT AGCCCACGGC AACGTCAGTG ATGCAGGAGC GAGGACACAG GGGCTCATTT 240 CATCTCCATC GGCCAATCCC TGATGATACC TTGAGAAACC AAGGTGCAGA GGACAGACTG 300 ATGAACACTG GTGTGGGGGG AAGCTTGTTG CATACAGGGA TGATCATTCT GTCATCAGGA 360 AGGCCGAGAC ATGAGGCAGG CTTTGGAGGC AGGAGTGAAA CAAGGTGCTA AAAGAGAAGG 420 ACTGCCTGTC ATTCACCAGT GCTGGGGGGG ATTTTTGGGG AAACGGGACT TGGGCTCTTA 480 ATATTCAACC TCTTTTCAAC AACTGTACCC CGAAGAGATA CTGAGGACAA AGCCTCCCTT 540 ATACGTAACT TCTCTCCTAA AATCAACTCT AACCCACTGC CACGTAGATG TTCAAACAAA 600 AAGAACGCAC ACCTTCTTTC CCATCCCCAT CCTGGCCAGG GAGGTGGGGA GGAAGTGTAC 660 GCAGTGCAGG GTGCGGTTCT ATCTCTGGGT CTGCCCCTTG CTGTCAGGCT GCTTTGGGCA 720 AATCCCTTAG TCTCTTGAGC TTCAGTTTCC TCCTCTACAC ATTGGCAGTA CCAAGAGCTA 780 CCATGAAGTT CACTGTGAGG ATTAGAATTA ACGCCTAGAA AATGCCTGAC AGTCTTAGAC 840 AGGGAGTAGC ACACAGGGAA TGGTGGTTTT TTTGTTTGTT TCTTTTTCTT TTTCTTTTCT 900 TTCTTTCTTC TTTTTTTTTG AGACAGAGTC TCACTCTGTC ACCCAGGCTG GAGTGCAGTG 960 GCGCAATACC AGCTCACTGC CAATCTTTGC CTCCTGGGTT CAAGCGATTT TCCTGCCTCA 1020 GCATCCTGAG TAGCTGGGAT TACAGGCATG CGCCACCATG CCCGGCTAAT TTTTTGTATT 1080 TTTAGTAGAG ATGGGGTTTC ACCATGTTGG CCAGGCTGAT CTTGAACCCC TGACCTCAGG 1140 TGATCCGCCT GCCTTGGCCT CCCAAAGTGC TGGGATTACA GGCACGAGCC ACCGTGCCCG 1200 GCCAACACTG TTTTATCACG TCTGCGCGCC AACTGCTCTT GGTTTGCGCA CCACCTGGAA 1260 AGGGGTGTGG CTTTCACTCA TTCTGGTACC AGGCACAGCA TGAACAAATA TTCAACAAGC 1320 AAACTGGCAG CATTCCTGGA TATCTTAGCT GCCTTGTTTG TCTTCCCAGA GCATGAGGTA 1380 GCCCTGTTTG GAACCTGACA CCAGCAAAAC AGGACGGCGC ATGGAACAGA CAAACATGCC 1440 CCGTGGTTCA GCCACAGTTT TTGGGCACAG ACTCCAGAGC ACTTCCTGGC CCAGGAAAGC 1500 AGCAAGCCAC TCCAACCTGG TCAGCTGCCA GGCTATGGTT CACATCTTAG GATTGAGACT 1560 TGGTTTCTGC TTCACAGACA GAACTAGAGG CAGAAAAGAA GAGAAAAATC AATACAGGCA 1620 CCCAGAGATG GGCTTACCTA GGGTCCTGGA AGATGCGAGA AGCCACAGTG CAGAGGACAG 1680 ACTGATGAAC ACACAGAGAA ATCACTTCTG CAAGAACCCA CTGATGTTTC ATGGTCTGAT 1740 CAAAATGTTT CACAATCAGC CCTCCTAGAC AAATGGCTCT GTGGGATGAC GCCATAGGCT 1800 TACGGGGAGG AGACAGGGAG TAGGAAGGAG AAAGGGAGAG GAAAAGGAGG GGGTAAGGAG 1860 GAAGATGAGG AGGCAGAGGG GGAGGGGGAG GAAGAAGAAG AATCACAATA ACATCAACAG 1920 CGAAGGCGAC ATGAAGGAGA GGGGAGGGGA GAGGGAGAAG GGAGGCAAAA GGAAGGGAAG 1980 AGAGAAAGGT TCAGAGTGGG TTGCACTCTG CCCAGCAGCC AAGTGTCCTG GAGTGAGGAG 2040 CCCATGGGAG TCCCCTGGAC ACTGTCAGAA TAAACAAATG AGCAGGACTC TTCCCCTCTT 2100 ACTGTCTCAT AAAGGCCTTG ATCCAGCAGA CTGGGCAGTC CAGTGGTTGC AGGAAGGGCC 2160 AGACCAGCCT GGGGCTAACA GTTCTGCAGC CAAGGCCCAC CGTGGTGCCC CCACCTTAGG 2220 ACAGGTTCCT CGGCTTTTCC TCTGGGACCC CCTCCCTGTG CCCCTCCAGC CTGGCCTCAG 2280 TTTTCCTACT CGGTTTCCCT ATGGGCCTCT CTGCACCCTT GTGCATGCTC ACAGAGTTGA 2340 AGGACTTGGA TTTTCTTAGA AGTTTTCCAA GAGGAAAAAC GATCTGTTGG CAATTGCAAA 2400 TACTTTAGAG TGTCTGCATA AAAGCCTCTC AACCTCACCC CACCCCCAGC TGGGCCTTCT 2460 CACCCTGATG TTCAGCTGCG CAAGTCACTC AGGCTTCTAG GATCTCAGAG TCTAAAAGAA 2520 ATCAGATGAG GCCCAAAAGA AATCAAGCAG AAGCCAAGAT TAAAATACAG TTGAGATCCA 2580 ACCTTTTACA CATCATACTC CTTCTGAACC TCCTGCAAAA GTCTTCTTGC CATCAGAAGA 2640 GCCATTACGT TTTAAAAACC CACCCCACAC AAGCACACCC ATACAAACAT ATCCAGTACC 2700 AATTATATGA 2710
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