Tag | Content |
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EnhancerAtlas ID | HS111-01691 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr15:85276690-85279170 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr15:85278456-85278474 | CATTCCTTCCCTCTTGCC | - | 6.17 | FOSL1 | MA0477.1 | chr15:85277511-85277522 | CATGAGTCACC | - | 6.62 | JUND | MA0491.1 | chr15:85277511-85277522 | CATGAGTCACC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr15:85277817-85277832 | TGAACTCCTGACCTC | - | 6.22 | SPIC | MA0687.1 | chr15:85278529-85278543 | CACAAGCGGAAGTA | + | 6.02 | ZNF263 | MA0528.1 | chr15:85277223-85277244 | GGAAAAGGAGGAGGAGAAGGG | + | 6.32 | ZNF263 | MA0528.1 | chr15:85277253-85277274 | GGAGAAGGAGAAAAAAGAAGA | + | 6.67 | ZNF263 | MA0528.1 | chr15:85277256-85277277 | GAAGGAGAAAAAAGAAGAAGA | + | 6.74 | ZNF263 | MA0528.1 | chr15:85277250-85277271 | GAAGGAGAAGGAGAAAAAAGA | + | 6.79 | ZNF263 | MA0528.1 | chr15:85277247-85277268 | GGAGAAGGAGAAGGAGAAAAA | + | 6.84 | ZNF263 | MA0528.1 | chr15:85277241-85277262 | GGGGAAGGAGAAGGAGAAGGA | + | 6.86 | ZNF263 | MA0528.1 | chr15:85277205-85277226 | GAAGAAGGAAGAAGAGAAGGA | + | 7.17 | ZNF263 | MA0528.1 | chr15:85277220-85277241 | GAAGGAAAAGGAGGAGGAGAA | + | 7.18 | ZNF263 | MA0528.1 | chr15:85277217-85277238 | AGAGAAGGAAAAGGAGGAGGA | + | 7.31 | ZNF263 | MA0528.1 | chr15:85277208-85277229 | GAAGGAAGAAGAGAAGGAAAA | + | 7.38 | ZNF263 | MA0528.1 | chr15:85277235-85277256 | GGAGAAGGGGAAGGAGAAGGA | + | 7.41 | ZNF263 | MA0528.1 | chr15:85277244-85277265 | GAAGGAGAAGGAGAAGGAGAA | + | 7.89 | ZNF263 | MA0528.1 | chr15:85277226-85277247 | AAAGGAGGAGGAGAAGGGGAA | + | 7.96 | ZNF263 | MA0528.1 | chr15:85277232-85277253 | GGAGGAGAAGGGGAAGGAGAA | + | 8.47 | ZNF263 | MA0528.1 | chr15:85277229-85277250 | GGAGGAGGAGAAGGGGAAGGA | + | 9.02 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_09489 | chr15:85276550-85282505 | CD14 | SE_11419 | chr15:85276610-85281334 | CD20 | SE_18983 | chr15:85276517-85281348 | CD4p_CD25-_Il17-_PMAstim_Th | SE_50869 | chr15:85277323-85279318 | Sigmoid_Colon | SE_53113 | chr15:85277860-85279325 | Small_Intestine | SE_63014 | chr15:85263877-85307023 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr15 | 85276994 | 85279157 | chr15 | 85277876 | 85278013 | chr15 | 85277388 | 85277598 |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I084733 | chr15 | 85276588 | 85280661 |
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Enhancer Sequence | GTATTAGGCA GGCAAGCTTT GGTGTTTTGG AGTCATATGA CCTGGGCTCA AATCCTAACT 60 CTGCCATTGA CTAGCAGTGT GATCTTGGGC GAATGACTTA GCTTCTCTGA GCCTCAGTTT 120 CCTCCTCTGT AAATTGGGAA TAACATATTC TTATGGAAAA TGTCTGGCCC ACAGAAGCTA 180 ATTACAATAG TATTATGCTG GCATCATACT CCAGTTGACT TTTTTTTTTT TTTTTTTGAG 240 ATAGCGTCTT GCTCTGTCAC CCAGTCTGGA GTCCAGTGCC CAGCTAATTT TTGTTTTGTT 300 TTGTTTTGTT TTTTGTATTT TTAGTAGATG CAGTTTTGCC ATGTTGGCCA GGCTGGTCTT 360 GAACTCCTGG CCTCAAGTGA TCAGCTCACC TCGGCCTCCC AAAGTGCTGG AATTATAGGT 420 GTGAGCCACT GCTCATGGCC TCCAGCTAAG TTTTTGAAGC CCTATTCCTC CCTCTCCTGC 480 CAGCTCTACA ACTGCTGCCT TTACCTTAGA AGAAGGAAGA AGGAAGAAGA GAAGGAAAAG 540 GAGGAGGAGA AGGGGAAGGA GAAGGAGAAG GAGAAAAAAG AAGAAGAAAA GAAGAAGAAG 600 AAGAAGAAGA AGAAGAAGAA GAAGAAGAAG AAGAAGAAGA AGAAGAAGAA GAAGAAATAG 660 CAGTAGTACA GCTTTTCTGA CCTTTAGAAA GAAATATACC TCATTTCACT CTGTTATTCT 720 TTCTGGTTAA TGTCTTACTT TTCCCTTTCA TTGCAAAGTC AGTGTTCTCA GATTGCATGT 780 GGTTTACTGC CTCACTGTTC TTTCTCCCTT TTCTTCTCTG CCATGAGTCA CCTGCTGTGA 840 CACTTTAGTG ACCCTTAAGA TACTTCAGTA AAGACCAGTG GGTTGGCAAA TCCAGCAAAT 900 CCCCCCCCCG CTTTTTTTTT TTCTGAGAGA GAGTCTCACT CTGTTGCCCA GTCTGGAGTG 960 CAGTGGCGTG ATCTTGGCTC ACTGCAACCT CTGCCTCCCA GGTTCAAGCA ATTCTCCCTG 1020 CCTCAGCTTC CTAAATAGCT GGGATTATAG GTGCCTACCA CCATGCCCGG CTAATTTTTG 1080 TATTTTTTAG TAGAGATAGG GTTTCACCAC GTTGGCCAGG CTGGTCTTGA ACTCCTGACC 1140 TCAGGTGATC GCCTGCCTTG GCTTCCCAAA GCAGTGGGAT TACAGGTGTG AGCTACCGTG 1200 CCCGGCCAAC TCTTTCTTTT CTTTTTTTAT TTGAGATAGG GTCTCACTTT GTCGCCCAGG 1260 CAGGAGTGCA GTGGCACGAT TATGGTTCAC TGCAGCCTTC ACCTGCTGGG CTCAAGCAAT 1320 CCTCCCACCT CAGCCTCTCA AATAGCTGGG ACTACAGGCA TGTGCCACAA TGCCCAGCTA 1380 ATTTTTTTAT TGAGACTGGG TTTCTCCATG TTGCCCAGGC TGGTCTTGAA CTCCTGGGCT 1440 CCAGCAATCC ACCTGCCTTG ACCTCCCAAA GTGTTTGGAT TACAGGCGTG AGCCACAATG 1500 GCCAGCCTCC CCTGTCTCTA TTCTTCCGGA TTTCACCACT GTGACATTCT GCACTCACCA 1560 CTTCCCCCAC CCCACCTTTT TTTTTTTTTT AATGCTTTTC TCCTGTAGCT CCCATGACCA 1620 CCAGAAGTTA CCCAACCAGG CAGATCAGTA TCCCTTATCA GCTCACCAGT CCTGAATAAT 1680 CCCTGACATT TGCATCTTCC TAGATCCCCT CTTTGAGACA GTGTGTTACA ACTTTTCCTT 1740 TTTCCTCACC CCTCCCCCCT TGGTGACATT CCTTCCCTCT TGCCTGCGGT TACTTCAGAG 1800 TCAGCACCTG CACCCACACT TGACTCCTCC CCTCCAGCTC ACAAGCGGAA GTATCTTCCT 1860 AGCTAAAGCC AGCCTCTCTG CGTTTGCTCT CGATCTCTCC CCTCCCACCA TTTGGCCCCC 1920 CTTAGGGGAC AGAACAGATC ATGACTGATG CACCTTCAGC CTCTCCTGCT TTACTTTAAA 1980 ATCTTGTCAT CCTTTAAAAT TCTTCCTTGC CCTCATCCGC CCTCCGCATA GTTACTGCCC 2040 TCTCTCTCCT CCCTCATTTC TGCCATCAAG CCCAAGCTCT CATGAAGCAT TCATTTAATC 2100 TTCACAGCAG CCCATGAGGA TGGTGTCAGT ATTGTCCCTA TAAAACAGAA GTGGAGTACA 2160 GTTGCTTTAT TAAACAAGGT CACCCGGCAG GGGTTTGAAG GCAGAGAACT GGGCTTAGGG 2220 TCTGTGCCCT TGACCACTAT GTCATACCAT AATGCATGCC TCATACTGGA TGGTGTCTGT 2280 TCCCAGCACT CAGCTCAGTG CCTTGCACAT ACATAGTAGG GGATTAATAA ATATGTCTGA 2340 CTAAATAAAT ACATGCTGCA AGTTCTTATT CTTTCACTCT TAGAATGACT CACTAGGCTG 2400 GGCACAGTGG CTCACGCCTG TAATCCCAGT ACTTTGGGAG GCTGAGGCGG GCGGATCATG 2460 AGGTCAGGAG ATTGAGACCT 2480
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