Tag | Content |
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EnhancerAtlas ID | HS108-06664 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr11:267060-270060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr11:269490-269511 | GTGTGGTTTCAGTTCCTGTTT | + | 6 | NFKB1 | MA0105.4 | chr11:267820-267833 | AGGGGAATCACCG | + | 6.25 | POU2F2 | MA0507.1 | chr11:269685-269698 | TTCATTTGCATTT | + | 6.59 | ZNF263 | MA0528.1 | chr11:267295-267316 | AAGTGAGGAGGAGGGGGGAGG | + | 6.01 | ZNF263 | MA0528.1 | chr11:267456-267477 | GGAGGAGGGGGAGGGGCGAGG | + | 6.04 | ZNF263 | MA0528.1 | chr11:267553-267574 | GGAGGAGGGGGAGGGGCGAGG | + | 6.04 | ZNF263 | MA0528.1 | chr11:267281-267302 | GGAGGAGTGGGGAGAAGTGAG | + | 6.09 | ZNF263 | MA0528.1 | chr11:267524-267545 | GGAGCAAGGAGGGGGGAGGAG | + | 6.09 | ZNF263 | MA0528.1 | chr11:267545-267566 | CGAGGAGGGGAGGAGGGGGAG | + | 6.12 | ZNF263 | MA0528.1 | chr11:267462-267483 | GGGGGAGGGGCGAGGAGGGAG | + | 6.23 | ZNF263 | MA0528.1 | chr11:267484-267505 | GGAGGGGGAGGGAGAGGGGAG | + | 6.27 | ZNF263 | MA0528.1 | chr11:267353-267374 | GGAGGAGGGGGAGGAGCGAGG | + | 6.28 | ZNF263 | MA0528.1 | chr11:267308-267329 | GGGGGAGGAGCGAAGAGGAGG | + | 6.2 | ZNF263 | MA0528.1 | chr11:267501-267522 | GGAGGAGCAACGAGGAGGGGG | + | 6.35 | ZNF263 | MA0528.1 | chr11:267330-267351 | GGAGGAGCGAGGGGGAGGAGC | + | 6.4 | ZNF263 | MA0528.1 | chr11:267559-267580 | GGGGGAGGGGCGAGGAGGAGG | + | 6.4 | ZNF263 | MA0528.1 | chr11:267453-267474 | CGAGGAGGAGGGGGAGGGGCG | + | 6.61 | ZNF263 | MA0528.1 | chr11:267311-267332 | GGAGGAGCGAAGAGGAGGGGG | + | 6.69 | ZNF263 | MA0528.1 | chr11:267340-267361 | GGGGGAGGAGCGAGGAGGAGG | + | 6.6 | ZNF263 | MA0528.1 | chr11:267427-267448 | GGGGGAGGAGCGAGGAGGAGG | + | 6.6 | ZNF263 | MA0528.1 | chr11:267350-267371 | CGAGGAGGAGGGGGAGGAGCG | + | 6.79 | ZNF263 | MA0528.1 | chr11:267298-267319 | TGAGGAGGAGGGGGGAGGAGC | + | 6.81 | ZNF263 | MA0528.1 | chr11:267518-267539 | GGGGGAGGAGCAAGGAGGGGG | + | 6.87 | ZNF263 | MA0528.1 | chr11:267359-267380 | GGGGGAGGAGCGAGGAGGGGG | + | 6.88 | ZNF263 | MA0528.1 | chr11:267376-267397 | GGGGGAGGAGCGAGGAGGGGG | + | 6.88 | ZNF263 | MA0528.1 | chr11:267393-267414 | GGGGGAGGAGCGAGGAGGGGG | + | 6.88 | ZNF263 | MA0528.1 | chr11:267410-267431 | GGGGGAGGAGCGAGGAGGGGG | + | 6.88 | ZNF263 | MA0528.1 | chr11:267550-267571 | AGGGGAGGAGGGGGAGGGGCG | + | 6.96 | ZNF263 | MA0528.1 | chr11:267535-267556 | GGGGGAGGAGCGAGGAGGGGA | + | 6.97 | ZNF263 | MA0528.1 | chr11:267327-267348 | GGGGGAGGAGCGAGGGGGAGG | + | 7.1 | ZNF263 | MA0528.1 | chr11:267476-267497 | GAGGGAGGGGAGGGGGAGGGA | + | 7.1 | ZNF263 | MA0528.1 | chr11:267362-267383 | GGAGGAGCGAGGAGGGGGGAG | + | 7.33 | ZNF263 | MA0528.1 | chr11:267379-267400 | GGAGGAGCGAGGAGGGGGGAG | + | 7.33 | ZNF263 | MA0528.1 | chr11:267396-267417 | GGAGGAGCGAGGAGGGGGGAG | + | 7.33 | ZNF263 | MA0528.1 | chr11:267413-267434 | GGAGGAGCGAGGAGGGGGGAG | + | 7.33 | ZNF263 | MA0528.1 | chr11:267343-267364 | GGAGGAGCGAGGAGGAGGGGG | + | 7.3 | ZNF263 | MA0528.1 | chr11:267430-267451 | GGAGGAGCGAGGAGGAGGGGG | + | 7.3 | ZNF263 | MA0528.1 | chr11:267487-267508 | GGGGGAGGGAGAGGGGAGGAG | + | 7.42 | ZNF263 | MA0528.1 | chr11:267521-267542 | GGAGGAGCAAGGAGGGGGGAG | + | 7.56 | ZNF263 | MA0528.1 | chr11:267481-267502 | AGGGGAGGGGGAGGGAGAGGG | + | 7.64 | ZNF263 | MA0528.1 | chr11:267472-267493 | CGAGGAGGGAGGGGAGGGGGA | + | 7.84 | ZNF263 | MA0528.1 | chr11:267440-267461 | GGAGGAGGGGGGGCGAGGAGG | + | 7.85 | ZNF263 | MA0528.1 | chr11:267538-267559 | GGAGGAGCGAGGAGGGGAGGA | + | 8.21 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_16128 | chr11:267513-270474 | CD4_Naive_Primary_7pool | SE_21864 | chr11:267477-270412 | CD8_Naive_7pool | SE_22226 | chr11:267090-270596 | CD8_Naive_8pool | SE_28519 | chr11:268667-269561 | Fetal_Intestine | SE_52556 | chr11:267492-273530 | Small_Intestine | SE_61820 | chr11:266425-273086 | Toledo | SE_62809 | chr11:266595-290841 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr11 | 268826 | 269269 | chr11 | 267611 | 268165 | chr11 | 269337 | 269903 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I000266 | chr11 | 266649 | 273455 |
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Enhancer Sequence | AAATAATGCC AGTGGGGGAA GCCCTCTGGC GCTTCCATTG CCTGTTTGAA AGTTACTGGG 60 CTCACTTGTT CGGGAAACAT CAGCTGCTCC CACTGGGTGC CAGGCCCTGT TCTAGGTGCT 120 TGGGAAGTGT CAGTGAGCAA AACAGACAAA TCTCCAGCCC ACATGGAGGG GTGAGGAGCA 180 AGGAGGAGGA GTGAGGAGCA AGGAGGAAGG GCAAGGAGCG AGGAGGAGTG GGGAGAAGTG 240 AGGAGGAGGG GGGAGGAGCG AAGAGGAGGG GGAGGAGCGA GGGGGAGGAG CGAGGAGGAG 300 GGGGAGGAGC GAGGAGGGGG GAGGAGCGAG GAGGGGGGAG GAGCGAGGAG GGGGGAGGAG 360 CGAGGAGGGG GGAGGAGCGA GGAGGAGGGG GGGCGAGGAG GAGGGGGAGG GGCGAGGAGG 420 GAGGGGAGGG GGAGGGAGAG GGGAGGAGCA ACGAGGAGGG GGGAGGAGCA AGGAGGGGGG 480 AGGAGCGAGG AGGGGAGGAG GGGGAGGGGC GAGGAGGAGG CGGGAGGAGC TGGACAGGAC 540 ATCGTGCCAG CCCGAGGGCG GAATGAACTT CAGAGAAGTT TGAGAGCAAA AGGTGCTTTG 600 CTGCTGTTAG ACCCTGAAAT TCCACGGGTC CCTGGACAGT TTTGGGAGCC GGGAGGGTGA 660 AGAGAGTGGA TCAAGCTTCG TGGGGTGGAC CCGGAAGAGA TGGGGCAGTG AATGGTTCTG 720 GGGGACTGCG GGAGCCTCCG GGGAGTGATT TTTTGCCCTG AGGGGAATCA CCGCAGCGGG 780 GACAAGGCTG GGGGAAAACA CTTCCTTCTG CAAGGGCACT GCTGAGCCTC ACTTGCTGGA 840 GCTTGCACTG TGCAACGGTA AATTCACGTT GTGTGCCCTC ACCTGAGCTT CTGATGAGGA 900 CGCTGGAGGG CTTGGCCCTT TGAAGTCCTC ACCTGTCCCT CCTTGGGCTG GGGGTGGTGA 960 CTAGGAGGGG CTGCACGGCT GCTGCCCGGG TTGGTCCCGG CCATCCCAGC TCCCTGGTAA 1020 ATAGGCTTCT CAAACTAGGA TACCTGGGCC TTGGGCGTTA CCTGCAAACC CTGTTCCTCG 1080 CTCTAGTTCC CCACTTCCAT CCCTCCTCTT GCCTCAGCCC TTCTCATCTC ACACGCCACA 1140 TGGGATCCAC CCTTTTTACG CATGTGCAGA GCGTGGCCCC TCTCTGATTC CCTTCCCCTC 1200 AGGAGAGCCG GACGTCTCCC TCCCTCACAC CCTCCCCAGC CCCACAGCAG CCCAGGGAGC 1260 CTTGCCCGCT CCTCGGCCCC CCTGGCTCTC CCAGCCACCC AGGCCTCCTG TGTCCTGAGT 1320 GGGCCAGCTC CTGCCAGACC ACGGCCCTGC CCTGCACCTG ACTGCGTCCC CACCGCGGAC 1380 CTGCCCCCTC GTTTATTCTC CTCTCTCCGC TCTGCTCTGT CCTTGGCACT GTTTTTGTTT 1440 GTTTTTTGTT TTTGTTTTTT GAGACGCAGT CTCGCTCTGT CACACAGGCT GGAGTGCAGT 1500 GGCGTGATCT CTGCTCACTG CAATCTCTGC CTCCTGGGTT CAAACTATTT TCTTGCCTCA 1560 GCCTCACGAG TAGCTGGGAT TACAGATGCC CGCCACCACG CCTGGCTAAT TTTTGTATTT 1620 TTAGTAGAGA CGGGGTTTCA CCATGTTGGC CAGGCTGATC TCGAACTCCT GACCTCAAGT 1680 GATCCGCCCG CCTCTGCCTC CCAAAGTGCT GGGATCACAG ATATGAGCCA CCGCGCCCCG 1740 CCCTTGGCAC TGTTTAATCC ATGTGTTGTT TATTTATGTA TCCTGTTTAT TTTCTGTCTC 1800 CCAACAAAGA CGTAGCTCCT TCTGGGTAGG GCATTTTGTT CATGCTCTCA GATGCCGCCT 1860 ACCGCCCTAG AGCAGGAAAT AGCGGTCAGC GCCAGCTGTG AGGAGCACAG CATTGCGGCC 1920 AACACAGGAG GCACTGACCA CGGGGCAGGC GCTATTTAAA AATCGTGGCA AAGGATCAGA 1980 CGTAACAGAA CTCTTTTTGT TTTAATCATT TTTAAGTGTG CAGTTCAATG ATGTTAGTTA 2040 CATGCACAAT ATTGTGTAAC CATCACCACT ATTTCCAAAA TCCTTTCTAT CCGTCAGACA 2100 GAAACTCCGT CCCCATTAAA CAGCAACTCT GCATTCCTCC GTCCCCCCAG CCTCTGGTCA 2160 CGTGTCTCAT CTACTTTCAG TCTCTACGGA TTTGCCTGTT CTAATTATTT CATAGAAGTG 2220 GATTCATACA GTACGTGTCC TTCTGTGTCA GGTTCATGTC ACTCAGCGTG ATGTGCCCAA 2280 GGTTCACCCA TGCGTCGGGC TCTCATTCCT GAATCGCATT TCTCTGTACG GATAGACTGA 2340 GTTTTGTTTG TCTGTTCACC TGTTTAGGAA CACTTGGTTG CTTCCACATT TTGACTGTTA 2400 TGAATAACGC TACTAGCAAA GTGAACACGA GTGTGGTTTC AGTTCCTGTT TTCAATTCTT 2460 CCGCGTCTTT TAAGAAAAAA CAAACTGTTT TCAACAGTTG CATCATTTTA CCGTCCCACC 2520 AGCAACATGG GAGGCTTCCC ATCACTTGTT TTCTTCATGT TTGTTTTGTT TAGTTGCATA 2580 ATAATTGCCA TCCTAGTGGA GGTAAGAAGG TATCTCACTG TTCTTTTCAT TTGCATTTTT 2640 GTAATGACTA ACGAGGTTGG GCAACTTTTC ACGTGCTTGT CAGTCATTCG CATCTTTTTT 2700 TTTTTTTGAG AAATGTCTAT TCAAGTCCTT TGCTCATTTT GAAATTGTGC TGTTTGGGTT 2760 TTGGTTGTTG ATTTGAAGGA GTCCTTTTTA TATTACGTAT ATGAATCCTT ACCAGATATA 2820 TGATTCGCAA ACATTTTCTC CCATTCTGTG GTGATCTCTT CAGCCCCTTG ATAGTGTCCT 2880 TTGATGCACA AAAGATTTTA ATTTTGATGA AGTACAATTT ATCTTTTTGT TGTTGTTGTC 2940 ATTGCCCATG CTTTTGGTGT TATATCTAAG AATCCAAGGT CGGCCGGGCA CGGTGGCTCA 3000
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