Tag | Content |
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EnhancerAtlas ID | HS133-05120 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr11:267400-268560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFKB1 | MA0105.4 | chr11:267820-267833 | AGGGGAATCACCG | + | 6.25 | ZNF263 | MA0528.1 | chr11:267456-267477 | GGAGGAGGGGGAGGGGCGAGG | + | 6.04 | ZNF263 | MA0528.1 | chr11:267553-267574 | GGAGGAGGGGGAGGGGCGAGG | + | 6.04 | 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 | chr11:267501-267522 | GGAGGAGCAACGAGGAGGGGG | + | 6.35 | ZNF263 | MA0528.1 | chr11:267559-267580 | GGGGGAGGGGCGAGGAGGAGG | + | 6.4 | ZNF263 | MA0528.1 | chr11:267453-267474 | CGAGGAGGAGGGGGAGGGGCG | + | 6.61 | ZNF263 | MA0528.1 | chr11:267427-267448 | GGGGGAGGAGCGAGGAGGAGG | + | 6.6 | ZNF263 | MA0528.1 | chr11:267518-267539 | GGGGGAGGAGCAAGGAGGGGG | + | 6.87 | 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 | chr11:267476-267497 | GAGGGAGGGGAGGGGGAGGGA | + | 7.1 | ZNF263 | MA0528.1 | chr11:267413-267434 | GGAGGAGCGAGGAGGGGGGAG | + | 7.33 | 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: 6 | 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_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: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I000266 | chr11 | 266649 | 273455 |
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Enhancer Sequence | GAGCGAGGAG GGGGGAGGAG CGAGGAGGGG GGAGGAGCGA GGAGGAGGGG GGGCGAGGAG 60 GAGGGGGAGG GGCGAGGAGG GAGGGGAGGG GGAGGGAGAG GGGAGGAGCA ACGAGGAGGG 120 GGGAGGAGCA AGGAGGGGGG AGGAGCGAGG AGGGGAGGAG GGGGAGGGGC GAGGAGGAGG 180 CGGGAGGAGC TGGACAGGAC ATCGTGCCAG CCCGAGGGCG GAATGAACTT CAGAGAAGTT 240 TGAGAGCAAA AGGTGCTTTG CTGCTGTTAG ACCCTGAAAT TCCACGGGTC CCTGGACAGT 300 TTTGGGAGCC GGGAGGGTGA AGAGAGTGGA TCAAGCTTCG TGGGGTGGAC CCGGAAGAGA 360 TGGGGCAGTG AATGGTTCTG GGGGACTGCG GGAGCCTCCG GGGAGTGATT TTTTGCCCTG 420 AGGGGAATCA CCGCAGCGGG GACAAGGCTG GGGGAAAACA CTTCCTTCTG CAAGGGCACT 480 GCTGAGCCTC ACTTGCTGGA GCTTGCACTG TGCAACGGTA AATTCACGTT GTGTGCCCTC 540 ACCTGAGCTT CTGATGAGGA CGCTGGAGGG CTTGGCCCTT TGAAGTCCTC ACCTGTCCCT 600 CCTTGGGCTG GGGGTGGTGA CTAGGAGGGG CTGCACGGCT GCTGCCCGGG TTGGTCCCGG 660 CCATCCCAGC TCCCTGGTAA ATAGGCTTCT CAAACTAGGA TACCTGGGCC TTGGGCGTTA 720 CCTGCAAACC CTGTTCCTCG CTCTAGTTCC CCACTTCCAT CCCTCCTCTT GCCTCAGCCC 780 TTCTCATCTC ACACGCCACA TGGGATCCAC CCTTTTTACG CATGTGCAGA GCGTGGCCCC 840 TCTCTGATTC CCTTCCCCTC AGGAGAGCCG GACGTCTCCC TCCCTCACAC CCTCCCCAGC 900 CCCACAGCAG CCCAGGGAGC CTTGCCCGCT CCTCGGCCCC CCTGGCTCTC CCAGCCACCC 960 AGGCCTCCTG TGTCCTGAGT GGGCCAGCTC CTGCCAGACC ACGGCCCTGC CCTGCACCTG 1020 ACTGCGTCCC CACCGCGGAC CTGCCCCCTC GTTTATTCTC CTCTCTCCGC TCTGCTCTGT 1080 CCTTGGCACT GTTTTTGTTT GTTTTTTGTT TTTGTTTTTT GAGACGCAGT CTCGCTCTGT 1140 CACACAGGCT GGAGTGCAGT 1160
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