Tag | Content |
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EnhancerAtlas ID | HS133-10741 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr16:373750-376000 |
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) |
RREB1 | MA0073.1 | chr16:373772-373792 | CCACCACACACACACACACA | + | 6.41 | ZIC3 | MA0697.1 | chr16:375299-375314 | TGCCCCCCGCTGCTC | + | 6 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_24104 | chr16:373786-376118 | Colon_Crypt_2 | SE_25025 | chr16:373765-376251 | Colon_Crypt_3 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr16 | 374352 | 374895 | chr16 | 374933 | 375274 | chr16 | 375625 | 375961 | chr16 | 374400 | 375188 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I000323 | chr16 | 373759 | 379105 |
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Enhancer Sequence | GCCTGGGCAA CAGAGTGAGA CTCCACCACA CACACACACA CACACACACA CACCAACAAA 60 ACAAAACACT GAGGGGTGTG ACTTGGGTTC TCACCTGCGT CTCTCTAGGA GCATAAGCAC 120 AGGTCTTCAC CACTGTGGGT GCAAAGGGAA AAGGTGTCAA CTGCGACAGG GGATGGAATA 180 CGGCACAGAA TGAGCAACCC ACCCTGGAGA CACCAGCCTG TGGGAGCCCC AAAGCCCACA 240 GGAGAGCCCC ATAGTCCATG GGGAGACCTG TCCATGGGAA GCCCCGTAGC CCACAGGAAA 300 CCCTGCAGAC CATGGGGAGC CCAGTGCAGG AGAGCCCTGC AGCCCACAAG AGTCACATCT 360 GAAATACCCG GGACCGTCCG CACTGACCAG CAGCCTCCAT GAGGGGCAGA TCTGGGGCCA 420 AGTGTCAGTG AGCCGCCTTA CGGGTCTTTA CGGGTCTTCC GGGCCACATT ACGGGTCGGC 480 ACTGGGCACG AGGCCACCTG CTCAAGGACG CCGATGCCAT GGCATGGGGG CTACATTTGC 540 TCTACAGGTC TCCTGCCGGA TCCTTTCTGA GCCCTCCTGG GAGGAGGCTG GGGGCCGGAA 600 TGCGGGTGCA TAGAAACGGC TGGAAGCAGC GCAGGGCAGA AGCGATATGG AAAGGCGGGT 660 CAGGCACAGG CCTCACAGGC CCGCGGTCCT CCGGGGAGGT TTGCAAGGAT CACATGGCCA 720 AGGGCACCAT GAGCAGCTTC CCAACCAACC CGCCCAGTGT CCCGCAGAGT TTGTGGAGAT 780 AAACAGAAGC TTGACAAACA CAACTGAGCA GAAAACGCCC GCAGGTGGTC AGTAGGCGCT 840 TCCAGTGTTA TCACAAGACC ACACGCCGCA CGTCAGCACA TGACACAGAC ACACTTACTT 900 GATCCCTGTT TTGACAAGCT AAGTCGTACT TTATACCAGG AGGAGGAGGG GCACCCCAGG 960 TGAGCGGTCC AATCCTCAGA CACGGCCAGT GCCATCAGCG ACCTGCATCC CGACCCCCCG 1020 GAACAGCACA GCCAGCAGAC AGAACCCGCC CTGCAGAGGC AGCTTCCGGC AGCCGCAGGC 1080 CCTTCCCAGG CCCAGCCCCC GAGTCCCGCG CAGGGAAAGG CTCTGCCCAA GCCTTCAGGG 1140 AGGCAGCAGC GCCCGGTGCA CAGTTCCTAA GGGCGCAGAA CTCCGGGATG AACAAAGGCA 1200 AGGAAACGGC TGTGTAAAAA TCAGCTCTAC TGACGCACGG CTGGGTGCTC AGCGGACCCG 1260 CACAGAACCA CAGTCCTACC TGGCACGTTC TGACGCGCAC CAGATCACAG CCTCAGCCCC 1320 GCGGGCGCGC CCCAGGAAAC CATGGCCTCA GCCCCGCGGG CGGCCCCGCA CCCCAGGAAA 1380 CCATCGCCTC AGCCCCGCGG GCGGCCCCGC ACCCCAGGAA ACCATCGCCT CAGCCCACAT 1440 ATTCAACCCG GAAGCCTGGG GAGGCTTCCC TTGGGGAAAT CCACCTGTCG CTCGAGGTCA 1500 GTCGGCCTTT TCTAGAATTC TGTATAAACG CAGTCTCATG GGGAGCTAGT GCCCCCCGCT 1560 GCTCCGGCGC CCCCTCCGCT CTGGCTTTCT TCACTGGCAC AGGATCCTGA GATGCACCCC 1620 TGCCTCCATG GTTATCAGCG ACTCATCCCT TTTATGCCGT GGCATGCCAG GATGCACCAC 1680 GGTGTTTTTC TCCAACTGCT TGGCAGTGCC ACTGGAGTTG GGGCAGCGCT TCCCAGCGGG 1740 CAGAGTTGAC CCCGAGGCCA ACAGCCAGGC CACAGCCAGC GCCCTCCCCA CGTCTCGCCT 1800 CCCCCAGTCC AGACACAAAC CTGGTCAAGG GCGCCCAGAC CAGGGCTCAA CCCACTGCCC 1860 GCAGGGGCCG ACTGCCAAGG AGCGGTCACC GCCCCAGAGT GATGGCTGCC ACAGCGTCGT 1920 GTGTACAACT TATGGTCTGT CCCACGTGGC TGCAGGCTCC AGCCCTGAGA AGAAGAGAGG 1980 AGAGCCATTC CCCAACACGG CACCTTGCTC TGTGTTAGCT CCATCTTCTC TCATGACGGG 2040 GCCTTCGGAA ACACCAAGAA ACGACCAAAG CAGACAGGCA CTGGGAGAAG CAGGACAAGC 2100 ATTTCCTCAC CTCACATGAA CTTCCATATG AATGTGACAA AGGCACAGCA CACAAAATGC 2160 AGATGCTGAC CACAGAGAGG GCCCCACTCA CTCACGCTGG CCACGAAAAG GCCCGCCCTG 2220 GTTCACACCG GCATGGAGAG GTCTCGCTTC 2250
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