Tag | Content |
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EnhancerAtlas ID | HS133-00017 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:1002860-1006050 |
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) |
KLF14 | MA0740.1 | chr1:1004737-1004751 | GTGGGGGCGTGGCC | - | 6.39 | KLF16 | MA0741.1 | chr1:1004739-1004750 | GGGGGCGTGGC | - | 6.62 | KLF5 | MA0599.1 | chr1:1004502-1004512 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:1004521-1004531 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:1004157-1004167 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr1:1004196-1004206 | GGGGCGGGGC | - | 6.02 | Klf1 | MA0493.1 | chr1:1005572-1005583 | TGGGTGTGGCC | - | 6.62 | NRF1 | MA0506.1 | chr1:1004721-1004732 | GCGCCTGCGCG | + | 6.14 | RFX1 | MA0509.2 | chr1:1004774-1004790 | CGTCGCCATGGTGACC | + | 6.11 | RFX1 | MA0509.2 | chr1:1004774-1004790 | CGTCGCCATGGTGACC | - | 6.12 | RFX2 | MA0600.2 | chr1:1004774-1004790 | CGTCGCCATGGTGACC | + | 6.2 | RFX2 | MA0600.2 | chr1:1004774-1004790 | CGTCGCCATGGTGACC | - | 6.2 | SP1 | MA0079.4 | chr1:1004499-1004514 | CAAGCCCCGCCCCTC | + | 6.34 | SP2 | MA0516.2 | chr1:1004498-1004515 | GCAAGCCCCGCCCCTCA | + | 6.23 | SP3 | MA0746.2 | chr1:1004738-1004751 | TGGGGGCGTGGCC | - | 6.57 | SP4 | MA0685.1 | chr1:1004499-1004516 | CAAGCCCCGCCCCTCAT | + | 6.24 | SP8 | MA0747.1 | chr1:1004738-1004750 | TGGGGGCGTGGC | - | 6.11 | ZNF263 | MA0528.1 | chr1:1003831-1003852 | CCTTCCTCCTCCTCCTGCTCG | - | 6.88 | ZNF263 | MA0528.1 | chr1:1003819-1003840 | CCCTCCCCATTTCCTTCCTCC | - | 6.89 | ZNF263 | MA0528.1 | chr1:1003825-1003846 | CCATTTCCTTCCTCCTCCTCC | - | 7.03 | ZNF263 | MA0528.1 | chr1:1003822-1003843 | TCCCCATTTCCTTCCTCCTCC | - | 8.3 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_24070 | chr1:1002554-1005867 | Colon_Crypt_2 | SE_24817 | chr1:1002490-1006081 | Colon_Crypt_3 | SE_27529 | chr1:1001798-1011077 | Esophagus | SE_34539 | chr1:1002321-1004360 | HCT-116 | SE_34539 | chr1:1004454-1006480 | HCT-116 | SE_41944 | chr1:1001963-1005965 | LNCaP | SE_58139 | chr1:1003761-1004209 | VACO_9m | SE_58139 | chr1:1004236-1004768 | VACO_9m | SE_58139 | chr1:1004812-1005267 | VACO_9m | SE_65935 | chr1:1001682-1006445 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 1003459 | 1003600 | chr1 | 1005293 | 1005547 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I001066 | chr1 | 1001837 | 1006486 |
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Enhancer Sequence | CTGTGGCTCC TCCCCGCGGG GCAGGGCCTC GCGGGCGCAG GGTGTACATC GCCTGCAGGG 60 CTGTCTGCAG GCCTGTCTGC AGGCCACGGT GGCTGCTTTC TGGGCCACGG TGCACCAGGA 120 GAACACGCGT GTCATCGTCA TGACCACCAG GGAGATGGAG CGGGGCCGGG TAGGGGTGCG 180 GTGCCAGTGC TCCCAGTGCC CATCCCACCC CGTGCATCTT CGGCTGCCCA AGGCCCTTCC 240 CGACCAGGCC AAGGAGGCTG TGGGACGCCG TGGGAGTGGG GAGGCTCCCA CAGAGCCCCG 300 TGGCTGCACG TACACACCTG CGTCTCTGCA GGTCGCAGGG GCGGGGTGCC GAGGTGCTGC 360 CAGCAAGGCT GATGCAAAGC GCTCCCCTCG GAACAAGTGT TTCCGGGACT GGCCAGAGCT 420 GCCCGGCAGC CAAGAGTTCG GCCGTGTGCA CATGCGCGTC CTCGGCAAGG GCCAGGCCCA 480 GGGCTACTGC GTGCGGGAGC TGCAGGTGTG GCGGCCGGGC CAGGTGAGCC TGGCGGCTGT 540 GGAGCGTGCC TGCTGTCGGC CTGCACTGGG AGACCCCACA CCTGCCTGCA TCCAACCCCA 600 CTGCCTTTGG GGGCTTCCAC ACCCCTCAAC CCAGGAGGTG CATTCCAAGC CTGGACAGGG 660 GTCACTGACG TGGCCACATT CTCAGCCCTG GGCTGGCGGC CGCTCCTCCC ACACACCTCT 720 CCAACTGCAG CTTTGGTCTC CGTTGTATAC CAGAGACGCC CATTTCTGCT CCGGGCAGAT 780 TACCTCGTGT TCCCTCCAGC CCCCGCCCAG TGTGTGTGGG GGGGTCCTCC AGGACCCCAT 840 GGACCCCTCA CATTTGGTTT TTCCTTATAA AATAACTGTC CTCACAGCCT GCTTCGCCCG 900 CCCCCAGCTC CCTCTTCCCT TCCCCAGGCA CCTGAGCCAC CTGGGGCCAT CTCGGCGCCC 960 CCTCCCCATT TCCTTCCTCC TCCTCCTGCT CGCCTTGGCT CCCGCAGCCC CTCCGCTTGG 1020 GCACTCCCGG AAACCCAGCT GTGCCTCAGC CTCCTCCTCC CACCCTGGGG TCACACTCAC 1080 CGCTTGCCCC GCTCAGGAGG AGCCACAGCG TACGGTGCAG CACTTCCAGT ACTTCGGCTG 1140 GCCGGACTAC GGCGTCCGGG CCGATCCCGC CGGCGTCCTC GGCTTCCGGG ACGAGGTGAA 1200 CCGGGCCCAG AGCAGCAAGC CGCGGGCCGG GCCCATGGTG GTGCACTTCA GCTGCGGCGG 1260 GGCGGGCCCA CGCGGGCTGT GCAGATGCAG GTGCGGCGGG GCGGGGCCAC GCGGGCTGTG 1320 CAGGTGCAGG TGCGGCGGGG CGGGGCCACG CGGGACGACG AGGGCGGAGC CATCGGGTGG 1380 GCGGGGGCGC CCCCGCCCCC GCCCCCCACT CTCGTCAAAG GCCGCCTAGT TTGTCCTCAG 1440 TGGGGGCATC GGATGCACGG GCACCATCAT CGTGATTGAC ATCCTGGTGG ACGTCATCCG 1500 CAGGCAGGGC GAGCCGCTCC ACTCTGGGTC CCCCCGCCCT GCCCTGCTAT AGCCCCACCC 1560 CTCCGGGCGA CCCCACCCCT CCGGACGACC CCACCCCTCA GGACGACCCC ACCCCTCAGG 1620 ACGACCCCAC CGCTACCGGC AAGCCCCGCC CCTCATCAGC AGCCCCGCCC CTGCCTGCCG 1680 GCACCTTCCC CCCATCCGTA GCCCCTCCCC AAGCGCGCTT GTCCGCAGGG CTGGACTGCG 1740 ACACCGACGT CCCGAAGACG ATCCAGCTGG TTTGGCGGCA GCACTGGGGA ATGGTGCAGA 1800 CGGAGGCTCC GTACAAGTTC ACGTACCTGG CGCTGCAGCG GCACATCCGG GGCGAGTAAC 1860 TGCGCCTGCG CGAGCAGGTG GGGGCGTGGC CCTGCGGGGC GTGGCCTGTG CGGGCGTCGC 1920 CATGGTGACC GGCGGCCCCT CCCCCCAGCG CGAGCCGCCT CAGGAGCGCG AGAACCAAAA 1980 CGTGGGCGCC GCCCCCCGCT AATCGGGTTG CAGCCCCCGG CTCCCCGGGC ATCCCCGGTG 2040 TGAGTGGAGC GCCGGGGCCG GTCCGGAGTC CTCTGGGAGG GACTGGGACG TGCGGGGTGC 2100 AGGGCTGAGC CGCTGCTCCG CGCGCAGAAC CCCGCAGCCC TGGGACGGCG AGGACGCGAA 2160 CCTGCGGAGC CGCGGGTGTC TGAGGAGCCG CAGGGAACCC CCGGCCTAGC CGCGCCCGCG 2220 TGTGGCCGGA GCTGCGGGCC GGGACTGTGT CCAGGACAGA GCCACAAGCT TGTCCCCAGC 2280 TCAGGGAGGT CCAGGGGCGG CAGAGGGAGC GACAGGCTGC GAAGCCCACC GGTGACCACG 2340 TGTGAACCCG CGTGCGCCCC CAGCTCGGCC ACTCCGTGCG GGTCTGCCCT CACCGCAGCT 2400 CCGGCCTGCC GGCCCTGCCT GCTCCCGTGG TCTGGGATGT GGCCCCGGTG AGGACCCGGC 2460 CCCATCAGGC ACAGGGTGGA TGTCTGTGGA GTGAGGTGTG TGTGACATAT TCATGTGACC 2520 ACCCGTGCAG CGTCACGCGC CTGGCCCTGC CGATGACAAG GGTGTGGGCC TGCGTGGGCA 2580 TGACTGTGTG TGTGACACAG AGTGATGTTG CTGTGACCCG TGGCTGCACT CCCCACATCA 2640 CCGGCTTTCA CAGCCTTCCG GTAAAGTGCT GTGTTCTCCC TTCTGTGTCT TCGCTGGGAC 2700 CTGGGGCAAG GGTGGGTGTG GCCCCCACAG CTGGAGTCAG CTTCTGTGGG GCCTTCCCGA 2760 GCCCTCCCCA CCCTGGACCA GAGGCCCAGC TGGTTGGAGC AGGAAGTACC TGGGCTCTGG 2820 GGTCAGGGAT GGGAAGGCTG AGGAGGCCTG CGTGAGCTGG ACCTGGCCTG GGCCCTCCTG 2880 GCCGTGCCTG CCTGGTGGTG CAGGATTCCT GGGGCTGATG ACAGACGGGG TAGGGCTGGG 2940 GTTGGCGAGC CTCCTGCCGA TACCTCACGT AGCTGACCTC TGACTCTTCC CCAGCCAGGC 3000 TGGCCCTGGG AGTTGCCGGA GAGTCAGTGG ATCTGCAGGC TGCACGCTGG CTGTTACCTT 3060 TGCTTCTGGG TTCCCACAGG GGTCATGGTT CTGTGGTTCT CCAGTCAGGG ACCCTAGCAG 3120 GGCCATGGGG CGTGACTTCC TGGAGGTGTG GCCTAGTATG GCCACGGCAG AGGATGGGGG 3180 AAGAGAAAGG 3190
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