Tag | Content |
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EnhancerAtlas ID | HS088-00033 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr1:1003440-1007120 |
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 | NKX2-5 | MA0063.2 | chr1:1006876-1006886 | CTCAAGTGGT | - | 6.02 | 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: 4 | Chromosome | Start | End |
chr1 | 1003459 | 1003600 | chr1 | 1005293 | 1005547 | chr1 | 1006044 | 1006328 | chr1 | 1003600 | 1006245 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I001066 | chr1 | 1001837 | 1006486 |
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Enhancer Sequence | CCTGCCTGCA TCCAACCCCA CTGCCTTTGG GGGCTTCCAC ACCCCTCAAC CCAGGAGGTG 60 CATTCCAAGC CTGGACAGGG GTCACTGACG TGGCCACATT CTCAGCCCTG GGCTGGCGGC 120 CGCTCCTCCC ACACACCTCT CCAACTGCAG CTTTGGTCTC CGTTGTATAC CAGAGACGCC 180 CATTTCTGCT CCGGGCAGAT TACCTCGTGT TCCCTCCAGC CCCCGCCCAG TGTGTGTGGG 240 GGGGTCCTCC AGGACCCCAT GGACCCCTCA CATTTGGTTT TTCCTTATAA AATAACTGTC 300 CTCACAGCCT GCTTCGCCCG CCCCCAGCTC CCTCTTCCCT TCCCCAGGCA CCTGAGCCAC 360 CTGGGGCCAT CTCGGCGCCC CCTCCCCATT TCCTTCCTCC TCCTCCTGCT CGCCTTGGCT 420 CCCGCAGCCC CTCCGCTTGG GCACTCCCGG AAACCCAGCT GTGCCTCAGC CTCCTCCTCC 480 CACCCTGGGG TCACACTCAC CGCTTGCCCC GCTCAGGAGG AGCCACAGCG TACGGTGCAG 540 CACTTCCAGT ACTTCGGCTG GCCGGACTAC GGCGTCCGGG CCGATCCCGC CGGCGTCCTC 600 GGCTTCCGGG ACGAGGTGAA CCGGGCCCAG AGCAGCAAGC CGCGGGCCGG GCCCATGGTG 660 GTGCACTTCA GCTGCGGCGG GGCGGGCCCA CGCGGGCTGT GCAGATGCAG GTGCGGCGGG 720 GCGGGGCCAC GCGGGCTGTG CAGGTGCAGG TGCGGCGGGG CGGGGCCACG CGGGACGACG 780 AGGGCGGAGC CATCGGGTGG GCGGGGGCGC CCCCGCCCCC GCCCCCCACT CTCGTCAAAG 840 GCCGCCTAGT TTGTCCTCAG TGGGGGCATC GGATGCACGG GCACCATCAT CGTGATTGAC 900 ATCCTGGTGG ACGTCATCCG CAGGCAGGGC GAGCCGCTCC ACTCTGGGTC CCCCCGCCCT 960 GCCCTGCTAT AGCCCCACCC CTCCGGGCGA CCCCACCCCT CCGGACGACC CCACCCCTCA 1020 GGACGACCCC ACCCCTCAGG ACGACCCCAC CGCTACCGGC AAGCCCCGCC CCTCATCAGC 1080 AGCCCCGCCC CTGCCTGCCG GCACCTTCCC CCCATCCGTA GCCCCTCCCC AAGCGCGCTT 1140 GTCCGCAGGG CTGGACTGCG ACACCGACGT CCCGAAGACG ATCCAGCTGG TTTGGCGGCA 1200 GCACTGGGGA ATGGTGCAGA CGGAGGCTCC GTACAAGTTC ACGTACCTGG CGCTGCAGCG 1260 GCACATCCGG GGCGAGTAAC TGCGCCTGCG CGAGCAGGTG GGGGCGTGGC CCTGCGGGGC 1320 GTGGCCTGTG CGGGCGTCGC CATGGTGACC GGCGGCCCCT CCCCCCAGCG CGAGCCGCCT 1380 CAGGAGCGCG AGAACCAAAA CGTGGGCGCC GCCCCCCGCT AATCGGGTTG CAGCCCCCGG 1440 CTCCCCGGGC ATCCCCGGTG TGAGTGGAGC GCCGGGGCCG GTCCGGAGTC CTCTGGGAGG 1500 GACTGGGACG TGCGGGGTGC AGGGCTGAGC CGCTGCTCCG CGCGCAGAAC CCCGCAGCCC 1560 TGGGACGGCG AGGACGCGAA CCTGCGGAGC CGCGGGTGTC TGAGGAGCCG CAGGGAACCC 1620 CCGGCCTAGC CGCGCCCGCG TGTGGCCGGA GCTGCGGGCC GGGACTGTGT CCAGGACAGA 1680 GCCACAAGCT TGTCCCCAGC TCAGGGAGGT CCAGGGGCGG CAGAGGGAGC GACAGGCTGC 1740 GAAGCCCACC GGTGACCACG TGTGAACCCG CGTGCGCCCC CAGCTCGGCC ACTCCGTGCG 1800 GGTCTGCCCT CACCGCAGCT CCGGCCTGCC GGCCCTGCCT GCTCCCGTGG TCTGGGATGT 1860 GGCCCCGGTG AGGACCCGGC CCCATCAGGC ACAGGGTGGA TGTCTGTGGA GTGAGGTGTG 1920 TGTGACATAT TCATGTGACC ACCCGTGCAG CGTCACGCGC CTGGCCCTGC CGATGACAAG 1980 GGTGTGGGCC TGCGTGGGCA TGACTGTGTG TGTGACACAG AGTGATGTTG CTGTGACCCG 2040 TGGCTGCACT CCCCACATCA CCGGCTTTCA CAGCCTTCCG GTAAAGTGCT GTGTTCTCCC 2100 TTCTGTGTCT TCGCTGGGAC CTGGGGCAAG GGTGGGTGTG GCCCCCACAG CTGGAGTCAG 2160 CTTCTGTGGG GCCTTCCCGA GCCCTCCCCA CCCTGGACCA GAGGCCCAGC TGGTTGGAGC 2220 AGGAAGTACC TGGGCTCTGG GGTCAGGGAT GGGAAGGCTG AGGAGGCCTG CGTGAGCTGG 2280 ACCTGGCCTG GGCCCTCCTG GCCGTGCCTG CCTGGTGGTG CAGGATTCCT GGGGCTGATG 2340 ACAGACGGGG TAGGGCTGGG GTTGGCGAGC CTCCTGCCGA TACCTCACGT AGCTGACCTC 2400 TGACTCTTCC CCAGCCAGGC TGGCCCTGGG AGTTGCCGGA GAGTCAGTGG ATCTGCAGGC 2460 TGCACGCTGG CTGTTACCTT TGCTTCTGGG TTCCCACAGG GGTCATGGTT CTGTGGTTCT 2520 CCAGTCAGGG ACCCTAGCAG GGCCATGGGG CGTGACTTCC TGGAGGTGTG GCCTAGTATG 2580 GCCACGGCAG AGGATGGGGG AAGAGAAAGG CCCCCTTTGT CAGCCCCCGG GCTCTGAACC 2640 AAGCTGAAGC CCTCCCCCTG GTCCAGCCTG CCCTGCCCCA AGTGTCCTGG GCCTCTCCCC 2700 ATCTCCCTGG GGAGCCTCAC ATTGCTGAGT CGCCAGCCAA CTCCAGAAAC CCCCAGCCTG 2760 TCTGCAGCCA GAGGGGCTGG GAGTTGGACC CCCTAGAACC TTGGGCCCAC CTGTCCCAGT 2820 GGCTGCTGGG AGTCTAATTC TGTCAGGGTA TCCTCTGGGT TGAGGCTGCA GCAGGGGCAC 2880 CCAGGGTGAG GCCCTCTTGC CAAAGATGGA TACAAATAAT TTATTTTAAA AGGTACAATT 2940 CACAAGGTTG GAGGGGTAGC TGGAAGTTTC TGTGGTTACC TTGCACTGGG GGGCTGCCCT 3000 GCCTCCACTC TCTCCCCACA GTCCGAGGGC AAGATGAGCA CCCCCACCCA ATGGCAGGAC 3060 CAGCCCTGCG GGGAAATGTC AGCATGAGTG GAAGCACGGC AAGGCCCCTT CCTTCTTGGC 3120 AAGGGGCTTC CCTGGCAGGC AGTTCACAGG GTGTGTGGGT GGGGGGGATG CTGACCAGCT 3180 GCTCTCCTGG ACCCTTCCTG TACGAGCCTG TTTTTTTTTG TTTTGTTTTG AGACAGGGTC 3240 TCCCTCTGTC GCCCAGGCTG GATGCAGTGG TGCAATCTTG GCTCACTGCC ACCTCCACCT 3300 CCCCGGTTCA AGCAGTTCTC CTGCCTCAGC CTCCCCAGTA GCTAAGAGGC ACCCACCACG 3360 ATGCCCGGTT AATTTTTGTA TTTTTAGTAG AGATGGGGTT TCACCATGTT GGCCAGGCTG 3420 GTGTCAAAAT CCCGACCTCA AGTGGTCTTT CTGCCTCAGC CCTCCAGAGT GCTGAGATGA 3480 CAGGCGTGAG CCACCGCGCC CGGTGAGACT GTGGTTCTTG GAGGCTTTGG GGATCCTCTT 3540 GTCCACCCCG TCAGGACCCA GCCTGGAGAA TGAGGGGTGG ACAAGCTAAA TGGAGCCTGG 3600 TCTTGGTGGG GCCCCGGTGG AGTCCTCAGA GATGCCAGGC TCCTTTCGCG TCCTCGGGGA 3660 CCGACTTCCA GTGGCTGCTG 3680
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