Tag | Content |
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EnhancerAtlas ID | HS030-00017 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr1:1003290-1006580 |
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: 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 | CAAGAGTTCG GCCGTGTGCA CATGCGCGTC CTCGGCAAGG GCCAGGCCCA GGGCTACTGC 60 GTGCGGGAGC TGCAGGTGTG GCGGCCGGGC CAGGTGAGCC TGGCGGCTGT GGAGCGTGCC 120 TGCTGTCGGC CTGCACTGGG AGACCCCACA CCTGCCTGCA TCCAACCCCA CTGCCTTTGG 180 GGGCTTCCAC ACCCCTCAAC CCAGGAGGTG CATTCCAAGC CTGGACAGGG GTCACTGACG 240 TGGCCACATT CTCAGCCCTG GGCTGGCGGC CGCTCCTCCC ACACACCTCT CCAACTGCAG 300 CTTTGGTCTC CGTTGTATAC CAGAGACGCC CATTTCTGCT CCGGGCAGAT TACCTCGTGT 360 TCCCTCCAGC CCCCGCCCAG TGTGTGTGGG GGGGTCCTCC AGGACCCCAT GGACCCCTCA 420 CATTTGGTTT TTCCTTATAA AATAACTGTC CTCACAGCCT GCTTCGCCCG CCCCCAGCTC 480 CCTCTTCCCT TCCCCAGGCA CCTGAGCCAC CTGGGGCCAT CTCGGCGCCC CCTCCCCATT 540 TCCTTCCTCC TCCTCCTGCT CGCCTTGGCT CCCGCAGCCC CTCCGCTTGG GCACTCCCGG 600 AAACCCAGCT GTGCCTCAGC CTCCTCCTCC CACCCTGGGG TCACACTCAC CGCTTGCCCC 660 GCTCAGGAGG AGCCACAGCG TACGGTGCAG CACTTCCAGT ACTTCGGCTG GCCGGACTAC 720 GGCGTCCGGG CCGATCCCGC CGGCGTCCTC GGCTTCCGGG ACGAGGTGAA CCGGGCCCAG 780 AGCAGCAAGC CGCGGGCCGG GCCCATGGTG GTGCACTTCA GCTGCGGCGG GGCGGGCCCA 840 CGCGGGCTGT GCAGATGCAG GTGCGGCGGG GCGGGGCCAC GCGGGCTGTG CAGGTGCAGG 900 TGCGGCGGGG CGGGGCCACG CGGGACGACG AGGGCGGAGC CATCGGGTGG GCGGGGGCGC 960 CCCCGCCCCC GCCCCCCACT CTCGTCAAAG GCCGCCTAGT TTGTCCTCAG TGGGGGCATC 1020 GGATGCACGG GCACCATCAT CGTGATTGAC ATCCTGGTGG ACGTCATCCG CAGGCAGGGC 1080 GAGCCGCTCC ACTCTGGGTC CCCCCGCCCT GCCCTGCTAT AGCCCCACCC CTCCGGGCGA 1140 CCCCACCCCT CCGGACGACC CCACCCCTCA GGACGACCCC ACCCCTCAGG ACGACCCCAC 1200 CGCTACCGGC AAGCCCCGCC CCTCATCAGC AGCCCCGCCC CTGCCTGCCG GCACCTTCCC 1260 CCCATCCGTA GCCCCTCCCC AAGCGCGCTT GTCCGCAGGG CTGGACTGCG ACACCGACGT 1320 CCCGAAGACG ATCCAGCTGG TTTGGCGGCA GCACTGGGGA ATGGTGCAGA CGGAGGCTCC 1380 GTACAAGTTC ACGTACCTGG CGCTGCAGCG GCACATCCGG GGCGAGTAAC TGCGCCTGCG 1440 CGAGCAGGTG GGGGCGTGGC CCTGCGGGGC GTGGCCTGTG CGGGCGTCGC CATGGTGACC 1500 GGCGGCCCCT CCCCCCAGCG CGAGCCGCCT CAGGAGCGCG AGAACCAAAA CGTGGGCGCC 1560 GCCCCCCGCT AATCGGGTTG CAGCCCCCGG CTCCCCGGGC ATCCCCGGTG TGAGTGGAGC 1620 GCCGGGGCCG GTCCGGAGTC CTCTGGGAGG GACTGGGACG TGCGGGGTGC AGGGCTGAGC 1680 CGCTGCTCCG CGCGCAGAAC CCCGCAGCCC TGGGACGGCG AGGACGCGAA CCTGCGGAGC 1740 CGCGGGTGTC TGAGGAGCCG CAGGGAACCC CCGGCCTAGC CGCGCCCGCG TGTGGCCGGA 1800 GCTGCGGGCC GGGACTGTGT CCAGGACAGA GCCACAAGCT TGTCCCCAGC TCAGGGAGGT 1860 CCAGGGGCGG CAGAGGGAGC GACAGGCTGC GAAGCCCACC GGTGACCACG TGTGAACCCG 1920 CGTGCGCCCC CAGCTCGGCC ACTCCGTGCG GGTCTGCCCT CACCGCAGCT CCGGCCTGCC 1980 GGCCCTGCCT GCTCCCGTGG TCTGGGATGT GGCCCCGGTG AGGACCCGGC CCCATCAGGC 2040 ACAGGGTGGA TGTCTGTGGA GTGAGGTGTG TGTGACATAT TCATGTGACC ACCCGTGCAG 2100 CGTCACGCGC CTGGCCCTGC CGATGACAAG GGTGTGGGCC TGCGTGGGCA TGACTGTGTG 2160 TGTGACACAG AGTGATGTTG CTGTGACCCG TGGCTGCACT CCCCACATCA CCGGCTTTCA 2220 CAGCCTTCCG GTAAAGTGCT GTGTTCTCCC TTCTGTGTCT TCGCTGGGAC CTGGGGCAAG 2280 GGTGGGTGTG GCCCCCACAG CTGGAGTCAG CTTCTGTGGG GCCTTCCCGA GCCCTCCCCA 2340 CCCTGGACCA GAGGCCCAGC TGGTTGGAGC AGGAAGTACC TGGGCTCTGG GGTCAGGGAT 2400 GGGAAGGCTG AGGAGGCCTG CGTGAGCTGG ACCTGGCCTG GGCCCTCCTG GCCGTGCCTG 2460 CCTGGTGGTG CAGGATTCCT GGGGCTGATG ACAGACGGGG TAGGGCTGGG GTTGGCGAGC 2520 CTCCTGCCGA TACCTCACGT AGCTGACCTC TGACTCTTCC CCAGCCAGGC TGGCCCTGGG 2580 AGTTGCCGGA GAGTCAGTGG ATCTGCAGGC TGCACGCTGG CTGTTACCTT TGCTTCTGGG 2640 TTCCCACAGG GGTCATGGTT CTGTGGTTCT CCAGTCAGGG ACCCTAGCAG GGCCATGGGG 2700 CGTGACTTCC TGGAGGTGTG GCCTAGTATG GCCACGGCAG AGGATGGGGG AAGAGAAAGG 2760 CCCCCTTTGT CAGCCCCCGG GCTCTGAACC AAGCTGAAGC CCTCCCCCTG GTCCAGCCTG 2820 CCCTGCCCCA AGTGTCCTGG GCCTCTCCCC ATCTCCCTGG GGAGCCTCAC ATTGCTGAGT 2880 CGCCAGCCAA CTCCAGAAAC CCCCAGCCTG TCTGCAGCCA GAGGGGCTGG GAGTTGGACC 2940 CCCTAGAACC TTGGGCCCAC CTGTCCCAGT GGCTGCTGGG AGTCTAATTC TGTCAGGGTA 3000 TCCTCTGGGT TGAGGCTGCA GCAGGGGCAC CCAGGGTGAG GCCCTCTTGC CAAAGATGGA 3060 TACAAATAAT TTATTTTAAA AGGTACAATT CACAAGGTTG GAGGGGTAGC TGGAAGTTTC 3120 TGTGGTTACC TTGCACTGGG GGGCTGCCCT GCCTCCACTC TCTCCCCACA GTCCGAGGGC 3180 AAGATGAGCA CCCCCACCCA ATGGCAGGAC CAGCCCTGCG GGGAAATGTC AGCATGAGTG 3240 GAAGCACGGC AAGGCCCCTT CCTTCTTGGC AAGGGGCTTC CCTGGCAGGC 3290
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