Tag | Content |
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EnhancerAtlas ID | HS110-00008 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr1:1002480-1006040 |
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 | Pou2f3 | MA0627.1 | chr1:1002525-1002541 | TATCATTTGCATAGCA | - | 6.09 | 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 | TTAAGCCACC AGGGCTCTTT GCATAATATT TGTGTGTCGT TTGCATATCA TTTGCATAGC 60 ATTTGCATGG ACTTGTTTGT CCTCTGTTAA CAGCAGCAGT TGGCCTCATT CCCTTTCAGA 120 CTGACCCTGA GGAGGAGCCG GGCCATGGCA GGGGCAGGGT GGACATCCCT TGTGGCCCTG 180 CCCCGCCGCA CCTGCACCTG CACAGCCCGC GTGGGCCCGC CCCGCCGCAG CTGAAGTGCA 240 CCACCATGGG CCCGGCCCGC GGCTCGCGGC TCGCGGCTCT GGGCCCGGTT CACCTCGTCC 300 CGGAAGCCGA GGACGCCGGC GGGATCGGTC CGGACGCCGT AGTCCGGCCA GCCGAAGTAC 360 TGGAAGTGCT GCACCGTACG CTGTGGCTCC TCCCCGCGGG GCAGGGCCTC GCGGGCGCAG 420 GGTGTACATC GCCTGCAGGG CTGTCTGCAG GCCTGTCTGC AGGCCACGGT GGCTGCTTTC 480 TGGGCCACGG TGCACCAGGA GAACACGCGT GTCATCGTCA TGACCACCAG GGAGATGGAG 540 CGGGGCCGGG TAGGGGTGCG GTGCCAGTGC TCCCAGTGCC CATCCCACCC CGTGCATCTT 600 CGGCTGCCCA AGGCCCTTCC CGACCAGGCC AAGGAGGCTG TGGGACGCCG TGGGAGTGGG 660 GAGGCTCCCA CAGAGCCCCG TGGCTGCACG TACACACCTG CGTCTCTGCA GGTCGCAGGG 720 GCGGGGTGCC GAGGTGCTGC CAGCAAGGCT GATGCAAAGC GCTCCCCTCG GAACAAGTGT 780 TTCCGGGACT GGCCAGAGCT GCCCGGCAGC CAAGAGTTCG GCCGTGTGCA CATGCGCGTC 840 CTCGGCAAGG GCCAGGCCCA GGGCTACTGC GTGCGGGAGC TGCAGGTGTG GCGGCCGGGC 900 CAGGTGAGCC TGGCGGCTGT GGAGCGTGCC TGCTGTCGGC CTGCACTGGG AGACCCCACA 960 CCTGCCTGCA TCCAACCCCA CTGCCTTTGG GGGCTTCCAC ACCCCTCAAC CCAGGAGGTG 1020 CATTCCAAGC CTGGACAGGG GTCACTGACG TGGCCACATT CTCAGCCCTG GGCTGGCGGC 1080 CGCTCCTCCC ACACACCTCT CCAACTGCAG CTTTGGTCTC CGTTGTATAC CAGAGACGCC 1140 CATTTCTGCT CCGGGCAGAT TACCTCGTGT TCCCTCCAGC CCCCGCCCAG TGTGTGTGGG 1200 GGGGTCCTCC AGGACCCCAT GGACCCCTCA CATTTGGTTT TTCCTTATAA AATAACTGTC 1260 CTCACAGCCT GCTTCGCCCG CCCCCAGCTC CCTCTTCCCT TCCCCAGGCA CCTGAGCCAC 1320 CTGGGGCCAT CTCGGCGCCC CCTCCCCATT TCCTTCCTCC TCCTCCTGCT CGCCTTGGCT 1380 CCCGCAGCCC CTCCGCTTGG GCACTCCCGG AAACCCAGCT GTGCCTCAGC CTCCTCCTCC 1440 CACCCTGGGG TCACACTCAC CGCTTGCCCC GCTCAGGAGG AGCCACAGCG TACGGTGCAG 1500 CACTTCCAGT ACTTCGGCTG GCCGGACTAC GGCGTCCGGG CCGATCCCGC CGGCGTCCTC 1560 GGCTTCCGGG ACGAGGTGAA CCGGGCCCAG AGCAGCAAGC CGCGGGCCGG GCCCATGGTG 1620 GTGCACTTCA GCTGCGGCGG GGCGGGCCCA CGCGGGCTGT GCAGATGCAG GTGCGGCGGG 1680 GCGGGGCCAC GCGGGCTGTG CAGGTGCAGG TGCGGCGGGG CGGGGCCACG CGGGACGACG 1740 AGGGCGGAGC CATCGGGTGG GCGGGGGCGC CCCCGCCCCC GCCCCCCACT CTCGTCAAAG 1800 GCCGCCTAGT TTGTCCTCAG TGGGGGCATC GGATGCACGG GCACCATCAT CGTGATTGAC 1860 ATCCTGGTGG ACGTCATCCG CAGGCAGGGC GAGCCGCTCC ACTCTGGGTC CCCCCGCCCT 1920 GCCCTGCTAT AGCCCCACCC CTCCGGGCGA CCCCACCCCT CCGGACGACC CCACCCCTCA 1980 GGACGACCCC ACCCCTCAGG ACGACCCCAC CGCTACCGGC AAGCCCCGCC CCTCATCAGC 2040 AGCCCCGCCC CTGCCTGCCG GCACCTTCCC CCCATCCGTA GCCCCTCCCC AAGCGCGCTT 2100 GTCCGCAGGG CTGGACTGCG ACACCGACGT CCCGAAGACG ATCCAGCTGG TTTGGCGGCA 2160 GCACTGGGGA ATGGTGCAGA CGGAGGCTCC GTACAAGTTC ACGTACCTGG CGCTGCAGCG 2220 GCACATCCGG GGCGAGTAAC TGCGCCTGCG CGAGCAGGTG GGGGCGTGGC CCTGCGGGGC 2280 GTGGCCTGTG CGGGCGTCGC CATGGTGACC GGCGGCCCCT CCCCCCAGCG CGAGCCGCCT 2340 CAGGAGCGCG AGAACCAAAA CGTGGGCGCC GCCCCCCGCT AATCGGGTTG CAGCCCCCGG 2400 CTCCCCGGGC ATCCCCGGTG TGAGTGGAGC GCCGGGGCCG GTCCGGAGTC CTCTGGGAGG 2460 GACTGGGACG TGCGGGGTGC AGGGCTGAGC CGCTGCTCCG CGCGCAGAAC CCCGCAGCCC 2520 TGGGACGGCG AGGACGCGAA CCTGCGGAGC CGCGGGTGTC TGAGGAGCCG CAGGGAACCC 2580 CCGGCCTAGC CGCGCCCGCG TGTGGCCGGA GCTGCGGGCC GGGACTGTGT CCAGGACAGA 2640 GCCACAAGCT TGTCCCCAGC TCAGGGAGGT CCAGGGGCGG CAGAGGGAGC GACAGGCTGC 2700 GAAGCCCACC GGTGACCACG TGTGAACCCG CGTGCGCCCC CAGCTCGGCC ACTCCGTGCG 2760 GGTCTGCCCT CACCGCAGCT CCGGCCTGCC GGCCCTGCCT GCTCCCGTGG TCTGGGATGT 2820 GGCCCCGGTG AGGACCCGGC CCCATCAGGC ACAGGGTGGA TGTCTGTGGA GTGAGGTGTG 2880 TGTGACATAT TCATGTGACC ACCCGTGCAG CGTCACGCGC CTGGCCCTGC CGATGACAAG 2940 GGTGTGGGCC TGCGTGGGCA TGACTGTGTG TGTGACACAG AGTGATGTTG CTGTGACCCG 3000 TGGCTGCACT CCCCACATCA CCGGCTTTCA CAGCCTTCCG GTAAAGTGCT GTGTTCTCCC 3060 TTCTGTGTCT TCGCTGGGAC CTGGGGCAAG GGTGGGTGTG GCCCCCACAG CTGGAGTCAG 3120 CTTCTGTGGG GCCTTCCCGA GCCCTCCCCA CCCTGGACCA GAGGCCCAGC TGGTTGGAGC 3180 AGGAAGTACC TGGGCTCTGG GGTCAGGGAT GGGAAGGCTG AGGAGGCCTG CGTGAGCTGG 3240 ACCTGGCCTG GGCCCTCCTG GCCGTGCCTG CCTGGTGGTG CAGGATTCCT GGGGCTGATG 3300 ACAGACGGGG TAGGGCTGGG GTTGGCGAGC CTCCTGCCGA TACCTCACGT AGCTGACCTC 3360 TGACTCTTCC CCAGCCAGGC TGGCCCTGGG AGTTGCCGGA GAGTCAGTGG ATCTGCAGGC 3420 TGCACGCTGG CTGTTACCTT TGCTTCTGGG TTCCCACAGG GGTCATGGTT CTGTGGTTCT 3480 CCAGTCAGGG ACCCTAGCAG GGCCATGGGG CGTGACTTCC TGGAGGTGTG GCCTAGTATG 3540 GCCACGGCAG AGGATGGGGG 3560
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