Tag | Content |
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EnhancerAtlas ID | HS073-00014 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr1:1001880-1006410 |
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: 9 | 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 | chr1:1004236-1004768 | 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 | GGGCTGGGGG TGGCCATCTC GGGCTCTGGG AAGGGGCCGG GGCTGTGAGC TGAAGGCTCC 60 ATCACCTCCA GATGCTGCAG CAGCAGGAAT GCCGGTTCCT GTACCCTCGG AAGGAGGGGC 120 AGAGTGTGGA GAACAAGCCC AAGAATCACT ACAAGAACAT CCTTCCCTGT GAGGGCGGAG 180 GCCAGGGCGT CACCCGTCGG GCCTGGGGGA GGTGGGGGGC AGGCCGAGCA TCTGCCACCG 240 CTGACCTGAG GCTCCCCCTT GCATACCCTG GACCCTCCAT CTCTGCTCAC CACAGGGTCT 300 GCGGGCAAAG AGGCAGGGTG AGGCCCACGA GCTGTGCCCT GGAGAACTGA GCGGCACCTC 360 CCTTCCCAGT TGATGCTACC CTTGAGTCAT CCTGCTCAAC GAGGATGACA GCGGGCCCGG 420 AGCCGACTAC ATCAGGGTGG GTGTGTGCGG GAGGCGGGGC CTGGGCCCAT TGCTCCTGGG 480 GGGCTCAGGA AGAACCAGGG TCCCCAAGGG AGGGGTGGGC GGCAGTCTCC AAGGGGTCCT 540 CAGAGAGGCT GGACGGGCAT TGGTCCTCAG CCCCTTGCTG GCCTGGAGTG AGGAGTGTGT 600 TTAAGCCACC AGGGCTCTTT GCATAATATT TGTGTGTCGT TTGCATATCA TTTGCATAGC 660 ATTTGCATGG ACTTGTTTGT CCTCTGTTAA CAGCAGCAGT TGGCCTCATT CCCTTTCAGA 720 CTGACCCTGA GGAGGAGCCG GGCCATGGCA GGGGCAGGGT GGACATCCCT TGTGGCCCTG 780 CCCCGCCGCA CCTGCACCTG CACAGCCCGC GTGGGCCCGC CCCGCCGCAG CTGAAGTGCA 840 CCACCATGGG CCCGGCCCGC GGCTCGCGGC TCGCGGCTCT GGGCCCGGTT CACCTCGTCC 900 CGGAAGCCGA GGACGCCGGC GGGATCGGTC CGGACGCCGT AGTCCGGCCA GCCGAAGTAC 960 TGGAAGTGCT GCACCGTACG CTGTGGCTCC TCCCCGCGGG GCAGGGCCTC GCGGGCGCAG 1020 GGTGTACATC GCCTGCAGGG CTGTCTGCAG GCCTGTCTGC AGGCCACGGT GGCTGCTTTC 1080 TGGGCCACGG TGCACCAGGA GAACACGCGT GTCATCGTCA TGACCACCAG GGAGATGGAG 1140 CGGGGCCGGG TAGGGGTGCG GTGCCAGTGC TCCCAGTGCC CATCCCACCC CGTGCATCTT 1200 CGGCTGCCCA AGGCCCTTCC CGACCAGGCC AAGGAGGCTG TGGGACGCCG TGGGAGTGGG 1260 GAGGCTCCCA CAGAGCCCCG TGGCTGCACG TACACACCTG CGTCTCTGCA GGTCGCAGGG 1320 GCGGGGTGCC GAGGTGCTGC CAGCAAGGCT GATGCAAAGC GCTCCCCTCG GAACAAGTGT 1380 TTCCGGGACT GGCCAGAGCT GCCCGGCAGC CAAGAGTTCG GCCGTGTGCA CATGCGCGTC 1440 CTCGGCAAGG GCCAGGCCCA GGGCTACTGC GTGCGGGAGC TGCAGGTGTG GCGGCCGGGC 1500 CAGGTGAGCC TGGCGGCTGT GGAGCGTGCC TGCTGTCGGC CTGCACTGGG AGACCCCACA 1560 CCTGCCTGCA TCCAACCCCA CTGCCTTTGG GGGCTTCCAC ACCCCTCAAC CCAGGAGGTG 1620 CATTCCAAGC CTGGACAGGG GTCACTGACG TGGCCACATT CTCAGCCCTG GGCTGGCGGC 1680 CGCTCCTCCC ACACACCTCT CCAACTGCAG CTTTGGTCTC CGTTGTATAC CAGAGACGCC 1740 CATTTCTGCT CCGGGCAGAT TACCTCGTGT TCCCTCCAGC CCCCGCCCAG TGTGTGTGGG 1800 GGGGTCCTCC AGGACCCCAT GGACCCCTCA CATTTGGTTT TTCCTTATAA AATAACTGTC 1860 CTCACAGCCT GCTTCGCCCG CCCCCAGCTC CCTCTTCCCT TCCCCAGGCA CCTGAGCCAC 1920 CTGGGGCCAT CTCGGCGCCC CCTCCCCATT TCCTTCCTCC TCCTCCTGCT CGCCTTGGCT 1980 CCCGCAGCCC CTCCGCTTGG GCACTCCCGG AAACCCAGCT GTGCCTCAGC CTCCTCCTCC 2040 CACCCTGGGG TCACACTCAC CGCTTGCCCC GCTCAGGAGG AGCCACAGCG TACGGTGCAG 2100 CACTTCCAGT ACTTCGGCTG GCCGGACTAC GGCGTCCGGG CCGATCCCGC CGGCGTCCTC 2160 GGCTTCCGGG ACGAGGTGAA CCGGGCCCAG AGCAGCAAGC CGCGGGCCGG GCCCATGGTG 2220 GTGCACTTCA GCTGCGGCGG GGCGGGCCCA CGCGGGCTGT GCAGATGCAG GTGCGGCGGG 2280 GCGGGGCCAC GCGGGCTGTG CAGGTGCAGG TGCGGCGGGG CGGGGCCACG CGGGACGACG 2340 AGGGCGGAGC CATCGGGTGG GCGGGGGCGC CCCCGCCCCC GCCCCCCACT CTCGTCAAAG 2400 GCCGCCTAGT TTGTCCTCAG TGGGGGCATC GGATGCACGG GCACCATCAT CGTGATTGAC 2460 ATCCTGGTGG ACGTCATCCG CAGGCAGGGC GAGCCGCTCC ACTCTGGGTC CCCCCGCCCT 2520 GCCCTGCTAT AGCCCCACCC CTCCGGGCGA CCCCACCCCT CCGGACGACC CCACCCCTCA 2580 GGACGACCCC ACCCCTCAGG ACGACCCCAC CGCTACCGGC AAGCCCCGCC CCTCATCAGC 2640 AGCCCCGCCC CTGCCTGCCG GCACCTTCCC CCCATCCGTA GCCCCTCCCC AAGCGCGCTT 2700 GTCCGCAGGG CTGGACTGCG ACACCGACGT CCCGAAGACG ATCCAGCTGG TTTGGCGGCA 2760 GCACTGGGGA ATGGTGCAGA CGGAGGCTCC GTACAAGTTC ACGTACCTGG CGCTGCAGCG 2820 GCACATCCGG GGCGAGTAAC TGCGCCTGCG CGAGCAGGTG GGGGCGTGGC CCTGCGGGGC 2880 GTGGCCTGTG CGGGCGTCGC CATGGTGACC GGCGGCCCCT CCCCCCAGCG CGAGCCGCCT 2940 CAGGAGCGCG AGAACCAAAA CGTGGGCGCC GCCCCCCGCT AATCGGGTTG CAGCCCCCGG 3000 CTCCCCGGGC ATCCCCGGTG TGAGTGGAGC GCCGGGGCCG GTCCGGAGTC CTCTGGGAGG 3060 GACTGGGACG TGCGGGGTGC AGGGCTGAGC CGCTGCTCCG CGCGCAGAAC CCCGCAGCCC 3120 TGGGACGGCG AGGACGCGAA CCTGCGGAGC CGCGGGTGTC TGAGGAGCCG CAGGGAACCC 3180 CCGGCCTAGC CGCGCCCGCG TGTGGCCGGA GCTGCGGGCC GGGACTGTGT CCAGGACAGA 3240 GCCACAAGCT TGTCCCCAGC TCAGGGAGGT CCAGGGGCGG CAGAGGGAGC GACAGGCTGC 3300 GAAGCCCACC GGTGACCACG TGTGAACCCG CGTGCGCCCC CAGCTCGGCC ACTCCGTGCG 3360 GGTCTGCCCT CACCGCAGCT CCGGCCTGCC GGCCCTGCCT GCTCCCGTGG TCTGGGATGT 3420 GGCCCCGGTG AGGACCCGGC CCCATCAGGC ACAGGGTGGA TGTCTGTGGA GTGAGGTGTG 3480 TGTGACATAT TCATGTGACC ACCCGTGCAG CGTCACGCGC CTGGCCCTGC CGATGACAAG 3540 GGTGTGGGCC TGCGTGGGCA TGACTGTGTG TGTGACACAG AGTGATGTTG CTGTGACCCG 3600 TGGCTGCACT CCCCACATCA CCGGCTTTCA CAGCCTTCCG GTAAAGTGCT GTGTTCTCCC 3660 TTCTGTGTCT TCGCTGGGAC CTGGGGCAAG GGTGGGTGTG GCCCCCACAG CTGGAGTCAG 3720 CTTCTGTGGG GCCTTCCCGA GCCCTCCCCA CCCTGGACCA GAGGCCCAGC TGGTTGGAGC 3780 AGGAAGTACC TGGGCTCTGG GGTCAGGGAT GGGAAGGCTG AGGAGGCCTG CGTGAGCTGG 3840 ACCTGGCCTG GGCCCTCCTG GCCGTGCCTG CCTGGTGGTG CAGGATTCCT GGGGCTGATG 3900 ACAGACGGGG TAGGGCTGGG GTTGGCGAGC CTCCTGCCGA TACCTCACGT AGCTGACCTC 3960 TGACTCTTCC CCAGCCAGGC TGGCCCTGGG AGTTGCCGGA GAGTCAGTGG ATCTGCAGGC 4020 TGCACGCTGG CTGTTACCTT TGCTTCTGGG TTCCCACAGG GGTCATGGTT CTGTGGTTCT 4080 CCAGTCAGGG ACCCTAGCAG GGCCATGGGG CGTGACTTCC TGGAGGTGTG GCCTAGTATG 4140 GCCACGGCAG AGGATGGGGG AAGAGAAAGG CCCCCTTTGT CAGCCCCCGG GCTCTGAACC 4200 AAGCTGAAGC CCTCCCCCTG GTCCAGCCTG CCCTGCCCCA AGTGTCCTGG GCCTCTCCCC 4260 ATCTCCCTGG GGAGCCTCAC ATTGCTGAGT CGCCAGCCAA CTCCAGAAAC CCCCAGCCTG 4320 TCTGCAGCCA GAGGGGCTGG GAGTTGGACC CCCTAGAACC TTGGGCCCAC CTGTCCCAGT 4380 GGCTGCTGGG AGTCTAATTC TGTCAGGGTA TCCTCTGGGT TGAGGCTGCA GCAGGGGCAC 4440 CCAGGGTGAG GCCCTCTTGC CAAAGATGGA TACAAATAAT TTATTTTAAA AGGTACAATT 4500 CACAAGGTTG GAGGGGTAGC TGGAAGTTTC 4530
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