Tag | Content |
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EnhancerAtlas ID | HS038-00013 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr1:1002170-1006620 |
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: 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 | CACAGGGTCT GCGGGCAAAG AGGCAGGGTG AGGCCCACGA GCTGTGCCCT GGAGAACTGA 60 GCGGCACCTC CCTTCCCAGT TGATGCTACC CTTGAGTCAT CCTGCTCAAC GAGGATGACA 120 GCGGGCCCGG AGCCGACTAC ATCAGGGTGG GTGTGTGCGG GAGGCGGGGC CTGGGCCCAT 180 TGCTCCTGGG GGGCTCAGGA AGAACCAGGG TCCCCAAGGG AGGGGTGGGC GGCAGTCTCC 240 AAGGGGTCCT CAGAGAGGCT GGACGGGCAT TGGTCCTCAG CCCCTTGCTG GCCTGGAGTG 300 AGGAGTGTGT TTAAGCCACC AGGGCTCTTT GCATAATATT TGTGTGTCGT TTGCATATCA 360 TTTGCATAGC ATTTGCATGG ACTTGTTTGT CCTCTGTTAA CAGCAGCAGT TGGCCTCATT 420 CCCTTTCAGA CTGACCCTGA GGAGGAGCCG GGCCATGGCA GGGGCAGGGT GGACATCCCT 480 TGTGGCCCTG CCCCGCCGCA CCTGCACCTG CACAGCCCGC GTGGGCCCGC CCCGCCGCAG 540 CTGAAGTGCA CCACCATGGG CCCGGCCCGC GGCTCGCGGC TCGCGGCTCT GGGCCCGGTT 600 CACCTCGTCC CGGAAGCCGA GGACGCCGGC GGGATCGGTC CGGACGCCGT AGTCCGGCCA 660 GCCGAAGTAC TGGAAGTGCT GCACCGTACG CTGTGGCTCC TCCCCGCGGG GCAGGGCCTC 720 GCGGGCGCAG GGTGTACATC GCCTGCAGGG CTGTCTGCAG GCCTGTCTGC AGGCCACGGT 780 GGCTGCTTTC TGGGCCACGG TGCACCAGGA GAACACGCGT GTCATCGTCA TGACCACCAG 840 GGAGATGGAG CGGGGCCGGG TAGGGGTGCG GTGCCAGTGC TCCCAGTGCC CATCCCACCC 900 CGTGCATCTT CGGCTGCCCA AGGCCCTTCC CGACCAGGCC AAGGAGGCTG TGGGACGCCG 960 TGGGAGTGGG GAGGCTCCCA CAGAGCCCCG TGGCTGCACG TACACACCTG CGTCTCTGCA 1020 GGTCGCAGGG GCGGGGTGCC GAGGTGCTGC CAGCAAGGCT GATGCAAAGC GCTCCCCTCG 1080 GAACAAGTGT TTCCGGGACT GGCCAGAGCT GCCCGGCAGC CAAGAGTTCG GCCGTGTGCA 1140 CATGCGCGTC CTCGGCAAGG GCCAGGCCCA GGGCTACTGC GTGCGGGAGC TGCAGGTGTG 1200 GCGGCCGGGC CAGGTGAGCC TGGCGGCTGT GGAGCGTGCC TGCTGTCGGC CTGCACTGGG 1260 AGACCCCACA CCTGCCTGCA TCCAACCCCA CTGCCTTTGG GGGCTTCCAC ACCCCTCAAC 1320 CCAGGAGGTG CATTCCAAGC CTGGACAGGG GTCACTGACG TGGCCACATT CTCAGCCCTG 1380 GGCTGGCGGC CGCTCCTCCC ACACACCTCT CCAACTGCAG CTTTGGTCTC CGTTGTATAC 1440 CAGAGACGCC CATTTCTGCT CCGGGCAGAT TACCTCGTGT TCCCTCCAGC CCCCGCCCAG 1500 TGTGTGTGGG GGGGTCCTCC AGGACCCCAT GGACCCCTCA CATTTGGTTT TTCCTTATAA 1560 AATAACTGTC CTCACAGCCT GCTTCGCCCG CCCCCAGCTC CCTCTTCCCT TCCCCAGGCA 1620 CCTGAGCCAC CTGGGGCCAT CTCGGCGCCC CCTCCCCATT TCCTTCCTCC TCCTCCTGCT 1680 CGCCTTGGCT CCCGCAGCCC CTCCGCTTGG GCACTCCCGG AAACCCAGCT GTGCCTCAGC 1740 CTCCTCCTCC CACCCTGGGG TCACACTCAC CGCTTGCCCC GCTCAGGAGG AGCCACAGCG 1800 TACGGTGCAG CACTTCCAGT ACTTCGGCTG GCCGGACTAC GGCGTCCGGG CCGATCCCGC 1860 CGGCGTCCTC GGCTTCCGGG ACGAGGTGAA CCGGGCCCAG AGCAGCAAGC CGCGGGCCGG 1920 GCCCATGGTG GTGCACTTCA GCTGCGGCGG GGCGGGCCCA CGCGGGCTGT GCAGATGCAG 1980 GTGCGGCGGG GCGGGGCCAC GCGGGCTGTG CAGGTGCAGG TGCGGCGGGG CGGGGCCACG 2040 CGGGACGACG AGGGCGGAGC CATCGGGTGG GCGGGGGCGC CCCCGCCCCC GCCCCCCACT 2100 CTCGTCAAAG GCCGCCTAGT TTGTCCTCAG TGGGGGCATC GGATGCACGG GCACCATCAT 2160 CGTGATTGAC ATCCTGGTGG ACGTCATCCG CAGGCAGGGC GAGCCGCTCC ACTCTGGGTC 2220 CCCCCGCCCT GCCCTGCTAT AGCCCCACCC CTCCGGGCGA CCCCACCCCT CCGGACGACC 2280 CCACCCCTCA GGACGACCCC ACCCCTCAGG ACGACCCCAC CGCTACCGGC AAGCCCCGCC 2340 CCTCATCAGC AGCCCCGCCC CTGCCTGCCG GCACCTTCCC CCCATCCGTA GCCCCTCCCC 2400 AAGCGCGCTT GTCCGCAGGG CTGGACTGCG ACACCGACGT CCCGAAGACG ATCCAGCTGG 2460 TTTGGCGGCA GCACTGGGGA ATGGTGCAGA CGGAGGCTCC GTACAAGTTC ACGTACCTGG 2520 CGCTGCAGCG GCACATCCGG GGCGAGTAAC TGCGCCTGCG CGAGCAGGTG GGGGCGTGGC 2580 CCTGCGGGGC GTGGCCTGTG CGGGCGTCGC CATGGTGACC GGCGGCCCCT CCCCCCAGCG 2640 CGAGCCGCCT CAGGAGCGCG AGAACCAAAA CGTGGGCGCC GCCCCCCGCT AATCGGGTTG 2700 CAGCCCCCGG CTCCCCGGGC ATCCCCGGTG TGAGTGGAGC GCCGGGGCCG GTCCGGAGTC 2760 CTCTGGGAGG GACTGGGACG TGCGGGGTGC AGGGCTGAGC CGCTGCTCCG CGCGCAGAAC 2820 CCCGCAGCCC TGGGACGGCG AGGACGCGAA CCTGCGGAGC CGCGGGTGTC TGAGGAGCCG 2880 CAGGGAACCC CCGGCCTAGC CGCGCCCGCG TGTGGCCGGA GCTGCGGGCC GGGACTGTGT 2940 CCAGGACAGA GCCACAAGCT TGTCCCCAGC TCAGGGAGGT CCAGGGGCGG CAGAGGGAGC 3000 GACAGGCTGC GAAGCCCACC GGTGACCACG TGTGAACCCG CGTGCGCCCC CAGCTCGGCC 3060 ACTCCGTGCG GGTCTGCCCT CACCGCAGCT CCGGCCTGCC GGCCCTGCCT GCTCCCGTGG 3120 TCTGGGATGT GGCCCCGGTG AGGACCCGGC CCCATCAGGC ACAGGGTGGA TGTCTGTGGA 3180 GTGAGGTGTG TGTGACATAT TCATGTGACC ACCCGTGCAG CGTCACGCGC CTGGCCCTGC 3240 CGATGACAAG GGTGTGGGCC TGCGTGGGCA TGACTGTGTG TGTGACACAG AGTGATGTTG 3300 CTGTGACCCG TGGCTGCACT CCCCACATCA CCGGCTTTCA CAGCCTTCCG GTAAAGTGCT 3360 GTGTTCTCCC TTCTGTGTCT TCGCTGGGAC CTGGGGCAAG GGTGGGTGTG GCCCCCACAG 3420 CTGGAGTCAG CTTCTGTGGG GCCTTCCCGA GCCCTCCCCA CCCTGGACCA GAGGCCCAGC 3480 TGGTTGGAGC AGGAAGTACC TGGGCTCTGG GGTCAGGGAT GGGAAGGCTG AGGAGGCCTG 3540 CGTGAGCTGG ACCTGGCCTG GGCCCTCCTG GCCGTGCCTG CCTGGTGGTG CAGGATTCCT 3600 GGGGCTGATG ACAGACGGGG TAGGGCTGGG GTTGGCGAGC CTCCTGCCGA TACCTCACGT 3660 AGCTGACCTC TGACTCTTCC CCAGCCAGGC TGGCCCTGGG AGTTGCCGGA GAGTCAGTGG 3720 ATCTGCAGGC TGCACGCTGG CTGTTACCTT TGCTTCTGGG TTCCCACAGG GGTCATGGTT 3780 CTGTGGTTCT CCAGTCAGGG ACCCTAGCAG GGCCATGGGG CGTGACTTCC TGGAGGTGTG 3840 GCCTAGTATG GCCACGGCAG AGGATGGGGG AAGAGAAAGG CCCCCTTTGT CAGCCCCCGG 3900 GCTCTGAACC AAGCTGAAGC CCTCCCCCTG GTCCAGCCTG CCCTGCCCCA AGTGTCCTGG 3960 GCCTCTCCCC ATCTCCCTGG GGAGCCTCAC ATTGCTGAGT CGCCAGCCAA CTCCAGAAAC 4020 CCCCAGCCTG TCTGCAGCCA GAGGGGCTGG GAGTTGGACC CCCTAGAACC TTGGGCCCAC 4080 CTGTCCCAGT GGCTGCTGGG AGTCTAATTC TGTCAGGGTA TCCTCTGGGT TGAGGCTGCA 4140 GCAGGGGCAC CCAGGGTGAG GCCCTCTTGC CAAAGATGGA TACAAATAAT TTATTTTAAA 4200 AGGTACAATT CACAAGGTTG GAGGGGTAGC TGGAAGTTTC TGTGGTTACC TTGCACTGGG 4260 GGGCTGCCCT GCCTCCACTC TCTCCCCACA GTCCGAGGGC AAGATGAGCA CCCCCACCCA 4320 ATGGCAGGAC CAGCCCTGCG GGGAAATGTC AGCATGAGTG GAAGCACGGC AAGGCCCCTT 4380 CCTTCTTGGC AAGGGGCTTC CCTGGCAGGC AGTTCACAGG GTGTGTGGGT GGGGGGGATG 4440 CTGACCAGCT 4450
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