Tag | Content |
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EnhancerAtlas ID | HS115-03633 |
Organism | Homo sapiens |
Tissue/cell | Kidney_cortex |
Coordinate | chr6:41470710-41473810 |
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) |
EN2 | MA0642.1 | chr6:41472903-41472913 | CCCAATTAGC | + | 6.02 | INSM1 | MA0155.1 | chr6:41472063-41472075 | TGCCTGGGGGCG | + | 6.14 | KLF16 | MA0741.1 | chr6:41470840-41470851 | GGGGGCGTGGC | - | 6.62 | RREB1 | MA0073.1 | chr6:41473245-41473265 | CCCCAATCTACCCCCACCCG | + | 6.07 | RREB1 | MA0073.1 | chr6:41473244-41473264 | CCCCCAATCTACCCCCACCC | + | 6.44 | SP1 | MA0079.4 | chr6:41470839-41470854 | TGGGGGCGTGGCTGC | - | 6.11 | SP2 | MA0516.2 | chr6:41470922-41470939 | GAGTGGGCGGGGGTAAA | - | 6.73 | SP3 | MA0746.2 | chr6:41470839-41470852 | TGGGGGCGTGGCT | - | 6.34 | SP4 | MA0685.1 | chr6:41470837-41470854 | GGTGGGGGCGTGGCTGC | - | 6.28 | SP8 | MA0747.1 | chr6:41470839-41470851 | TGGGGGCGTGGC | - | 6.11 | ZNF263 | MA0528.1 | chr6:41472731-41472752 | TCCTCCTCCTCTCCTCCCTCC | - | 6.01 | ZNF263 | MA0528.1 | chr6:41472737-41472758 | TCCTCTCCTCCCTCCTCTCTC | - | 6.1 | ZNF263 | MA0528.1 | chr6:41472730-41472751 | TTCCTCCTCCTCTCCTCCCTC | - | 6.42 | ZNF263 | MA0528.1 | chr6:41472743-41472764 | CCTCCCTCCTCTCTCTCCCTC | - | 7.02 | ZNF263 | MA0528.1 | chr6:41472747-41472768 | CCTCCTCTCTCTCCCTCCTTC | - | 7.68 | ZNF263 | MA0528.1 | chr6:41472716-41472737 | TCCTCCTCCTCGTCTTCCTCC | - | 8.6 | ZNF263 | MA0528.1 | chr6:41472734-41472755 | TCCTCCTCTCCTCCCTCCTCT | - | 8.96 | ZNF263 | MA0528.1 | chr6:41472719-41472740 | TCCTCCTCGTCTTCCTCCTCC | - | 8.99 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_27953 | chr6:41470176-41473777 | Fetal_Intestine | SE_28956 | chr6:41470148-41472895 | Fetal_Intestine_Large | SE_28956 | chr6:41472929-41473990 | Fetal_Intestine_Large | SE_31492 | chr6:41470133-41471273 | Gastric | SE_31492 | chr6:41471288-41473818 | Gastric | SE_65317 | chr6:41471357-41473703 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I041502 | chr6 | 41470110 | 41474146 |
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Enhancer Sequence | GGTACGAGGA TGACAACACC TAGCCAACCC GCGGAGAAGG CGGTGAGCTG GGTGACCTCC 60 TGGAGCTGCA AGAGTTTGTG CCTGCTGAGG CCTTGCTCCA CCGAGTCTTG GGGGGAGGCA 120 GCTGGCGGGT GGGGGCGTGG CTGCCAAGGA AGTGGGTGTC GGGTACTGGG CGGGGGACAG 180 AGCTAGGTCA CAGTCGAGGT TTTCACTGAC CCGAGTGGGC GGGGGTAAAG GGAATTCGTA 240 AAAAGTTTCT TTCTTCATTA ATGGCCTTTT TTCCCTATCC GAGAGCCTGG GCGCGGGAGG 300 GAGCGAAGAC GGCCGGGGGC AGGGCAGGCC CTCCGCAAGT GACACTTAAT TCCCGGTCTG 360 GACTGGGCCG GCGCTTGAAA GCAACTAAAT TAGCAAAACA GAAGTCAACT GTCGATTGCT 420 TCATTGGAGG ATTAAGTGTG ATAAATGGGG GGTTTGTTCG CTCTCCGGTC CAGATGTTGT 480 GTCTAAGTAA GGGTTTTTTC AAAAAAAAGT TTTTTTACAT TCTTGGCCCA GGGCCCATAT 540 ATATTTTGGA TACTGCTGGG AGTATATAAT ATCATTGGAA AATGATGCGG TCTGCTAACC 600 TTTTAAATAA CATTTCCTCC CTCCTCTATT TTCTAATAGT TTGTTTTTCT TTCCATGTTT 660 GCCTTTTATT GGGGGAAATT TTTTTTGGAA ATTAATGAGG CTCAAGTTTG GAGACCAAAA 720 TAAAAAAGGG GTGGGGGAGT GTGAGAGGTG GATGGGGTGT GGAATGAAGC TGGGTGGAGG 780 GAGGGCTACT CTTTGTGTGT TTTAAAGCGC TCCTGGTTTG ATTTTTTTTT TCTTGTAATT 840 TTCTCTGCCG AGGCTGCCCG CGGCCCTCCG GCGGGGCTGC GCGGTGGCGC GCGCGGGAAG 900 GGCGCCCGGG ACTCTCCGCC GCGCCGGGCA CCCGCTCGCC CTGCCCGGGC CGTGGGGCTG 960 CGCGCCGCTG GCCTCCGGGA AGAACCTGCC ATTCCCCCTG CAGCCGAGTC CGACGTGAGA 1020 GGGGGTGGGG GTGGGGGCGC CTCCTTCCTG AGTGAAACCT ACGGAATCCG GCAGGAATTC 1080 GGGCCTCCCA GATTTAAGAA AACAAACAAA GGAAAGATTG TCAGAGAGGG GCCGCCAAGA 1140 GCCGCCGGGC CGCCGCACTG CCCTCCGCCC TCACCCCCGG GGCGCCCGGG CCTCCCAGCG 1200 GGGGCAGAAC GCGAGGCTGG GGGGCTCCCC CGGGTGGTCC CCGGTGGGCT TCCCTGCCCT 1260 GGGTCTTGAC TAACCTGTGT TGAGTCATCC TCCTGTCTCT AGAGCTGAAG AGGCCCCAGG 1320 GCGCATAGGA AAGGAGGGTG CTGCCGAGGT GGCTGCCTGG GGGCGGGCCC TACAGGGGTC 1380 ATTTGGGGCA TCCCCTGCCT CTAGGCAAAT CCCCACGGAG CCCCATCCCG CACCCTCCCG 1440 CAGTGTCCAG GGCGAACCCC TGTCCCCAAG CCCAGGCTTA GGAGTGAAAT CTCGACGGCT 1500 CAGGTTCCTT CTCTACGCAG TCCCCCAGCC AGACTAGGAA TGGATCACCG CGCGGGTGGG 1560 CTCAGTTCCC GGCTTCGCCC GGGTCTAGGA AGAATGATAA AAAGTGAGAA TGTAAAGGGA 1620 GGAGGTACTA TAAAACAAAA GGGGTTAGAC ACCCATCAGG CAGCTGCGAC CCGGTGGTAA 1680 ACATGAGCGT CTCCTGTGCT CCCACCGCCT GCGTTCTTCC CGGCCGCGTC CACGTTGGTT 1740 TCCTTCTCGT TGTCTTGGTC TCTCCTGATT CTGTTCTCGT GTCAGTCTGC CCTGCCTCTG 1800 TTACTCCAAA TCTCTGTGGT CTCTCTCCCT CTCTACCTTC TCTGTCTCCT TCTGAATCTG 1860 AATATGGCTC AGTGCTTCTG GCTTTCTCTT TGTCTCTGAA GCTATCTCTC TGAGAATGTC 1920 TCTGTCCCTT TCTGTCTGCC CCTCTTCGTG TTTCTCTGTC TCAAGCTGAC GCTGTCTCGT 1980 GGCCTGTCTC ACTGTGTCTT CTTCTGTCCT CCTCCTCGTC TTCCTCCTCC TCTCCTCCCT 2040 CCTCTCTCTC CCTCCTTCGT ACCCCCCCCC GCCCCACTAT TCCCCTCCAT CTCTCCACCC 2100 TGCCCCCGCC TTAGGTAGCC CAGCGGGCGG GCGCCCGGCC AAGGCCGCCC TGGGCAGGGC 2160 CTTACTGGCG CTGACAGAGC CTCGCGCCCG CGGCCCAATT AGCGCGCGGC GCGAGGGACG 2220 CGGCATCTGG AATTGCGCTG CGCTCACGGC CAAGGCCGAT TGTTTAGTCT GCGCGGCGGG 2280 GCGGGCGGCC CGCGCGGTGG CCCCACATCT GGAGCCTCGG CCAGACGGCC CTGCTGGCGG 2340 CTGGCCGGGG TGCGTGTGCA TTTTTAACTC TGGGATTTGC TGACAAGTTA AGAAGTCAGA 2400 AAGTCAGTGA CGGCGGGAAC TGGCGAGGCG CTCAAGGAAG GGAGGGGCAG GCGGAGGCTC 2460 GGGCGCATCA GCCGCGGCGG AGACATGCTT GGGGGAGCGC ACAGCAGCTC CGTGCTTTGG 2520 CCCAGCGCGG CCTTCCCCCA ATCTACCCCC ACCCGTAGCT GCCCAGCGCC GCAGCCACGC 2580 GTTGACTTTT CTTCCTTCCC GGTCTTTATC CTCTCCCACT TCTCCTTTCT CTTCATTTAG 2640 TCCCTGAATT ATCCCGAAAT CCCACACTTC CCAGCTGGCC AGAGCTCCTT GGAGGTCAGC 2700 CTCTAAGAGG GAAGCCCTGG AGTCTTAGGG CTCCCACGCT CTGGAGGAAA CACAAAGAGG 2760 GCCAGAGAAG GCCAACAAAT TGCCCGGAGG TGGCTCAGCA GTTGAGCGGC AGAGCTAGGA 2820 CCAGAGGCCA ACTCTCTTGA CCCCTAATAG GGTTCTTGGC ACAGCTCCGG GTCCCCCTTG 2880 GGGCTGATCC AATGTGAGCA TTCTCACATT GTCAGAGTTC CTTCCCATCC TTTAAAAACG 2940 TGCTTTTGCA CTTCCACTCA TTCATTTCAC AAATATCTGT AGCACACTGT GTGCCCAGCC 3000 TGGGAAACAC AGCGGTAAAC AAGACAGGCA CGTCCTTGTG CTGCAGAGCT TACATTTTAG 3060 TGGAGAAGAG AGACAGAAAC TACGCAGCAA ACAAACTATC 3100
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