Tag | Content |
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EnhancerAtlas ID | HS044-07764 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr2:218722110-218724700 |
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) |
KLF4 | MA0039.3 | chr2:218723112-218723123 | CCACACCCTCC | + | 6.32 | POU2F2 | MA0507.1 | chr2:218724639-218724652 | CTTATTTGCATAT | + | 6.57 | ZNF263 | MA0528.1 | chr2:218724083-218724104 | TCTCCCCCTTTCCCCTCCACA | - | 6.1 | ZNF263 | MA0528.1 | chr2:218723234-218723255 | GAGGGAGGAAGCGGAGGGAAG | + | 6.56 | ZNF263 | MA0528.1 | chr2:218723220-218723241 | GAGGGAGGGAGGGAGAGGGAG | + | 6.72 | ZNF263 | MA0528.1 | chr2:218723224-218723245 | GAGGGAGGGAGAGGGAGGAAG | + | 6.84 |
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| Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
SE_00005 | chr2:218676398-218731742 | Adipose_Nuclei | SE_00853 | chr2:218721535-218725039 | Adrenal_Gland | SE_01533 | chr2:218716763-218725202 | Aorta | SE_05795 | chr2:218714016-218724645 | Brain_Hippocampus_Middle | SE_26107 | chr2:218722029-218724987 | Duodenum_Smooth_Muscle | SE_26522 | chr2:218721570-218724529 | Esophagus | SE_29627 | chr2:218721207-218726387 | Fetal_Muscle | SE_36939 | chr2:218685985-218724919 | HSMMtube | SE_40583 | chr2:218693978-218725316 | Left_Ventricle | SE_42142 | chr2:218709673-218725303 | Lung | SE_46178 | chr2:218722338-218724831 | Osteoblasts | SE_46622 | chr2:218722262-218723377 | Ovary | SE_46622 | chr2:218723412-218724005 | Ovary | SE_46622 | chr2:218724137-218724594 | Ovary | SE_48080 | chr2:218698688-218725214 | Psoas_Muscle | SE_48661 | chr2:218719000-218725195 | Right_Atrium | SE_49571 | chr2:218721446-218724052 | Right_Ventricle | SE_51206 | chr2:218689199-218725234 | Skeletal_Muscle | SE_53299 | chr2:218722086-218724414 | Spleen | SE_54481 | chr2:218719922-218727178 | Stomach_Smooth_Muscle | SE_64002 | chr2:218722436-218724501 | HSMM |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I217845 | chr2 | 218709821 | 218725149 |
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Enhancer Sequence | TCAGTGCTCT TGTCCCTAAT GCTGCTTCAA GGTGAAGATG GCTGGGGCTG GAGGCATTGG 60 AAGGTGGACT CTCCAACTAT GTCTGTGGAC CCAGAACCAC AGGACAACAT AATATATGGT 120 GCTTCTGTCA AGCGATGATG ATAAATGTGT CCCCGGACCC TCCTTAGGAA GGACCCGTGG 180 CAATTGTCCC AGGTATCTTC TTACTTGAAT TCATACCATG CCCTCCATAA AAAGGGAGTA 240 GGAGCAGAAA ACCTGATCGT GACCTTGACT TCAGTCCCGA GAGACCAGGG GCCTGGAGGG 300 CAAGTGATCT GCCCTGCCCT GGATGGCCCA CGCCTGCAGG GCAAATGTGA ATTCTCAGAC 360 CCAGCCTCCT GACTCCGGCC TGGCCTGTGT TCCCCCCAGC CTGAAGCTAT AACCCGAGCC 420 TGGCACTCCC ACCCCTACCC TCAGCCTATA CGGGCAGCAG ATATCACAGG CACACTCAGG 480 ATGGTAAAAA TAGCTCCAGA GCCCACAACA AGCTGAAGTC CTTCTCTGCC AGGCCAGGGT 540 GCCAGCCTGG GCACTCAGAG ATCCCTGGCT AGAGGAGAGT CAAGCTGCCA AAATCTCTGC 600 CAAAGTCAGG AGAAAGCCGT GAATGGGAGC CCACAGGAGG CCGGTGGGGA ATGGTGAGCA 660 CTGGAGGTGC CCCAAAGCTC AGGCCAAAGA TGCAGGGAGG GGGCGTCCTG AATAACATCT 720 CACCAGAGCT ATCCATGCAT CCACCTCATT CCCTCTGCCA ACCCCATTCG CGCACAAGAC 780 GAACCGTTAC CCCCACAAGA CTTAGGACAA CTCAGACACA CGGCCCCCCC ACCAACCCAG 840 ATACCCTCGC CCTGAAAGCT ATGGCTCTTA CGTGTCCCAG AAGCAAGTCC AGGAAGGGGA 900 CCACCAGGCC CGTCACATCC ACATCAGACA GCAGCACAGC GGGCCACAGC CCCACTCAGC 960 CACAAGCCCT TCCAAGGTGG GGTCGTGACA GAGCCTGCCC CTCCACACCC TCCCAGCACA 1020 GAAGCACGAG CACCCCAGCC CAGATCCAGC AGAAAGCCAC ACAAGAACAC TCACAGGCAA 1080 AACAACTGCC CAGCAGACAC TTACCCTCTG GAGGGAGGGA GGGAGAGGGA GGAAGCGGAG 1140 GGAAGCCCGC TCTGATTTGA TCCTGGTGCC CCAAGTTCCC AATAATTCCT ACATGGCTGC 1200 AGCTCCAAGT GCTGTCTGTG TCCTACTCAA GCTCCCTCCG ACTGTCAGGG GTGGGAGGAG 1260 CCAGTGCCGC CTGCCTGCCC ATGTACACAC ACACACACAC ACACACACAC ACACCCCACT 1320 CCCTCCCTCC CTCCACTCTC CTGCACGCTC TCTCCCCAGC TCAGCTTGCT CTGCCTCACT 1380 CTGGCTTGTA GGAAGCCAGT GGGATAAAAC TGTCTGTAAT TTCAGCCAGC TGGGTCCCCA 1440 GGGCTTCACT TATCATCCTG CAGCTATGCC GTTCTTGAAT GACATCACGG TGGCTTCCCA 1500 AGCCCTTCAC TCCCACCGGC CGGGAGTCAG GAAAAGTGGC CAGCCCAGTC CAACTCCAGC 1560 CCCAACCCCA GCCCAGCCCC AGCCCCAGCC CCAGCCCCTG CTCAACTCTC ACCCAGCACA 1620 GTCTAGCCCA GCCTGGTCCC AGCACAGCCC AGCCCAGCCC CACCGGGTCC CAGTCCAGCC 1680 CAGCCCAGTC CCAGTGTAGC CCAGCCCAGC CCCAGTCCCA AACCCATGGC AGCCCCAGTG 1740 CCCTGAAGAG AAGCAGGGAG AGAATCTGGG AGCAAAGTGA AACTGAGCCC CAAGCGGAAA 1800 GGCAGGGATG CAAGGGCCAG AGAGGGAGGG GAGAGAGGTC CTATGAGGGT ATTGAGATTT 1860 ATTTCCCCAA ATTTTCCACA TTTTTTTTCC ATTCTCAGCA AATGGAAGGC AGAACAGATG 1920 ACAACAATTT TCCAGCTGCT GAACAATAAG GTGGAAATCT TTTTTTCCCT CTCTCTCCCC 1980 CTTTCCCCTC CACAGGGCAG AGTCCAGGAG CCAGAACACT TCCTTGGCTT GGAAAAGGAA 2040 AAAGAAAAAA CCCCACAGGG TCCTGCACTT CCCAGAGGTG AACACAGGAC CTGAATAGAA 2100 GGACTGGGGT GTCACCCAGG CAGGGCTCCA GGAGGGGACA GGAGCCCCAA CATGAAGTTC 2160 TCAGTGCAAA GCTTTGGATT CTGGCTTGGC AACTTGACAT TTTGGAGGGC CTAACTTTGG 2220 GAAGGCCAGT GTGTGTCTGG CCAGGTATAT TGATCCTCCA GGCCACCTGA GATGCTTCCA 2280 ATTGACTGGC TATTGGTATT CTGTTTGTTC CCATCTGTGG AAATCATGAA TAGCAGAGTA 2340 TCACTTTTCA GAGTTCGCAA TGCCTCACCC TCGTTCCCAA CCACCCAGAT CCGAGAGCCA 2400 TGCAGCTGAA AGGCAGGTGA ACGGCCCTCA AGTTCCCACC ATTATCCTGA TGTGCCCTGG 2460 AAAGTGCCAG GAGTCCCTAA CTGATAATAA GACACCAAAT CCCCACTCTT ATTAACATGT 2520 TGTTTGTGAC TTATTTGCAT ATCAATTGAA TCTCCCAACC CAATTCTCAG AGTGGACAGG 2580 AGGTGATCTG 2590
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