Tag | Content |
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EnhancerAtlas ID | HS051-23605 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr6:43742120-43743740 |
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) |
KLF16 | MA0741.1 | chr6:43742693-43742704 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr6:43742693-43742703 | GCCCCGCCCC | + | 6.02 | SP3 | MA0746.2 | chr6:43742692-43742705 | CGCCCCGCCCCCC | + | 6.11 | ZNF263 | MA0528.1 | chr6:43742212-43742233 | TGGGGAGGAAGGGGAAGGGGC | + | 6.48 | ZNF263 | MA0528.1 | chr6:43743707-43743728 | GAGGGAGGAGTGAGGGGGAGG | + | 6.86 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_00396 | chr6:43736316-43745488 | Adipose_Nuclei | SE_01192 | chr6:43737139-43746428 | Adrenal_Gland | SE_23526 | chr6:43737293-43742678 | Colon_Crypt_1 | SE_23526 | chr6:43742693-43743493 | Colon_Crypt_1 | SE_24121 | chr6:43742273-43743294 | Colon_Crypt_2 | SE_24895 | chr6:43737183-43743933 | Colon_Crypt_3 | SE_28417 | chr6:43733443-43743448 | Fetal_Intestine | SE_31486 | chr6:43733978-43746297 | Gastric | SE_40138 | chr6:43736992-43743467 | K562 | SE_40829 | chr6:43735857-43749621 | Left_Ventricle | SE_42766 | chr6:43736785-43746029 | Lung | SE_47663 | chr6:43741555-43743392 | Pancreas | SE_47663 | chr6:43743479-43743786 | Pancreas | SE_48225 | chr6:43736672-43749155 | Psoas_Muscle | SE_48830 | chr6:43735975-43746480 | Right_Atrium | SE_49610 | chr6:43742655-43743332 | Right_Ventricle | SE_51234 | chr6:43736064-43746936 | Skeletal_Muscle | SE_52912 | chr6:43736153-43744457 | Small_Intestine | SE_56485 | chr6:43735203-43744983 | u87 | SE_56977 | chr6:43737921-43744654 | VACO_400 | SE_60925 | chr6:43736759-43743185 | DHL6 | SE_65246 | chr6:43735577-43753935 | Pancreatic_islets | SE_67504 | chr6:43735203-43744983 | u87 | SE_69158 | chr6:43736725-43743662 | H9 |
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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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Enhancer Sequence | ATCACGAAGG TGAGTCCCCC TGGCTGTTGG ATGGGGTTCC CTGTCCTCTC AGGGGATGGG 60 TGGATGGCCT AATTCCTTTT TCTTCAGAAC TGTGGGGAGG AAGGGGAAGG GGCACAGGAA 120 TATAAGGATC AAGAAAGAAA GAGCTGGGCA CCACGAGGTT CACCCTCAGT TTCGTGAGGA 180 CTCTCCGCTG TTCAGGTCTC TGCTAGAAGT AGGACTTGTT GCCTTTTTCT TCTGCTCTTT 240 CCAGTAAAAT TTTATTTGGA GAAGGAGTCG TGCGCACAGA GCAGGAAGAC AGTGTTCAGG 300 GATCCTAGGT GTTGGGGGAA GTGTCCCTTG TTTCCCCTAG CTCCCAGGGG AGAGTGGACA 360 TTTAGTGTCA TTTCCTATAT AGACATGTCC CATTTGTGGG AACTGTGACC CTTCCTGTGT 420 GAGCTGGAGG CACAGAGGGC TCAGCCTAAT GGGATCTCTC CTCCCTTCCC TGGTTTGCAT 480 TCCTTTGGGG GTGGAGAAAA CCCCATTTGA CTATGTTCGG GTGCTGTGAA CTTCCCTCCC 540 AGGCCAGCAG AGGGCTGGCT GTAGCTCCCA GGCGCCCCGC CCCCCTGCCC AACCCCGAGT 600 CCGCCTGCCT TTTGTTCCGT TGTGGTTTGG ATCCTCCCAT TTCTCTGGGG ACACCCTGGC 660 TCTCCCCACC ACTGACTGTG GCCTGTGCTC TCCACCTCTG GGGAGGGAAG GCCCTGGGGT 720 CTTCCTTCCC GCGAGTTTCC CTGACCTAAA TCTGGCGTGG CTGGGTAGTG GCCAGCAGTG 780 GTGATGCCCA GCCTGTTCTG CCTCCTCCTT CCCCACCCCA GGAGCCCTTT CCTTGGCCTA 840 GGACCTGGCT TCTCAGCCAC TGACCGGCCC CCTGCTTCCA GTGCGCCACT TACCCCTTCC 900 AGCTTCCCAG TGGTCTCTGG TCTGGGAGAG GCAGGACAAA GGTCTTTGTT TGCTGGAGAA 960 AAGGTTGTCT GCGATAAATA AGGAAAACCA CGAAAGCCTG GTTGTTGGAG TGTACGTGTG 1020 TGCTCCCCCA GGCAGTGGAG GCCAGCCCTC CTTGGAGGGG CGGCTGCCTG ATGAAGGATG 1080 CGGGTGAGGT TCCCCGCCTC CACCTCCCAT GGGACTTGGG GATTCATTCC AAGGGGAAGC 1140 TTTTTGGGGG AATTCCTACC CCAGGTCTTT TTACCCTCAG TTACCAACCC CTTGCCCAGG 1200 CCAGACCTTC CTGCTATCCC CTCCTGGGCC ACAAGCCTGG CCCTCCTCTG TCCCAATTGT 1260 GATGAAGGGG CAGTTCAAAA CTTCTTGATT AGTCATCTTC TCCCCTATCG ACTTGGCTTT 1320 AAAAAATGAC CTTTTCAGAC TTCTAGTCTC GTTCACTCTT TTTGATGATG CTTTGCCGTA 1380 ACCCTTCGTG GGTAGAGAAG GATTCTGTGC CCATTGGTGG TCTGGATAAA AGAAATAGAG 1440 ACCTCACAGG AAGCAGTGGA CTGGCCTGTT TCCCCACTGT TCTTTCTGTT TTCACACCTG 1500 TGGCCTTCTC CCCACCTTCT TCCCAATCAA CCTATTGTGT ACATAGCCCC CCTCATTGTC 1560 CTTTATTCTT CTGGAAAGCA GACCTTGGAG GGAGGAGTGA GGGGGAGGCT CAGCTGTGGT 1620
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