Tag | Content |
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EnhancerAtlas ID | HS094-25672 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr22:31645980-31647130 |
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) |
Stat6 | MA0520.1 | chr22:31646353-31646368 | ACTTCTCAGGAAGAG | - | 7.07 | ZNF263 | MA0528.1 | chr22:31646982-31647003 | GAGGGAGCAAGGGAATGAAGA | + | 6.17 | ZNF263 | MA0528.1 | chr22:31646975-31646996 | GGAGGAAGAGGGAGCAAGGGA | + | 6.3 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_26106 | chr22:31645649-31647755 | Duodenum_Smooth_Muscle | SE_27205 | chr22:31643647-31647694 | Esophagus | SE_27790 | chr22:31643391-31650686 | Fetal_Intestine | SE_28888 | chr22:31643343-31650784 | Fetal_Intestine_Large | SE_31902 | chr22:31643646-31647232 | Gastric | SE_37292 | chr22:31642944-31647660 | HSMMtube | SE_42312 | chr22:31643665-31647360 | Lung | SE_52405 | chr22:31644955-31648226 | Small_Intestine |
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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 | AGCTTTTTCT GTCTTCCTGA CTTTCTCTCA TCCTTCAGGG GGCTGCAGGT TTGTTTTCTT 60 CTCCTAGTGG AGAGGAAATT CTCAGGTTTG TTTTCCTCTC CTAGCAGAGA GTAAAAAAAG 120 GGATAGTTTG CCTGACTTGT TGAAGGTGTG GCTGAGATTG TTTTCTAAAG AGCCAATGGA 180 AATTGATCTT GAGTTTAGGA GAAAGCTTTT ACATGTGGAA TTAAGATGCC AAGTGTTGAA 240 GTAGCCACAT TTCAGGTCCT CATTAATTTC TCTTAATCCT GGGAAGGCAG CTTAGGAGAA 300 GGGTTGTTCC TTTAGGAGCC AGGAACTATA CCCCTTTTAC CCTTGGAGAG GCAGGGAAGC 360 CAGGGAGGAC ACAACTTCTC AGGAAGAGGA GAAGCTAGAG CAGATAGTGA ACTCTCAACC 420 TGAACCTTTA AGGGCCAGAC CACTAATGCC ACCCAAGTCC ACCTGCCGTT TGTCTTGTTC 480 TGTCCCAGGC TTTCTGGAGA ACCTGATCTT CTTGCCCCTA CCCCCAAGCT CCGTTTGCCC 540 AGCTAGAGTC TGGGGGGTAC TGACTGACTT TCGTAGACAT TCTTCCCTTC CCCAAATAAG 600 AGGCCACATT CCTGAAGTCA CTTCTGAAGA GATAGCTGCC ACACAGGGCT CTTTCCCCCC 660 AGGGAGGGAC CACCCAGACC CTCTGCTCTC CCAGGTATCC GTTACCACAT CACTACCTGG 720 TCAGAAAGCT GTTTCTGCCA TTAGCCCCTC CCTCTTTTAT TATAGGATAT CCTCAAGGGC 780 TCCTCTTTGG GCCTCAGTTT CATCCTTGGC AGAAAGTAGA AGCTAGACTT CTTGGGCTCC 840 TGAACAGGGT CCTTGCTGGA TTCTGTGAAA CAAATTAAGT TCTTGACCCT AGGCCTCTGG 900 GGGAGTACAA AGTCTATGGG AGTTCTGGGG CTGTGGTTGC AAGGAAAGTG ACGCAACCAG 960 ATTCCATGGG GACATGATCA GGCGTGACAT GTGAGGGAGG AAGAGGGAGC AAGGGAATGA 1020 AGAATACAAC TTCTGTGTCC CATACACCCC TGCCTGACAG GCCATACATA CTCAGCAGAG 1080 AATGCACTGT CTTTCCTACC ACACTAGCGT GAGAAGTGAG CTGCAATTAC CACTGTGCTT 1140 CCAAGTAAGA 1150
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