Tag | Content |
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EnhancerAtlas ID | HS050-43632 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr21:41775800-41777220 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TCF7L2 | MA0523.1 | chr21:41776112-41776126 | TAACTTCAAAGGGA | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_43411 | chr21:41775334-41777445 | MCF-7 |
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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 |
GH21I040403 | chr21 | 41775658 | 41777252 |
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Enhancer Sequence | TGATGAAGAA AATATCTTAG AAAATAATAT GAAAATCAGG CATGTCTGTT TCCAAATCAT 60 TCATCATCAT CATGATCACC ATCATGGCTA CAACTTACTG AACTACCTGT TCAGCATTGT 120 GCCAAGAAAC TGACATAGAT TATCTATGTT AATTCCCTTT TTAACATAAA TGAGAAAGCC 180 CTGAGATGGA CTGCTGTGTC CCTTGCTGAC TCTCTTATTT CTCTCTTATT TCAGACCTAT 240 AGCTTACACT TTTCCTGTCT TCTGTGAACA CAAGTTCATG ATACTGCATT TAACAATTGC 300 CTCAATAAAG GTTAACTTCA AAGGGATTCA TCTATGGTAC AAACAAAATG CTGCTACGAG 360 GCACTTTACA TTTGCAAAAT GTTCTGGAAA TGTACATAAA TAGCAAAGTG AAACAGTTAA 420 GATACTGTTT CAGATTCTGT GAACCAAGAG GCGGTTGGAG ATCTCTTAGA TCAAAGATTT 480 TAGAGGAATT TTGGACAATT TTGCAAGTGA TTTCCTAAGA TCCAGTCTCT TGACTAGTTA 540 TAAACAATTG TGTGTTCACT GGGCCTCTTG AGGGCAGAAG AGCAAACATT AAGCACAAGG 600 CTAAAAGGGT TTCCTTGGAA ACCTGGTGTT TCTTTAATAC AGCACAAGTC CCTTAACACG 660 TCACAGATTT TCCAGGCTCC TCCTGTGTGT CTCTGAAAAA CCTGCTCTTT GAATTGCACT 720 TAAATAAACA CAGGGAATAA TTCCACTTTT AGATATCCTC TCCGGAAAGT TCTATCATTG 780 CCAACACTCC ATTTAACACA TAGGGCTTGT CATACACCAG GCTCCAGGCC AGGGGTTGGA 840 TATAGAATAG TGAGTGGAGG AAGGCGTGGT CCCTCCTTGA CTGGAGCTCA CTGTGCTGTC 900 ATCCTCTAGG AAAGTCTCCT CAGTTTGCAC TCCTGGCACT GTTTGCTTCA AATTCATTTC 960 CATTTTGATT CAATGGATGG ATCATCTTTC CTAAAATGAC TGATATTCAT GAGGTCAGCA 1020 GGCACACCCA GTAACAGACC TAGGCAATAG ATTCTAGGAT CTCAGAGACA TATGAAATAA 1080 TTTAGTGTGG TTACAGCAAG GCTTTTAATT TGCTTCAGTA CAAAATATGT ATTATTCAAG 1140 TTGAGCTATT TTGGTTTTTC AACTGGGCAG CTGGCTCCCG TATAACAGAA GCCATGAAGT 1200 ATGGGAGATG CAAAGGTGAA TGGGACATAG CCCATGGCCC CCAGGAACTG AGAATCTAGT 1260 GGCGTATATT GTCTAGTAAA AATAATAATT TTCATACTGA GTGATGCTTA TGTTCTGAAA 1320 GCACTGAGCA GAGGTAGACC CTGGGAAAAT GTAACAGGGT CTTTCATGCA TTAAACTGGG 1380 ATCAGAGCAG CCATCTTACC ATATTATCCC TCTGAGACCT 1420
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