Tag | Content |
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EnhancerAtlas ID | HS187-08962 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr16:374500-376180 |
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) |
Nr2f6(var.2) | MA0728.1 | chr16:376136-376151 | GAGGTCAGGAGTTCA | + | 6.22 | ZIC3 | MA0697.1 | chr16:375299-375314 | TGCCCCCCGCTGCTC | + | 6 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_24104 | chr16:373786-376118 | Colon_Crypt_2 | SE_25025 | chr16:373765-376251 | Colon_Crypt_3 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr16 | 374933 | 375274 | chr16 | 376000 | 376139 | chr16 | 375625 | 375961 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I000323 | chr16 | 373759 | 379105 |
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Enhancer Sequence | CGCCCAGTGT CCCGCAGAGT TTGTGGAGAT AAACAGAAGC TTGACAAACA CAACTGAGCA 60 GAAAACGCCC GCAGGTGGTC AGTAGGCGCT TCCAGTGTTA TCACAAGACC ACACGCCGCA 120 CGTCAGCACA TGACACAGAC ACACTTACTT GATCCCTGTT TTGACAAGCT AAGTCGTACT 180 TTATACCAGG AGGAGGAGGG GCACCCCAGG TGAGCGGTCC AATCCTCAGA CACGGCCAGT 240 GCCATCAGCG ACCTGCATCC CGACCCCCCG GAACAGCACA GCCAGCAGAC AGAACCCGCC 300 CTGCAGAGGC AGCTTCCGGC AGCCGCAGGC CCTTCCCAGG CCCAGCCCCC GAGTCCCGCG 360 CAGGGAAAGG CTCTGCCCAA GCCTTCAGGG AGGCAGCAGC GCCCGGTGCA CAGTTCCTAA 420 GGGCGCAGAA CTCCGGGATG AACAAAGGCA AGGAAACGGC TGTGTAAAAA TCAGCTCTAC 480 TGACGCACGG CTGGGTGCTC AGCGGACCCG CACAGAACCA CAGTCCTACC TGGCACGTTC 540 TGACGCGCAC CAGATCACAG CCTCAGCCCC GCGGGCGCGC CCCAGGAAAC CATGGCCTCA 600 GCCCCGCGGG CGGCCCCGCA CCCCAGGAAA CCATCGCCTC AGCCCCGCGG GCGGCCCCGC 660 ACCCCAGGAA ACCATCGCCT CAGCCCACAT ATTCAACCCG GAAGCCTGGG GAGGCTTCCC 720 TTGGGGAAAT CCACCTGTCG CTCGAGGTCA GTCGGCCTTT TCTAGAATTC TGTATAAACG 780 CAGTCTCATG GGGAGCTAGT GCCCCCCGCT GCTCCGGCGC CCCCTCCGCT CTGGCTTTCT 840 TCACTGGCAC AGGATCCTGA GATGCACCCC TGCCTCCATG GTTATCAGCG ACTCATCCCT 900 TTTATGCCGT GGCATGCCAG GATGCACCAC GGTGTTTTTC TCCAACTGCT TGGCAGTGCC 960 ACTGGAGTTG GGGCAGCGCT TCCCAGCGGG CAGAGTTGAC CCCGAGGCCA ACAGCCAGGC 1020 CACAGCCAGC GCCCTCCCCA CGTCTCGCCT CCCCCAGTCC AGACACAAAC CTGGTCAAGG 1080 GCGCCCAGAC CAGGGCTCAA CCCACTGCCC GCAGGGGCCG ACTGCCAAGG AGCGGTCACC 1140 GCCCCAGAGT GATGGCTGCC ACAGCGTCGT GTGTACAACT TATGGTCTGT CCCACGTGGC 1200 TGCAGGCTCC AGCCCTGAGA AGAAGAGAGG AGAGCCATTC CCCAACACGG CACCTTGCTC 1260 TGTGTTAGCT CCATCTTCTC TCATGACGGG GCCTTCGGAA ACACCAAGAA ACGACCAAAG 1320 CAGACAGGCA CTGGGAGAAG CAGGACAAGC ATTTCCTCAC CTCACATGAA CTTCCATATG 1380 AATGTGACAA AGGCACAGCA CACAAAATGC AGATGCTGAC CACAGAGAGG GCCCCACTCA 1440 CTCACGCTGG CCACGAAAAG GCCCGCCCTG GTTCACACCG GCATGGAGAG GTCTCGCTTC 1500 TGTTTTAGCA ATACTGACAA CTGGCCCCCA TTCATGCAGA TGCTGTCACT TATATACTAT 1560 ATATATAACA AGGGCCAGGC GTGGTGGCTC ATGCCTGTAA TCCCAGCACT TTGGGAGACT 1620 GAGGTGGGCG GATCATGAGG TCAGGAGTTC AAGACCAGCC TGGCTAAAAT GGTGAAACCC 1680
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