Tag | Content |
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EnhancerAtlas ID | HS051-07328 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr13:42954280-42955580 |
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) |
NFYB | MA0502.1 | chr13:42955491-42955506 | AAATGCACCAATCAG | + | 7.1 | SP8 | MA0747.1 | chr13:42955366-42955378 | CCCACGCCCCCT | + | 6.04 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_32561 | chr13:42950092-42955938 | GM12878 | SE_66702 | chr13:42954075-42955424 | Jurkat |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr13 | 42954449 | 42955216 | chr13 | 42954492 | 42954777 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I042379 | chr13 | 42954121 | 42955490 |
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Enhancer Sequence | TCTAAAACTA AAAGAAGGAA TATGCTTAAG AGATCTGTTG TACAACATGG TAACTGCAAA 60 AGTCACAGCA AGTTAGTAAT GGAGCTACTT TATAATTTAC TTTCATCCTA CCCTCAATTA 120 ATTTACTGGA ATTCAACTAC TGGGTAAAAG AAAACAAACA GAGAGGGCTT AGGGCAGATA 180 TCATGGGTCC TGGACCATTA AGCCTCAAAC AGTCCAGCCT TGCTAGAAAG TTTAGGGGAA 240 GAATTATGTG TTTAAAATAA ACCTTAAAAA ATTGAAGTAT TATGATCATA CAGAAAAGCG 300 CACAGTCACC AGTGTTCAGC TTGATGAATT ATGACACAGT GAGCACACCT GTATTAACCA 360 CAGCCAAGGT CAAGAAACAG AACTTCATCA TAACCCCAGA GGTTCCCTTG TCCCACTCAC 420 TGCCAGCCCT GGTTTCTCTT CCTCCCTCTT GTAAACGATT TTAATGATTT TCCAGCCTCC 480 CTCAGAGAAG AGAAGCACTT TGTTCAGGAG GCCTGGCCGA GGCTGGTGGA AGAGTGGAGG 540 AATCAACTGA AGAATTAATT GAAAGTCATA GAGAAACAAT GACCAACAAA GAATTGGGAG 600 AACAGACACA GAATTGTATA CGTATAGCCT TTTATTCCAG GCAGTATTCT AGGAACAGTT 660 TAAGACATTT TTAAGGGCAT TTTCCACTCT TTACGATTTT CACTTGAGTA CTGTTTAGGT 720 TTTAACCAAA CTTCGTGTCA TCTTAAATCG CCCTGAGAAC CGGCGGGGGT TCTCTGCTCA 780 GCGGAGGCTG AGGCTCTCAG CTGGCTCACA GCTTTAGGGA AGCTGCTACT TCCTCCTACT 840 CACCTGCCCT TGAGCGCAGG GTGCACAGAG GGGAGGGGGC AGAGAGCAAG ACGACTGGGC 900 CAGCTCAGAG CCAGACAGTC CTACCTCAGT TTACTCATTC TGTCTCAGGG ATGAGAGATG 960 AACAAGGTCC CTAGAAAGAG AGTGAGTTGA TTCAGCTGCC CTAGGGAAAC AGCTCCATTC 1020 TGCTTATGGC CTCAGCCAAC TGAGGTCCAC AGTGCCAGAT AACCTCACCC CAGCGTGGGG 1080 CTGCGGCCCA CGCCCCCTCG TGAGAGGTGA AGCCAGCAGG ACTTCCTGGG TCCAGTGGAA 1140 CTTGGAGAAC TTTTCTGTCT TACAAGAGGA TTGTAAAATG CACCACTCAG CACTCTGTAG 1200 CTAGGATTGT AAAATGCACC AATCAGCACT CTGTAGCTTC CTAGAGGTTT GTAAAATGCT 1260 CCAATCAGTG CTCTGTAAAA ATGCACCAAT GGATGGTCTG 1300
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