Tag | Content |
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EnhancerAtlas ID | HS076-37109 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr21:36880460-36881620 |
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) |
POU2F2 | MA0507.1 | chr21:36880637-36880650 | CTAATTTGCATGT | + | 6.2 | TBX21 | MA0690.1 | chr21:36880677-36880687 | AAGGTGTGAA | + | 6.02 | TBX2 | MA0688.1 | chr21:36880677-36880688 | AAGGTGTGAAT | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_25514 | chr21:36872696-36883946 | DND41 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr21 | 36880713 | 36881139 | chr21 | 36881031 | 36881190 | chr21 | 36881422 | 36881515 |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I035508 | chr21 | 36880500 | 36881949 |
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Enhancer Sequence | TCAGATGACA TTTTTATTAA TACTTAAAAA CTGATACTTA AAAAATTCTT AAAAAAACAT 60 AATTACAGTC TGAAATATAA TAGATTCTCA AAGAAAAGTA CACATTCTCC TTTCCTCTTC 120 ATTTAGCATC TGTTGTTGGC CAAACAACAG ATGACGCCTT GCCTTCAGGG TAAAAATCTA 180 ATTTGCATGT AGGCGCTTGA ATGAAATTAA GCTCCACAAG GTGTGAATAA CAAGGGGTGG 240 CCTGCTCTAG TGACAACAGG CAGCTCTTCT CAAACAAGGA CGTTGAAAGC TTGTTAGTGC 300 TAACTGAACT ACTTTGCAGC GTATATCCCC ATCTGGAGGC CGACATCAAA TTTGAGAGTC 360 ACAAAGAAAC ACAAAGGTCA TTGTGGCAAA CCAGGGCCGT GGCATTGCAC AATTCTAGCC 420 AGAGGCCAGA CTCCTCAAAG TCTAGATGAA TGGTGCCCCC TGGAGCTGTG CAGTGCACAA 480 CGTGTGCATC TGGATAGGTC AGTCCTGAGG CCAGCCGACT CATTTTATAA GGCAAGAAAC 540 TGCAGCCCAA AGAATATATA TGCCTGGTTG GAAGTTAAGC AATGAGGCAC ATTTCAACTC 600 AATATGAAGA AAACATTTTT GAAACAGGAA GCTGTCAAAG ATGATGTTGG TTGACTCAGG 660 AGGTAGTGAG GACCAGTTAC AGGACATTTG CAAGCCTAGG CTGCTCTACC ATCTGGTATG 720 GACTTTCAGA GGGGGCTTGA AATTAAGGTG TGGGTAGGGG CTGGCCTCCA TAGCTGTTAA 780 GGTTTTTCCC AACCCTCAAC TAAGGAATCC ATTGTTCAAA CACAAGTCTT CAGGCTACTG 840 AGCACCAATC AAGGTATGGG GACCCTGAAA GGCAATAGAA ATCAAAAGAT CTATTTTGAG 900 AGGGCTCTAA CTTAACAACA GGAGGCAGCA ACATCAGTGA CTTTCTCAGC TGCTACAAAA 960 AGTAAACCAT CGTCAGACAC AATTTTCCCA TTCTCCCCCC TGCACTTGCG TCATACCCAA 1020 CTTCCCCTTC CCCTCAACAC TGCAGAACTT ACTGATAACT AAGCCATGTC TACCCCTCTA 1080 GGAGTAGTTC AAGAGTCCTG GTAAAGACCT AACAGGAAGT AGAAATTACA TATGAGCAGC 1140 ATGTGTGTGT GCATGTGTAT 1160
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