Tag | Content |
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EnhancerAtlas ID | HS108-25999 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr21:36880580-36881700 |
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 | ATTTAGCATC TGTTGTTGGC CAAACAACAG ATGACGCCTT GCCTTCAGGG TAAAAATCTA 60 ATTTGCATGT AGGCGCTTGA ATGAAATTAA GCTCCACAAG GTGTGAATAA CAAGGGGTGG 120 CCTGCTCTAG TGACAACAGG CAGCTCTTCT CAAACAAGGA CGTTGAAAGC TTGTTAGTGC 180 TAACTGAACT ACTTTGCAGC GTATATCCCC ATCTGGAGGC CGACATCAAA TTTGAGAGTC 240 ACAAAGAAAC ACAAAGGTCA TTGTGGCAAA CCAGGGCCGT GGCATTGCAC AATTCTAGCC 300 AGAGGCCAGA CTCCTCAAAG TCTAGATGAA TGGTGCCCCC TGGAGCTGTG CAGTGCACAA 360 CGTGTGCATC TGGATAGGTC AGTCCTGAGG CCAGCCGACT CATTTTATAA GGCAAGAAAC 420 TGCAGCCCAA AGAATATATA TGCCTGGTTG GAAGTTAAGC AATGAGGCAC ATTTCAACTC 480 AATATGAAGA AAACATTTTT GAAACAGGAA GCTGTCAAAG ATGATGTTGG TTGACTCAGG 540 AGGTAGTGAG GACCAGTTAC AGGACATTTG CAAGCCTAGG CTGCTCTACC ATCTGGTATG 600 GACTTTCAGA GGGGGCTTGA AATTAAGGTG TGGGTAGGGG CTGGCCTCCA TAGCTGTTAA 660 GGTTTTTCCC AACCCTCAAC TAAGGAATCC ATTGTTCAAA CACAAGTCTT CAGGCTACTG 720 AGCACCAATC AAGGTATGGG GACCCTGAAA GGCAATAGAA ATCAAAAGAT CTATTTTGAG 780 AGGGCTCTAA CTTAACAACA GGAGGCAGCA ACATCAGTGA CTTTCTCAGC TGCTACAAAA 840 AGTAAACCAT CGTCAGACAC AATTTTCCCA TTCTCCCCCC TGCACTTGCG TCATACCCAA 900 CTTCCCCTTC CCCTCAACAC TGCAGAACTT ACTGATAACT AAGCCATGTC TACCCCTCTA 960 GGAGTAGTTC AAGAGTCCTG GTAAAGACCT AACAGGAAGT AGAAATTACA TATGAGCAGC 1020 ATGTGTGTGT GCATGTGTAT GTGCACATGC ATGTGTGTGG TATGTATGTA CACGTGTGTG 1080 TGTGTGCATG CACACACTGC ATGGGTGTAT TTCCTTAAGC 1120
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