Tag | Content |
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EnhancerAtlas ID | HS080-19363 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr2:111616590-111617670 |
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) |
ZNF263 | MA0528.1 | chr2:111617103-111617124 | GAGGAAGGAGAAGGAGGAAAA | + | 6.36 | ZNF263 | MA0528.1 | chr2:111617102-111617123 | GGAGGAAGGAGAAGGAGGAAA | + | 6.66 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_25457 | chr2:111613774-111620073 | DND41 | SE_31274 | chr2:111615418-111620099 | Fetal_Thymus |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I110857 | chr2 | 111615499 | 111617608 |
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Enhancer Sequence | ATTTCTATAT GACAATTAAA GGTCAAATTG CAAAGTTGAA TCAGTTATAG CTCTGCGTTT 60 AGGATACGTT CAACCTGAGC TGATTTTATC TGCCTGGGCT TTGTAAAATG TTAGTATTTG 120 CATAGTGAGT TTAAAAACAG AAACCTTTTG CATAACCATA TTTGAAAAAT CCAAAACAAA 180 GAGAAAGAGA ATGGACTGAT GATATGAAAA GATGCCATTT GACCGGACGC TGTGTAGTCT 240 GGGTGGCTTT TGTGGCAGTT GTGCTGCTTC TGAGCGTAGC TTTCTAGAGT GTGCGAGTGG 300 TGGCTAGATG TGCTTTGTTT CGTGTGCTGT GCATTTCAGT GCTATGTGAG GATCCATCTG 360 ACCCCAATAC ATTTTATTTG ACATGCACAG CTGGGTTGCT GGAGGATAGT TCAGGCCATT 420 AACAAGAAGG CAAAAGAAAA CACAGACAAT CTATTCATCA GAACACTATG AAAGGGAGAC 480 TTATTGGGGC AAGCTCTGGC AAGAGCACAC CTGGAGGAAG GAGAAGGAGG AAAACCAACT 540 GGGTGCCTAG GGAGAAGGGC GGAGGAAATG CAGCTGCTGT TGACGGCAGC CGGCTGCATG 600 GAGAGGGGCT TTGCCAGTGG TGAAACCCGA TTCCATTTCC AACTTGTGGA ATCGTATTTT 660 AGGATGCTCT GCAAACAAGA GGGTTGGATG GCAGACATAA GGTCTTATTT GCTGAGGGGT 720 CTTTGCTCAC CAGGCGCTTG GCACCCCAGC AGGACCCCAG GCTAAGGAGT GTGATGCTCA 780 CCTTGCATCT GAGGGTGGCA ACCAAGTTCC TGGCCTGTGG GATCAATGCT AGGACTCCCC 840 AGGCATCCCT CAGACTCACC GAAGAGGGAA GAGAGGAGGC GGCTTCTAGA ATCCTTGGAA 900 AGCCATTTCC TTGCCCTTCT TCAGCCACAG AGATGCCCCA GTAACCTCAG CCCGGTTCTC 960 ACAACCTGCC TACTCCCAAC CCTGTCTTTC CCTTCCTGCT TCCTATCTGT GACTTTGCAG 1020 CACTGGTTTC ACATTTTGTG CTTTTATCCA GTATAAGATT TCCATTTGTG TGTGCTGTGG 1080
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