Tag | Content |
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EnhancerAtlas ID | HS141-11262 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr2:231321600-231322820 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr2:231322246-231322257 | TTCTGTGGTTT | + | 6.32 | Sox3 | MA0514.1 | chr2:231322597-231322607 | CCTTTGTTTT | + | 6.02 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_09384 | chr2:231320724-231324992 | CD14 | SE_10266 | chr2:231321351-231322930 | CD19_Primary | SE_10885 | chr2:231272649-231341656 | CD20 | SE_18487 | chr2:231320965-231325165 | CD4p_CD25-_Il17-_PMAstim_Th | SE_22757 | chr2:231321449-231322907 | CD8_primiary | SE_53670 | chr2:231321492-231324812 | Spleen | SE_62343 | chr2:231275151-231339482 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 231322204 | 231322520 | chr2 | 231321800 | 231322600 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I230456 | chr2 | 231321647 | 231323115 |
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Enhancer Sequence | TCTGCATAAG GCAGTTTGTT ATCTCCATTA CTTTGGGGTC TGCTATGGGG AGATTATTGT 60 GTTCTTTTGG TCATGTTGTG TCTCTTTGGT TTTTATGTTT CTTGTTGCCT TACATTTATG 120 TCTGTACATT TGAGAAAGTA GAAACTATTC TAGTCTTTGC AGGCTGACTT TGTCTGGGAA 180 AGCCTTTCAC CCTATTTAAA GATTCTAAGA TGGCCATCTG GCATGGTACA AGGGCAGGCT 240 TGCTGCTAGA GTCCTCAAGC AGGCTAGTCT GGTGCCTAGG ACAACCAGTG GGCAGGTCTG 300 TGCTGGGGGA AACCTTGAGC CAGAATCTGC AGGGCTCTAC ACCACTGATG CAGGCTTCTT 360 CAGGCACTTC AGTAGGCATG AAGCCCAGTG CTATTGAAGC CAGCTTGCTG CTAGGATGGG 420 CCTCAAGCCC AGTGCCACTT GGTCCAGTTT GGCACTCGGT CTGGTCTGGA TCATGGGTTC 480 ACTGAGGCTG AAATAGTGCT GTAGGAGGCT GAAGACTGAG TTCGCAGGGC TGGCCTGAGT 540 CCTGGGGCTG CAGGATTTAG GTTGGGGTCA GAGTGAGCTT GGAGGTTCAG ACCATGGGTA 600 CTGGCTAGAG TCTGGGGCTT TGGGAGCTGG GTTTTACTGA AGTCGGTTCT GTGGTTTGGG 660 TGTAAGGCAA AGTCTGGTGC TCACTTCCTT CTCCTTTCCC CAAGCATATT GTATCTTGCT 720 CAATGCTGTG CTTCCTGGAG TTGGGGAAGA TGACACAGTG AAACTTTTCT TCCTGCCCTT 780 TTCAATGTGC TCTTTCTTAT TTCTGTGTTT CACTCAGGTG CTGTGATCTT TCATCTGGTT 840 TCCTCAGCTC TTGCAAAGGT ATTTTCATGC ATAGGTCGTT GTTCACATCA GTGTTTCTGC 900 AGGGGATGGA GGGCTGGAGA GTCCTATTCT CCCATCTTGC TCTACTTCTC CCCAATTTTC 960 TAATTATATC TTTATTTTTC TATAAGGGCA AAACTTCCCT TTGTTTTCTC ATACTAACTG 1020 CCTACACTCA TCCAAGACAC ACAGACTTTG TTCACAGCCT CTGGCTGCTT TTAACAGGTA 1080 TGAGATGGAA GGGAAAAAGA GAGTGAGTCT TTTTAACAGA GGGACTGTCC CTGGTTAGAG 1140 AATGCAAGAA GAAAGAATAC AAAAGAGGTC AACTAGGGAA TATTAAATAA CAAAACACAG 1200 TTGACCCCTG GACACTGTGG 1220
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