Tag | Content |
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EnhancerAtlas ID | HS022-05158 |
Organism | Homo sapiens |
Tissue/cell | CD4+ |
Coordinate | chr16:1407730-1408900 |
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 | chr16:1408804-1408817 | TTAATTTGCATTT | + | 6.25 | Zfx | MA0146.2 | chr16:1407757-1407771 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_01156 | chr16:1404853-1409582 | Adrenal_Gland |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH16I001356 | chr16 | 1406640 | 1409035 |
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Enhancer Sequence | GTCTCGATCT CCTGACCTCG TGATCTGCCC GCCTCGGCCT CCCACAGTGC TGGGATGACA 60 GTCATGAGCC ACCGCGCCTG GCCTCGACTT TATTATTAAT ACGGTAAAAC TACAGAGAGT 120 TTGAAACATC AGTCTGGGGC GTCCTCCTCT AACCAGTGCA CTTGCTGCTG CAGCGCAGGC 180 CCTTCAGGGG ACGGGGATGG GGGCCAGTCC CCTCCCTGCC TCCACGGCCC AAGCCCCAGC 240 CTTCCCCACA GTCCTGGAGG ATGGCCCGTG GCTGACAGTC TCGGTGGGCG CTGTGTTAAG 300 GTGGCGTCCC CAGCCAGGTC CCGACTCCCC AGCTTAAAGA ACAGGGTGGC TGCTGTGGCT 360 TGACTCACGA GTTGCCACTG GCCTTGATGT GTACACGCCC TTGCTCTAGC ACTGCCTGGG 420 GCTGGCCTGG CTGGAGGGTA GGGACGCTGC ACGCCTTCCC TCTTCCCCCA GGCGCTGGTG 480 ACACTGCCCT GCAACCGTCA GCACCATCAT CTCCACAACT TGCTCTGTCC CCTTCAAACC 540 CTGACTCCCA GCTGCCCCGC TCCCCCAGCC CCGGCACCCA CCATTCTGCT GTCTCTGAAC 600 TTGGCTATTC ATAGACGTCA CATAGGTGAC TCATAACTGT GTGCGACCTT TTGTGTCTGA 660 CCAACTCCTC TTGGCACAGT GTCCCCAAGG TCCCCCAGGC TGGAGGCTCT CAGTGCTTCC 720 TTTTTATATG GCTGAGGACT GTTCCACTGC AAGGACAGAC CACGTTGTTG TTTACCCGTC 780 ATCTGTCCAT GGACACTGGA GTGGCTTCCA CCCTCTGCCT GGGAATAGGC TGCTGTGAAC 840 TTGGGTGTAA ATATTTGAGT CTCTGCTTCC AATTTCTGAG AGTAGCTTTG CTGGATCTTA 900 TTAGAATTCC ATGTTTAGCT TTTTGAGGAA CCACCAAACT GTTTGCATAG TGGCTGCACC 960 GTTTCCCATT CCAGCCAGCA TTGCACGAGG GGTCCAGTTT CTCCACATTT TCACCAACAC 1020 TGTTTTTTGC TAACAGCCAT CCTAGTGGGT GTGAAGCGGT ACCTTAGGGT TGTTTTAATT 1080 TGCATTTCCC TAATGATCAG TCATGTGGGA TCTTTTCAGT TGCTTATGGT GTTTGTCCTT 1140 TTTTTTTTTT GAGATGGAGT CTCACTCTGT 1170
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