Tag | Content |
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EnhancerAtlas ID | HS022-06952 |
Organism | Homo sapiens |
Tissue/cell | CD4+ |
Coordinate | chr19:8444430-8446060 |
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) |
SPI1 | MA0080.4 | chr19:8445064-8445078 | AGCTTCCGCTTTTC | - | 6.09 | STAT3 | MA0144.2 | chr19:8444996-8445007 | TTTCTGGGAAG | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 8444800 | 8445225 | chr19 | 8446008 | 8446058 |
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Enhancer Sequence | ATGTGGGTGG GGCCAAATAA GGGAATAAAA GGCCACCCGA GCCAGCAGCA GCAACCCACT 60 CAGGTTCCCT TCCACGCTGT AGAAGCTCTG TTCTTTCACT CTTCGCAATA AATCTTGCTG 120 CTGCTCACTC TTTGGGTCCG CACCACCTTT ATGAGCTGTA ACACTCACCG CAAAGATCTG 180 CAGCTTCACT CCTGAAGTCA GCGAGACCAC GAACCTACCA GAAGGAATAA ACTCCAGACA 240 CATCCAAACA TCAGAAGGAA CAAACTCCAG ACACACCATC TTTAAGAACT GTAACACTCA 300 CCGTGAGGGT CCACAGCTTC ATTCTTGAAG TCAGTGAGAC CAAGAACCCA CCAATACTGG 360 ACACATTTTG GCGACCACGA AGGGACTATC GCCTATCACC AAGCGGTGAG ACTATCGCCT 420 ATCACCAAGC GGTGAGTACC ATCGGACCCC TTTCGCTTGC TATTCGTCCT ATTTTTCCTT 480 AGAATTTGGG GGCTAAATAC CGGGCACCTG TCGGCCAGTT AAAAGCGACT AGCGCAGGTG 540 CTGGACTAAA GACATGGGTG TGAGGCTTTC TGGGAAGGGG CTCTCTAACA AACCCCGACT 600 TTTTGGAGTT GGGAGCGTTA GTTTGCCTGG AACCAGCTTC CGCTTTTCCT GTACTTCTGG 660 GCTGAGTCGA GGGTTGACAG GAAAGCCATT CAGCTCTGGG GTCTTGACAA CAAGTTGGTT 720 GATCCTGTGG CCATGAGCAG AACTCTCAAA GTCATGTCGC CCAAGTGAGA CTCGCCCATC 780 TATCCTATCT GTCCTGACCC TTGCCTCCTG GGTCCTAATG CCTGTCAGAC AAACTTCCTC 840 TCGCCTCTCT TCTCCGAGGC TAGTCCCACC TCTAAAAACC ACTCCCTGTC TCTGGTGCTT 900 TTCTAGTTTC TCCTATAAGA ATGACTTCTA GTATAAACTT CAGGACTCTG TTACCTTCTT 960 TAGGCACCTA GGCTCACTAA TCAGAAAGAC ATAATTTTTG CCCAAAGCCC TGTTGTAGGG 1020 GGGCTATCTG GAATTTTAGG ATCCCTCCTC AGACAAGCAG GACTAATAAA AGCTATTCCT 1080 GAAGCTAGGA TATGGGGAGC CTCAGAAATT GTATTCTTCC TATTCATATA AGTGAGGACA 1140 AAAGGTGTCA CTCTTCCAAC CCTGGAGATC CCTTCCTTCC CTCATGGTAT GGCCCTCCAC 1200 TTCATTTTTG GGGCATAACA TCATTGTAGG AAATTGGTAA GGTCCCAATA CTAAAAGGAG 1260 AATGCTTAGG ACTGTAACAG GTTTTCGAGA ATGTGTTGGT AAGGGCCACT AAATCCAATT 1320 TTTCTCGGTC ATCTTTGTGG TCTAGGAGGA CAGGCAAGGG TGCAGGTTTT TTGAGAATGC 1380 GTTGGTAAGG GCCACTAAAT CCGACCTTCC TCGGTTCTCC TTGTGGTCTG GGAGGAAAGC 1440 TACTGTTTCT GCTGCTGCGT TGGTGAGTGC AACTATTCCA ATCAGCAGGG TCTAGTGACC 1500 ATTACGGGTT CTTGGGCAGG GGTTGTTTCT GCTGCTGCAT CAGTGAGCGC AACTATTCCG 1560 ATCAGCAGGG CCCAAGGACC ATTGTGGATT CTTGGGCAGG GGGAGAAGAA AAACACACCA 1620 AAATCGTGGG 1630
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