Tag | Content |
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EnhancerAtlas ID | HS182-12496 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr2:85402420-85403580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Ar | MA0007.3 | chr2:85402685-85402702 | AGGTACACCCTGTTCTT | + | 6.49 | Ar | MA0007.3 | chr2:85402685-85402702 | AGGTACACCCTGTTCTT | - | 7.04 | NR3C1 | MA0113.3 | chr2:85402685-85402702 | AGGTACACCCTGTTCTT | - | 6.06 | SOX10 | MA0442.2 | chr2:85403018-85403029 | GTCTTTGTTTT | - | 6.14 | Twist2 | MA0633.1 | chr2:85403394-85403404 | ACCATATGTT | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I085174 | chr2 | 85401720 | 85403770 |
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Enhancer Sequence | TATGGTTGGC TGAGCTAGCT GAAAAATTAC CCGAATTTTG ATAAAAATTT GAACCATGGA 60 TTTCCTTTCT GACCATGCCT AGCTGTGTAA ATTCCACAGG ATAGTAACAG GTGCCTGGCC 120 ACCATCCAGC AAGACCCCTG ATAACGTCCA TGCAGTGGGG AGCCACGGGG GCAAGTGCTT 180 CCCCTCCCTC CTGGTCATAG GCTTGAGCAT GGGTAGCCAG GATGGGGGGT GGGTGCAACT 240 TGAGATAAGC AAATCGACAA CAATGAGGTA CACCCTGTTC TTTGTCCTCT TGTCAACTTG 300 TGATTTCCCG ATGGATCAGG TAATCCCCAG TAGCAGATAA CTCAGTTGAA TTTTTTCACT 360 GTCGCTGTTA TCTGTATTCA TTGTCTGCCT AAATAGTAGT GAACAGAGAA AAAAAGAACA 420 TTAAAATAGG AAGCTGGGAA TGACAGGAAG AGGGACTGTA GGCCTGGTAA ACAAAAGTTG 480 GCTGTAACAT GAGCCAGGAT ATGGAAGCGT GACCAATACT TTGGACTCTC TCAATGCTGG 540 CCCTCTGCGG TTCATGGCTC TCCTCCCTTT CTCGCTGTCA CCAGCCACGT TTAGGTCAGT 600 CTTTGTTTTT GGCTGTTGTT CCTGAAGACG CATTTATCAG GTGGATCTCT TAAAATCAGG 660 GTTAGGGATT GGAAGTCTAG CTGGGACAAT TCCTGTGAAG ACAGACTTCC TTCTGATGAA 720 ATATTTACTA GCTTTTGTAG GAAGCCATCT CCTCCTCTTT GCTGTGATAA GAGGTACTCC 780 CCACCTTTCT GTCTCATGGC AAGGGTGGAA ACTGATGATA TTTGTAGGGC ATACTGGGGT 840 GAGCCAACAG GCTGGAGGCA GCCAACCCTG GGCATGCAAA GAAGCACCGT TTGGAAGCTC 900 TGGTGTAGCT CTCGTGCAGC AGCAGTCCAG GCCCTGGGAC ATCTGAGTTT GAGGCTTCAG 960 TCCTCCGCTG ACTGACCATA TGTTTACACT GCAGCCTGTT GTGGTATGAA ATGAGATCTG 1020 GAAGCACCTG AGCTCCCCAG TGTCTGCAGG TAGATGATTA TTTAATACCC TCTTCCCATA 1080 CATCTTCATG GTCAGGAGAC TGGACCTTGG CAATTCTGTT ATTAGACAGC TCCACTCGTA 1140 GGGAATTTCT CCCTTATATT 1160
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