Tag | Content |
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EnhancerAtlas ID | HS051-16420 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr2:192604050-192605370 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr2:192604798-192604813 | TCATGAGTCAGCAAA | + | 6.22 | Sox6 | MA0515.1 | chr2:192604683-192604693 | AAAACAATGG | - | 6.02 | ZNF263 | MA0528.1 | chr2:192604157-192604178 | GCCCTCCCCTGCTCCTCCTCC | - | 6.8 |
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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 |
GH02I191740 | chr2 | 192604941 | 192605090 |
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Enhancer Sequence | CATGACGTTC CCATTATTCA CATGGCTACA ATACTGCCCC TCCTCTCAAC TTTCTATTCT 60 CTTTCCAAGG CAGTCCATCC AAACCACACC TTCTCCCAGA TTTGCCTGCC CTCCCCTGCT 120 CCTCCTCCAG CCTTCCTGTT CTATTCCATT CCTTGGTCTG CAGCTCTCTG CCCTCTTGGC 180 TCTTTTCTCT TTACCAAGTG CCCTGCGTGA GCATAAGGAA GGGCCTAGAA GGGAGCAGCC 240 ATCAAGCCAT CTCTTGAAAT TGGCAGAGAA GAAAGATGAT GAATATACAA TATTTTTAGC 300 TCTGTCAAAT AGACTCAAAC CCAATCTAAT ACACATTTAG AACTCGGACT CTGCCTACAA 360 AGAATTGGTT GCTATCAACC TTTACTCCTT TCTTACCACC TTTCCCTCAA CACTTCTTGT 420 TCTATCTGCT TTGCTGTATG CCATTTCCTT GGGGAAAGTA ATCAGAAGAG CTGGAGGCTA 480 CTGCAGGAGA TGGGGTCCTG AATGGCTCTT CAGAAGGAGG GGGCTTAGCT TGATTCTGGG 540 GTGGTGCATT GGCACAGAGA GAAACTGTTG GCTGTCCCAC TAAGTAGACA CCTAAATTTG 600 GGAGGGCAGT TGCAAGCCAG GTGGGGGAGG AGTAAAACAA TGGAGCAGTG AAGATGTATA 660 TTGAGTTTGA GAGCAGACAA AGATAAATTT GTCAATATGA AAGAAGGAAG AGAGCAAAAC 720 ATAACTAGAG CAGGTGTCAC AATTGAGGTC ATGAGTCAGC AAAGACTAGA CTGAAGGTAC 780 AAGAGATGAG GAAGACATTC AAGGGGGAAG GGTGGGGCAA TGGAATCAAA CACACAGGAA 840 GAAGGCCTTC AAATTTTATA CCACCATGGT TTAGTCCTTT TAAGAAACTT TCTTATGTGG 900 TATTTATGGT GGATTGTGAA CATGGCTTGT CTTTTCTAAG CTCCTTGAGG CTGTGTTCTG 960 AGTTTGGTTT GCCCTTGTTG TGGAAAATGT GGTGAGTCTC ACATACTCCC AGCTGTCTGC 1020 TGGTTGTCAT GCAGCATACA TCCAGAAGGG CATTGGGTAG TATTGAGTGA GTAGGAGGAG 1080 ACAAGGAAGC CTGGCTGTTG GGTGAGCAGA GGGTGAAATA CTTAATCAGG TCTTGAAAAT 1140 TTTTATGAAA AGTCTAACTC CAGTATTTTT TGGAAATTTC GATGATATTG GTATCATCCA 1200 ATTTGTATAA TCCAAGTCTA ACAGGTCTTG CTGCTCTCTG CTTATTTAAG AATAATGTAT 1260 TTAAATACGA TCAAGTGTGA TAATCTTAAC TATCACCTTC TTTATCTCTT ATCACCCTGA 1320
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