Tag | Content |
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EnhancerAtlas ID | HS182-13474 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr2:242302320-242303890 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr2:242303117-242303138 | AAAGTGAAAGTGACACTGATA | - | 6.34 | IRF1 | MA0050.2 | chr2:242303111-242303132 | GCTTTGAAAGTGAAAGTGACA | - | 6.37 | IRF2 | MA0051.1 | chr2:242303115-242303133 | TGAAAGTGAAAGTGACAC | + | 6.34 | PRDM1 | MA0508.2 | chr2:242303120-242303130 | GTGAAAGTGA | - | 6.02 | ZNF263 | MA0528.1 | chr2:242302668-242302689 | CCCTCTTGCTTCCTCTCCTCC | - | 6.84 |
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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 |
GH02I241363 | chr2 | 242302561 | 242303678 |
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Enhancer Sequence | TGTATTTTAA AATGCATGGA TGTGGAGCTG TGGTTCTGGG AGGTGGAGGG AGCATACTCC 60 ATCTTGCCTC TCCCACTGTC TGTGGCTGTA AGACCTGGAC ATGTGCATGG AGCAGCTGTT 120 GAGGACTCCG ACAAGTAAAC GGTAACAGGC GGATGGGAGA GAAGGCCAGA ATTTGAAGCA 180 CCACTTTGCA CCAGTAGTGA GTTTCTTGTC TTCCCTTCAG CATCCCCTGC CCTGGACTCT 240 GGCTGTCCAA AACCTGAAGG CAGGTACCCA GTATGAACAG GGAGAGCTAC AGAGTAGTTT 300 TGTAGTTGGG CCCCAAGACA GAAAGTGGGA GAAAGCCATT ATTTTTTTCC CTCTTGCTTC 360 CTCTCCTCCA CTCAGCCCTG CAGTGGCAGG AGTGTGTGAA CACCTAAAAC TCTTAGGGAA 420 TGGGGAAAAC CCCAGTTGCC TTTTTATTCT CTTCCCTCCT GCAGCTCAGT CCCAGGCAAG 480 ATGCAGGCAC AAGAATAGCA TGGCTAAACG GAGTAATTAA AGCCGTAGGT TTCTGGTTGG 540 AGTCTGAAAA GGGGAGCCCA GGTCACTGGA AGGGATACTA GGGAGATTCC AGAGAGGGAA 600 TTGCTCAGGA AAGTGACCCC ATGAAGTTGT TAGTTAACTT ATAGGCTCAA CACTGAGCTA 660 TGCACGCGTG ATGTGAGCCA GAACAGGTTG CCAAAGACGG AACTCGGCTA TGGGATAGAC 720 CATCGCCTGG AAGGCAGGCT GGCCACCAAG CAAGTAGGGA CCGCAGGACA TTGCTGAGGA 780 GCACTGCAAA GGCTTTGAAA GTGAAAGTGA CACTGATACC ATGTTCTACA GAAGGCTGGT 840 CAGGACCTGG GGACTGAATC CAGCCAGGCC AGTGCCTGCT CAACAAAATA CCAGCATTCC 900 CCATAGGATT TAAACAAGAT CAAGAGTCTC TAAGAGTGTG ATGTTAAAAA TGTCCAGGAT 960 ACAATGCAAA ATTTACTCAG CATGTGAAGA ACCAGGAAAA TAACTCGTGA AAAAAGACAC 1020 AGGCTAAAGC TGAGGTGGTG CCTATGTTGG AATTATCTGA TAGACTGTGG TCTGCAGATT 1080 TGTGGCCTCC ATGAGCTTGA CCTCCTAGTG TTTATCCTGG GAGTATGTGA CTGATTTGGC 1140 AAAAGCACAT TGCAGATGTA ATGAAGGGTA CGAATCAACT AGCCTGGATT CGTTGTCTAG 1200 ATTATCCAGG TGGGCCTTAG GTAATTATAT GAGCCTTTAA AAGCAGGGAT CTTCCTCCAG 1260 CTGGTAGCAG ATGGGGAAGG CAGAGAGACT GGAAGTATAA GAAGTTTTCA ACGTAACATT 1320 TCTGGCATGG AAGATGGAAG GGGCCATGAG CCAAGGAATG AGAATGACAA ACAGCTGACA 1380 GCCAGCAAGA ACTAAGGACC TCAGTCCTCT ACCCACACAG ACTTGAATGA GCCTGTAAGT 1440 GTATTCTCCC CCAAGGAAAT CCACATAAGA CCCCAGGTCA GCTGACACCT TGACTTAGAC 1500 CTTTTGAGAC CCTAAGCAGA GAATTCTGGT GAGTTACATT ACACTCAAAC TTCTAACCCG 1560 TAGACACTGT 1570
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