Tag | Content |
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EnhancerAtlas ID | HS196-15788 |
Organism | Homo sapiens |
Tissue/cell | ZR75-1 |
Coordinate | chr2:160105730-160107220 |
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) |
IRF1 | MA0050.2 | chr2:160106423-160106444 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 160105959 | 160107201 | chr2 | 160106082 | 160106269 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I159248 | chr2 | 160105445 | 160107579 |
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Enhancer Sequence | TTAAACTTAA TGAAACTGGA TATATTTGCT GATTCTTGTA AGAAACACAA TCACAAATAA 60 AGCTCATCTG TTTGTCCAAA CCATAAACAG TTTCACTTGT TTTTATTCTT AACTTTAAAA 120 GATTTTTAGT TTTAGAAAGT CTAATGAATT TTAGGAATTT TAGAATTATT GGCTGTTTAC 180 ACTTTTAGAA CTAGTTGACA GTTCTACTTT AGGTTGAAGT GGGTAGAAGA ATTAGATTTC 240 AGAATGCCTT ACAGTTACTA GAAAAAGCCA AACCAACTTT CTTTCTGTTG GGAGGTAATG 300 CTCCATGAGG TTTATACATG TCTTAGGACA CCCTGTGTTT CAGACAGTCT TCTTGAGGAT 360 GTCTGAAAAC ATCCTTGGAA GCTAGAGATA GTGCGTCCCT CCCTGTGGGA GGGCAGATGT 420 TTCCTGACTA CTATAATGTC TTGCCTCTTG GGGGCTATTT GCTTAGCCCC CTCATAAGAC 480 TGGGGGTTTC CCAAGCTCAG GGCTCCTCAG CTGTGACATA AACATAAACC ACCACCATGA 540 AACTTACTTA AGAGGGAAAG GGGAGGCTGG GTACAGTGGC TCATGCCTGT AACCCCAGCA 600 CTTTGGGAGG ATTAGGCAGG TGGATCACTT GAGGTCAGAA TTTCAAGACC AGCCTGGCCA 660 ACATGGCAAA ACCCCATCTC TATTAAAAAT ACAAAAAAAA AAAAGAAAGA AAGAAAAAAA 720 ATAGCTGGAT GTGTTGGCAC ATGCCTGTAA TCCCAGCTAC TCGGGAGGCT AAGGCAGGAA 780 CTTCACTTGA ACCCAGGAGG CGGAGGTTGC AGTGAGCTGA GATGGCGCCA CTGCATTCCA 840 GCCTGGGCGA CACAGTGAGA CTCTGCCTCA AAAAAAAAAA AAAAAAAAGA AGGGAAGGGA 900 AAACAATCAG AACCTGAAGT GCAAGTGTCT GCTGTGTCAC GAGTAATAAA CCGTTTGAGT 960 CAGTCAGGGC TCATTGCCCA CATTCATGTG AATGTGGCAA GTTACCCTAG CAGCTTCCTG 1020 CCACCAAAGG GCTGCTTTCC TCTGACTTCC TTCCAATGGG ATATGCTGAA ATGAAACTGA 1080 GGATTTTTAA AACAATTTTT TTTAAAGTGT CACAAACAAA TCAATGATTT CTTTACATGT 1140 TGAATATGAT TTTGCAAAAA TATTTATAAC TTAAAAAGAT TCCCTCAAAT TCTTTATGAA 1200 ATCACCATCC AGTTTCAAGA GAAAGCTATT TCAACACAAA GTACTCAAAA GTGCTTAGTT 1260 AGGGAAGTAC CTCTAAAATG CAGCACAGTG TTAGCTGATC ACCACAGCCA GCCTTGAATG 1320 TAACAAATCA GAGAATGGTC ATGACAGTTT ATCGAGTCCA CCTCTTCCCA GAATGTCCCA 1380 TTCACAATGC TGTGTTTTCC AAGGGTTAGC TGAGCTGTAT TTTTATTTTG CCAGGCAAAT 1440 ACAGTGGAAG GTTTACGAGG AGTTATAATG ATGGATCATG TATTCTAAGC 1490
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