Tag | Content |
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EnhancerAtlas ID | HS105-46415 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:176097360-176098990 |
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 | chr2:176097814-176097835 | AAAAAAAAAGAAAAAGTAATT | - | 6.22 |
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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: 2 | ID | Chromosome | Start | End |
GH02I175233 | chr2 | 176097961 | 176098090 | GH02I175234 | chr2 | 176098221 | 176098370 |
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Enhancer Sequence | GTTAGCCAGG ATGGTGTCGA TCCCCTGACC TTGTGATCTG CCCACCTTGG CCTCCCAAAG 60 TGCTGGGATT ACAGGTGTGA GCCACCACGC CTGGCCAAAT CAATGTCATT TAAAGCAATA 120 TCCAACACCA TCTAATTAGC ATTCCTGAAT TATAAAATAA ATTGGCCAGG TACAGTGGCT 180 CACACCAGTA ATCCCAGCAC TTTGGGATGC TGAGGCGGGC AGATAACCTG AGTTCAGGAG 240 TTTGAGACCA GCCTGGCCAA CATGTTGAAA CTCCATCCCT ACTAAAAATA CAAAAATTAG 300 CCAGGCATGG TGGCGGGTGC CTGTAGTACC AGCTATTTGG GAGGCTCAGG CAGGAGAATT 360 GCTTGAAGCC GGGAGGCGGA GGTTGCAGTG AGCAGAGATT GTGTCATTGC ACTCCAGCCT 420 GGGCGACAAG AGCAAGACTT CATCTCAAGA AAAAAAAAAA AAAGAAAAAG TAATTATTTA 480 AGTAGAAATA ACATGTGATG CCATATTTCA AAGGCCTAGA GCAGAGGTTG GCAAACGCTT 540 TCTGTAAAAC ATTTACAGAT AGTAAATATT TTAGGTTTTG TAGATCATAC AGTCTTTGTT 600 GAAATTACTC AACGATGCCA TTATAAAGTG AAGGCAGCCA TAAATTATAC GCAAAAGAAT 660 GAGCATGAAT ATGTTCCAAT AGAACTTTAT TTACAAAACA AGGCAGTGGG CTGAATTTGG 720 CCTTCAGGCT GTGGTTCTCT GACCCTGGCT AAGGGTCCTG TATTTTATAG ATTTTAAGTA 780 ATGTTTGTAT ATATAAAGTG ATGCTTGCTT TAAAAATGCT TACTTTAAAA ATGCAGATAA 840 TCTTTTGTTT GGTTAGTTTT ATTTTTCTTT TAAATAGCCC TTACATATTT AACTAAAGTG 900 AATGTAAATA TAAGTGACAG GGTAGTTCTA GAGATATGTA TGTGGTCTGG CAAGAGTTCA 960 TATAATATGA CTCATCTCAG TTACCTCATC TGTAAAATGG CATACGACAT AATCCTTATT 1020 TAATTGCTAT TTCCAAACTA GTGAACTTGG GGATGATAGT AGGATGCACT AAAGACATGC 1080 CAGGCATACT ATTTATTTAG TGATGAGTTT GTTATATGTA TCTGCTTCTT TATTTTGTAC 1140 CTTGAGAATG CCAAGTTTCT ATGCCAGCCT CTTGTGTGGC CTTCTGTGAG TTATTTCTGC 1200 TCCTTTATCT GAATGATAAA GAATGATGCT TACCTGCATC TTATGGGTGT GGCATGGAAA 1260 TCTCTAGGGA TTTGCCAAAT GTCATCTAGC ACTTAAATGC CGTTGGAAAT TGGACATGTC 1320 CGCACACTTT AATTGTTGCG TACTGATGAC TACCAGGCCT CAGTCTTGTG GCTTTCCATC 1380 AGACAACCTG AGAAGGGAGA TAAAAACAAA AGAAAACTAA CAAAGCAGAA AAAGAAAGAT 1440 GATAAAAGGT AAGGATAATG GCTGAGTGGA TAATGGCAGG AGACATCTTT AGCTACCATG 1500 AAAAGTATTA AGCCAATGTG TTTGTTGAAT TCATTTTGCT GGTGGTCACT TTGTGTTCAT 1560 TCTGAACATC CAGCAGTTAG CTAAGTAAAG ACACATGACT GATGAAAGAA GAAAGGGAAC 1620 TATTTTTACA 1630
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