Tag | Content |
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EnhancerAtlas ID | HS103-25880 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr9:102975580-102977020 |
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) |
ALX3 | MA0634.1 | chr9:102975663-102975673 | TTTAATTAGA | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 102976586 | 102976842 | chr9 | 102976036 | 102976466 |
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| Number: 2 | ID | Chromosome | Start | End |
GH09I100214 | chr9 | 102975499 | 102975593 | GH09I100213 | chr9 | 102975661 | 102976716 |
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Enhancer Sequence | ATCCATTTTA TAACCCCTGC TCACCTCTCT GATCTTACTT TTCACTTCCT CTTACAGTGC 60 ATTTCTTTTC TTTTTTCTTT TTTTTTAATT AGAGAAAGGG TCTCACTATG TGGCTCAGGC 120 TGGTTTCTAA CTCCTGGGCT CGAGTGATCT GCCCACCTTG GCCTCCCAAA GTGCTGGGAT 180 ACAGGCATGA GCCACCATTC CTGGCCCTTA CAATGCATTT CATATTACAA TGATATTGAA 240 TTATTTGCGG AGTTTGAGAT GAGATTTTAC CCTAAATATA AGCTAAGAAG TTAGTCTGTT 300 ACTGTTTCAT GGATGCTAAC AATAGATACG AGACTCCGCA GTCAGAGACA AAGTAGTTTA 360 CTACTCACAA CACAGCAAAA AGAATGAGCA CCACGTCTAT GCTTCCCTTG CCCCCAGAGA 420 ACATGTGGAA GTTGCAGAGG CTGCACACAG TGGGTTTTCA TCACAACTGA GGAACACCGA 480 ACTTCAGGAA TCTACCACTT TTATAGTAAG CACTTAGTAA GCCCAGAGGA AGACATTACC 540 TCATCTCTCC AGTTGCTTGT TGCAAACACA ACCCTGAAAA ATTACCTAAG TAAAGAGTGG 600 CCAAGACTTT GCATTCTTGG CATACCCAGT AAGAACGTTT AGGAATGCTT CAGGCCCATG 660 GTAGATTGAC TCTTCCAACA ACCCATCCCT CAGCCCAGCA TTGTCTTGAC ATGAGTATGC 720 CACTACATCA GCTACTTTTA TTTATCTTAC CAAGAGAGAC TAGGACCATC GCTTTAATTT 780 GTCTCATACA GCACTTACTT AACAAGACTC CAAGTAGCAG GATAAAAACA TCCTGTAATA 840 TTGGTATCAA CTATGTCCCT CAGTATCTTG GACTAAATCA ACTGTGAATA AGCCCCAGAG 900 GAGAAAGTAG ATCTTACTTT ATACAGCTAG GATGTAATCT AAGTCTGGTC TGTTATCTAT 960 TTTGACCCAT GCAAGGGAGT TTAGACTGAC ATGCTAATCT TTGGCCTCGT TGCAGATAGT 1020 TACAGGAGGC GCTAGATTAC AGGGGCCAAA AAGCAACCCC CAAGCTCAAA GGTGGAATAC 1080 ACCATGGCCT ACTCTTTCCT ACATACAAAC ATGTAGCCTA AAGAGGCTGA AATAAAGAGT 1140 CACTTTATTT CAGGATTTGT CATTAAACTT GGATCAACCA TTACATTGAT TTGTCTAAGC 1200 CACATGGGCA GTATCACTAA GTAGTTGTTA CTTCAGTTGC CATGCATGGC ATAATCCAAA 1260 GCTGCTCACA TGTCAGAAGA AGCATATGGA TTTGTGTACA TCAGATTAAA ATAAGGTTGT 1320 GCCAGTCCCT TTGCTTCCAT GTATACAACG GGGTCCACAT TCAGGAGCTG TCATTGATGG 1380 TATCAAGCAC AGCAAAAGAA TTAAGAACCA CCAATGCCCA TGTGAATTTT TCTGTTTCAT 1440
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