Tag | Content |
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EnhancerAtlas ID | HS098-04165 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:180529220-180531330 |
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 | chr1:180530861-180530871 | TTTAATTAGA | - | 6.02 |
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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 |
GH01I180560 | chr1 | 180530065 | 180530884 |
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Enhancer Sequence | ACAGAGGAAA AAAGTGAGGC TTAGAGAGGG TAAGTTGACA AGAATTAGTA AGTGGCAGAA 60 ATGGAATCAA AATGCTATTT TGTCTCCCCA AGATATGAGC TGAGGGAGCA AAACAAAATA 120 AGAATGTAAG GGCATCCAGG GTGGAGGTGA AAGGGATCAA GAGAATGAGG GTGAGGCACA 180 GAGATAAAGT AGGTGATATC GAGGAGTTCA GAAAATGAAG CCCACAAGCA CTCGATATAA 240 GAACTGTGTA TCTCTTCAGA GCAAGGGCAG TTCCTGGGAG GCACTGTGCC AGCCAGGAGG 300 TAGTTAGAAT CTACAGGAAT GCGAGGTCAT AGAACCAGGA TCATACAAAG TCTAGAGTGC 360 ACAGGGCATT ACCCTACTGT TTAGCTGTTC CTCCTAGGGT GTCTCAAAAA GAGCAGATAC 420 ACTAGAAGTT ATATTTAGAG ATACCTGGCA TTTGGATTTT TAGCTGTACC TCAGAGTTCC 480 AAAGAAATAA AGATATGTCT CTTCTCTGGC CCAGCAATTA CTGAAATGGT TTTATTTTAT 540 AGATCTACAT AGTTCACATA CATTAGAAAT GACTTTGTAT AACCTACACC TTTACTGGCT 600 AAGTTAGCAG AGAGAACATT CAGCCCACTA AATGTTCAGC AGTATTTACT TAGTTTACAA 660 GCTGTTGCAA CTTTGCCCTC CAACAAATTA TGTTAGTACT AACCTAACAG CTTATAAAAT 720 AATACTTCTA TAGTTAGTAA CTTACATAGT AATCAAACTC CTTTTAGAAG TGTATAGTTT 780 TTGGCAAATT AAATTATGTT TAAATATCTG CTGAATTCAA CTTGTTCTAG GAATACCAAA 840 GAACGCCACG CTTACATTTT TTAAAGGTTT TATATGGTAA GTCATCTTAG GGTAGGGAAA 900 ATCTGAATTG GCCTTTCTAT TTTCAGTCCT ACGGTGGGGC TTGAGTCACT GCATTCCAGG 960 CTCAGTGAAT TAGTGATAAT AGAAAAGGGC ACAAAAAGGC TATCAGGAAC CAGGGTTATC 1020 TGGTATATTT GCTCTGCTCT TCCCTGGCAC CTCTCAGTTG CTCCTGCCTG AGCATGCTCC 1080 TCTTTTCCAT CTGTGTTGTT TTTTACCCCA GCATACTGTT GGAAGGGTTG CTCGAAGGCA 1140 TTTGACTGAA GGGTACTTGG AAAGACCAAA CCCAAACCAC AGTAGTGACC AGATACTTAG 1200 TGGCAGCCCC AGCTGCAGTT ATGGCAAGAA GTGGCCAAGG AGGGGAATCA CCATGACCAC 1260 AGAGGATGCA GTGGGCATTA GGGACCTGGC ATTTGCTGTC AGAACAATCC AGTCAGGGTA 1320 ACAGGTGGTG TTGCAGGAGA TGGGTGGAGC ACACAGCAGG GATTTGGGGA ACAGGAGATC 1380 CATGGATATC TACACATGCT GACAGCTCTC AGCATCGGGT TATCTGGCAG CTCAGAGCAG 1440 TTGCTTTGCC TGGAGTGGTT GGGTACTCAG CCTGGCTGAG GCTTGTCTGG GAGAACTTTC 1500 TCTGTCATTG TTCATCTTGA TCTGTGAGAA GCTGTAGGTG CCCCTAAGGC TCAGTGGGAA 1560 GATAAAACCC CAACAAGTTG GTCTGGAAAA TCGAAGACCA GCAAGTGGGT ATGGTCATAA 1620 TAATTTTAAT TTTATTTTTT TTTTAATTAG AGTTCTGGCC AGGTGCAGCG GCTCACGCCT 1680 GTAATCCTAG CACTTTGGGA GGCAGAGGCT GGCAGATAAC CTGAGGTCAG GAGTTTGAGA 1740 TCAGCCTGGC CAAAGTGGTG AAATCCTATC TCTACTAATA ATACAAAAAA TAGCCGGACA 1800 TGATGGTGAG CACCTGTAAT CCCAGCTACT TGAGAGGCTG AGGCAAGAGA ATTGCTTGAA 1860 CTAGGGATGC TGAGGTTGCA GTGAGCTGAG ATTGCACCAC TGCACTCCAG CCTGGGCGAG 1920 AAGAGTGAAA CTCCATCTCA AAAAAAAAAA AAAATAGAGT TCGCTTTTCC TTTTTGGCCT 1980 TCCTAGACTG CGCAGGTGTC AGCAGGAGGA CCAGCCATCC ACTTTGGCTA TGGCAGCAAG 2040 GCTTTCTGGT CAGTCTGGAA ATCAGTAGGT ATGGAGATTG GCTTGCAAGT ACTCATCAGA 2100 GCTCCTATTT 2110
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