Tag | Content |
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EnhancerAtlas ID | HS133-11069 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr16:18057470-18059890 |
Target genes | |
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) |
Atoh1 | MA0461.2 | chr16:18059658-18059668 | AACATATGTT | + | 6.02 | Atoh1 | MA0461.2 | chr16:18059658-18059668 | AACATATGTT | - | 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 |
GH16I017964 | chr16 | 18058201 | 18058350 |
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Enhancer Sequence | GGTTTCCTAA AGGATGGGGA AGTGAAAATA TTCACTTTGT ACCACAGAAA ATGAAGAAAG 60 TGCCCAACCG TGCTCTGAAA GGCCTCAAGA CTTAGCTTCC AGTTTTGTAC ATCACTTCTA 120 GCGTATCGTC TTAGAGAGGG CAGTCAAGAC ACGTATATTT CAGCATTTTT CTTTTTTCAA 180 GACAGAGTCT CACTCTGTCA CCCAGACTGG AGTGCAGTGG TGTGATTTTG GCTCACTGCA 240 ACCTTTGCCT CCCAGGTTCA AGTGATTCTC CTGTCTCAGC CTCCTGAGTA GCTGAGACTA 300 CAGGCATGCA CAACCATGCC CGGCTAATTT TTGTATATTT AGTAGATATG GGGTCTCACT 360 GTGTTGGCTA GACTGGTCTC AAACTCTTGA CCTCAGGAGA TCCACCCGCC TCAGCCTCCC 420 AAAGTGCTGG GATTACAGGC GTGAGCCACC TCACCTGGCC AGCATTTGTT TCTTTTGACT 480 TCAGGTCCTC TCTGAGGACC AAAGAGCCTT CCTCTTGCCA CTCAGCACTT CCTCTAGCGC 540 CTCCAGGAGC TGGGGCATGA GGAGGATCTG TCATGAAACT CTATGGTCTA AGTTGGCCAG 600 GCTTGCACAT TGGTATGCGA AAAGGCCTTT TGGAATTTAG AAAGGGCAAA CAAATGCAGA 660 AGCATTTATC TTGTAATAAA GTTTGGCTTT AAAGATAATT GTCTTGCCAT TTCCTGGAGA 720 AAAAAAAATA AGTCATCTTT GAAACTCAAC ATTGAATGAT GAGCTTTGTT CCATTCCATA 780 GCGTCCTCTC CTTCCCTAGG GCAATGTCTC ATGGCTTAGC TTTTGTAACA CAAGGAGTGC 840 CGAGAAGAAA GAAACTGGCT GTTAAGGGAG TAATTAATCA CCAAGAGGTA TTTCAAAAAC 900 ATTAAACCTA TCATATTTGT TGTGTGTACA GTTTGTACAT ATGTGTGTGT TTGTGTGTAT 960 TTGTACACAA ATGGTCCATG TTCTACACCA TGGGTTTCCA AACTATGCCC CACAGTCCAA 1020 GTCCAGCCTG CCTCCTATTT TTTGTTGTTG TTATTTTAGT GTGTTTTACA ATTTTTTTAA 1080 ATTGTGTTGA AATACACATA ACAGGCTGGG CATGGTGGCT CAGGCTGTAA ACCCAGCACT 1140 TTGGGAGGCC GAGGCAGGTG GATCACGAGG TCAACAGTTG GAGACCAGCC TGGCCAACAT 1200 GGTGAAACCC CATCTCTACT AAAAATACAA AAATTAGCCA GGCATAGTGC TGTGCACCCT 1260 GTAATCCCAG GTACTTGGGA GGCTGAGGCA GGAGAATTGC TTGAACCCGG GAAGCAGAGG 1320 TTGCAGTGAC GTGAGATCAT GCCACTGTAC TCCAGCCCGG GTGACAGAGC AGGACTCCAT 1380 CTTGGGAAAA AAAAACACAC ACACACACAC AACATAAAAT TTACCATCTA AGTCATTTTA 1440 AGTGTACAGT TCAGTGTCTT TAAACACACT CATAATGTTG TACAACCATC ACCACCATCC 1500 AACTCTGCAA TTCTTTTCCT CTTGTAAAAC TGAAACTCCA TACCCATTAA ACAACTCCCC 1560 ATTTTCCCCT TCCCTCAAGC CCAACAACCA CCATTCTATT GTCTCTATGA ATTTGAATAT 1620 AAGTACCTCA TACAAATAGA ATCGTACAGT GTTTGTCTTT TGTGACTCGC TTGTTTCACA 1680 TGGCATAATA TCCTCAAAAT TCATCCATGT TGTAATGTAT GTCAGGATTT CCTAAGGCTG 1740 AACAATAGCC TATTATACAT ACGTACGTAG CACATCTTGC TTATTCATCC ATCAGTGGAT 1800 GCTCTCACAT TTTAGCTATT GTGAATAAGG TTGCCACGGA AGTCGATGTA AAAATAATCC 1860 CTTTGAGACC CTGCTTTCAT TTAATTATTT TTTGGTATGG CTAGCAAGCC GAGAATGATT 1920 TTTACATTTT CAGATGATTG AGGGGAGGGG GAACAAAAGA AGAAGAGTAT TTGGTGACAT 1980 ATGAACAACT TTTGAAATTC CAAGTTCAAT ATGTATGAAG TTTTATTGGA ACACAGCCAT 2040 ATGAATTCCT TTGTGTGTCG TCCATCGTTG CTTTCACACA CGAGAAAAGA AACCATACAG 2100 ACCACAAAGC CTCTTACTAT CTGGTCTTTT AAGAAAAAGT TTGCCAACCC CTTTTGTATA 2160 CTGGTTGGCA CTTTGTTTTT TTATCTTAAA CATATGTTGG AGATCATTTC ATATCATACT 2220 CCTCCTACTT GAGTCTACTT CTTTCAAAAA GGTTGTTTCA GAAATTTGCT GTTACAAACA 2280 ACACCATAAT GAATATTCTA AGACATCTAG CCTTCTATAT ATAACATGTC TCTCTCTGAA 2340 CCTCCCATCC CCTACATACA CACAGACACA GACACACAGA CACACACAGA GACAACCATG 2400 AGCCCCTTGA AAACAGTGAC 2420
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