Tag | Content |
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EnhancerAtlas ID | HS133-07216 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:26390520-26393250 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYB | MA0502.1 | chr12:26392297-26392312 | ATGTCAGCCAATCAG | + | 6.03 | RARA(var.2) | MA0730.1 | chr12:26392894-26392911 | AGTTCATCTATAGGTCA | + | 6.14 | TFAP4 | MA0691.1 | chr12:26393015-26393025 | AACAGCTGAT | + | 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 |
GH12I026238 | chr12 | 26391098 | 26393585 |
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Enhancer Sequence | TGAAGTCTTC TGTTTAACAA GACTCTCTGA CTGAGGGATG AGGAAGCCTG GAGTCACTTT 60 TGTGGGACAA GGGCTGGTCC TTCCTCTCCC ACAGGAAAGC CTGCTGGAGA GGAAGGCAGG 120 GCCCAGAATG GGACTGAGAC CCACCTGGTG CTGCCAGGAA TTGTGGAGGA GACTTAGACA 180 ATACCCAACG AGGCAACTGA ACAAGGAGAG GTCAGTGGGC GCTTTAGAGA CCCCAAACCT 240 AGAGACTTTG GACAGCACCT CTCTCTAGGC AGGGTGCCTT GTTTACTCTG TTTGATTTCC 300 TACCCAGACA TTTCCCCCCA GAAATTCTCA CTGTGTTGTC TTTGCTTGGC CAGGTGTGAT 360 TGTAGAGAGC AGGAGGAGGA CTCTCAAGGA CCACAGGGGA CAGTGGCACT GTGACCAGAG 420 AAGATGAGAA TAATCTTGTG AAATCCACCC CCAAGTGGTC TCTCTACGTT TTCCTAGACA 480 TGTGTTTGTT AGAGCACGGT TACCCAGGGA GGGCCTGAAA GTGGTGCGCC AGCCATAGTG 540 AATTATCATA AGCAGAGGAA GCAGAGTCTG AAAATTATGT GATTAAAGCT GTCACTAACC 600 TCAGTGGATT AGTTTTCATT CTTTCACTCA GGTATTTTTA CAAAATAGAT AACGTTCCTT 660 CCTCAGATAC TTTTGCTCGC AAGAGTAGAC TTAATTTTTT ATTAATTTTT CCCTAGATTG 720 CAACAAAGTG ACAAAAGGAT GGTTATAAGA TTGTAAAAGG AGAGATCACT GCTTCATTTT 780 AATATGGGGA AGCTTAGGAC TTGGGACATT GAGCATGGCT ATTTAACCAG TGGCAGGGAA 840 TGTGCACTCT GGCAAATGCA GGGAGGAGTG ACATCATGAG TGTACTTGGT GGCTGGACAA 900 GGTGCCCACA AGTGAAAACG TGGATTCCAT TTGGCCTGGC TTGAATTACA AGTAAAAGCA 960 TTGCTCCTGG TACAATTCAC GCCCACCCAC CACTAGATTT TAATATTGTT CCAGACATTC 1020 CGGGAGAAAC TATTAGAAAG GCTCTCTCCA CCTGATTCAT CTCTCTGTCC CCTCCTGGGA 1080 TCCCTCTGCT CCTCCAGATA AGAAACTTCC TCCCCCAACC TTATTCCACA GCAAAATCTG 1140 CCCCTCCTTC ATTTCCTGTC CCATTTCTAT GGGACTCTAT TAAGATATTA TTGACTCAAG 1200 TGCTCATGCT GAATACAGAG ATTTCTTCAT AAATATGGTT TTCATTTTAA CAGGCTATTT 1260 CTAACAATCA GAAAAACTTT CAGATCCAGA GAAATGCGGC ACCCTGCCAA GGAGTGGAGA 1320 CCCACCCAGT CATCCTTCAA ACTCACCATG TAGGTGGCCA CCCACTCTGT CTGACCAGAA 1380 TTATCAGACT TTCAGGGCTC ATGGGACTTG GAGAACATGG ACCATCAGCC CCAGCCCTGG 1440 CTGTGGCTTG GAAACCTGTG TGGATCTGTG GCTAAACAGG TTGCTGGTTA CAACTCTGTG 1500 CTCAGACTGG TGGAAGGGAG GTATCCAGAA GAAGCTGGCA GGAAGGGATT TTTCCTCCCA 1560 TGATTTCAGA GGACATTTTA CTGTGGAAGA CAGGATGAGT GAAAGGGAAG AATTCATGCA 1620 GAACCTCTTT GCTCCCAGGG CCCGGCTCCC TAAGCATTCC TTGTGACAAC TCACCAAGGT 1680 TGACTGGCTT TGCTCAGACC CCTGAGCTTC TCTATTCATT CCACACAGAA CACCCTCAGA 1740 TACTGGCTGG GCTTCACAGT GCTGCCCAGA GGAGGACATG TCAGCCAATC AGCAGGAAAG 1800 ATGCTCATTT CTTGTTGAAA AAGTCCCAAA TTGTAACTTA ACAGGGTGAT CTCTCTCTCA 1860 CTCTCTCTCT CTCTTTTTTT TTTTAATTTC CAGAATGTGT TTTTCCCCTA GAGTCCTTGA 1920 GCACAGACCT GCGGTTTTCT CTCTCCTGGT TTTACAGTCT ATCTGCCTCA AGCCAAGAGA 1980 CTTGGCTCTG CTCCCCCCTG ACTCAGAGTC TCGGCTGGTA GCTGAACCCA GGAAGCCCTG 2040 GCCCCACGTC TCTCCCTGGA ACCACCAGAC CACACAGCCT CCTGTGCTCA ACCCTTTGGC 2100 TGGGTGTCCT GCCTCCTCTT TGTTTGGAAA GAGATGTCTT ACGTAACTCC ACAACCTTCT 2160 AAAGGCTCCA TTGTCTTCCA CTTGGGAGAG CTCAAAACAA CCCATTAGTG ACTTATGACT 2220 TATCACAAAG AGAATCTATT GCCCACATAT CCACAGCCCC CATGGAGCTA GCCTCACCTA 2280 TCTTACTTAG ATCAATAATC AACAATGAGA CTTAATGACT TGTGGTCTTT GGGAAATTAT 2340 AAGTTCAGTA CAAGGTGCAG GAAATACAAA GGCTAGTTCA TCTATAGGTC ACGGTACTTC 2400 GCCCAGGCAG CACATGAAAG TCATTTGTAA TTCAAGATTG AGACAGGCAT AAACAATTCT 2460 GATCTGATTA TTCTTTTACT AATCTGATTT TGATAAACAG CTGATGAAAA TGGAAGGTGT 2520 CTGGTCATCA GAGGAGAGAT ACTCAGGCAG TGAAATAAGT TTTCCTTATC TCACTGGATA 2580 GGGATTTATT TCAAGGCTCC TATTAATAGC CCCTAATGCC AAGAACTGTG ATCGCTGCCC 2640 TGGACTGCAA GAGCCTTCTG AGCAAAATGA CAGAAACCCA TTGGGTAGGG CATTCTCCTT 2700 CATTTTTATT TTCTATAAGT CTCTGATTAG 2730
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