Tag | Content |
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EnhancerAtlas ID | HS133-18962 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr20:34604850-34607010 |
Target genes | Number: 17 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Stat4 | MA0518.1 | chr20:34606257-34606271 | TGATTTCCTAGAAG | - | 6.24 |
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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 |
GH20I036017 | chr20 | 34604983 | 34606470 |
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Enhancer Sequence | TTTGCCTATG ATCCCAGCTA CTTGGGAGGG TGGGGTGGGA GGATTGCTTG ACCCTGTGAA 60 GTCGAGGCTG CAGTGAGCCA TGATTGTGTT ACTGTACTTC AATCTGAACA ATAGAATGAG 120 AGCCTGTCTC AAAAAAAAAA AAAAAAAAAT GCAGTTGTGG GAGCGAGGGC AGTATGGATG 180 ACCACGCTTG GCTATGAGCT GATCACTATG GAAGCTGGGT GGCAGGTGCC AGAGCTGAAT 240 GAGAGGAGGA GGAGCAGTGT GCGGGTGCAG AGGTAGGGCA GGAGAAGGGA TTTCAGGAGG 300 AGCAATGGGC CTTCGGCCTC CCTGTGCCTG CAGAGGGCTG TCTCCTGAAG CCTCATGTGT 360 GGTTATTCAG CATCTGGGAA ACTGTTCCCT CACCAAGCCC TCTCCTCTGT TCCTCTGTCA 420 CTATCTCCAA GGTTGTCCTT ATGCCATTCT CCCCCTGTGT TATGGTGGAC TGTGCATGCT 480 CCTTCCCTCC ACTCACACCA GCCTGTATGT CCTCAGGGCT GGGAAGGTCA GTCCAGTACT 540 GTCTGGGAGG TCCAGTCCCT AGCACAGCCC TCTGTCAATG CTGATTATTT TTTAGCTCTT 600 AGAAATTTCT TCCTTTTGTT TAGTAAAACA TTGCCTCCTA CAACTTTAAA CTAGCTCCTC 660 TCCTCTCCCT GCCCTGTTCC CCAAAACAGA AGAAATCCAC TTCCTTAGCA TGTGATGCCC 720 TTAGGTATTT AAAGAATGCT GTTTTGTTTT TCATTCAACA TTTATGTAGC CAGGCACAGT 780 GCCAGTGTTC CGTTAATTAT TTTCATATTC ACGCAGAGTG GCCTCCATTC CTTCGGTCAT 840 TCTTCAAGGG GCGTAATTTC CAGCCTTCCA GCCTATTGCT CCTCCTGGAA AGCCCTTCTG 900 CCTGCCCCAC CTCTGCGCCC ACACACCGCT CCTCCTGCCA CTCAGCTCTG TCACCTGCCT 960 CCCAGCCTCC ATAGTGATCA GCTCACAGCC AAGCGTGGTC ACCCACACTC CCCCTGCCCC 1020 CACTACTGGA TTCATTGTTT TAGTGGTCTT ATTTTTTAGA ACAGTTTTTA GATTTACAGA 1080 AAAATTGAGA AGATAGTACA GAGAGTCCCC ATATGCCCCA CGCCCAGTTT CCCCTGTTAT 1140 TAACATCTTA CATTTATACG TCTTTGTTAG AGTTAGTGAA GGTGGTGTCT GCTTCACTTC 1200 AATTTATTAA TGTTTCAGAG TAAGGTGCTC AGAGATGAAC ACAGGGCACT AAGGGACAGG 1260 GAGGCCTGGG CAGGATGGAG GCACGAGGAT GGAAAAGGCC TTGCTCAGTT TGGTAGGCAG 1320 TGACAGGAGG GGAGGCTGTG TCAGGAACAG GAACAACAGG GTCTGTTTTG TCCAGGCCCT 1380 GCAATGCTGG AACAGGGAGT AAGGCCTTGA TTTCCTAGAA GTCCTGGAAG GCTTTGGGTG 1440 GGGACTTAGC ACAAGGACCT GGCTGCTGCT TCCCACATAG GGCCAGCACA TAGAAAGCCT 1500 TCAACAAATA TTTGTTAACA TGACCCCTTT GAAGAAAATG TCTGCGGATG CCTTCGTGAG 1560 GTGCCTGTGG TAGGACTCTG AGCTCCCTGT GTTGAGGCCC TGGCTTCAGC TGTAGGAGAA 1620 TGAGAGTGGT AACTGCTTGA CTGAACCCGC CCCCTGGAAG GTGGGTCACA TCGTCCTCAC 1680 CCTTGGGAGT AGCAGTGTGG AGCTGGGTCA GCCCTGGGAG CAGCAGAGGG TGGGGCCTAG 1740 GGTGGAGGGA CCCAGGTTTT GAGCCAGGAG ATATAGGAAG TCCAACTTCT CCAAGGAACA 1800 GGCAGGCTGA GGCCTCTGAG GTGGTCAAGA CTGGGCAGGC CAGAGCCATG GGCAGCGCAG 1860 AAGAGAGGTG GCAAGCAGCA TTTCTTATTT TCATTCTGCT TCTAATAGTT AGCTGTGTGG 1920 CCACGGGCAA ATCACTTTCC CTTTCTGAAT CTATGTCATG GGAAAATGAG GAGATTCATC 1980 TGGGTGAGCT GCCACCTCTA AAGTTGTGTG GCTCCATTTG GGTCACTCAT TCAGCAGATA 2040 TTCCTTGAGC ACCTACCATG CTCCAAGCAT GGAACAAAGT GCCATTGTGG CTGAGTAGAC 2100 TGACGTAATT CCTGCCCTTA TGGGGCTTAT GATCTAGTCA GGACAGACAA CAAACAGATA 2160
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