Tag | Content |
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EnhancerAtlas ID | HS133-18544 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr20:5200260-5202640 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MIXL1 | MA0662.1 | chr20:5201988-5201998 | TCTAATTAAC | + | 6.02 | Nr5a2 | MA0505.1 | chr20:5202533-5202548 | CTTGACCTTGGACTT | - | 6.29 |
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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 |
GH20I005219 | chr20 | 5200632 | 5202242 |
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Enhancer Sequence | TATGAATTTT TCAGCAACCA TGCCAACTGG CCACCGTGAT CATTTCGCTC AAGCATTCTC 60 AGCCTAGGTG TTCTGGTCCT CTCTCATCTC CTGCCTCCAT CTGGCTGTAT GGACAAAAGG 120 GTGCCATCGA ATCCTCTGGG CTGTGGTTTC CGGTAAAATA ATGGGTTTGA ACTGGATGAT 180 TTGAGTCTCC CAGATCCGAA TTTTAGTCTC CCAAGTCTTT GATTTTTTTG TCGTCTAAAT 240 CTCTACCTTC ACATGGCCAA GCTTCAAACA GGCTATATTA TAAACGGGAC ATATTAGCAG 300 AGTAGTTAGT GATTCCCTTT GTGGAGTCCC TGTCTCCACT GCTTGTAGCA GAAGCCATCA 360 GTGACCAGCC TAAGCTCTTG AAACTGACTG TTCCAGGTCA CACCAACTGT ACTCCACTGT 420 GAGCTCCTGG GCCTTTGTGC TGGAGGGTTT TCTATCCACC AGGGATGGGC GGGCTGGAAG 480 GTGTGAGGAG TGTGTGTCCC TGGGAGTGGC CTTCAGCCAA TGATGTGTGA GAATTGGATA 540 AATAATCCAG CTCCTTTTCC CCTCTGGGGT GTAACTCCCA GGGGTGTTCT ACCCTGTCTC 600 CCAGAGTTAT CCCACACGAT TGAGCCCCAG TTGCCCAGGG TCCTGTCCTG CCCATTAACA 660 CTTCCTATCA TCCCTCTATT GCTCACTCCA CTACCCCTTC CCAGTGTTTC CTGGGATCAC 720 CTCCCTAATC ATCTACTTGT ACTCAAATCC CTGCCTTGGG CTCAACTTCT GGGGGACTCT 780 GACTTCTCCT GCTGACTTCT TCTCAGCAGG CACAGAGCCT GCTGCCTCCA GGCAGCTGAA 840 AGCACCTCAT GCATGTGCTT GTTGGGTTCT CTTTCTCTGT ATGGGCGGAG TACTGGCCTC 900 CACCCTCCCT TCCCATTGCT TCATATGTCC TTCTATGGGC TCCTCTTTCC CCTATATGGC 960 TAGGACCCAT TTCCTCCCAC TTCCCCTTCC ACAGTCTCCA CTTTTCCCCC AAGCCTCAGG 1020 AAGCAATGCC AACATTACTA TGCAGTGCAG TTTAACTCTT CTTTATCCTT ACCTCTCTCA 1080 CCTAAGCTAT TCACATGGGG ATCTTCACCT TCTTGACCAG CCCCACCCTT CAGGACTCTA 1140 AGATAAGCAA AACAATAGGT CTCCCCTGCA CATGTGCCTC CTTCTCTGGG TTTGAGCTAC 1200 TGCACAAACT GTAAGTAGTT AAAAAATGTG TTTTCCTTGT CACGTTGGAC TCTGTGAGCT 1260 CAAAGTCTAC CCCGAAGGCT TCATACCACA GCTGGAAATT GCGTTTTATT CACAAAGCAT 1320 CCAGGATATG ACGCATTTCA TATCCACATG AATGACAACG AGCAAAGAAA CAGACAAATT 1380 GTACGAAAGA ATAATGTTCC TTCTTCCTGG AAATTTTCTA AAAGGGATAG GATGAGAACT 1440 CTGGGTCTTA TTATTTTAAA AAAATGCCAT ACAGCCTCAA ATTGCCCATC AACCTCAAGC 1500 ACACACTTGA ATGTATAATT TTTCTTGAAT ATCCAGCGTA TAAATATTAG CTTCCATGTC 1560 CTTGACTAGA GTAATAGCAT GGACAGACTG TGGAAAGGCT GAACTGCCTG CCTGGAGGCA 1620 AGTTGTGTTT GAAATAAATA ATGCATTTCA TAATCCCATG TGACATCATG TTCTATGGAG 1680 CCTTGAGAGA TGTAATCTAC TACCATTACT CCACGCTCCT CAAGCATTTC TAATTAACTC 1740 AAGAACTGTG GGCCCTGTGT GGAGCTGAGG ACGTAGAAGA ATCGGTGGGG GACAGGGGGG 1800 ATATGGGGGA GAAGGACAAA CCAGAAAGGT TTTTGCCTTC CTTCTCAGTC CTCATCTTTG 1860 CCTTGGCCAT TGCAGTCCAA CTCTTTGCCT CAAAGATAAG GAAACAAAAC AAAACAGCTA 1920 ATTGTAAATC TATCCACCTA AACATCTAAC CCTGGTGCTA TGGTTTGAAT GTTTGTCTTC 1980 TCCAAAACTC ATGTTGACAT TTAACCCCCA ATGTGGCAGT ATTGAGAGGT GGGGTCTTTA 2040 AGAGGTGGTT GGGTCATGAG GGCTCAGCCC TCATGAATGG ATTAATGCAT TCATGAATAG 2100 AGGGTTAACA CATCAATGAG TTATCATGGG AGTGGGACTG GTGGCTTTAT AAGAAGAGGA 2160 AGAGAGACCT GGGCTAGCAC ACTCAGCTCC TCACCATGTG ATGCCCTGAG CCACCTCAGG 2220 ACTCTGCAGA GTCCCCACTA GCAAAGCAAG AAGGCCCTCA CCATATGCAC CCCCTTGACC 2280 TTGGACTTCT CAGCTTCCAT AACTGTTGGA AATAAATTCC TTTTCTTTAT AACGTACCCA 2340 GTTTCAGATA TTCTTTTCCA AACAACAGAA AATGGACTAA 2380
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