Tag | Content |
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EnhancerAtlas ID | HS133-28863 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:77037720-77039520 |
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) |
FOXP1 | MA0481.2 | chr7:77038808-77038820 | AGGTAAACAGAA | + | 6.14 | Mecom | MA0029.1 | chr7:77038185-77038199 | AAGACAAGATAAAA | + | 7.52 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_09437 | chr7:77036479-77046770 | CD14 | SE_35338 | chr7:77035582-77041626 | HepG2 | SE_55764 | chr7:77036386-77044193 | u87 | SE_67674 | chr7:77036386-77044193 | u87 |
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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 |
GH07I077408 | chr7 | 77037519 | 77041619 |
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Enhancer Sequence | TTATCCAAAA TTATGGCCGG CACAGTGGCT CACGCCTGTA ATCCCAGCAC TTTGGAAGGC 60 TGAGGTAGAT GGATCACTTG AGGCCAGGAA TTCAAGAGCA GCCTGGTCAA CATGGTGAAA 120 CCCAATCTCT ACTAAAAAAT ACAGAAAATT AGCTGGGCAC GGTGGTGCAC ACCTGTAATC 180 CCAGCTACTC AGGAGGCTGA GACAGGAGAA TCACTTGAAC CCAGGAGGTG GAGGTTGCAA 240 TGAGCCGGGA TTGAGCCATT GCACTTCAGA CCAAGACTCT GCCTCCAAAA AAAAAAAAAA 300 AAAAAAAAAA GAAAAGATAA ATTGCTTAAA TTTGACTCAT TTTTCCCATA CAGGAATAGT 360 TTTTACATGT TAATTACATT GATTATGACA AATTCTAATA TTCAGACAAA ACATATGCAA 420 ACTATCTGTA ACTCAGCAAA TTTCTGTCTG TATTCCTAAA AGGAAAAGAC AAGATAAAAA 480 ATAAGGATAA TTGGTGAGCT GGACACCTGC ACTGGAGCTG GAGGTGGGAA ACATTTAGAG 540 AGAGGAAGAC CAGGTTTCAC TGAGAACTTA GACATCATCC TGAGATCTCT CTTCCCCACC 600 CCTCACAAGC AGCAGCTTAG TGGGTCTCCT AGGGGCAGGG CAAAGGGATA GGGCAAAGTG 660 TTTTCTATAC ATGGGTATAA ACGTTTGTCA GTATATTGAC ATGTATATGG AGCTGTCAGA 720 CTCACTTCAC ACTGAAGGAT AATAAGGATA ATAATTTGGT CTCTTAGGAG ACTAGGATTT 780 AAATAATCAG TTCATGGGCC AAGCATGATG ACTCACGCCT GTAATCTCAG CACTCTGGGA 840 GGCCAAGGTG GGAGGATGGC TTGAGCTCAG GAGTTCAAGA CCAACCTGGG CAACACAGCA 900 AAACCCTGTC TCTTAATAAT AATAATAAGC TTATGGCTAA GTAGGCCTTC ACAATTTAGA 960 GAGTTCTCAT TTCTATCTCA TCTGCATTGT ATAAGGTATT CCAGGCCTAC TATACTTTTC 1020 AATGAGATAA TGATACTTGA CCAATATACA GTGAAAAGGT GGCGTAGACT GAACTCAAAC 1080 CTAGAAAAAG GTAAACAGAA CAATGGACTG AGTGTTCTGT ATCAAGCTTA CAATGAGAAA 1140 ATGGGTAATT ACTCAAAAGT CCTTTGAAAG GCAGATATTG TAGACATCTA AAGAGAATTT 1200 CAGTGAGTTT GTTCATCCTG TACACGACTC AAAACTTCTG GAATGCAATG TGTCAATATT 1260 TTGAGAAGTA TTTTTTTTCT TTCAAGATTA TAAGTATGCG AGGAGAGATC GTCGCAAAAG 1320 TACAGTTAAA AGGTTTCGGC TAAGATAAGA ACTCCTTCAC AAGAAATCTT GCTAAATCCA 1380 ATTTACTTGC AAAAGCGTAT CTATTTTCAG ATTACTATAA TACTAAGAGA AAAAATTCTC 1440 CAACAAACGC AGATTACAAT AAATGACACA TTTTTATCCC ATTAAACTAG TGGTTCTCAA 1500 CTCTGGCTGT CTTAAAATCA TTAAGGGAGC TTTTAAAAGA ACACTGATGC CCCAAGCCAT 1560 ACCCAGGATA TTCTGATTTT ATTGAGCTGG TGTGGAGCCC ACTCTCTGGT GTACATGTAT 1620 GTGTTTTAGA TTCCCTGGGT GATTCTAATG TACAGCCAGG GTTAAGAACC ATTGAACTAC 1680 AAATGTACAT TACATATTAA GCAATATTTG TTAGAGGGCA TAACTTGGAC CATCTTATAA 1740 TATAACCATG GTAGACAGAG AGTTGAAAGA AATAAAAATA ATGTTTTCAT GGGAACATTA 1800
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