Tag | Content |
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EnhancerAtlas ID | HS133-04516 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr10:64875170-64876500 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr10:64875211-64875221 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr10:64875211-64875221 | GGCACGTGCC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr10:64875288-64875303 | TGATCTCTTGACCTT | - | 6.93 |
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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 |
GH10I063113 | chr10 | 64873341 | 64876466 |
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Enhancer Sequence | GCGATTCTCC TGCCTCAGCC TCCTGAGAAG CTGGGACTAC AGGCACGTGC CATCACGCCC 60 AGCTAATTTT TGTATTTTTA GTAGAGACAG GGTTTCACCA TGTTGGCCAG GATGGTCTTG 120 ATCTCTTGAC CTTGTGATCC ACCTGCCTTG GCCTCCCAAG TGCTGGGATT ACAGGTGTGA 180 GCCACAGCAC CCAGCTGAAG TTATATTTTA TAGATAGAAA AAAGGCAGCA CTACTGGTGC 240 ACCAGAAGCT GAGTGGTCCA AGGACATTAG GATTCTGGAG GGTTCGCTTC AGCTTCCTTT 300 TTTGAGAAAC ACTAACTTAG TACAAAGTCG ATTGAATCAT TGCCTTTCTG CATTTATTTG 360 ACTGCCGTTT CCCAAATGTC AGCTTACTGA ATAAAAAACT ACCCTGAAAT TCTGCTTTCC 420 TTGGACTCTC CTCTATTGAA CTTGGTTGAA TAGAATGCCT GACTCCTGCC TAACTTGGCT 480 TTGTTCACCC TGGCTCAGGC TGAAGCAACT GGACAAGTTG GCTCAGAGTC CGAGGAGTTA 540 GAGCCTGCTG ACCTCACAGC TACCCTCCCC CTTCTCACAT GGCCAGTTCC TGCCCAGTCT 600 AGTTTGTGAA TAGTTCTTGG AAAATACCCT GGAGGAGAAT AGAGTCACTA ACAATAGCGA 660 CTCTCTTTTT AGCCTGAACC TCTTAGTACT CAGGACTGTG AACCTAGGAA AACCAAAAAT 720 AACAAATGTA ATTGCAGTGG GTTACCCTCT ATTTCTATTA TTACCAACAT CCAGTCATTC 780 TGGTAGATAT TTAGCTGCTT GTCGTGGAAA AATAACTGGG TTTATAACCA GACAGAGCTA 840 GATTCAAGAC CTAGCTCAGC CATTTATTAA TTTTATGACA TTGGACAAGT CCCTAATTTG 900 AGCCCGTTAG AATTGAAAGA GGGAATGTAC ATGTAAGTGC TTGGAAACGT GCAAAGTATT 960 ATACAGTACA AAGTCAAACC ATTAATATTG GGAAATAGGG ATAATTTGAA AGTTTCAGGA 1020 AACAGAATAA TTTAATTGTT CAAAAAACAC TTGAATCAGC CCGAAGCAAA ATGGGGCTTA 1080 CTAGTCAACA CCAGTCTTAA AAATAAACAA CTAAACTATA CTGTAGTTAG TTTCTGTTTA 1140 AAGTTAAAGG CAGTCTTCCC TTTTGTTCAT GATGAAGTTG GAAATGGGGA AGGACTTATC 1200 AGATCCTTTC ATATCAGGGA ATGACGCAGA AGGATGATGG GCCCTCACAC CTATTAAGTA 1260 CAGGAAAGAT GGCCATTGCT TACATGCTGG CTCTGCTGGC AAACTGTTTT TTTTTTTTTT 1320 TTCTCTGAAG 1330
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