Tag | Content |
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EnhancerAtlas ID | HS133-31603 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr9:34083980-34085580 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TBX21 | MA0690.1 | chr9:34084047-34084057 | TTCACACCTT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 34084140 | 34084483 | chr9 | 34084504 | 34085140 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I034083 | chr9 | 34083801 | 34087753 |
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Enhancer Sequence | GTCCACACCT CTCTTGGAGA GTGGAATCAT AAAAGAGCTC ACAACTCCAT CTCCATCTTG 60 AGTTCAGTTC ACACCTTTCT CTCCAGTGGT AGTATTCCTA TGTCTCACAT TTCTTTCATT 120 GGATTCTTCT TTGGAGGAGC TAAGGGCAGA ACCAAGCTAA GAAACCTGAG CAATTTATTG 180 TCTTCATCAC TGGTTTCAGA ATTAGCAGCC TATGTTTCCA TCCTCCCAAA CATTTCAGTT 240 ATCTCAGCAC ACTAGCGTGA AGAAAGATAT GAATGAACTA GCATGAAGCA AATAACACTG 300 AGTGATTCCT TCTCCTGTCC ACCCCCCACT CCTCATTGTT GTCTTCTAGA TACCAGCAAC 360 TGAAAAGCAG AACAAAAACA CTTGGATCGT AGGCTAACTC CTAAAAGATT GATCCCTGGT 420 GCTGATACAG GTATGGACAT CCTGACTTGC TATTTCTGGG TATCTGCACG AGGAATGGCA 480 GCTGGATCAG AGTGGCCTGG ACTGCGGGCA GTCTTTAGTT TTATTAGGAA CACAGGGCCA 540 GATCAATAAT CAATTAGAGT TGGCAGGGGA CCAGGGACTT GGAGCATAAA CAAGTCATGA 600 AGGGCTAAGA ATTCAGTTCA GCTACAAAGC CTCCTGTAGA AGGACCCAAA GGATGAGGAG 660 CCAGCAGACT ATTTGGAATA AGGCATGTGG CATGCGGCCT GAGACAGAAC AAGAAGTGCC 720 TGAGAGAGAA CAAGAAGTTC TTTCACAGAA GGGAGTAGGG ACTGCTGGCT AAAAAGGGAC 780 CCCATAAAGC CCACAAAGCC CTTCTGTGAT ACATGCTTTG CTGGAAAGTC TGGCTGGAAA 840 GTGGGAGCAA GGCCAAGATT CCATGGAGGC CAGAGGCCTA GACCAAGTCA ACCCCACATT 900 CCCTAAGTCA CCTTTCTTTG TGAGCATGTT CTATGGAACA AGTCCCATAG TAAAATACCA 960 AAAACCTAAG AGTTCAGTTG CACATGTGTA CCTTTTTCCT TTTATAAATA TTCATGACTC 1020 CTCCTATAGC TTATTAAATA CATATATTCA GCCACCTTGT TCAACATAAA TTCCTGTCCC 1080 CTTTGCCCCT CCCTCAGTTT GTGTTTCTGA CTTCTGGCCA GAGGCTGTAC TTCCCAGACT 1140 GTCAGAATGG CCACCCTGCA GACTGCAACC CTTTGAGAAA TAAAGCTCTC CTTTCCAATT 1200 TTTAAAAATA AAAAAACCTG ATGGTAAAGG AATGAAGCTG CTTTTGTTCT AATCTGCATT 1260 TCCCAAAAAT GATTTGACAA TATATTTTGT TTGGAGATGG AGTCTCACTC TGTTGCCCAG 1320 GCTGGAGTGT AGTGGCACAA TCTCGGCTCA CTGCAACCTC TGCCTCCCAG GTACAAGCAA 1380 TTCTCCTGCC TCAGCCTCCC AATAGCTGGG ATTACAGGCA CCCGCCAACA CGCCCAGCTA 1440 ATTTTTGTAT TTTTGGTAGA GATGGGGTTT CACCATGTTG GCTGGGCTGG TCTCAAACTC 1500 CTGACCTCAG GTGATCCACC CACCTGGGCC TCCCAAAGTG CTGGGATTAC AGGTGTGAGC 1560 CACTGCACCC GGCTGACAAT GAAGATTTTA CAAATACCTT 1600
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