Tag | Content |
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EnhancerAtlas ID | HS193-10297 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr14:70367530-70368960 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MITF | MA0620.2 | chr14:70368792-70368810 | AATGGTCATGTGACTTAT | + | 6.32 | MITF | MA0620.2 | chr14:70368792-70368810 | AATGGTCATGTGACTTAT | - | 6.32 | SOX10 | MA0442.2 | chr14:70368434-70368445 | GTCTTTGTTTT | - | 6.14 |
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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 |
GH14I069901 | chr14 | 70367861 | 70369209 |
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Enhancer Sequence | TGTGCTTGCC ACAGCTGATT AAACTCATGG CCACATGCCA CAATGGCCTG GTCTAGCATG 60 ACCTTTAGTC ATGCCAGCCT GTAACTGGCC ATTATTAGCA AAATCTTATC CTCTTCTTCG 120 AGGACAGATT TTTCTTACCC TCTTCTTGTT TTTGGGTTGG AGCTGCTCCT TTACTGACAT 180 GAAATTGGGA ATCTCAACTG GGCAGCTGCA GTTCTAAAAA GATGATGTCC AATTCCATGG 240 AAGACCAAGT CTTAAGGGTC ACATGCAACT GCTATACCAT GTGATGAAAT TTAAAATGAG 300 AGATATCTTT TCTCAGCTCC TTCTCCCATA CTCAGGAGAT GTCCAGGAAG ATGAAGAGAA 360 GTGCTATAGC ATAAATTAGT AATAGTCCAT GAGGGTCCAA AGAGAAGGGC TGCTTGAATT 420 GTTAAGGTAC ATTTGCCCTC TGACCATCTT TGTTCAGGGC CTGAAGCACA GCTCTAACCA 480 GGAGGTGCAT TTTGACTCAT TTCCTCACTC CTTTGTTCAG CCTTTGACTC ATTCATTCAC 540 TTGTTGTGGA TATCCTAATT TCTGCAGTTT AAACTGTAAA TATTCTTGGG GATGGAACTA 600 TCTGAGGTGG TCTGGGAATT ATTAATTTAC TGATGGCACA CATCTTCACA TTGTCCCTCA 660 GCCTTCATGT AGTTCTGGCC CAGTTGCTTC TAAGATTTTA TGAGTTGGCC TATAATGGGG 720 CTGTGGAAAG TAAGGGGGAT GTTGTGTTTG CATCTGTTCC AGAAAAAAAC TCTGAGTTAA 780 AAGTATTCTG ATTCCTATTA GGGTAGGACA TCTTAGGGAG GAATTTGACA AATGTCTGAG 840 AAAGAATATC TTTTGCCAGA TTGAAGAATT GTGCAAGTGC ATATTGCAAA AGGCTTTGTC 900 CTATGTCTTT GTTTTTCAAA TGCACAAGAA GCTGTTCAGT GGTGCACACA CCACCCCGCT 960 GGGAAACAGG GACTTGTCAG CTGGCAAAAT TCCATGATGC ATTGGGAGAG GGAAATTCAG 1020 TGCATTCTTT GGTGGCTCTT TGCCTTGTCA CCATCTTGAG ATGCCTATTG TAGGAAACAT 1080 CTGTTGTTTT GGTCTGCCCA GCCTCTACTC TGTCTTTTCT GGCAATAGAA TCTCTACTTT 1140 CCTTTGGGGA ACACCGTCCC TCACTCTACT CTTCATAACT TGAGTGGACT GATCCCACCT 1200 CCCAGTTCTA GGGTGAATGC ATGACCCAGG CCTGATCAGT GTATGCCCTC CTCTGGTTTA 1260 GGAATGGTCA TGTGACTTAT GCTGGACCAG TGGATTCAAT TTGGAGACTT TTTATTGAAA 1320 CTCTGGAGAA AGACAAGCCC TGGGGTTTGT ATGCTCTAAA GATGTAGGCC TGTAGTCATT 1380 GGTAGTTATT TGGTCACTAT GAAGGAAAAG CTTGCTTCAA AATAAATCCA 1430
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