Tag | Content |
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EnhancerAtlas ID | HS105-24833 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr14:70367660-70368840 |
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 | TTTCTTACCC TCTTCTTGTT TTTGGGTTGG AGCTGCTCCT TTACTGACAT GAAATTGGGA 60 ATCTCAACTG GGCAGCTGCA GTTCTAAAAA GATGATGTCC AATTCCATGG AAGACCAAGT 120 CTTAAGGGTC ACATGCAACT GCTATACCAT GTGATGAAAT TTAAAATGAG AGATATCTTT 180 TCTCAGCTCC TTCTCCCATA CTCAGGAGAT GTCCAGGAAG ATGAAGAGAA GTGCTATAGC 240 ATAAATTAGT AATAGTCCAT GAGGGTCCAA AGAGAAGGGC TGCTTGAATT GTTAAGGTAC 300 ATTTGCCCTC TGACCATCTT TGTTCAGGGC CTGAAGCACA GCTCTAACCA GGAGGTGCAT 360 TTTGACTCAT TTCCTCACTC CTTTGTTCAG CCTTTGACTC ATTCATTCAC TTGTTGTGGA 420 TATCCTAATT TCTGCAGTTT AAACTGTAAA TATTCTTGGG GATGGAACTA TCTGAGGTGG 480 TCTGGGAATT ATTAATTTAC TGATGGCACA CATCTTCACA TTGTCCCTCA GCCTTCATGT 540 AGTTCTGGCC CAGTTGCTTC TAAGATTTTA TGAGTTGGCC TATAATGGGG CTGTGGAAAG 600 TAAGGGGGAT GTTGTGTTTG CATCTGTTCC AGAAAAAAAC TCTGAGTTAA AAGTATTCTG 660 ATTCCTATTA GGGTAGGACA TCTTAGGGAG GAATTTGACA AATGTCTGAG AAAGAATATC 720 TTTTGCCAGA TTGAAGAATT GTGCAAGTGC ATATTGCAAA AGGCTTTGTC CTATGTCTTT 780 GTTTTTCAAA TGCACAAGAA GCTGTTCAGT GGTGCACACA CCACCCCGCT GGGAAACAGG 840 GACTTGTCAG CTGGCAAAAT TCCATGATGC ATTGGGAGAG GGAAATTCAG TGCATTCTTT 900 GGTGGCTCTT TGCCTTGTCA CCATCTTGAG ATGCCTATTG TAGGAAACAT CTGTTGTTTT 960 GGTCTGCCCA GCCTCTACTC TGTCTTTTCT GGCAATAGAA TCTCTACTTT CCTTTGGGGA 1020 ACACCGTCCC TCACTCTACT CTTCATAACT TGAGTGGACT GATCCCACCT CCCAGTTCTA 1080 GGGTGAATGC ATGACCCAGG CCTGATCAGT GTATGCCCTC CTCTGGTTTA GGAATGGTCA 1140 TGTGACTTAT GCTGGACCAG TGGATTCAAT TTGGAGACTT 1180
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