Tag | Content |
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EnhancerAtlas ID | HS129-30948 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr6:3918940-3920070 |
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) |
TFAP2A | MA0003.3 | chr6:3919448-3919459 | TGCCTGAGGCT | - | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 3919215 | 3919391 | chr6 | 3919432 | 3919937 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH06I003918 | chr6 | 3918864 | 3920592 |
|
Enhancer Sequence | TAGAATGCCC TTGGCCAGGA GGAGGAGTCC ATTCCATTGG CTGGGGTTGC TTAGAATTTG 60 ACTTTTGGTT TACAGCTACA TGGTAGAGCC TATTGCTCCT AGGCTACAAA CCTGTATGTT 120 AGAGGTGGCG AATATCTGAT TTACCGGTGG CAAATCCATA TGGAGCAACC TCAATTCTTG 180 CCTCCTCAGA AGAAAGAATT CAATTGAGGG GTATAAGGCA GAAAAAGAGA CCGAGGCAAG 240 TTTCAGAGCA GGAGTGGAAG TTTATTAAGA AGCTGTAGAG TAGCAAAGAA AGGAAAGTAC 300 CGTTGGAAGA GATCCAAGTG GACACTTTGA AGGTCAAGTG TGGCATTTGA CTTTTTGACT 360 CGGGGTTTTA TATGTTGGCA TATTTCCAGG GTCTTGCATC CCTTTTCCAT GGTTCCTCCC 420 TTAGGGTGGG CTGCCTGCAC GTGTGGTGGC CTGTTAATAC TTGGGAGGTG AGCATGCGCA 480 GTGTGTTTAC TGGAGTTGTA TGCATGCTTG CCTGAGGCTT CCTTCCCTTC CCTGGCGGAA 540 TGTCCCAGGA AGGTCCTTCT TCGCCATTTT GTTTCTTAAT GTGCATGCCT GAGCCTACTC 600 ACCGAATTCC TGAGCTGCCA ATTACCAATT TCAAGTATTT TTTATATATT GTGAAATTGC 660 CTCTCCCTGG GCCTGTGACC AATTATCGCT CTAGTGTGAC AGTTGTGGGC CATCAGGAAA 720 TTGCCTCTCC CTGGCTCCAG CTGCCAATTA TTATTTTTAG AGAGGCACTG TGACAACTGC 780 CTGACTATCA CCTGATGATC ACTTGACATT CCTGGTAGGT GGGGGGAGGG AGCCCTCTCC 840 TGCCCCACTC ATGCCTGGCT AGCTACCTAC TATCACATGT GCAGCATGTT ACTGTGCTGA 900 ATACTATAGT CAATTATAAC ACAATGGCGA GTATTTGCAT ATCCAAACAT AGAAAAGGTA 960 ATGGGTTGGT CTTGGATGTT TCAACACCTA CAACATCACT AGATGACAGA AAACTTTCAG 1020 CTCCATTACA ATCTTATGGT ATTGTTGCAG GACTTTTTCT TAGTTCAGCT AAAGACAGGG 1080 TTCTTTGTCC CATGGCCATA AAAATTCAGG CTTGCAAACA ATTTGAATGG 1130
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