Tag | Content |
---|
EnhancerAtlas ID | HS105-85608 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chrX:152198970-152201630 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2A | MA0003.3 | chrX:152199763-152199774 | TGCCTGAGGCT | - | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH0XI153032 | chrX | 152200413 | 152201681 |
| Enhancer Sequence | CCCTCATCCC ACATCAGGAT CGGGGCCCCC CACCTCCCTC CAAAGGGCCC TGGCCACCAC 60 CATCAGCCCT TCCCGGTGAC CCAGATGACC ACGTTGATAC CAAATGGGGT TGGGGGAGGC 120 ACCCCTGCTT TGCACCCAGT GCTGCACCCA GCCCCAGCCC CAAACCCTGC CGTCTCTGGG 180 GGGCTGGCCA GGAGGGAGCC CTGAGTGGCC AGCTGCGACC TGGGTGGGGG CACCTGAAGA 240 TGTCTGTCCC CCACCCCTTG TCCTGGGTTG GGAGAGACAG GGGAAAGAGG TCCTCTCAAG 300 GGTGCCAGCT GCCTGGGTCT CCCAAGAGGG TTGCCCCATT TGCCGTCCCC GGGGCAGGCT 360 GCCCCCTGTT CTGGGAAGCC CACCCTCACC TGTTTAGGCC CCGTAGTGAC CCACGCGCCC 420 AGCAGACGCC CACCCACTGC TAGCTGTCGT TCCTGTGCAA AGTTGTGTGT TGTGCACCCA 480 CCCGGGCGGC CGCCACTAGG CCCGGGGCAT GTGCTGTGAG CTTCCTGTGA GCCCAGGTTC 540 TGCTCACTGC TGTCTGTCCT GCATCTTAAA CACCACCTCT GCTTTCCTGG TGTAGATCTA 600 GGCCAGTGGC TGCTTGTTCT CGTGGAGCTG TGTGTGTTCT TCTCTGAGCT GCTCCTCCCC 660 GGAGGCCCCC AGCACAGACC CAGGAGATGG CCGGAAGGAG GAACCAGGGC GCGGCCAATG 720 CTCACCCTGT GACCACGATG GTAACCATGA CTGTGGGAGG AAGAGCCGGA CCCGGGACGG 780 AGTGGGGCTG CCCTGCCTGA GGCTCCCAGG AGAGCTTTAT GCTTTGGCAT TCCACCCCTG 840 TTGTTACTTG TGACTGTTTC CTCGCCCTGG TGGGCTGTTC CCTGCTGTGT TTACTGGTGT 900 CCTGTGACTG TCTGTGATGA CTATAGGGCA GGGCCCTGCC CCAGCAGATG GGCTTGGGAG 960 GGGGCTCCCT GAAGCCGGTG GACACTGCCA GAGTCCACCG TCCTGGCAAG AGGCGGGCCC 1020 TGGGGCCCTC GGGAAGGAGG GAGGTGGCAG TGGGGTCGGC AGCAGGACGG GGGTAGACGA 1080 GGCGCCTTGC CAGGAACCCC AGGAGGAGGG ATCCTAGGAC CTGTGTCCTG TAGTGGCTGT 1140 TTGCAGTTTC TCTCTGTGTT GTGGTTCCCT TCTTTTCAGT GATTTCGGTA CACGTTTCTC 1200 TTCAATAAAT TTCATTCCAT TTTCCAGCCG GTCTCGCCTC TGCTGTGGGA AACTAGTGGG 1260 AAAGGTCTCT TTGGGATAAA ATGGAAGTTG GGGGACAACA GTGGCCTGGA ATTCTGACCC 1320 TATTGTGCTC ACTGGGATAC GGTCAGGGCA TAGTAGGCCA GCGATTGTAG AGAATGACCT 1380 AACTGTGATG GTGGTTCCAA CCCAGAGTCA GTGGCTTATG AGGATGAGGA AAGAAACCAA 1440 GCTGAACATG CTGGATGGTG CCAGTTGACG GAACACTGCC GTGCGAGGGC AATGTGTGGC 1500 TTGCTCCCCA GGGCATGCAT GGAGGCTCCC AGAACGAAGT GCATAAGACG TGGAAGGGCA 1560 GGCAGGGGAC AGCAGGCTGG GGCGGAGGCC TGGGTTGAAG CTCTAGCATA GACATCTTTT 1620 TAACTGTTCC TCAGTTCCTC ATGTTTATCC TGTGTGTGGA GCTTTCACCA TCTCTTTGGA 1680 AAGACAGAAG AGATGGATAA GGAAAAGGAG TAGAACAGAG CGGCACCCCT TGCCTTCCCC 1740 AGAGTCTGGG TAGCGGGCGC AGGACGTGTC GCCTGTCCAA ATGCGCAACT TTCACCAGTG 1800 TACGCTACGC GTGCGCGCCT GTGCACCTTG ACGAGCACGC AGCCGTCATG AGTGCGCCTG 1860 GGCACGCCGC CATTTCCTGC AGCCGCGACA GCACGGTCGT ATATTTCCGG TTGTCATTTT 1920 ATTCTTTTTG AGAAATGGTC TCGCTCTGTT GCCTAGGGTG GAGTGTAGTG GCGCTGTCAT 1980 AGCTCACTGC AACCCAGACC TCCTGGGCTC AAGCGATTCT CCCGCCTCAG CCTCCCGACT 2040 AGCTGGGACC ACAGGCGTGC AACCACCATA CCCGGAACCA CAGTCACAGT CGGTCGCAGT 2100 GCCCGCTGGG AAAATGCGAC CGTCCACAAA GCGAAACGGC CATCGGGGCG AGTTCGGCCT 2160 CGGCGGGGAT TCTCCTGAGG TCACGCCCGC TCTGGCCGCC AGAGGACGCC CGAGGATCAC 2220 GAATGGGCCC GAGGAGCTGG CTGCCCCTTC CCACGCTCAA GGTCTGCAGC CGTGGCCAGA 2280 GTGGCCTTGG GGTGACCGCG CGTGGACCGT CGCCGGCGGG AGGGAGCGCG GTCCCGCGGG 2340 GGCCGAACGG GGCTCCTGTG GCCTGAGCTT GTTTCGCAGG GAGCCCTGGC GGCCATGGCT 2400 CTGGGACACC AGACAACGGT CGTCAGGGCT GTCCAGGGTA AGGGGGTGTG GACGTGCAGA 2460 CAGGGAGGGC AGCTGGACCC TCCAACCATG CTGGGCCCTC GGGCTGACCG GGGCTCGTCT 2520 GTGGGGCTCA GTGAGGAGGG ACTTTGTTCC CTAGGAGTTT GATGAGGGAG CGCCATGGGG 2580 GTGGCGTCAT CCTGACATCC TGCAGGGCAG TGGAGCCTTA CTTTCCCTAG CCCCAGAGAT 2640 CATGAAGTCT CTCTTTGTTT 2660
|
| |
|
|
|