Tag | Content |
---|
EnhancerAtlas ID | HS129-24364 | Organism | Homo sapiens | Tissue/cell | MCF10A | Coordinate | chr22:41983460-41985720 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr22:41983892-41983907 | GATTAAAAATTAACT | + | 6.21 | SPDEF | MA0686.1 | chr22:41985107-41985118 | CACATCCGGGT | - | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 41983691 | 41984236 | chr22 | 41984800 | 41985077 |
| Enhancer Sequence | AAAAGATATT AGCCAGGCAT GGTGGCACTT GCCTGTAGTC CCAGCTACCA GCTACTCCAG 60 AAGCTGAGGC GGGAGAATCA CTTGAGCCCA GGAGTTCGAG GCTGCAGTGA GCTGTGATAG 120 CGCCACTGCA CTCCAGACTG AGTGACAGAG TGAGACCCCG GTCTCTAACA ACAACAACAA 180 CAAAATAGCA TCACAATCAA GTTGATTTTT GAGGAGCCAA AGAACAATAA CAAAAATAGC 240 CTCACAAAAC AATGCTTAAT ATTTGCTCTG GGCAAATAGA TCCAGATAAA GGCCTGGAGG 300 GAAGCCACAC CACAGTAACC ACATTAACTT GGGGAGCCGG CCAGGCTCCC CAAGTGCGGT 360 CAGAGTGGAC TTTACCCTTC TCTGTTACGT TTCCATTCTT TACCAGGAGA GTGTGCTCAT 420 GAAAATGTGT ACGATTAAAA ATTAACTTTC AAAAGGCACT AAGCACAGAG GCTGGCCCGT 480 AGACAAATTA ATAGGCTGTT CTTATTCAGG TTGTTATGTT TGTGGAGCAA AAGGTCAGAG 540 GGAGGAGTCA GAACTGTGCC TAGGCCCTGC CACTTTTGTT CCAGTTCTTT TATTCATTTA 600 TTTGTTTGTT TGAGACGGAG TTTCACTCTT GTTGCCCAGG CTGGAGTGCA ATGGCACAAT 660 CTTGGCTCAC TGCAACCTCC ACCTCCTGGG TTCAATCGAT TCTCCTGCCT CTGCCTCCCC 720 AGTAGCTGGG ACTACAGGCA CACGACACCA CGCCCATCTA CTTTTTGTTT TGTTTTGTTT 780 TGAGACTGAG TCTCCCTCTG TCGCCCAGGC TGTAGTGCAA TGGCACATTC TCGGCTCACT 840 GCAACTTCTG CCTCTCGGGT TCAAGTGATT CTCCTGCCTC AGCCTCCCGA CTAGCTAGGA 900 TTACAGGTGC ATGCCACCAC GCCTGGCTAA TTTTTTGTAT TTTTAGTAGA GATAGGGTTT 960 CACGATATTG GTCAGGCTGG TCTTAAACTC CTGACATCGT GATCTGTCTG CCTCGGCCTC 1020 CCAAAGTGCT GGGATTACAG GCGTGAGCCA CTGAACCCAG CCTAATTTTT GTATTTTTAG 1080 TAGAGACGGG GTTTCACCAT GTTAGCCAGA CTGATCTAGA ATTCCTGACC TCAGGTGATC 1140 TGCCCACCAT GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GACCCACAAG CAAATGGCCC 1200 ACCTTTGCTC CAGTCCTGCT ATCTTCCTCC CGGATCCACC CCTGCAGGAA GGCCTCCAGG 1260 GCCCAAGCCA GGGCAACTTC ACCACAGAGG ATGGGGAGGG GCATTCGGGA CCTAAGAGAG 1320 GAGGCTAAGA CCTGGGTTCC CATCAGCCAC TGCCCAGTAA AGCCCATCCC ACTGCTCCCC 1380 CACGCTAGGA GACCTGTTGG TTGGTCCTTG AGGCCCCCAG ACTGGAGGGT GGGTTACCCA 1440 CAGGGAGGGC ATGAATGAAG CCTGCTTACT GATGCATCCA GCTGGTGAGG GGGCTTTTGG 1500 GGACTCACTC ACAATGAGAC CCAATGGGAG AAAAACTGAG CAGAGGTAAG AGGCTCAACA 1560 CAGCGAGAGT CTTTAGAAGA AAACTAGACT CTTACCCTCA CTATTCCTCA GTGTCCTCAC 1620 AGCAAACAGG CTAGGCCTGG AGCCTCTCAC ATCCGGGTGG GTAGAGCTCA TAAACGAATT 1680 TGAAAAGAAG CCCTCTCTGC TCCACGACTG GGGGTGGAAG GTAAAGTGGG TGATGGGGCT 1740 TCAGAAACTA GACCCAGTCC CAGGCCTGCA AAGGTCGGGG TGGGAAGACT CCGAGACGCC 1800 CTGTCTCCCA CCAGATGATG ACTGACGCTT GGCTGTGTGC TTGTGTGCCT GGAACCCCGG 1860 TTCAGAAGCC AGCTCCGACC ACTGGTGTGT CGTAGGGCTG AACTAGGGTG GGATCCCCAG 1920 CTCAGGAGGC GGGGGCGTCC GTGAGCCAGG CCTTAGCGGC GTGTGACAGC CTCCGGGGAG 1980 GGAGGGAGCT AGGCCCCTGC TCGCAGCCTC CTCCCTCCAG TACTGGATCC AACCCCAGCA 2040 CTCCCAAGCA GAACACAGGC AAGGACGCTG CGGGGTCAGT GACGTGAGGG CCAGGTCCCC 2100 TCACTCCCGG TGGGTGGCCC CGGATGTCAG GGGGCCGGGT ACCGCCGCAT CCCACACTCG 2160 GTCCCCGGGT GTCCACGGTC ACGCTGCTGC AGACCCCACA CTCAGCCTCG GGGGTGTCCG 2220 CGTGACACTC CCGGTGGGAG CTTCCAATCT TCAGGGTCCT 2260
|
| |
|
|
|