| Tag | Content |
|---|
EnhancerAtlas ID | HS129-01553 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:96939120-96940600 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr1:96939533-96939547 | GAGAGATGACTCAG | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 96939421 | 96939993 | | chr1 | 96940024 | 96940438 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I096472 | chr1 | 96937662 | 96940758 |
|
Enhancer Sequence | ATCCTACATG CACATTAGAA AGCATCTTGG GAGCTTTGAA AATACTTACC AAAGTCGATC 60
CCCATGCACA GAGAGTCTGT TTTAATTGAC AGGGAGGTGG AGTTCCAGTA TTAGTTTGTT 120
GTCATTGTAT TGTTTTGTTT TGTAAGATCC TTAGATTATT CTAATGAGTA GCCAAGGCTA 180
AGAGCCACTG GTCTAGTCCA AATTCTCTTT TAACCGAGGA AAAACTGAGG TACAGAAAGA 240
ATAGGCTAAA GCCCAAGGCT AAGCAGTGAG GTCCTGGCAA AATTGGGATT AGAACCCCAC 300
ACACCTCCTG ACTCCCATTG CAATGCTTTC TGATGCACAA TGAATTCAGG AACAATGGGG 360
GAGACACTTT TGCATTTAGA CACAGCCTCA GTGATCCCAG GGAGTGAGTC GGTGAGAGAT 420
GACTCAGATG TGAATTCCCC GCTGACTCCC ATTTTCATCC CCTTGGGCAG TGTGTAGGAG 480
AGGTATAACT GCATGAAGAG AGCATTGTCA AAGAAAATAT CCTGGCTGAT CTATTTTAGT 540
TAAAACAGCT TTTTCCCCCC AGGTACTGTG AGATTGCTTG TCTGTCAGGG TGTTGGCCTT 600
GAGCAGGAGC TGGGCACCAG GGAAGGTGTT TTCAGTGGAG GGAGAAAATA GAAATAAAAA 660
GGAGGGCTAA GCCACAGGGT GCTGGGAGCA GAGGGAGTGA GCGCTGTCTG CTCAGCGGTG 720
TGTTCTTCAT TGCAAATATC TCTGGGCTAA AGCCGATCCT CTGCTTTCAC AGCGCCAGTT 780
GAAATTAGCA TTTCTCACGT CCCAGGATTT GTCTATCGTT ATTCAGAGTA TCGCAGTAAA 840
CTCATCCAGT TCTTCTGAAA TTGTGTTATG AGTTTATGCT CTTTTAAAAA TTCAGGCTGC 900
TCTCTGGAAG AAGCGGGTGA ATCTGAATAA CAAATAACAT ATACCAGAAT CCAAATGTCA 960
GGACCTGGGT CTGTCCCTAA AGAGCAGAGG CTAATGGCAG TGAAAAAGGG CTGCAGAGGT 1020
ATCTGGGCAT AGCTAAAGGA TGATTCTAGG TGTCAACGGC AACAGAGTGG AAAGAGGGAG 1080
GTTCTAATGA GGGCGGTAGG AAACCAGCGG GAAAAACTGG AAAAGTAAAA TTGCTGGTTA 1140
TTTGTGAGAA GGAGGGTAAG TTTCCCCAGA CTGATTCAAA ACTCTTAACT TGAGGAAGAT 1200
GGCTTGTCTC TCAAGTTAGT CATTTCTTGG CATAGTGGTA GCCACCTTGA CTATGGGCAT 1260
TTCAGTGAAT TCCCTGTCTT TCTTGCTTAA TGGTAGGTGT CATGGGTGTG CCACTTCCTG 1320
ACAGATTTTG TTTACAGGAT CCTCTATTCC AAAATTTTAA TGTACCTGCC AATCACCCAG 1380
GGATTTTGTT GTGATGTAGA TTCTGATTTA CTGGGTCTGG GGTGAGGCCT GAGTTTTTAC 1440
ATTTCTAGAA ATTTCCTCGG GTGATGCTAA AGCAGCAAGT 1480
|
