| Tag | Content |
|---|
EnhancerAtlas ID | HS129-16712 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr18:8960610-8961990 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Hnf4a | MA0114.3 | chr18:8960863-8960879 | AGGGTCAAAGTCTGGA | + | 6.07 | | POU2F2 | MA0507.1 | chr18:8960620-8960633 | ATAATTTGCATAT | + | 6.44 | | PPARG | MA0066.1 | chr18:8961957-8961977 | CGTGAGTCACTGTGCCCCAC | - | 6.23 | | PPARG | MA0066.1 | chr18:8961958-8961978 | GTGAGTCACTGTGCCCCACT | + | 6.97 |
|
| | 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 |
| GH18I008960 | chr18 | 8960448 | 8962013 |
|
Enhancer Sequence | GAATTTGTGC ATAATTTGCA TATGTTTGTG CAGAATTTGT ATTTGAGACA GGAACAGTAT 60
GTGGGAAAAG TTATTATGTC TGTTTTAACG CCTATTCCAG CATGAACATA TTTTAAAACC 120
CATAGAAATA CATTTTAAAA TCATAAATAA CAGCAACAAA TAAAGTCTTT TGATAGGTTT 180
ATTTCCTTCA TTTGCCAGAG TAATTACGGT AATTCCCAAA TGACCAATTT GAACAACGAA 240
GCCTCTTGTT AGTAGGGTCA AAGTCTGGAT CCGTTAACAG CGGCATTCCT GTCAAAATCT 300
GATCTTTCCT CTAAGTGCCC AAATAGCCTA GGTGTACTAG ATACCATTCT TCATGTCTCT 360
AATACGTGCA AACAGACCTG ACAACTATTT CAGAACCTAG AAAGGCCAGC CAAAAGTTAG 420
TCATTAACTA AGCAGGATAA ATCTTAATCA ACTGAATAAA TGCAAAGTAT GTAACATTTT 480
AAGTAAAACA AACAGGGTAG AGTTAACCAA GAGCCCTTAC GGGAGGAAAA AAATCATTAT 540
TTCTTCCTTC GGGTGAGGCA AAAACCGTTT CTTTAAACTT GAAATGCAAA GAGCATTCAT 600
TTATATATTT CAGGATTAGA TTCCGGTCTC AGACTGATAT GCATTTCTTA AATGTGTCTT 660
ACATTTTCCC TGTTGAGAAA GTGGGTGAAT CAGAACTGAC TCAGGCCAGA CACACCACAG 720
GGAGAACAGG TCAGCACTAG AGTGAGAATG TCTAGTATGC TACCTTTATT CTGTATTACT 780
ATGATCCATG TCTATTTTGT GTTAATTATT GCTTGTCCAA AGGGACCACC AGAAAAATCT 840
GTTGATCAAG CAAATCTAAG TATATTAGAC CTACAGCAGT AAGGGACAAT ACTACAGTGT 900
CAGTCTTAGA AGTGTCTCAA AACAGAGAAA TTAGGAAAGG GTGTTGGAGG GTGTTATGGC 960
CCAGATTATA TGATTTTAAG GCATGTCTTG CAAGGCAAGA AACGAGATTG GGCAAAATTA 1020
AGATATAATA GTCTTGAAGA GGTGAACACA AGAGGGTGAG GGTCTTTTGT TTTGGTTTGT 1080
TTTGAAACAG AGTCTCACTC TCTCACCTAG GCTGGAATAC AATGGTGCCA TCATAGCCCA 1140
CTGCAGCCTC GAACTCCTGG GCTCATGCTA TCTTTCTGCC TCTGTCTACT GAGTAGCTAG 1200
GATTACAGGT GTGGCACCAC AGCCAGCTAA TTTTTTAGTT TTTATTTTTG TAGAGATGGG 1260
TTCTCACTAT GTTGTCCAGG CTGGTCTTGA ACTCCTGGCC TCAAATAGTC CTCCCATCCC 1320
AGCCTCCCAA AGTGCTGATA CTACAGGCGT GAGTCACTGT GCCCCACTGA GATGAGGGTC 1380
|
