| Tag | Content |
|---|
EnhancerAtlas ID | HS129-10935 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr13:111537550-111538870 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr13:111537898-111537919 | AAAGAAAAAAAGAAAGAAAGA | - | 6.34 | | Nr2f6(var.2) | MA0728.1 | chr13:111537681-111537696 | GAGGTCAAGAGATCG | + | 6 | | TBX2 | MA0688.1 | chr13:111538221-111538232 | TTTCACACCTC | - | 6.14 | | Zfx | MA0146.2 | chr13:111537659-111537673 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr13 | 111537631 | 111537770 | | chr13 | 111537982 | 111538100 | | chr13 | 111538209 | 111538695 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH13I110887 | chr13 | 111538401 | 111538590 | | GH13I110886 | chr13 | 111538801 | 111540747 |
|
Enhancer Sequence | ATGCACTTTT AAGAGATCAG TGTGTAAGCA GGGCATCTTT TGAAAAAAAG AGAGAGAAAA 60
AAAAAAGGGC TGGGCATGGT GGCTCATGCC TGTAATCCCA GCACTTTGGG AGGCCGAGGC 120
GGGTGGATCA CGAGGTCAAG AGATCGAGAC CGTCCTGGCC AACATGCTGA ATAAATACTA 180
CTAAAAATAC AAACATTAGC CAGGCGTGGT GGCGAGTGCC TGTAGTCCCA GCTACTGGGG 240
AGGCTGAGGC AGGAGAATCA CTAGAACCCA GGAGGCGGAG GTTGCATTGA ACAGAGATTG 300
CGCCACTGCC CTCCAGCCTG GTGACAGAGC GAGACTCCAT CTAAAAAAAA AGAAAAAAAG 360
AAAGAAAGAA AAAGAAAAAA GAATGGGAGA GGGGGGTGGT GGAAGAGCAG ATCCCCCAAG 420
TGTGCCAAAG TCGTCTCAAC CTCCAGGAGC CTTCATGGCA CGCAGACACA GAGAACCTGC 480
AGCCAAGAGC GGGTCAACGT TTGCTCCTCC CACAGGCTGC AATCCTGCAA AGCCACACAC 540
GAACACGGTT TGTACAAAAG AGTGGACTTT GATGGGAATA CAATGCAGAC AGCTTAAAAT 600
ACCTACACAC TCAATTGGCG TTCAGATGCC AATGTTCCCC GGATAAAGTG GCAACTAGGG 660
GTTACCTGCA ATTTCACACC TCTGAAAAGC AGGTTAGAAA ACCGCAACAG AGAAGAGCTT 720
CACGAAAGCT GGGGTGTTTG TCTTCTCCTT CACTAGGCCC AGTACCTAGA ATAGTACTCA 780
CATCAGCAGA TGAAGCCCAC CCACTAGCCA GGAGAAACAA AAACACAAGG TAAACAAAAA 840
CAAATGATCA GTAGCTGGCA TAGCCTGTAA TACAACCTGA GGAGTCACAA CCATCCAGGC 900
AGGCCTGGCC ATGCGAGGTG CAGGGACATG CACCCTGAAG GCAGAGGTGC CACTAGGGGC 960
CGGAAGAGCC GCGTTAAGGG CAGCCCAGGG AAGAGGCAGC GGGAAACACA CTAGTCTCCC 1020
AGCAACAATT AATCCTGTAA CTATAAGGCT CACAGTGACC AGGGACCTCT CAGAAACTGC 1080
TCCATTGAGT AGATGCATCT TTTGTTAATG CAGATGGTTT CTCTAATAAA GCAGGATAAG 1140
AATGAAAGGC TTCCATATTT TACCAATCAA GATTCTATTG TGGGAATCAT TCCAACAGAA 1200
CCTTAGAATT TCATTCCATC TCCATAGATA CAGCCTCTCT ATACGGTGTA GTTCCCACAA 1260
CCAGCTGTCA CAGAGCCTTG GATAATGCTG TTTCACGAGT GCCACCTTCT TCATTCCTAG 1320
|
