| Tag | Content |
|---|
EnhancerAtlas ID | HS164-01506 | Organism | Homo sapiens | Tissue/cell | Raji | Coordinate | chr10:26703530-26704940 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr10:26704332-26704347 | AGGTCACATTGGCCT | + | 6.81 | | Foxo1 | MA0480.1 | chr10:26704365-26704376 | TCCTGTTTACA | + | 6.62 | | Nr2f6(var.2) | MA0728.1 | chr10:26704490-26704505 | TGATCTTCTGACCTC | - | 6.15 | | RARA | MA0729.1 | chr10:26704487-26704505 | AAGTGATCTTCTGACCTC | - | 6.4 | | RREB1 | MA0073.1 | chr10:26704642-26704662 | CTCCCACACACCCACTAACC | + | 6.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr10 | 26704321 | 26704463 | | chr10 | 26704592 | 26704694 |
| Enhancer Sequence | CTGTAATCCC AGCTACCTGG GAGACTGAGG CAGGAGAATC ACTTGAACCT GGGAGATGGA 60
GGTTGCAGTG AGCCAAGATC GCACCATTGC ACTCCAGCCT GGGCAACACA GCGAGACTCC 120
ATCTCTAAAT AAATAAATAA AGTGTATTTC TGGCTGGGCA CAATGGCTGA CGCCTGTAAT 180
CCCAGGACTT TCGGAAGCTG AAACAGGAGG ATTTCTTGAG CGCAGGAGTT CAAAATCAGC 240
CTGGGCAACA TAGCAAGACC CCATCTCTAT AACATAAATA AATAAAATGT GTTTCTACCT 300
GGTGTGGTGG CTCATGTCTA TAATCTCAGT GCTCTGGGAG GCTGACGTGG GAGGATCATT 360
TTAGGCCAAG AGTTTGAGAC CAGCCTGGGC AACATAGTGA GATCCCAGCT CAACAAAACA 420
TTAGAATAAT TAGTTGGGCA TGGTAACATA TACCTGTAGT CCCAGCTACT AAAGAGGCTG 480
AGGTGGGAGG ATCGTTTGAG TCTGGGAGTT CAAGGTTACA ATGAGCTATA ATCGGGCCAC 540
TACACTCCAG CCTGGGCGAC AGAGCAGGAC TGTCTCAAAA TAACAATAAT AATAATAAAA 600
TGAAATGTAT TTATTTGCTA TGTTCATTGG AAGAATATTG CATAGTGTCT GAAGATTGCT 660
GCATGAGCAG AAATAGAGTG CAGAGTCTTT GAGGTCCCCA GAATGGGACA ATGACATGCT 720
CATCGAGGTC TTCTCTAAGC ATGTTGGCCT CACTGCCTGG TCCTGGGCAC AATTCACAAG 780
TGAAGGCACC ACTAGAGTGT GAAGGTCACA TTGGCCTGAA GTTACTCACA TCTGTTCCTG 840
TTTACAGCTG TCAAAGCCAT CTTGAATATG TTGCCATCTG CACACCAACC TTGTGATGAG 900
GGCAGGAAGG CATTATGATT GGTGTCATTT TACAGTCCAG GTGCTGGTAA GACCATAAAG 960
TGATCTTCTG ACCTCTTTCT TCTCATGTTT CACAGTCTGA TCTGGGTGTT TAAACTGACT 1020
ACTTCACACT ACCTCTCTTA GAAAAGGAAG AACCAATTTA GAACAATGTG CTTGGAGAAA 1080
TGAAGACTCC CTACGTTCCC TCCGCTCTCT ACCTCCCACA CACCCACTAA CCCCTACTAC 1140
AGCTATGCCC CGGTGTCTTC AGGGAGCTCA CCCAACAGGA GCAAGAGGAC TTCTTTAAGC 1200
TGAGACTGCA AAGGTCAGAG ACACCACTCA GCAAAGAGCC AGGAGGTGTG CATTCTAAGC 1260
AGCAAAGCGG TTCTCAATAT TCAGGAAAAG ACCAGATGTG GGGGCTCATG CCTGTAATCG 1320
AAGCACTCTG GGAGGCCAAG GCGGGAGGAT CCCTTGAGGT CAGGAGTTTG AGGCTGCAGT 1380
GAGCTACAAT GGCACCCCTG CACTCCAGCG 1410
|
| |
|
|
|
