| Tag | Content |
|---|
EnhancerAtlas ID | HS136-13821 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr3:112484940-112487250 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr3:112486469-112486487 | ACTTCCCTCCCTCCCTCC | - | 6.05 | | POU4F2 | MA0683.1 | chr3:112486709-112486725 | TTGCATATTTAATCAT | + | 6.1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 112486003 | 112486364 | | chr3 | 112486008 | 112486559 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I112767 | chr3 | 112485848 | 112486654 |
|
Enhancer Sequence | TGAAATTAGT TTGATAGATG CAGTTCACAA TTTTTAAATA AAAAAAAATA GAAAGCATTA 60
AAGTAGAAGA TAGATGGTAC AGGTAGATAT TGTTTCACAA ACTTTTTTCA ATGTGTGTAT 120
GTCTTTGTAA AGCAAATATT TCTTCCCATG ATCACAGTTA GAAAGGTTTA AAAACTTTTT 180
CCATGGTCTG AATGTTCGTG TCCCTCAGTT CATAGTTGAA ATTGAATCCC CACTGTGGTG 240
GTATTAAGAG TTGGGGCCCT TGGGAGGTGA TTAGGTCATG AAGGCAGAGC CTTTATGCAT 300
GGAATTAGTA TTCTTATAAA AGAGACCCAA GGAGCTTATA AGTCCCTTCC TCCATGTGAG 360
GACACACAGA AGGTGCCGTC TATGAGGAAC AGGACCTCGC CAGACACTAG ATCTACTGGT 420
GCCTTGATCT TGGACTCCCC AGCCTGCAGA ACTGTAAGCA TTACATTTCT GTTGTTTATA 480
AATTACCCAG TCTAAGGCAT TTTGCTATAG CAGCCTGGAT GGATTGAAAC GAGCTTTGCG 540
TTAGGACTTG GGCCCGGAGT AAGAGCAGGG TAACACGAGG GGTCTGAAAG ATCATTGGAG 600
AAAAGAACAG GGCAATGATG GGGACAGGTA GGTGCTTGGG TGGGTACCAA AGAGAATTCT 660
TTTCACACTT CTGCCAAATT CCTGCACATA TATGCATGTA CACCAAACCA TACCACACTC 720
TACATACACA TTTGCCTATT CCTAACACCA CTGTTCTAAA TTCCTAATAT GTTTCCAATT 780
GCTGCCTCCA GCATAAGTGC CAGATTCCAT CCTTGATCTG AGAGAATCTT GGAAAATGTC 840
AGTCCAGGTG GATGTCCACA GGAAGAACAT TAGGAACAAA GAGAGACCTC TGTTTCTTTC 900
TTGAGCTGGG TGTAAACACT AATGCGAGAG TGATCAACCC CCTTGTTTAC ATACCTTCCT 960
ATTTTAGAGT TTCTGCTTTG GAATATTTAG ATTAACAAGA ATATCATATG TACAAATATC 1020
ACAAGAAGAA AGTCTCCAGT TTTAGGTTAG ATTGCTAAGC AGTTGTAATT CAAATATGAG 1080
AAAACTTGAA GTTTTATGTT CTTAGCCACA TCATGTGCTC TACAAATGTT GCGACAGTCT 1140
TTCCTAAGGA AGGTCCAGTT AAACCGCAGC CTCCTCTCAG TTCTCTCTAA ATCCAGCAGG 1200
GAGTGTGTGT GTTGTTCCTT CTCCCTGTGT CTTGATCTCA AGAGGTACCT TAGGAAGGCT 1260
GCAGTTGGAC AGCTGAGCCA AAGCCACAAA GACCACATTT AACTCTCCTC ATTTGGGTAC 1320
ATTTGACATG TTCTCTCATC TTATCACCAT GGAAATCCCA CAGAGAGAGT GTGAGTGAGG 1380
GAGAGGGGAA CTGAAAAGGA CTCACCCACA AGACATTACT GCCACACCCA GAAGCAGGTT 1440
GGTGAGAGGT GGAAGCAGCC CCCTAGGTCT CCTCAGCTGC TGGGTCTAAC CAGCCCCTCA 1500
TAGGGTGTGG GATGCTCAAC CCTGTCCCAA CTTCCCTCCC TCCCTCCTGT GGGGCTAAAA 1560
GGCAGCCTCA GCTCCATTCT TCAAGCTTCT TTCCTTGCAT TCCTCCCCTG ACCCTCAGCC 1620
CCATGACTCT GTCCCATAAT ATTTACCTGC AGTAGGCAGA TGTTCAGATC ACCTCACCCA 1680
GGAAACCTCC CTCAGAAAAC TTTGCTTCTT CTATTACCCT CTGAAAATTT TATTTCTATA 1740
ATTATTTATC TTAATTTTGG TGAGCCTTGT TGCATATTTA ATCATTAGCA TCCTACTGGT 1800
TTTTTGTACT ACACTATTTC TTCGTGTTCC TGTTCAAGCT ACCCTACAAA AACCAACTAT 1860
CCTGCCAGCT TGGCAGAGTG CCTTTATATT TCATAGATGC TGCCTGATTC ATGAATTGCT 1920
AACAAAAGCC AGTTAGATTA TTGAACTACA TCTATTGAAA TTTTGTTTTT TGACATTGTA 1980
AGTATGAAAA AGAGCCCCAA GAATATTTGA CATAGAACAC AAAGGTAGCC CAGGAGTGGG 2040
GTGTATGAGG TCAAGAGAAT GGAAAGGGCT GGGCGTGGTG GCTCAAGCCT GTAATCTCAG 2100
CACTTTGAGA GGCCGAGGTG GGCAGATCAT GAAGTCAGGA GATCGAGACC ATCCTGGCTA 2160
ACACGGTGAA ACCCTGTCTC TACTGAAAAA ATTAGCCAGG TTTGATGGCA CACACCTATA 2220
GTCCCAGGTA CTCGGGAGGC TGAGGCAGGA GAATCGCTTG AACCTGGAGG CGGAGGTTGC 2280
AGTTAGCCGA GATCGTGACA CTGCACTCCA 2310
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