| Tag | Content |
|---|
EnhancerAtlas ID | HS047-18401 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:15808430-15809510 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELK1 | MA0028.2 | chr2:15809113-15809123 | ACCGGAAGTG | + | 6.02 | | ERG | MA0474.2 | chr2:15809113-15809123 | ACCGGAAGTG | + | 6.02 | | ETS1 | MA0098.3 | chr2:15809113-15809123 | ACCGGAAGTG | + | 6.02 | | FEV | MA0156.2 | chr2:15809113-15809123 | ACCGGAAGTG | + | 6.02 | | FLI1 | MA0475.2 | chr2:15809113-15809123 | ACCGGAAGTG | + | 6.02 | | ZNF263 | MA0528.1 | chr2:15809328-15809349 | GGTGGAGTAGGGGGCAGAGGG | + | 6.02 |
|
| | 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 |
| GH02I015668 | chr2 | 15808725 | 15808924 |
|
Enhancer Sequence | ATTTTGGCAC AGAGGAGCCT AATAGGATTG GGGGATGTTG AGTAAGAGGA TGTGGTTGGA 60
GAAGGAAATG GCAGGGAAGA GCCTTGTAAG GAAGATCTCA AAGGAGTGGA TCTAACAACT 120
CTAGTTACTG GGCAAGTATT GAGGATATTT TTTTAGGTAG GGTATGTAAT AAGATGTGTG 180
TTTTAAAAAT GTATGCGAGA GGCTGCTTCC ACTGTTAATC TGGTTTGATA ATTGCGAAAG 240
CCTCTGTCGA CAACAAAGAT CTGAATGTTA GTGAGCAACA AGCCGACAAA ATATTCCCCA 300
CACAATGACA AAAGCATATA CAAAGGTGGC TGAAACATAG CTGGGTTTGA AATGCCTCTG 360
TCTGTCCTGT CTGGGAGTGA GGCTGTCGAA TCCCTCCCCT CCTCTGGGGA GGCTGTCTGT 420
CCTCATGGGA GCCGCAGGTC CAATATTTTT GTGCTTGAAA ACCCTGCCCT CGTCCACCCC 480
AGGCGGCTCA CAGCTTTCAA CAGAGGATTA CTTAGAATAA CAAGTTAATG ACTGTCCTTG 540
GATTAGCTGA AGTTTGCTGG GAGAAGCAGA CATGCTCAGA GTTCATTTCA CTCAAGTCTG 600
ACGTGGGTGA GTTGAGAAAA CACGTTGCAA ATTCCATCCT AGGAAAACAA GAAAAGAATT 660
CTTCACGATG TCAAAGCAGC ATCACCGGAA GTGTGTGTGA AAATGGAGCT TCCTTTAAAA 720
CTATAAAAGC ATTTGTGCCT ATCTTCTGAG TGTGGCAGAG TGTCTGGGTG GCAGACCTAC 780
CTGGGAAATG ACAAGCAGGC CATGGGCTCT GTTGTTCTTA GGGTCAAATG ATCTGGGGCC 840
CCACAGGAAA CAGCTGGGGG TTTAAGTGTG AACCTGGAGT GGGGAGACGT GGATCAGGGG 900
TGGAGTAGGG GGCAGAGGGA GACAGAGGAG AGGCACCGCT GACTCTACTC AGTCAACACC 960
AGAGACCACC AACAGCCCAA GCTTCTAGCA GCTCCCTGCT CCCAGCCCTC CAGCCAAACC 1020
TGTCTGATTC TCTTCTAGGT TCTGCAGGTG TCTATGCTCC TTCATTCATT CACGCAATAA 1080
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