| Tag | Content |
|---|
EnhancerAtlas ID | HS134-00413 | Organism | Homo sapiens | Tissue/cell | Mesendoderm | Coordinate | chr1:19002670-19003550 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:19002988-19003009 | AGGGGAGGGGAGGGGAGGGGA | + | 6.91 | | ZNF263 | MA0528.1 | chr1:19002886-19002907 | GAGAGAGGGTGGGGAGGGGGG | + | 6 | | ZNF263 | MA0528.1 | chr1:19003013-19003034 | GGGGGAGGAGAGGGGAAAGGA | + | 7.47 | | ZNF263 | MA0528.1 | chr1:19002983-19003004 | GGGGGAGGGGAGGGGAGGGGA | + | 7.81 | | ZNF263 | MA0528.1 | chr1:19003016-19003037 | GGAGGAGAGGGGAAAGGAAGG | + | 7.82 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 19003028 | 19003200 | | chr1 | 19003200 | 19003400 | | chr1 | 19002800 | 19002935 |
| Enhancer Sequence | TCCCCCTGCC ATCTTCGCCT TGCTTTATTT ATACATTCGT CCTCAAACAA TGGCAATAAA 60
CTCTTTCCCA GAGTGTTGCA AATCAGAAAT TTGTCCACAT TTTTCCACCA CCTTCCACTG 120
TGGACCTGCT CTGCCTGGGA ACGGCCCATC CAGGCCAGCT GGAGAGGGCT GGGTTGCAGT 180
AGATTGATGG GGGCACGACA GGTTGGGGTT GCTGGGGAGA GAGGGTGGGG AGGGGGGCAG 240
CGGGAGAATG CACCATGAAA GGCCTCTCGC TGCCCAGCGA CCAGCCGGAG ACACAAGAGG 300
CCCATGAGTG GCTGGGGGAG GGGAGGGGAG GGGAGGGGAA GTTGGGGGAG GAGAGGGGAA 360
AGGAAGGATA AGTCTTCCCC ACCCCCTTCT CCTAAGAGGA AAAGAGGGGG ATTGGGGGAT 420
CCTGGGAGGC AGGGCAGGCC CCAGGCAGAA TGGGAGGGTG ATGAAATTGG TCCTTCCCCT 480
CCCCCACAGG AAGCAGATGA TCTCAGGGTG TCCTGTAGCT CATGCTGCAC ACGCAACTTA 540
GGATCATAGT CCCTTCTGAA ACTCCTCACC ACCCCCACCA GTCAATGATC CTTTCTCCAG 600
CAACAGGCAT TGTTGAGAGC CAGCCCCGCT GTATGCCTGG CACTGTCCTG AACCCTGAAG 660
GTGGAGTTTA TCCATCAGAT ACAGCCCAGA CCCCTTCTCA GGGGGCTGTT CTTTGAGATC 720
CAGGAAGACC CCTTGGTTTT AGGGGTAGGG AAAATGCAGC TCAGAGAGGG GTTTAGAGGT 780
GAAGTCAGGG ACAAACTTCA GGGTTTCAAC CCCAAGCCCC CTCGTCTTTA CAGCCAGCCC 840
ACGGGCTCCT GGGGGATGCC CCTCTGGGCA AGGTGAAGAG 880
|
| |
|
|
|
