| Tag | Content |
|---|
EnhancerAtlas ID | HS060-18266 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr19:49918250-49919570 |
Target genes | | Number: 35 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| YY1 | MA0095.2 | chr19:49918875-49918887 | CAAGATGGCTGC | + | 6.74 | | ZIC1 | MA0696.1 | chr19:49919076-49919090 | CACAGCAGGTGGTA | - | 6.35 | | ZIC3 | MA0697.1 | chr19:49919075-49919090 | GCACAGCAGGTGGTA | - | 6.17 | | ZIC4 | MA0751.1 | chr19:49919075-49919090 | GCACAGCAGGTGGTA | - | 6.07 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ACGGTAGGCA GTCCCCAGCA CCCCTCCCCA GTCCCCATCC ACTCCACACC CACAGAGGCT 60
GAGTCGTTTC AACTCTTCCC AAGCCCCAGC CTCACACTCC AACTCCTCAG GAGCAGAGAG 120
AAAAATCATT TGGCCAAGAG ATAACAAGGC CTTTGCTGTA GCTAATGAGA GCGATGGTGA 180
GGTGGGGGGA GGCCTGGAGG CTAGTGGGCG GCCAGGCTGC TCCCAGGGGA CCCTCCCAGC 240
CACACACACA GGGCTGCAGC CACCACACCG CAGGCCTCAT AGACGTGGCT ACACCCCCGG 300
ATTGCATAAA TGCACACGCA CATGCGCCCA CACTCGGGAG AGGTTGGGCC GGCCCTCCCC 360
AGCCAGCCTC AGAACTCCCT GGGGGCGTAG TGCCCGCAGC CCCCCTGCCT GCAGCCACAC 420
AGGCCAGTTC CTCTGCTCCT CAGAGCCCAG TGCCCGGTGG GGGTTAAGAT TTCCATTCTC 480
AGGCAAGGAC GGGGAAAGAA ACTTGGTAAG GAGAGGTGAG GAGCCCTCAG TTGTGAGCTG 540
AGGAATGCAG GAGCTGGGCT GGAGTCTGCC TGTTGTGGGT CAGGCACTGT CAGGGCCCCT 600
GGGGCTCTTC AGGGTCCAAA CCGGCCAAGA TGGCTGCCTC CAGGACACTC AGCTCCCAGC 660
ACCCTGGCCC CGAAGCCCAC CTCCTTCAAC ATACTACACT CCCTTGCAGA GACTGGGGCT 720
CCACCTCAGC TTCCTCACAG CTCACATGGG CATAATCTCT TCCTTGCTCC CAGGGTGGGG 780
AGGAGGGTTA AGGACTATGT CATAAAGGGC CTGGGTCCCT GCCTGGCACA GCAGGTGGTA 840
GAGGTGAAGA TATTGATTGT GATTGGTGTT CTGTTTTTAT TTACTGCCAT TATCATTGTC 900
ATTCATCATC CTCATCTGTG TTAAAAAGGT ATGGGGGTAG GAAAGCCAAA GACCCATAGA 960
GGGGAGGCCC TTCCGGGGAG ACATGGGGGA TGAGGCGGTG CAGTGGGTGG GGCCTGGCCC 1020
TGGAGGAACA GCTGGGGCTT TGATCTTTGA ATCCTCAGAT GAAGTGTTGG AATTAATCAG 1080
TGAATTTAGT GTGGTTGCTG GGTGAAAGAT CAAAATAAAA AATCATATTT CAGTATAGCA 1140
ACCATGAGCA ATTAGAAAAA TAAATTTGTA ATTATACCAT TTATAATGGC ATGGTGTTTT 1200
GTTTTTGGTT TTTGTTTTGA GATGGAGTCT TGCTCTGTCG CCAGGCTGGA GTGCAGTGGT 1260
GCGATCTCGG CTCACTGCAA GCTCCACCTC CCAGGTTCAC ACCATTCTCC TGCCTCAGCC 1320
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