| Tag | Content |
|---|
EnhancerAtlas ID | HS060-13025 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr16:47607990-47608970 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr16:47608638-47608652 | AATCCCATGGGAAT | + | 6.64 | | EBF1 | MA0154.3 | chr16:47608638-47608652 | AATCCCATGGGAAT | - | 6.6 | | Nr2f6(var.2) | MA0728.1 | chr16:47608049-47608064 | TGAACTCTTGACCTC | - | 7.64 | | RARA | MA0729.1 | chr16:47608046-47608064 | TCTTGAACTCTTGACCTC | - | 6.45 |
|
| | 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 |
| GH16I047573 | chr16 | 47607399 | 47609219 |
|
Enhancer Sequence | CAGCTAATTT TTGTATTTTT AGTAGAGACA GGGTTTCGCC ATGTTGACCA GGCTGGTCTT 60
GAACTCTTGA CCTCAGGTGA CCCACCCGTT TCAGCCTCCC AAAGTTCTGG GATTACAGGC 120
ATGAGCCATC ACTTCTCATA TGCTCCTTGT GGCTCACCAA ATCAGCACCA GTGCTTGGTA 180
GGGTTGAGAC ATTCCCCTGT GGCCTGGATT GCCCAGTTCC CCAGTGTCAA TGTGTAATCA 240
TGGAGGCAGT CTCCCCGCTT TCACACCCTG GAGACATATT TTCACCTGAC TCACCATGTA 300
GGTTGCCACC CACAGCTTTC AAAGTGTCTG AAGTTTCTTT CATTTTTTCT GTTGAGTTAC 360
TGTGTTTCTT CTTGGATAAA AGTTTACAGC ATAAATCTCT GCACGTTATT TTGCTCTTTG 420
CAAGTGGGTG AGGCATGCTA ACAATGCCTC CAATCTGGAG CCTGGGTAGT TTATAAAGAA 480
AAGAGGTTTA TTTGGCTCAC AGTTTTGCAG GCTGTATATA CAAGAAGCTC AGGACAGAAG 540
ACTAAGTGGA ACTGGAGTAT AGAAATCACA TGACAAGAGA GGGAATAATA GGTGCCAGGT 600
TCTTTTCAAC AACCAGTTCT CACGGGAACT CAGACTAAGA ACTCACTCAA TCCCATGGGA 660
ATGACACCAA GCCATTCATG AGGATCCTGA CACCTCCCAC CTTGCCACAC CTCCAACATT 720
GGGGATCAGA TTTCAACATG AGACTTGGCA GGATCAAACA AACCACATTC AAATCATAGC 780
ATATGTCATC TGCAAAGAAA CAGTTTCATT TCTACCTTTC TCAGCTATAT TCTTTTTATT 840
TCCTTTTCTT GCCCTATTTT ACCACATAGA ACTTCCAGTA CTATGTTAGT CATGGTGAGA 900
GCAGACATTT TTGTTTTGAG AGGGAGCATT CAGTTTTTCT TTCACCATCA AGTAGAGTTA 960
GCTGTAGAAG TTTTGTAAAT 980
|
