| Tag | Content |
|---|
EnhancerAtlas ID | HS024-01421 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr1:226221400-226222860 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DUX4 | MA0468.1 | chr1:226222154-226222165 | TGATTAGATTA | - | 6.32 | | EWSR1-FLI1 | MA0149.1 | chr1:226221451-226221469 | GGAAGTAAGGCAGGAAAG | + | 7.66 | | IRF1 | MA0050.2 | chr1:226221935-226221956 | TTTTTCTTTCTTTTTTTTTTT | + | 6.59 | | KLF4 | MA0039.3 | chr1:226222483-226222494 | ACAGGGTGTGG | - | 6.14 |
|
| | 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 |
| GH01I226033 | chr1 | 226220902 | 226224392 |
|
Enhancer Sequence | TCTAGATTCA ACTAGTTTGT TTAAGAGGTG ATTGCGGGAA GACTAGAGTG GGGAAGTAAG 60
GCAGGAAAGG GAAGGAAGCC AAGAAAAGGA ACATTATTAA GCAAGTTGCT TCTGTGTAAC 120
TGCAGCTGGG GTTCAGTCCT ACTGGGGACC CTGGGAGACA GTGCAGAACA TGCCTCTGAG 180
CTTTCCTACC CAAGAGGTGA GGAAGATGGG GAGCCTCCGG TTTCCATCCA TCATTGGCTG 240
AGGCCTGCTC GTAGGGTCAG TAACCCTTCA GCATGTCTGT GTCTCAGGTG GAAGGAAAAC 300
TGTCAGGTGA AGAATCCCAG GTGCTTGCAG TAGGACAGCC ACTGGAATGT ACTGGAATGC 360
TGAATGACAA GGGGATATGG ATCCCAAAAG AATTTCTGAG CTCCCTTTAA GGAACAGACT 420
CTAAAGTGGT CCCCATGATC TCCACCTCCT AGTAACTCAC ACCTTTGTAT AATCATATAA 480
TTCCCTCCCT TTGAGTGTGG GTGGGTCCAG TGACTGCTTC TTTTTTTTTC TTGTTTTTTT 540
CTTTCTTTTT TTTTTTTTTT TTTTTTTTTT TTTTTTAAAG AGATGGGGTC TCACTGTGTT 600
GCCTTGGCTA GAGTGCAGTT GCTGTTCACA GATGCAATTA TAGCCCACTA CAGCCTCTAA 660
CTCCTGGGCT CAAGCAATCC TTTTGCCTCA GCCTCCCAAT CTAAGACTAC TTCTAACCAA 720
CAGAATATGG CAAAGGTGAT GGGCTGTTAG TCTGTGATTA GATTACATTA TATACAATTC 780
TACCCCACTA GCTCTGTTCC TCCCTTAGTG GCTTTGAGGA AGCAAGCTGC TATTTTGTAA 840
GAGGACCTAT CAAGAGGTCC ACATGGCCAG GAACTGTGAG CAGCCTCATA GAGCTAAGGG 900
CAGCTAACAG TCAGCAAAAA TCCAGGCCCT TGGTCTTACA GCAGCAAGGA ACCAAATTCT 960
GCCAACAACC CGAATGAGTT TGGCAGCAGA TCTGTCACTA GTCAGGCCTC CAGATGGAGC 1020
TGAGCCACGG CCGACACCAT GATGACAGCC TTGCGGCCTG CACTATGCCC AGGCCCCTGA 1080
CTCACAGGGT GTGGGATAAT AAAGGGAAGT TGTTTTAAAC TAGTGCATTT GTCGTAATAC 1140
GTTATGCAGC ATAGGAAACA AATATGCTCC CTTATCCTAT AAGCCTCCAA TCTGAGCAAG 1200
ATGGCCTCAG CCCTTCTGCT TTTTCTTCTG ATAACCTTTA CTCCATGTCC GCTAATGAGC 1260
AATTCTTTTT TATCTTATTT TATTTTATTT ATTTTATTTT TTTAAGACAG GGTCTCTGTC 1320
TGTTGCCCAG GCTGGAGTGC ACTGGCATGA TCATAGCTCA CTGCAGCCTC GACCCTGGCT 1380
CAAGTGATCG TCCAACCACA GCTTCCCGAG TAGCTGGCAC CACAGGTGTG TGCCACCACA 1440
CCCGGATTTT TATAGGTTTT 1460
|
