| Tag | Content |
|---|
EnhancerAtlas ID | HS098-36334 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr22:19732450-19734260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr22:19732560-19732572 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr22:19732564-19732576 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr22:19732568-19732580 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr22:19732572-19732584 | GTTTGTTTGTTT | + | 6.32 |
|
| | 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 |
| GH22I019744 | chr22 | 19731879 | 19734350 |
|
Enhancer Sequence | AGTTGGGGAG CTAGAGGCCG GGACAGGAGC TGAGGGCCAG AGGGGACTCC GGAGAACACT 60
GGATCAAGTG CCATCAGCTG GGCTAGTTGA AGAGTTTTGT GAGGGTTTTT GTTTGTTTGT 120
TTGTTTGTTT GTTTTTGCGG GAGGGGTGGA ACAAGGACCA GCATGCAGGG CAAGATGAGG 180
CCTGAGGGTG GAGGGGACAG AAGAGCCCTG CCGGGACAAG GGACACAGGG ACATCGGTTA 240
GGTTTGGACC CATGCACAAG GGCTCAGCCA CGCTGCCAGT GCCAGACTGG CCCCCCTTCC 300
TGGGGCGTGG CAGCACATTC AGTTATGGGC ACAGGCAACG GCAGGGGCCA GGGCTGCCTC 360
GAGCAGGGGA GGCTGGGCAC CCAGCTGTCC TGTGAGGACA CACCACCCCA CCCTCAGACC 420
GTGCCACTGG ACACTCACAT GACCCAAGTC TGGCCGCTTG CTCACTGGCA CCCCTGCCAA 480
TCATGCTGAC CTTCTTCCCA CTAGCACCTG CTGGGAGCTG ACAGAGGTCT CTATTCCCAG 540
CCAGGCGCCT GCTCAGGTTA TATTTAGGCC ACAGGGGTGG GAGCTGGGCC TCTGACCCCC 600
ACCATGCCCA AGCAGGGGCA GCTGGGCTGA CGCCGTGGGT TGCTCACTGC CTGCAGGGCC 660
CCTCCCTCCA GGCCTTGTCC TCTCATCCAT CGGCCATGTG CAGGCTGGGA GGCGCGGGCC 720
GGCCATGCTT CATATGGGAA ACAAGCTAGT CTGGCTTTGA GCTCCTGGCC TCGGGACGAT 780
GGGGGCTGAT GGCACCAGAA ACTCTAGGGA GGCCAGCACA AGGGGACAGG CCCGGGAGCT 840
CAGGTTGGGT GGGGGGCTGG CGGGAGGCCC AGCCCAGCCT TTCAGCTCCG GAGGCTCAGA 900
CGTGCCATGA GGTCATTCCC TCCTGGGAGC TCCCAGAGCC CTGCCCGAGG GGATGCTGAG 960
CCCCAGGCCC TTCCTGCCCA GCCGGGGCTG GATCCCTCTT TTCCCTCCTG CTGCCCAGGC 1020
AGGATGTTTC CAGGGAGGAA ATGGCTCCTG GGAGGCCACC CCACCCCCGC TGGAGTCTAG 1080
GGCCACTTCC TGCCCCGCAT GGGCCTTGGT TCTGCCCCCA GTCTGCCAGC CTGGGCCAGA 1140
TCCCAGATTT CCTGTCCCTA CAGCATGGAG AGGCAGAGGT GTCTCGGCCT CAACCAGCCT 1200
GGGAGGCACA GTCGCAACCT CCTGGACCCC AGGACCTGAG AACCTCCCCC TGGAGCCCCA 1260
CTTCCCTTGC CCCACAACCC TGGTCAGAGG GAGGCACGAC CTGCCCTGCC CCCATGCCCA 1320
GCCTTCCCCA GCGCCACAGA GCCTCCTTCA TATAGGTTCC GCTTGGGTAC CAGCTGCTGC 1380
TCCACCGCCC ATCTCCATGG GGCCCGCGGG CCTGGGCCAT CCCCAGCCCA CCCCAGGAAG 1440
CTGAATGGCT GCATCGAAGC TCCCTTTTGG CTACAATCCT GCAGGGCTGG CCTTGGACCA 1500
GCGGGTTAGC CTGGATCTGA TGGGCCCTCC TAGCAGAGGT CATCACCCGG CTCCGTGGGC 1560
AGCCCCATCC CCAGGGGAGG TCAATCAGCT CAGTCCTCAC CCACCCTATT CAATGGGGCT 1620
TCCTGCCGAC CCCAGATCTG GGTGAGTGTC CTGGTCACCG CCCCCTCGAC CACCACCCCA 1680
TGCAGCAGGA AACACGTAGC TGGGGGGTTG TGGGGCTTCA GGACTGGGAT TGGAGAGGCT 1740
GACAGCAGGG CTCAGGGCTC TCGGCGGAAG TGGGGCCTCA GCCCACTCAG AGGTCCAGGA 1800
AGTGGGGGTC 1810
|
