| Tag | Content |
|---|
EnhancerAtlas ID | HS052-15729 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr17:27703080-27704500 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX5 | MA0510.2 | chr17:27703092-27703108 | AGTTGCCATGGCACCC | - | 6.1 | | RFX5 | MA0510.2 | chr17:27703092-27703108 | AGTTGCCATGGCACCC | + | 6.31 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 27703183 | 27703308 | | chr17 | 27703475 | 27703981 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I029376 | chr17 | 27703238 | 27704454 |
|
Enhancer Sequence | ACCGTTTCTT TGAGTTGCCA TGGCACCCAA AAGACAAAGT TGGGGGGCTG TCTATTAGTG 60
AATGATTAGG AGCCAAATAA AAAGGAAAGT TCTTTGAGGG AAGGCTGGGG TTGTTTGGGG 120
AGCGGGGTGG AGCTGGGTGT TTAAGTATTG ATATAGGGTT AATCCAGACA ACTCTTGGCA 180
TGACCCATAC ACAAGCAACA AAGACCAGAA CAAACAGGAA GGCTTACCTA GGAGCTTTCC 240
AGCATGGTTT CTTCTTCCTA ATTGCCTACG TCTAAGAGAG ATCTGAGTAA GTGACCAGAG 300
GAGAGGTCTG AAGCTAGCAA CTGTTCAGCA CTGAAAATGT TAAGTATTAA TGGTGCCCTG 360
TAGGGACAAA AAGAGTCTTT GGGCTCCTCA GAAAGTGAGG GAACAGCAGG AGCTGCCTGT 420
ACCTGAATAA AATTCACCAG GGAGGTGAGT GAGATTTCTG TTTGGGATGA ATTCCTGGTG 480
ACACAGCCAT ATGGCTTTTA CTGACTGCCA TCCTCCAGAC AGTATACTCT TTTTGGGGAG 540
AAGCTAAAGT ATACAGAAGA TTGTGCTTTC CTCACTGTCA TCTTTAATCC CTCCCCCATC 600
ATTAGCTGGA ACTCTTAAAT GAAGACTCAA GTGTCCCAAT CTATCCTTCC AGCCTGAATT 660
CCTGCCCAAG ATCAAGGGTC CTCCTTCCCT TTCCCCAAGC CACTTCCCCA CATCTCTGAT 720
TTTCTCCCTA GAGTAGGAGG CTCCAGGGGA CCACAGCTGA CTCTGCCAGG CACAGAGGGT 780
TGAGTCATTC TGCAGGCGTC AGAGCTGTTA GCAACAGCTC TGCTGATCTG TATGCAGCTC 840
CAACTCCCTC TCCAGTTCAG AGTTTTGGAG CCGTCTTGTT CAAAAGTAAA GAACAGAACA 900
CAGATGGCTG GTAACAGGAT CCCACAGGGG CCTCCTTTCC CACTGAGCCC ATCCTGCTAA 960
TCCTTTTACA GAAGACAAAA TAAATGGTGA GTAGAGAGAG AGGAAAAAAA AAAAGAGTAT 1020
CGGCTTCTGC ACTGTTCTGT GGGTCCTAGT GGAAGGTCTC TGGTAACAAC CCCAAGCTAC 1080
TCACTAAATT TCCTAGGCAT ATTCCCTTCC TGATCCTTCT TTCTCTTCAT CCACTTCATT 1140
TCCCTTCCAA TCTCCCATTC TCCAACCCAG TTTCCTTTTC TCTGTAGTAT CTATTAATCT 1200
GATGGAGTAT TTTGCCCAAA TGCCTTCTAT TTGTGCCAGG CAATTCTAAT CCTTATGTGT 1260
ATAGGACAAT CAAAAATACT AGGAGTTCTT GGCTGGGCGC GGTGGCTCAC GCCTGTAATC 1320
CCAGCACTTT GGGAGGCCGA GGTGGGCGGA TCAGGATGTC AGGAGATCGA GACCATGCTG 1380
GCTAACACGG TGAAACCCCA TCTCTACTAA AAATACAAAA 1420
|
