| Tag | Content |
|---|
EnhancerAtlas ID | HS073-11657 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr5:131693610-131694800 |
Target genes | | Number: 16 | 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) |
| IRF1 | MA0050.2 | chr5:131694771-131694792 | ATTTCCTTTCCCTTTCAGTTT | + | 6.84 | | Sox3 | MA0514.1 | chr5:131694730-131694740 | CCTTTGTTTT | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_25154 | chr5:131693653-131695507 | Colon_Crypt_3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr5 | 131693684 | 131693784 | | chr5 | 131693910 | 131694525 | | chr5 | 131693745 | 131694100 | | chr5 | 131694113 | 131694404 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I132357 | chr5 | 131693240 | 131695295 |
|
Enhancer Sequence | GAGAGGCTGA GGCAGGAGAA TCACTTGAAC CAGGGAAGCG GAGGTTGCAG TGAGCCAAGA 60
TCACACCACT GCACTCTAGC CCGGGTGACA GAGTGAGACT CTGTCTCAAA AAAAAAAAAA 120
AAAAATTCTT GCATCAGTGG GCTTAGTCTA GCCTGGTTAT AAACTCCTGC TTGTGGCCTT 180
AGCAACTTGC CCAGTGCTCC CCTGGGGCTT AGCCCTGTGG AGGCTGAAAC CCAGGTCAAA 240
GTCATGTTCT CCAATCCAGA GCTGGGTGTC TCTCTCACTT CCTTTGAGCA GCAATCACCT 300
CTACCCTGAT TTAGACCAAG CCAAGCTTGC TATGCTGAGG TAACTTAGCT TATCACCAAG 360
GTTATATTTA ACAGACTGCT GAAAGGATTA TAAAAAATTA TGGGGATTTG AACTATCACC 420
CAATGCCTCC GTCTGTTGAC ACAGACAAGT TTAAAGCTTG ATTTTGTGAA CCTTGAGATG 480
ATCTTCCTCC AGCACTGCAA ATGTAATCCT TCTCATCTAA AACTCCCATT CTAATGCCCT 540
ACTGTGCTCC TGCCCCTGCA GAGCCCTCCA GCTCACCCTC CTGCAGTTGT CTTCTCTGTG 600
ACTGAGTCCT CTGCAACACA TATTCCATTG TAGACATGCA ACTCTCCTCT TTCAAGTACA 660
TCCCTGGTTG TTCTCTCCAT CTCCTTTCCT TGATAGAGAT CTGGCTTCTT TCTGAGCACT 720
CCACTAGCCT CATGGCTCTG TCTCTCAAAG GAAGGCTACT CATTTTGCAC TATCCATGAT 780
CCTGGAAGAC AAGAGCTGAG CAGGCTCTCA GCATTCTCCT TGCTTCCCAC TGCCATTTCT 840
AAATCATAAC TCCTTCACCT TCACATACAT AAAAGACCTG CTCAGGTTTG TGCTGTGCCC 900
TCCTGGTTGC TGTTACCAAC ATCTGCCTGG TTGGTTATCC ACATTCTGTG AGCTCTCTGA 960
CACCCAGCCC AAGGTGCTGG TGACTTTTGT GCTCAGGAAG ATGAGTAGTG CTACACCTTA 1020
GCCTCGCAGT ACTTGACCTT CACCTATACT TCACACTCTT GCTGCTGAGG ACACACCCTG 1080
GGCCTCTCAT CAGTCACAAC AGCTCCATCT CACTCTAGGA CCTTTGTTTT CCTCCCAACT 1140
CTTCAGCTCT CACCTGATAT CATTTCCTTT CCCTTTCAGT TTATACCTTG 1190
|
