| Tag | Content |
|---|
EnhancerAtlas ID | HS116-27772 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr5:131693710-131695180 |
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 | 131693910 | 131694525 | | chr5 | 131693745 | 131694100 | | chr5 | 131694113 | 131694404 | | chr5 | 131694495 | 131694889 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I132357 | chr5 | 131693240 | 131695295 |
|
Enhancer Sequence | CTGTCTCAAA AAAAAAAAAA AAAAATTCTT GCATCAGTGG GCTTAGTCTA GCCTGGTTAT 60
AAACTCCTGC TTGTGGCCTT AGCAACTTGC CCAGTGCTCC CCTGGGGCTT AGCCCTGTGG 120
AGGCTGAAAC CCAGGTCAAA GTCATGTTCT CCAATCCAGA GCTGGGTGTC TCTCTCACTT 180
CCTTTGAGCA GCAATCACCT CTACCCTGAT TTAGACCAAG CCAAGCTTGC TATGCTGAGG 240
TAACTTAGCT TATCACCAAG GTTATATTTA ACAGACTGCT GAAAGGATTA TAAAAAATTA 300
TGGGGATTTG AACTATCACC CAATGCCTCC GTCTGTTGAC ACAGACAAGT TTAAAGCTTG 360
ATTTTGTGAA CCTTGAGATG ATCTTCCTCC AGCACTGCAA ATGTAATCCT TCTCATCTAA 420
AACTCCCATT CTAATGCCCT ACTGTGCTCC TGCCCCTGCA GAGCCCTCCA GCTCACCCTC 480
CTGCAGTTGT CTTCTCTGTG ACTGAGTCCT CTGCAACACA TATTCCATTG TAGACATGCA 540
ACTCTCCTCT TTCAAGTACA TCCCTGGTTG TTCTCTCCAT CTCCTTTCCT TGATAGAGAT 600
CTGGCTTCTT TCTGAGCACT CCACTAGCCT CATGGCTCTG TCTCTCAAAG GAAGGCTACT 660
CATTTTGCAC TATCCATGAT CCTGGAAGAC AAGAGCTGAG CAGGCTCTCA GCATTCTCCT 720
TGCTTCCCAC TGCCATTTCT AAATCATAAC TCCTTCACCT TCACATACAT AAAAGACCTG 780
CTCAGGTTTG TGCTGTGCCC TCCTGGTTGC TGTTACCAAC ATCTGCCTGG TTGGTTATCC 840
ACATTCTGTG AGCTCTCTGA CACCCAGCCC AAGGTGCTGG TGACTTTTGT GCTCAGGAAG 900
ATGAGTAGTG CTACACCTTA GCCTCGCAGT ACTTGACCTT CACCTATACT TCACACTCTT 960
GCTGCTGAGG ACACACCCTG GGCCTCTCAT CAGTCACAAC AGCTCCATCT CACTCTAGGA 1020
CCTTTGTTTT CCTCCCAACT CTTCAGCTCT CACCTGATAT CATTTCCTTT CCCTTTCAGT 1080
TTATACCTTG TGATCCCTCC AGCCCATTCA TACTCTTGCC ACTACCCCAG TCCTTTTGTT 1140
TACTAGTCTT GCAAAGGCTA AGCTCACAAT AAGTCAAACC ATTTTACTCT TCACTCTCAA 1200
TCCAGGATGC TGACTTAAGA TACAAGAAAG AAGGGGGGCT GTTGATGGGT GCAAGGAAAC 1260
ATGGGTTGAG AGAGTAACAA GTGGGCTGAG GGTCCAATTG TGATTGGAAA TGTAAATGTG 1320
TCAAGACACC AACTCACATG GTTGTGTGAT TTCCTCCAGT GACCCAGGGT AGGAGTACAG 1380
TGACCAAATG GTTGGATTTA GGGCCTTGCA GTAGAGGTGA ATGGAATGAT AAGACAACGA 1440
AGGAACTGAG ATAGACGGAA GCAAAGGGCC 1470
|
