| Tag | Content |
|---|
EnhancerAtlas ID | HS047-21481 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr20:48381350-48382730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SRF | MA0083.3 | chr20:48382416-48382432 | AGACCATATAGGGTAA | - | 6.07 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_10052 | chr20:48380887-48386644 | CD14 | | SE_26706 | chr20:48381248-48383112 | Esophagus | | SE_53571 | chr20:48381334-48383258 | Spleen |
|
| | 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 |
| GH20I049762 | chr20 | 48379421 | 48394150 |
|
Enhancer Sequence | TATTTTTAGT AGAGATGGGG TTTCACCATA TTAGCCAGGA TGGTCTCGAA CTCCTGACCT 60
TGTGATCCGC CTGCCTCGGC CTCCCAAAGT GCTGGGATTA TAGGCATGAG CCACCGCGCC 120
CAGCAGAAAG GAGTTTTAAT CATTACTTAA TCCAACGCTT TTTTGTTGTT GTTGAAGAGG 180
GAAAACTGAA ACGGGAATGT AATTTGCTCA GGATCACATG GCCAAGTTGT AGAATCAGGC 240
TGCACTCTAG CCTGGGTGAC AGAGGGGGAC TCCATCTAAA AAAAAAAAAA AAGAAAAGAA 300
AGAAAAAGAA ATTATTAACA ATGAAAATTA AAACAAATAA AAATGTTAGA GGCTAGACTC 360
CACAGCCAGC CCACTCTCAC CCTCTGTGTT GTAAATGCTT GCATGAGGCT TCAGGCAACT 420
TTCAGGCTGA CAAGGAAGTT TACAGCACCC AGTCCATAGT GGGAGTGTCC TAATGAATGA 480
TGAATGCTTA TCGTGTGCAA CAGCTTTTTC TTCTTCTTCT TTTAAATGAC CTGGTCAGCA 540
GGAAGTAGCA AGAGCTTCTT AATAGAACAT TGGGGGAGCC AACTGGGAGA GGCTCAACCA 600
GCTTTTGAAC CAGAATAATC TCCGAGAAGT CACAGCCTTT TTTGTTTGGC CCTCTTTTCC 660
TGCAGGTGGA TTCATTAGAG TACTTTGAGT TGCATGTAAG GAGACTGGGT CAAGAGGGCC 720
TTAAGTGACT AGAGTACTTA GTATTATCTC AGGTAACAAT ACACCAATAG GTGGACTGTT 780
TCAGGGTTGG CTATTTCAGC GTCTCAGTTC TGGGGTATTG GATTAGCTTG TTACTGGACA 840
GGGGTCCCAA TCCAGACCAC AAGAGAGGGT TCTTGGATCT CGCGCAAGAA TAAATTCAGG 900
GTGAGTCCGC ATAGTAAAGT GAAAGCAAGT TTATTAGGAA AATAAAGGAA TAAAGAATGG 960
CTACTCCATA GACAGAGCAG TCCTCAGAGT GCCTGGTTGC CCATTTTTAT GGTTATTTCT 1020
TGATCATATG CTAAACAAGG GGTGGATTAT TCATGCCTCT CCTTTTAGAC CATATAGGGT 1080
AACTTTCTGA GGTTGCCATG GCTTTTGTAA ACTGTCAGGG CACTGGTGGG AGTATAGCAG 1140
TGAGGATGAC CAGAGGTCAC TCTCATCGCC TTCTTGGTTT TGGTGGGTTT TGGCAGGCTT 1200
CTTTACTGCA ATCTGTTTTA TCAGCAAGGT CTTTATGACC TGTATCTTGT GCTGACCTCC 1260
TGTCTCATCC TATGACTTAG AATGCCTAAG TGCCTGAGAA CATATCCCAG TAGGTCTCAG 1320
CCTTATTTCA TACAGCCCCT ACTCAAGACG GAGTTGCTCT GGTTCAAATG CCTCTAAGCT 1380
|
