| Tag | Content |
|---|
EnhancerAtlas ID | HS060-22366 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr21:30677780-30679160 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| YY1 | MA0095.2 | chr21:30678615-30678627 | CAAGATGGCTGC | + | 6.74 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_09591 | chr21:30669827-30682369 | CD14 | | SE_45766 | chr21:30676593-30681045 | Osteoblasts |
|
| | 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 |
| GH21I029304 | chr21 | 30676832 | 30679645 |
|
Enhancer Sequence | TAGTTTGTCT TTTTCCAGAC CCCAGAAAGG CTGGGCCACC TTTTCTTCTT TGAGCAGGTT 60
GGCAACAGTG GTCACAAATA GCAGAGGAGC TGAGATTCTA GAGAGCTATC CTACCACTGC 120
TTCTCAGATG CCAGTGTGGA AACAGCCTCT TCTTTTTTGT TGAATTAGCT TGGAACAGCT 180
CTCTAATCTC TGAAGAGTGA GGAAAAACTG TGTTTTTAAG TTTCAAGGCT AAGGCACTGT 240
GTTCTCTTTT CTCCCTGTTC CTGCTGCTGT TCTCCCCCAA CTCACATGAA CGCATACTTA 300
ACTTTCAGTG TATGTGGACA GTAGGGTTGC TAAATTCATG TCAATATTTG TGGCATTCCT 360
ACATGTTAGG CATTTGGTTT ACATTTAACT TATGAAACAA ATGTTTAGGC TTTTATAAGC 420
CAGGAACTTT TCCAGATATT GGCAATAATG AACTTTTCAG AAGTTACAGT CTAATAGACA 480
GGCAAACTAT TCCCATAGCA TGCTATAGTA GCAACATGTA AAATGTGCTG TGGAACCACA 540
GACTATTAAA AGCCTAAGTT TTGGGAAATC AAGAAAGCCT TAGGGATGTT TAGTGATGAA 600
TGCATAGGTT AGTGGAGGAA ACAACTTGTA TCAACTCAAT TTGAGAAGCT TAGCTGTGAA 660
TAAGAGGAGA GAGAAATAGA TTTTAGTAGG GAGAAGTTGG GTCAGGAAGA GTGTGTGTGT 720
GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTATTTAAAA ATCCAGTCAA TGGAAAAAGG 780
TTGAAGATGC AGGCAACGTC CTTGTTTTGT CCTTGGCAAG TTCCTCTTAT GGTTGCAAGA 840
TGGCTGCCAC AAGTTCAAGT GTCACAAGAA AATATGACTT AAGTTTCCTG GAAGAAGACA 900
CACTTTTTTT TTTTTTTTCC TAGGTTGTTG CTATCAGTGA GAAAAATTTT TCCCTAAAGC 960
CTCATAGCAG ATGCTACCTT GTCCCTCTCT CCTCTCTTCA TAGGTCAGCA TTGCACACAA 1020
GCCAGTGCCT AAATGAGTCA AGGTCAAGGG GAATAGTACC GCTGTGATTG GCATAAATGG 1080
ATCGTGATTC ATCTTAGGTT GTGGCTGGGG TCTACTTCCT TGGAAGTTGA TGGCCTCGGG 1140
TTGAGAGTAG ATACGTGAGC ACAGTCAGGG TTTGGTTAGA AAGTGAGGGG GTGAATGGTG 1200
TTGTGCAGTT AACAGTGACA TCCTTGTCTA CTAGTTCTGC CACCACTACA CTTAGATACA 1260
AACTTCGGAG GAGAAAAAGA AAATGTGCTT GCCTTTGGAT TTGGAATTTT AGGTGACTTT 1320
TTTTCCTCTT ATATGCCATT TCCTTCTATG ATCAAGTAGC ACTTTTACAA TCAAATCAAA 1380
|
