| Tag | Content |
|---|
EnhancerAtlas ID | HS187-21749 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:131234010-131234710 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F1 | MA0024.3 | chr6:131234013-131234025 | AATGGCGCCAAA | + | 6.11 | | E2F4 | MA0470.2 | chr6:131234012-131234026 | GAATGGCGCCAAAT | - | 6.95 | | PRDM1 | MA0508.2 | chr6:131234531-131234541 | TCACTTTCAC | + | 6.02 | | SP1 | MA0079.4 | chr6:131234456-131234471 | AGTGGGCGGGGTTTA | - | 6.64 | | SP2 | MA0516.2 | chr6:131234455-131234472 | AAGTGGGCGGGGTTTAC | - | 7.29 | | SP4 | MA0685.1 | chr6:131234454-131234471 | TAAGTGGGCGGGGTTTA | - | 6.88 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 131234304 | 131234668 | | chr6 | 131234380 | 131234589 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I130911 | chr6 | 131232799 | 131235285 |
|
Enhancer Sequence | TTGAATGGCG CCAAATTGAA AAGAAAAAAA AAGTCCCCAG AATATTAACA CAGAGAAATT 60
AAGAGAAAGT GCTGGTCTTA AAGACAGACC CTTCCAAATC CCCAATTTCA TTAAGTGTGA 120
GCAGTGATAC AGATCCCCAG TACAGAAGAG CAACAAAGGA CCCTTCTCTG TTCCAGAAGA 180
TGGTGGAAGC TTGTGAACCC AAGGACTAAC CCTGTGTCCC AGCCACCTGG CACCTTCTAT 240
TCTCACCTAA AGCACCCGGC CCTTGTACAA ATTACCTAAC AGTTTCTATA GGGCATGGTA 300
AGAGTCAGCT CTATAAACCC AGCAATATGA GTGAAAAGTC AGACAGCCAA ATTCAGACTT 360
GGTGTCATTC TCAGGCCACT TTCCACAACA CTGCCAGACA GATTACTGAA GGCTGAAATG 420
GCTTACTTTC AACCATCCAA AGACTAAGTG GGCGGGGTTT ACCTGATGTG ATCAAACAGC 480
AGCATGACTT CCTCACCGCG TTTTCCCTTT CCTAACCACA CTCACTTTCA CACTGTAAGT 540
TCCATTCCTG CCAAGCATTA GGCTGTCTTC TCACTCCCCA GTACTACAAC TTTGCAAGGG 600
CTGGAACAGA CCATATTATT TATATCTTCC AGGGTACTTA ATACAGTTTT AGGCAACCAG 660
TGAGAACTAA ATTAATACCT GCTGACTGAT ATATGCCCCT 700
|
