| Tag | Content |
|---|
EnhancerAtlas ID | HS187-07269 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr14:35723580-35724470 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr14:35723590-35723602 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr14:35723594-35723606 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr14:35723598-35723610 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr14:35723602-35723614 | GTTTGTTTGTTT | + | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr14:35723816-35723831 | TGAACTCCTGACCTC | - | 6.22 | | RELA | MA0107.1 | chr14:35724134-35724144 | GGAAATTCCC | - | 6.02 |
|
| | 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 |
| GH14I035254 | chr14 | 35724121 | 35724210 |
|
Enhancer Sequence | TTGTTTGCTT GTTTGTTTGT TTGTTTGTTT GTTTTGAGAT GGAGTTTCGC TCTTGTTGCC 60
CAGGCTGGAG TGCAATGACG CAATCTCAGC TCACCACAAC CTCTGCCTCC CGAGTTCAAG 120
CGATTCTCCT GCCTCAGCCT CCTGAGTAGC TGGGATTACA GGCATGCGCC ACCACTCGCA 180
GCTAATTTTG TATTTTTAGT AGAGATGAGG TTTCTCCATG TTGATCAGGC AGGTCTTGAA 240
CTCCTGACCT CAGGTGCTCC ACCCGCTTTG GCCTCCCAAA GTGCTGGGAT TACAGGCATG 300
AGCCACCGCG CCCAGCCCAC TCTCCTGTTT TAAATCCTTT GATTTTCCCC CATTGCTTTC 360
AGGCAGGAAA AGACTTTATA CAACTTATAA AGACCCCTGG GATCTAACCC TTGCATTCAT 420
TTCCAGTCTT ATTTCTGGCA CGTCCCATGT CATCCTCCCA CACCTCTGCT TGAGTCACAT 480
TTGACACCTT GCAGTTCCTC AAATTCAGTG TGCTAATAAA GAGCCTCCAC CTTCAACTTG 540
CTGCTCCTGT TCTTGGAAAT TCCCATTCCT TGCCGGGCTA GTTCATCTGA AAACTCAGCT 600
CTGCTGTCAC TTCCTCTGTG GTGACTTCCC TGACCACCCT CCTCACCCAC AGTCTGATTG 660
AAGTGCCCAT CCTTTGTGTT CCATCTTAGT GCATACATTA TATTATATTA ATTTGACTGC 720
AAAGACCTTG AGGTTAGAGA TAACTGTGTT TGGTTGTTTT TTTGTTTTTT TGAGATGGAG 780
TCTCACTTTG TCTCCCAGGC TGGAGTGCAG TGGCGTGATC TCGGCTCACT GCAACCTCTG 840
TCTCCTGGGT TCGAGCAATT CTCCTGCCTC AGCCTCCCAA GTAGCTGGGA 890
|
