| Tag | Content |
|---|
EnhancerAtlas ID | HS059-13628 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr14:35723240-35724460 |
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 | AACTGGCCGC CTACTAGATC TCTCCCACCT TGAGATATCA AAAGCTCCTC CTCTCATAGA 60
CTCTATCTTG GTACCATCAT CTATCCAGCT GTCCAATCTG TCTTGCTTTA TCCCTCTCCT 120
TGTTTCCCAC ATCCAGTCAG TGACTAAGTC TGCTCAATTC TGCTTTACTA ACTCACAAAG 180
AGCTCTGTTC TTTTCATTTT TACTGCCAGT TTTCTCATTA TCTCTTGCCT GAATTACTGC 240
AGAAGCCTCC TAATTGATCT CCCTTTTGTG GCCCAGCCTT CATGCAGTCC ACAATTTTGA 300
TCTCTCTAAA ATGGAAGTCA TGTCAGTCTC CTGTTTTGGT TTGTTTGCTT GTTTGTTTGT 360
TTGTTTGTTT GTTTTGAGAT GGAGTTTCGC TCTTGTTGCC CAGGCTGGAG TGCAATGACG 420
CAATCTCAGC TCACCACAAC CTCTGCCTCC CGAGTTCAAG CGATTCTCCT GCCTCAGCCT 480
CCTGAGTAGC TGGGATTACA GGCATGCGCC ACCACTCGCA GCTAATTTTG TATTTTTAGT 540
AGAGATGAGG TTTCTCCATG TTGATCAGGC AGGTCTTGAA CTCCTGACCT CAGGTGCTCC 600
ACCCGCTTTG GCCTCCCAAA GTGCTGGGAT TACAGGCATG AGCCACCGCG CCCAGCCCAC 660
TCTCCTGTTT TAAATCCTTT GATTTTCCCC CATTGCTTTC AGGCAGGAAA AGACTTTATA 720
CAACTTATAA AGACCCCTGG GATCTAACCC TTGCATTCAT TTCCAGTCTT ATTTCTGGCA 780
CGTCCCATGT CATCCTCCCA CACCTCTGCT TGAGTCACAT TTGACACCTT GCAGTTCCTC 840
AAATTCAGTG TGCTAATAAA GAGCCTCCAC CTTCAACTTG CTGCTCCTGT TCTTGGAAAT 900
TCCCATTCCT TGCCGGGCTA GTTCATCTGA AAACTCAGCT CTGCTGTCAC TTCCTCTGTG 960
GTGACTTCCC TGACCACCCT CCTCACCCAC AGTCTGATTG AAGTGCCCAT CCTTTGTGTT 1020
CCATCTTAGT GCATACATTA TATTATATTA ATTTGACTGC AAAGACCTTG AGGTTAGAGA 1080
TAACTGTGTT TGGTTGTTTT TTTGTTTTTT TGAGATGGAG TCTCACTTTG TCTCCCAGGC 1140
TGGAGTGCAG TGGCGTGATC TCGGCTCACT GCAACCTCTG TCTCCTGGGT TCGAGCAATT 1200
CTCCTGCCTC AGCCTCCCAA 1220
|
