| Tag | Content |
|---|
EnhancerAtlas ID | HS049-03849 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr19:8218740-8220370 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr19:8220352-8220364 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr19:8220356-8220368 | AAACAAACAAAC | - | 6.32 | | Klf1 | MA0493.1 | chr19:8220196-8220207 | AGCCACACCCT | + | 6.02 | | MYC | MA0147.3 | chr19:8219939-8219951 | GGCCACGTGCCC | + | 7.22 | | RREB1 | MA0073.1 | chr19:8220191-8220211 | CCCCCAGCCACACCCTCACC | + | 6.1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH19I008155 | chr19 | 8219073 | 8219130 | | GH19I008154 | chr19 | 8219326 | 8220561 |
|
Enhancer Sequence | CCATCTAGTT TTTTTTTTTT CTTTTTCTTT TTCCTTTTTT TTTTTTTTTT TTTTTTTTTA 60
GATGGAGTCT TGCTCTGTCT CCCAGGCTGG AGTGCAGTGG TGCCATCTCG GCTCACTGCA 120
ACCTCCACCT CCCAGTTTAA GTGATTCTCC TGTTTTAGCC TCCTGAGTAG CTGGGATTAC 180
AGGTGCCTGC CACCACGTCT GGCTAATTTT GTATTTTTAG TAGAGATGGG GTTTCACCAC 240
ATTGGCCAGT CTGGTCTTGA ACTCCAGACC TCAGGTGATC CACCTGCCTC GGTCCCAAAC 300
TGTGGGGATT ACAAGTGTGA GCCACCGCGC CTGACCCCTA GTGGATGTTC TCTTTTTTTG 360
GTTTTTGTCC TCCCCGGACC GCCCCCGCCC CGAGATGCAG TCTTGCTCTG TCACCCAGGC 420
TGGAGTGCAG TGGTGGGATC TTGGCTCACT GCAACCTCCT CCTCCTGGGT TCAAGGAATT 480
CTCCTGCCTC AGCCTCCTAA GTAGCTGGGA TTACAGGCGT GTGCCACCAC ACCCGGCTAT 540
TTTTTTTTTT TTTTTTTTGT ATTTTTAGTA GAGATGGGGT TTCACCATGT TGGTCAGGCT 600
GGTCTCGAAT TCCTGACCTC ATGATATGTC CGCCTTGGCC TCCCAAAGTG CTGGGATTAC 660
AGGTGTGAGC CACTGCACCT GGCCCCTAGT GGGTTTTAAA ATTACAGTGT CACCTGTTGC 720
TGTCACCTGT TGCCTTCCCA TCATTCCCAG TTCCTGTGAC GTTGTCACCT GTTGCTGTCA 780
CATTGTCACA CTATTAATGT CCCCCAGAAC TGTCCCCCCC CGCTGCTGCC ACTGTCATCC 840
CGTTAAGGTC ACTGTGAGTC ACGCCAGCCC CACCCTCCGT TTGACTTTCT GAGCAGCCAT 900
GGAGCCCCCC CTCATAGGCG GGACTTGACT GTGTGCACCC AGAGCCAGCA GACCCCAGAT 960
GTTCATTAGC ATGAGCTCGA GGAAGGCATG GAGACAGGAG TGGGCAGGGT GTGCCCAGGA 1020
GCACAGGGTC AAGGCTGGGG ACAAGGAGAT GGGAGGAGGG ACGGGGAGAT GCCTGCAGTC 1080
TATGGTGTGT GGAGTGCGCT GGGCCAGCCT AGGCCAGGGT GGCTTGGGGA CAGAGCCCTC 1140
TTTGTATAAG CACAGGAAGC AGCTGGGAGT CAAAGCATTG CATACAACGC CAGGAGTTTG 1200
GCCACGTGCC CAGGAATGAG GCTTGGAGCG GGGAGGGAAG CCGCAGAGGA CCCAGGAAAG 1260
CTCTGAGGAA GAGATCAAGC TGGATCCTCA CAAGAGACCC TGAAGACAGG CTCTGATATC 1320
ATCCCATTAC ACAGATGAGG AAACTGAGGC ACAGAGCCAC CACATCGCCC ACTGGGACCC 1380
CACCACCAGG AAAGAATACA GGCAAATCTG AACCCAGGCC ACAAAGCTGG AACCTTCCCC 1440
GTGGCCTTGG GCCCCCAGCC ACACCCTCAC CCCATTGCCT TGATGTTCTA GCTGGGGGAC 1500
CTGTCTAGGG TCCATATACA ATATATTATT TCTCTTTCTA ATAAACACAC ATGTTTGCAC 1560
CTTTATACAT TGTTCTGTAT TTGCCCTATT TCCTCTTTGT AAAAATAATT AAAAACAAAC 1620
AAACAAACAA 1630
|
