| Tag | Content |
|---|
EnhancerAtlas ID | HS146-01698 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr10:32110680-32112190 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr10:32112153-32112165 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr10:32112157-32112169 | AAACAAACATAC | - | 6.37 | | JUN | MA0488.1 | chr10:32111314-32111327 | ATGATGATGTCAT | + | 7.52 | | JUND(var.2) | MA0492.1 | chr10:32111313-32111328 | AATGATGATGTCATA | + | 8.12 | | MEF2A | MA0052.3 | chr10:32111890-32111902 | ACTATTTTTAGA | - | 6.02 | | NEUROG2 | MA0669.1 | chr10:32112007-32112017 | AACATATGTC | + | 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 |
| GH10I031822 | chr10 | 32110957 | 32112312 |
|
Enhancer Sequence | TACATGGAAT TTATTTGTGG AATCATAATA AAAATCACAA TAGAAATTGT AACTGTATTC 60
TACAAAGTCT TTGCCTGAAG TACCATTGTC AATCGAAAGA CAAATTAAAC ATAAAGCTAT 120
ATGTTGGGCA TAACTTTCTG AGCAGAAATG ATGTATTGCA AATGTTACCA AACTTGAACA 180
TACATTTAAC AAAATGACAA AAATCAATTA TTTAATTTAT TGTCATCATA CACGCTGTAG 240
ATGGGTAGCT CTAAGCTAAG ATACAAATAA GCAACCAAAT AAGATATAGC AATTAAATAT 300
AAATACAATG ACATGACATG GAATGCTAAA AAAAAAAAAT GCAATCAGTA TAGCTGGCAA 360
CATTTCGTTA GTTATTATTT TCCAAAATCT AGTCCCACTT TTCTCTACTG TAATCAACCT 420
CCCCACCAAT GTATTCATCA CAAAGAAAAC AGAATTATTG TGGCAAAGGG CATGCAACAG 480
GAACACATAC AGTGACAGCT GAAACAGGAT CAGACTTTAC ATATGCAACA GCAGGCCGAC 540
GACGGACAGA GTGTTTCCAA GAAGAAAGCA GCGAAAGCAA GAGCTCAGAG ACTGAGCCTT 600
GTTGGCAGAA GGACTTGATG GAAAAGGGAA GAAAATGATG ATGTCATAAC AATGCACAAC 660
AGCAAAATGA CACACAAGAG AAAAGCATAA TGGAACCAGA CAAGACAAAG ATACAATTCT 720
ATATGCAGAC ATACAACATA AGCAAAGCTC AACTTCCAAA TAACTTTGCA AAGGTCCTAG 780
AATTTATCCT GATGATTATT ACATAAATTT ATGTTTCATT TTTAAGATGA ATGCTTTATA 840
GAATTTATCT TAAACAGACT TGTGTTAGCC ATTGGGAGGA ATCATGTCAG GCCCTTTACG 900
ATCTTGATTA GACCCTGTCC AAAATCCCCT AGCTTCCTCC TCGTGACCTG CTGAGTAGTA 960
TCTTCTGGTG TCCCTTTCCA AGTCATCTGT TGGGAGTAGC CCTACCATCT AGCCTGCCTT 1020
TCCCTTCCTC TAGGACACTG ATACTTCCTC TAGGAGACAG GGAATTTTGT CCTCTGGGGG 1080
ACATCTGGTA ACGTTTGGAG ATATTTTTAG TTGTCACAAC TAGAGGCGGA GTGCCAGTCA 1140
TCTGCTAAAC ACCCTACCAC GCAAAGGACA GCCCCACCGA CAACAAATAA TTATCTAGCC 1200
CAAAAGAGTG ACTATTTTTA GAAATTTGAA AGCATGTACA AATGAATGTT TGAATAACTA 1260
CCAATATTTA TGGGTTGATT TTTTAAATGC TCAAGGAATA TGATGAATAA TAACTGAAAA 1320
GAAGCACAAC ATATGTCATG TCACACTGAA CCTGTTCACT TGTCAGTCTT CCCCACTACT 1380
ACGTAAGCTT TGAAGCCAGG GACCATGTTA TTTCTTTCTA AACCCAAAGC TTAACAATGC 1440
CCAGAACACA GCAGGCTTTT AGGTCTGTTG AACAAACAAA CAAACATACA AACATACATT 1500
TCTGAAGTGA 1510
|
