| Tag | Content |
|---|
EnhancerAtlas ID | HS034-31101 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr9:131814210-131815600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx2-5(var.2) | MA0503.1 | chr9:131815134-131815145 | CTTGAGTGCCT | - | 6.14 | | Zfx | MA0146.2 | chr9:131814348-131814362 | CCCGCCTCGGCCTC | + | 6.01 | | Zfx | MA0146.2 | chr9:131814645-131814659 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | 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 |
| GH09I129051 | chr9 | 131814117 | 131815639 |
|
Enhancer Sequence | TCTCCTGCCT CAGCCTCTGG AGTAGCTGGG ACTACAGGTG CCTACCACCA CGCCCAGCTA 60
ATTTTTTTGT ATTTTTAGCA GAGACAGGGT TTCACTGTGT TAGCCAGGAT GGGCTTGATC 120
TCCTGACCTC GTGATCCGCC CGCCTCGGCC TCCCAAAGTG CTGGGATTAT AGGCGTGAGC 180
CACCGCGCCC AGCCTGTAAT TTATTTATTT TTAAGGTGTG GCCTCACTCT GTTTTCCAGG 240
CTGGAGTGCA GTGGCGTGAT CTTGGCTCAC TGCAGCCTCC ACCTCCTGGG TTCAAGCGAT 300
TCTGTCTCAG CCTCCTGAGA AGCCAGAGTC AGAGGTGCCT GCCAGCACGC CCGGCTAATT 360
TTTGTATTTT TAGTAGAGAT GGGGTTTTAC CATGTTGGCC AGGGTGGTCT CGAACTCCTA 420
ACTTCAAGTG ATCCACCCGC CTCGGCCTCC CAAAGTGCTG GGATTACAGG CTTGAGCCAC 480
CACACCCAGC CTACAGTGAA TATTTATTAT TGCAATATCA GGAAAGGAAA ATGAAGTTAA 540
AAGGCTAAAA TTTAAATTTT TGTGGCCAGG CACGGTGCCT CACACCTGTA ATCCCAGCAC 600
TTTGGGAGGC CGAGGCAGGA GGACCAGTTG AGCCCAGGAA TTTGAGGGGA TGGGGCCACT 660
TTTGGCAGCG GAGGTAGAAG GAGGAGGGAG GATTTCTCTG CCTATTCCTC CCTCACCCTT 720
GCCTTCATTC CTCTACCCGT GTGTCCCATT GGCCGAGAGC CAGCTGGCAG GGGGACCTGG 780
GAAACAGGTT GCAGAACAAG GGGAGGGCTG TGTCTGGCAC AGCTGGTAAC AAGTTGAAGG 840
TGTCCATGCT CTCTGTCCCT GCTGGGGCGT GAGCTCAGGA TGTGAAGGTC AGGGAAATAC 900
CTGAGGTTTG AAGTGACTCA AACCCTTGAG TGCCTGCAGT TGCAGCTGCG TCAGGTCCTG 960
TCTGCGAGTC GGCAGGGAAC GGGCACCTGT AGGAGTGTGT TGGTGAGGGG GACTCAAGGG 1020
AGGTAGCTTT ATTTCCCAAA TTGTATTTCT TGCTAAAAAC TATATCTGAA AATGATAGAA 1080
TTTGCATTGT TTTCCTTGTT GTGAAAGCAA TTACATATTC CTTATCAAAT AATGAAAAGT 1140
ACAGAAATAG GAAAGAGAAG GGGGTGTAAA ATAGTCTGAT CCCAGACTCT GATCAGACAG 1200
CCCATGGTTG TGTGGTGTGG CACCCTCGGC CTCCTGGAGC ACTGGCGCTC TGTGGGGGCG 1260
CCAGCACCAG CTGTTCAGGC CTGGTCCATA GTAGGTGCTC AGTTAATGAT CTGTGGCATA 1320
TCTACATGCC AGGACGCCTA CAACCTTACA ATCCTACAAG GGGTGCCTGC AGCCCTTCAT 1380
CCAGGCATCA 1390
|
