Tag | Content |
---|
EnhancerAtlas ID | HS176-04300 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr10:3710340-3711580 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CEBPA | MA0102.3 | chr10:3710701-3710712 | TGTTGTGCAAT | - | 6.14 | KLF5 | MA0599.1 | chr10:3710975-3710985 | GCCCCGCCCC | + | 6.02 | ONECUT3 | MA0757.1 | chr10:3711184-3711198 | TCTATTGATTTTCT | - | 6 |
|
| 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 |
GH10I003667 | chr10 | 3709730 | 3711884 |
|
Enhancer Sequence | CTCCCAAAGT GCTGGGATTA CGGGCGTGAG CCACCGTGCC CAGCCTTTTG TGGACATTTT 60 AAACAGCAGG GAAATTAATC CTGAGCAATA AAAAATAAAT AAATAAATAA ATAAATCATG 120 GTTTTTATTT GAATCTTAAA AAAACAAAAC GAAACATGTT TTCACTTTTT TTTTTCCTTA 180 TCTAATTTGG CTACTGCTTC ACTTTCTCTG CCACCTCTCT TACTGCAGTT TCAACTAAAT 240 GACTAAGCAA ATTAGATCTT GAGTTGCTTT TCTGGAATGC GGAGAGTTGG AGAATCAGAT 300 AAAAGTCGAG GTATCTCTCT CTTCAGCAGC TTCCAGATCG GGGGCTGGAG CTGAGCGGGG 360 GTGTTGTGCA ATCCCGTACT GTTGTCGAGC AGGCTTCAGT TCAGGGAGAC CAGGCAGGCT 420 GAGGCCCAGG AGAGTGCCCC CTTGCATCTG CCCTGGGGGA AACTCTAGAA GGGGTAGAGA 480 AAATCCGAGA AGAAAGGATA TTTTTACACG GTAGGATTGT ATTTTTATCC CCGGAGGCTT 540 GCTGAACGCA AGTTTCTGGG TAAGTTACAC AATACAGGAA AAGTAACTGT TTAGCGTATA 600 GGTGATACGT GTTGGAGGCC AGAGCGCTCT GCAAAGCCCC GCCCCTGTGT GTGTTGTGTG 660 GTCTGAAAAC AAAGAGCAGG CATCACCTTC TGGAGGTGAG GCTGGCCCGG GACTCAGATG 720 GCTCTAACTC TGCGGGTCGC CTGCCCAGAG GCTGCACTTC AGCCGGCGGG GAAGCCAGGA 780 TGGATCTTAA GTCATTCGAT TCTCAGGCCA TAGGTTGTTG CCAAACTGCA GCCTGGAAAA 840 ATAGTCTATT GATTTTCTGA GTCAAATAAA GTTATGTTAA TGTAGAATTA AATAGATAGT 900 CACATAGCTG TAACATCCCC AAAGATGGAA ATACTACACA TCAAATGTGC CTGTGGTCTC 960 TTTGTTCATC TGTTCCTTCC TGTTCTTACT GCTATCAGAA AAAAACATAC CTAGCATTGC 1020 TAAATAAGGC TTGAGAAACA AGCGTGTTTT GTAAATAGCA CATCTTCGTA CAAACTCATA 1080 TAATATTTTC AAACCCTGAA GTCGCTTGCA TTTTTCTTCG CTATTCACAG CAACTCTGCA 1140 AGATGCTCCT CACATTGGGT TTAAATTGTG ACATCATATC CAAATTATGT CCCCTTGGGC 1200 AACTCAACTA AACTCTTTTC CCCGTTTCTT CATCTCTAAA 1240
|