| Tag | Content |
|---|
EnhancerAtlas ID | HS105-41828 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:12964180-12965780 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr2:12964732-12964750 | AGAAGGAGGGAAGAAAGG | + | 6.75 |
|
| | 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 |
| GH02I012824 | chr2 | 12964201 | 12965530 |
|
Enhancer Sequence | ATGGGTCCTT TCCAGGATCA TGATGTGAAG GAAAAGGTGG AATATTGGGC TGCATTTGTG 60
GTGCTCTGCC AGTGCAGGTG AGGAGTGTGT GAGCATCCTA GGAGTGCATC CAGGTAGTTA 120
GGAGGGAGAG GACAACACAT AGTCTCCTAG GTGCAGGCGG CGGGGGAAGT CCGGTGGACA 180
CCTGTGAAGC TAAGTTCCAG GACCTTCTGG GGGCTGTGGA GAGGAAGGGG ACCTTCTCCA 240
GAGGGGCCGT GTTGATTGAC TCATTCTTCT CTGACTCCTC AGAAGCCAGT TCATTGCAGT 300
AGAGGGGCTG TCCTGCAAGT CATATGCTTC TCCTCCTTGC CTTAACTACA GGAATTCCAA 360
GATGTTTACA CAAACTTCAA GGAGTGAACC AAGTTATTAA AAGAGTAGCA ATTAGGGTGG 420
CCCATCCCAG CAATTTAGTT TCCTGTCTAA GGAAGCATGA AGGGGGAGGG GTTTCCAGGG 480
AGGGGAGAGG GAGGGAGCAT TCTTGTCTCC TGATTGGACC GCCCCAGGAT TTCCATTTCT 540
GAACACAGAC ACAGAAGGAG GGAAGAAAGG TTGCCAGATG CCAGCTCCCA GCTCCCTGGA 600
GGAGTTACTC GCCGCCACAG ATGCTCCAGC AGCTGGTTGG GCCCCTCCTC AAAGTGTCTC 660
TCCTGCTTCC TTCTTTTGGG GGATTCTGGC TCAGCTTTGA AAGCCTTTTG GCATCTTTTG 720
CCTGCCTCCA AAAATTAAGC TGTGTTGGAA GCTGCCTGAT AAATCACTCT TTGCACCGTG 780
GCTGCCATGG GGCTTGCAGA GAGTGGCTGC CTAGTGATTT ACCGCGGCTG TCTGAGAGGG 840
CTTTTCCAAG CAGCCAGCGT AGACCAGGGA GTCATCTCTG GCAAAAGGAG CATTTTGTCT 900
AGCTCAAATG GACACTACAG AGAGGAAGTG GGATTGCTTT GTTCAAAACT TGTTGGTCAT 960
CCATTCCTCA AGCCAGCCGG AATCTCCAAG TTCATTTCTT CCATGCAACT TGAGCTCAAG 1020
AAAAGAGGTC CAGAAAAGTG GTTTTTCATG ACAGGCCTGC TGGAGCCTTT CCTAGGGGAA 1080
GGAGAACTTT CTGGTTCTGA ACTGCAGTTA CACAATGCTG GGCAGGCCCT CTGATTTGTG 1140
GTCATAGTTT CCCAGAACCC CAAGGGACCC ATCCAGGAAA ACGCCCATGT CCCCTCGCCT 1200
GCGTTGTCAT CTGCTCCCTC CCAAGGGGAT TTTGTTTCCT TGATTGTGTT CCATAGTGGC 1260
TGTTGGAAGT CAGGTGCCCT GGACGCAGCT TGGACAGGAA CCATGTGGTG TGAGGACCTG 1320
AGCCTTGTGC ATACGTGGCT TTTGCTTCTG GTTCTGGCTT GACAGTGTGA CGAGTTAATT 1380
AACCTCTTTC ACCTCTAAAT CTTCATCTCC ATTATCAGAA TAATAAGCTC TTCCTTGAGA 1440
AATTGTTGTT TCGACGAAGC CTCATATAGT TAGCACAAAG TAGATGGAAG AGTAGATCCA 1500
AATAAAATAT TTTTAAACAA TATTTTGTTG CTTGTTTTCT GTTCTTGTTT TTGTGGGGTT 1560
TTTTTTTGTT TTTTGTCTTT TTCCCTACAA ACAGGTTTTC 1600
|
