| Tag | Content |
|---|
EnhancerAtlas ID | HS098-28938 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:12964220-12965760 |
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 | AATATTGGGC TGCATTTGTG GTGCTCTGCC AGTGCAGGTG AGGAGTGTGT GAGCATCCTA 60
GGAGTGCATC CAGGTAGTTA GGAGGGAGAG GACAACACAT AGTCTCCTAG GTGCAGGCGG 120
CGGGGGAAGT CCGGTGGACA CCTGTGAAGC TAAGTTCCAG GACCTTCTGG GGGCTGTGGA 180
GAGGAAGGGG ACCTTCTCCA GAGGGGCCGT GTTGATTGAC TCATTCTTCT CTGACTCCTC 240
AGAAGCCAGT TCATTGCAGT AGAGGGGCTG TCCTGCAAGT CATATGCTTC TCCTCCTTGC 300
CTTAACTACA GGAATTCCAA GATGTTTACA CAAACTTCAA GGAGTGAACC AAGTTATTAA 360
AAGAGTAGCA ATTAGGGTGG CCCATCCCAG CAATTTAGTT TCCTGTCTAA GGAAGCATGA 420
AGGGGGAGGG GTTTCCAGGG AGGGGAGAGG GAGGGAGCAT TCTTGTCTCC TGATTGGACC 480
GCCCCAGGAT TTCCATTTCT GAACACAGAC ACAGAAGGAG GGAAGAAAGG TTGCCAGATG 540
CCAGCTCCCA GCTCCCTGGA GGAGTTACTC GCCGCCACAG ATGCTCCAGC AGCTGGTTGG 600
GCCCCTCCTC AAAGTGTCTC TCCTGCTTCC TTCTTTTGGG GGATTCTGGC TCAGCTTTGA 660
AAGCCTTTTG GCATCTTTTG CCTGCCTCCA AAAATTAAGC TGTGTTGGAA GCTGCCTGAT 720
AAATCACTCT TTGCACCGTG GCTGCCATGG GGCTTGCAGA GAGTGGCTGC CTAGTGATTT 780
ACCGCGGCTG TCTGAGAGGG CTTTTCCAAG CAGCCAGCGT AGACCAGGGA GTCATCTCTG 840
GCAAAAGGAG CATTTTGTCT AGCTCAAATG GACACTACAG AGAGGAAGTG GGATTGCTTT 900
GTTCAAAACT TGTTGGTCAT CCATTCCTCA AGCCAGCCGG AATCTCCAAG TTCATTTCTT 960
CCATGCAACT TGAGCTCAAG AAAAGAGGTC CAGAAAAGTG GTTTTTCATG ACAGGCCTGC 1020
TGGAGCCTTT CCTAGGGGAA GGAGAACTTT CTGGTTCTGA ACTGCAGTTA CACAATGCTG 1080
GGCAGGCCCT CTGATTTGTG GTCATAGTTT CCCAGAACCC CAAGGGACCC ATCCAGGAAA 1140
ACGCCCATGT CCCCTCGCCT GCGTTGTCAT CTGCTCCCTC CCAAGGGGAT TTTGTTTCCT 1200
TGATTGTGTT CCATAGTGGC TGTTGGAAGT CAGGTGCCCT GGACGCAGCT TGGACAGGAA 1260
CCATGTGGTG TGAGGACCTG AGCCTTGTGC ATACGTGGCT TTTGCTTCTG GTTCTGGCTT 1320
GACAGTGTGA CGAGTTAATT AACCTCTTTC ACCTCTAAAT CTTCATCTCC ATTATCAGAA 1380
TAATAAGCTC TTCCTTGAGA AATTGTTGTT TCGACGAAGC CTCATATAGT TAGCACAAAG 1440
TAGATGGAAG AGTAGATCCA AATAAAATAT TTTTAAACAA TATTTTGTTG CTTGTTTTCT 1500
GTTCTTGTTT TTGTGGGGTT TTTTTTTGTT TTTTGTCTTT 1540
|
