| Tag | Content |
|---|
EnhancerAtlas ID | HS108-36071 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr6:161202940-161204050 |
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 | chr6:161203851-161203869 | CCTTCCTCCCTCTCTCCC | - | 6.27 | | EWSR1-FLI1 | MA0149.1 | chr6:161203847-161203865 | CCTGCCTTCCTCCCTCTC | - | 6.33 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGTAGTAAAT AATTCTCATG AGATCTGATG GTTTTATAAC AGGAAACCTC TTAGGCTTGA 60
CTCACATTCT GTCTTGTCTG CCAACATGTA AGACATGCAT TTGGCCTTCC ACCATGATTA 120
GGAGGCCTCC TCAGTCACGT GGAACTGTGA GTCCACTTAA CCTCTTTTTC TTTATAAATT 180
ACCCAGTTTT GGGTACGTCT TTATCAGGAG AATGAAAACG GACTAAAACA GTATCCAACA 240
CCAGGACGAT GCATGCACAT CAACTAATAC TAAGGGAAGA TCCCACAAGC CTAGAGTGGG 300
GACTAGGCTG GGAAAAGGCT AGGACTTAAG GCAGGAGCAA GAAATCTAGA CAAGGAAAAA 360
AGGCAGAGAC TTAAGACAGA GGTGGGAACT TCAGGAAAGA GTTTGATGTC ATAGCAACTC 420
AATGCAGAAC TCTTGGAAAG CTGTTGACTC TCTCCCTTTC AACAGCCTGC TCTGCCTTAT 480
CTTTCAGAGC ATACTGTCTC TCTGTGTAAA TTCTCTGCTC TCTATCTTCC TTCCATAAAT 540
TGTCTTTTTT GGCTAAATTA GTCACTTAGC AGAATTCTTT CTCCGAAGTA AGACAAAGAT 600
CTGAGGATTC TTCCACTTCC AGATAACACT GTATTCATTA ATATAGTAAC ACAGGAGTGG 660
TGACATCATT CTAACCTGTT TATCAATCTA GTTAATCTTT TAATATATTG AAATCTGTGA 720
ATGGAAAAGT TTTTTATATA ATTTCAACTT TTGAGATTTG GAGGTACATA AGCAGGTTTG 780
TTACATGAGT AAATTAGCCT CTTTTGGCCT CTCACCCTGT GAAGATTGCG TGACACTGAG 840
GTTTGAGGCA CAAATGATCT CATTACCCAG CTAGTGAGCT TCATACCCCA CAGGTAGTTT 900
TTCAGCCCCT GCCTTCCTCC CTCTCTCCCG GCTCTAGTAG TTGCCAGTGT GTCTTTTGTT 960
GCCATCTTTA CGTCCATGTT TTGAAGTGTT TTCTTCATTA AATATCTTGA TTCATAGCTA 1020
TGCATTCTGC TTCCAGTAAA GCAGAAAGTT TTATTTGACT AATATGAACC AAATAGATAA 1080
AAAAAGAACT CATGACAATC AGACTTGGTT 1110
|
