| Tag | Content |
|---|
EnhancerAtlas ID | HS041-20850 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr8:131060040-131061260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MSC | MA0665.1 | chr8:131060102-131060112 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr8:131060102-131060112 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr8:131060102-131060112 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr8:131060102-131060112 | AACAGCTGTT | - | 6.02 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_37698 | chr8:131059446-131061495 | HSMMtube | | SE_58319 | chr8:130983513-131114285 | Ly1 | | SE_59893 | chr8:131020352-131075191 | Ly4 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 131060097 | 131060737 | | chr8 | 131060466 | 131060676 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I130047 | chr8 | 131059654 | 131061032 |
|
Enhancer Sequence | AGGTGAAAGT TTTGGCCTCC TGAGCTTCAG ACCAGGGTTT GCTATGTGGT AAGATTTTGC 60
AAAACAGCTG TTTATCTGAG CTTTAATTCT GGTGTTCAGG AGCTCAAGTG TTTGTGTACG 120
GGCTGCTGTG CTCACACACA GACATGCACA CTCTGCTTTC TTCTCAGTCA CTCACATTGT 180
ACGTGCACCA AGTCACCCTG TGTGCCAGCT CCACCTCTAG CTCCCAAGTG CACAGTGGCT 240
GTCCATGACA TGTTATGAGA AATGCTCGCT GTGGGGCCCT CTGGCAAATG CCTTAATTTC 300
CGAATCCGGA ACTTCATTGC CCTTCATGGT TCACCCCTCC CTGGTGCTGA CCTAATGGTA 360
GAGGGCCGGG ACAGGCCAGC TTTGACCAGC AGCAGCCAAG AGGCAGCAGA GGGTTGTGGC 420
CAGGAGCTCC ATGGCTGAAC CCTGATGTCA GGGCTCAAAA TTCTTGCCTC CACCCTTCAT 480
GAGTGACTTG ACTTTTTGGC ACGCCACGGC TCAGCTGCTC TGAGTATCAG TCTCCTAATC 540
TGTGAACGGG GAAAGTAACA GTCCCTGCCT CTCAGTACTG CTGAGAGAAC TGCAATCGTG 600
CTGCTCAAGC GCTTGGCCTG GTGCTCAGCC CCCGTGGAGG CCTCAGTATG ATGAGCTGCT 660
GGTGGTCCAC GGATCCGCCT GCACAGAGTG CTCCTCAGCA CAGCACAGGG ACTTTGGGGC 720
TGGTCCTGCC TGCCTTCAGT CTGCCGTTTC CTTCTCCTGT CTGCTCCATC TGTTGCAGGG 780
ATGCCACCCC ATCCCAGCAG CTTTGCAGGA GCTCAATCTG TGCAGGCTCC TAGGATGAGC 840
TACGCTCCTT TCTTCAGGCA GCTCCCTGCC AGGTGAACTC TACAGTCATC ATTACTTACC 900
TGTGTTTCTC CGCTTCTCAG GGACAGAATA TGGGGCTGTC TTTGCAACCA AAGGCCTGGC 960
ACTGTCTAGA CAAAAATGGA ATGCTTGTGG ACCATGTGAG CCTCAGGTGT GTAAGAGTAA 1020
GGTGACCTAA TTTAGTGGAC TTCACCTCCA TCCCAGGCAG CTGGCTGGAG AGGCCAGGCC 1080
TCTGTGGGAG GGACACGTGC TCAGACACCC CTGCTAGAGA TGTGAGCCCA TTCACTCCAA 1140
ATTACCCACA GACTGCATAA TGAGGAGAAT CAAAGATTTC CATGGGGTCG GAGAACACAT 1200
GGGGGGGCAG AGGAGAACAC 1220
|
