| Tag | Content |
|---|
EnhancerAtlas ID | HS034-31381 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr9:140633840-140635240 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr9:140634317-140634335 | GGCAGGGAGGAAGGAGGA | + | 6.21 | | MYC | MA0147.3 | chr9:140635045-140635057 | AGCCACGTGCTC | + | 6.04 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_11232 | chr9:140631344-140634115 | CD20 | | SE_32711 | chr9:140631342-140634659 | GM12878 | | SE_59172 | chr9:140631350-140657613 | Ly3 | | SE_62965 | chr9:140561512-140658488 | Tonsil |
|
| | 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 |
| GH09I137739 | chr9 | 140634187 | 140635286 |
|
Enhancer Sequence | TAGGTCATAA AGCAGTTTGA GTGTCCACAC TTGTAGGTTG CTGCTGGGTT CAGTGTCCAC 60
ACTTGGGTAG AAGCTGCAGG TCCCTGCTTG GTACAGTGTC CACACTTGAG TAGAAGCTGC 120
AGGTCCCTGC TGGGTTCAAT GTTCACACTT GGGTAGAAGC TGCAGGTCCC TGCTGGGTTC 180
ATTTTCCACA CTTGGGTAGA AGCTGCAGGT CCCTGCTGGG TTCATTGTCC ACACTTGGGT 240
AGAAGCTGCA GGTCCCTACT GGGTTCATTG TCCACACTTG GGTAGAAGCT GCAGGTTGCT 300
GCAGAAGTTG CAGTGCTTCC CTTGCGCTTT TTTGCTGGTG ACCACAGGAC ATGCCCAGAG 360
TGGAGGCCCT GCCTTTTGCT TTGTGAGCTT GGAGTGTTCG TGCCTTCTGC ATAGGTGGGT 420
GGGAACAGTG CCAAATACTG ATCCTGAATG GCCTGGGGTC TCTGTGTGGA CTTGTCGGGC 480
AGGGAGGAAG GAGGACGGTG TCTCTGATGG CAGGGAACAG TTCTACAGGT GCTGCTGTCC 540
AGGCATGAGG CCTGGACATA GAGCTGGGCC CTGCTCTATG TGACCTGAGG ACAGAAGCCC 600
TTGTGAGTGG CAGAGTTGTG GTGGTGACCA CGCAGACTGC TGTGTTTCCC GTGCACTTGC 660
TTTTTTCCCT CACTTCCAAC CTCCCATCCA CCTTGTCTGC CCTCTGGAGC CTGTCGCCTT 720
TCTTCCTTGT CCACACCTCT TCTACCCAGC AGCCCAGCCT TCCTGCAGAG CAGCTGGGCA 780
GTGCCCACCC CCACCCCACG CCCATTTCCA CTCCTGGCAC TATTTTTCCT GGAACTGTCT 840
GTTCCACACT GTCCTATGCC TGGGCCTCCC CGAGCGTCCT GTGAGATGCC AGTTGGCGAG 900
AGTCTTTGCT CGGGGTCCTG AAGCCCCCCC CTCGCCCCCC TTCTTGATGT TCTCCACCAG 960
GATTCTCCTG TGCCAGATCC CATCTGCAGG GCACTGGCCC CGCTTCTTTG AGGCCTGGAC 1020
TGCAAATCCT CCTTCCAAAG AGGCCCTCGA GCCTCTTCGA AGCTTACTGC CAGCCGTCCT 1080
GCAGTTTTCT TTCTCCTGGC CCCTGATGAC GCTGAATCCC AGCCGTCTGG CTCAGGGCCA 1140
GACCCCTTCC CTGGACACAG CTGGAAGTCC CCCTGCAGGA CTGAAGCGGC TCCTCTTCAC 1200
ACTTCAGCCA CGTGCTCAAA CACTTTCAGG TCCTTAATAG ATTCTACATT TCTGAAAGTC 1260
ATCCATAGAT GTTTCTCTAC TATTTAATGT GTAGCAAATT TTATACCTAA CATCTGTTTC 1320
ACACATACAA CCTGTCACTC AGTAAGAGGC CCTTAGACAC CATTCTTCAC TTGTTTGCAG 1380
CAGACAGACT TCCTGACATG 1400
|
