| Tag | Content |
|---|
EnhancerAtlas ID | HS098-21184 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr16:11086410-11087530 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arid5a | MA0602.1 | chr16:11086755-11086769 | CTAATATTGAGAAC | + | 6.64 | | KLF14 | MA0740.1 | chr16:11086812-11086826 | CGGGGGGCGTGGCC | - | 6.32 | | KLF16 | MA0741.1 | chr16:11086814-11086825 | GGGGGCGTGGC | - | 6.62 | | SP1 | MA0079.4 | chr16:11086813-11086828 | GGGGGGCGTGGCCAA | - | 7.4 | | SP3 | MA0746.2 | chr16:11086813-11086826 | GGGGGGCGTGGCC | - | 7.22 | | SP4 | MA0685.1 | chr16:11086811-11086828 | TCGGGGGGCGTGGCCAA | - | 6.64 | | SP8 | MA0747.1 | chr16:11086813-11086825 | GGGGGGCGTGGC | - | 6.44 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_39078 | chr16:11084028-11088306 | IMR90 |
|
| | 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 |
| GH16I010990 | chr16 | 11084434 | 11088171 |
|
Enhancer Sequence | AGATAACATT AAATGGTTTT ATTCACTCAA ATAATATTGT GCTGGGTGAC ACTTGAGTTC 60
TGGGTGGGTC ATTTTCTGAC ATGAGCAGAA TGTGCTCCAT CTGTGAGGCA GAGGCTGGCT 120
GCCATACTTA CCCTTGTGCA CTCCCTGCCT CGAGTAATTG TTGAGCCCCT ACAAGTTGCA 180
GGCAGGTGCT GTGAATGAAC AAGACATCTG TCCCTTCCCT GATGATCTAT TTGTGGGGGA 240
TAGACAGTAA GCCAGCTCAT CCTCACAAAT TTAAGATTTG GATATGGGAA GGAAATAGAA 300
GCAACTTTGG GAGGTATGAT GAGGGAAGCC CTCTAAGGAG GGAGCCTAAT ATTGAGAACT 360
GAGGTCAGGG AGCTAGGCCT GCTGAGAGTT GAGGGGTTGG GTCGGGGGGC GTGGCCAAAA 420
CATGAGAAAT GGTGAGTCAG AGGCCTCTGT GGGAAGGAGT TGGGTGTATA TGGGATCAGG 480
AGAGAGGCCA GCATTCAAGA AATATCCTGG GTTGGTGGAA GAGAGGGACG GTTTTCGTTT 540
TATAGAAGAT GAACCTGGCT GGGCTTGGTG GTTCATGCCT GTAATCCCAC CACTTTGGGA 600
GGCCGGTGTG GGCAGATCAC TTGAGGCCAG CCTAGACAAC ATGGTAAGAC CCTGTCTCTT 660
CAAAAAAATA CAAAAATTAA CCGGGCGTGA TGATGCGTAC CTGTGATTCC AGCTACTCAG 720
GAGGCTGAGG TGGGACCATC TCTTGAGCCT GGGAGGCGGA GGTTGCAGTG AGCCATGATC 780
ACACCACTGC ACTCCAGCCT GGGCAATAGA GTGAGACTGT CTAAAAAAGA AAGAAAAGAA 840
GTCAAGCTTA CTTGTTTGTC TCATTGAACA TCTCATTTCA CGCTCATAAT GAAAGAGAGC 900
GAGGTGGTGT TATTGTCACA CGCTCCCCAT AAGGAAGCCA AGGTTCCGTG ATTGTTCCTT 960
TGGGATTGCA GGTGACTAGC CCCAAATCTC ACACTGTTTC TATTCCAAGT CTTTTTATCA 1020
CCACTTGCAA TTATGTTTTC CAGTTTGGCA TGAGATGTCA GGGCAGTGTA GCATTTTGGG 1080
CTGTTCTGAG TAACAGAATA ACCAGTGTTT CACAGTTCAT 1120
|
