| Tag | Content |
|---|
EnhancerAtlas ID | HS098-08912 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:268720-269550 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr11:269490-269511 | GTGTGGTTTCAGTTCCTGTTT | + | 6 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_16128 | chr11:267513-270474 | CD4_Naive_Primary_7pool | | SE_21864 | chr11:267477-270412 | CD8_Naive_7pool | | SE_22226 | chr11:267090-270596 | CD8_Naive_8pool | | SE_28519 | chr11:268667-269561 | Fetal_Intestine | | SE_52556 | chr11:267492-273530 | Small_Intestine | | SE_61820 | chr11:266425-273086 | Toledo | | SE_62809 | chr11:266595-290841 | 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 |
| GH11I000266 | chr11 | 266649 | 273455 |
|
Enhancer Sequence | TCGAACTCCT GACCTCAAGT GATCCGCCCG CCTCTGCCTC CCAAAGTGCT GGGATCACAG 60
ATATGAGCCA CCGCGCCCCG CCCTTGGCAC TGTTTAATCC ATGTGTTGTT TATTTATGTA 120
TCCTGTTTAT TTTCTGTCTC CCAACAAAGA CGTAGCTCCT TCTGGGTAGG GCATTTTGTT 180
CATGCTCTCA GATGCCGCCT ACCGCCCTAG AGCAGGAAAT AGCGGTCAGC GCCAGCTGTG 240
AGGAGCACAG CATTGCGGCC AACACAGGAG GCACTGACCA CGGGGCAGGC GCTATTTAAA 300
AATCGTGGCA AAGGATCAGA CGTAACAGAA CTCTTTTTGT TTTAATCATT TTTAAGTGTG 360
CAGTTCAATG ATGTTAGTTA CATGCACAAT ATTGTGTAAC CATCACCACT ATTTCCAAAA 420
TCCTTTCTAT CCGTCAGACA GAAACTCCGT CCCCATTAAA CAGCAACTCT GCATTCCTCC 480
GTCCCCCCAG CCTCTGGTCA CGTGTCTCAT CTACTTTCAG TCTCTACGGA TTTGCCTGTT 540
CTAATTATTT CATAGAAGTG GATTCATACA GTACGTGTCC TTCTGTGTCA GGTTCATGTC 600
ACTCAGCGTG ATGTGCCCAA GGTTCACCCA TGCGTCGGGC TCTCATTCCT GAATCGCATT 660
TCTCTGTACG GATAGACTGA GTTTTGTTTG TCTGTTCACC TGTTTAGGAA CACTTGGTTG 720
CTTCCACATT TTGACTGTTA TGAATAACGC TACTAGCAAA GTGAACACGA GTGTGGTTTC 780
AGTTCCTGTT TTCAATTCTT CCGCGTCTTT TAAGAAAAAA CAAACTGTTT 830
|
