| Tag | Content |
|---|
EnhancerAtlas ID | HS182-03298 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr11:267540-268560 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFKB1 | MA0105.4 | chr11:267820-267833 | AGGGGAATCACCG | + | 6.25 | | ZNF263 | MA0528.1 | chr11:267553-267574 | GGAGGAGGGGGAGGGGCGAGG | + | 6.04 | | ZNF263 | MA0528.1 | chr11:267545-267566 | CGAGGAGGGGAGGAGGGGGAG | + | 6.12 | | ZNF263 | MA0528.1 | chr11:267559-267580 | GGGGGAGGGGCGAGGAGGAGG | + | 6.4 | | ZNF263 | MA0528.1 | chr11:267550-267571 | AGGGGAGGAGGGGGAGGGGCG | + | 6.96 |
|
| | Number of super-enhancer constituents: 6 | 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_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 | AGGAGCGAGG AGGGGAGGAG GGGGAGGGGC GAGGAGGAGG CGGGAGGAGC TGGACAGGAC 60
ATCGTGCCAG CCCGAGGGCG GAATGAACTT CAGAGAAGTT TGAGAGCAAA AGGTGCTTTG 120
CTGCTGTTAG ACCCTGAAAT TCCACGGGTC CCTGGACAGT TTTGGGAGCC GGGAGGGTGA 180
AGAGAGTGGA TCAAGCTTCG TGGGGTGGAC CCGGAAGAGA TGGGGCAGTG AATGGTTCTG 240
GGGGACTGCG GGAGCCTCCG GGGAGTGATT TTTTGCCCTG AGGGGAATCA CCGCAGCGGG 300
GACAAGGCTG GGGGAAAACA CTTCCTTCTG CAAGGGCACT GCTGAGCCTC ACTTGCTGGA 360
GCTTGCACTG TGCAACGGTA AATTCACGTT GTGTGCCCTC ACCTGAGCTT CTGATGAGGA 420
CGCTGGAGGG CTTGGCCCTT TGAAGTCCTC ACCTGTCCCT CCTTGGGCTG GGGGTGGTGA 480
CTAGGAGGGG CTGCACGGCT GCTGCCCGGG TTGGTCCCGG CCATCCCAGC TCCCTGGTAA 540
ATAGGCTTCT CAAACTAGGA TACCTGGGCC TTGGGCGTTA CCTGCAAACC CTGTTCCTCG 600
CTCTAGTTCC CCACTTCCAT CCCTCCTCTT GCCTCAGCCC TTCTCATCTC ACACGCCACA 660
TGGGATCCAC CCTTTTTACG CATGTGCAGA GCGTGGCCCC TCTCTGATTC CCTTCCCCTC 720
AGGAGAGCCG GACGTCTCCC TCCCTCACAC CCTCCCCAGC CCCACAGCAG CCCAGGGAGC 780
CTTGCCCGCT CCTCGGCCCC CCTGGCTCTC CCAGCCACCC AGGCCTCCTG TGTCCTGAGT 840
GGGCCAGCTC CTGCCAGACC ACGGCCCTGC CCTGCACCTG ACTGCGTCCC CACCGCGGAC 900
CTGCCCCCTC GTTTATTCTC CTCTCTCCGC TCTGCTCTGT CCTTGGCACT GTTTTTGTTT 960
GTTTTTTGTT TTTGTTTTTT GAGACGCAGT CTCGCTCTGT CACACAGGCT GGAGTGCAGT 1020
|
