| Tag | Content |
|---|
EnhancerAtlas ID | HS182-03624 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr11:35351820-35353190 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr11:35352723-35352741 | CCTCCCTTCCTCACTTCC | - | 6.9 | | HSF1 | MA0486.2 | chr11:35352323-35352336 | GAAGCTTCTAGAA | - | 6.28 | | ZNF263 | MA0528.1 | chr11:35352723-35352744 | CCTCCCTTCCTCACTTCCTCC | - | 6.27 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_09894 | chr11:35352062-35353427 | CD14 | | SE_59963 | chr11:35326350-35353415 | Ly4 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 35352000 | 35352622 | | chr11 | 35352025 | 35353057 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I035329 | chr11 | 35351432 | 35353869 |
|
Enhancer Sequence | ACTTCCCCAC TCCCCTAAGC CCATCAAAGA CTGCCTTTCT CACTTTCAAC CTCCAGCACG 60
TCAGATTCTA CCAGAGCTGA GGCTTCTGCC CTGCCTTTGA AAAACTGAAG GGCATAGGTA 120
ATTTCACAGT AGAGAAAGAA GGTGGTAGGG AGTACTGGTA ATGAATAGAA CCATTTATTG 180
ACTTTTTATT CTGTACCAGT GATAGGTAGA GTAATGCCCC AACAAATGTC CATGTCCTAA 240
TCCCCAGAAC CTGTGGATGT GTCAGATTAC ATGGCAAAGG GGCTCTAAGG CTGCAGTTGC 300
AAAGAAGGTT GCTAATCAGC TGACCTCAAG ATAGGGAGAT GCGCCTGAAT TCTCCAGGTG 360
GGACCAGTGG AATCACAGGG GTTCTTATGC ATGAAAAAGG GAAACAGAAA AGAAAGAACT 420
GAAGGATGGC AGCATGACAA AGACACAGCC CAATGTTGCT GGCTCTAAAG ATAAAGGAAA 480
GGGCCAGGAG CCAAGGCATG TGAGAAGCTT CTAGAAACTG GCAAAGGCAA GGAAACAGAC 540
TCCTCCTCCG AGCCTCCAGA AAAGAATGCA GCCCTGCTGA CACCTTGATT TTAGCCCAGT 600
GAGACCCAAC TCAGATTTCT GGCCTCCAGA ACTATATGAT AATAAGTTGT CTTGTCTTAA 660
GCCTCTTGAT TTGTGATCAT TTGTTACTGC AACAATGGGA AACTAAGGTA GTACCAGACC 720
TTATGCTACA CTATCTCATT TGTTGTTTAC AAAAAGCCTC AGCAGAAGGT GATAGACATA 780
GAGAGTTTCC TGTCCACACC CACACCTCTG CTGCTTCTAG AAATCTGCTC AGAGAAGCAG 840
CATGCTCAGC CAGACACTGC TTCTCAGCCT CCCTTCCTGA GATGTAGGCT GAAGTGTTCT 900
GCTCCTCCCT TCCTCACTTC CTCCTGCCCT AGAGAAATGC AGACCAAAGT AACATCTTTC 960
TCTCTTTAGC TAATCACGTG TTTAAAAGGC TCAGCAACAC CATGCCTCTA AATGGCTTCC 1020
ATCGCCCATG GAAGCCTTTC AAGGCCTCCC AGAGGACTTG TGCAGTTCTT TACTTTGGTT 1080
CCTTCTAATG AGCTGCTAAA TTTGTGGCTA TTGAAAGTGA ACTAAACATC CAGTCCCTGT 1140
TGATCCCAGC AGTCCAGTCA GTTTACTGAC TGCCCAACTG CTTCTCAACT AGTTTGATCT 1200
GCTAAATTTA CAAGTGATAA ACTGAGCCAT CCAGTCACCC CTGAAGGGTA ATGTTCTCAC 1260
CAGGAGAATT TCTTCTTAAG AGAAGAATGT ATATTTATCA CTCTGGTAGC TTGTGGAGAC 1320
AGGCTGGTTC ACAGGGCTTT GTGCTGATAT GGCACAGTCC ACAAGTGCAA 1370
|
