| Tag | Content |
|---|
EnhancerAtlas ID | HS182-04161 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr11:75040860-75042030 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr11:75041401-75041421 | CCCCACCCCACCCCATAACA | + | 6.79 | | RREB1 | MA0073.1 | chr11:75041411-75041431 | CCCCATAACACCCCACACCA | + | 7.01 |
|
| | Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
| SE_03287 | chr11:75041374-75041920 | Brain_Angular_Gyrus | | SE_04031 | chr11:75040313-75041841 | Brain_Anterior_Caudate | | SE_04951 | chr11:75038698-75042281 | Brain_Cingulate_Gyrus | | SE_05927 | chr11:75039003-75042234 | Brain_Hippocampus_Middle | | SE_07907 | chr11:75038776-75042175 | Brain_Inferior_Temporal_Lobe | | SE_09621 | chr11:75038907-75042083 | CD14 | | SE_13044 | chr11:75040931-75042114 | CD34_Primary_RO01480 | | SE_13386 | chr11:75038965-75042257 | CD34_Primary_RO01536 | | SE_14290 | chr11:75039890-75042323 | CD34_Primary_RO01549 | | SE_23271 | chr11:75039239-75042140 | Colon_Crypt_1 | | SE_24003 | chr11:75041047-75041451 | Colon_Crypt_2 | | SE_24003 | chr11:75041600-75042140 | Colon_Crypt_2 | | SE_25192 | chr11:75039037-75042197 | Colon_Crypt_3 | | SE_25898 | chr11:75038978-75042365 | Duodenum_Smooth_Muscle | | SE_26962 | chr11:75041074-75042209 | Esophagus | | SE_28109 | chr11:75039189-75042419 | Fetal_Intestine | | SE_29208 | chr11:75039169-75042452 | Fetal_Intestine_Large | | SE_31429 | chr11:75039234-75042571 | Gastric | | SE_41608 | chr11:75041068-75041957 | LNCaP | | SE_42220 | chr11:75039229-75042237 | Lung | | SE_47208 | chr11:75032345-75042889 | Panc1 | | SE_49998 | chr11:75038987-75042142 | RPMI-8402 | | SE_50175 | chr11:75039169-75042236 | Sigmoid_Colon | | SE_52494 | chr11:75039154-75042185 | Small_Intestine | | SE_54712 | chr11:75038901-75042420 | Stomach_Smooth_Muscle | | SE_59773 | chr11:75038940-75077709 | Ly4 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr11 | 75041227 | 75041400 | | chr11 | 75041400 | 75041600 | | chr11 | 75041361 | 75041638 | | chr11 | 75041069 | 75041957 |
|
Enhancer Sequence | ACTCCATCTC TACAAAAAAT TTTAAAATCT ACCCAGGCAT GGTAGCACAT ACCTGTGCTA 60
CAAGTCTCAG CTACTTGAAA AGCTGATGCA GGAGGATCAC TTGACCCCAG GAGTTCGAGG 120
CTGCAGTGAG ATGTGATTGC ACCACTGCAC TCTAGCCTGA ATGACAAGAC TGAGACCCTG 180
TCTCTAAAAA AAAAAAAAGT CACTACTGCC TCTCAGACTC CCTTTCACAC ATGACAGAGG 240
CCTGACAAAT TTGCACTGAA TGAATAAATG AACGAACGAA CAATCTGTCA CTCATTTCCC 300
AACTTCTAGC CTCTCTCTTC TAGTCTATTT ACCTACACAG CTGCCACGTG AACCTTCAGA 360
TCCTGCTGCT CCTGCAAGCT GTGTGTTCAG ACAAATTGCT GAACTTAGCT GAGCCTTCAA 420
TTCCTCAACT ACAAACAGGG ACTCTACTTG GGTAATTAGG AAGATTGAAA GAAAGCATAA 480
GCACAGCATC TCAAGGGCTA AGGAGGAGTC CAGGAAAAGC TGTTGAAGGA AAGCTGTTTC 540
TCCCCACCCC ACCCCATAAC ACCCCACACC ACCCTGATCC TCTAATCTCT CTGTTCCAAA 600
GGCTGCAGGA AAGAGCCCAG CCCCTGGGCT GGCCCCTGGC TATATGTAAA TGTTTATGCC 660
AAGCCCAGCC TCCTAAGGAC AAGTTATTTG CTTTGCTTGT AATTAATTGC AGAAGGCCTG 720
CCTGGGTAAT AAACTCTGCC GAAGAAATAT AAACAGTTTG CACAGAGCTT CAAATCCATT 780
GTGAGGCCAA GAGAAAGGGT CTGCTAGGAA TGGAATGTTC TCCCCAGTCT TCCTCTAAGC 840
TGGAGGCAGA GAGATCACTG AAGGTCAGAA CTGAGAGGAC CCTTGGAAAT CATTTGAAAA 900
ATAGCACCTG GCATCATGAC CTTGTTCCAG GCCCGGCTGA GCACTTGCTT TATATGGTAC 960
AGCTATTTTC CCATTCTAAA GATGAAGAAA CTGAAGCTGA ATGAAAGTGG CAGGGAACTT 1020
TCCCCAACTA GAAGGCAGCT GGGCTGAAAG TTGAATCTGG CTGGACTTTA GAGAAAAAGA 1080
AAGACAGCCA TTCATTCAAC AAAAATATCC CGTGTCCCCC GTGCCAGACA CTGGTACCTG 1140
GTGACACAGC TCCTGCAGCA CTTGCATTCC 1170
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