| Tag | Content |
|---|
EnhancerAtlas ID | HS190-12970 |
Organism | Homo sapiens |
Tissue/cell | Treg_cell |
Coordinate | chr9:92051930-92053560 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr9:92052405-92052425 | CCCCCACCCAGCACCAACCC | + | 6.66 |
|
| | Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
| SE_03177 | chr9:92048344-92053491 | Brain_Angular_Gyrus | | SE_03905 | chr9:92046545-92053775 | Brain_Anterior_Caudate | | SE_04779 | chr9:92038176-92053883 | Brain_Cingulate_Gyrus | | SE_05782 | chr9:92038008-92053861 | Brain_Hippocampus_Middle | | SE_06723 | chr9:92046697-92053775 | Brain_Hippocampus_Middle_150 | | SE_07735 | chr9:92046339-92053618 | Brain_Inferior_Temporal_Lobe | | SE_09037 | chr9:92051844-92052149 | Brain_Mid_Frontal_Lobe | | SE_09170 | chr9:92052077-92053725 | CD14 | | SE_11886 | chr9:92051227-92053330 | CD3 | | SE_14475 | chr9:92051443-92053297 | CD4_Memory_Primary_7pool | | SE_16354 | chr9:92051528-92053432 | CD4_Naive_Primary_8pool | | SE_16924 | chr9:92052250-92053193 | CD4p_CD225int_CD127p_Tmem | | SE_17355 | chr9:92032066-92053749 | CD4p_CD25-_CD45RAp_Naive | | SE_17792 | chr9:92047985-92053851 | CD4p_CD25-_CD45ROp_Memory | | SE_18250 | chr9:92048668-92053803 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19118 | chr9:92051964-92053297 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20089 | chr9:92050886-92053432 | CD56 | | SE_21155 | chr9:92051412-92053610 | CD8_Memory_7pool | | SE_21665 | chr9:92051772-92053329 | CD8_Naive_7pool | | SE_21969 | chr9:92051498-92053290 | CD8_Naive_8pool | | SE_22409 | chr9:92049770-92053658 | CD8_primiary | | SE_26933 | chr9:92049392-92053607 | Esophagus | | SE_32149 | chr9:92049473-92053449 | Gastric | | SE_33121 | chr9:92048376-92052618 | H1 | | SE_41833 | chr9:92049918-92052874 | LNCaP | | SE_50088 | chr9:92050024-92053515 | Sigmoid_Colon | | SE_52548 | chr9:92050161-92053181 | Small_Intestine | | SE_53415 | chr9:92052345-92053066 | Spleen | | SE_60002 | chr9:92014899-92064443 | Ly4 | | SE_62222 | chr9:92014516-92154755 | Tonsil | | SE_68703 | chr9:92047240-92053642 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr9 | 92052114 | 92052760 | | chr9 | 92052785 | 92053119 | | chr9 | 92053103 | 92053397 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I089433 | chr9 | 92048651 | 92053272 |
|
Enhancer Sequence | GACAGCTCAG TCAAGAGGTA GCAATGAGGG CAAACTTGGG AGGTGAGCAT GCACAGAGCT 60
GCTGGACAGT GCTGCAGCGA GATGGCCTGC TCCCAGCTGG GCAGACGACC CTAAAACAGG 120
AAGCACGTGG CCTCTTTTGT TAGGGGCTGC AGGGCCCTGG CTGCTCTGCG GGCCAGCATG 180
CCCACCCCCA TGAGTGGCCT GATCCTAGTG GGCATTGCAC AGTGCAATGA AGTGTGGCTC 240
GTGCAGCTCT GGCAGTTTTT ATTTTTCTGC AGGCCAGGTT TTCCTCCCAC AGCGGCAGGC 300
ACCTGCCCTC AGCCTGTAAG GAAGCGCGAT GCAGTGAGTA TTGCCCAATC TTGGTCGCCC 360
ACACTTGGTC TTGAATAAGC AAACAACCAC AGGACAAGCA GCAGGGCAGG TGTGAAGCTC 420
GCCCTGAGTC TCTGACACTG CAGGTGTGGC CTCCAGATCC CAGCCTCTGC ACCCACCCCC 480
ACCCAGCACC AACCCTAGCA GGCGGCAGCG ACAGGCACTC CCACTGCTGC GGTGCGCCCT 540
GAGAGGGGAG GGCACAGGCC TGGCGCATGA CTGGGCTCAG TGACACGGGC ACCTGCCCAT 600
GTGTGCCAGC GGCAAGGGGC ACAGGTTCCC GGTGCTGCCT CTGGTCAAGG GGTCCCAGGG 660
AGGGAGGTCT GGCTGATGTG TCCAGGTGCT AAAGGAAGGT AGCAACGTGA CTTGAGCAGG 720
CACAGGTGAC AGCCACACAA ATGAGGTCTC TGAGCCTCGG AGATGAACAA GACAGGGACA 780
CTGTATAAAA GATGTGGTGC TCTGCCCTGG TCCGCAGCTC GGGACATAGC CAGGACAGGG 840
ACATGCTTGA ACCCAGATAC CAAGTCTAAA ATTCCTTAAA TTGAGCAACT CAGTCCCAAG 900
GATGAGCCAT CCAACCTGCT AACATGCACA GTGCCATCTG GCACCAGGCT CTGCGCCCTT 960
CTCGCTGGAA GATTTCTAAT AACCTACAGG GGTAGGGATA GAAGGGCAGG GCCATCTCAG 1020
CAAGATGCAG AGAGGAACCA GAGGACACTT TACCCAGTAG GGCACCCAGA TGCTGTGGAG 1080
GGAGCAGCCT CCCTGGGGGC TGAGTGTGGA AGAGGGAAGA GGGAAGCAAC AAAGGTGCAC 1140
TGTAGAGAAT ACTCAAGCCA AGCGCCCTGC TTCTCTCCTG GGAGCCTTTT GTGGCCATGA 1200
AGGCAAGTTT TAAGTTTGGA GATGAGAAAC TGGAGACCCA GGAAGGGTGA AGAGTGAAGG 1260
GCTGGGGGCC TCAGCTGGTG CTGGACTTGT GCTCATGTGG ATGCCACACT CAGGCTGGCC 1320
TGGAGAGAGC TTTCAGGGTG GAGCACCTCC CATGGCAGCT CGTGATGGCT GCATCACAGA 1380
ATGCAACAAG AAGGTGAGCA GGACGACATT CACCGCGGGA GCCTGGTGAC TGCAACTCCT 1440
GCTCACGACA GAGCTGGGGT CATGCAATTA GATAAAATAT TAATCCAGTA CATCACGGGC 1500
TGAAAGCTAT GCCAGTCAAA CCCACATTAT GAAGCACTTT ATTCTGTCGT TCCTGAGACA 1560
AACAACATTT CTAGTGTTAG GGATATTTGA GGCAAAAAAT CGAAGTATTC TTTATGTTCT 1620
TTGACTAGAA 1630
|
