Tag | Content |
---|
EnhancerAtlas ID | HS183-13393 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr9:123629240-123631080 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr9:123630294-123630305 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr9:123630294-123630304 | GCCCCGCCCC | + | 6.02 | MEF2C | MA0497.1 | chr9:123630353-123630368 | TTCTATTTTTGGAGA | - | 6.04 | PLAG1 | MA0163.1 | chr9:123630945-123630959 | CCCCCTCGGGCCCC | - | 6.65 | SP3 | MA0746.2 | chr9:123630293-123630306 | TGCCCCGCCCCCC | + | 6.01 |
|
| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_11823 | chr9:123630403-123631214 | CD3 | SE_13925 | chr9:123630290-123631203 | CD34_Primary_RO01536 | SE_15579 | chr9:123630324-123632151 | CD4_Memory_Primary_8pool | SE_16326 | chr9:123630227-123632358 | CD4_Naive_Primary_8pool | SE_16854 | chr9:123630351-123631205 | CD4p_CD225int_CD127p_Tmem | SE_17311 | chr9:123629326-123633344 | CD4p_CD25-_CD45RAp_Naive | SE_17766 | chr9:123629615-123633170 | CD4p_CD25-_CD45ROp_Memory | SE_19108 | chr9:123630361-123632185 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20050 | chr9:123630318-123632258 | CD56 | SE_20898 | chr9:123629968-123631224 | CD8_Memory_7pool | SE_21944 | chr9:123630159-123632244 | CD8_Naive_8pool | SE_22312 | chr9:123630271-123632788 | CD8_primiary | SE_26718 | chr9:123629785-123632615 | Esophagus | SE_27931 | chr9:123630320-123632218 | Fetal_Intestine | SE_28718 | chr9:123630212-123631214 | Fetal_Intestine_Large | SE_30939 | chr9:123630434-123631230 | Fetal_Thymus | SE_39875 | chr9:123627352-123629663 | K562 | SE_39875 | chr9:123630415-123631192 | K562 | SE_50248 | chr9:123630276-123631237 | Sigmoid_Colon | SE_52520 | chr9:123630305-123631188 | Small_Intestine | SE_53449 | chr9:123629999-123632594 | Spleen | SE_55104 | chr9:123630521-123631203 | Thymus | SE_59300 | chr9:123630370-123667495 | Ly3 | SE_59862 | chr9:123630341-123667956 | Ly4 | SE_60687 | chr9:123630207-123668046 | DHL6 | SE_61111 | chr9:123630545-123707493 | HBL1 | SE_61770 | chr9:123630310-123667005 | Toledo | SE_62230 | chr9:123630172-123700621 | 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 |
GH09I120865 | chr9 | 123627353 | 123629663 |
|
Enhancer Sequence | CATCTGGAGA GACAGAGGAG CCAAGGTCAG CCAGGACCAC ACCCCCAGTC AGGTATGAGC 60 TTCGGCAACC TTTCCCAAGT TAAATTTGCC CTCCACTGGC AGAAAGGGAA GAGAATTCAG 120 TTACTGAGCA CTTAGGCTGT GCCAAGGGAG GACCTGAGAG TTGGACATAT ACTCTCATTT 180 CACCTCACCA CCTGGTAAAA GATGGGACAC TGTCCCCATA TTACAGATAA GTCACAGGTG 240 AAATGGCTTG CCCTAGCTCA CAGGCAAGTG GAGGATGGTG ATTCAAATTC TGGTTTCCCT 300 AACTTCAGAG GCTGTGCTCT CCTTGCCATG CCACAATGAA GCCACCATTT CTGGACTTGC 360 TGCTTCCCAA ACACTGCTGA CAGGGAAACG TTTGCCTTGG AGACTTCACG GGAGAATAAT 420 GGTTTCTGTA AGCTGCACGG GGGCAAGACT ACATCTGGCT TTTCTCACCT GCAACTGTAT 480 CTGGCCTATC ATGGTCATCC AACAACTATT CATGGAATAT GAAGAGCAAA ATGCTCAATG 540 CTTCATTGAC ACCTTGTCAG GTGAGCTCCA GGTTAAAACG CAGATTCCTT GGTCCACTGC 600 AGACCTATTC AATCTTTGGG GAAGCCTCTG GGATGCATTT TTAACAAGCA TCCTGTGCAA 660 CTCTGCCCAT AGGCGTTGAG AAACACTGCA TTAATGCAGG AAAGGTTTCC ATAAGCATTT 720 CTCCATCTGA CAATACTTGG GGAAGCTCAT GGGCCTGAAG TTAAGGTTAA GCCCATTTGA 780 GAGATGAAGT AGTTCAAGCT TTGCCCAAGT TACCCAGCTG GAGCTTGGGG CTGAGATTCA 840 GGACTTCAGG GGGTCCTGAC GGCTGAACTT CCTGAGGGCA GAGACCCTCC CTCTTACATC 900 TGTGGTTCCT TCCACAATGC CACGTGCACT CAGCCCAAAG AAGCAAGCTC AACTGCCATG 960 GCTACATAGA GGCCCAGGTC GGCAAGGAAG AATCAAAGAC TCTTGCCGCA GAGCCAGGAC 1020 AAGAATTCCC TCCACAGTGG CCCCGACATA GCATGCCCCG CCCCCCGGCC CCCTACCCCT 1080 GCCTGATTGC ACATCTCCAG GGAAAAGAAT CTTTTCTATT TTTGGAGACA GGGTCGTCCT 1140 GCTTTGTCGC CCAGGCTGGA GTACAGTGGC ATGATCACAG CTCACTGCAG CCTCCATCTC 1200 CCAAGCTCAA GTGATCCTCC CACCTCAGCC TCCTACGAAG CTGGGACTAC AGGCGTGTGC 1260 CACCGCGCCA GGCGGGAAAA GGATCTTCAT ATCTCACCAG CAGCCGGTTC CACTGACTCT 1320 GACTGTGAAA AGGTTATCTT GACTTTCATG CATTAGTACC ACCACTACCA CCAGTAACAG 1380 CTCACATTTT TTTTGTTTAC CAAATGCCAG GCACTATGAG AACCTCTATG TGAATTACGT 1440 AATTCATGCT CTGCTCATAA TCACCACATG ATGGGGAAAC TATTCAGAGA GCTGAGGCTA 1500 AGGGGTTGCA CAGCTGGTAA GGAGCAGAGC TAGGACGTGG ACGTCCTGGG AGGATTCGCA 1560 CTGTGTCCGG CCCAGGCTCT TAACCACTCT TCAATACTTC CTCGTTTCCT ACAAAGCTCC 1620 AAGGTAACAC CTCTGCCCTC CAGCCCTGCT CCACAGTGCT AGATGCCACG CGGAGCCGGC 1680 CTTCTGTTCT CCCCTTGAGG TCCCGCCCCC TCGGGCCCCA CCCCGAGCCC TTCCCTTCAG 1740 GGACCGCCCC TTGAGGCCTC GCCTCCTCAG GTCCTGTTCC CGAGGCCTTA CTATTCCCTC 1800 CTCCCCACCC CGCCCCTCCA CAGGGTGCTT CTCGACCTGC 1840
|