| Tag | Content |
|---|
EnhancerAtlas ID | HS052-07172 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr11:75036530-75038060 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr11:75037534-75037555 | ACAGGGAAACTGAAACAGAGA | - | 6.36 |
|
| | Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
| SE_00135 | chr11:75036513-75038138 | Adipose_Nuclei | | SE_03287 | chr11:75036636-75037918 | Brain_Angular_Gyrus | | SE_04031 | chr11:75036345-75038085 | Brain_Anterior_Caudate | | SE_04951 | chr11:75034663-75038287 | Brain_Cingulate_Gyrus | | SE_05927 | chr11:75034576-75038325 | Brain_Hippocampus_Middle | | SE_07122 | chr11:75036347-75038077 | Brain_Hippocampus_Middle_150 | | SE_07907 | chr11:75035020-75038317 | Brain_Inferior_Temporal_Lobe | | SE_13044 | chr11:75036022-75036699 | CD34_Primary_RO01480 | | SE_13386 | chr11:75034550-75037272 | CD34_Primary_RO01536 | | SE_14290 | chr11:75036781-75037569 | CD34_Primary_RO01549 | | SE_23271 | chr11:75036602-75038082 | Colon_Crypt_1 | | SE_24003 | chr11:75036640-75037365 | Colon_Crypt_2 | | SE_24003 | chr11:75037483-75037767 | Colon_Crypt_2 | | SE_25898 | chr11:75036317-75038204 | Duodenum_Smooth_Muscle | | SE_26962 | chr11:75036593-75037381 | Esophagus | | SE_26962 | chr11:75037469-75038141 | Esophagus | | SE_31429 | chr11:75027974-75038240 | Gastric | | SE_41608 | chr11:75036701-75037438 | LNCaP | | SE_41608 | chr11:75037518-75037958 | LNCaP | | SE_42220 | chr11:75036533-75038074 | Lung | | SE_46889 | chr11:75036773-75037203 | Ovary | | SE_47208 | chr11:75032345-75042889 | Panc1 | | SE_49998 | chr11:75036567-75037958 | RPMI-8402 | | SE_50175 | chr11:75036544-75038029 | Sigmoid_Colon | | SE_52494 | chr11:75036574-75038096 | Small_Intestine | | SE_54712 | chr11:75035877-75037659 | Stomach_Smooth_Muscle | | SE_65484 | chr11:75033887-75038053 | Pancreatic_islets |
|
| | 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 |
| GH11I075322 | chr11 | 75033560 | 75038244 |
|
Enhancer Sequence | AACTTTTGTA TTTTTAGTAG AGACAGGAGT TTCACCATGT TGGCCAGGCT GGTCTCAAAC 60
TCCTGACCTC AAGTGATCTA CCTGCCTCAG CCTCCCAAAG TGTTGGGATT ATAGGCGTGA 120
GCCACCATGC CTGGCCCAGT TTACTTTTTA TAAAATAAAT CTCAACAGGC ATGACACTTT 180
AAGCCCATCC AAAATATAGA CTAGTGAACT CTGCGGCTCA TGCTAAGAAC AGGTAGGGGC 240
TGAGGCCACC AAAGCCGCTC CCCAAACCAG GCTTGGCCAT TACCTTCCAG GCACCCCCAG 300
GCATGCCCCA GCCTCTCTCT GGACCTCACT AACCTTGTGC GTAAAGGGAC CTCTGAGATC 360
CCTTCTGGAC CTCACGCCCA GGGCTCTCTG GTCTGACCCT GCCAGTGCTC AAAGCAAAAG 420
CCCCAGGCCC AACTCGGGCC GGCTGACTCA GAGGCTTGGA GGTTAGAAAA CAGAAGAATC 480
TCAGAGCTCA GCCAGGCTGA CCTCTCCCAT GACAGGTAGG GAAACTAAGG CCTAGGATCT 540
TTCCTAAGGT CCCCTCAAAC CTAGGGCACC AGCTCCCAAG CCTAGGGCAT TTTCTAATGC 600
CTTGAAGGAG CTCTGCAGGG TCCCAGGGGA GGTGGTGCCT GCTCAGGCAG CTCTGGAGAA 660
GCAGGAGGTG ATGAAGAATT TTCATTAACA GCCAAGGCTC CAGGCTGGGA GGAGGAGGGT 720
GCTGCCGGAG GATGTGCGAG AGCTCCTGAG AGAGGCACTG AGTCATGCTT GCAGCTGCGT 780
CCCCAGAAAG CAGCCCAGGG CCTGGCACAG CGTGGGTGTG CAGTAAATGA ACAAATAAAT 840
AAAAATGTGA ATGAGTGATA ACAACAGCAG CTAACACGTA GTACTTACTT TGTGCCAAGC 900
ACTTTACAAA TATTAACTCA TTTAATCCTA ATGGAAACAT TAAGATTCCC ATAACAAAAG 960
ATGAAGATTC TCATAATAAA AATTTTGTTA TTCCTCTTTT ATAGACAGGG AAACTGAAAC 1020
AGAGAGAGGT TAAATAACCT GCCCAAGGCC ACACAGCTTG GGCAGTGTGG GAAGTCTGGC 1080
AGTCAACCTT GGTCTTAACC ACTCTGCCTC CCACTCAGCA CCCTTACCTG CCACAGCCTC 1140
TCTCCCACAC ACCGTCTCCA GCAGTCTCAC CCTAACGCCC ATGTCTCATC GCAACCCCAT 1200
CCCCTCTTAC TACACACTGC CTTTTTAAAA TTACTGTCTT TTTTTTTTTT TTTTTTTGAG 1260
ACAGGGTGTC ACTCCAGCCC AGGCTAGAGT GCAGGGCTGC AATCATGGCT CACTACAGCT 1320
TCAACCTCCT ACCTCAGCCT CTCGAGTAGC TGGGACTACA GGCATGCCCC ACCACACCCA 1380
TGCCTAATTT TTGTATTTTT AGTAGAGATA GAGTTTTGCC ATGTTGCCCA GGCTCATCTC 1440
AAAGGCCTGA GCTCAAGTGA TCTGCCCATC TTGGCCTCAC AAAATGCTGG GATTACAGGC 1500
ATGAGCCACC ATGCCCAGAC TCTTGTTATT 1530
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