Tag | Content |
---|
EnhancerAtlas ID | HS034-13439 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr17:80255160-80256620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EHF | MA0598.2 | chr17:80256139-80256151 | TACCCGGAAGTT | + | 6.27 | ELF3 | MA0640.1 | chr17:80256139-80256152 | TACCCGGAAGTTG | + | 6.22 | ELF5 | MA0136.2 | chr17:80256140-80256151 | ACCCGGAAGTT | + | 6.14 | JUN(var.2) | MA0489.1 | chr17:80255371-80255385 | AGAAGATGAGTCAG | + | 6.12 | NR3C1 | MA0113.3 | chr17:80255424-80255441 | GGGAACACAATGTCCTG | - | 6.21 | NR3C1 | MA0113.3 | chr17:80255424-80255441 | GGGAACACAATGTCCTG | + | 6.5 | NR3C2 | MA0727.1 | chr17:80255424-80255441 | GGGAACACAATGTCCTG | - | 6.31 | NR3C2 | MA0727.1 | chr17:80255424-80255441 | GGGAACACAATGTCCTG | + | 7.17 |
|
| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_00818 | chr17:80255887-80256080 | Adipose_Tissue | SE_00818 | chr17:80256274-80256826 | Adipose_Tissue | SE_10769 | chr17:80254688-80257502 | CD19_Primary | SE_12141 | chr17:80254519-80257876 | CD3 | SE_15773 | chr17:80254447-80257503 | CD4_Memory_Primary_8pool | SE_17230 | chr17:80254412-80257607 | CD4p_CD225int_CD127p_Tmem | SE_17429 | chr17:80253981-80262450 | CD4p_CD25-_CD45RAp_Naive | SE_18092 | chr17:80253986-80258182 | CD4p_CD25-_CD45ROp_Memory | SE_18707 | chr17:80253900-80262110 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19245 | chr17:80254090-80257868 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20291 | chr17:80254220-80257864 | CD56 | SE_21847 | chr17:80254455-80257781 | CD8_Naive_7pool | SE_22123 | chr17:80254024-80257918 | CD8_Naive_8pool | SE_22786 | chr17:80254381-80257761 | CD8_primiary | SE_23169 | chr17:80254105-80257136 | Colon_Crypt_1 | SE_23832 | chr17:80255090-80257082 | Colon_Crypt_2 | SE_25627 | chr17:80254016-80265092 | DND41 | SE_26885 | chr17:80254243-80257487 | Esophagus | SE_28208 | chr17:80255246-80256802 | Fetal_Intestine | SE_29286 | chr17:80255088-80256871 | Fetal_Intestine_Large | SE_34851 | chr17:80253979-80257835 | HeLa | SE_41785 | chr17:80254937-80256957 | LNCaP | SE_42530 | chr17:80254128-80257686 | Lung | SE_47542 | chr17:80255074-80256844 | Pancreas | SE_53499 | chr17:80254021-80257645 | Spleen | SE_55236 | chr17:80254169-80257671 | Thymus | SE_58167 | chr17:80255745-80256249 | VACO_9m | SE_62764 | chr17:80249594-80262297 | Tonsil | SE_65283 | chr17:80254425-80257995 | Pancreatic_islets | SE_66650 | chr17:80255005-80257528 | Jurkat |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 80255798 | 80256475 | chr17 | 80255299 | 80255755 |
|
Enhancer Sequence | AATTATCACC CATCCATGGC TCCCAGCTAT GCCACAGTGA CTGCAATCCT AAGATTGGGC 60 ATCCGGAAGG ATGGCCCAAC ACCGTGCCAC CCTGCAGCTT TGCCGCAAGC TGCCCTGGGT 120 CCTGCATCCT CTTCGAGGTG GAATGAGAAC ACAGCCGAGA GCTCAGGATC TTCCAACTGC 180 TGCCCACAGT GGCAAAAAGA AACCTGGTGG GAGAAGATGA GTCAGACGGA GCCAGGAGCC 240 CGCGGCCGGT GACGCCAGCG GTGGGGGAAC ACAATGTCCT GTGGGTGATC GGTGAGCGAG 300 CGGACGGTGG ATTTCTCCTG CAGTCGGTGG CAGGAAGGAT GTCATCACGC GCTATTTTGT 360 GACCAGCCCC TGGACCACAA CTCACGTGAG CAGAAGGGCT TTCTTCTTTG CTTAAGATGT 420 CTGTGCTTGC AAACTTACTG GCCACAGGTA CAAGGAGGTT TTCTTTGCTT ATGTTCATAT 480 TAAACATGTT AATAAAGGTT TTTCTTATTG TCCTTGTTTT TACATTTATA AATTACTCAT 540 AAGCTGACGA AACAGAAAAC AGAGACTCAT CTCCGGTTCC CGGTACAGTG AGGTGAGAGC 600 TGCTGTGCTG GGTGCGGGAA GCGCCTGGCC CCAGGTTCCT CCTGGACGGA GGCCAGAAGG 660 GCTGAGCAAG AGCCAGCGAG GCTGGGGAGG AGGAGGAGGC GCTGGAACAG GAACGGCCGG 720 CCGGGAGGGG CGAGGCTGGG GGACAGTCAC GCAGGGCTGA GGCGGGCGTG TGGTGCGGGA 780 GCGTGTGTGT GCAGGAAGCT TGTGTGCGTG CGTGTGGGGA GCGGGTCTGG TGAGGGCGCA 840 CTTGGGCCTG AGCCCCTTCC GGCCCCTCGT GTTTGCTGGA GGCTGCGTGT GCTGTGTCCC 900 CACCCCAGAT GCTTGCCCTG AGGGGCAGGT TTCCATCCAA CACCCCGATT GTCTCCTTCA 960 GTAAACCCCC GGCACCGTCT ACCCGGAAGT TGTGGGCTGG GAGGGATGAC ATGCCCTGGG 1020 GACTGTGAGC AGTGGAACCC ACGTCATTGC AAGGAAATGA TCACACAAAC ACCAGCTCGG 1080 CAGAGTGGAA CCTTTGCCAA ACCTCAGAGC TGCAGCGAGC GGCTGGGCAA CCTTCCTGAG 1140 GACGGCGCCC CCTCGCCCAG CTCCAAGCTC CTCCCTGTCC CCACAGGATA TCCCTGGACC 1200 TGGCGGGTCA CTCTAGCCAG AGCAGCCTTC CACAGTCCTC CAGGGTCAGA GCTACAGTTG 1260 AGGACCCTGT AGGTGGTAGA GGTGCCCGGG GCCGGGCTCT GGGGCTGGCA GAGGCAATGT 1320 CAGCGCCTGC CACCTGCGAT GTGGCCAGGG AACTTGGGGC TGAGCAAGGG CACAGAGGGG 1380 AGAGTGTGGC ATGAGGGAGA GGCGGGACCC CGCAGAGGCT CCCACACCTT CCAAGGCAGC 1440 AGAGGAGAAG GGGAGGCTGC 1460
|