Tag | Content |
---|
EnhancerAtlas ID | HS139-24552 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr18:9115500-9117830 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr18:9117498-9117519 | CAGACAAAAGTGAAAGTCAAG | - | 6.23 | Nr2f6(var.2) | MA0728.1 | chr18:9117253-9117268 | CGATCTCTTGACCTC | - | 6 |
|
| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_00349 | chr18:9115861-9120474 | Adipose_Nuclei | SE_09486 | chr18:9115219-9120218 | CD14 | SE_10610 | chr18:9115721-9121785 | CD19_Primary | SE_11126 | chr18:9100942-9124322 | CD20 | SE_12132 | chr18:9115785-9122093 | CD3 | SE_13114 | chr18:9117228-9120036 | CD34_Primary_RO01480 | SE_13362 | chr18:9115877-9120374 | CD34_Primary_RO01536 | SE_14419 | chr18:9115669-9121941 | CD4_Memory_Primary_7pool | SE_15563 | chr18:9115860-9120733 | CD4_Memory_Primary_8pool | SE_16604 | chr18:9115994-9119428 | CD4_Naive_Primary_8pool | SE_16911 | chr18:9115896-9121792 | CD4p_CD225int_CD127p_Tmem | SE_17425 | chr18:9112592-9123232 | CD4p_CD25-_CD45RAp_Naive | SE_17858 | chr18:9114467-9123254 | CD4p_CD25-_CD45ROp_Memory | SE_18293 | chr18:9112472-9123378 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19258 | chr18:9115706-9120102 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_21116 | chr18:9115562-9119259 | CD8_Memory_7pool | SE_22523 | chr18:9115687-9123222 | CD8_primiary | SE_25822 | chr18:9115474-9120407 | Duodenum_Smooth_Muscle | SE_32657 | chr18:9115694-9119675 | GM12878 | SE_43370 | chr18:9116511-9117810 | Lung | SE_43499 | chr18:9112603-9123280 | MM1S | SE_45431 | chr18:9116606-9118447 | NHLF | SE_46129 | chr18:9115724-9119908 | Osteoblasts | SE_51563 | chr18:9115710-9120127 | Skeletal_Muscle | SE_58595 | chr18:9094528-9148577 | Ly1 | SE_58828 | chr18:9047588-9150664 | Ly3 | SE_62260 | chr18:9060747-9148643 | Tonsil | SE_65021 | chr18:9115905-9120119 | NHEK | SE_67311 | chr18:9112603-9123280 | MM1S |
|
| 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 |
GH18I009112 | chr18 | 9112600 | 9121919 |
|
Enhancer Sequence | GCTTTATCCT CATTTTGTAC TGCAGGAAAA ATACCTAGGT TAGAATTACT AAATTAAAAA 60 ATGGACACTT GGGGCCAGGC GCAGTGGCTT ACGCCTGTAA TTCCACCACT TTGGGGAGCT 120 GAGGCGGGCA GATCACTTGA CATCGAGAGT TCAAGACCAG CCTGACCAAC ATGGAGAAAC 180 CCCGTCTCTA CTAAAAATAC AAAAAATTAT CCAGACGTAG TGGCACATGC CTGTAATCTC 240 AGCTACTTGG GAGGCTGAGG TAGGAGAATC GCTTGAACCC GGGAGGCAGA GGTTGTGGTG 300 AGCCGAGATC ATGCCATTGA ACTCCAGCCT GGGCAACAAG AGCGAAACTC CGTCTCCAAA 360 AAAAAAAAAA GACACTTATT TAGGCTTTCC ATATATCATG GTAATTTGCT TTCTAAAAGG 420 CTATATGAAT TTTTAAGTGT GCTTGTTTCT CTATATGCTC AACAGAATGG AATGCTATCT 480 TAAAAGAAAA AAGATACTTG GTAGTTTGAT AACTAGTAAT GTTATTTTAA GTTGTATGTT 540 TTTAGTTACT AGTAAGCAGT TTGAATTCTG TGAAACTTTT GTTCATGATC TTTACTCATT 600 TTTTAAGTGC ATTTATGATC TCTTCAGGCT ATTAGCCTCT TGTCATCAAA TGTGTGTAAG 660 ATTTAAGACT CATCACTGTC AAGTTAATGG ATGAGTTCTC AGAGGCAAAG GCTTTATAGA 720 GAAAAGAAGA TAGGAGTGTG AACTGAGCCC TGAGGACAGC CTGCAAGGAG TGGATAAAAA 780 GCCAATAAAC AGAAAATGTT AGTGTTCAGA AATTAGGAGA AGACTGAATA CTTTCCCTAC 840 TCTTAAAATT AATCCTTTTA TTATAAGTAT ACAGTCTTTT CTCTCAGAAT TTAGTTAAGT 900 AACTCACTGA TGTTACTCAA AAATTGTTAC TCGATTAAAA AAATTTTCTG AGCTAAGATG 960 ACAGTGACTG TCTTCTAAAT TTTAGTTTCA GTTAATTTTT CAAAACAAAA CCAACACAAT 1020 CAAAGCCCCC TTGTGCACCT CTGACTGTAT CCCTCCCTGC CTTCCAATTA TCCTGAAATT 1080 GATATTTATC ACTCCCATCT TTTGTACGTG TGTCTCACAT CCTGTACCTT AGTCTTTTCT 1140 TGTTAATTAA AGCAGATGTT CCATGTAAAC TTATTTATTA ATATTTCTTC AACTGAAATA 1200 TCATTTGGAC CTAGGGTAAA GTTAAATATA CTATTGTGTT ATATTACTCC GTTTACTTTC 1260 TTCTATGTTT GCCTTTGAAT TGTCCAACTC TTTGCTAGTT CCATGCTTGG TTTAACCCAG 1320 CCAGTGTTCT GCCGTCTGTG GTTAGTAGAA CTCAGAAATT GGAGGAATCC AGAACAGTAG 1380 TTGAAATACT TGGGGGCGGG GGACAGGGTA GGAGTGGAGG GTAGGAGCAA GAGGGCAAAG 1440 AGAAATGAAA TGCAGCTGAG AGAATAATCA GATTCCTTCC AAAGCAACTG AACATTGTCA 1500 GTCCGCATAG CATCATAAAT AGCTTTCTGA AACTACTTTT TTTTTTTTTT TTGAGACGGA 1560 GCCTTGCTCT GCTGCTCAGG CTGGAGTGCG GTGGCGCGAT CTCGGCTCAC TGCAACCTCT 1620 GCCTCCCAGG TTCAGGCGAT TCTCCTGCCT AAGCCTCCCG AGTAGCTGGG ACTACCAGCG 1680 TGCGCCACCA CGCCCAGCTA ATTTTTGTGT TCTTAGTAGA GATGGGGTTT TACCATGTTG 1740 GCCAGGATGG TCTCGATCTC TTGACCTCGT GATCTCCTTG CCTTAGCCTC CCAAAGTGCT 1800 GGGATTACAG GCATGAACCA CCACACCCGG CCAGAAACTA CTTTTTACGG CTGGAGTTTC 1860 AGAACTAATT TAGTAAAGGA TTGAAAAGGA AGGAGGATAC AGTTGACTCA TTTGTACAGA 1920 GTATATGACT CATTTGTACA GAATGAAAAC ATGTTTATGA AGGTTCACAC TAAGTGAAAG 1980 CTGGCATCCA AGTTGATTCA GACAAAAGTG AAAGTCAAGA AGTTAATAGT ACATTAATTC 2040 TCCAAATGCA TGCCAGCAGA GCGTGGCAGG AAGGTACACA AGTCAGCAGA TCTGGGTTGT 2100 CCTGGTTCTC CTATTGACTC GTGTGTGTGA TGTTAGGTGG GTGAATCTTG GCTTTGAATC 2160 TCCATTTGTA AAATAACTCT CCTGAAATAG AGATGGATAG GGTAGAATAC CATATTTCTT 2220 AAGATCTTTT ATAAGTTGAT TCCATTGTTG TAAATTATGA ATCCTAAAGT ATTTCTTTAT 2280 GAAAAATTTT TTAAGGCTAT GATTTACTAA ACTTTCTTAA AATTTTAAAT 2330
|