Tag | Content |
---|
EnhancerAtlas ID | HS178-07245 |
Organism | Homo sapiens |
Tissue/cell | Skeletal_muscle |
Coordinate | chr14:70109470-70111110 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr14:70110478-70110489 | TGTGACTCATT | + | 6.62 | Lhx3 | MA0135.1 | chr14:70111067-70111080 | GAATTAATTAATT | + | 6.29 | Lhx3 | MA0135.1 | chr14:70111071-70111084 | TAATTAATTAATT | + | 6.78 | Lhx3 | MA0135.1 | chr14:70111068-70111081 | AATTAATTAATTA | - | 6.78 | Lhx3 | MA0135.1 | chr14:70111072-70111085 | AATTAATTAATTA | - | 6.78 | POU6F1 | MA0628.1 | chr14:70111069-70111079 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr14:70111073-70111083 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr14:70111069-70111079 | ATTAATTAAT | - | 6.02 | POU6F1 | MA0628.1 | chr14:70111073-70111083 | ATTAATTAAT | - | 6.02 |
|
| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_01046 | chr14:70110138-70110582 | Adrenal_Gland | SE_09201 | chr14:70108212-70112690 | CD14 | SE_10433 | chr14:70109353-70109933 | CD19_Primary | SE_10939 | chr14:70097782-70144384 | CD20 | SE_13365 | chr14:70109682-70112060 | CD34_Primary_RO01536 | SE_18280 | chr14:70108409-70112458 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19536 | chr14:70108460-70111344 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20540 | chr14:70110135-70111078 | CD56 | SE_25838 | chr14:70109458-70112328 | Duodenum_Smooth_Muscle | SE_26683 | chr14:70109494-70110077 | Esophagus | SE_26683 | chr14:70110099-70111239 | Esophagus | SE_27827 | chr14:70109436-70111309 | Fetal_Intestine | SE_28670 | chr14:70109369-70111474 | Fetal_Intestine_Large | SE_31600 | chr14:70109253-70112057 | Gastric | SE_32500 | chr14:70108473-70110405 | GM12878 | SE_40959 | chr14:70109593-70111025 | Left_Ventricle | SE_42217 | chr14:70109356-70110934 | Lung | SE_50082 | chr14:70109370-70112379 | Sigmoid_Colon | SE_51685 | chr14:70109453-70111341 | Skeletal_Muscle | SE_52366 | chr14:70109354-70112180 | Small_Intestine | SE_53514 | chr14:70109476-70112577 | Spleen | SE_58413 | chr14:70076448-70170966 | Ly1 | SE_59839 | chr14:70072682-70121076 | Ly4 | SE_60579 | chr14:70076514-70162614 | DHL6 | SE_62292 | chr14:70076365-70194637 | Tonsil |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 70110235 | 70110559 | chr14 | 70110611 | 70110850 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH14I069642 | chr14 | 70108957 | 70112389 |
|
Enhancer Sequence | CTATTTCTGA CTCTGAGTGA GTTCTAGGGG TTGTGCCACC CACTTCTTTC TGATCATTAT 60 TTTCCCACCC TTGCTAGTTT CCTCAGAGGC ATGCACAGAT CAGTACTCAG CCCAAAACTC 120 AAAGGGGTCC CTCTGCAGAT GTTTGGTGGT TTTGCTCTTT GCAGCTCTCT CCTTTTCAAT 180 TAATTTGCCC TGCAAATTCT AGCCACTTGG GCCTCTCCAA ATTTCCAACT CTGTTTTTTC 240 AACTGAGTGA CATTGCTGAA CTCTTTCAGG TTTCTCTGCC CTACCCTATG GTCTGGAAAC 300 TCTCAAGGGA GTTAAGTGGG GCAGTAGTAG GGCTCACTGC GTTTTTTCCC CCATTTCTCA 360 AGGATTACTG CCCTGTGCTG CCTGTTGTCC AATGTCTGAA AACCGTTATT TTATCTGGTT 420 TTTCAGTTGT TTAGGGAAGG AGAATAAGTT GAGTCCCCAT TATTCCACCA TGACTAGAGG 480 TAGATATTCC TCAGCTGTCC CTCAAATCAG GTATTAACCT TGGATGTCTT TTCCTTCTGT 540 GTTCACTTAT TGAAACATGG ATCATTTAGA CAAATCTTAT GGTAATTCAG CCAGATTCAC 600 ATCATGTCAG TTTGCCAAAT ATTTATCTGG CACCTGCTAT GTCCAAAAGA ATAGTATAGC 660 CAGTATCTTG CTGAACGTGG TATAATCTGT AACTTTACCC ATATTCTAAT GCTGCACCTT 720 CTAGCAGAAG ATTCTGTGCA TCCTGACATG CATGTGACAC AAATACACTT TGAGTCTTCT 780 TCCTGTACCT CCTGATCATG GTCCCATTAA ACCTGGGCAA ACAACTGAAC TAACTAGTCA 840 GAATTGGTGA GCAAACAGCA GGTGCTTGGC TGTCTGCCTA TTCATGAGTC AGGCCCAGAC 900 AGCCGTGTGT GGGGAGGGAA GAGAGCATTA AGTCTCTGTG TGTGGGTGAG CACCTCCATT 960 TTACCTGGCC TTATTCTGTG CCAGATACTA TATTCAATTT CAAAAATGTG TGACTCATTG 1020 ACTCTGTAAT TCCATGAAGT ATAGGTCTGT TACCTCAATT TTATATGTGA CAAACAGAGG 1080 CTCACAACAG TAAAGCAGCA TACCTAGGCC CTGTGAGAAG CTAGAGGTAG AGTCAGGATT 1140 TGAATTCCCT TTTGTGTGAC TCCAGAGACT ATGTACTATT CACTAGACTA CATTGATTGA 1200 CCCTGTAATT TTCTCTGTCA CTTCCCTCTT CTGGACTCCA GCTTATCTTC CTGTTTTATC 1260 TTTGACACGT TGGCTGTATA TCTCCCATGA CTTTTCACTT TGTACCTCAT GTTGTAATTA 1320 TTTGTGTTTG TGTCTTATAT ATATACACAA TATACAGTAG ACCGTAAACT CTTAAGGGCG 1380 TATGCTTCCT TTACCTCTCA AGGAATCTCG TACATGTAGG TGCCCAATGT ATGTGTTGAA 1440 TAGTCACTGA GTTCCTTAAG AAAGAAGCAT GTTAGGAATG AGTTCATAAG CCCTGTCTGG 1500 AGGGAAATAT CAAATTCTCT CATTAATTTA TGATGTTTCT TCTTCATCTT CTCTGTGTTT 1560 ATCATAATCC CTTTTAACAT ATTCCAGAAT GTTGCCTGAA TTAATTAATT AATTATGGCT 1620 GGGCACGGTG GCTCACACCT 1640
|