Tag | Content |
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EnhancerAtlas ID | HS059-42799 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr7:44661580-44663910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXF2 | MA0030.1 | chr7:44662014-44662028 | CTTGTTTACCTTTA | - | 6.96 | Lhx3 | MA0135.1 | chr7:44663131-44663144 | AAATTAATTAATC | + | 7.82 | POU6F1 | MA0628.1 | chr7:44663133-44663143 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr7:44663133-44663143 | ATTAATTAAT | - | 6.02 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_09293 | chr7:44656533-44664867 | CD14 | SE_12002 | chr7:44661970-44664769 | CD3 | SE_14587 | chr7:44661595-44666552 | CD4_Memory_Primary_7pool | SE_15490 | chr7:44662284-44664805 | CD4_Memory_Primary_8pool | SE_16434 | chr7:44661773-44664498 | CD4_Naive_Primary_8pool | SE_16951 | chr7:44661854-44664820 | CD4p_CD225int_CD127p_Tmem | SE_17851 | chr7:44660970-44667023 | CD4p_CD25-_CD45ROp_Memory | SE_18656 | chr7:44661057-44666341 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19294 | chr7:44661232-44666908 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20655 | chr7:44662135-44663196 | CD56 | SE_21218 | chr7:44661809-44663212 | CD8_Memory_7pool | SE_22840 | chr7:44661619-44664737 | CD8_primiary | SE_24636 | chr7:44662278-44662951 | Colon_Crypt_2 | SE_26120 | chr7:44660088-44663486 | Duodenum_Smooth_Muscle | SE_27427 | chr7:44661906-44662995 | Esophagus | SE_27654 | chr7:44653619-44664659 | Fetal_Intestine | SE_28557 | chr7:44653546-44666729 | Fetal_Intestine_Large | SE_32407 | chr7:44662061-44663077 | Gastric | SE_34691 | chr7:44659818-44663107 | HeLa | SE_37328 | chr7:44659783-44663176 | HSMMtube | SE_40682 | chr7:44660511-44661823 | Left_Ventricle | SE_40682 | chr7:44661832-44663053 | Left_Ventricle | SE_42075 | chr7:44662099-44663009 | LNCaP | SE_42544 | chr7:44660490-44663115 | Lung | SE_43768 | chr7:44661678-44664721 | MM1S | SE_46384 | chr7:44661325-44663119 | Osteoblasts | SE_48519 | chr7:44661882-44663185 | Psoas_Muscle | SE_50531 | chr7:44661881-44663149 | Sigmoid_Colon | SE_52560 | chr7:44661291-44663148 | Small_Intestine | SE_52560 | chr7:44663429-44664614 | Small_Intestine | SE_53907 | chr7:44660114-44664683 | Spleen | SE_62947 | chr7:44653723-44680812 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr7 | 44662824 | 44662939 | chr7 | 44663549 | 44663779 | chr7 | 44662048 | 44662924 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I044613 | chr7 | 44653472 | 44666508 |
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Enhancer Sequence | ATGTGGAAGG GGCCACTTTG GGAAGAACAG ATGAAATTGG TGTTTTACGA TTGTCAGTTC 60 AGTGCCTGTT AATTGGGCTA TTGCAGCAAC TGAATACTGA TAGTTAATGA GGTGATGCTA 120 TTGTTTTCTG GGAGAAAACC CAACTCAGAG GCAATTGGGT ATTTAATATT GCCTTAATAA 180 TGACATTAAA GGAAAAAAAT GAACATTTTC CTTTGAGCCT GAGAAATTAA AAAAAAAATA 240 GCATAAAATG AAGCAACAGT AGTATTTTTG CTGTCAATGT TAGGGCTGTT TGTCTTCCTT 300 AAATATATCA GTGGAAAAAC TTGGAGTGTA GTTGGAGGTA GGAAGAACTA CCGAATTAAC 360 TTAAAACTTT TGATTTCTAA AGTGAAAACC CAGGGGTAAA GATTGCATTC CCTAATTATA 420 TCCAGAATAT ATTGCTTGTT TACCTTTAAT TTGTAAGGAG CAAGTTTTTG TTTGTTGTTC 480 AGTTTGTTTT TAAAGAATAT GTTCTGCTGT TTACTTTTGC TGACCTATCT CTTCTCAGTG 540 GAGCAGGCCA GAGGTGAATG CAGGACACTC TAAGCCCTCT CTCTTGGTGT CCCTTAAGTG 600 TATTCTGAGC ATATTTGGGC CAAGAGGAAG TTTCTGATAA ATAATATAGA AGATATTTTT 660 ATGTAACAGT TATTTCTGGG TAATTCACAC TATGTTTCAG AGCTTGGATT TTCTTCGGGT 720 AGGTGTGGAC ATGGAGTGTA GTTCTAACTT TACAACCAGA GCACCTGCTT TGAGACAAAT 780 TCATGAGCAA CCATGTAGGC CAGCAAGCAC CTTTTTTTCC ACAGGCAGCG TCCTTGTGAA 840 CTTTCCGCTT GGATCCTGAC TCTGCTGTTA GTAGCCTATG ACCTTGGATG AAATGTAAGG 900 GAATAGAAAC TGAAGCTATC TGTAAAGTGA AAGAGCTGGT GCCTGCCTTA TTGGGAGCCT 960 CTGGGTTTAT GTATGAGTCA GATGCGTAGA GTTGCTCACC ATGGAGGGCC CAGGGTAGGC 1020 AGGCATTATT GAACAACTGC TCCATGTGCT CTTTTCAATC TTTGCAGACC CCACCCACGT 1080 CTCCCTTGCT CAGACCTGGC TCCCCATGGC TTATGAAAGG GGGCTGAGTG CAGAAGGTGG 1140 CAGGCAGGAC ACTGGACAAC CCTCTGTGGC TTTTCCTTAC CCTTCGTAGT ACCATGAGAT 1200 TCTGGCTCTT CCCGTCTCTG TGTTTCTGCC TATGGGTCCT TCCACATGCA GTGCCTCGTC 1260 TTCCCTCCTT CCCATCCATG TCCTTTTGTC TTCAGGCACA CCCACTTGGA AGGAGCCCAT 1320 CCTCTCACAG GGTCTGCTGG CATATTCTGC ACCTCTCAAG TACTCATATT TCCTCTGCAA 1380 TCTTTTCTAT GTTGTTTTTC CTCTGCTCAA GGGTAAATTG AGAGTAAGGA AAGTATTTTT 1440 CTAATTTCTT TGTATTTTCC ATAATATTGT AAGTACAGCA GGTACTCAGT AGTTTCTGGA 1500 CAGATTAGAA AATGTTTTAC TTATTCTCCA ATTAATCCTA ATCCTAATTC TAAATTAATT 1560 AATCCTTGTT GCCTTTCTTC TAATTGTTTT ATATATATGT AATATGTAAA TTTAAAGAAC 1620 ATCGTATGTT TATCATCTTA GCCCTTAAAC TAGATTTAAT GGTTTTTTGT TTTGTTTTGT 1680 TTTGAGACAG AGTCTCACTC TGTTGCTAGG CTGGAGTGCA GTGGTGCAAT CTCGGCTCAC 1740 TGCAGCCTCC ACCTACCAGG TTCAAGCAAT TCTCCTGCCT CAGCCTCCCA AGTATCTGGG 1800 TCTACAGGCA TGCACCACCA CACCCAGCTA ATTTTTGTAT TTTTAGTAGA GATGTGGTTT 1860 CACCATGTTG GCCAGGATGG TCTTGATCTC CTGACCTCGT GATCCACCCG CCTTGGCCTC 1920 CCAAAGTGCT GGGATTACAG GTGTGAGCCA CCGAGTCTGG CCTAGATTTA AATTTTTAAG 1980 TGAAGATGGT AATATCTGCA ACTGTGCACT CACCTTCCTT GGGCTCGCAC AGGCATCCTG 2040 TGTTAGTAGG TGCAAGAGTG TGTTTCAGTT TCACACAGTC ACAGCTCTGT TGTGCTCTCA 2100 GGCACATGAA CTGGTGGCAC TGAGCAGGTA GCACTCTTGT GAATACATTT ATAGGCCAGG 2160 GTCTTTCTCC TCAACAATTA GAGTTGAACA TGTTTTGTTT TTGTTTTTGT TTTTCTAGTA 2220 GCTTTTAAAA AAAAATTATC CTTTCTCTAG AGCATCAGGA TCTAGTAGCC TTGTCTCCTA 2280 AATACTCATT TTTAAAACCT TTCTTTCTTG TTTTTTTTTT TTTTTTTTTG 2330
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