Tag | Content |
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EnhancerAtlas ID | HS187-22637 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr7:44661960-44663910 |
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: 31 | 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 | chr7:44661832-44663053 | 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 | AGTGAAAACC CAGGGGTAAA GATTGCATTC CCTAATTATA TCCAGAATAT ATTGCTTGTT 60 TACCTTTAAT TTGTAAGGAG CAAGTTTTTG TTTGTTGTTC AGTTTGTTTT TAAAGAATAT 120 GTTCTGCTGT TTACTTTTGC TGACCTATCT CTTCTCAGTG GAGCAGGCCA GAGGTGAATG 180 CAGGACACTC TAAGCCCTCT CTCTTGGTGT CCCTTAAGTG TATTCTGAGC ATATTTGGGC 240 CAAGAGGAAG TTTCTGATAA ATAATATAGA AGATATTTTT ATGTAACAGT TATTTCTGGG 300 TAATTCACAC TATGTTTCAG AGCTTGGATT TTCTTCGGGT AGGTGTGGAC ATGGAGTGTA 360 GTTCTAACTT TACAACCAGA GCACCTGCTT TGAGACAAAT TCATGAGCAA CCATGTAGGC 420 CAGCAAGCAC CTTTTTTTCC ACAGGCAGCG TCCTTGTGAA CTTTCCGCTT GGATCCTGAC 480 TCTGCTGTTA GTAGCCTATG ACCTTGGATG AAATGTAAGG GAATAGAAAC TGAAGCTATC 540 TGTAAAGTGA AAGAGCTGGT GCCTGCCTTA TTGGGAGCCT CTGGGTTTAT GTATGAGTCA 600 GATGCGTAGA GTTGCTCACC ATGGAGGGCC CAGGGTAGGC AGGCATTATT GAACAACTGC 660 TCCATGTGCT CTTTTCAATC TTTGCAGACC CCACCCACGT CTCCCTTGCT CAGACCTGGC 720 TCCCCATGGC TTATGAAAGG GGGCTGAGTG CAGAAGGTGG CAGGCAGGAC ACTGGACAAC 780 CCTCTGTGGC TTTTCCTTAC CCTTCGTAGT ACCATGAGAT TCTGGCTCTT CCCGTCTCTG 840 TGTTTCTGCC TATGGGTCCT TCCACATGCA GTGCCTCGTC TTCCCTCCTT CCCATCCATG 900 TCCTTTTGTC TTCAGGCACA CCCACTTGGA AGGAGCCCAT CCTCTCACAG GGTCTGCTGG 960 CATATTCTGC ACCTCTCAAG TACTCATATT TCCTCTGCAA TCTTTTCTAT GTTGTTTTTC 1020 CTCTGCTCAA GGGTAAATTG AGAGTAAGGA AAGTATTTTT CTAATTTCTT TGTATTTTCC 1080 ATAATATTGT AAGTACAGCA GGTACTCAGT AGTTTCTGGA CAGATTAGAA AATGTTTTAC 1140 TTATTCTCCA ATTAATCCTA ATCCTAATTC TAAATTAATT AATCCTTGTT GCCTTTCTTC 1200 TAATTGTTTT ATATATATGT AATATGTAAA TTTAAAGAAC ATCGTATGTT TATCATCTTA 1260 GCCCTTAAAC TAGATTTAAT GGTTTTTTGT TTTGTTTTGT TTTGAGACAG AGTCTCACTC 1320 TGTTGCTAGG CTGGAGTGCA GTGGTGCAAT CTCGGCTCAC TGCAGCCTCC ACCTACCAGG 1380 TTCAAGCAAT TCTCCTGCCT CAGCCTCCCA AGTATCTGGG TCTACAGGCA TGCACCACCA 1440 CACCCAGCTA ATTTTTGTAT TTTTAGTAGA GATGTGGTTT CACCATGTTG GCCAGGATGG 1500 TCTTGATCTC CTGACCTCGT GATCCACCCG CCTTGGCCTC CCAAAGTGCT GGGATTACAG 1560 GTGTGAGCCA CCGAGTCTGG CCTAGATTTA AATTTTTAAG TGAAGATGGT AATATCTGCA 1620 ACTGTGCACT CACCTTCCTT GGGCTCGCAC AGGCATCCTG TGTTAGTAGG TGCAAGAGTG 1680 TGTTTCAGTT TCACACAGTC ACAGCTCTGT TGTGCTCTCA GGCACATGAA CTGGTGGCAC 1740 TGAGCAGGTA GCACTCTTGT GAATACATTT ATAGGCCAGG GTCTTTCTCC TCAACAATTA 1800 GAGTTGAACA TGTTTTGTTT TTGTTTTTGT TTTTCTAGTA GCTTTTAAAA AAAAATTATC 1860 CTTTCTCTAG AGCATCAGGA TCTAGTAGCC TTGTCTCCTA AATACTCATT TTTAAAACCT 1920 TTCTTTCTTG TTTTTTTTTT TTTTTTTTTG 1950
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