Tag | Content |
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EnhancerAtlas ID | HS047-30809 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr7:44661250-44663020 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXF2 | MA0030.1 | chr7:44662014-44662028 | CTTGTTTACCTTTA | - | 6.96 |
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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 | chr7:44660432-44661811 | Psoas_Muscle | SE_48519 | chr7:44661882-44663185 | Psoas_Muscle | SE_50531 | chr7:44661881-44663149 | Sigmoid_Colon | SE_52560 | chr7:44661291-44663148 | 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: 2 | Chromosome | Start | End |
chr7 | 44662824 | 44662939 | chr7 | 44662048 | 44662924 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I044613 | chr7 | 44653472 | 44666508 |
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Enhancer Sequence | TCATGAGGTC AGGAGTTTGA GACCAGCCTG GCCAACATAA TGAAACCCTG TCTCTACTAA 60 AAATACAAAA ATTAACCAGG TGTGATGGCA TGCACCTGTA GTCCTAGCTA CTCGGGAGGC 120 TGAGGCAGGG GAATTGCTTG AACCTGGGAT GGGAGGTTGC ACTGAGCCGA GATCACACCA 180 CTGCACTCCA GCCTGGACTA CAGAGCAAGA CTCCGTATCA AAAAAAAAAA ATCTCCAGCT 240 GTTGTGGCAG CTCTGCTGGG CAGCACTTAA CTATGTGTCA GATTCAGTGA CTGCGGATAG 300 CAAAATGTCA TGATTTACTT AAACAGGATC ATGTGGAAGG GGCCACTTTG GGAAGAACAG 360 ATGAAATTGG TGTTTTACGA TTGTCAGTTC AGTGCCTGTT AATTGGGCTA TTGCAGCAAC 420 TGAATACTGA TAGTTAATGA GGTGATGCTA TTGTTTTCTG GGAGAAAACC CAACTCAGAG 480 GCAATTGGGT ATTTAATATT GCCTTAATAA TGACATTAAA GGAAAAAAAT GAACATTTTC 540 CTTTGAGCCT GAGAAATTAA AAAAAAAATA GCATAAAATG AAGCAACAGT AGTATTTTTG 600 CTGTCAATGT TAGGGCTGTT TGTCTTCCTT AAATATATCA GTGGAAAAAC TTGGAGTGTA 660 GTTGGAGGTA GGAAGAACTA CCGAATTAAC TTAAAACTTT TGATTTCTAA AGTGAAAACC 720 CAGGGGTAAA GATTGCATTC CCTAATTATA TCCAGAATAT ATTGCTTGTT TACCTTTAAT 780 TTGTAAGGAG CAAGTTTTTG TTTGTTGTTC AGTTTGTTTT TAAAGAATAT GTTCTGCTGT 840 TTACTTTTGC TGACCTATCT CTTCTCAGTG GAGCAGGCCA GAGGTGAATG CAGGACACTC 900 TAAGCCCTCT CTCTTGGTGT CCCTTAAGTG TATTCTGAGC ATATTTGGGC CAAGAGGAAG 960 TTTCTGATAA ATAATATAGA AGATATTTTT ATGTAACAGT TATTTCTGGG TAATTCACAC 1020 TATGTTTCAG AGCTTGGATT TTCTTCGGGT AGGTGTGGAC ATGGAGTGTA GTTCTAACTT 1080 TACAACCAGA GCACCTGCTT TGAGACAAAT TCATGAGCAA CCATGTAGGC CAGCAAGCAC 1140 CTTTTTTTCC ACAGGCAGCG TCCTTGTGAA CTTTCCGCTT GGATCCTGAC TCTGCTGTTA 1200 GTAGCCTATG ACCTTGGATG AAATGTAAGG GAATAGAAAC TGAAGCTATC TGTAAAGTGA 1260 AAGAGCTGGT GCCTGCCTTA TTGGGAGCCT CTGGGTTTAT GTATGAGTCA GATGCGTAGA 1320 GTTGCTCACC ATGGAGGGCC CAGGGTAGGC AGGCATTATT GAACAACTGC TCCATGTGCT 1380 CTTTTCAATC TTTGCAGACC CCACCCACGT CTCCCTTGCT CAGACCTGGC TCCCCATGGC 1440 TTATGAAAGG GGGCTGAGTG CAGAAGGTGG CAGGCAGGAC ACTGGACAAC CCTCTGTGGC 1500 TTTTCCTTAC CCTTCGTAGT ACCATGAGAT TCTGGCTCTT CCCGTCTCTG TGTTTCTGCC 1560 TATGGGTCCT TCCACATGCA GTGCCTCGTC TTCCCTCCTT CCCATCCATG TCCTTTTGTC 1620 TTCAGGCACA CCCACTTGGA AGGAGCCCAT CCTCTCACAG GGTCTGCTGG CATATTCTGC 1680 ACCTCTCAAG TACTCATATT TCCTCTGCAA TCTTTTCTAT GTTGTTTTTC CTCTGCTCAA 1740 GGGTAAATTG AGAGTAAGGA AAGTATTTTT 1770
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