Tag | Content |
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EnhancerAtlas ID | HS059-03667 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:198633140-198634590 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2C | MA0497.1 | chr1:198634478-198634493 | ATTTTAAAAATAGAT | + | 6.19 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_09213 | chr1:198631253-198635605 | CD14 | SE_10200 | chr1:198633097-198634455 | CD19_Primary | SE_10874 | chr1:198579403-198671825 | CD20 | SE_11822 | chr1:198632977-198635318 | CD3 | SE_12868 | chr1:198633279-198633841 | CD34_Primary_RO01480 | SE_13336 | chr1:198632957-198634303 | CD34_Primary_RO01536 | SE_14067 | chr1:198633220-198633914 | CD34_Primary_RO01549 | SE_14382 | chr1:198631677-198635440 | CD4_Memory_Primary_7pool | SE_15805 | chr1:198632921-198633915 | CD4_Naive_Primary_7pool | SE_16283 | chr1:198633568-198634777 | CD4_Naive_Primary_8pool | SE_16874 | chr1:198633038-198634380 | CD4p_CD225int_CD127p_Tmem | SE_17305 | chr1:198604496-198661531 | CD4p_CD25-_CD45RAp_Naive | SE_17776 | chr1:198604306-198639795 | CD4p_CD25-_CD45ROp_Memory | SE_18245 | chr1:198604293-198639821 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19200 | chr1:198630752-198635295 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19995 | chr1:198620471-198643645 | CD56 | SE_20746 | chr1:198633171-198634478 | CD8_Memory_7pool | SE_21924 | chr1:198633003-198635203 | CD8_Naive_8pool | SE_22285 | chr1:198604395-198665148 | CD8_primiary | SE_25576 | chr1:198633136-198634475 | DND41 | SE_31026 | chr1:198633117-198634311 | Fetal_Thymus | SE_49861 | chr1:198631695-198634219 | RPMI-8402 | SE_58290 | chr1:198564715-198671046 | Ly1 | SE_59080 | chr1:198588455-198654514 | Ly3 | SE_59608 | chr1:198585244-198671628 | Ly4 | SE_60444 | chr1:198588133-198656098 | DHL6 | SE_61004 | chr1:198588339-198656148 | HBL1 | SE_61429 | chr1:198565046-198658062 | Toledo | SE_62210 | chr1:198565497-198666528 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 198633275 | 198633927 | chr1 | 198633320 | 198633627 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I198660 | chr1 | 198629438 | 198661503 |
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Enhancer Sequence | GCCTTTAGTT CATGGAAAGA AAAGTATGTT AAAGATGCTA TGGGGGTGAA GAGAATGATA 60 AATATTATTA TTTAAGACAA TGTTTGCTAT AATTTTTATA TATCAAATAA GTTTATATGT 120 TCTCAGAAAA TTGGTCTTTG AATAATTGAG GACAGTGTGG GTTTTTATTC TGTTTCTGGA 180 AGGCGGTGCC TGTGGCTGTG AGAAATAAGG AACAGACCAT CTTCCCACAT TTGAGAGGGA 240 ACTATACAAA AATGGGAAAA TATTTGTTTT AAATATCTTT TGGATGTGAA TTTTGTCATA 300 ATTGCAAACT GTTTTGGCAG CAAAACGAAT TATTTCGGTA GCAAGAAGAG ACTTAACGAT 360 GCTATGTGGG AGAAAAACTA AGTCCCTACT ATCTTTCTGA GAGCACGTCT CAGAGGACAT 420 GATGTGATCC TGTAAGTTTG TAGCAATCTT ATTGTGCCCC AGTGCAGACA CTCCTTCCTA 480 CTTCCCTGTA GAAAACAGAA CTGTTTTTTT AAAATTCTTT CTCAACTACC ATTTTTAATA 540 GTCATGTTAC TTGATGACAA AATCTGATAC AGTGGCCTTT AATACTATAT AGTGAATGAT 600 TTTTGAAAAT TTGGAAAACT CTAACCGAAA TATACCAGGA ACTGCTCTCC TCTTCATCTC 660 AGATGTCTAC TTCCTCTTCA GACCTGTGTG TGAAGCTCTA GAATAGGCTG TTTGGGAAGA 720 CTACAAAATC TCCTCTCCGA GGTCCCTTAT AACCCTGATA GTTGCTAGAT TTGAAATCAA 780 GGATTTATTC TCCCCCTGCC CTGAGCCTCT CCCTTATGTC CACATAGGCT CTAGCATTGG 840 AAGAAATATT TTAAGATCTC TTTCTTTTTG ACTTTGTGAT ACTCCCATAT TAAAAATGGC 900 TTATGACAGG AAAAGGACAA ATATGCTATA TTTTTTCCCT TAAGGCTAAT GTTCTCGGGA 960 CTACCATGAA AAATCCAGGT ATCCTAATCT GGAGGGTTAC CCTTTGGATC TGAATGGGAT 1020 TGGAGTCAGT ACAAGGGGTG GGGAGTGTTT TTAGAACATC CCGGCAGCAT TTTTTTTTTT 1080 TTTTTTTTTT TTTTTTGAGA CGGAGTCTCG CTCTGTCGCC CAGGCTGGAG TGCAGTGGTG 1140 CAATCGCGGC TCACTGCAAG CTCCGCCTCC CGGGTTCACG CCATTCTCCT GCCTCAGCCT 1200 CCCGAGTAGG GGGGACTACA GGCGCCCGCC GCCACGCCTG GCTAATTTTT CTTTTTTTTT 1260 TTTTGTATTC TTAGTAGAGA CGGGGTTTCA CCGCCCTGCT GCCTTTTAAA GCAATTTAAT 1320 ACATGAGTTA AATATCATAT TTTAAAAATA GATTTTATTT TTTATTATAA TTTTGATGAA 1380 TGCATTTTTG TCAAAGTTGT CAAAGTCAAG AAGTCATTAT TGAGACCCTG AGGGTAAGGC 1440 AGGAGCCAAG 1450
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