| Tag | Content |
|---|
EnhancerAtlas ID | HS093-02554 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr1:198589850-198591100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ETV6 | MA0645.1 | chr1:198590193-198590203 | CACTTCCGCT | - | 6.02 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_09213 | chr1:198588981-198592120 | CD14 | | SE_10200 | chr1:198588027-198594672 | CD19_Primary | | SE_10874 | chr1:198579403-198671825 | CD20 | | SE_11822 | chr1:198587521-198595241 | CD3 | | SE_13336 | chr1:198589295-198591554 | CD34_Primary_RO01536 | | SE_14382 | chr1:198587909-198593024 | CD4_Memory_Primary_7pool | | SE_15405 | chr1:198587286-198591751 | CD4_Memory_Primary_8pool | | SE_15805 | chr1:198588242-198592643 | CD4_Naive_Primary_7pool | | SE_16283 | chr1:198588465-198591973 | CD4_Naive_Primary_8pool | | SE_17305 | chr1:198587675-198600249 | CD4p_CD25-_CD45RAp_Naive | | SE_17776 | chr1:198587525-198598559 | CD4p_CD25-_CD45ROp_Memory | | SE_18245 | chr1:198586009-198601808 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19200 | chr1:198588420-198594418 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_19995 | chr1:198587255-198594711 | CD56 | | SE_20746 | chr1:198588472-198591608 | CD8_Memory_7pool | | SE_21924 | chr1:198588052-198594703 | CD8_Naive_8pool | | SE_22285 | chr1:198585323-198601107 | CD8_primiary | | SE_31026 | chr1:198588235-198592906 | Fetal_Thymus | | SE_39433 | chr1:198589254-198591591 | Jurkat | | SE_49861 | chr1:198588569-198593134 | 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 | | SE_66263 | chr1:198589254-198591591 | Jurkat |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I198617 | chr1 | 198586995 | 198595024 |
|
Enhancer Sequence | TTAAGAAGAT AAGGTCAGTT TTGTCATTGA TCTGGTCCTA TTCACCTTGT TTTTCTCTCT 60
TAAATTATTT CTTTACCATT GTGGAGATAA TCAACCGCAT GGTGTCATCA CTCATTTATC 120
TCTAAGCATA ACAGACATTT TCAACCCATT TCAGGTGTCC TCAAATTATT CATTTTTTAT 180
TTAAATGAAG AATTGTCCAG AGTTAGCATG TAAATATTAG CTAAGGGCAG GATGTGTGTG 240
TGTCATGGAG GGGAGGACCT CTCCTGTTTA GGAGGAACTG CTGGCCCTAA TATGCATGTC 300
ACATACATAT GAACCTTGAT CGGCTGTCAT GCGGAAGGAA TTACACTTCC GCTGGCCTCC 360
CCTACCACAA CCACAGGTGG AATCTAAGCT AGGCACTGAA CTTGGCTCAC ACAGCTGTGA 420
GCTTGCGCTG AGTCTCATCC TTTGCTGTGG AACTCCCTCT GCTGCTTCCT GCCCCAGCAA 480
ACTCCCCTCT ACCCAGCCAC TGGAAAGGAG TCCCACAGGA GGGGAGGGAC AGTAGAGTAG 540
AGCCCAGCTT CTCTGTCCAA CACATAAAAG CTCTGAAAGG CAGTTATAAA AGGCTGAACT 600
GGGAGCAGGT ATTGTTAAAA AGGGAACCAC TGACTTCCTG TGAGCACATG TTCCTGTCTC 660
ACTCTTGCTC TGCAGCACAG TAGAGGCTGT TTAGTTCATC ACAAAGGAAG TGCATCAGCA 720
CTCCTGAAGA TGCTACTCTA AGGGCACCTT TGAGTTGTGG GCCAGGAAGG CATTCCATAG 780
TAAGACGAAG GAAAGGCCAA GTTCCTATTG TTAGCGTCAC TATGCTTCTG GTTTTATAGT 840
TTCCTAAGTT ATTGCCACAG GTCATGGATC TGTGGCGCTC AAATGTTCGC TCACAAGGTT 900
CACAGCACAT TCTTTGCAGT TGCACCACCC AGCTAGGAGG GGCGAAACCA ATGGAGCATT 960
TTAGGCAGAG CTCATTTCCG CCCACATCAA AAGTAAGAGA GAAGTTTGTG GAGAGCTACA 1020
TTTGAGCCCT CCATTAGCTG TTTTACATCT TGTAGGCCAA GGTGACACTT TCTACACTAT 1080
GTGCTGGTGA GATACCACAT GGACAAAATG TTGTAGAGGA CCCAGCCTGA AAAATGCTCA 1140
GGCTTTAAGT CTGAGCAATC TCCACCACAT CTCTACTCCA CATCCCACCC CTCCTGGAAT 1200
TTTAAGTCAG GAGACACATT GTGAGTGCAT GGACAAAATA AAGAAAAGAA 1250
|
