| Tag | Content |
|---|
EnhancerAtlas ID | HS060-05528 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr11:44594110-44597290 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crem | MA0609.1 | chr11:44594785-44594795 | TATGACGTAA | + | 6.02 | | KLF4 | MA0039.3 | chr11:44595168-44595179 | CCACACCCTCT | + | 6.02 | | KLF5 | MA0599.1 | chr11:44594574-44594584 | GGGGCGGGGC | - | 6.02 | | Nr5a2 | MA0505.1 | chr11:44596590-44596605 | AAACTCAAGGTCAGA | + | 6.07 | | RREB1 | MA0073.1 | chr11:44596112-44596132 | CCCCAAAAAACCCCCCAAAC | + | 6.52 |
|
| | Number of super-enhancer constituents: 19 | ID | Coordinate | Tissue/cell |
| SE_10955 | chr11:44585347-44606263 | CD20 | | SE_14978 | chr11:44594539-44596937 | CD4_Memory_Primary_7pool | | SE_18030 | chr11:44593108-44597614 | CD4p_CD25-_CD45ROp_Memory | | SE_18725 | chr11:44593177-44599224 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19325 | chr11:44586077-44599410 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_25709 | chr11:44586950-44600967 | DND41 | | SE_27056 | chr11:44594021-44601651 | Esophagus | | SE_32002 | chr11:44594025-44594815 | Gastric | | SE_32002 | chr11:44594861-44597255 | Gastric | | SE_39624 | chr11:44593301-44602114 | Jurkat | | SE_42483 | chr11:44594870-44596126 | Lung | | SE_52138 | chr11:44594818-44597200 | Skeletal_Muscle_Myoblast | | SE_53218 | chr11:44594138-44596110 | Small_Intestine | | SE_55965 | chr11:44594177-44599445 | u87 | | SE_62566 | chr11:44577989-44637584 | Tonsil | | SE_63922 | chr11:44594804-44597961 | HSMM | | SE_65536 | chr11:44594271-44595894 | Pancreatic_islets | | SE_65536 | chr11:44596629-44602221 | Pancreatic_islets | | SE_66474 | chr11:44593301-44602114 | Jurkat |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 7 | Chromosome | Start | End |
| chr11 | 44594314 | 44594766 | | chr11 | 44594392 | 44595143 | | chr11 | 44595147 | 44595263 | | chr11 | 44595610 | 44595895 | | chr11 | 44595924 | 44597228 | | chr11 | 44596231 | 44596678 | | chr11 | 44596848 | 44597017 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I044572 | chr11 | 44593907 | 44601798 |
|
Enhancer Sequence | CTTGGAGGGA GTGCCTATGG TAGGAGCGTC CATTGTCCGC AGCCGCCCAG GCTGGGAGAC 60
AAGAGTTAGA TATGAATAGG AGTGTAATCC GCCTTCCCAT GCGGTGGGCA CACCCTGAGC 120
GTTGGGTGGT GTGTAGAAAG CTTTTGAACA GTAGTTGAGA TCAAGTTCCT TAATGACCAT 180
TCTGAGCCTC AGTTTCCTCA TCTGTGAAAT AGGGATGGGC TGCTGTGAGG GTTAAATGAG 240
CTAAACACAT ATTGAATATG GAGCTCTAAA TGGAAGCCGG TGGAAGAAGG TGGCTTTACA 300
TCTGGGGTCC AGAGGGCTTG CTGACTGGCC TGTCCTGGAC CTGGCAGAGT TACCCGTCCC 360
GCCACAGGAC GTGCTGGACA GGAGGCAGCC TCCTGCAGGA CCAGGTAGCA GGAGCAGAGA 420
ACAGCCCAGA CAGAACTCTC CCTGCGGGCA ATTTGGCTCT GCGAGGGGCG GGGCCCCACT 480
GAGTCTGCCC TATGTGTCTC TAAGACGAAC CAATCATAAG CCTCCCAGGG CGTGGCGTGA 540
AGCGGGGATT TGGTAGGGGA GCGCAGAGCG AGGCCTGAGG TGTTTCCCTG GCAGAGGTCC 600
CTCCACTGGG AAACAAACGG AGAGGGGAGT ATGTGTTCCC ACGTGTACAC ATAAACCGTT 660
TTGAATGATA CCTGGTATGA CGTAAGCACT CAATAAATGT TTGTTGTTGC TGATAATAAC 720
AATTGGTAAA TTATACTAGT ACAGTTGGAA AACCACCTCC CACTCACTGT CTTAAAAGGT 780
GGAATATAAG AATGCTTTTG CAGTGGGACC TATGAGACAT CATCGTATAT AGAGGAAATA 840
GAAACTTGGC AGGGGAGGTT TGATTTATCT GAGGTCATGG AGCAAGTGGG TGTCTAGGCC 900
TTGAGTCACC TTTGGACATG TAGATAGCCC ACCTCCCTGA CCCCTGGCCT TTCTGAACAC 960
ACAGCAGTGG AGTAACTGAG GCAGGGAGGA TGTGTCCTCT ACTCTGAACT AGTCACTTAT 1020
TTTCCATCCG AAAGCCCCTC TTATCTGCTT TCTCTGCCCC ACACCCTCTC CTGGCATGGT 1080
TGAGCAAGTC TCCTTGTTTG CCAGGAGACG GTATGGCATG GCACTGTGGT TCTCAAAATG 1140
TGTGCCTATC AGGAATCCCT AACCATCCCT GCAAGTTGCA GTCAGGGAAA CACTGGGGCT 1200
GTGCCTACAG CTTGGGGTTC TAGCTTCTCA GGCATTGATG TCAGCCAGGC CTAGCTATGG 1260
GCACAGTGTC TGTTCACCTC TGGGCAAGTT TCTTGGCCTC TCAGAGTCTT GGTTTTTATG 1320
AGGATTAAAT GAGATAATGC TGGTAAAATG CTTCGTGGCA GGCCCAGGGA AGAGTGCACC 1380
CTCAATGAAG CCAGAGGTTA AGGGTGGTGA TGATGAGCAA AGGCTGCTCC TGTCATTACT 1440
TCTGGGGAAA TGATAGGGAG TCTTCCTGTC CGAAGGCTGA GGTCCCTGAT CTGGAGTGAG 1500
GGAGCTTTCC GGGGTTGCTT GAAGCTCTGC TGGGGGGTCA GCAGAAGACT TAGATTCTCT 1560
GTAGTCTTGG TCCCCAGACT ATCTGAACCC AGCCTTGAGC TGGGTGCTCT TGGCATAGAG 1620
TTGAGGGCAA AGTTGAGGGC TTACGTCTAG AGTCACAGGA TCTTGGTGTT GTGAGAAGCT 1680
CTGTGGTCCA TCCAGTCAAC CTACCTGCCC AGTCTGATCC CATGGACCAC ATCCAGCCTT 1740
TGCTCGCACA CCTCAAGGCT TGGAAAGCTC ATGATTTTTT ATTTCTGGAA AGAACTGACT 1800
CTTAGAAAAT AGGGGATAGA ATCTGAGCAA ACCCACCCAC CCTTGGCTTC CCCATTTTGA 1860
TCCTGATCTT GCTTGTTGGA ATTACACACA ATGTGGAAAC ACCCTGGTGG GACCAAATCT 1920
TGTAGCAGAA GACCCCAGGC CAGCGATTCT GACATAGGAA GGAGATTTTT CTTTTAAAAA 1980
CTTTATCTAA ACCAAATGGC TACCCCAAAA AACCCCCCAA ACTTTCTGAT TATTGAAGAA 2040
AGAGGGTTTT TTTTGTGTGT GTGGAAAAAT TCAGGCGGTA AAGAACAGAC CTGCAGGAGG 2100
AAATAACTGC TCAGAGATAA CTGCCGTGAG CAGTTTGGTG TTTTGGCCTT AAAGACACAC 2160
ACATACAAGA TTGGGATTGT ACCACACAAA CCACTTCCTG CACTGCCACT TTTGACTGAG 2220
TGCTGTATAG GGAGGGTTTT CCCATGTGAT TGAGCATTCT TCTCCAGCAA GTTTCCCAGC 2280
TCTGTAGTAT TGCACCATAG GAATCTTCTG TGACCTGGTT AAGCATTCCC CAGCCATTGC 2340
ACATTTAGGC CCTTTGAATT TTTCATTAGT ATCCACATTG CTATAATGAT CGCCTTGTCC 2400
CTATGTATAT TTTGTACTCA ACTCTAATGA GCTCCATGGA ATGAATTTCT AGAAGTGGCT 2460
TTCCAGCTCA GATGGTTTTT AAACTCAAGG TCAGAGGACC AGAATCTCCC ACCATAACCA 2520
GTCTCCCAGT TTCGCTTCAG CCCTACTGGT GGGGGAGCGT TCTGTCTGTC CCTGGTGCTA 2580
GTTGGCCTAC CCACAGGAGG AGGAGGAGCA GGCTTTTAGG GTATGTGTAT CTGTGAAAGA 2640
GAAGGAGATG GAGAAAGGCA GATAGATATA GGGGAGTGTT TTCTCTTCAA TTACAGTCTG 2700
ATTTTGACCC TCTCCTCTCT GGGAGCCTGT GGTGTCATTA ACTAATCATG GGCTCTCTTT 2760
ACTATTTAAT GACCTCTCCC CACAGTGACT CCTTCCTCCC CAACAGTCTC CTGGAAAGGA 2820
GGAGGTGGGA AGATGAGTCA GTGGGGGAAA GTTTCTCCAG AGTAGGTGGT GGGTGTTGCA 2880
GTGGTTCTCA AACTCTGACA TGCATCAGTC CCTTGGATGG CTTATGAAAG CACAGATTGC 2940
TTGGCCCCAC CCCCAGGTTT CTGATTCTGT GGGTCTGGGG TACTGCCTGA GAATGTGCAT 3000
TGCTAACACG TTCCCAGGGG ACGCTGCATC TGCTGGCCCT GGACCACACT TTGGGTACCA 3060
GTAAAGTAGT GGGATGGGGC AGGGTGGGGT TCTGTGGTGA GTTTCAGCTC CTGGTGTTGC 3120
TGACAGTAGG AACCTTGTCC TGTTTAATAA AGGCTCATCT TGTGAGGCCT GAACTCACCT 3180
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