Tag | Content |
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EnhancerAtlas ID | HS068-05665 |
Organism | Homo sapiens |
Tissue/cell | GM18526 |
Coordinate | chr9:123637740-123639360 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PLAG1 | MA0163.1 | chr9:123639226-123639240 | CCCCCGAGAGCCCC | - | 6.35 | Zfx | MA0146.2 | chr9:123638610-123638624 | CAGGCCGGGGCCGC | - | 6.79 |
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| Number of super-enhancer constituents: 34 | ID | Coordinate | Tissue/cell |
SE_11823 | chr9:123637655-123639687 | CD3 | SE_13925 | chr9:123636768-123641379 | CD34_Primary_RO01536 | SE_15226 | chr9:123634985-123642730 | CD4_Memory_Primary_7pool | SE_15579 | chr9:123637916-123639531 | CD4_Memory_Primary_8pool | SE_16326 | chr9:123637738-123639482 | CD4_Naive_Primary_8pool | SE_16854 | chr9:123637455-123639673 | CD4p_CD225int_CD127p_Tmem | SE_17311 | chr9:123634993-123643597 | CD4p_CD25-_CD45RAp_Naive | SE_17766 | chr9:123634294-123642934 | CD4p_CD25-_CD45ROp_Memory | SE_19108 | chr9:123637391-123641414 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20050 | chr9:123637382-123641113 | CD56 | SE_20898 | chr9:123636462-123642473 | CD8_Memory_7pool | SE_21944 | chr9:123638042-123639525 | CD8_Naive_8pool | SE_22312 | chr9:123636734-123642480 | CD8_primiary | SE_26718 | chr9:123637091-123641239 | Esophagus | SE_27931 | chr9:123634310-123641616 | Fetal_Intestine | SE_28718 | chr9:123633996-123641611 | Fetal_Intestine_Large | SE_30939 | chr9:123636787-123642410 | Fetal_Thymus | SE_39503 | chr9:123636935-123638708 | Jurkat | SE_39503 | chr9:123638731-123639497 | Jurkat | SE_39875 | chr9:123634346-123642044 | K562 | SE_43652 | chr9:123634250-123641808 | MM1S | SE_50248 | chr9:123636006-123642006 | Sigmoid_Colon | SE_52520 | chr9:123635149-123641908 | Small_Intestine | SE_53449 | chr9:123637553-123641189 | Spleen | SE_55104 | chr9:123637181-123641403 | Thymus | SE_59300 | chr9:123630370-123667495 | Ly3 | SE_59862 | chr9:123630341-123667956 | Ly4 | SE_60687 | chr9:123630207-123668046 | DHL6 | SE_61111 | chr9:123630545-123707493 | HBL1 | SE_61770 | chr9:123630310-123667005 | Toledo | SE_62230 | chr9:123630172-123700621 | Tonsil | SE_66426 | chr9:123636935-123638708 | Jurkat | SE_66426 | chr9:123638731-123639497 | Jurkat | SE_67222 | chr9:123634250-123641808 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | ATCGATTTCT CTCTCCCTGC CTGTGGTACT GCCTTCATGC ATCTCAAACT CCTCCAAGCA 60 ATTAGTTGCC ACAGCCGGCC CATTTTAAGT GCCATGATTT CTGGCTTTCC AGCTCTAGCT 120 TCCATCCTCC TGCCCTGGTC TCAGTTCAGG CCTCATCTTT TGCTTGGGCC ATTCATTCAT 180 TCATTCATTC ACCCAATAAC AGTTTCCTGG GCCTTGTGCT TACCTCCACT AGGCACCTAG 240 GGTGGGGAAC GGTACTACCA GCACCCAGTG CTAAACAGGC CGTTCCTGCA TTCCTGCCTC 300 TCCACCAGAC TCTTCCGCAG GGCCACCAAT TTCCTTCCAG AAACTTTCTG GGGCTCCCCA 360 CTGCCCTCAC TGGTGCTCAA AGCCGTCCCT AACGCCCCCT CCTTTCTGCT GGGCTCACCT 420 GGCTCCAAGT CCCTCCACAT GCTCTCCACT ACAGCCACAC ACAGCCTCTC TCTTTCCCCG 480 CGGGCCTACT CGGGTCTCCT CCTTGTGGCC ATGGCGCTGG GCACCTGGTG TTGTGACTAT 540 CTGTTCACAG GGAGAGAGTC CAGTGCCTGT TTCTGTGTGG TGCGTGTGTG TACTCCTGTG 600 AGACTGGGCA GGATGATGTC TACGGCATTG TGCCAGGGAG TGTGTGAAGC TAAGTATGTG 660 CGGGGCCCTG GGGCGAGCCA GGCACTGCAG GGGTCTCGGC TCCCCAGATG GTGGCGTGGC 720 CACGACCTTC TCCACCCCCA CTCCCATCTC CTTTTTCTCC AGCGCAGAGC GCACAGGCTC 780 CCGGGCAGGG GATGCGGTCT GAATCCCTGT CCTCTCCCTG CCACCTGGCT CGCCCGGCGC 840 TGCGAGGTCC CCGCCCGCCC GGCCAGGGGC CAGGCCGGGG CCGCTGCAGG TTCACAAACT 900 GACACTTCCT CTCCCGCTGC GCCTCTAGGA GCCGGCCGGG TCGCCGCACC CGCCTCCACC 960 CTGGCCGGGC GGGGGCCCCC GGGTGGCGCC CCCCCAGCCC CCGCCTCCGT CCTCCCGGAG 1020 CGGGCCCCCG CGGGCTGTGA TTGGCTGATT CAAACCCATT TGCAAAGAAA TGCCTGTTTG 1080 CGGGTTCCCG TCTGCGTCCA GTTCAAATCC GCGGCACCGG GAGCGCGGGG CCGGGCGGGG 1140 GCAGGAAGCG AGGATGATTC ATGCGCCGGG GCCTCTCCCA GGGCGGCCGT TGGCTTTTTA 1200 AAAAGGATGT TCAGGAGGGG GGAAAAAGCT TGCAGAAGCA CCCCCTTCGG GTTCAGCGCT 1260 CCTCTCCTCA GTCGCTCGGA CGCCAAGCCT CCCCCATCCC AACCCTGCCG CAGCCTGACT 1320 TCGGACGTGA GCGAAATGCC AAACGCCCGT CTGTCCTTCC CCCACCCCGA TAGGAAAATT 1380 AAAGATCGGG GGCGAGGAAG AACGACCTGT CACCCATGCC CCCCGGGGCT CGGGAACCCG 1440 GGTGGGGCCC CTCTGCCCCG CAGGTAACCT GCACCCCCGG TCCCCACCCC CGAGAGCCCC 1500 GCTCCGCAGG AGTCTCACCC CCCGGAGGCG TTCGGGCCGC CAAAGTTCAG GGAGATTTCG 1560 AAAAGAGAGG GATGAGGGCC GGGAGGGGAG AGCGTGGCGG GGAGTCCGCC CAACAGCGCA 1620
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