Tag | Content |
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EnhancerAtlas ID | HS134-30190 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr2:70334960-70337440 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESX1 | MA0644.1 | chr2:70335613-70335623 | GTTAATTGGT | - | 6.02 | HES2 | MA0616.2 | chr2:70336601-70336611 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr2:70336601-70336611 | GGCACGTGCC | - | 6.02 | KLF5 | MA0599.1 | chr2:70336206-70336216 | GGGGCGGGGC | - | 6.02 | NR2F1 | MA0017.2 | chr2:70335322-70335335 | CAGAGGTCACAGG | + | 6.19 | POU4F2 | MA0683.1 | chr2:70337170-70337186 | GTGCATATTTAATAAA | + | 6.51 | RREB1 | MA0073.1 | chr2:70336054-70336074 | TGTGTGGGTGTGTGGTGGGG | - | 6.68 | RREB1 | MA0073.1 | chr2:70336052-70336072 | TGTGTGTGGGTGTGTGGTGG | - | 7.62 | Zfx | MA0146.2 | chr2:70336205-70336219 | CGGGGCGGGGCCTG | + | 6.18 | Znf423 | MA0116.1 | chr2:70335934-70335949 | AGCCCCTAGGGTGGC | + | 6.17 | Znf423 | MA0116.1 | chr2:70337159-70337174 | GCACCCCAGGGGTGC | - | 6.32 | Znf423 | MA0116.1 | chr2:70337159-70337174 | GCACCCCAGGGGTGC | + | 7.52 |
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| Number of super-enhancer constituents: 17 | ID | Coordinate | Tissue/cell |
SE_03004 | chr2:70335365-70336160 | Bladder | SE_08976 | chr2:70335702-70336032 | Brain_Mid_Frontal_Lobe | SE_11876 | chr2:70334952-70336502 | CD3 | SE_11876 | chr2:70336603-70337538 | CD3 | SE_15476 | chr2:70335123-70336775 | CD4_Memory_Primary_8pool | SE_16420 | chr2:70335113-70337034 | CD4_Naive_Primary_8pool | SE_16927 | chr2:70335400-70336482 | CD4p_CD225int_CD127p_Tmem | SE_19261 | chr2:70334981-70337422 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_21576 | chr2:70335226-70336530 | CD8_Naive_7pool | SE_21995 | chr2:70334869-70336793 | CD8_Naive_8pool | SE_23504 | chr2:70335181-70336532 | Colon_Crypt_1 | SE_24093 | chr2:70335260-70336387 | Colon_Crypt_2 | SE_25188 | chr2:70335628-70336458 | Colon_Crypt_3 | SE_25929 | chr2:70334878-70336553 | Duodenum_Smooth_Muscle | SE_28737 | chr2:70334137-70340794 | Fetal_Intestine_Large | SE_34548 | chr2:70334331-70337725 | HCT-116 | SE_47654 | chr2:70334994-70336517 | Pancreas |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 70336386 | 70336532 | chr2 | 70335985 | 70336314 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I070107 | chr2 | 70334334 | 70341628 |
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Enhancer Sequence | AAAGAAATGA AATTAGCTCA GTGTGGTGGC TGGCGCCTGT AGTCCCAGCT ACTCCAGGGG 60 CTGAGGTGGA AGGATTGCTT TAGCCTGGGA GTTCGAGGCT GCAGTGAACC GTGATTGCGC 120 CACTGCCCTC CAGCCTGGGC GACAGAGCGA GACCTTGTCT CAAAAAAAAA AAAAAAGAAG 180 AAGAAGAAGC CACTAAGCTA AGAGGTAGGT ACTAAGTTGA AGGGGAGACA GAATGGAGAT 240 AAGGATTTGG GTTTTTTAGG TGGTAGTGAC ACAAGGATGT TCATAAGCTG AAGAAGAAAA 300 GACCAACAAA CAGACTAAAC ATTTGAGAAT GAGACAGAGG AAAAAGCATA CGGAGCAAAG 360 CACAGAGGTC ACAGGGTGTG TGGCCAGCAG TGGTGGGGAC GCTGCTAGCT TTCTCTGAAG 420 TGGGAGAAAA GGAGTGTTCC TTTCCCTGCA CTTTCTCAAC CACACTGACT GAGGAAGGAC 480 AGAGGGGGCC CAGAGAGCAG TGGGGGTGTC CAATCACTGT TCTTGGGCCT GGAAACTGTT 540 GGGGCTGTGG ACCCCAGAGT ACTGAAGGAC TGCTGGACGG AGCGTATGGC TCCATCTGAG 600 CCTGTAAATC ATAAATCTAC CTGGTCAAAG AGTAAAGGCC TCAAAGGTTC TGAGTTAATT 660 GGTCTGGTTT TTGACCTGAG CATCAGAAAT TTTTTAAGCT CCCTGAGTGA GTCTAACATG 720 CAGCCATGGT TGAGAACCAC TGGGGTTAAG AAGTGAATTG AGACGTATGG AGACTTAAAT 780 CTCCAACCCT GGGTGGGAGG ACAAGGAGAG GCTCTGCCGC CCTGGCTGGA ATAGTGGGGC 840 CCTGTTTGGG TTGTGGACGT CCCTTCAGTC ACAGGAGGAT GAATTCCTGC CTTGTTCCTT 900 TGGTCGGATC TGAATTCTTC CCCAACCTCC CGCCCTAACT GATAGCATAC AGGGCTTCCC 960 AGACAGAGAC CATCAGCCCC TAGGGTGGCA GAGAAAGGCC AGGTTCAGGA ATGTGACATT 1020 AATTATGACA AACAATATGT TCTCCCACTT AAGAACTAAG CCTGGTTGGC TGCGCATGTG 1080 CGCGCGCGTG CTTGTGTGTG GGTGTGTGGT GGGGTATGTG TGTGTCCGGG GCTGCCGATT 1140 CAACTGAAAA ACAAAAGCGG CTCTGAGTCT GAAGCTAAGG TTTAACAAGT GACCAAGATG 1200 ACTCATGCTG CTTGGCTGCA AAGGCCACAG GGCTGCCACC CCCAGCGGGG CGGGGCCTGG 1260 GTGGGAAGAG TCACAGGTAC AGAGGCTCCT GTGACATTCA CACTCTGCCC CTGCATCGGC 1320 TGCCTTTGGG GCCAAATACT TTTGTGAAAA TTAAGACAGA AGGCCGGGTG CGGTGGTTCA 1380 CGCGTGTAAT CCCAGCACTT TTGGAGGCCG AGGCAGGCGG ATCACGAGGT CAAGAGATGG 1440 AGACCATCCT GGCCCACATG GTGAAACCCT GTTTCTACTA AAAATACAAA AATAGGCAGG 1500 GCGTGGTGGC TCACGCTTGT AATCCCAGCA CTTTGGGAGG CTGAGGCGGG CAGATCACGA 1560 GCTCAGGAGA TCGAAATCAT CCTGGCTAAT ACGGTGAAAC CCCGTCTCTA CTAAAAATAC 1620 AAAAAATTAG CCGGGTGTGG TGGCACGTGC CTGTAGTCTC AGCTACTCAG GAGGCTGAGG 1680 CAGGAGAATT GCTTGAACCC AGGAGGTGGA GGTTGCAGTG AGCCAAGACT GCGCCACCTC 1740 ACTCCAGCCT GGCAACAGAG TGAGACTCCA TCTCAAAAAA AAAACAAAAA CAAAAACAAA 1800 AAGTAACTGG GTGTGGTGGC CCGCACCTAT AGTCCCAGCT ACTCGGGAGG CTGAGGCAGG 1860 AGAATCACTT GAACCCAGGA GGCGGAGGTT GCAGTGAGCC GAGATCGTGC CACTGTACTC 1920 CAGACTGGCG ACAGAGCCAG ACTCCCTCTC AAAAAAAACA AAAAACAAAA AAGAACCAGA 1980 AAATGTAACT TTCTTCCTAT GGTCATAAAT CTGGTGTAAG CAGGCAAGTC AAAGCGATGT 2040 TGAAGCCAAT GGATCTTGCA AAGGCATGGC AATGTTTGCA CAAGGATGGG ATATAGTAAG 2100 TTAAAATACA TTGGCTTTTT CCAAACGGGC TCAAACTGGA AGAGAAGGTC TAAGCAGAGC 2160 ATGTGCTGCT GTCAGGAGGG TTCCTCAGCA GGAGACAGGG CACCCCAGGG GTGCATATTT 2220 AATAAAAACT TACAATATGC AGGTTTTGGG ACATGAAGGA AACATTTAAC CTGTCCTGTC 2280 CAACACGGCA GCCACTTGTC ACATGCGGCA GTTGAATACT TGGAATATGG CTAGTCTGAA 2340 TAAAGATGTA AAACATACGC CGGATTTTAG ACTTAGTACA GGGGTGGGAA AGAGTTTAAA 2400 ATAGCTCAGT ATAGGCCGGG CACAGTGGTT CACACCTGTA ATCCCAGCAC TTTGGGAGGC 2460 CAAGGTGGGC AGATCACCTG 2480
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