Tag | Content |
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EnhancerAtlas ID | HS105-06545 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr1:204416790-204418310 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-3 | MA0672.1 | chr1:204417337-204417347 | TTCAAGTGGT | - | 6.02 | Six3 | MA0631.1 | chr1:204417428-204417445 | GACAGGGTATCACCATG | + | 6.11 |
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| Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
SE_00064 | chr1:204415801-204417319 | Adipose_Nuclei | SE_00064 | chr1:204417530-204422553 | Adipose_Nuclei | SE_03975 | chr1:204415223-204416998 | Brain_Anterior_Caudate | SE_04850 | chr1:204414465-204417204 | Brain_Cingulate_Gyrus | SE_04850 | chr1:204417565-204418666 | Brain_Cingulate_Gyrus | SE_05834 | chr1:204414554-204422838 | Brain_Hippocampus_Middle | SE_06778 | chr1:204414634-204417237 | Brain_Hippocampus_Middle_150 | SE_07775 | chr1:204414572-204417332 | Brain_Inferior_Temporal_Lobe | SE_07775 | chr1:204417757-204421412 | Brain_Inferior_Temporal_Lobe | SE_10255 | chr1:204417782-204418559 | CD19_Primary | SE_10905 | chr1:204414650-204438582 | CD20 | SE_25125 | chr1:204416348-204417318 | Colon_Crypt_3 | SE_25125 | chr1:204417816-204422942 | Colon_Crypt_3 | SE_26688 | chr1:204416875-204421560 | Esophagus | SE_28866 | chr1:204417158-204423024 | Fetal_Intestine_Large | SE_30246 | chr1:204415638-204416972 | Fetal_Muscle | SE_31610 | chr1:204417780-204422694 | Gastric | SE_34711 | chr1:204415846-204421729 | HeLa | SE_40776 | chr1:204415081-204417377 | Left_Ventricle | SE_40776 | chr1:204417564-204421617 | Left_Ventricle | SE_42225 | chr1:204414898-204417247 | Lung | SE_42225 | chr1:204417746-204421550 | Lung | SE_48201 | chr1:204414946-204421702 | Psoas_Muscle | SE_48746 | chr1:204414986-204417248 | Right_Atrium | SE_48746 | chr1:204417807-204421419 | Right_Atrium | SE_50149 | chr1:204415315-204422829 | Sigmoid_Colon | SE_51536 | chr1:204415200-204417241 | Skeletal_Muscle | SE_51536 | chr1:204417745-204423045 | Skeletal_Muscle | SE_52421 | chr1:204416678-204422949 | Small_Intestine | SE_58430 | chr1:204415099-204506026 | Ly1 | SE_59794 | chr1:204415680-204491493 | Ly4 | SE_62377 | chr1:204415291-204492168 | Tonsil | SE_65868 | chr1:204415035-204417231 | Pancreatic_islets |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH01I204445 | chr1 | 204415101 | 204423341 |
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Enhancer Sequence | GGCCTTGTCC CTCCCTCACT TTCCCTCAGG TTCTTTGTAA AATAGCCCTG TTAGACTTGG 60 TGATCTCTAA AGTCCTTTCC AGCTATAACT CTCAGCAAAA AATGAGAGGG AAACAAAAAG 120 AGAAAAAGAA TGGACATGTG AGGAAGAGGT TCGGTGGAGA TGCACCTTGG TGAGGGGTGA 180 GGGGACAAGC CCCAGCCAGA ACTCTGAACA GAGGTGTCAC CCAGCTGAAA CACGGGGTGC 240 ATCCAGGCTG AGTCCGGGGT GACTTCCATG GGGTGCCAGA GGACACTGCT GCCAGAGGGG 300 AGGCAAGACC ACACACTGGG AGAAGGCCCT GGGACACTCG GTCCCTACTC TATGCCACCA 360 GATGTTCATC CTACTAAAGT ATCAGAGCTG AGTGAGCCAA GTCTCCAAAG GAGGTCTACT 420 TTCTTTCATT CAAAAAACTT ATTTATTTAT TCATTTATTT ATTTATTTTG AGACAGAGTC 480 TTGCTCTGTC ACCCAGGCTG GAGTGCAGGG GTGTGATCTC GGCTCAGTGC AACCTCTGCC 540 TCCCCGGTTC AAGTGGTTCT CATGCCTCAG CTTCCTGAGT ACCTGGGATT TACAGGCACC 600 CGCCACCACA CCCAGCTAAT TTTTGTATTT CTAGTAGAGA CAGGGTATCA CCATGTTGGC 660 CACTCCTGAC CTCAAGTGAT CCCCCTGCCT CAGCCTCCCA AAGTGCTGGG ATTGCAGGCA 720 TGAGCCACCA CACCCAGCCT CATTCAACAA ATATCTATTG AATCCTAACA TGTGCCAGGC 780 ATTTTCTAGA GTCTGGGCAT AAAGCAGCAA ATAAGACAGA CAAAAATTAG CCGGGCGTGG 840 TGGTGTGCGC CTGTAGTCTC ATCTACTCGG GAGGCTGAAG TGGGAGGATG ATTTGTGCCT 900 GGGAGGCAGA GGTTGCAGTG AGCCAAGATT GTGCCATTGC ATTCCAGCCT GGGTGACAGA 960 GATCCTGTCT CAAAAAAAAA AAAAAAAAAA CCTGCCTCAG GGAGCTTTCA TTCTATGTCA 1020 ACATTCATAC TCCATACCAA AGTATCTCAT AACCACAAGA AGGGGAAGCT GGGAACTGAG 1080 AAGTGCACCT TGGGCGTGAC CAGCTCCTCC TCTTCTCCCT GGAGAATAGG TCCATCCTGC 1140 CAAAGCACTG AGTCACTGGC AGGGGCAAAG GTGTCCCCTC AGGCCCCAAG AGGACCCAGG 1200 TCAGGTTTGA TCAGACTTAG ACGTATGAAG ATTCAATACA AGGGACTCAG AAGCTGAGCC 1260 CTGAATGCAG AGGGTCTCAG ACCCCATCTT CAGGCTCCAC GAAATCAATT TAACCTCCAG 1320 GAGATGGGAG ATGGATACCC CAGAGCTCAC CTCACAATCC ACATCTAACC ATATTCCCTC 1380 AGTTGCTTCA GTCACATCAT CCTCCCATGC TTGAAGTTCT AGCACTCTCT CCTGCTGTCC 1440 CAGCCCAAAT CTCCAGGAGA AAAATGTAGA GTTGACTGGA ATGGTCTTGC TGGTGACTGG 1500 GAGGGAAGGG CTAAAGCCTC 1520
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