Tag | Content |
---|
EnhancerAtlas ID | HS128-01781 |
Organism | Homo sapiens |
Tissue/cell | MCF-7 |
Coordinate | chr1:204416710-204418310 |
Target genes | |
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 |
|
| Number of super-enhancer constituents: 34 | 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 | chr1:204415095-204416911 | Gastric | 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 |
|
| 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 |
GH01I204445 | chr1 | 204415101 | 204423341 |
|
Enhancer Sequence | GGGATGAGAT CAGGGATGTG AGGAGAGAAA ACAGGCAGCG TGTGTGGACT CCCAGCTTCT 60 TTCTCTCACC CCAGCATTCC GGCCTTGTCC CTCCCTCACT TTCCCTCAGG TTCTTTGTAA 120 AATAGCCCTG TTAGACTTGG TGATCTCTAA AGTCCTTTCC AGCTATAACT CTCAGCAAAA 180 AATGAGAGGG AAACAAAAAG AGAAAAAGAA TGGACATGTG AGGAAGAGGT TCGGTGGAGA 240 TGCACCTTGG TGAGGGGTGA GGGGACAAGC CCCAGCCAGA ACTCTGAACA GAGGTGTCAC 300 CCAGCTGAAA CACGGGGTGC ATCCAGGCTG AGTCCGGGGT GACTTCCATG GGGTGCCAGA 360 GGACACTGCT GCCAGAGGGG AGGCAAGACC ACACACTGGG AGAAGGCCCT GGGACACTCG 420 GTCCCTACTC TATGCCACCA GATGTTCATC CTACTAAAGT ATCAGAGCTG AGTGAGCCAA 480 GTCTCCAAAG GAGGTCTACT TTCTTTCATT CAAAAAACTT ATTTATTTAT TCATTTATTT 540 ATTTATTTTG AGACAGAGTC TTGCTCTGTC ACCCAGGCTG GAGTGCAGGG GTGTGATCTC 600 GGCTCAGTGC AACCTCTGCC TCCCCGGTTC AAGTGGTTCT CATGCCTCAG CTTCCTGAGT 660 ACCTGGGATT TACAGGCACC CGCCACCACA CCCAGCTAAT TTTTGTATTT CTAGTAGAGA 720 CAGGGTATCA CCATGTTGGC CACTCCTGAC CTCAAGTGAT CCCCCTGCCT CAGCCTCCCA 780 AAGTGCTGGG ATTGCAGGCA TGAGCCACCA CACCCAGCCT CATTCAACAA ATATCTATTG 840 AATCCTAACA TGTGCCAGGC ATTTTCTAGA GTCTGGGCAT AAAGCAGCAA ATAAGACAGA 900 CAAAAATTAG CCGGGCGTGG TGGTGTGCGC CTGTAGTCTC ATCTACTCGG GAGGCTGAAG 960 TGGGAGGATG ATTTGTGCCT GGGAGGCAGA GGTTGCAGTG AGCCAAGATT GTGCCATTGC 1020 ATTCCAGCCT GGGTGACAGA GATCCTGTCT CAAAAAAAAA AAAAAAAAAA CCTGCCTCAG 1080 GGAGCTTTCA TTCTATGTCA ACATTCATAC TCCATACCAA AGTATCTCAT AACCACAAGA 1140 AGGGGAAGCT GGGAACTGAG AAGTGCACCT TGGGCGTGAC CAGCTCCTCC TCTTCTCCCT 1200 GGAGAATAGG TCCATCCTGC CAAAGCACTG AGTCACTGGC AGGGGCAAAG GTGTCCCCTC 1260 AGGCCCCAAG AGGACCCAGG TCAGGTTTGA TCAGACTTAG ACGTATGAAG ATTCAATACA 1320 AGGGACTCAG AAGCTGAGCC CTGAATGCAG AGGGTCTCAG ACCCCATCTT CAGGCTCCAC 1380 GAAATCAATT TAACCTCCAG GAGATGGGAG ATGGATACCC CAGAGCTCAC CTCACAATCC 1440 ACATCTAACC ATATTCCCTC AGTTGCTTCA GTCACATCAT CCTCCCATGC TTGAAGTTCT 1500 AGCACTCTCT CCTGCTGTCC CAGCCCAAAT CTCCAGGAGA AAAATGTAGA GTTGACTGGA 1560 ATGGTCTTGC TGGTGACTGG GAGGGAAGGG CTAAAGCCTC 1600
|