Tag | Content |
---|
EnhancerAtlas ID | HS048-03159 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:204416770-204418310 |
Target genes | Number: 11 | Name | Ensembl ID |
|
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: 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 |
|
| 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 | TTCTCTCACC CCAGCATTCC GGCCTTGTCC CTCCCTCACT TTCCCTCAGG TTCTTTGTAA 60 AATAGCCCTG TTAGACTTGG TGATCTCTAA AGTCCTTTCC AGCTATAACT CTCAGCAAAA 120 AATGAGAGGG AAACAAAAAG AGAAAAAGAA TGGACATGTG AGGAAGAGGT TCGGTGGAGA 180 TGCACCTTGG TGAGGGGTGA GGGGACAAGC CCCAGCCAGA ACTCTGAACA GAGGTGTCAC 240 CCAGCTGAAA CACGGGGTGC ATCCAGGCTG AGTCCGGGGT GACTTCCATG GGGTGCCAGA 300 GGACACTGCT GCCAGAGGGG AGGCAAGACC ACACACTGGG AGAAGGCCCT GGGACACTCG 360 GTCCCTACTC TATGCCACCA GATGTTCATC CTACTAAAGT ATCAGAGCTG AGTGAGCCAA 420 GTCTCCAAAG GAGGTCTACT TTCTTTCATT CAAAAAACTT ATTTATTTAT TCATTTATTT 480 ATTTATTTTG AGACAGAGTC TTGCTCTGTC ACCCAGGCTG GAGTGCAGGG GTGTGATCTC 540 GGCTCAGTGC AACCTCTGCC TCCCCGGTTC AAGTGGTTCT CATGCCTCAG CTTCCTGAGT 600 ACCTGGGATT TACAGGCACC CGCCACCACA CCCAGCTAAT TTTTGTATTT CTAGTAGAGA 660 CAGGGTATCA CCATGTTGGC CACTCCTGAC CTCAAGTGAT CCCCCTGCCT CAGCCTCCCA 720 AAGTGCTGGG ATTGCAGGCA TGAGCCACCA CACCCAGCCT CATTCAACAA ATATCTATTG 780 AATCCTAACA TGTGCCAGGC ATTTTCTAGA GTCTGGGCAT AAAGCAGCAA ATAAGACAGA 840 CAAAAATTAG CCGGGCGTGG TGGTGTGCGC CTGTAGTCTC ATCTACTCGG GAGGCTGAAG 900 TGGGAGGATG ATTTGTGCCT GGGAGGCAGA GGTTGCAGTG AGCCAAGATT GTGCCATTGC 960 ATTCCAGCCT GGGTGACAGA GATCCTGTCT CAAAAAAAAA AAAAAAAAAA CCTGCCTCAG 1020 GGAGCTTTCA TTCTATGTCA ACATTCATAC TCCATACCAA AGTATCTCAT AACCACAAGA 1080 AGGGGAAGCT GGGAACTGAG AAGTGCACCT TGGGCGTGAC CAGCTCCTCC TCTTCTCCCT 1140 GGAGAATAGG TCCATCCTGC CAAAGCACTG AGTCACTGGC AGGGGCAAAG GTGTCCCCTC 1200 AGGCCCCAAG AGGACCCAGG TCAGGTTTGA TCAGACTTAG ACGTATGAAG ATTCAATACA 1260 AGGGACTCAG AAGCTGAGCC CTGAATGCAG AGGGTCTCAG ACCCCATCTT CAGGCTCCAC 1320 GAAATCAATT TAACCTCCAG GAGATGGGAG ATGGATACCC CAGAGCTCAC CTCACAATCC 1380 ACATCTAACC ATATTCCCTC AGTTGCTTCA GTCACATCAT CCTCCCATGC TTGAAGTTCT 1440 AGCACTCTCT CCTGCTGTCC CAGCCCAAAT CTCCAGGAGA AAAATGTAGA GTTGACTGGA 1500 ATGGTCTTGC TGGTGACTGG GAGGGAAGGG CTAAAGCCTC 1540
|