Tag | Content |
---|
EnhancerAtlas ID | HS038-17671 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr5:139055980-139059150 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PLAG1 | MA0163.1 | chr5:139058399-139058413 | CCCCCTTGAGCCTC | - | 6.35 | RARA(var.2) | MA0730.1 | chr5:139057466-139057483 | TGACTTCTAATTGACCT | - | 6.09 | ZNF263 | MA0528.1 | chr5:139056449-139056470 | TCCCCTTTTCTCTGATCCTCC | - | 6.01 | ZNF263 | MA0528.1 | chr5:139056078-139056099 | CTCCTCCCCATCTCCTCCTCA | - | 6.04 | ZNF263 | MA0528.1 | chr5:139056025-139056046 | CCCACCTCCTCCCCAGCCTCC | - | 6.09 | ZNF263 | MA0528.1 | chr5:139056005-139056026 | ATCTCCTCTCCAGCCTCCTCC | - | 6.33 | ZNF263 | MA0528.1 | chr5:139056052-139056073 | CCTCCCCCCAAGCCCTCCTCC | - | 6.56 | ZNF263 | MA0528.1 | chr5:139056137-139056158 | CCCTCCTCCCCAGACTCCTCC | - | 6.78 | ZNF263 | MA0528.1 | chr5:139056031-139056052 | TCCTCCCCAGCCTCCTCCCCA | - | 6 | ZNF263 | MA0528.1 | chr5:139056064-139056085 | CCCTCCTCCCCAGGCTCCTCC | - | 7.08 | ZNF263 | MA0528.1 | chr5:139057518-139057539 | GGAGGAGGGAGGGGGTGAGCA | + | 7.24 | ZNF263 | MA0528.1 | chr5:139056028-139056049 | ACCTCCTCCCCAGCCTCCTCC | - | 7.2 |
|
| Number of super-enhancer constituents: 46 | ID | Coordinate | Tissue/cell |
SE_00187 | chr5:139052580-139059377 | Adipose_Nuclei | SE_03140 | chr5:139056046-139056660 | Brain_Angular_Gyrus | SE_03140 | chr5:139056739-139059366 | Brain_Angular_Gyrus | SE_03865 | chr5:139055996-139061963 | Brain_Anterior_Caudate | SE_04768 | chr5:139026027-139072090 | Brain_Cingulate_Gyrus | SE_05771 | chr5:139026065-139074431 | Brain_Hippocampus_Middle | SE_06683 | chr5:139027027-139071104 | Brain_Hippocampus_Middle_150 | SE_07722 | chr5:139028082-139075240 | Brain_Inferior_Temporal_Lobe | SE_08785 | chr5:139056815-139058122 | Brain_Mid_Frontal_Lobe | SE_08785 | chr5:139058627-139059015 | Brain_Mid_Frontal_Lobe | SE_11063 | chr5:139026860-139059578 | CD20 | SE_13414 | chr5:139056780-139058400 | CD34_Primary_RO01536 | SE_13414 | chr5:139058435-139059304 | CD34_Primary_RO01536 | SE_20188 | chr5:139056880-139059135 | CD56 | SE_25255 | chr5:139058189-139058964 | Colon_Crypt_3 | SE_26221 | chr5:139056720-139057563 | Duodenum_Smooth_Muscle | SE_26778 | chr5:139056356-139058039 | Esophagus | SE_27739 | chr5:139056202-139058212 | Fetal_Intestine | SE_28684 | chr5:139056665-139058254 | Fetal_Intestine_Large | SE_29581 | chr5:139056057-139058505 | Fetal_Muscle | SE_30930 | chr5:139056057-139058331 | Fetal_Thymus | SE_31417 | chr5:139056046-139059186 | Gastric | SE_33677 | chr5:139055902-139059162 | H2171 | SE_34346 | chr5:139057922-139059244 | HCT-116 | SE_36941 | chr5:139027373-139059446 | HSMMtube | SE_40649 | chr5:139056032-139059400 | Left_Ventricle | SE_41599 | chr5:139057494-139058017 | LNCaP | SE_42197 | chr5:139056073-139059249 | Lung | SE_45813 | chr5:139056829-139059282 | Osteoblasts | SE_47229 | chr5:139058326-139059295 | Panc1 | SE_47460 | chr5:139056059-139056464 | Pancreas | SE_47460 | chr5:139056780-139058230 | Pancreas | SE_47460 | chr5:139058237-139058680 | Pancreas | SE_48055 | chr5:139055919-139062629 | Psoas_Muscle | SE_48579 | chr5:139055935-139059336 | Right_Atrium | SE_49460 | chr5:139056809-139057877 | Right_Ventricle | SE_51090 | chr5:139055934-139059157 | Skeletal_Muscle | SE_53351 | chr5:139057715-139058567 | Spleen | SE_54845 | chr5:139055998-139057753 | Stomach_Smooth_Muscle | SE_55117 | chr5:139056107-139056654 | Thymus | SE_55730 | chr5:139057497-139059261 | u87 | SE_58504 | chr5:139012442-139092243 | Ly1 | SE_63555 | chr5:139056584-139057808 | HSMM | SE_65250 | chr5:139036623-139059169 | Pancreatic_islets | SE_67548 | chr5:139057497-139059261 | u87 | SE_68692 | chr5:139057230-139059117 | H9 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr5 | 139058350 | 139058600 | chr5 | 139056887 | 139057262 | chr5 | 139057354 | 139058068 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH05I139676 | chr5 | 139056126 | 139059178 |
|
Enhancer Sequence | AGGCCTCCTC CGCAGATTCC TCCCCATCTC CTCTCCAGCC TCCTCCCCAC CTCCTCCCCA 60 GCCTCCTCCC CACCTCCCCC CAAGCCCTCC TCCCCAGGCT CCTCCCCATC TCCTCCTCAG 120 TCCTTCTCCC CAGTGTCCTC CCCACCCTCG TCCCCAGCCC TCCTCCCCAG ACTCCTCCCC 180 ATCTCCTCCC CACCTCCTCT TCTCAGGCCT TGGGCTACAC AGTGGGTCTG ATCTGGTCTC 240 CTCGCCACTT CTCCTCTACC CTTCCCTCTG CCTCCCTCTC CTGTGGGCAT GCCCAGCTGC 300 CTTCTGGGAT TCCCTCCTTA GGGCTGTTTC CTTGTCTTTT AGACCCTCAA GTCCCTGAGC 360 CTGGACAAGG TGTCCTGGGT CCCTGGGTCT CTGAACCCTG TTACCCCAGA CACTGCTTCC 420 CATGACACTG TCTCCACTAA CCTTGACCCT CTGCCCCTTC CTCTCCAGCT CCCCTTTTCT 480 CTGATCCTCC CCTCTAGTTC TCTGTCTCAT GATTCTGTCC CCACCACCTG TCTCTATTCT 540 GCCCCCGCAT GCCCCTCTGC CCCCCAGCTT TCCATGACTC GTCCCCCCTC AGCCCCCCGT 600 GCTCTGTCCC CGCCCGTCAG CCCCTGGTCC CAGCTCCCGG CTGGCCGGCT CCTGCATGGA 660 CAAAGGGGTC CTTTGTGGGC TGACCGCGGC TGGCGGGGCG GCGGGGCGCT GGCTCCGCAT 720 TGCTGATGAA ACGGAGCCCT TTGTTGTCCC TCCTCAGGCG CAGTATTTCT TTTTGGGGGC 780 TGGATGTGTT CCTGGCAGGG CCGATGATGG ATGCGCCCGC CGCCGCCCGC CTGCCCGCCA 840 GCTTTCCCTC CCGCTCATTC CCGCTCCGCT TCAACGCAGC CCTGACTCCT CCCCTGCTGC 900 CTGGGCACTG CCAGGCCCTT CCTGGCCTGG AAGGGGATGG CTGTGTGCCC TAGAGTAGAA 960 GACTGGGACC TGGGAGAACG TCCCCTCTAT GTCCTCCTCT TCCATGAGTA GGGCAAATGG 1020 GGCTTTTGGT CAGGGGTCCA CTGGGACCAG GACATCAGTT TTTCCTAAGG TCTGAAGGAG 1080 AAGATGAGCC AGGTATCAGG GCCGATTTGG AACAAGCTTG AGGACCAGAT GTTCATGTCT 1140 GTCTACTCTG GATTTGAAAA CAGAGTTGTC CCTGTGAGCC AGTCCCTCCG TGTACCCACC 1200 TCCCTTCAAC TTCTGTGGCT GAAAAACCAT AGTGTTCTGC CTGCAGCACC TGTTTGGTGA 1260 CATATCACAT CCTCTGGTCC CAAGCTCAGT ATGTCCCAGG ACCTCAGAGG CTGGGGGTGG 1320 GTGGGCCCTG AAGAAGGATA GAATAGTGGA AGATCAGAGA AATTCCAAGA GAGGAACAGA 1380 ACATGAGGTT TGGTCCCCAC CAGGAGAGAC TCAGGACGGA GACAAAAGCC GAGACACTCA 1440 GCCAGAGCGC CAGCCCTGAG CGCAGGCCGG CTGTGTTGGA AGGAGCTGAC TTCTAATTGA 1500 CCTGCCCGCC CCGCACGCAG AGCCAGATCC TGGAGCTGGG AGGAGGGAGG GGGTGAGCAG 1560 AGCAGGAACA GCGTTAATGC AGCTATCGAT TTCTGCCACC AGCCAGCAGG CCGCAGAGGC 1620 GGGGGACGCA CACAGGGGCT GGGGCGCAGC CTGCTCCCCT CCCCATCTCT GCAGCCCACA 1680 AGACACCTGC CTTCTGCCTT CTCCCCTCAC CCAGTATCTG GGCTGCCGGG GTTGTCGTCC 1740 AGGGCAGGGC AGATGAGCTT AGTTGGGCAG GAGCTGGATG AGCTGACTTG ACGGTTTTTG 1800 TCCCTGATCT CACTGACCCT GGTCCCCAAC AACTAGCCAG GGTCACTGAT TCCTGAAAGG 1860 GTCACCAGTC TCTGAGGAGA GGGGCTGAAA AGACCATCCT GGTCTTGGCC GTTATGAGGT 1920 GGGAGGGAAC ACAGCTATCC TTGGACACAC ATGGTCTTCT TGCTTCAGCT CTGACCTCTG 1980 ATGCCCCCCA ACCCAGCCTG GATTCCCTGC CAGGGCCCCC CGGCTCTGTC CTGGTGGAAT 2040 CTGCCATCTT GCCCAGCTCT TCCTCCTCAC CCATTTCCCT CTGCTAGGAA GGAGCCCTAG 2100 GTGGTCTGGT GCCCACTGGG GAGGGACAGG GAGTATCTGA CTGTTGATGG CGGCTACTCG 2160 CCTCACCCTA GAGACAGAGC TTTTCCTTTC CCCACACCCG GTCCTCTTTG GCCACTCCTT 2220 AGTCCTGGGG AAGCCCCCCC TCCCCCCCGC TTGGGGCCTC AGTTTCCCCC TCTGTAAATG 2280 CAGAGGGTTG GACTAGATGC TCTCTTGGGA CAGGCTTGAG TCCTGTGACT AGGGGGGTTT 2340 TGGGGTTGCC TGGGGACAAA GATCCAGTGT GTGCTGCCCT CAAGCCCAGG GCGTGATGGG 2400 GCCCGCCAGA TGTGCGCCTC CCCCTTGAGC CTCCAGCTGC TCTGGGGCTG GGCCCTGTCC 2460 TCCCACCCCT CTCTTGGGGC ATGCTAGGCC ACAGCAGGCA GACAGGGAAG CAAGGCTGGA 2520 GAGCCGGGAC TGATGAGGAA ACCGCCGCCT TGCTCCATCT GGCCCAGTCC CTTCAGCTGA 2580 GGAGGCAGCT CAGACGCCTT AGCCTTGAAA CCTGAGTAGA GCAGGCCCTG CCCCGGGATG 2640 GGCTGCCTTG GAAATATGGA GGTGGCCAGA GGACAGGCTC CTGCTGGGCT CCATTCCCTT 2700 GAGGGTCACG CCTACTCCTC AGTGCCAGCC TGCCCCAGCC AGAGGTCCCT CCTGGCAACA 2760 GCCCACCCCG GCTCTCTGGG TTCTCACTGA GACCTCCACC CAGGCCCTAC TCTGCAGGCC 2820 TTGTGAGGCC TCTGCCCACC ACCGCCCCCA ATCTGGGAGC CAGGCCAGAG CACCACAGTG 2880 AGGCCTGAGT AGAGACAAGA ATGAGGTCTG AGACGATAAT GATTGTGGTT CGGGGGTTGA 2940 GAAGGAAGCG TGTGCCAGGG TGTGCACAAG CATGTCCTCT CACTGTGGCA GGGGACGGCT 3000 GGTCCTCTGG CCCTGTGCTG CTCGCCCTGT AGCAGGCGGG GAGAAGATCC CTGAAATAAG 3060 GGTTCTGCAC TCATTGGCAA ACTGGGTTAC ACAAAGGCAA CCAGGTTCCT TTGCCTGCAG 3120 GACATGTCAG AGCCTTGAAA TAACTGATGT GTATTAGTAA TCCCCAGATG 3170
|