Tag | Content |
---|
EnhancerAtlas ID | HS017-00421 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr1:21643140-21645480 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr1:21644930-21644945 | AGGTCAGCCTGGCCT | + | 7.13 | KLF4 | MA0039.3 | chr1:21644137-21644148 | CCACACCCTCC | + | 6.32 | Klf1 | MA0493.1 | chr1:21644135-21644146 | AGCCACACCCT | + | 6.02 | MITF | MA0620.2 | chr1:21644318-21644336 | ACAGGTCATGTGACTTCT | + | 6.53 | MITF | MA0620.2 | chr1:21644318-21644336 | ACAGGTCATGTGACTTCT | - | 6.53 | SREBF1 | MA0595.1 | chr1:21645053-21645063 | GTGGGGTGAT | - | 6.02 |
|
| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_00105 | chr1:21640019-21654616 | Adipose_Nuclei | SE_00854 | chr1:21642962-21648227 | Adrenal_Gland | SE_01643 | chr1:21642185-21648218 | Aorta | SE_02944 | chr1:21642987-21644019 | Bladder | SE_02944 | chr1:21644056-21645524 | Bladder | SE_03598 | chr1:21643482-21644096 | Brain_Angular_Gyrus | SE_03598 | chr1:21644394-21645277 | Brain_Angular_Gyrus | SE_04518 | chr1:21643279-21645748 | Brain_Anterior_Caudate | SE_05710 | chr1:21643177-21645586 | Brain_Cingulate_Gyrus | SE_05944 | chr1:21639044-21646536 | Brain_Hippocampus_Middle | SE_08398 | chr1:21643228-21645720 | Brain_Inferior_Temporal_Lobe | SE_26127 | chr1:21642960-21646679 | Duodenum_Smooth_Muscle | SE_26770 | chr1:21642974-21647847 | Esophagus | SE_28486 | chr1:21644573-21646764 | Fetal_Intestine | SE_29337 | chr1:21644662-21646709 | Fetal_Intestine_Large | SE_31433 | chr1:21643029-21648183 | Gastric | SE_39164 | chr1:21643088-21645576 | IMR90 | SE_42174 | chr1:21642958-21646742 | Lung | SE_44380 | chr1:21642937-21647054 | NHDF-Ad | SE_45045 | chr1:21643168-21646698 | NHLF | SE_46660 | chr1:21643074-21643434 | Ovary | SE_46660 | chr1:21643459-21645622 | Ovary | SE_47592 | chr1:21643574-21645731 | Pancreas | SE_48583 | chr1:21642944-21648219 | Right_Atrium | SE_50108 | chr1:21643010-21645670 | Sigmoid_Colon | SE_52633 | chr1:21642919-21645734 | Small_Intestine | SE_53334 | chr1:21642938-21645903 | Spleen | SE_54639 | chr1:21639148-21648300 | Stomach_Smooth_Muscle | SE_56171 | chr1:21642916-21645508 | u87 | SE_65263 | chr1:21643359-21649820 | Pancreatic_islets | SE_67931 | chr1:21642916-21645508 | u87 | SE_68932 | chr1:21643728-21645709 | H9 |
|
| 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 |
GH01I021312 | chr1 | 21638973 | 21657659 |
|
Enhancer Sequence | TGGAAGTCCC ACACAGCATG TGCTGTGGTT GTGAATGAGA AACAGCCTAA ATGCCCATCT 60 ATAGGAGCCT GGATAAACCA CAGGAGAGCC ACATCATGGG ATGGAATACT ACACGGTAAT 120 GAAAACCAAG TGGCTGCAAC TCAAACAACA GGAAGACAGA AAAGCTGCAG AAGTCAACAT 180 GGAGCCTCCA ATCAATTATT GAAAGTTCAA AAACAGTGAG CAACATCATA CCTATGTATC 240 ATTTAGGGAG GCAGAATCAG GCTGCGCTTG GTGGCTCACA CCTGTAATCC CAGCACTTTG 300 GGAGGCCGAG GTGGGCGGAT CACCTGAGGT CAGGAGTAAC AGTATCAAGA CAGTCACTGA 360 AGAGTCTCTC CCAGTCTCTT CCCCTGGGAG AGAGAGTGGT AAGAAACGGA CTGGGGGTGT 420 GGGGGTATGG GGGATTCAAC TGCATTTGGG ATGTTTTATT CCTTAAGCTG AACACTTACA 480 TACCAGTGTT TGGTTTTACT GAGCCTGATG CTTTTAATAT GTCTGAGATA TTTTGCTACC 540 CACCAGAATA GGTCAGACAG ACTTGGGCTT CGAGCCAGCC CTGTGCTTTG CTGCCATGCG 600 ATCCTAGTCT TCTCTGTGAA GTGGGAATCC TATCGCCCAC TGTTAGCTCC CGGGACTCTT 660 CTGAGAATTA AACAAGGTCG TGTCTGCAAA GGGCCTGGCA TCCGGTGGCT GCCATTGTTC 720 CTGCTGCTGT TGGGAGGGTC TCCCAAAATG AACAGACAGA GGGGAAGGCC AGCTCGCAGG 780 CCTCAGATGG GGAAAAGGGT TTGCTTGTCA CAAGGCCAGT CCAGCCCGCG GCGACGCTGA 840 GCTGGTGACG CATCTGCAGC TCTGGGGATT GAGCAATCTT GGTCCCCTGA CCGGGATGGA 900 GTCATGGGCC CAGGCTGGCT GGAGCCCCTC TACTGCTCCC CACCCGCTTC TCAGACTTTG 960 TGTTCCTGGC CTTCTTGGGA CCCCTCCAGG CTGGCAGCCA CACCCTCCCC TCTGTGAGCT 1020 AGGCAGGAAA GCCCGGTTCC ATTCCTGCCC AGTTCTCTTC GGCCTCTCCT GAGCCCCTGC 1080 TCCCCAACTC AAGGTGGGGT CCTAACCACC TTGCATCCAA ACAGATCCTC TGGAGACGCA 1140 CGAGTGGGTC AGGGCAGTCA AGAGCTGTGC AGGCTCAGAC AGGTCATGTG ACTTCTGTAG 1200 GTCCCTGGCT TTAGCAGGTG TGGCCGAAGG TGTGGGGTGC CAGTGTCTGT CTCCTGGTTC 1260 AAATCCAGGC TCGGGGTGTG ACCCCAATGT TCTTGAACTT AAATCAGAGC CACCGCGATC 1320 TCTTTCTCGA AGTGGGGACA AAACACATGC AAAGCAGGGC CTGCCCCTCC AAGGTGCACC 1380 TTGAAGGTAT CAGACGGCAT GGACGAGGTC CCCTCGCTGG CTGCTGTGAC GGTTAAACGA 1440 TTCTTCCCAG CTCTGCACAA CTCAAGTGAT AGCTGTTGGA CTCGGAGATG AACAAGAGTG 1500 AGGGAAACGG TGGGGGAGAG CAGTGGGCAA GACCTGGCGT GGCAAGTGGG GAGCAGGAGG 1560 CCCTCGTGTG GACTCGCAGA GACCCAAACC CAATGAAACA AGTACCCTGC TGGCGCATGT 1620 GCAGGAACTG ATCAGCGTTC CTGAGGGCCC AAGGACATTT CCAGGGCACA GCTTGGGGAG 1680 GGCAGCAGAG TGGGAGCAGC TGTGAAATTG GGTTTCAGGT CATGACGCAG TTGGGGAACT 1740 TATTTCCTTC ATCCCTGCCC TTTCCTGACC CTGTCCCACT CCCTTAACAA AGGTCAGCCT 1800 GGCCTAGGGG TGTCCTCCCT GGAGACCTCC CCTCCCTTGT GCCTCAGCCT CTCACTGTCT 1860 TTGGGGCAGA CATTTCTCCG CTCTGGGCTT CAGTTTCTCT ATCTGTAAAA TGGGTGGGGT 1920 GATATTTCAG GCCTTAGCAA CTTCTAAAAT CCCATTTTTT GAAGATTTAG AACCAGTGAG 1980 CCTTCCTGAG GCCCACTTCA CAAGCCTATC CAAGCAGAGG TGGCAAAATC CTCCTCCCTG 2040 GGTGAGAGGC AGGCGACACC CCTGAGTTGG TCACACCAGC CTTCCAAGGA GCTAACCCGA 2100 CCTGACAGTC ACTTCAGCCT GGCCAGGCCC CCAGGCAGTG TGCCAAAAAG CGGACGGGGG 2160 AGGGGATTTG CAGCAAGAGC TACAGCTCCC CAGAGGCCGC ACTTCTGTCG GGGGAGACGC 2220 TGAGCGAGGG TCAGAAGAAA GTCAGCATGG GAAATGTGAC GTCAGCAGAG GCAGATGCGA 2280 AGGAATACTA TCCGAAAATG CTTCCGTAAA CTCACCCTCC CAGGAAGCCA AATTCTGTGG 2340
|