Tag | Content |
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EnhancerAtlas ID | HS019-07871 |
Organism | Homo sapiens |
Tissue/cell | CD20+ |
Coordinate | chr19:4374820-4376640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr19:4376254-4376265 | CATGAGTCACC | - | 6.62 | JUND | MA0491.1 | chr19:4376254-4376265 | CATGAGTCACC | - | 6.02 | ZEB1 | MA0103.3 | chr19:4375085-4375096 | CCCACCTGCCC | + | 6.14 |
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| Number of super-enhancer constituents: 37 | ID | Coordinate | Tissue/cell |
SE_00671 | chr19:4372603-4377782 | Adipose_Nuclei | SE_00953 | chr19:4369010-4378529 | Adrenal_Gland | SE_03081 | chr19:4373372-4375693 | Bladder | SE_05654 | chr19:4369240-4377898 | Brain_Cingulate_Gyrus | SE_06216 | chr19:4367183-4378196 | Brain_Hippocampus_Middle | SE_08374 | chr19:4369264-4378128 | Brain_Inferior_Temporal_Lobe | SE_12525 | chr19:4374150-4375101 | CD34_adult | SE_12525 | chr19:4375113-4375691 | CD34_adult | SE_12525 | chr19:4376053-4376297 | CD34_adult | SE_12525 | chr19:4376307-4376536 | CD34_adult | SE_12725 | chr19:4373541-4375388 | CD34_fetal | SE_12725 | chr19:4375391-4375655 | CD34_fetal | SE_12725 | chr19:4376134-4376375 | CD34_fetal | SE_14750 | chr19:4367713-4381827 | CD4_Memory_Primary_7pool | SE_26598 | chr19:4366396-4381720 | Esophagus | SE_27964 | chr19:4373020-4377930 | Fetal_Intestine | SE_28734 | chr19:4372075-4378347 | Fetal_Intestine_Large | SE_30332 | chr19:4367899-4377712 | Fetal_Muscle | SE_31749 | chr19:4372054-4378341 | Gastric | SE_37296 | chr19:4367503-4381769 | HSMMtube | SE_38442 | chr19:4373325-4377704 | HUVEC | SE_40064 | chr19:4371892-4377882 | K562 | SE_41739 | chr19:4374225-4375739 | LNCaP | SE_41739 | chr19:4375788-4376658 | LNCaP | SE_42702 | chr19:4371440-4378535 | Lung | SE_44622 | chr19:4371840-4377656 | NHDF-Ad | SE_45249 | chr19:4372679-4376637 | NHLF | SE_47754 | chr19:4373974-4376769 | Pancreas | SE_48336 | chr19:4367194-4378514 | Psoas_Muscle | SE_49011 | chr19:4372055-4378263 | Right_Atrium | SE_53019 | chr19:4371950-4378408 | Small_Intestine | SE_53804 | chr19:4371474-4376759 | Spleen | SE_57120 | chr19:4373475-4378484 | VACO_400 | SE_57934 | chr19:4373729-4376544 | VACO_9m | SE_64150 | chr19:4373205-4378580 | HSMM | SE_65589 | chr19:4367712-4380728 | Pancreatic_islets | SE_69091 | chr19:4373604-4377851 | H9 |
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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 |
GH19I004367 | chr19 | 4367437 | 4382197 |
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Enhancer Sequence | CACATGGGTG TGGGGGAGGC TGCGGGCTGC GCCTGGTGGC CGTATGGGGC CTAGGCTGGC 60 CAGTGCTGCC CAATGGTGGG GGCTCCCTCA CCGCCCGTCT GGCAGAAGCC ATGGGCCACA 120 CGCTGTCCCA GCACATGGTG GCAGGGCGGT GACCTGGGCT CGGCTCTAAT GACCGGCAGC 180 CCTGGGGCTC CCATCACCAC TACCAGTCTG CCCAGGAGGC AGCAGAGCAC TGAGCCCGAC 240 CTGCTCCCCT CGGGCACCTA CGAGACCCAC CTGCCCCTCC ATGCGTGGGG GAGAAGGGGT 300 GCCCTCTGCT GTGGAAAGCT GGGACCTACT GTCTGTGGTG CGAGGCTGAC CCCACAGAGC 360 TCCAGGACAA CCCCGAGAGG AGTGGACAGA GCCAGCCGGG CCCTCCAGCC CCCACCTGGC 420 CCAGCTGCCG CCTCTGGGCA GATGTCTCCA CTTGATAAAC AGGACAGCTA AGGGCCTAGG 480 AGAGACATGC CTGGCCCAAG GCCAGACAGC AGGAGTGGCT AGGAAGGTCA AGGGATCCCC 540 ACTGCAGGCC CCACCAACCC TGGCTCTGCC TGGAATGCAG TCAGGGCAGG TGGAAGGGGA 600 GGGGCAACGC CCCAGGGCTG GGCGAGGAAT CTGGGAGCAG GTGGGAAGCT CATGCTACCT 660 TCCCAGGAGA CGGGAGGACA GGCCTGCCAA CCAGGGGGCT CAGCTATGTG GGACACACGC 720 TCCCACCCTT GCCCTTGCAC AGGGTTTCAT CCAAACATGG AGATGCCAGT GAGTGCCTGG 780 GGCTCCTCTC CCAGGAACAA ACCACACCCA GAGCTCCAGC CCGAGCGAAC ACATCTACAT 840 GAAAATCAGC CTCATGCATC ATGCATTGTA ATTTCTCATC TTGGGGACCA GGCAGGAGGG 900 CTGTGTGACA TACAACTGGT AAAATCAGTT TCCGATGAAA ACTTATAAAA GGAAAAAGCC 960 AACCCACAAA CAAATGAGGC GATAAATCCC CTGAGGCTCC GCCTGGCAGG GAAACACCAG 1020 CTCTGCAGCA CTGAGCACAG GCTGGTGTTC CCACTGGGGG CAGCATGGAG GATCTGCGTC 1080 CAGGGGGCAG AGTGTGATGA CATCACCCAC ATGCACAGGA ACGATAAGGC TTTCTTAAAA 1140 AACGATCTTT TCTCAACAGC TCCTCAAAAG GAGCTGAGGC AATGCATAGC CCTGCAGGAA 1200 GAGACTGGAA ATGGTCTTGG AGAGAGAACT GCGGGGCATG GTGACAGCGG TGAGAGGCTG 1260 CAGGTGCACA GATCTCAACG AGGGGCCGTG AGTTCCCTCA CTCCCTGAGA GCTGAGGAGA 1320 CTTGCCCGAA AGCCCAGAGC CCTTCCTGAG ACACAGAAAC CATCTTCACC ATCTCTAAGA 1380 TCCCTTCCAT TTCTGAAGGA CTTCCATTTC TTTGTGACTG TGGGCCACCA TGGGCATGAG 1440 TCACCTGTCA CCAGAGCCTG GTGTCCCTGT GCAGCTGTGC CAGGTGGGCA GAGGAGACAG 1500 GTGAAGGCAC ATTCCTCAGC GCCCGCTCAC AGCTCTGCCC ACCGTGCATT CTGTAGAGAA 1560 CCTCAGCGCC CTCCTCCCTG CCGGCAGCCA GGCAGGGATT TAGGTGGTTT CTGTTTGGCC 1620 TCCAGTGCTT GCCTCTCCCG TGTCCTATCC GCCCAGACCT CAGACCTCAG AGAAGCCTCC 1680 TCCCACAGGA AGCTCTCCTG ATTGATCCCC ATCACTGGTC TCCTCACCTT CTCCCAACAC 1740 ACCACTGATG CCTCCTCTCT CGTGCGCCTG CCCCTTCACA CTTCATCTTA CACCCCCATC 1800 TGCCTGGGCG GCCCCCCCAT 1820
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