Tag | Content |
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EnhancerAtlas ID | HS022-06888 |
Organism | Homo sapiens |
Tissue/cell | CD4+ |
Coordinate | chr19:4375100-4376620 |
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 |
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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 | chr19:4375113-4375691 | 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 | chr19:4375658-4375829 | 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 | ATGCGTGGGG GAGAAGGGGT GCCCTCTGCT GTGGAAAGCT GGGACCTACT GTCTGTGGTG 60 CGAGGCTGAC CCCACAGAGC TCCAGGACAA CCCCGAGAGG AGTGGACAGA GCCAGCCGGG 120 CCCTCCAGCC CCCACCTGGC CCAGCTGCCG CCTCTGGGCA GATGTCTCCA CTTGATAAAC 180 AGGACAGCTA AGGGCCTAGG AGAGACATGC CTGGCCCAAG GCCAGACAGC AGGAGTGGCT 240 AGGAAGGTCA AGGGATCCCC ACTGCAGGCC CCACCAACCC TGGCTCTGCC TGGAATGCAG 300 TCAGGGCAGG TGGAAGGGGA GGGGCAACGC CCCAGGGCTG GGCGAGGAAT CTGGGAGCAG 360 GTGGGAAGCT CATGCTACCT TCCCAGGAGA CGGGAGGACA GGCCTGCCAA CCAGGGGGCT 420 CAGCTATGTG GGACACACGC TCCCACCCTT GCCCTTGCAC AGGGTTTCAT CCAAACATGG 480 AGATGCCAGT GAGTGCCTGG GGCTCCTCTC CCAGGAACAA ACCACACCCA GAGCTCCAGC 540 CCGAGCGAAC ACATCTACAT GAAAATCAGC CTCATGCATC ATGCATTGTA ATTTCTCATC 600 TTGGGGACCA GGCAGGAGGG CTGTGTGACA TACAACTGGT AAAATCAGTT TCCGATGAAA 660 ACTTATAAAA GGAAAAAGCC AACCCACAAA CAAATGAGGC GATAAATCCC CTGAGGCTCC 720 GCCTGGCAGG GAAACACCAG CTCTGCAGCA CTGAGCACAG GCTGGTGTTC CCACTGGGGG 780 CAGCATGGAG GATCTGCGTC CAGGGGGCAG AGTGTGATGA CATCACCCAC ATGCACAGGA 840 ACGATAAGGC TTTCTTAAAA AACGATCTTT TCTCAACAGC TCCTCAAAAG GAGCTGAGGC 900 AATGCATAGC CCTGCAGGAA GAGACTGGAA ATGGTCTTGG AGAGAGAACT GCGGGGCATG 960 GTGACAGCGG TGAGAGGCTG CAGGTGCACA GATCTCAACG AGGGGCCGTG AGTTCCCTCA 1020 CTCCCTGAGA GCTGAGGAGA CTTGCCCGAA AGCCCAGAGC CCTTCCTGAG ACACAGAAAC 1080 CATCTTCACC ATCTCTAAGA TCCCTTCCAT TTCTGAAGGA CTTCCATTTC TTTGTGACTG 1140 TGGGCCACCA TGGGCATGAG TCACCTGTCA CCAGAGCCTG GTGTCCCTGT GCAGCTGTGC 1200 CAGGTGGGCA GAGGAGACAG GTGAAGGCAC ATTCCTCAGC GCCCGCTCAC AGCTCTGCCC 1260 ACCGTGCATT CTGTAGAGAA CCTCAGCGCC CTCCTCCCTG CCGGCAGCCA GGCAGGGATT 1320 TAGGTGGTTT CTGTTTGGCC TCCAGTGCTT GCCTCTCCCG TGTCCTATCC GCCCAGACCT 1380 CAGACCTCAG AGAAGCCTCC TCCCACAGGA AGCTCTCCTG ATTGATCCCC ATCACTGGTC 1440 TCCTCACCTT CTCCCAACAC ACCACTGATG CCTCCTCTCT CGTGCGCCTG CCCCTTCACA 1500 CTTCATCTTA CACCCCCATC 1520
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