Tag | Content |
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EnhancerAtlas ID | HS117-03301 |
Organism | Homo sapiens |
Tissue/cell | LHCN-M2 |
Coordinate | chr19:4373340-4375720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr19:4374747-4374758 | CTGAGTCACCC | - | 6.02 | JUNB | MA0490.1 | chr19:4374747-4374758 | CTGAGTCACCC | - | 6.02 | NFE2L1 | MA0089.2 | chr19:4374761-4374776 | AGGTGACTCAGCAGT | + | 6.66 | ZEB1 | MA0103.3 | chr19:4375085-4375096 | CCCACCTGCCC | + | 6.14 |
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| Number of super-enhancer constituents: 34 | 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 | chr19:4373622-4374001 | CD34_adult | SE_12525 | chr19:4374150-4375101 | CD34_adult | SE_12525 | chr19:4375113-4375691 | CD34_adult | SE_12725 | chr19:4373541-4375388 | CD34_fetal | SE_12725 | chr19:4375391-4375655 | 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_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 | TGGGAGTTCT GAGAGCCCTG GATTTGCCAC TGTCCTTCGA GCCTCCAGCC TCTCAGTAGA 60 GATCTCCCCT CCTGTCCATC AAGGCTGAAT GGTTTTTAAA AAGCAGCCTT TGGGAACGGA 120 GGCACTGAAA ACAATGAATC AAGACAAAGT TTCTGAAATT ATTTTCTCAC GGAAACCCCA 180 AACCAGACGC TGCCACCATG GCCAGATTGG GCACCCGGGG ACAGCCACAG ACCCACCTCT 240 GTGGCGGGTC AGGCGCTCCT CTGGGAACCA AGCTCTGGCA GCAAAAGGAC AGTGGCTCTG 300 GAAGCCCCAG GCGTCCTCTC AGCCAAAGGG GCAGTCCCTT GGGCCTGGGC TGGCAACCGA 360 GATACCGGCT CTGGACTGGA ACCAGAATGG GCTCTGCCTC AGACCAGGCC ACAGAGGGCC 420 CCCTGAGAGC CCGGCTTCCC CACGGCCCCC AGGCTGTGGG GACAGGCCTG CCACAGACTT 480 CCTGGCCAGA GGTGTGGCTG GGTGCCATGG TAGGGAAAGA CAGCCAGACA TTGGGGGCCA 540 TGGTGCGGCC CGGCCACCGC AGTCTAAATC GCCTTGGGGG TGCGTTTCTG CCAACTGTGG 600 TGCTGGCCAT TCATGCCGTC TCTCAGGCTG TCGGGCCCTG CCCTGCCTGA CTCCTGGCTC 660 TTGGAGCTGG AGAAAGGACT CTCAGATTGG CAGAGAGCGA TAAATGCTTT GTTGTGTGCG 720 CGGCAGCGAG CCGATGTCAT TTGAAGTCAC AGCACATGAA AATGAGGGGG AGAAAAAAAC 780 TTAGGCAAGA GAAATCCTCC AGATGGGCCC TGGAGGCCCC ATCCAAGAGT CTGAGGCCAA 840 CACATCAGGG GAACTGGAAG CAGAGAGGGA ATCAGCCACT GGAAAGAAGT CACGCAGACG 900 AAGTGGTGAC AGCCACGACA GGAAATTGCT CAGCGGTGGC CACAACAGAG TGGCAGCCAG 960 GGGCCAGGGG CCAGCTCTGT GACCATCCCC GAGAGAGAAA GGGGACATTC AGGCCTGGTC 1020 TATGATGGTC TGGTGGCCGG AGGCTCCGTG AGGGCAGCCC CAGGGCCAGA AGGACCTCTC 1080 CTGTGCTGAC AGCAAAGTCA CCAGCGGGAG TCCAGCCCAC ACTGCCTTTC TGATGAGGCC 1140 TCCAGCTCTG GCTGCTGACT TTAAACCCTA AGGAACCCTG TGCAGGGCCT GCATCCCGGA 1200 AGGCCTCCAC CAGCCCGAAC CTGGCCCGTC CGCCCTAGAT GGGGCAATCG GCGTTTCTCC 1260 CGGGACAGCC TCCTCCCTGG CCTCCTGGCC CTCGTCTGCA TTGAGAGGCT TGGCCTCTGG 1320 TCCGCATGCT GCCCTTCCCG TGCTGTGGCC TTGCAGCCCG GCCTCTCCCC TGCTGTCCCC 1380 CTTGGCTCTG GCCTGGCCCC TGGGCCCCTG AGTCACCCCT GAGGTGACTC AGCAGTCCTT 1440 GGAAACGCAT GCCGAGGACG CACCCTGCCT GGCCCAGCTC CACATGGGTG TGGGGGAGGC 1500 TGCGGGCTGC GCCTGGTGGC CGTATGGGGC CTAGGCTGGC CAGTGCTGCC CAATGGTGGG 1560 GGCTCCCTCA CCGCCCGTCT GGCAGAAGCC ATGGGCCACA CGCTGTCCCA GCACATGGTG 1620 GCAGGGCGGT GACCTGGGCT CGGCTCTAAT GACCGGCAGC CCTGGGGCTC CCATCACCAC 1680 TACCAGTCTG CCCAGGAGGC AGCAGAGCAC TGAGCCCGAC CTGCTCCCCT CGGGCACCTA 1740 CGAGACCCAC CTGCCCCTCC ATGCGTGGGG GAGAAGGGGT GCCCTCTGCT GTGGAAAGCT 1800 GGGACCTACT GTCTGTGGTG CGAGGCTGAC CCCACAGAGC TCCAGGACAA CCCCGAGAGG 1860 AGTGGACAGA GCCAGCCGGG CCCTCCAGCC CCCACCTGGC CCAGCTGCCG CCTCTGGGCA 1920 GATGTCTCCA CTTGATAAAC AGGACAGCTA AGGGCCTAGG AGAGACATGC CTGGCCCAAG 1980 GCCAGACAGC AGGAGTGGCT AGGAAGGTCA AGGGATCCCC ACTGCAGGCC CCACCAACCC 2040 TGGCTCTGCC TGGAATGCAG TCAGGGCAGG TGGAAGGGGA GGGGCAACGC CCCAGGGCTG 2100 GGCGAGGAAT CTGGGAGCAG GTGGGAAGCT CATGCTACCT TCCCAGGAGA CGGGAGGACA 2160 GGCCTGCCAA CCAGGGGGCT CAGCTATGTG GGACACACGC TCCCACCCTT GCCCTTGCAC 2220 AGGGTTTCAT CCAAACATGG AGATGCCAGT GAGTGCCTGG GGCTCCTCTC CCAGGAACAA 2280 ACCACACCCA GAGCTCCAGC CCGAGCGAAC ACATCTACAT GAAAATCAGC CTCATGCATC 2340 ATGCATTGTA ATTTCTCATC TTGGGGACCA GGCAGGAGGG 2380
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