Tag | Content |
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EnhancerAtlas ID | HS049-03767 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr19:2047070-2050750 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr19:2049721-2049732 | CTTTCCCGCCC | - | 6.32 | EWSR1-FLI1 | MA0149.1 | chr19:2048783-2048801 | GGAGGGAAGGAAGGGGGG | + | 6.89 | EWSR1-FLI1 | MA0149.1 | chr19:2048779-2048797 | GGGAGGAGGGAAGGAAGG | + | 8.45 | TFAP2C | MA0524.2 | chr19:2049807-2049819 | TGCCCTGGGGCA | + | 6.44 | TFAP2C | MA0524.2 | chr19:2049807-2049819 | TGCCCTGGGGCA | - | 7.22 | ZNF263 | MA0528.1 | chr19:2048777-2048798 | GGGGGAGGAGGGAAGGAAGGG | + | 7.67 | ZNF263 | MA0528.1 | chr19:2048780-2048801 | GGAGGAGGGAAGGAAGGGGGG | + | 8.87 |
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| Number of super-enhancer constituents: 61 | ID | Coordinate | Tissue/cell |
SE_00410 | chr19:2040386-2053186 | Adipose_Nuclei | SE_00877 | chr19:2043921-2052778 | Adrenal_Gland | SE_02925 | chr19:2048869-2051301 | Bladder | SE_03565 | chr19:2048324-2050846 | Brain_Angular_Gyrus | SE_04258 | chr19:2046741-2052500 | Brain_Anterior_Caudate | SE_05392 | chr19:2047378-2051239 | Brain_Cingulate_Gyrus | SE_06065 | chr19:2039897-2052942 | Brain_Hippocampus_Middle | SE_07327 | chr19:2047327-2052628 | Brain_Hippocampus_Middle_150 | SE_08493 | chr19:2047327-2052448 | Brain_Inferior_Temporal_Lobe | SE_08907 | chr19:2049401-2049912 | Brain_Mid_Frontal_Lobe | SE_08907 | chr19:2049934-2050697 | Brain_Mid_Frontal_Lobe | SE_10185 | chr19:2047987-2054377 | CD19_Primary | SE_11386 | chr19:2039336-2059166 | CD20 | SE_11985 | chr19:2046880-2047770 | CD3 | SE_11985 | chr19:2048045-2050917 | CD3 | SE_14045 | chr19:2049408-2053107 | CD34_Primary_RO01536 | SE_14636 | chr19:2046521-2051249 | CD4_Memory_Primary_7pool | SE_17004 | chr19:2048366-2052914 | CD4p_CD225int_CD127p_Tmem | SE_17626 | chr19:2038511-2053432 | CD4p_CD25-_CD45RAp_Naive | SE_17917 | chr19:2046688-2053390 | CD4p_CD25-_CD45ROp_Memory | SE_19564 | chr19:2046765-2052948 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20037 | chr19:2048084-2051202 | CD56 | SE_20925 | chr19:2047955-2052980 | CD8_Memory_7pool | SE_22582 | chr19:2046785-2050922 | CD8_primiary | SE_23148 | chr19:2047060-2052907 | Colon_Crypt_1 | SE_23772 | chr19:2047435-2051308 | Colon_Crypt_2 | SE_25073 | chr19:2047159-2052899 | Colon_Crypt_3 | SE_26566 | chr19:2038851-2054518 | Esophagus | SE_28069 | chr19:2048918-2051185 | Fetal_Intestine | SE_29067 | chr19:2049038-2051201 | Fetal_Intestine_Large | SE_29903 | chr19:2049126-2050917 | Fetal_Muscle | SE_31409 | chr19:2043840-2053094 | Gastric | SE_34292 | chr19:2046713-2063146 | HCT-116 | SE_34839 | chr19:2046910-2047939 | HeLa | SE_34839 | chr19:2048987-2051185 | HeLa | SE_39943 | chr19:2049362-2052838 | K562 | SE_40728 | chr19:2042250-2052968 | Left_Ventricle | SE_41572 | chr19:2043959-2052890 | LNCaP | SE_42204 | chr19:2043982-2052921 | Lung | SE_46685 | chr19:2048280-2051328 | Ovary | SE_47494 | chr19:2046951-2051306 | Pancreas | SE_48086 | chr19:2036911-2052819 | Psoas_Muscle | SE_48699 | chr19:2046500-2052937 | Right_Atrium | SE_49469 | chr19:2046990-2048075 | Right_Ventricle | SE_49469 | chr19:2048799-2051277 | Right_Ventricle | SE_50075 | chr19:2046933-2053000 | Sigmoid_Colon | SE_51187 | chr19:2038576-2052883 | Skeletal_Muscle | SE_52407 | chr19:2046849-2048378 | Small_Intestine | SE_52407 | chr19:2048606-2053006 | Small_Intestine | SE_53798 | chr19:2037650-2053000 | Spleen | SE_54890 | chr19:2046717-2052159 | Stomach_Smooth_Muscle | SE_55272 | chr19:2049431-2052904 | Thymus | SE_57445 | chr19:2046970-2048317 | VACO_503 | SE_57445 | chr19:2048510-2051278 | VACO_503 | SE_57963 | chr19:2049496-2049996 | VACO_9m | SE_57963 | chr19:2050058-2051212 | VACO_9m | SE_59032 | chr19:2040556-2063003 | Ly3 | SE_59944 | chr19:2041147-2096724 | Ly4 | SE_60429 | chr19:2041140-2096762 | DHL6 | SE_65305 | chr19:2038632-2051258 | Pancreatic_islets | SE_68856 | chr19:2049853-2051215 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr19 | 2047200 | 2048200 | chr19 | 2047311 | 2048451 | chr19 | 2049976 | 2050209 |
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Enhancer Sequence | TCACAGGTGT GGGCCACATG TGGAAGGCGT GAGGCCTCCT AGCACCTCAG CAAGGCAAGA 60 TCAGGGGACG CAGAGTCTCT TAGGGGGTCC ATGGAATTTG CCAACCCAGG GGGTGATTCT 120 GTCCCCCAGG AGACACTGGG CCATGTCTGG GGACATCTGT GGTTGTGACC GGTTGGGGGA 180 GCTCCTGGCA CGGAGTGGGG TGGGGCAGGG GTGCTGCTCA GCACCCTGCA GTGCCCAGGA 240 CAGCCCCACC CCAGAGAAAG ATGGGCCCCA ACCTCCACAG GGCCGTGGGG AAGACCTCCT 300 CCCACCTGCA GAGCCCTGGG GGCCTCTGGG AAAGGGGTGC ATTGCGGGGA GGGGACAGAC 360 ACAAGCAGCT GGCTCTTGGG AACCCTGCCT CTGATGCCAG GATTGAGTCA CCGTGGGGCC 420 CAAGCCGTGT CTTGCACCTC CGTCTGCTTG TCCACAGAAT GGGGACGGCT GACCTCTGGG 480 GCGGGTCGCG GGGATCAAAG GCAGCGGGGC AGTGGGAAGG AGGTGAGTCA CTAGGCGGGC 540 TGCCAGCCTG GTGGCTGTGC CTGCTTTCCC ACGGCCTCCT GGGCCATCTC AGGGCAGCTG 600 AGTCCTCCCT GGGCCTCAGT TTCCCCCATC TAAGATGGCA CACAACCACC TCTCCTTCCC 660 CTAAGCTGCT CCCCTCCCTT TCGCTCAGTG CCTGGGGCTG GCGGGGTAAG AATTCAGTGC 720 CTGGTGCTCT GGGGCCTGCT GAAGGTGGGG GCTCTGCTTC CATCACCCCT GCCTTCTGCC 780 CCTACCCAAG CCCAGACACC TGCATTCCTC CGCCCATGTC CCGCAGCTGC CCGGCACACC 840 TTTCCCCTGC CAGCTCTGTG CACCTACGCC CCCGCCACCC ACCAGAGGCT CATCTGCTTC 900 CAGCCCCCCA ACCCCGCAGC TACCAGTTAC CGAGTCAGTA TACACAGTGC TGTACTGGTC 960 CTGGGGGCTC ACGGGAGAGG CACCCACAGG CGCGAGTGTG CCAGGCCCTG CCCAGACCAC 1020 ATCCTGCACT CTCCCATTTC AGTGCCAGAC ACCCCTGGAG GGAGCCCCTG GTGGGCCCTG 1080 ATACCCGGCT AAGGAAGCCG CCTTGGGCCC TGGGGGCCAG GATTCAAATC CAGGCCTGTT 1140 GCACTGGGCA GGCTGGGGCT GGGTCATTTC TTGACCCAGC CCCAGGACCA TGGGAGCAAG 1200 ACCCTGACCA GGGTGCAAGG AACAGTGCAG ATTAGAGTAG GCTTTGCCCA GCCCCCGTGG 1260 AAGATGGTGG CATACATATG TACGTTTCCA CAGAGCAAAT GGCCCAGCGC AGGGACTGCC 1320 GGCCCTTTAC GAGGGGCCGG GCCTTTGAAG CTGGGGAACC GAGGCCCGGT CAGGTTCCTT 1380 GTACCACTGA GCTCTCACTC AGCTTCACCC GTCTGGGTGA ACCCAGGCGG GAGGGGCCCA 1440 CAGAGGTGGC GGGGGTCCCA GTCCCAGTGA GGATGCTGGC TGCTCTGGGC CAAGTCACTG 1500 CCCCTCTCTG GGCCCCAGAC AACCTGAGTG GGGCTCTAAC AAGAGGGTCG TTCAGCAGAA 1560 GTGAGACTCC AGTGGAGCCC GTGGGAGACC CAAGGCCAGG AGATGGGTGG AGGCCAGAGG 1620 GCAGAGTCTG GGAGGGGCCG TGAGCCAAGC TGCCCTCCTG CCTCCCCACC CACCCTGGCT 1680 CGGGCAGATA GCTACCAGGA GGCTGCTGGG GGAGGAGGGA AGGAAGGGGG GGGCTCCAAC 1740 TAGCCCCCAT GGGAGTCAGC ATTCCCATAA GGCTCCTGTC CAGAGGCCCC TGGTGGCCCT 1800 GGGGCAGCCA CCACAAGGCA GGTGACCAGG GTCTAAGGCC AGACTGGAGT TCACCTGCTG 1860 TCTGACCTTG GCCTAGTGAC CTCACCCTGG GGTCTGTCAG CGGTGAGACG GGAGGCAGCT 1920 GCCCCCAACT CGTGGGAGCT CACGAGAGTG AAATGACCTA AGGGGCCACA GAGCCCAGCG 1980 TGAGCTCCTG GCCCTGTCTG GCCACCGTTC CCCTGTGCCA GCCACAGCCT CCAACTCAGC 2040 AAAGCTACAG ATGGACGGCC GCAGCCACCA CAGCGGAGGG GCCAGGCACC ACGAGACTCC 2100 GCGGCCTCCT CGCCCGTGTA CAGGGGAGCC CCAGGCACAC GCGCCTGCAG TCTCAGAGCC 2160 TCACTTTCCC ATCTGCGAAC GGAAAGAAAC CCAAGGCACC CACAGACGTG CCTCCCTGCT 2220 GGGCTGCTGC CTGCTGGAGG CAAGGAGAGT ATTTCAGGAG AGGTGGCCCC AATCCAGGGA 2280 GCAGCCGTGC ATGGTGGGGG CTGTGGGGGG AGATTCCTAG AGCAACCGGT CCCGGCCACC 2340 TGGAGGAACA CCTCACAGCC AGGACTGCCT GCCAGGCCCT CCTCCACCAA GACGCCCACC 2400 TTCCCAGCTC CCAGCCAGGC TGCCCTGGCC ATGCACAGAG GCCGGCCCAC AATCCTGGGC 2460 AGTGTGGGCG GTCCTGGTCC CACTGTTCTA GGTCTGGCTG TGGGACTCGA GTCAGCAGGC 2520 CTTGGCAGGA GGTGGCTGGA ACCATCTAGA AAGTTCAAGT GTGCTTTAGC TGCCTGGCTG 2580 GCCCCATGCA CTGACTCTGT ATCAGCTCAT GCCTGGCCCT AGGAGGGAGA AGACCACTGT 2640 CAGGTCCTCC TCTTTCCCGC CCAGCCCCTG ACACTCTGAT GGTGCCAGGC CTGCTGCCCT 2700 AGGGGAAAAC TGGGCAGGGG TGGCAGGGGT GGAGTGCTGC CCTGGGGCAC TGGCTGGACA 2760 GACCTGGGAA TTCTTCCCAG TCTCTCTTTG CTCCTCCCAC CCTGGAGCAC CGCGTTGTGT 2820 GTACACACAA GACAGAGACA CACACACACA CAAACACACA CACATACACT CACACTCTCT 2880 CTTCCTCTCT CCAGTCCTGC CTTCCCTACC GGGCAACAGG TCCCTGCCCA AGGAAGCCCA 2940 GTGAAGCGAT TACATAACCC CGGCCTGAGG GGTGGGGCGG GCCGGCTGAC ATCACTGCGT 3000 CCCCTGGGCC AGGTCCTGCG GGGCCCCTGC CCAGCACCTG CCCTCCCCTT CCCCCCCAAG 3060 ATTTGCTCAT CTGAAACCAG CACTCAACAG CAGTCACCAC CCGGGCTGCG CAGAAACTTC 3120 CCGCTCCGAC AGGAAACAGC ACTTGGGCCT GGGGTGTCTG CGAAGTGCAG GGCTGAGGGG 3180 ACATCCCATC CCCTCCCCCA CGGCACAGGC CCCCTGGGGG TGGGTGCACC TGACCAGCCC 3240 GGCCTGGGGA TTCTGAAAGA AAGTCCCCAG AAGCCACATG GAGGTGGGAA TGGGACTGTG 3300 GCCCGCTGAC CCGTCCCCAC CAGGGCACAA CCAGCTGGAG CTTGCAGGGG ACACCCCCCA 3360 TAAGCCACAT GCAGCGACTG GGACAGGACT GCAGCCTGCT GACCCCCCAG AACATACCCG 3420 GCGGGGGCTT GCAGGGGACA CACAGCCTGG TGCCCTGACC CGGAGGGGGC TCCTGCTCCC 3480 AGCCTCACTT GGGGGTCCTG GAGGAAGGAC CCGGCGGCCA TGGCTGGAGA GAGGACTGTG 3540 GCCTGCTGAA CCCCCATCCT CGCACACCGA CCCCGCTTCA GCGCACGGCC GGCCCGGGCA 3600 GCCCCGGGTG TAGGGCGGGG GCCAGGCACG AGCCCCGGGA GCCGATCTTA GGGGCGGGCC 3660 CCGCGCCCCC CACGCCGGCC 3680
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