Tag | Content |
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EnhancerAtlas ID | HS116-16767 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr19:5948440-5951400 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXF2 | MA0030.1 | chr19:5950718-5950732 | AATGTTTACCTTTC | - | 6.05 | RAX | MA0718.1 | chr19:5949385-5949395 | GCCAATTAAC | + | 6.02 | ZNF143 | MA0088.2 | chr19:5950232-5950248 | CAGTGCACTGTGGGTC | - | 6.53 | ZNF263 | MA0528.1 | chr19:5951051-5951072 | GAAGGAAAAATGGAAGGAGGG | + | 6.07 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_01024 | chr19:5948476-5949078 | Adrenal_Gland | SE_04361 | chr19:5947171-5955190 | Brain_Anterior_Caudate | SE_05659 | chr19:5945996-5950306 | Brain_Cingulate_Gyrus | SE_05659 | chr19:5950684-5955150 | Brain_Cingulate_Gyrus | SE_06265 | chr19:5945643-5950568 | Brain_Hippocampus_Middle | SE_06265 | chr19:5950740-5955430 | Brain_Hippocampus_Middle | SE_08492 | chr19:5947293-5955433 | Brain_Inferior_Temporal_Lobe | SE_14928 | chr19:5948279-5951623 | CD4_Memory_Primary_7pool | SE_19010 | chr19:5947302-5951564 | CD4p_CD25-_Il17-_PMAstim_Th | SE_31266 | chr19:5948408-5951040 | Fetal_Thymus | SE_31728 | chr19:5948458-5949058 | Gastric | SE_31728 | chr19:5949063-5950804 | Gastric | SE_42610 | chr19:5948400-5952995 | Lung | SE_49179 | chr19:5949584-5950677 | Right_Atrium | SE_49179 | chr19:5950899-5953604 | Right_Atrium | SE_50862 | chr19:5948360-5950702 | Sigmoid_Colon | SE_50862 | chr19:5950825-5955957 | Sigmoid_Colon | SE_53195 | chr19:5948414-5950798 | Small_Intestine | SE_53195 | chr19:5950822-5955239 | Small_Intestine | SE_54374 | chr19:5949171-5950504 | Spleen | SE_54374 | chr19:5950971-5952414 | Spleen | SE_54795 | chr19:5945993-5955320 | Stomach_Smooth_Muscle | SE_55382 | chr19:5948477-5950686 | Thymus | SE_65343 | chr19:5945660-5950661 | Pancreatic_islets | SE_65343 | chr19:5950845-5953189 | Pancreatic_islets |
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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 |
GH19I005945 | chr19 | 5945921 | 5956215 |
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Enhancer Sequence | GCGACAGAGC GAGACTCCAT GTCAAAAAAA AAAAAAAAAG ATAAATTCCC CCTAGAAAAC 60 TGGCAACCAA GCGGTGTACC AGGGCCTCAG TGAGTCTGGC AAGTTAGAAA ACCTGGCTGG 120 TCATGGCTGG ATACCTGGGA TACAAAATAA ATGATGGGCC AGTTCAATGC TTTTTATTCT 180 GTGGCAGAGG CAACCAGCTC AGAAATTCTT GTCAAAAGGG CAGGCCCTGA GAAAAGCAAG 240 TGAGAGGTGG CTTCCAAAGT TGAGGGGTGC TGAGGGTCAA ATCCTGTGCA GGGGCTGGAA 300 GGTGGGGGGA AGCTGTCTGG CCAGAGGGAT TCATTCCAGA ACCTCCTTAA GCTCCCTGGT 360 GGGTCTAATA AACATATCTG AAGCTCGGCA GGTCCTTGGC AGGGAGCTTC AGTCCAGTAC 420 AATTCCACCA GGCTCGCAGT GAGTGCCCAG AGCTGCCTGC TTTCTCCACA TCAAACAGAG 480 AACTTAATCG GGATGTGGTT TGGTCTTCTT CAGACTGTCT TCTGAAAGCC AGGAAGTCTG 540 ATATATAGAG ACTTTTTCCT GGTACTGACT CTTCCATGGC CAGGGTTCTG ACGAGACTAA 600 AAGATGGTAA GGGCCCTTTA CAAGTAACAA TTCAGCGCAC CACTGTTTAT CATCAAGAAC 660 TCTCAGCTTT ATATTCCCCC CAGGGACCAT GGAATAAAGT GAACAGACTA GATGTGACGG 720 ATGAGACCTG CCGGGTAACA TGGGGGTGGT TTCCTGAACA CCAGTGTGAT ACAGAGTGAG 780 ACCCAAATTT CTTCTGATGC AAACGAAAAC GGTCTGAGTT CACACACACG AAAAAGGCTC 840 AGGCCAAGAA GCAGTTGGCA TCGGGTTCCA TCTGACTTGA TCTATGGCCT AACTAACCTA 900 AAATAAAGTT TACTTTGCTC TGAGCAGGCC CGATTAGTAG AGAAAGCCAA TTAACAGGAG 960 CCCTTAGCAA CCAGTCAGGG TGTTCTCTGC AGACAGCCTG AGGGAAGAGC CCTGGTCAGC 1020 TCAGAGCTGT CACAAGGGGC TTGACAATGG CTCTCCTGGG GCTCCTGAAA GTGGGTGTCC 1080 AAAAGTTACG AGTGCTAAAA CTACAAGGTG CATGTTATGC ACATGGCCAC CAGAGCTACA 1140 TTGGAACATT TACATACTGC TCTATGCAGC CTCCAATCCT GGCTCTCCCA CGGTGCCCAC 1200 AAGCTCATCC CAAGGCTCCC TGCCATACAG CTTCACCTTC CACCTGCCAG TGTGGGGGAC 1260 TGCTTGAATT TCTCAGGATC AGAGCCTCAG ACCCAAAGTC CATGAGAATC AGGATGCTGA 1320 GATCTACCTG GGCTGGCCAG GCCAAAGAGA TGAACATGTG GACGAGGTGA GGCCCCTCCA 1380 GACACTCCAA CATGGGCCTC TGTGAGAAGT ACGCAGGGCA CAGAACAGCG CGTGTGCTCT 1440 TGAAGAGCAC CTGCTGTCAC AAAAACTCTG TGATGCACTT GTTTGCTACT CTCATTCTAG 1500 AACCTGTCAC CTCTGCAGCT GGAGAGTCCT ATGTGGGCTG CATTTTTCAA ACCCAGGCAC 1560 CTGCAGAAGG CCTCTGGGGG GGACCCTAAA GACCATCTGT TCCCAGACAG CTGAAGACGG 1620 AAACCTGAGA ACACCATTTC CTGTGCTCTC AAAGACCAGA GGTGCAGTAA CTCACCATAC 1680 CTGACTCAGG AGAAGTTTCC GGCAGCCACT CTGCCAACAA AAGAAGGACG CAGCCACCTC 1740 CTAATTCTTG CTCTGGCGGC AGTCACGTGC GCTCATGGGA GGGCTGTACT CCCAGTGCAC 1800 TGTGGGTCAA GTGCCTCCTG GCTGGACTCC TTCCCGCGGC TCCCGTGTCT CACTACCCCA 1860 AACCCACTTT TGTGCCACGA AGGCCACTAC TGCCGTTACC TCCCCCACAC CCATAGCCTA 1920 TGGCACAAGT AAAGACTGTT GCTTCTTTTT CCATCACACA CTGACTCCTC CAAAATGTTA 1980 ACACAGGACT CCAACCCACC CCTGGCTGAA CAGTGCTTCC TAAGTGTCCT GAGGTTTGGT 2040 GGCTGTAGCT GAATGTTAAC AGTTTCCTTA AAAACCGGGG ACTGTTGTGT GCTAGAAAGA 2100 ACGCTGAGGT CCGGGATAAG GTTTGGGACC GTACCAGCCT GGAAGGCTGC CTGGTGCTCA 2160 GGCGGTAGAG CTGGGTCCCT TCTTTTCTTG TTAAGAGTCC TTTTTCCCTG TCCTGAGAAT 2220 AGGGGTCTTC TGTCATGAGT TACCTACAGG ATGGAGTTTT CAATCCTGAA TGTAGGATAA 2280 TGTTTACCTT TCCCAATTTA TCAAACTTCA AAAACCCAAG ACATTTCTTG TTCTTGAGAG 2340 TTCACAATCT TCTCCACCTA TAATCTTCAA AAGGCTTCTT AATACAAAGA TAAAGGGCTC 2400 AGGGGATTCC TTCTGGGTTC AAAGGAAGAG TCTTTTCTTC TTCCTGCTTT GATTGAAGAC 2460 AATCAGTTCA CTGCCTTAAC CACAGTCCAA ACACAATCAG TCTTGCAAAG CAATCTGTGT 2520 TGGAGAGTGC CTCTTCCTAG ATATCAAAGG AAGCCTTAGC TTCTTGGGTT TCTAAGACGC 2580 TAAACTTGAA TGCCCGCATT CAGGGAAACA AGAAGGAAAA ATGGAAGGAG GGTGAAGGGG 2640 TCAAATTAGG TTTGGAAGGT TCTACTTCAC ATGACTCAAT TCCTCCTGAC CCCTCGTGTC 2700 TTTTTTGGGA AACAGGATTC ACCTCTTGCT GTGGGTATAT ATTCCCACGG CAATTTAGAA 2760 AAGGCTAAAA GGGGATTCGA TCTTCCCTGA CTTTTCAGCA GCATGAATTA AAGCGAGCTG 2820 GAAGAAATCC TTGTCATCTT TTAAGTTACC ATTAGCTGCT TACAATTAGC TAGGGCCAGG 2880 ATCTGAGGGA CCCGAAGGGA AAGTGGCTGG TCTGGGTTGG GCTCCCCCTG GGCGGTAGGA 2940 GTGCCGGGTA GGTGTGGACT 2960
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