Tag | Content |
---|
EnhancerAtlas ID | HS187-11815 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr19:5948430-5951400 |
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 |
|
| 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 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH19I005945 | chr19 | 5945921 | 5956215 |
|
Enhancer Sequence | TCCAGCCTGG GCGACAGAGC GAGACTCCAT GTCAAAAAAA AAAAAAAAAG ATAAATTCCC 60 CCTAGAAAAC TGGCAACCAA GCGGTGTACC AGGGCCTCAG TGAGTCTGGC AAGTTAGAAA 120 ACCTGGCTGG TCATGGCTGG ATACCTGGGA TACAAAATAA ATGATGGGCC AGTTCAATGC 180 TTTTTATTCT GTGGCAGAGG CAACCAGCTC AGAAATTCTT GTCAAAAGGG CAGGCCCTGA 240 GAAAAGCAAG TGAGAGGTGG CTTCCAAAGT TGAGGGGTGC TGAGGGTCAA ATCCTGTGCA 300 GGGGCTGGAA GGTGGGGGGA AGCTGTCTGG CCAGAGGGAT TCATTCCAGA ACCTCCTTAA 360 GCTCCCTGGT GGGTCTAATA AACATATCTG AAGCTCGGCA GGTCCTTGGC AGGGAGCTTC 420 AGTCCAGTAC AATTCCACCA GGCTCGCAGT GAGTGCCCAG AGCTGCCTGC TTTCTCCACA 480 TCAAACAGAG AACTTAATCG GGATGTGGTT TGGTCTTCTT CAGACTGTCT TCTGAAAGCC 540 AGGAAGTCTG ATATATAGAG ACTTTTTCCT GGTACTGACT CTTCCATGGC CAGGGTTCTG 600 ACGAGACTAA AAGATGGTAA GGGCCCTTTA CAAGTAACAA TTCAGCGCAC CACTGTTTAT 660 CATCAAGAAC TCTCAGCTTT ATATTCCCCC CAGGGACCAT GGAATAAAGT GAACAGACTA 720 GATGTGACGG ATGAGACCTG CCGGGTAACA TGGGGGTGGT TTCCTGAACA CCAGTGTGAT 780 ACAGAGTGAG ACCCAAATTT CTTCTGATGC AAACGAAAAC GGTCTGAGTT CACACACACG 840 AAAAAGGCTC AGGCCAAGAA GCAGTTGGCA TCGGGTTCCA TCTGACTTGA TCTATGGCCT 900 AACTAACCTA AAATAAAGTT TACTTTGCTC TGAGCAGGCC CGATTAGTAG AGAAAGCCAA 960 TTAACAGGAG CCCTTAGCAA CCAGTCAGGG TGTTCTCTGC AGACAGCCTG AGGGAAGAGC 1020 CCTGGTCAGC TCAGAGCTGT CACAAGGGGC TTGACAATGG CTCTCCTGGG GCTCCTGAAA 1080 GTGGGTGTCC AAAAGTTACG AGTGCTAAAA CTACAAGGTG CATGTTATGC ACATGGCCAC 1140 CAGAGCTACA TTGGAACATT TACATACTGC TCTATGCAGC CTCCAATCCT GGCTCTCCCA 1200 CGGTGCCCAC AAGCTCATCC CAAGGCTCCC TGCCATACAG CTTCACCTTC CACCTGCCAG 1260 TGTGGGGGAC TGCTTGAATT TCTCAGGATC AGAGCCTCAG ACCCAAAGTC CATGAGAATC 1320 AGGATGCTGA GATCTACCTG GGCTGGCCAG GCCAAAGAGA TGAACATGTG GACGAGGTGA 1380 GGCCCCTCCA GACACTCCAA CATGGGCCTC TGTGAGAAGT ACGCAGGGCA CAGAACAGCG 1440 CGTGTGCTCT TGAAGAGCAC CTGCTGTCAC AAAAACTCTG TGATGCACTT GTTTGCTACT 1500 CTCATTCTAG AACCTGTCAC CTCTGCAGCT GGAGAGTCCT ATGTGGGCTG CATTTTTCAA 1560 ACCCAGGCAC CTGCAGAAGG CCTCTGGGGG GGACCCTAAA GACCATCTGT TCCCAGACAG 1620 CTGAAGACGG AAACCTGAGA ACACCATTTC CTGTGCTCTC AAAGACCAGA GGTGCAGTAA 1680 CTCACCATAC CTGACTCAGG AGAAGTTTCC GGCAGCCACT CTGCCAACAA AAGAAGGACG 1740 CAGCCACCTC CTAATTCTTG CTCTGGCGGC AGTCACGTGC GCTCATGGGA GGGCTGTACT 1800 CCCAGTGCAC TGTGGGTCAA GTGCCTCCTG GCTGGACTCC TTCCCGCGGC TCCCGTGTCT 1860 CACTACCCCA AACCCACTTT TGTGCCACGA AGGCCACTAC TGCCGTTACC TCCCCCACAC 1920 CCATAGCCTA TGGCACAAGT AAAGACTGTT GCTTCTTTTT CCATCACACA CTGACTCCTC 1980 CAAAATGTTA ACACAGGACT CCAACCCACC CCTGGCTGAA CAGTGCTTCC TAAGTGTCCT 2040 GAGGTTTGGT GGCTGTAGCT GAATGTTAAC AGTTTCCTTA AAAACCGGGG ACTGTTGTGT 2100 GCTAGAAAGA ACGCTGAGGT CCGGGATAAG GTTTGGGACC GTACCAGCCT GGAAGGCTGC 2160 CTGGTGCTCA GGCGGTAGAG CTGGGTCCCT TCTTTTCTTG TTAAGAGTCC TTTTTCCCTG 2220 TCCTGAGAAT AGGGGTCTTC TGTCATGAGT TACCTACAGG ATGGAGTTTT CAATCCTGAA 2280 TGTAGGATAA TGTTTACCTT TCCCAATTTA TCAAACTTCA AAAACCCAAG ACATTTCTTG 2340 TTCTTGAGAG TTCACAATCT TCTCCACCTA TAATCTTCAA AAGGCTTCTT AATACAAAGA 2400 TAAAGGGCTC AGGGGATTCC TTCTGGGTTC AAAGGAAGAG TCTTTTCTTC TTCCTGCTTT 2460 GATTGAAGAC AATCAGTTCA CTGCCTTAAC CACAGTCCAA ACACAATCAG TCTTGCAAAG 2520 CAATCTGTGT TGGAGAGTGC CTCTTCCTAG ATATCAAAGG AAGCCTTAGC TTCTTGGGTT 2580 TCTAAGACGC TAAACTTGAA TGCCCGCATT CAGGGAAACA AGAAGGAAAA ATGGAAGGAG 2640 GGTGAAGGGG TCAAATTAGG TTTGGAAGGT TCTACTTCAC ATGACTCAAT TCCTCCTGAC 2700 CCCTCGTGTC TTTTTTGGGA AACAGGATTC ACCTCTTGCT GTGGGTATAT ATTCCCACGG 2760 CAATTTAGAA AAGGCTAAAA GGGGATTCGA TCTTCCCTGA CTTTTCAGCA GCATGAATTA 2820 AAGCGAGCTG GAAGAAATCC TTGTCATCTT TTAAGTTACC ATTAGCTGCT TACAATTAGC 2880 TAGGGCCAGG ATCTGAGGGA CCCGAAGGGA AAGTGGCTGG TCTGGGTTGG GCTCCCCCTG 2940 GGCGGTAGGA GTGCCGGGTA GGTGTGGACT 2970
|