Tag | Content |
---|
EnhancerAtlas ID | HS103-11384 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr19:5948620-5951400 |
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 | GTGGCAGAGG CAACCAGCTC AGAAATTCTT GTCAAAAGGG CAGGCCCTGA GAAAAGCAAG 60 TGAGAGGTGG CTTCCAAAGT TGAGGGGTGC TGAGGGTCAA ATCCTGTGCA GGGGCTGGAA 120 GGTGGGGGGA AGCTGTCTGG CCAGAGGGAT TCATTCCAGA ACCTCCTTAA GCTCCCTGGT 180 GGGTCTAATA AACATATCTG AAGCTCGGCA GGTCCTTGGC AGGGAGCTTC AGTCCAGTAC 240 AATTCCACCA GGCTCGCAGT GAGTGCCCAG AGCTGCCTGC TTTCTCCACA TCAAACAGAG 300 AACTTAATCG GGATGTGGTT TGGTCTTCTT CAGACTGTCT TCTGAAAGCC AGGAAGTCTG 360 ATATATAGAG ACTTTTTCCT GGTACTGACT CTTCCATGGC CAGGGTTCTG ACGAGACTAA 420 AAGATGGTAA GGGCCCTTTA CAAGTAACAA TTCAGCGCAC CACTGTTTAT CATCAAGAAC 480 TCTCAGCTTT ATATTCCCCC CAGGGACCAT GGAATAAAGT GAACAGACTA GATGTGACGG 540 ATGAGACCTG CCGGGTAACA TGGGGGTGGT TTCCTGAACA CCAGTGTGAT ACAGAGTGAG 600 ACCCAAATTT CTTCTGATGC AAACGAAAAC GGTCTGAGTT CACACACACG AAAAAGGCTC 660 AGGCCAAGAA GCAGTTGGCA TCGGGTTCCA TCTGACTTGA TCTATGGCCT AACTAACCTA 720 AAATAAAGTT TACTTTGCTC TGAGCAGGCC CGATTAGTAG AGAAAGCCAA TTAACAGGAG 780 CCCTTAGCAA CCAGTCAGGG TGTTCTCTGC AGACAGCCTG AGGGAAGAGC CCTGGTCAGC 840 TCAGAGCTGT CACAAGGGGC TTGACAATGG CTCTCCTGGG GCTCCTGAAA GTGGGTGTCC 900 AAAAGTTACG AGTGCTAAAA CTACAAGGTG CATGTTATGC ACATGGCCAC CAGAGCTACA 960 TTGGAACATT TACATACTGC TCTATGCAGC CTCCAATCCT GGCTCTCCCA CGGTGCCCAC 1020 AAGCTCATCC CAAGGCTCCC TGCCATACAG CTTCACCTTC CACCTGCCAG TGTGGGGGAC 1080 TGCTTGAATT TCTCAGGATC AGAGCCTCAG ACCCAAAGTC CATGAGAATC AGGATGCTGA 1140 GATCTACCTG GGCTGGCCAG GCCAAAGAGA TGAACATGTG GACGAGGTGA GGCCCCTCCA 1200 GACACTCCAA CATGGGCCTC TGTGAGAAGT ACGCAGGGCA CAGAACAGCG CGTGTGCTCT 1260 TGAAGAGCAC CTGCTGTCAC AAAAACTCTG TGATGCACTT GTTTGCTACT CTCATTCTAG 1320 AACCTGTCAC CTCTGCAGCT GGAGAGTCCT ATGTGGGCTG CATTTTTCAA ACCCAGGCAC 1380 CTGCAGAAGG CCTCTGGGGG GGACCCTAAA GACCATCTGT TCCCAGACAG CTGAAGACGG 1440 AAACCTGAGA ACACCATTTC CTGTGCTCTC AAAGACCAGA GGTGCAGTAA CTCACCATAC 1500 CTGACTCAGG AGAAGTTTCC GGCAGCCACT CTGCCAACAA AAGAAGGACG CAGCCACCTC 1560 CTAATTCTTG CTCTGGCGGC AGTCACGTGC GCTCATGGGA GGGCTGTACT CCCAGTGCAC 1620 TGTGGGTCAA GTGCCTCCTG GCTGGACTCC TTCCCGCGGC TCCCGTGTCT CACTACCCCA 1680 AACCCACTTT TGTGCCACGA AGGCCACTAC TGCCGTTACC TCCCCCACAC CCATAGCCTA 1740 TGGCACAAGT AAAGACTGTT GCTTCTTTTT CCATCACACA CTGACTCCTC CAAAATGTTA 1800 ACACAGGACT CCAACCCACC CCTGGCTGAA CAGTGCTTCC TAAGTGTCCT GAGGTTTGGT 1860 GGCTGTAGCT GAATGTTAAC AGTTTCCTTA AAAACCGGGG ACTGTTGTGT GCTAGAAAGA 1920 ACGCTGAGGT CCGGGATAAG GTTTGGGACC GTACCAGCCT GGAAGGCTGC CTGGTGCTCA 1980 GGCGGTAGAG CTGGGTCCCT TCTTTTCTTG TTAAGAGTCC TTTTTCCCTG TCCTGAGAAT 2040 AGGGGTCTTC TGTCATGAGT TACCTACAGG ATGGAGTTTT CAATCCTGAA TGTAGGATAA 2100 TGTTTACCTT TCCCAATTTA TCAAACTTCA AAAACCCAAG ACATTTCTTG TTCTTGAGAG 2160 TTCACAATCT TCTCCACCTA TAATCTTCAA AAGGCTTCTT AATACAAAGA TAAAGGGCTC 2220 AGGGGATTCC TTCTGGGTTC AAAGGAAGAG TCTTTTCTTC TTCCTGCTTT GATTGAAGAC 2280 AATCAGTTCA CTGCCTTAAC CACAGTCCAA ACACAATCAG TCTTGCAAAG CAATCTGTGT 2340 TGGAGAGTGC CTCTTCCTAG ATATCAAAGG AAGCCTTAGC TTCTTGGGTT TCTAAGACGC 2400 TAAACTTGAA TGCCCGCATT CAGGGAAACA AGAAGGAAAA ATGGAAGGAG GGTGAAGGGG 2460 TCAAATTAGG TTTGGAAGGT TCTACTTCAC ATGACTCAAT TCCTCCTGAC CCCTCGTGTC 2520 TTTTTTGGGA AACAGGATTC ACCTCTTGCT GTGGGTATAT ATTCCCACGG CAATTTAGAA 2580 AAGGCTAAAA GGGGATTCGA TCTTCCCTGA CTTTTCAGCA GCATGAATTA AAGCGAGCTG 2640 GAAGAAATCC TTGTCATCTT TTAAGTTACC ATTAGCTGCT TACAATTAGC TAGGGCCAGG 2700 ATCTGAGGGA CCCGAAGGGA AAGTGGCTGG TCTGGGTTGG GCTCCCCCTG GGCGGTAGGA 2760 GTGCCGGGTA GGTGTGGACT 2780
|