Tag | Content |
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EnhancerAtlas ID | HS087-11258 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr19:45958500-45959930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr19:45959150-45959161 | CTGAGTCACCC | - | 6.02 | JUNB | MA0490.1 | chr19:45959150-45959161 | CTGAGTCACCC | - | 6.02 | MYC | MA0147.3 | chr19:45959266-45959278 | GGGCACGTGGCC | - | 7.22 |
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| Number of super-enhancer constituents: 39 | ID | Coordinate | Tissue/cell |
SE_01498 | chr19:45958813-45960047 | Adrenal_Gland | SE_02108 | chr19:45958499-45960183 | Aorta | SE_02406 | chr19:45958430-45960350 | Astrocytes | SE_03036 | chr19:45958768-45959960 | Bladder | SE_06640 | chr19:45958730-45960254 | Brain_Hippocampus_Middle | SE_09930 | chr19:45956713-45960693 | CD14 | SE_11261 | chr19:45958545-45960135 | CD20 | SE_13038 | chr19:45958977-45959634 | CD34_Primary_RO01480 | SE_14395 | chr19:45958713-45960104 | CD4_Memory_Primary_7pool | SE_19219 | chr19:45958648-45960125 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20014 | chr19:45958474-45960238 | CD56 | SE_20748 | chr19:45959094-45960173 | CD8_Memory_7pool | SE_22333 | chr19:45958933-45959876 | CD8_primiary | SE_23143 | chr19:45958333-45960000 | Colon_Crypt_1 | SE_23745 | chr19:45958435-45960006 | Colon_Crypt_2 | SE_24769 | chr19:45958330-45960073 | Colon_Crypt_3 | SE_26771 | chr19:45958314-45960076 | Esophagus | SE_29756 | chr19:45958492-45960156 | Fetal_Muscle | SE_31887 | chr19:45958242-45959952 | Gastric | SE_34472 | chr19:45958815-45960056 | HCT-116 | SE_35967 | chr19:45958253-45960308 | HMEC | SE_38090 | chr19:45957862-45960688 | HUVEC | SE_39922 | chr19:45958724-45960027 | K562 | SE_41239 | chr19:45958731-45960085 | Left_Ventricle | SE_44217 | chr19:45958500-45960314 | NHDF-Ad | SE_44830 | chr19:45958669-45960328 | NHLF | SE_45809 | chr19:45956766-45960850 | Osteoblasts | SE_47661 | chr19:45958424-45958684 | Pancreas | SE_47661 | chr19:45958698-45959895 | Pancreas | SE_48343 | chr19:45958657-45960059 | Psoas_Muscle | SE_49047 | chr19:45958609-45960056 | Right_Atrium | SE_50737 | chr19:45958444-45960123 | Sigmoid_Colon | SE_51420 | chr19:45958482-45960430 | Skeletal_Muscle | SE_52836 | chr19:45958420-45960076 | Small_Intestine | SE_53558 | chr19:45958651-45960115 | Spleen | SE_57973 | chr19:45958776-45959093 | VACO_9m | SE_57973 | chr19:45959154-45959797 | VACO_9m | SE_64393 | chr19:45958339-45960189 | NHEK | SE_65504 | chr19:45958083-45960176 | 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 |
GH19I045453 | chr19 | 45956370 | 45960535 |
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Enhancer Sequence | TTAGATAGGG TCTGGCTCTG GCTCTGTCAT ACAGGCTGGA GCACAGTGGC ATGATGACAA 60 CCCACTGCAG CCTTGACCTC CTGGGCTTAA GTGATCCTCT TGCCTCAGCC TCCTGAGTAG 120 CTGGGGCTAC AGGCTTATTT TTTTGTAGAG ATGGGGTCTC ACTCTGTTGC CCAGGCTGGT 180 CTCAAACTTC TGGGCTCAAG CAATCCTCCT GCCTTGGCTT CCCAAAGTGC TGGGTTTACA 240 GGAGTGAGCC ACCATGTCTG GCCATTTGAG GAAATTTTTA TTTTTGTCTG TCTTGTTTCC 300 TGCTCTGTCC CCAGCACCTA GAGTGTGTGA CTGCAGTGTG TGTGTGTGTG TGTGTGTGTG 360 TGTGTGTGTG TGTGTAGGTG TGCTGATTAA ATATTTGAAT GGCTGATTGA ATGAACGAAT 420 GAATGTCATC CTACAACCAC TTGTGAGTCC TGGTCTTAGG GGAAGGCTGG GCTGGGGCCC 480 TGGCCTCTGG GATCCCTCTT GTGCCAGTCC CCCAGCCCTG CTGTTCCCAC AGCTCTGTGC 540 TGAAGAGGGC GTGGAGGGGG CCAGGGAAGG GAGTGTCAGG CAGCCAGCCG GCTGCCTGCC 600 CTGGACAGCA GCCCAGAGTG TCTGCAGGAG GGAGAGGGTA GTTCAGGAGC CTGAGTCACC 660 CTGGGAGAAA CCCCAGCCAC ATACCTGGCC GCTGACATCA CCCGGCCAGG GCACCCCCGG 720 CAGCCTAGAC AAGCTGACTG AATCACAGGC GGAATTCAGC CACCCCGGGC ACGTGGCCTG 780 CTGTGACCCC CCGCAACACC CCCGAGTGGC CGTCTGGCTG CGGGGGTTGG GCCGGGCACA 840 CAGGGGTCAG TGAGGGGGCA TGGGGCCTGA GTCAGGGACA GGGTGGCTAC AGCCAGAGAC 900 CACCCAGCCA CAGGCGTCCA TGTGGGGCAG GAAGGAGAAA GTTTGGGAAG GAGAGCCTGT 960 GGGGAGGCCC TGGCGGGTGA GGAGGAAGCA CGTGTGGGTG TGACGGGGAG GCTGCGGCTT 1020 GTGGGCAGCG GCTGGGCGAC CCACAGGGGT GGGATGGGGT CTGAGTGTTT GCGCAGAGAA 1080 TCACCAAATC GTAAGAGACT TGGTCGTAAG AGTCAGTCAG GAGGACAATG GAATCACCAA 1140 TGTGCTTACA CACGCAAAGG CACACACGCA CACTCAACAC CCGGCCTGGG GAGGCCCTGA 1200 CTCCACCCAC CCCAGGCCAG CGGGGCCTCA CTACCCATAA GCCTGCAAGT TCCCTAAGGG 1260 ACTGAGGCCT AAGGGACAGT TTCCTCATCT GTTGAGTGGG GGTATTAACA AGCATTATTA 1320 GGCCAGGCAC AGTGACTCGT GAGGCAGAGG TAGGCGGATC CCTTGGAGGC CAGAAGTTCA 1380 AGACCAGCCT GGACATCATA GCAAGACCCC TTCTCTACAA AGAAAAAATT 1430
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