Tag | Content |
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EnhancerAtlas ID | HS040-18683 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr19:45958410-45959920 |
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 | CCGGGTTCAA GCGATTCTCC TGCCTCAGGC TCCCAAGTGG CTGGGATAAC AGGTGCCCAC 60 CACTACGCCC AGCTAATTTT TTTTTTTTTT TTAGATAGGG TCTGGCTCTG GCTCTGTCAT 120 ACAGGCTGGA GCACAGTGGC ATGATGACAA CCCACTGCAG CCTTGACCTC CTGGGCTTAA 180 GTGATCCTCT TGCCTCAGCC TCCTGAGTAG CTGGGGCTAC AGGCTTATTT TTTTGTAGAG 240 ATGGGGTCTC ACTCTGTTGC CCAGGCTGGT CTCAAACTTC TGGGCTCAAG CAATCCTCCT 300 GCCTTGGCTT CCCAAAGTGC TGGGTTTACA GGAGTGAGCC ACCATGTCTG GCCATTTGAG 360 GAAATTTTTA TTTTTGTCTG TCTTGTTTCC TGCTCTGTCC CCAGCACCTA GAGTGTGTGA 420 CTGCAGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTAGGTG TGCTGATTAA 480 ATATTTGAAT GGCTGATTGA ATGAACGAAT GAATGTCATC CTACAACCAC TTGTGAGTCC 540 TGGTCTTAGG GGAAGGCTGG GCTGGGGCCC TGGCCTCTGG GATCCCTCTT GTGCCAGTCC 600 CCCAGCCCTG CTGTTCCCAC AGCTCTGTGC TGAAGAGGGC GTGGAGGGGG CCAGGGAAGG 660 GAGTGTCAGG CAGCCAGCCG GCTGCCTGCC CTGGACAGCA GCCCAGAGTG TCTGCAGGAG 720 GGAGAGGGTA GTTCAGGAGC CTGAGTCACC CTGGGAGAAA CCCCAGCCAC ATACCTGGCC 780 GCTGACATCA CCCGGCCAGG GCACCCCCGG CAGCCTAGAC AAGCTGACTG AATCACAGGC 840 GGAATTCAGC CACCCCGGGC ACGTGGCCTG CTGTGACCCC CCGCAACACC CCCGAGTGGC 900 CGTCTGGCTG CGGGGGTTGG GCCGGGCACA CAGGGGTCAG TGAGGGGGCA TGGGGCCTGA 960 GTCAGGGACA GGGTGGCTAC AGCCAGAGAC CACCCAGCCA CAGGCGTCCA TGTGGGGCAG 1020 GAAGGAGAAA GTTTGGGAAG GAGAGCCTGT GGGGAGGCCC TGGCGGGTGA GGAGGAAGCA 1080 CGTGTGGGTG TGACGGGGAG GCTGCGGCTT GTGGGCAGCG GCTGGGCGAC CCACAGGGGT 1140 GGGATGGGGT CTGAGTGTTT GCGCAGAGAA TCACCAAATC GTAAGAGACT TGGTCGTAAG 1200 AGTCAGTCAG GAGGACAATG GAATCACCAA TGTGCTTACA CACGCAAAGG CACACACGCA 1260 CACTCAACAC CCGGCCTGGG GAGGCCCTGA CTCCACCCAC CCCAGGCCAG CGGGGCCTCA 1320 CTACCCATAA GCCTGCAAGT TCCCTAAGGG ACTGAGGCCT AAGGGACAGT TTCCTCATCT 1380 GTTGAGTGGG GGTATTAACA AGCATTATTA GGCCAGGCAC AGTGACTCGT GAGGCAGAGG 1440 TAGGCGGATC CCTTGGAGGC CAGAAGTTCA AGACCAGCCT GGACATCATA GCAAGACCCC 1500 TTCTCTACAA 1510
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