Tag | Content |
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EnhancerAtlas ID | HS179-15779 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr19:45958530-45960090 |
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: 38 | 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 | chr19:45958698-45959895 | 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 | ACAGGCTGGA GCACAGTGGC ATGATGACAA CCCACTGCAG CCTTGACCTC CTGGGCTTAA 60 GTGATCCTCT TGCCTCAGCC TCCTGAGTAG CTGGGGCTAC AGGCTTATTT TTTTGTAGAG 120 ATGGGGTCTC ACTCTGTTGC CCAGGCTGGT CTCAAACTTC TGGGCTCAAG CAATCCTCCT 180 GCCTTGGCTT CCCAAAGTGC TGGGTTTACA GGAGTGAGCC ACCATGTCTG GCCATTTGAG 240 GAAATTTTTA TTTTTGTCTG TCTTGTTTCC TGCTCTGTCC CCAGCACCTA GAGTGTGTGA 300 CTGCAGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTAGGTG TGCTGATTAA 360 ATATTTGAAT GGCTGATTGA ATGAACGAAT GAATGTCATC CTACAACCAC TTGTGAGTCC 420 TGGTCTTAGG GGAAGGCTGG GCTGGGGCCC TGGCCTCTGG GATCCCTCTT GTGCCAGTCC 480 CCCAGCCCTG CTGTTCCCAC AGCTCTGTGC TGAAGAGGGC GTGGAGGGGG CCAGGGAAGG 540 GAGTGTCAGG CAGCCAGCCG GCTGCCTGCC CTGGACAGCA GCCCAGAGTG TCTGCAGGAG 600 GGAGAGGGTA GTTCAGGAGC CTGAGTCACC CTGGGAGAAA CCCCAGCCAC ATACCTGGCC 660 GCTGACATCA CCCGGCCAGG GCACCCCCGG CAGCCTAGAC AAGCTGACTG AATCACAGGC 720 GGAATTCAGC CACCCCGGGC ACGTGGCCTG CTGTGACCCC CCGCAACACC CCCGAGTGGC 780 CGTCTGGCTG CGGGGGTTGG GCCGGGCACA CAGGGGTCAG TGAGGGGGCA TGGGGCCTGA 840 GTCAGGGACA GGGTGGCTAC AGCCAGAGAC CACCCAGCCA CAGGCGTCCA TGTGGGGCAG 900 GAAGGAGAAA GTTTGGGAAG GAGAGCCTGT GGGGAGGCCC TGGCGGGTGA GGAGGAAGCA 960 CGTGTGGGTG TGACGGGGAG GCTGCGGCTT GTGGGCAGCG GCTGGGCGAC CCACAGGGGT 1020 GGGATGGGGT CTGAGTGTTT GCGCAGAGAA TCACCAAATC GTAAGAGACT TGGTCGTAAG 1080 AGTCAGTCAG GAGGACAATG GAATCACCAA TGTGCTTACA CACGCAAAGG CACACACGCA 1140 CACTCAACAC CCGGCCTGGG GAGGCCCTGA CTCCACCCAC CCCAGGCCAG CGGGGCCTCA 1200 CTACCCATAA GCCTGCAAGT TCCCTAAGGG ACTGAGGCCT AAGGGACAGT TTCCTCATCT 1260 GTTGAGTGGG GGTATTAACA AGCATTATTA GGCCAGGCAC AGTGACTCGT GAGGCAGAGG 1320 TAGGCGGATC CCTTGGAGGC CAGAAGTTCA AGACCAGCCT GGACATCATA GCAAGACCCC 1380 TTCTCTACAA AGAAAAAATT TAAAAATTAG CTGGATGTGG TGGTGTGCAC CTGTAGTCCC 1440 AGGTACTCAG GAGGCTGTGG AGGGTGGATT GCTGGAGTGT TGGAGTTTGA GACTGCAGTG 1500 AGCTATTGAT TGCACCACTG TACTCCAGCC TAGACAACAG AACAAGATCC TATAGCAAAA 1560
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