Tag | Content |
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EnhancerAtlas ID | HS108-20645 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr19:45958560-45960080 |
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 | CCCACTGCAG CCTTGACCTC CTGGGCTTAA GTGATCCTCT TGCCTCAGCC TCCTGAGTAG 60 CTGGGGCTAC AGGCTTATTT TTTTGTAGAG ATGGGGTCTC ACTCTGTTGC CCAGGCTGGT 120 CTCAAACTTC TGGGCTCAAG CAATCCTCCT GCCTTGGCTT CCCAAAGTGC TGGGTTTACA 180 GGAGTGAGCC ACCATGTCTG GCCATTTGAG GAAATTTTTA TTTTTGTCTG TCTTGTTTCC 240 TGCTCTGTCC CCAGCACCTA GAGTGTGTGA CTGCAGTGTG TGTGTGTGTG TGTGTGTGTG 300 TGTGTGTGTG TGTGTAGGTG TGCTGATTAA ATATTTGAAT GGCTGATTGA ATGAACGAAT 360 GAATGTCATC CTACAACCAC TTGTGAGTCC TGGTCTTAGG GGAAGGCTGG GCTGGGGCCC 420 TGGCCTCTGG GATCCCTCTT GTGCCAGTCC CCCAGCCCTG CTGTTCCCAC AGCTCTGTGC 480 TGAAGAGGGC GTGGAGGGGG CCAGGGAAGG GAGTGTCAGG CAGCCAGCCG GCTGCCTGCC 540 CTGGACAGCA GCCCAGAGTG TCTGCAGGAG GGAGAGGGTA GTTCAGGAGC CTGAGTCACC 600 CTGGGAGAAA CCCCAGCCAC ATACCTGGCC GCTGACATCA CCCGGCCAGG GCACCCCCGG 660 CAGCCTAGAC AAGCTGACTG AATCACAGGC GGAATTCAGC CACCCCGGGC ACGTGGCCTG 720 CTGTGACCCC CCGCAACACC CCCGAGTGGC CGTCTGGCTG CGGGGGTTGG GCCGGGCACA 780 CAGGGGTCAG TGAGGGGGCA TGGGGCCTGA GTCAGGGACA GGGTGGCTAC AGCCAGAGAC 840 CACCCAGCCA CAGGCGTCCA TGTGGGGCAG GAAGGAGAAA GTTTGGGAAG GAGAGCCTGT 900 GGGGAGGCCC TGGCGGGTGA GGAGGAAGCA CGTGTGGGTG TGACGGGGAG GCTGCGGCTT 960 GTGGGCAGCG GCTGGGCGAC CCACAGGGGT GGGATGGGGT CTGAGTGTTT GCGCAGAGAA 1020 TCACCAAATC GTAAGAGACT TGGTCGTAAG AGTCAGTCAG GAGGACAATG GAATCACCAA 1080 TGTGCTTACA CACGCAAAGG CACACACGCA CACTCAACAC CCGGCCTGGG GAGGCCCTGA 1140 CTCCACCCAC CCCAGGCCAG CGGGGCCTCA CTACCCATAA GCCTGCAAGT TCCCTAAGGG 1200 ACTGAGGCCT AAGGGACAGT TTCCTCATCT GTTGAGTGGG GGTATTAACA AGCATTATTA 1260 GGCCAGGCAC AGTGACTCGT GAGGCAGAGG TAGGCGGATC CCTTGGAGGC CAGAAGTTCA 1320 AGACCAGCCT GGACATCATA GCAAGACCCC TTCTCTACAA AGAAAAAATT TAAAAATTAG 1380 CTGGATGTGG TGGTGTGCAC CTGTAGTCCC AGGTACTCAG GAGGCTGTGG AGGGTGGATT 1440 GCTGGAGTGT TGGAGTTTGA GACTGCAGTG AGCTATTGAT TGCACCACTG TACTCCAGCC 1500 TAGACAACAG AACAAGATCC 1520
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