Tag | Content |
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EnhancerAtlas ID | HS098-28156 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr19:45958510-45960000 |
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 | TCTGGCTCTG GCTCTGTCAT ACAGGCTGGA GCACAGTGGC ATGATGACAA CCCACTGCAG 60 CCTTGACCTC CTGGGCTTAA GTGATCCTCT TGCCTCAGCC TCCTGAGTAG CTGGGGCTAC 120 AGGCTTATTT TTTTGTAGAG ATGGGGTCTC ACTCTGTTGC CCAGGCTGGT CTCAAACTTC 180 TGGGCTCAAG CAATCCTCCT GCCTTGGCTT CCCAAAGTGC TGGGTTTACA GGAGTGAGCC 240 ACCATGTCTG GCCATTTGAG GAAATTTTTA TTTTTGTCTG TCTTGTTTCC TGCTCTGTCC 300 CCAGCACCTA GAGTGTGTGA CTGCAGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG 360 TGTGTAGGTG TGCTGATTAA ATATTTGAAT GGCTGATTGA ATGAACGAAT GAATGTCATC 420 CTACAACCAC TTGTGAGTCC TGGTCTTAGG GGAAGGCTGG GCTGGGGCCC TGGCCTCTGG 480 GATCCCTCTT GTGCCAGTCC CCCAGCCCTG CTGTTCCCAC AGCTCTGTGC TGAAGAGGGC 540 GTGGAGGGGG CCAGGGAAGG GAGTGTCAGG CAGCCAGCCG GCTGCCTGCC CTGGACAGCA 600 GCCCAGAGTG TCTGCAGGAG GGAGAGGGTA GTTCAGGAGC CTGAGTCACC CTGGGAGAAA 660 CCCCAGCCAC ATACCTGGCC GCTGACATCA CCCGGCCAGG GCACCCCCGG CAGCCTAGAC 720 AAGCTGACTG AATCACAGGC GGAATTCAGC CACCCCGGGC ACGTGGCCTG CTGTGACCCC 780 CCGCAACACC CCCGAGTGGC CGTCTGGCTG CGGGGGTTGG GCCGGGCACA CAGGGGTCAG 840 TGAGGGGGCA TGGGGCCTGA GTCAGGGACA GGGTGGCTAC AGCCAGAGAC CACCCAGCCA 900 CAGGCGTCCA TGTGGGGCAG GAAGGAGAAA GTTTGGGAAG GAGAGCCTGT GGGGAGGCCC 960 TGGCGGGTGA GGAGGAAGCA CGTGTGGGTG TGACGGGGAG GCTGCGGCTT GTGGGCAGCG 1020 GCTGGGCGAC CCACAGGGGT GGGATGGGGT CTGAGTGTTT GCGCAGAGAA TCACCAAATC 1080 GTAAGAGACT TGGTCGTAAG AGTCAGTCAG GAGGACAATG GAATCACCAA TGTGCTTACA 1140 CACGCAAAGG CACACACGCA CACTCAACAC CCGGCCTGGG GAGGCCCTGA CTCCACCCAC 1200 CCCAGGCCAG CGGGGCCTCA CTACCCATAA GCCTGCAAGT TCCCTAAGGG ACTGAGGCCT 1260 AAGGGACAGT TTCCTCATCT GTTGAGTGGG GGTATTAACA AGCATTATTA GGCCAGGCAC 1320 AGTGACTCGT GAGGCAGAGG TAGGCGGATC CCTTGGAGGC CAGAAGTTCA AGACCAGCCT 1380 GGACATCATA GCAAGACCCC TTCTCTACAA AGAAAAAATT TAAAAATTAG CTGGATGTGG 1440 TGGTGTGCAC CTGTAGTCCC AGGTACTCAG GAGGCTGTGG AGGGTGGATT 1490
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