| Tag | Content |
|---|
EnhancerAtlas ID | HS082-17179 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr19:45958020-45960220 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr19:45959150-45959161 | CTGAGTCACCC | - | 6.02 | | IRF1 | MA0050.2 | chr19:45958311-45958332 | TCTTTCTTTCTTTTTTCTTTT | + | 6.11 | | JUNB | MA0490.1 | chr19:45959150-45959161 | CTGAGTCACCC | - | 6.02 | | MYC | MA0147.3 | chr19:45959266-45959278 | GGGCACGTGGCC | - | 7.22 |
|
| | 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 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I045453 | chr19 | 45956370 | 45960535 |
|
Enhancer Sequence | ACCTGAGGTC TGGAGTTCGA GACCAGCCTG GCCAGCATGG CAAAACCCTG TCTTTACTAA 60
AAATACAAAA AAAATTAACC AGGCTTGGTG GTGTGTGCCT GTAATTCCAG CTACTCGGGA 120
GGTTGAGGCA GGAGAATAAC TTGAACCCGG GAGGTGTGGG TTGCAGTGAA CCGAGATCAT 180
GCCACTGCAC TCCAGCCTGG GCGACAGAGT GAGACTTTGT GTCAAAAACA ATAATAATAA 240
TAATAATAAT GCACTAGGTG CAGATACTGA TAAAGGCTTT GTGAGGAATT TTCTTTCTTT 300
CTTTTTTCTT TTTTTTTTGA GACAGAGTCT CACTCTCTTT CCTGGCTGGA GTGCAGTGGC 360
ACGATCTCGG CTCACTGCAA CCTCCGCCTC CCGGGTTCAA GCGATTCTCC TGCCTCAGGC 420
TCCCAAGTGG CTGGGATAAC AGGTGCCCAC CACTACGCCC AGCTAATTTT TTTTTTTTTT 480
TTAGATAGGG TCTGGCTCTG GCTCTGTCAT ACAGGCTGGA GCACAGTGGC ATGATGACAA 540
CCCACTGCAG CCTTGACCTC CTGGGCTTAA GTGATCCTCT TGCCTCAGCC TCCTGAGTAG 600
CTGGGGCTAC AGGCTTATTT TTTTGTAGAG ATGGGGTCTC ACTCTGTTGC CCAGGCTGGT 660
CTCAAACTTC TGGGCTCAAG CAATCCTCCT GCCTTGGCTT CCCAAAGTGC TGGGTTTACA 720
GGAGTGAGCC ACCATGTCTG GCCATTTGAG GAAATTTTTA TTTTTGTCTG TCTTGTTTCC 780
TGCTCTGTCC CCAGCACCTA GAGTGTGTGA CTGCAGTGTG TGTGTGTGTG TGTGTGTGTG 840
TGTGTGTGTG TGTGTAGGTG TGCTGATTAA ATATTTGAAT GGCTGATTGA ATGAACGAAT 900
GAATGTCATC CTACAACCAC TTGTGAGTCC TGGTCTTAGG GGAAGGCTGG GCTGGGGCCC 960
TGGCCTCTGG GATCCCTCTT GTGCCAGTCC CCCAGCCCTG CTGTTCCCAC AGCTCTGTGC 1020
TGAAGAGGGC GTGGAGGGGG CCAGGGAAGG GAGTGTCAGG CAGCCAGCCG GCTGCCTGCC 1080
CTGGACAGCA GCCCAGAGTG TCTGCAGGAG GGAGAGGGTA GTTCAGGAGC CTGAGTCACC 1140
CTGGGAGAAA CCCCAGCCAC ATACCTGGCC GCTGACATCA CCCGGCCAGG GCACCCCCGG 1200
CAGCCTAGAC AAGCTGACTG AATCACAGGC GGAATTCAGC CACCCCGGGC ACGTGGCCTG 1260
CTGTGACCCC CCGCAACACC CCCGAGTGGC CGTCTGGCTG CGGGGGTTGG GCCGGGCACA 1320
CAGGGGTCAG TGAGGGGGCA TGGGGCCTGA GTCAGGGACA GGGTGGCTAC AGCCAGAGAC 1380
CACCCAGCCA CAGGCGTCCA TGTGGGGCAG GAAGGAGAAA GTTTGGGAAG GAGAGCCTGT 1440
GGGGAGGCCC TGGCGGGTGA GGAGGAAGCA CGTGTGGGTG TGACGGGGAG GCTGCGGCTT 1500
GTGGGCAGCG GCTGGGCGAC CCACAGGGGT GGGATGGGGT CTGAGTGTTT GCGCAGAGAA 1560
TCACCAAATC GTAAGAGACT TGGTCGTAAG AGTCAGTCAG GAGGACAATG GAATCACCAA 1620
TGTGCTTACA CACGCAAAGG CACACACGCA CACTCAACAC CCGGCCTGGG GAGGCCCTGA 1680
CTCCACCCAC CCCAGGCCAG CGGGGCCTCA CTACCCATAA GCCTGCAAGT TCCCTAAGGG 1740
ACTGAGGCCT AAGGGACAGT TTCCTCATCT GTTGAGTGGG GGTATTAACA AGCATTATTA 1800
GGCCAGGCAC AGTGACTCGT GAGGCAGAGG TAGGCGGATC CCTTGGAGGC CAGAAGTTCA 1860
AGACCAGCCT GGACATCATA GCAAGACCCC TTCTCTACAA AGAAAAAATT TAAAAATTAG 1920
CTGGATGTGG TGGTGTGCAC CTGTAGTCCC AGGTACTCAG GAGGCTGTGG AGGGTGGATT 1980
GCTGGAGTGT TGGAGTTTGA GACTGCAGTG AGCTATTGAT TGCACCACTG TACTCCAGCC 2040
TAGACAACAG AACAAGATCC TATAGCAAAA AAAAAAAAAA AAAAAAATCA CTATTATTGT 2100
AATAGCTATG CTTACGGGGA ACATACTTTC TGCCAGGTGC TGTTCTAGGC ATTCTACATT 2160
TTTTTTTTTT AAATAATGGA GATGACGTCT CACTATGTTT 2200
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