Tag | Content |
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EnhancerAtlas ID | HS076-29900 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr19:45942680-45943990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr19:45942877-45942896 | GGGCCACCAGGGGGCGCGG | + | 7.19 | MEF2B | MA0660.1 | chr19:45943185-45943197 | GCTAAAAATAGT | + | 6.11 |
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| Number of super-enhancer constituents: 40 | ID | Coordinate | Tissue/cell |
SE_01498 | chr19:45942833-45944111 | Adrenal_Gland | SE_02108 | chr19:45942659-45944793 | Aorta | SE_02406 | chr19:45942626-45944083 | Astrocytes | SE_03036 | chr19:45942873-45943894 | Bladder | SE_06640 | chr19:45942245-45944998 | Brain_Hippocampus_Middle | SE_09930 | chr19:45942427-45943956 | CD14 | SE_11261 | chr19:45942250-45944562 | CD20 | SE_12309 | chr19:45943141-45944010 | CD3 | SE_14395 | chr19:45942417-45944510 | CD4_Memory_Primary_7pool | SE_16220 | chr19:45942579-45943820 | CD4_Naive_Primary_7pool | SE_16563 | chr19:45942537-45943950 | CD4_Naive_Primary_8pool | SE_17214 | chr19:45942536-45944077 | CD4p_CD225int_CD127p_Tmem | SE_19219 | chr19:45942438-45944101 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20014 | chr19:45942216-45944187 | CD56 | SE_20748 | chr19:45942289-45944277 | CD8_Memory_7pool | SE_21766 | chr19:45942403-45943715 | CD8_Naive_7pool | SE_22333 | chr19:45942181-45944271 | CD8_primiary | SE_23143 | chr19:45942794-45943873 | Colon_Crypt_1 | SE_23745 | chr19:45942805-45943742 | Colon_Crypt_2 | SE_24769 | chr19:45942653-45943882 | Colon_Crypt_3 | SE_26771 | chr19:45942658-45944815 | Esophagus | SE_29756 | chr19:45942465-45944778 | Fetal_Muscle | SE_31887 | chr19:45942664-45943954 | Gastric | SE_34472 | chr19:45942692-45944959 | HCT-116 | SE_35967 | chr19:45942563-45943789 | HMEC | SE_38090 | chr19:45942414-45944040 | HUVEC | SE_39922 | chr19:45942598-45944765 | K562 | SE_41239 | chr19:45942635-45944849 | Left_Ventricle | SE_44217 | chr19:45942733-45944784 | NHDF-Ad | SE_44830 | chr19:45942605-45944087 | NHLF | SE_45809 | chr19:45942415-45944792 | Osteoblasts | SE_47661 | chr19:45942791-45943591 | Pancreas | SE_48343 | chr19:45942343-45944744 | Psoas_Muscle | SE_49047 | chr19:45942813-45944746 | Right_Atrium | SE_50737 | chr19:45942718-45944750 | Sigmoid_Colon | SE_51420 | chr19:45942394-45944499 | Skeletal_Muscle | SE_52836 | chr19:45942665-45944567 | Small_Intestine | SE_53558 | chr19:45942445-45944250 | Spleen | SE_57973 | chr19:45942871-45943474 | VACO_9m | SE_65504 | chr19:45942507-45944327 | 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 |
GH19I045439 | chr19 | 45942259 | 45944857 |
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Enhancer Sequence | TGCAGTGGCT CAGGCCTTTA ATCCCAGCAC TTTGGGAGGC CGAGGTAGCA GGATCGCTTG 60 AGCCCAGGAG TTCTAGACAA TCCTGGGGCA ATATAGCGAG ATTCTATCTC AAAGAAATAA 120 TCATAATCAT AATAAAAATA AATGAATAGA TAAGCTGAGA CGGACTCAGG CCCAGCTCCT 180 GCCTGCGATC CCTGCGGGGG CCACCAGGGG GCGCGGCGCC CCTGCCCAAA ACTCCGCCGT 240 CGGCTCTGAA CCCCGGCGGA CGCGTCCCGA CGCCCCTGGA AGATTCTGCG CCCTGCCGGC 300 TCGCCGGCGC CCGGGAGCCC GGGAGGCGGG TGTGCACGCG GGGTGTCCAG GGCGCCCCCG 360 ATCGAGGCCC CCTCGCCGTG CCTCGGGGTA GGGGGACGGC TGTGACTCAG GCGCGCGCTC 420 CTCCCCGGGG CCCTCAGTGG TCGCGAGGGG GCGCGCACGG CCTCGGGAAC CCGCGCGGCG 480 CCGCGTCCAT TTTTACCCCA GCTCCGCTAA AAATAGTTGC CGCGCTCCGA GCCGAGCCCG 540 AAATAGCGGC CCCCAGATAA GGCAGGACGA CTCAGCGCTT CCGGGGAGCG GAAGGGGGAG 600 CGCGCGGGGG GAGCGGTGCT GGGCGCAGCC CGGCCGAGCA GGCGCCGCTG TCCCCAGCGC 660 ACCCCCACTC TGCCCTGGCG GTCACACTCG CCCCCGACTG CGACCCCGCC CCGCCGCTAG 720 CCTGGCTGCC TTCCTACGTC CCCCACATTG TATCCTCATC CCCTGTCCCC CATCCTCAGC 780 TTCACCTCCA TTCCTCATCA TAACTCCCCC CTCCCCTACA CCCCCAGCGA TGTCCCCCAC 840 TGGTACTCAT CCGCATCCCC CAGCCTGTCC TACTCCTGTC CCTATTTCCC CTCTCCACCC 900 TCATCGCCAA TCTCCTGTCG TCCTGAATCT GCCCCTTACC ATCTCTGTCC TCAAGGCCAA 960 CCTTTATGGG GGCAGAGCAG GGCGAGAGGA TCACAGGGAG TCAGGAGACC TGCGGGCTGA 1020 GGGCTGAGGG CTGGGGGTGA GGATCTGATT TCTTGGTTTG TTTCTACTGT GGGCAGGGGT 1080 AGGCTTAGAT CTGGGGGTTG GAGCATGGGA CACTTCAGTC TGGCCTAGTC TTCAGAGCTG 1140 AGGCGAGGCA TGGCCAGCAT CACGGCTCAT TCTGTGACCA GGGTCGGGGC TCAGGCTGGG 1200 GAAGGATGAC CGTCTTTGTC ACCAAATTTG ATCACTGTGT CACCAGAGTT AGGGCTCAGC 1260 CTTGAGCCGT TTCTTTATTT ACCCACCTCC ACTAATATTT TTTATTTCAG 1310
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