| Tag | Content |
|---|
EnhancerAtlas ID | HS117-04660 |
Organism | Homo sapiens |
Tissue/cell | LHCN-M2 |
Coordinate | chr3:46967620-46968560 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr3:46967659-46967673 | AGAGGGGCGTGGCT | - | 6.25 | | Zfx | MA0146.2 | chr3:46967719-46967733 | GGCGCCTGGGCCTG | + | 6.41 |
|
| | Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
| SE_00943 | chr3:46966307-46969328 | Adrenal_Gland | | SE_02008 | chr3:46966356-46969637 | Aorta | | SE_10127 | chr3:46964000-46982704 | CD14 | | SE_11155 | chr3:46963907-46992913 | CD20 | | SE_13638 | chr3:46967735-46969552 | CD34_Primary_RO01536 | | SE_14564 | chr3:46966688-46969464 | CD4_Memory_Primary_7pool | | SE_18708 | chr3:46966449-46969796 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_20061 | chr3:46966255-46969830 | CD56 | | SE_22640 | chr3:46967131-46969404 | CD8_primiary | | SE_23114 | chr3:46967107-46969663 | Colon_Crypt_1 | | SE_23749 | chr3:46966359-46969563 | Colon_Crypt_2 | | SE_26114 | chr3:46968072-46971522 | Duodenum_Smooth_Muscle | | SE_28630 | chr3:46967051-46969812 | Fetal_Intestine_Large | | SE_30558 | chr3:46966747-46969559 | Fetal_Muscle | | SE_31407 | chr3:46966210-46969802 | Gastric | | SE_32585 | chr3:46966448-46975230 | GM12878 | | SE_38780 | chr3:46966789-46969421 | HUVEC | | SE_40617 | chr3:46966281-46970663 | Left_Ventricle | | SE_42118 | chr3:46964238-46969951 | Lung | | SE_48306 | chr3:46966313-46969573 | Psoas_Muscle | | SE_48684 | chr3:46966340-46969754 | Right_Atrium | | SE_49453 | chr3:46966340-46969606 | Right_Ventricle | | SE_50160 | chr3:46966963-46970076 | Sigmoid_Colon | | SE_52388 | chr3:46967352-46970127 | Small_Intestine | | SE_53507 | chr3:46967172-46970034 | Spleen | | SE_58746 | chr3:46966845-47032612 | Ly1 | | SE_59412 | chr3:46966960-46998383 | Ly3 | | SE_59747 | chr3:46966600-47033537 | Ly4 | | SE_60850 | chr3:46965041-47030117 | DHL6 | | SE_62445 | chr3:46966331-47033109 | Tonsil |
|
| | 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 |
| GH03I046924 | chr3 | 46966329 | 46982223 |
|
Enhancer Sequence | AGTGACATGT GGACAGAGAA GCAGGTGCTG GAGGGCTCCA GAGGGGCGTG GCTGCCTACA 60
GCTGTGGGAA TGTGGAGGGG AGACACTCCA GGAGGAGGTG GCGCCTGGGC CTGCAATGAC 120
GCGGACAGGG TCAAGGCACA AAGCACACGA GAGGCTGACT CAGCTCCAAG ACTGTTGAGA 180
GTGGCCAGTG AGGGCTGTGA AAATAGGCAT GACCATGTGC AAGGCTGGGA AGGCCACAGT 240
CCACCAGGAC AGCAGTGAGA ACTGAACAGC CCCAAAGGCC TCCATGAAGA GAGAGGAGCC 300
ACAAGGGGCC AGAATCTCCC GGCAGGAGCT GCGGCTAGCT ACTATGTTTT TATGTTCTTC 360
CTGCCTCAGT CTTTTCAGGC AGGGGTGGCT GAACCAAGAA CTCACTGGGG TCCTCTCTGG 420
CTCAGGGGCT CATCAAATCC TAGCCCCACA CACACAGAAG CAGGCTCCCA GGAAAATGTG 480
TCCCTGGTAA CTCCACAGGG CGGCAGGGCG AGAGGTCCTG GGGGCTGCAG GGTCTAAGAA 540
AGGCAAGGCA GAGGCAGTGG GACAGACCCC TAGCCCCAGG GGATGCAGGA GTGGCCCCTC 600
AGATGCTGGC CAGGTGAGAC TAGGCCGCAG GTCCTCCTCC TTCCCCAGTA CCTCTTTCGG 660
TTCTTGACCA GTGGTCCCTC AGAAAAGTCC TGGGCCTCTA AGGCAGGAAA CAATTTCCCA 720
ACAGGCCTCC CACAGTCTGC CATCTCCCAA GCCCTCTGTC TGGACCAGGT AAAAGTGCTG 780
CTGACTTCCT CAGGCCCTGC AAAAGCAAGC TTTCCCAGAG GCAGGGGTGT CTGTGGCTAC 840
ACAGCTAGCA AGCGGCAGTG CTTTGGACTC AGGGGCTTTC AGATGCTATT CACTCTCCTA 900
TTTAAGGGCT CCACCTGCTT CCTGCCCCCA GCTTACTTAC 940
|
