| Tag | Content |
|---|
EnhancerAtlas ID | HS158-38557 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr3:46967120-46968830 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr3:46968561-46968579 | ATCTCCTTCCTTCCTGCC | - | 6.36 | | KLF14 | MA0740.1 | chr3:46967659-46967673 | AGAGGGGCGTGGCT | - | 6.25 | | TFAP2C | MA0524.2 | chr3:46967532-46967544 | TGCCCTGGGGCT | - | 6.11 | | 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: 4 | Chromosome | Start | End |
| chr3 | 46968009 | 46968296 | | chr3 | 46967600 | 46968800 | | chr3 | 46967558 | 46967892 | | chr3 | 46967181 | 46967944 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I046924 | chr3 | 46966329 | 46982223 |
|
Enhancer Sequence | ATTTCCTCTG CACTCTCTGG AGATAGCCTG GTAAGGAGGA GAAGCACAGA ATGGAGTGTC 60
ATCAGGCAGG CCCCTTGGCA CCGTCCCCTG CCACTTAGCG GGACTGGCTG CCCTCCAGAG 120
GCCCTGTCTA CTCTGTTGGA GTACGGTTCT CTTCCAGAGC TGGGCCAAGG ACGCCTAGGG 180
AGCATTCACA GGGTGTCTCT CCTGGATCAT CCCATTTGAC AGATAAGGGG ACTGGAGGTC 240
AGAGAGACTG TACCCTTTTC ATAGGATCAC ACAGCAGTGG CTGCACATCT TAGCTCAAGG 300
CAATGTATAA CTCCCAGCCA GGGCTAAAGC TCCTAGGCTG AGTGATTCCC AAAAGAGAAG 360
GCCAGTGGTC ACCCACAAAT TCCCCAAGTC TGGCCCCTCT TCAGAGCCTT CCTGCCCTGG 420
GGCTCATGCC ATGGAATACG CCTCAACTAC TTAGAGAAAA GCATCTGGGT GTGCTGGGCC 480
AGGGGCATGT GGCAGTGAGG AGTGACATGT GGACAGAGAA GCAGGTGCTG GAGGGCTCCA 540
GAGGGGCGTG GCTGCCTACA GCTGTGGGAA TGTGGAGGGG AGACACTCCA GGAGGAGGTG 600
GCGCCTGGGC CTGCAATGAC GCGGACAGGG TCAAGGCACA AAGCACACGA GAGGCTGACT 660
CAGCTCCAAG ACTGTTGAGA GTGGCCAGTG AGGGCTGTGA AAATAGGCAT GACCATGTGC 720
AAGGCTGGGA AGGCCACAGT CCACCAGGAC AGCAGTGAGA ACTGAACAGC CCCAAAGGCC 780
TCCATGAAGA GAGAGGAGCC ACAAGGGGCC AGAATCTCCC GGCAGGAGCT GCGGCTAGCT 840
ACTATGTTTT TATGTTCTTC CTGCCTCAGT CTTTTCAGGC AGGGGTGGCT GAACCAAGAA 900
CTCACTGGGG TCCTCTCTGG CTCAGGGGCT CATCAAATCC TAGCCCCACA CACACAGAAG 960
CAGGCTCCCA GGAAAATGTG TCCCTGGTAA CTCCACAGGG CGGCAGGGCG AGAGGTCCTG 1020
GGGGCTGCAG GGTCTAAGAA AGGCAAGGCA GAGGCAGTGG GACAGACCCC TAGCCCCAGG 1080
GGATGCAGGA GTGGCCCCTC AGATGCTGGC CAGGTGAGAC TAGGCCGCAG GTCCTCCTCC 1140
TTCCCCAGTA CCTCTTTCGG TTCTTGACCA GTGGTCCCTC AGAAAAGTCC TGGGCCTCTA 1200
AGGCAGGAAA CAATTTCCCA ACAGGCCTCC CACAGTCTGC CATCTCCCAA GCCCTCTGTC 1260
TGGACCAGGT AAAAGTGCTG CTGACTTCCT CAGGCCCTGC AAAAGCAAGC TTTCCCAGAG 1320
GCAGGGGTGT CTGTGGCTAC ACAGCTAGCA AGCGGCAGTG CTTTGGACTC AGGGGCTTTC 1380
AGATGCTATT CACTCTCCTA TTTAAGGGCT CCACCTGCTT CCTGCCCCCA GCTTACTTAC 1440
CATCTCCTTC CTTCCTGCCA GGGCCCCTGA GCCTGGAGCC TTGGGGCTGG GCTGAACCAC 1500
TGCGGGCGAT GGGGCAGTAC CAGCATAGCC TGTGTGGAGG AAGCCCACCT GCACTCCCAG 1560
AAGGCCCAGA GATACCCCAC CCCGTCCCCC ATCCTTGAAC ACCTGCCTCG GGCCTGGAGG 1620
TACATGTCAG GTCACAGAGG TACAGGGAGA CAAAGTGGGG CATGACTGGG TGCAAAGGCT 1680
TTCGTTCACA ACAGGGTGGG GAGAAATGAG 1710
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