| Tag | Content |
|---|
EnhancerAtlas ID | HS051-19490 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr3:46967030-46969950 |
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 | AGAATAGAGG GAACAAGCAG AGATGAAGTC AGTGTGTGAC ATGGTCTCAT TCATTCATTC 60
ATACAATTTG CATAGCCCGT GAATTCCTGA ATTTCCTCTG CACTCTCTGG AGATAGCCTG 120
GTAAGGAGGA GAAGCACAGA ATGGAGTGTC ATCAGGCAGG CCCCTTGGCA CCGTCCCCTG 180
CCACTTAGCG GGACTGGCTG CCCTCCAGAG GCCCTGTCTA CTCTGTTGGA GTACGGTTCT 240
CTTCCAGAGC TGGGCCAAGG ACGCCTAGGG AGCATTCACA GGGTGTCTCT CCTGGATCAT 300
CCCATTTGAC AGATAAGGGG ACTGGAGGTC AGAGAGACTG TACCCTTTTC ATAGGATCAC 360
ACAGCAGTGG CTGCACATCT TAGCTCAAGG CAATGTATAA CTCCCAGCCA GGGCTAAAGC 420
TCCTAGGCTG AGTGATTCCC AAAAGAGAAG GCCAGTGGTC ACCCACAAAT TCCCCAAGTC 480
TGGCCCCTCT TCAGAGCCTT CCTGCCCTGG GGCTCATGCC ATGGAATACG CCTCAACTAC 540
TTAGAGAAAA GCATCTGGGT GTGCTGGGCC AGGGGCATGT GGCAGTGAGG AGTGACATGT 600
GGACAGAGAA GCAGGTGCTG GAGGGCTCCA GAGGGGCGTG GCTGCCTACA GCTGTGGGAA 660
TGTGGAGGGG AGACACTCCA GGAGGAGGTG GCGCCTGGGC CTGCAATGAC GCGGACAGGG 720
TCAAGGCACA AAGCACACGA GAGGCTGACT CAGCTCCAAG ACTGTTGAGA GTGGCCAGTG 780
AGGGCTGTGA AAATAGGCAT GACCATGTGC AAGGCTGGGA AGGCCACAGT CCACCAGGAC 840
AGCAGTGAGA ACTGAACAGC CCCAAAGGCC TCCATGAAGA GAGAGGAGCC ACAAGGGGCC 900
AGAATCTCCC GGCAGGAGCT GCGGCTAGCT ACTATGTTTT TATGTTCTTC CTGCCTCAGT 960
CTTTTCAGGC AGGGGTGGCT GAACCAAGAA CTCACTGGGG TCCTCTCTGG CTCAGGGGCT 1020
CATCAAATCC TAGCCCCACA CACACAGAAG CAGGCTCCCA GGAAAATGTG TCCCTGGTAA 1080
CTCCACAGGG CGGCAGGGCG AGAGGTCCTG GGGGCTGCAG GGTCTAAGAA AGGCAAGGCA 1140
GAGGCAGTGG GACAGACCCC TAGCCCCAGG GGATGCAGGA GTGGCCCCTC AGATGCTGGC 1200
CAGGTGAGAC TAGGCCGCAG GTCCTCCTCC TTCCCCAGTA CCTCTTTCGG TTCTTGACCA 1260
GTGGTCCCTC AGAAAAGTCC TGGGCCTCTA AGGCAGGAAA CAATTTCCCA ACAGGCCTCC 1320
CACAGTCTGC CATCTCCCAA GCCCTCTGTC TGGACCAGGT AAAAGTGCTG CTGACTTCCT 1380
CAGGCCCTGC AAAAGCAAGC TTTCCCAGAG GCAGGGGTGT CTGTGGCTAC ACAGCTAGCA 1440
AGCGGCAGTG CTTTGGACTC AGGGGCTTTC AGATGCTATT CACTCTCCTA TTTAAGGGCT 1500
CCACCTGCTT CCTGCCCCCA GCTTACTTAC CATCTCCTTC CTTCCTGCCA GGGCCCCTGA 1560
GCCTGGAGCC TTGGGGCTGG GCTGAACCAC TGCGGGCGAT GGGGCAGTAC CAGCATAGCC 1620
TGTGTGGAGG AAGCCCACCT GCACTCCCAG AAGGCCCAGA GATACCCCAC CCCGTCCCCC 1680
ATCCTTGAAC ACCTGCCTCG GGCCTGGAGG TACATGTCAG GTCACAGAGG TACAGGGAGA 1740
CAAAGTGGGG CATGACTGGG TGCAAAGGCT TTCGTTCACA ACAGGGTGGG GAGAAATGAG 1800
GAAGAGAAAC TGGGTGTGGG AAGAAAACTG CAGGGATTAG TAAGAAAAAA AACTGTCGCT 1860
TTCAGAAACG GTCTCCAGGG TTCTGTGAGA AATCAGAAGG AGAGAGGAGA GGCCACAGGG 1920
AACTGTACCC AGAACTCACA GCAGCAACAC GCACCCATGC CTCCAGACCC ACCCACTGCC 1980
CGAGGCTTCA GAAGGCCAAC TGGAGGAGTG AACCAGAAGC AAGAGGCGGG AGCAGAGCCT 2040
TGCGCCCACT GTGCCCTGCC ACCCCCAGAG CGGAGCACTG GCCAAGCAGC CAAGAACATC 2100
TAGATCCCGA CCACCATGGG AAGGTCTCAT TCTGGGCCTC AGTTTCCACA TTTAGAAACA 2160
TTACGGCTGT GCTGGGTGCA TCCAGCTCTA TCAAGCTGGG TCCACGCCCT CCCCAGACTC 2220
ACTCTTGGAG GGTTAATCTG ATGTGCAGCC ACTGTTGTGT GATCGCGTGA AAATGGTGCA 2280
GTCTCTGACC TCCAGTCCCC TTAGCGTGGA GAGCTAAGAG ACTTCCCCTC CCTAATGCCC 2340
ACTTAACTGC CCACCCCCGG AATTCCACCA CTACCAAAGG ACAGGAGTCT CTGGGAGAGG 2400
TCAAGGAGCA TGGGGGGGTT CAGCTTGGGG ACCTGGCCTT TCCAACACAG GCCCAAGATT 2460
TAACCTCCCT TATAAAAGCA GGTGGATCAC TTTAGGTCAG GAGTTTGAGC CCAGCCTGGC 2520
CAACAGGGCG AAACCCGGTC TCTACTAAAA ATACAAAAAT TAGGTGGGTA TGGTGCCACA 2580
TGCCTGTAAT CTCAGCTATT CAGGAGGCTG AAGCAGGAGA ATCGCTTGAA CTGAGGAGGC 2640
AGAGGTTGCA GTGAGCTGAG ATCGCACCAC TGCACTCCAG CCTAGGCTGC AGACTGTCTC 2700
AAAAAAAAAA AATGTATATA TATGTATTTT AAATGGCTTT AGAGAAGTAC CAAGACAGCA 2760
AGGATTTCAG GGGCTGCAAT CATGGAGATA AGGGAAGTAC AACAAAGTGA GCCTGACATC 2820
ACGTCCCTCT TTCCCCTTAA AGCATGTCTA TTTACATGCA GCAGCTGAAA AGCTGAGAGA 2880
CTGAGCAGAG CTTCCCATTA GGTTGATGCA AAAATAACTG 2920
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