Tag | Content |
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EnhancerAtlas ID | HS187-17076 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr3:46968230-46970380 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr3:46968561-46968579 | ATCTCCTTCCTTCCTGCC | - | 6.36 |
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| Number of super-enhancer constituents: 32 | 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_20061 | chr3:46970016-46975395 | 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_42118 | chr3:46970032-46992962 | 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 |
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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 |
GH03I046924 | chr3 | 46966329 | 46982223 |
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Enhancer Sequence | CAGGTGAGAC TAGGCCGCAG GTCCTCCTCC TTCCCCAGTA CCTCTTTCGG TTCTTGACCA 60 GTGGTCCCTC AGAAAAGTCC TGGGCCTCTA AGGCAGGAAA CAATTTCCCA ACAGGCCTCC 120 CACAGTCTGC CATCTCCCAA GCCCTCTGTC TGGACCAGGT AAAAGTGCTG CTGACTTCCT 180 CAGGCCCTGC AAAAGCAAGC TTTCCCAGAG GCAGGGGTGT CTGTGGCTAC ACAGCTAGCA 240 AGCGGCAGTG CTTTGGACTC AGGGGCTTTC AGATGCTATT CACTCTCCTA TTTAAGGGCT 300 CCACCTGCTT CCTGCCCCCA GCTTACTTAC CATCTCCTTC CTTCCTGCCA GGGCCCCTGA 360 GCCTGGAGCC TTGGGGCTGG GCTGAACCAC TGCGGGCGAT GGGGCAGTAC CAGCATAGCC 420 TGTGTGGAGG AAGCCCACCT GCACTCCCAG AAGGCCCAGA GATACCCCAC CCCGTCCCCC 480 ATCCTTGAAC ACCTGCCTCG GGCCTGGAGG TACATGTCAG GTCACAGAGG TACAGGGAGA 540 CAAAGTGGGG CATGACTGGG TGCAAAGGCT TTCGTTCACA ACAGGGTGGG GAGAAATGAG 600 GAAGAGAAAC TGGGTGTGGG AAGAAAACTG CAGGGATTAG TAAGAAAAAA AACTGTCGCT 660 TTCAGAAACG GTCTCCAGGG TTCTGTGAGA AATCAGAAGG AGAGAGGAGA GGCCACAGGG 720 AACTGTACCC AGAACTCACA GCAGCAACAC GCACCCATGC CTCCAGACCC ACCCACTGCC 780 CGAGGCTTCA GAAGGCCAAC TGGAGGAGTG AACCAGAAGC AAGAGGCGGG AGCAGAGCCT 840 TGCGCCCACT GTGCCCTGCC ACCCCCAGAG CGGAGCACTG GCCAAGCAGC CAAGAACATC 900 TAGATCCCGA CCACCATGGG AAGGTCTCAT TCTGGGCCTC AGTTTCCACA TTTAGAAACA 960 TTACGGCTGT GCTGGGTGCA TCCAGCTCTA TCAAGCTGGG TCCACGCCCT CCCCAGACTC 1020 ACTCTTGGAG GGTTAATCTG ATGTGCAGCC ACTGTTGTGT GATCGCGTGA AAATGGTGCA 1080 GTCTCTGACC TCCAGTCCCC TTAGCGTGGA GAGCTAAGAG ACTTCCCCTC CCTAATGCCC 1140 ACTTAACTGC CCACCCCCGG AATTCCACCA CTACCAAAGG ACAGGAGTCT CTGGGAGAGG 1200 TCAAGGAGCA TGGGGGGGTT CAGCTTGGGG ACCTGGCCTT TCCAACACAG GCCCAAGATT 1260 TAACCTCCCT TATAAAAGCA GGTGGATCAC TTTAGGTCAG GAGTTTGAGC CCAGCCTGGC 1320 CAACAGGGCG AAACCCGGTC TCTACTAAAA ATACAAAAAT TAGGTGGGTA TGGTGCCACA 1380 TGCCTGTAAT CTCAGCTATT CAGGAGGCTG AAGCAGGAGA ATCGCTTGAA CTGAGGAGGC 1440 AGAGGTTGCA GTGAGCTGAG ATCGCACCAC TGCACTCCAG CCTAGGCTGC AGACTGTCTC 1500 AAAAAAAAAA AATGTATATA TATGTATTTT AAATGGCTTT AGAGAAGTAC CAAGACAGCA 1560 AGGATTTCAG GGGCTGCAAT CATGGAGATA AGGGAAGTAC AACAAAGTGA GCCTGACATC 1620 ACGTCCCTCT TTCCCCTTAA AGCATGTCTA TTTACATGCA GCAGCTGAAA AGCTGAGAGA 1680 CTGAGCAGAG CTTCCCATTA GGTTGATGCA AAAATAACTG TGGTTTTTGC CATTGAACAT 1740 AGTGGCAGAA ACCACAATTA CTTTTGCACC AACCTCATAT AATCTCATGG GCCTGGAGAG 1800 AAAAAAAAAA GTGTGTTTAA GCAGAAACTA AAACAGACTA CTGACTTCTC AACTGCAACT 1860 ATGGAAACCA TAAGACCATG AAATGGTATC TCAGAAGTGT GGACAAAATA AATGTCACAC 1920 AAAATTCTAA ATCTAGTTAA GAAGCCTTCA AGAGAAAGAC TTTTTCAGAC AAAGAAAGGT 1980 TAGGAGAATC AGTTATCAGT GAATCCGTTA TTCAAGAAAT ACTAAAAGGA ATACTTTAGG 2040 CTAGAGGAAA ATGATCTCAG ACGGAAACAT GGAATTGCAG GGAAAAAATA AAATGCCTCA 2100 GAAAGGGTAA ATACAATGGC TTGTGTCTGT AATCCCAGCT ACTTCGGAGG 2150
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