| Tag | Content |
|---|
EnhancerAtlas ID | HS104-40407 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr3:46967100-46969520 |
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 | CATAGCCCGT GAATTCCTGA ATTTCCTCTG CACTCTCTGG AGATAGCCTG GTAAGGAGGA 60
GAAGCACAGA ATGGAGTGTC ATCAGGCAGG CCCCTTGGCA CCGTCCCCTG CCACTTAGCG 120
GGACTGGCTG CCCTCCAGAG GCCCTGTCTA CTCTGTTGGA GTACGGTTCT CTTCCAGAGC 180
TGGGCCAAGG ACGCCTAGGG AGCATTCACA GGGTGTCTCT CCTGGATCAT CCCATTTGAC 240
AGATAAGGGG ACTGGAGGTC AGAGAGACTG TACCCTTTTC ATAGGATCAC ACAGCAGTGG 300
CTGCACATCT TAGCTCAAGG CAATGTATAA CTCCCAGCCA GGGCTAAAGC TCCTAGGCTG 360
AGTGATTCCC AAAAGAGAAG GCCAGTGGTC ACCCACAAAT TCCCCAAGTC TGGCCCCTCT 420
TCAGAGCCTT CCTGCCCTGG GGCTCATGCC ATGGAATACG CCTCAACTAC TTAGAGAAAA 480
GCATCTGGGT GTGCTGGGCC AGGGGCATGT GGCAGTGAGG AGTGACATGT GGACAGAGAA 540
GCAGGTGCTG GAGGGCTCCA GAGGGGCGTG GCTGCCTACA GCTGTGGGAA TGTGGAGGGG 600
AGACACTCCA GGAGGAGGTG GCGCCTGGGC CTGCAATGAC GCGGACAGGG TCAAGGCACA 660
AAGCACACGA GAGGCTGACT CAGCTCCAAG ACTGTTGAGA GTGGCCAGTG AGGGCTGTGA 720
AAATAGGCAT GACCATGTGC AAGGCTGGGA AGGCCACAGT CCACCAGGAC AGCAGTGAGA 780
ACTGAACAGC CCCAAAGGCC TCCATGAAGA GAGAGGAGCC ACAAGGGGCC AGAATCTCCC 840
GGCAGGAGCT GCGGCTAGCT ACTATGTTTT TATGTTCTTC CTGCCTCAGT CTTTTCAGGC 900
AGGGGTGGCT GAACCAAGAA CTCACTGGGG TCCTCTCTGG CTCAGGGGCT CATCAAATCC 960
TAGCCCCACA CACACAGAAG CAGGCTCCCA GGAAAATGTG TCCCTGGTAA CTCCACAGGG 1020
CGGCAGGGCG AGAGGTCCTG GGGGCTGCAG GGTCTAAGAA AGGCAAGGCA GAGGCAGTGG 1080
GACAGACCCC TAGCCCCAGG GGATGCAGGA GTGGCCCCTC AGATGCTGGC CAGGTGAGAC 1140
TAGGCCGCAG GTCCTCCTCC TTCCCCAGTA CCTCTTTCGG TTCTTGACCA GTGGTCCCTC 1200
AGAAAAGTCC TGGGCCTCTA AGGCAGGAAA CAATTTCCCA ACAGGCCTCC CACAGTCTGC 1260
CATCTCCCAA GCCCTCTGTC TGGACCAGGT AAAAGTGCTG CTGACTTCCT CAGGCCCTGC 1320
AAAAGCAAGC TTTCCCAGAG GCAGGGGTGT CTGTGGCTAC ACAGCTAGCA AGCGGCAGTG 1380
CTTTGGACTC AGGGGCTTTC AGATGCTATT CACTCTCCTA TTTAAGGGCT CCACCTGCTT 1440
CCTGCCCCCA GCTTACTTAC CATCTCCTTC CTTCCTGCCA GGGCCCCTGA GCCTGGAGCC 1500
TTGGGGCTGG GCTGAACCAC TGCGGGCGAT GGGGCAGTAC CAGCATAGCC TGTGTGGAGG 1560
AAGCCCACCT GCACTCCCAG AAGGCCCAGA GATACCCCAC CCCGTCCCCC ATCCTTGAAC 1620
ACCTGCCTCG GGCCTGGAGG TACATGTCAG GTCACAGAGG TACAGGGAGA CAAAGTGGGG 1680
CATGACTGGG TGCAAAGGCT TTCGTTCACA ACAGGGTGGG GAGAAATGAG GAAGAGAAAC 1740
TGGGTGTGGG AAGAAAACTG CAGGGATTAG TAAGAAAAAA AACTGTCGCT TTCAGAAACG 1800
GTCTCCAGGG TTCTGTGAGA AATCAGAAGG AGAGAGGAGA GGCCACAGGG AACTGTACCC 1860
AGAACTCACA GCAGCAACAC GCACCCATGC CTCCAGACCC ACCCACTGCC CGAGGCTTCA 1920
GAAGGCCAAC TGGAGGAGTG AACCAGAAGC AAGAGGCGGG AGCAGAGCCT TGCGCCCACT 1980
GTGCCCTGCC ACCCCCAGAG CGGAGCACTG GCCAAGCAGC CAAGAACATC TAGATCCCGA 2040
CCACCATGGG AAGGTCTCAT TCTGGGCCTC AGTTTCCACA TTTAGAAACA TTACGGCTGT 2100
GCTGGGTGCA TCCAGCTCTA TCAAGCTGGG TCCACGCCCT CCCCAGACTC ACTCTTGGAG 2160
GGTTAATCTG ATGTGCAGCC ACTGTTGTGT GATCGCGTGA AAATGGTGCA GTCTCTGACC 2220
TCCAGTCCCC TTAGCGTGGA GAGCTAAGAG ACTTCCCCTC CCTAATGCCC ACTTAACTGC 2280
CCACCCCCGG AATTCCACCA CTACCAAAGG ACAGGAGTCT CTGGGAGAGG TCAAGGAGCA 2340
TGGGGGGGTT CAGCTTGGGG ACCTGGCCTT TCCAACACAG GCCCAAGATT TAACCTCCCT 2400
TATAAAAGCA GGTGGATCAC 2420
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