Tag | Content |
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EnhancerAtlas ID | HS196-18955 |
Organism | Homo sapiens |
Tissue/cell | ZR75-1 |
Coordinate | chr3:46971640-46974120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nkx2-5(var.2) | MA0503.1 | chr3:46972492-46972503 | AGGCACTCAAG | + | 6.14 | SOX10 | MA0442.2 | chr3:46973700-46973711 | AAAACAAAGCA | + | 6.02 | Znf423 | MA0116.1 | chr3:46972788-46972803 | TCACCCCTAGGGTGC | - | 6.46 |
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| Number of super-enhancer constituents: 37 | ID | Coordinate | Tissue/cell |
SE_00943 | chr3:46971562-46975179 | Adrenal_Gland | SE_02008 | chr3:46971380-46975339 | Aorta | SE_10127 | chr3:46964000-46982704 | CD14 | SE_11155 | chr3:46963907-46992913 | CD20 | SE_13638 | chr3:46971550-46974655 | CD34_Primary_RO01536 | SE_14564 | chr3:46971566-46975300 | CD4_Memory_Primary_7pool | SE_18708 | chr3:46972575-46975234 | CD4p_CD25-_Il17-_PMAstim_Th | SE_20061 | chr3:46970016-46975395 | CD56 | SE_22640 | chr3:46971928-46975052 | CD8_primiary | SE_23114 | chr3:46971617-46975208 | Colon_Crypt_1 | SE_23749 | chr3:46971711-46973448 | Colon_Crypt_2 | SE_23749 | chr3:46973449-46975042 | Colon_Crypt_2 | SE_26114 | chr3:46971685-46975312 | Duodenum_Smooth_Muscle | SE_27403 | chr3:46970664-46979932 | Esophagus | SE_28630 | chr3:46971492-46975383 | Fetal_Intestine_Large | SE_30558 | chr3:46971654-46978550 | Fetal_Muscle | SE_31407 | chr3:46970646-46975250 | Gastric | SE_32585 | chr3:46966448-46975230 | GM12878 | SE_38780 | chr3:46970749-46974865 | HUVEC | SE_40617 | chr3:46970726-46975377 | Left_Ventricle | SE_41619 | chr3:46971597-46975216 | LNCaP | SE_42118 | chr3:46970032-46992962 | Lung | SE_47478 | chr3:46971661-46973453 | Pancreas | SE_47478 | chr3:46973781-46974777 | Pancreas | SE_48306 | chr3:46971528-46975218 | Psoas_Muscle | SE_48684 | chr3:46971559-46975364 | Right_Atrium | SE_49453 | chr3:46971538-46972807 | Right_Ventricle | SE_49453 | chr3:46972817-46973621 | Right_Ventricle | SE_49453 | chr3:46973793-46975177 | Right_Ventricle | SE_50160 | chr3:46971539-46975248 | Sigmoid_Colon | SE_52388 | chr3:46971545-46975260 | Small_Intestine | SE_53507 | chr3:46970696-46975269 | 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 | AGGCATGAGC CACCATGTCC AGCTCTGAGT GATTTTTACT TGCTTCTCTG ATTTTCTGTA 60 GTTTCCGGAA TTTCTAATCA GTATTCTTCC TACACAGAAA CAACCAACGA AGTACTCAAA 120 AACATAAAGA GGAAACAGGC AGAGGGGCCA TAAGGCAGCA GAAGACTGTG GCAGGGTTCT 180 GAGTCAGGCA GCACCAGCAC CTCAGCTCTG CTGGTGGCCA GTCTCTGTGG CTTAGGGCCA 240 GGCTGTCCCC TAGCCAAAGG GAAGCAGAGA CCAAGCCATG CTTTTTTGGG GCTTTCTGCC 300 CCCAGAGTCT ATGGGAAGGA GGGCAGCCCA GAAAGCCCAA TGGCTTCTAA GACACTATCC 360 TTTGCACCAA ATGCCCTAGG CCACCCAAAG TCCACCCTAT ACCGGCAGCC AGTGTCTGGG 420 TGGAGCTTTG CTGTCTCTCC ACAGGAGCAG ACACATCAGC CACCTCAGTG CCTCCACTGG 480 CCCTCCCTCT GACTCAGGGA CCCCAGTGTC CCCAAAACAA GTCTAAGCTT CTTCACGTGG 540 TCCTGGCCCC ACAGCCTGCT CACCCCCTCA GCTACACACT TCCCCGTCCA TCACGCTTAA 600 AGAGCCAGCT CCAGGAGGTG GCCCTGTGGG CCCCTCCCAG TGTCCCTACT CACCCTGAGG 660 CACAGTAACC GCCCTTCTCC TGGGCCCCCT TTGCCCCACT TGCCTCTCTA CCCTCTCCAC 720 AGCAGGCCCC ACTCCATGCA CGTGGCCCTG TGTCGGCTGC ATGTCTGTCT TTCACAGCCT 780 GCCCTAAATG CACCAGGCAG CTCCAGGAGG GGCTCAGCAT ACATTGCCTC AAGCTGGATA 840 AAGGAATTCA GAAGGCACTC AAGAAAGAGC TTTATGGGTA GCCTGGGGCT CTCTGAGCCT 900 TTCAATGACT TGAGAAGACA TTTGGAAGCA AAGAAGTTGT GCCCAGCAGA GAGGGCAGGA 960 ATGTGGCTGG GCCGGGGCAG CCAACCCCTA AGCAACTTCT TTGTGGCAAA GCAACAGGGA 1020 ATGCCAAGTT TGCATTCCAT AGAGTTTCCT TCTAAAATGG GTAGCTGACC TTTTCTATTT 1080 ACTTTACTCT GCTTCAGGCC AGCTGCAGGA GCCCGGGACA TGGGCTGGCC AGGGAGGTTC 1140 AGGGGAAATC ACCCCTAGGG TGCTTTTTCA CATGTGCCAA TGAGAGGAAG CAGGTGGAGA 1200 AAGTTGATGT TCTCTGTCAA GTATAGAACC AGAGTAGAGT TCTAGAATGG CGAAATGAAA 1260 GGAAGCTTTG AGATTATGAA TCTGATCCAA CCCCATCACT GGCAAACTGG CCTCAAAGCC 1320 TACACTGCTC ATGGGGGTTT CATGGCCCCT GGTCCACTTC ACTCACTCAT GCTACCAGGC 1380 TTATCCTTTG GGGCGCTAGC CTCCCTTCTC ATCCCTTATA TCTTGAGGCT ACTCCACATT 1440 CACCTGCTGC CCTGGGCCCC TGGAGGGAGG CAGAGAGGAT AAGGACAGGA CAGTCCCACA 1500 TGGCCTGTTC CCTGAGAACA AGGTCCTCCA CCTGGCCACC CTGGTCCCTC CTGGCCATAC 1560 AGGCCCCATC AAGGGCCAGA GAGAGAACTG CTGTGAGGCA CTCCTCCTAG TAACAGACCA 1620 CAGGGAAGGC CACGCCCAGG ATGCGCCTGC AGGCCTTGCA GAGGCCACCA CTGACCAGAG 1680 AGACTGGCAA CTTTGATCAA AGAACACTTT CATTTTTAAT ATTCAGAGTA CAGAGACACT 1740 GGAGCTCTGC CAGGAAAACA CACTCATGAC ACTCAGACAT GCCCCTAATA ATCCTCTGTT 1800 TGCTTTAGGC TCTGCACATA GAGACCTACC CCTTGTCCCC AATATAAATA ACAAGGCTTC 1860 AGTTGCTGCT GCCAGAGGCC AGACTCGACA GAAGCATGAA AATGAGGGGA GAGGCAACTA 1920 CCCCAAATGA GGTACACAAC TGCTCTAGAG GCTGATCTGG TCTTTCTTTC AAGGGCCATT 1980 AAAATGTTCA AACTCCCTGA CCCGGTAACC CTGCTCTGGG GAAATTATTC CATAGAAATA 2040 GTAACAAGAC AGGAGCAAGC AAAACAAAGC ATTCTATATA CGCACGATCC TGGCAGCATA 2100 ATTCATAATA GCTACAACAC CTCTGGGATC TCTTCTGGCA GAGTGCCCTA GAGTGGCCTA 2160 AAGTACCACC AGGCTATGAG GGCAAAGGAC AATTTAGTAC AGGGATGTTT TTGTTTGGTG 2220 GTTGATATTT TTCTTTAGAA CACTCAATGG CTGGCTTTGC AGCAAATGAG ACTTTTAAAG 2280 AGCCCAGTGG CTTCCCCACT CGTGGGCAGA GGAGACTGTC CTCCAGCTGT CACCCAGCAA 2340 GGCAACTGTG GCCCCAGCCT GAAGAACGGG TACAGTGTAA GGCAATAAAA CCTCCCTTCC 2400 CTTCTCTTAT CCAGCCCACC CCAAGCCTCC TGTCCTTCTG GCCACACAAA GAGGACAAGG 2460 TCTATTGGAG CACATGACAC 2480
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