Tag | Content |
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EnhancerAtlas ID | HS104-42180 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr3:141084670-141087460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MNX1 | MA0707.1 | chr3:141084835-141084845 | TTTAATTACC | - | 6.02 | RUNX1 | MA0002.2 | chr3:141085695-141085706 | AAACCACAGAG | - | 6.14 | RUNX1 | MA0002.2 | chr3:141085680-141085691 | AAACCACAGAA | - | 6.32 |
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| Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
SE_01738 | chr3:141085024-141088687 | Aorta | SE_02348 | chr3:141083880-141089733 | Astrocytes | SE_03218 | chr3:141085077-141089138 | Brain_Angular_Gyrus | SE_04033 | chr3:141084847-141089397 | Brain_Anterior_Caudate | SE_05020 | chr3:141084656-141089895 | Brain_Cingulate_Gyrus | SE_06003 | chr3:141084757-141090012 | Brain_Hippocampus_Middle | SE_06927 | chr3:141084727-141089400 | Brain_Hippocampus_Middle_150 | SE_07904 | chr3:141084758-141089393 | Brain_Inferior_Temporal_Lobe | SE_15060 | chr3:141084789-141089312 | CD4_Memory_Primary_7pool | SE_21172 | chr3:141084779-141089349 | CD8_Memory_7pool | SE_27685 | chr3:141083798-141089529 | Fetal_Intestine | SE_28664 | chr3:141083959-141089855 | Fetal_Intestine_Large | SE_32498 | chr3:141086653-141089187 | GM12878 | SE_36772 | chr3:141083866-141089271 | HMEC | SE_37751 | chr3:141084178-141089545 | HSMMtube | SE_38384 | chr3:141084411-141089627 | HUVEC | SE_38859 | chr3:141084454-141089731 | IMR90 | SE_40294 | chr3:141085108-141089363 | K562 | SE_43497 | chr3:141086620-141090041 | MM1S | SE_44200 | chr3:141083519-141089889 | NHDF-Ad | SE_44940 | chr3:141084055-141089459 | NHLF | SE_45548 | chr3:141083332-141090208 | Osteoblasts | SE_52056 | chr3:141084656-141089224 | Skeletal_Muscle_Myoblast | SE_52489 | chr3:141084918-141088791 | Small_Intestine | SE_55659 | chr3:141083394-141090015 | u87 | SE_58225 | chr3:141085077-141086586 | VACO_9m | SE_58225 | chr3:141086598-141088278 | VACO_9m | SE_61127 | chr3:141079164-141144945 | HBL1 | SE_62287 | chr3:141079553-141134828 | Tonsil | SE_63852 | chr3:141084634-141089224 | HSMM | SE_64416 | chr3:141084544-141089108 | NHEK | SE_67139 | chr3:141086620-141090041 | MM1S | SE_67471 | chr3:141083394-141090015 | u87 |
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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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Enhancer Sequence | ACACTAAAAC CCATTGAATT GTACACTTTA AGTGAGTGAA CTTTCTGATA TGTAAATTAT 60 ACCTTAATAA TTTTTTTTAA AGAGAGGGAA TAAAATGAGA GAAATCTAAG TCAACAAGTA 120 TAGACAAGTC TTCCAAGGAA TTCCTTGCAT TCATAAAGGT TTGGTTTTAA TTACCAGCAT 180 TTAACTGCAT TTGTTGTAGC AAAGGAGGAG GATGCTCCAC TTCACGTAGA GACCAGGGAA 240 GTGCCATTGT ACTTACTTCT CTGTATCTCC AAGTGGATAT TTTTCCCAGT TCTCTGATTT 300 TATTTTCACT GTTAGTATCA ACCCCAGAGC ATATAACCCA AGAATCTGTG TCTCACTTAA 360 GCTTACTGAT CATTTCTGCT TCTTTTCTTT ATTTTTCTGT TCACATTATC CTGATAGGAT 420 GCAGGGTGAA GAAATAATCA GCCTCTGTTC ATCTTATTAG AGAAATAAAT ACCTGTGTAT 480 ATGAAGCAAG CAAGGCCACT GAGTCTTTGG GGAAACAGAG CAGGGAGGTG CCCAGAGGCA 540 TTTTCTGCAG AGAAGGAAGA AAAGAATAAA CAAGTCTTCT GCCAAAAATG CCTGGAACTT 600 AAAGCGATTT CCTCAGCCCA AGATCAGGCT GTGTGCAGAC ACTGACAGTG AACCTGATCA 660 GTTGCTGCTG CTCCCTTGAT TAAAAGCATG TAGCTTTCTC TCTTGTGAAA TTCACCTCTA 720 TAAATTCCAC CTGCCTAGGG ATTCAAACTA CATGGAACAA GTGCAATTCC TCAGAGTGGC 780 AACTGGCAGA GCTCCCAGGA ACAAGGTAGA ACTACACAAT GTCCCAGGCA TCAGAGGCAT 840 AGATTGCCTG AGTCAGGGAG AGTGGTCTCT GTGACCTGAC ACCCCACCCA CAGTGGGAAG 900 GAAAGCTGTG GGTGTGTTAT CAAGGAGGCC TCCACAAGGG GCTGGAAATT CCTGGTTTTG 960 TCTTCCTCTT GGAATGAGAC ATTTACTCTA AGAGAATCAT GGAAAAGTAC AAACCACAGA 1020 ATCATAAACC ACAGAGGGAG AAGCTACCTC GTAGGTCATT CTTATGCTGG GCCCAGATAC 1080 CCCGATAAGC AGATGTTCTC TTCTCACCAC CCCTCCTCGC CTTTGCTTGC CCACAGCCAT 1140 TGCCAGGACT CTTCCTCAGG CCCAGAAAGG CAGCTGATTC CTGGTAGGAG GGCGCTAAGA 1200 GTAGAAAGTA ACTACCATTG TCAGGTCCAG ATCTGTTCCC AATCCCTTCT CACTCCTCCT 1260 GCACTCTAAA ACCACACCAC AGTTCCAACT CTTTCTGAGT CTGGAATCTT TGAGAGTGCC 1320 GTCATGTCCT TCTTCCTGTA GCCTTCTTGT CCACCCCAGA TGGACTGACC CTCCCACCTA 1380 CATCCATGAG GCCAGAAGGC AACAAAGACA AGCGTGGACT CTGGCTCCCG CCGAGGTACT 1440 CTGTACCCCG TGGCTCTCGG ATTTTGCATC TACCACATGC CACAGGCTTG CGTCCATCCG 1500 ACCTCCCTAG TTTCTCATCC CCACTTGAAC CTGATGACTG ATTCGCCCTC CTGGCTACGC 1560 TGAGTAAGCC ACCCACTTGC CAAACCTCAG ACCTGGTGTT GACGCAGTAA GAAGGCATGA 1620 GGCCCATGTT GCCAGAACAT TCCTAATTGT TTCATTGTTT CCTTGTAGGA TGTGGTTTCA 1680 AGTCCCATCT TTGTCTCTTT TCTCCTGGCC AGGTTGCCCT TGGTCAATAT TCCTTCATTC 1740 ACTCCAGCCA CTCAGCACCG TGATTAAGAA AACAGGATGT GAGATTAGAT GATCCAGGCT 1800 CTGCCATGAA CTAACTAGCT GTGAGGCTTT AGAGAAGTGT CTTAACCTCT CTGAGCATCC 1860 ATTTCTTTCT CTATAGCATT AGGAATATTA ATAGTACCTA CCTCACAGCT TTTTTGTTGT 1920 GATAATACCA ATAAATGAAA TAATCTTCAT AAAGCACAGA GGCTTGAATG TTCACTCTAA 1980 GTATTTAATA TGTGTCCTCT ACTATTTTAT TTTACAATTA TCATTCCTTA ATTCATCATA 2040 TAATTACCAA GCCTCATGCC AGGCACTGAG ATATAAATAT CCCCTTTAAA GAGTGGTCAT 2100 GTCTTAAATC CAGGAAGAGC TAGTTCATGT TGGCACCCAG GGTAGGGAGC GAAGCCCAGG 2160 GCCACAGCAC AGAGGCAGAG GAGAATAGAC ACTGACCACC AGGAGCTGCC CGGGGATGGT 2220 GACAAAAGTG CCTTCCACCT TTCCGCATCT CTTTCAATAC CACTGCAACT CCTTGAGTAA 2280 GGTGGGCACC ACACAGAAGA AGGGGGATGG CAGAGGGGCA GTGAGAGGTC CCCAGGGAAA 2340 CACCCTCTTC TTCTTCCCTG CTTCTCTGAC AGAGCACGGC CATGCCTCTG CCATGCAGGA 2400 GGGTGATGTC CTTTGGGGAG GCCTTGTTGA ATCTGTCTGG GGCTGTTCCG GAAGTAGGAA 2460 GGGCGGCTGG GGGTGGGGAG ACGGCAGGAA TGTTCTCCTG GCCTGCTGGT CTGTGCCGGC 2520 GAGTGTGCTG AGAGGAGGGC CTCTGGACAT CAAAGGTTCC TTTTGTCCCC TTCCGAGTGG 2580 CAGGGCAGCC CGGCCCGGGC TGCTGGCGAT GACTCAGGCC TGGCCCTGAC GTCACCCACG 2640 CCCGGCCACT GGCCTCCCTC TGAAGCCAGG AAACTAGTTG GGGAGTGGCA CTCGCAGCTG 2700 CAGCAAATCT CAAAATAAAG AGGCAACGGC CTTTCTCTTC CTCTCCATCT CCCTATAGCA 2760 CACCTTTTAT TTCTTTTCTT CTTTTTTTTA 2790
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