Tag | Content |
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EnhancerAtlas ID | HS176-27504 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr3:141084720-141087460 |
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 | TGTAAATTAT ACCTTAATAA TTTTTTTTAA AGAGAGGGAA TAAAATGAGA GAAATCTAAG 60 TCAACAAGTA TAGACAAGTC TTCCAAGGAA TTCCTTGCAT TCATAAAGGT TTGGTTTTAA 120 TTACCAGCAT TTAACTGCAT TTGTTGTAGC AAAGGAGGAG GATGCTCCAC TTCACGTAGA 180 GACCAGGGAA GTGCCATTGT ACTTACTTCT CTGTATCTCC AAGTGGATAT TTTTCCCAGT 240 TCTCTGATTT TATTTTCACT GTTAGTATCA ACCCCAGAGC ATATAACCCA AGAATCTGTG 300 TCTCACTTAA GCTTACTGAT CATTTCTGCT TCTTTTCTTT ATTTTTCTGT TCACATTATC 360 CTGATAGGAT GCAGGGTGAA GAAATAATCA GCCTCTGTTC ATCTTATTAG AGAAATAAAT 420 ACCTGTGTAT ATGAAGCAAG CAAGGCCACT GAGTCTTTGG GGAAACAGAG CAGGGAGGTG 480 CCCAGAGGCA TTTTCTGCAG AGAAGGAAGA AAAGAATAAA CAAGTCTTCT GCCAAAAATG 540 CCTGGAACTT AAAGCGATTT CCTCAGCCCA AGATCAGGCT GTGTGCAGAC ACTGACAGTG 600 AACCTGATCA GTTGCTGCTG CTCCCTTGAT TAAAAGCATG TAGCTTTCTC TCTTGTGAAA 660 TTCACCTCTA TAAATTCCAC CTGCCTAGGG ATTCAAACTA CATGGAACAA GTGCAATTCC 720 TCAGAGTGGC AACTGGCAGA GCTCCCAGGA ACAAGGTAGA ACTACACAAT GTCCCAGGCA 780 TCAGAGGCAT AGATTGCCTG AGTCAGGGAG AGTGGTCTCT GTGACCTGAC ACCCCACCCA 840 CAGTGGGAAG GAAAGCTGTG GGTGTGTTAT CAAGGAGGCC TCCACAAGGG GCTGGAAATT 900 CCTGGTTTTG TCTTCCTCTT GGAATGAGAC ATTTACTCTA AGAGAATCAT GGAAAAGTAC 960 AAACCACAGA ATCATAAACC ACAGAGGGAG AAGCTACCTC GTAGGTCATT CTTATGCTGG 1020 GCCCAGATAC CCCGATAAGC AGATGTTCTC TTCTCACCAC CCCTCCTCGC CTTTGCTTGC 1080 CCACAGCCAT TGCCAGGACT CTTCCTCAGG CCCAGAAAGG CAGCTGATTC CTGGTAGGAG 1140 GGCGCTAAGA GTAGAAAGTA ACTACCATTG TCAGGTCCAG ATCTGTTCCC AATCCCTTCT 1200 CACTCCTCCT GCACTCTAAA ACCACACCAC AGTTCCAACT CTTTCTGAGT CTGGAATCTT 1260 TGAGAGTGCC GTCATGTCCT TCTTCCTGTA GCCTTCTTGT CCACCCCAGA TGGACTGACC 1320 CTCCCACCTA CATCCATGAG GCCAGAAGGC AACAAAGACA AGCGTGGACT CTGGCTCCCG 1380 CCGAGGTACT CTGTACCCCG TGGCTCTCGG ATTTTGCATC TACCACATGC CACAGGCTTG 1440 CGTCCATCCG ACCTCCCTAG TTTCTCATCC CCACTTGAAC CTGATGACTG ATTCGCCCTC 1500 CTGGCTACGC TGAGTAAGCC ACCCACTTGC CAAACCTCAG ACCTGGTGTT GACGCAGTAA 1560 GAAGGCATGA GGCCCATGTT GCCAGAACAT TCCTAATTGT TTCATTGTTT CCTTGTAGGA 1620 TGTGGTTTCA AGTCCCATCT TTGTCTCTTT TCTCCTGGCC AGGTTGCCCT TGGTCAATAT 1680 TCCTTCATTC ACTCCAGCCA CTCAGCACCG TGATTAAGAA AACAGGATGT GAGATTAGAT 1740 GATCCAGGCT CTGCCATGAA CTAACTAGCT GTGAGGCTTT AGAGAAGTGT CTTAACCTCT 1800 CTGAGCATCC ATTTCTTTCT CTATAGCATT AGGAATATTA ATAGTACCTA CCTCACAGCT 1860 TTTTTGTTGT GATAATACCA ATAAATGAAA TAATCTTCAT AAAGCACAGA GGCTTGAATG 1920 TTCACTCTAA GTATTTAATA TGTGTCCTCT ACTATTTTAT TTTACAATTA TCATTCCTTA 1980 ATTCATCATA TAATTACCAA GCCTCATGCC AGGCACTGAG ATATAAATAT CCCCTTTAAA 2040 GAGTGGTCAT GTCTTAAATC CAGGAAGAGC TAGTTCATGT TGGCACCCAG GGTAGGGAGC 2100 GAAGCCCAGG GCCACAGCAC AGAGGCAGAG GAGAATAGAC ACTGACCACC AGGAGCTGCC 2160 CGGGGATGGT GACAAAAGTG CCTTCCACCT TTCCGCATCT CTTTCAATAC CACTGCAACT 2220 CCTTGAGTAA GGTGGGCACC ACACAGAAGA AGGGGGATGG CAGAGGGGCA GTGAGAGGTC 2280 CCCAGGGAAA CACCCTCTTC TTCTTCCCTG CTTCTCTGAC AGAGCACGGC CATGCCTCTG 2340 CCATGCAGGA GGGTGATGTC CTTTGGGGAG GCCTTGTTGA ATCTGTCTGG GGCTGTTCCG 2400 GAAGTAGGAA GGGCGGCTGG GGGTGGGGAG ACGGCAGGAA TGTTCTCCTG GCCTGCTGGT 2460 CTGTGCCGGC GAGTGTGCTG AGAGGAGGGC CTCTGGACAT CAAAGGTTCC TTTTGTCCCC 2520 TTCCGAGTGG CAGGGCAGCC CGGCCCGGGC TGCTGGCGAT GACTCAGGCC TGGCCCTGAC 2580 GTCACCCACG CCCGGCCACT GGCCTCCCTC TGAAGCCAGG AAACTAGTTG GGGAGTGGCA 2640 CTCGCAGCTG CAGCAAATCT CAAAATAAAG AGGCAACGGC CTTTCTCTTC CTCTCCATCT 2700 CCCTATAGCA CACCTTTTAT TTCTTTTCTT CTTTTTTTTA 2740
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