Tag | Content |
---|
EnhancerAtlas ID | HS082-37537 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr9:127027740-127031170 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gabpa | MA0062.2 | chr9:127028731-127028742 | CCGGAAGTGAC | + | 6.14 | MYCN | MA0104.4 | chr9:127030909-127030921 | GGCCACGTGGTG | + | 6.07 | MYCN | MA0104.4 | chr9:127030909-127030921 | GGCCACGTGGTG | - | 6.07 | Nkx3-2 | MA0122.3 | chr9:127030559-127030572 | ATTAAGTGGTTTA | - | 6.92 | RUNX1 | MA0002.2 | chr9:127029896-127029907 | TTCTGTGGTTT | + | 6.32 |
|
| Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
SE_01861 | chr9:127028027-127030811 | Aorta | SE_02294 | chr9:127028292-127030548 | Astrocytes | SE_03002 | chr9:127027842-127028520 | Bladder | SE_04593 | chr9:127028891-127030342 | Brain_Anterior_Caudate | SE_06625 | chr9:127028933-127030320 | Brain_Hippocampus_Middle | SE_09789 | chr9:127025946-127031287 | CD14 | SE_23712 | chr9:127027894-127031158 | Colon_Crypt_1 | SE_24006 | chr9:127027853-127028277 | Colon_Crypt_2 | SE_24006 | chr9:127028617-127030420 | Colon_Crypt_2 | SE_26169 | chr9:127028464-127031167 | Duodenum_Smooth_Muscle | SE_27460 | chr9:127028546-127029502 | Esophagus | SE_27460 | chr9:127029577-127030298 | Esophagus | SE_29975 | chr9:127028907-127030325 | Fetal_Muscle | SE_31765 | chr9:127027836-127031189 | Gastric | SE_36996 | chr9:127027502-127031245 | HSMMtube | SE_38009 | chr9:127027450-127031685 | HUVEC | SE_38868 | chr9:127028106-127031763 | IMR90 | SE_42506 | chr9:127027674-127031138 | Lung | SE_44293 | chr9:127028727-127031058 | NHDF-Ad | SE_44809 | chr9:127028276-127028828 | NHLF | SE_44809 | chr9:127029011-127029548 | NHLF | SE_45648 | chr9:127018281-127031420 | Osteoblasts | SE_47283 | chr9:127027822-127030793 | Panc1 | SE_47557 | chr9:127029471-127030049 | Pancreas | SE_50283 | chr9:127027697-127031101 | Sigmoid_Colon | SE_51779 | chr9:127028340-127030620 | Skeletal_Muscle_Myoblast | SE_52726 | chr9:127027715-127030348 | Small_Intestine | SE_54297 | chr9:127028449-127030673 | Spleen | SE_59258 | chr9:127016097-127031007 | Ly3 | SE_60141 | chr9:127018983-127030974 | Ly4 | SE_60448 | chr9:127019058-127056389 | DHL6 | SE_63558 | chr9:127028209-127030812 | HSMM | SE_65907 | chr9:127028092-127030478 | Pancreatic_islets |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 127028281 | 127028331 | chr9 | 127028725 | 127030267 |
|
Enhancer Sequence | CAGTGAGCCG AGATGGCGCC ACTGCACTCC AGCTTGGGCA ATAGAGTGAG ACTCCGTCTC 60 AAAAAAAAAA AGACAAGTTT GTCTTGCTTT AAAAAAAAAA ATACCTCTCC TTTTACAGAT 120 GGCGACACTG AGGCCCAGAG AGACATCATG ACCAGCCTCA GGTCCCACAT GCAGCCTGCT 180 GCTCTGTAGC CTAAATCAGA TCACTGTCCC AGCTTTCAGG TCAAGGCTCT GGTTGTGACA 240 CCTGGGCCTG GACTGCGGGT GAAAAGTTTT GATGCAAAAA CACAGACCGT CCATTGTCCT 300 ATGGGCTAAG TGGACTCCCT TCTGCTAACC AGAGATGCTT GTGCTGGCTG GTGTGTGGCA 360 CGTTATCTCA TTCTTTCATG ACGTATGTCC GGATGGAAGT CCTGGGTCAG GCATTGTGCT 420 GGGAGCCCAC ACGAAGACCC TCTAATGGCC CCACCCATTG GCCTCTCACC ACCTGGTGGG 480 GACAGAGGCT GTCACAACCC CTTCTTAGGT GCTCTTGATC AATTTGCAGG TGGCATTTTT 540 TGGGATGTAG TCTCTGGGGA AGTAGGAGAG CTTCCGGCAG TGAGGGGTGT TTGAACCCAC 600 CTGGAGGGAG ACGTGGGGTT TGCCAGAGGG CTGAGAGGGC TGGGGTGAAG GGCAGGTAGA 660 CCCCAAGGTG GAGAGGCAGG TGGGGCCGGT GGGTGAGAGG TGGGGCTGTG GAACTTCCTC 720 CTGCTTCTTT GGCCTTTGCT CCTGTCGGTA GATGGCCTTA CCAGGCACTT ACTGTGGGCC 780 ATGTTCTAAT CTAACCCTTA ACCTGAGGGA ACTCACTTCA TCCTCCCAGT GATGCCGTGA 840 TGTGGGTATC GTTCTGCCCA TTTTATAGAT GAGGAAACAG AGACCCAGAG AGTCCAGGAT 900 CTGTGGTGCT TGACGAGCAT CAGCCTGAGT GCTGTGAGGA CACCCACAGC ATGGGGGTCT 960 GAGCTGAAAA TTGGAGGACA GAGGCTGCCC TCCGGAAGTG ACCAGGATGT GCCCTCAGGA 1020 AGTGACCAGC TGCCCAGCTC AGGACCTGTG TGAGGGCCCC CAGGCAGCTG GAAGGAACAG 1080 TGTGCACCCA GGTACCATGC CAGGGCCCCT GAGCATCCGT CTTGTCATCG CATAGTTGTA 1140 ACCTGCCTCA CAGACTGAAC ATGCACTCTA GAAGGGGATG GGACTTGGTC TGTGGACCAC 1200 AACAGTGTTC TCCATGGCCA GCATTGTGCC TGACACATAG GAGGAGCTCA ATTAATATTT 1260 GTTGAGTGAA TGGGAAGTTT TAAGTAGGCA CGCGGCCGGA TCCTTGGAGA ATGTTTATAT 1320 GGAGTGAACG AATCTGTTAG CAAACGTTCC TCACTCCCCT CAGTGGGCTG TGCAGGGCTG 1380 TATTGAGCTG AGCTGGCCCT TCCCTGGGAG AAGAGGTTTC TTAGAGAAAT GCTCATCCTC 1440 GAATTATTCC AATGAGGAGG AACCTAAGCC CAGAAGGGCT CTACCTCCCA GAGTTACAGG 1500 CTCTCCTTCC TATGCCCCTT CCCTGCCGAG GCAGCTCCCA CATGTCTGCA TAGGAGGGCT 1560 TTGGGTTGGA ATGGGTCAGT GCTGTGTCTT AAAGCTGCAT TTTCTACCAA GCACACACTT 1620 TGTTTAGAGG GCATATCTTT TGGGGTTGCT TTGAGGAAAG GCTAACCAAG CCACCTCTGA 1680 GCACAGACAT GACTTTTTGG CAAATGAGCA GGACCCCAGA TTACACCCCA TCTTAGAAAG 1740 TAGGAAACCC AGCATTGAAA GAGGAAAGAT TCTGCAGCTG ATGTGGCCTT GGCGGGCCAC 1800 CAGCGTGGGT GCCCAGATGG CAGGATCACT GGGCACCACA TGGCACACAG AAGAGAGCAA 1860 AGGAGAGGGA GTCCGCCCCT GGGCTTGGCA GGTCCGGTCG AGTCCGCCTG GATTCAGTTA 1920 CAACAGGACC TCGAGTGGGC ACGGCGTGCC GGACTGAGTC AGTGTGTGTA CATTTCCTTT 1980 GTTCGTCTCC TCCGGGAATG TAGTGGCCTT TTGTGTGTGT TTTAAATGCC AGCCTCCTTA 2040 CCTAACCCAA GAGGAAATGA GGACTGGGTT TTTGTCTGTG CAGACGCTGG GACAAGTGTG 2100 GGAGCCGCCT GCTCTTGGAG CCAGCCTAGT GGTGACAGCG TGGCATTTGG AAAACATTCT 2160 GTGGTTTTCT CCAAGGGGTG ATGGGCACAC CAGGTGCTGG GCCGCCCCTG AGCTGGCCAC 2220 TGGGACCCTG AAATGAGGAA GCCCTGTGAC CAGGTTTCAT GATGCCATTC AGCAAGGGAC 2280 GGCTGAGCAC CACATGCCTT CTTGGCCCCT GGGGAAACAC ACAGGAATCA GATGAGGTCC 2340 CTGCCCCGTC TTCCTGGGGA AACATGCAGA GAAAATACTT GTACTCTGAG CTAACACCTT 2400 TCACTCGCAC AGACCTTTAT GGTGTTCTGT GTCTTCAGAC ATTGATCACC TGTAGGTGAG 2460 ACACATCATG GCCCCACTTT CCAAACTCCC AAACGGGCTG TGATCTGTAG AAGTATTTAG 2520 TGCCATTCAG GGACAGGAGA GATGGTTTGG AAGATGCTGT CTGCTGTGCG AAGTCTCTGG 2580 ATGCTCAAAT GGCTTATGGG GTGGCATCTT TGAAATTACC CAGTCCTGAA AATTTCAGGA 2640 CATATGGTCA CTGTGATGTG CTAATGTTAG CAATTGAGAT ATTTAATGAC CCAGAAAAAC 2700 CCCTTTTCCT ACCCAGTGCA GGTTACTGGA GAGCCTTTAT TTCTCAGGAG GAGGGTCTTA 2760 CACAGTGTAA TTTGGACCAG CAGATAGGGA GTCATTATCC CTCATTCATT TATTAGCTAA 2820 TTAAGTGGTT TATCTGGTCA CACATTTACT CCTTCAATTG CCATTCATCC AGCACTGTTT 2880 GCTGATGTAC CTGGCCTGGT GCTGGGTACT GGGGGTGGAA TGAAACAGAA CAAATATGAC 2940 TGAGTCCCTA CTGTGTGCCA GCCCATAGGG TGTGCTGTGT GCCACAGGTG AATGCATTCA 3000 CTTCCCAGTG GACATTTAAC AACCACCTAC TGTGTGCAGA CTCATGGAGA TGCAGAAATG 3060 CAAATGGCAC AGTCCGTAGT GGTTTGGACA CTTGTGGTGT TTTGATGGGG TCTTTAGTCC 3120 TGGCTCTCTC TCTGCTTGCT GTGATATACC CAGTCAGCCA CTGTTCACAG GCCACGTGGT 3180 GACGTCCCCA GAATGAACCA GAAACAATCC AGATGCCCCA GGAACCGACG TGAGAACAAG 3240 GCATCCCCTT CACACGTTGT GTCTCAGTTC AGCGTCTTGC CACCACCCAG CATTTTGAGA 3300 CAGAATGTGA GATCGCGTGG TTGGCTAAAT ACATAAATAT TTTATGTCTC GATATTCTGA 3360 AAATGAAGCC CAAATGCACA GAACTGCAGC ACATCAGTGC TATAGATCAT ATGTTATAAT 3420 AATCTGATGA 3430
|