Tag | Content |
---|
EnhancerAtlas ID | HS053-17624 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr17:76385680-76388550 |
SNPs | Number: 3 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MSC | MA0665.1 | chr17:76386414-76386424 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr17:76386414-76386424 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr17:76386414-76386424 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr17:76386414-76386424 | AACAGCTGTT | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr17:76387247-76387262 | TGAACTACTGACCTC | - | 6.07 | Nr2f6(var.2) | MA0728.1 | chr17:76385915-76385930 | TGAACTCCTGACCTC | - | 6.22 | PBX1 | MA0070.1 | chr17:76387405-76387417 | TTTGATTGATTG | - | 6.18 | RARA | MA0729.1 | chr17:76387244-76387262 | TCTTGAACTACTGACCTC | - | 6.1 | STAT3 | MA0144.2 | chr17:76386545-76386556 | TTTCTGGGAAG | + | 6.02 |
|
| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_00336 | chr17:76386145-76387299 | Adipose_Nuclei | SE_02571 | chr17:76385876-76387594 | Astrocytes | SE_02571 | chr17:76387662-76388894 | Astrocytes | SE_09402 | chr17:76385796-76387196 | CD14 | SE_09402 | chr17:76387807-76389155 | CD14 | SE_29662 | chr17:76385844-76387171 | Fetal_Muscle | SE_31461 | chr17:76385841-76386644 | Gastric | SE_31461 | chr17:76386651-76387098 | Gastric | SE_36965 | chr17:76385256-76389565 | HSMMtube | SE_38195 | chr17:76385655-76388714 | HUVEC | SE_39141 | chr17:76385846-76387683 | IMR90 | SE_40802 | chr17:76385837-76387196 | Left_Ventricle | SE_42104 | chr17:76385811-76387176 | Lung | SE_44143 | chr17:76385692-76388854 | NHDF-Ad | SE_44787 | chr17:76385822-76389178 | NHLF | SE_45620 | chr17:76385671-76389091 | Osteoblasts | SE_50089 | chr17:76385808-76387604 | Sigmoid_Colon | SE_51088 | chr17:76385682-76386847 | Skeletal_Muscle | SE_51835 | chr17:76385676-76389059 | Skeletal_Muscle_Myoblast | SE_52389 | chr17:76385878-76387198 | Small_Intestine | SE_53327 | chr17:76385698-76387613 | Spleen | SE_55689 | chr17:76385830-76387298 | u87 | SE_55689 | chr17:76387543-76388371 | u87 | SE_58926 | chr17:76309354-76389031 | Ly3 | SE_63627 | chr17:76385676-76389073 | HSMM |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 76386233 | 76387019 | chr17 | 76387917 | 76388443 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I078387 | chr17 | 76383643 | 76389156 |
|
Enhancer Sequence | CGTGAGCCAC CGTGCTCGGC CCCTTTTTTT TTGAGACGAA GTCTCACTCT GTCACTCAGG 60 CTGGCATGCA GTGGTGCAAT CTTGGCTCAC TGCAACCTCC GCCTCCTGGG TTCAAGCGAT 120 TCTCCTGCTT CAGCCTTCCA AGTAGCTGGG ATTACAGGCA TGTACCACCA CACCCAACTA 180 ATTTTTTTGT GTTTTTAGTA GAGACGGGGT TTCACCATAT TGGCCAGGCT GGTTTTGAAC 240 TCCTGACCTC AAGTTTTCTT CCCGCCTTGG CCTCCCAAAG TGCTAAGATT ATAGGCATGA 300 GCCACTGTGC TGGGCTGCGG CTCTCAGCTT CTTTGAAGGC CGCGTGTGGA CTGACCACAT 360 GACCTGGAGC AGTACAGCGG CACCTGATTT TTGGATGGTC TGAGAGATGG CAGAAATGCT 420 GTGAGGCAGG GGAGACATTG ATTTTATGCT GCTGTTGCCT GTTCCCCCGC CCCCGACCAT 480 GTTTCATTAG TGAATATGAG ACTCTAGGCC CCTTGGGGCC TCGGGTTGAT GGGTTGCTGT 540 GCACCTTTCC CATTGTCCGG TGGTTTCTGC TGCACTGAAG GGTCCTTCGC TCTCCTCTCT 600 TGAGCTTTGC AGGAGGGTGG CCCAGGATTT GGGAAACCCA GGCAGCGAGC CCTGCGTTAC 660 ACATCTAGGC CCTTCATCTG CAAGCTGATG CCTGTGAGTG TCATCACCCC CTCTAGAGAC 720 GGGGGTGGGG GAGGAACAGC TGTTTCCCAC CTCTGCACTG GGTGGCCACG GCCAGTCGCA 780 GACTTCCAGG ATCCACAGAG GCAGCACCTT CTGCTGTTGA CTAAGGTTTT CTTGGCAGTG 840 AATCGGCAGT GACAGACCGG TGGGCTTTCT GGGAAGTGCA GCTGTGGGCC ATCTGTTGTC 900 TGTGCAGGGA CATTTACGAA GCCTGGGAAG ATTGAGGGCT TTATCATGAA GCAAGTGAGT 960 GAAATCATCT TCCTGGAATT TGTGGCCATT CAGGCCTTGG GATGTTTGAG CATCCTCTCC 1020 CCCACGTCCC TCTTGAGGTC ACACACTGAA GAGGATTTTC CTGCTGCTGT TTGCAGGACT 1080 AGGATTCATA GTAGGTCAGG TCTGTGTGGG GCTCTGGGTG TGCGGTCCCT CCACCCCCAT 1140 CTCCCGCAGG TTTTTAGTCA TTGAGCAGCA GAAATGAAGT TCTGTGGGCA GAAATTCATC 1200 TCCTTCAGCC TTGGCCTCAG TGGAGTGTGG AGTCCGCTGG GGTGCAGCTT TATGTGGTCG 1260 AGCTAACACT GGCCAGAAAT GGTGTGTGAC CCCACCAAAC AGGATGTGTC TGATGGTGAA 1320 TGAGTATGGC TCATCATCAC TCTTTTTTTT TTCTTCTTTG AGATGGAGTC TTGCTCTGTT 1380 GCCCAGGCTG GAGTGCAGTG GCACCATCTC AGCTCACTGC AATCTCCGCC TCCCAGGTTT 1440 AAGCGATTCT CCTGCCTCAG GCTCCTGAGT AGTTGGGATA ACAGGCATCT GCATCATGCC 1500 CGGCTAATTT TTTTGTATTT TTATTTTTAG TAGAGATGGG GTTTCACCAT GTTGGCTAGG 1560 CTTATCTTGA ACTACTGACC TCAGGTAATC TGCACGCCTC GGCCTCCCAA AGTGGTGGGA 1620 TTACAGGCGT GAGCCACCGT GCGCGGCCAC GGCTCATCAT CACTCTTGAG AGGAGCTCAT 1680 TTGCTCCCGT CTCTCCCTGC TCCAGCTTTT CTTTCCGAGT CTGATTTTGA TTGATTGAGA 1740 CAGGGTCTCG CTGTGCCACC CAGGCTGGAA TGCAATGGCA TGATCATAGC TGGGAGAACA 1800 GCCTTGAACT CTTGGGCTCA GGAGATCCTC CTGCCTCAGC CTCTTGAGTA GCTGGGACTA 1860 CAGGTTTGTG CTACCATGCC CAGGTAACTT TTTTTTGAGA CAGAGTCTCG TTCTGTCACC 1920 CAGGCTGGGG TGCAGTGGTG CGATCTCGCC TCACTGCAAC CTCCACCTCC CTGGTTCAAG 1980 CAATTCTCCT GCCTTAGCCT CCCAAGTAGC TGGGACTACA GTCACATACC ACCACGCCCG 2040 GCTAATTTTT GTATTTTTAG TAGAGAGGGG GTTTCACCAT ATTGGTCAGG CTAGTCTCAA 2100 ACACCTGACC TTAGGTTGTC TACCTGCCTC GGCCTCCCAA AGTGCTGGGA TTACAGGTGT 2160 GAGCCACTGC ACCCAGCCTG CCCAGCTAAT TTTAAACAAT TTTTTGTAGA CACTGGGTCC 2220 TGCTATATTG CTCAGGCTGG TCCTGAGCTC CTTGACTCAA GCATTCGTCC TGCCTTGGCC 2280 TCCCAAAGTG CTAGGATTAT AGGCCTGAGC CACCATGCTC GGCATAAATT GGATTTTTAA 2340 AGAGAAAAGT TTCTTTTTCT GGGTGCTTCC TTGAATAGAA ATCTTGTTTA TCTCATGAGT 2400 CATAAAGCGG GGCATCTGGG CTGTAATCAT CAGACTTCTG CCAGACTTAC CCTTCTGCTA 2460 GGTGTCTTTT AGTGGTGGCT GCAGGCAAAT ATTTTTGAGG TAGATTCATT AGAACGTTGC 2520 CATGTGGTAG CTAACCATGT GGTAGCTTTT ATGAGTTTAC TTGTGGATGC TCTAAATTTG 2580 GTTCCTGAGT TGTTTGGAAT TAAAGTTTGG GATTTATCTA TAGGTATTGA CACTTCTCAA 2640 GTTGCTCAGT TAGTAGGCTC TTTAAGGAAT AAGAGGAAAG GGGGCTGAAG GAAAAATCCT 2700 TTAGCAGAGC TTGAGTTGGG CTCACTTTTT AAAATGTTCT AGAAAATCTG ACATTCATAA 2760 CACAAGCAAC GCACCCATCT CCCAGCCCCT CTTCACTCCC CAGTAACTGA GGGGGGCTTC 2820 TGCAGAAGTA TTTGAGGTAT TTGAGGTGTG ACCCAGTTGC ATATTTCTTT 2870
|