Tag | Content |
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EnhancerAtlas ID | HS053-00576 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:21660460-21663410 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:21661045-21661063 | GGAAGCGAGGGAGGCAGG | + | 6.22 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_00105 | chr1:21656775-21671990 | Adipose_Nuclei | SE_00854 | chr1:21660236-21662991 | Adrenal_Gland | SE_01643 | chr1:21660262-21662754 | Aorta | SE_02944 | chr1:21660560-21662580 | Bladder | SE_03598 | chr1:21660541-21661932 | Brain_Angular_Gyrus | SE_04518 | chr1:21660215-21662707 | Brain_Anterior_Caudate | SE_05710 | chr1:21660439-21662968 | Brain_Cingulate_Gyrus | SE_05944 | chr1:21659989-21673592 | Brain_Hippocampus_Middle | SE_08398 | chr1:21660398-21662710 | Brain_Inferior_Temporal_Lobe | SE_08982 | chr1:21661732-21662044 | Brain_Mid_Frontal_Lobe | SE_26127 | chr1:21660172-21662296 | Duodenum_Smooth_Muscle | SE_26770 | chr1:21660268-21662706 | Esophagus | SE_28486 | chr1:21660184-21661733 | Fetal_Intestine | SE_29337 | chr1:21660165-21661628 | Fetal_Intestine_Large | SE_31433 | chr1:21660241-21662714 | Gastric | SE_42174 | chr1:21660216-21662835 | Lung | SE_44380 | chr1:21660201-21662771 | NHDF-Ad | SE_45045 | chr1:21660317-21662260 | NHLF | SE_46660 | chr1:21660404-21662544 | Ovary | SE_47592 | chr1:21660300-21662327 | Pancreas | SE_48583 | chr1:21660227-21662766 | Right_Atrium | SE_50108 | chr1:21660245-21662740 | Sigmoid_Colon | SE_52633 | chr1:21660234-21662726 | Small_Intestine | SE_53334 | chr1:21659249-21662815 | Spleen | SE_54639 | chr1:21660115-21662959 | Stomach_Smooth_Muscle | SE_54639 | chr1:21663094-21674002 | Stomach_Smooth_Muscle | SE_56171 | chr1:21660198-21662906 | u87 | SE_65263 | chr1:21660486-21671744 | Pancreatic_islets | SE_67931 | chr1:21660198-21662906 | u87 | SE_68932 | chr1:21660639-21662409 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 21660622 | 21661187 | chr1 | 21661800 | 21662962 |
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Enhancer Sequence | AGGTGCTACC ATCATCCCAT TTCATAGAGG AGAAAACCGA GGCTCAGAGA TGGTCACTCA 60 CCAAAGGTCA CCCAGCTGGG ACTAAGTGAC AGAGCTGGGA CTACAACCCA CATCTGTCTG 120 GCTCCAAAAC CTCCATACCT CCATCTTATC TAGAAAGAGT GCTGGATGAG GAGTCTAGAA 180 TCAGGGTCTA AGTCCTGCCT CTAACCTGCT GTATAGCCTC AGGTAAGTCT CTTTCCCTTT 240 GTGAGCCTTG GTCTGCCCTA TGAGGAAGTT GGCCTAGATG ACCTCCAAGT CCCACCTCCT 300 GTGACTCTGT GAGCTCTCAT GCCCTCCTCT CTCTGGCTCC CAGCCACCAC ACCGGAAGCC 360 CAACAGGATG CCGAGTAACC ACCCACTGAA CACTCAGGGG CGAAGGAAGA TGAAGTGCCG 420 CTTTCTCATG GCCATCTTCC ACCAGACCAG CCCAGGAAAC AAGGAACCAC AAAGCCACAG 480 GATTCCCTCC AGCGTGGCCG TGTGAACAGC AGCCCTGGAG CAGAGGGGCT GGGCATCCCC 540 TTGCGGCCAT CACTTCCTAT GCCCTCACTT CTCGGCAGGG TGTGCGGAAG CGAGGGAGGC 600 AGGCTCCAGC TCAATGCCCT CTGGCTCTGT TTCTCTGGGT CCCCAGGGGC TGGGACGGTG 660 GGAACTGGTC ACTCTGGGAG AATCCCAAGC CCACCCCGGA AGGCTGAGTT GAAGTGGAGG 720 TTCAGACAGG TCTGTCTGGC TCCACAGGTA ACTTTTGCCC ACTGTGCTCT GCTGCCAGCA 780 AGGTCTCGAA GCATCTGGGA TGCCTGGCTA CCTCTCTCCC ATCCCTGAAG TAGCAGCCAA 840 AATCCCAGAT CCTGCAGAAA CCTACGCCTC CTCAGCCTCA GGACAGACGA ATATCCTGAG 900 GCCCGCGCTC CTGCCTCCCT CCTGCCCCCT ACAGTCCATG CTCTACACAG CAGCCAAGGT 960 CTTTCCAAAC AGAAACCAAG CCCAGTCGCC CCTCAACGTG GGGTCCTCCA GTGGCTTCCC 1020 ACCACTATTA GAACGAAATG CTGACCCCTG CCCCACAGAC AAGGCTGTCC ATGGCTTGCC 1080 CCTCCAGGCC CACCTCTCCC TAGCCTTCCC TCCACCCTCC ACTGCCTCTG CCCGGCCACA 1140 CCAGCGTTCA CCCCCTACAT GTGCCAAACT TGCTGTTCCG GCAGCCGGGA ACTCTCATCT 1200 CCCCCGCCCC CGTCTTTGCC CGGCTGCCCC CTCCTCAACC TTCATGTCCC AGCTCAGACA 1260 TCACCTCCTT TCCTGGCCGC TCCTCTAGAG CGGCCCCCTC CCCTCACAGC CACTCTCCAC 1320 CACATCGCCC TGTTTTGTCT CCTTTCTTCT CTCGGAGCGA TCCTTCTGGT GGGTGGCTTT 1380 GCCTGTTTGG TCTCCAGCTT CCTCCCCTAG AGTGCAGCTC CTTAGGGGCA GGCATGTGAC 1440 TGCTCCATTC TCTTCTGTCC CCACAATGAG GCAGGGCCTC CTTGGGTGCT CACAACCCTG 1500 AAGATGAGGA CGCTGCAGCC CTGAGAGGTG GATTGAGCCG CCCAAAGTCC CAGAGCCAGG 1560 GAATAGCAGG GTTCAGACCG AGGGCGACCT GATGCCAAGC CTCAGTGGGT GGGGGGCTCT 1620 CACGGCTGGG GGCCTACTCT GGAGGGCTCT CACCCAGGGT GGACAGAGTC GCAGTGAGGC 1680 TCTTAGGGCG GGTACCAAGA ATGAAGGGCC CACCAGCTTT CCCAAATGGT CCTTCTGCAA 1740 GCTACAGGCC AGCTGAGCTC CTGCCTGGGG TGGGTGAGAC CCTGGGGGTG AAGAGGCACC 1800 AAACACCAGG AGCAAAGGCT CCCAAATGAG GGAGACCACA GACACAGGGA GCTGGGAAGC 1860 TTCGACCCAC CCAGTGCTTG ACGGAAGGGG AAAGTGAGGA CTATGGAGGG GAAGGGACTT 1920 GCCTGAGGTC ACACAGCCAA TCAGTGGGTC TCCAGGGAGG GAGGCCCTTC CCTACCCTGC 1980 AGAACAGCAG GCGAAGCCCA AAGCCCAGGG TCTGGGCAGA GTGCCAGCCC AGAACTGCCA 2040 GGCCCTGGGG GCAGGGGCAG GGCTACAGAG TGAATCTGGG GCATTAAGAC AAAGAAAGGA 2100 CTCAAATTTC TTCCTTCTTT CAAAAAACAC TTGAGACAGG CAGTGTCTCA TACCTGTAAT 2160 CCCAGCACCA TGGAAGGCTA AGGTGGATGA ATCACTTGAG CCCAGGAGTT CAATACCAGC 2220 CTTGGCAACT AGTGAGACCT TGTCTCTACA AAAAAATATC AGAAAATTAG CTGGGTGTAG 2280 TGGTGCACCT GTGGTACCAG CTACTCAGGA GGCTGAGGTG GGAAGATCAC TTGAGCCCAT 2340 AAGTTCAAGG CTGCAGTGAG CTGTGTTCAT GCCACTGTAC TCCAGCCTGG GTGACAGAGT 2400 GAGAGACCCT GTCTCAAAAC CAAAACAACA AAAAACATTC ACTGAGGCCG GGCGTGGTGG 2460 CTCACACCTG TAATCCCAGC ACTTTGGGAG GACGAGGTGG GCAGATCACC TGAGGTCAGG 2520 AGTTCGAGAC CAGGCTGGCC AACATGGTGA AACCCCGTCT CTACTAAAAA TACAAAAAAT 2580 TAGTCGGCTG TGGCCGGGCG CGGTGGCTCA CACCTGTAGT AATCCCAGCA CTTTCGGAGG 2640 CCGAGGTGGG CGGATCACGA GGTCAGGAGA TTGAGACCAT CCTGGCTAAC ACAGTGAAAC 2700 CCTGTCTCAA CTAAAAATAC AAAAAATTAG CCAAGCGTGG TGGCGGGCAC CTGTAGTCCC 2760 AGCTACTCAG GAGGCTGAGG CAGGAGAATG GCGTGAACCC AAAAGGTGGA GCTTGCAGTG 2820 AGCCGAGATC GCGCCACTGC ACTCCAGCTT GGGCGACAGA GCGAGACTCC AGTGTGGGGG 2880 ACAAAGCGAG ACTCCGTCTA AAAAAAAGAA AAAATTTGCC TGGTGTTGTG GCAAACGCCT 2940 GTAATCCCAG 2950
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