Tag | Content |
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EnhancerAtlas ID | HS043-03618 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr1:204445720-204448470 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:204448382-204448403 | TCCTCCCCTCTTCCCTCACCC | - | 6.43 | ZNF263 | MA0528.1 | chr1:204448378-204448399 | TTCCTCCTCCCCTCTTCCCTC | - | 6 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_00064 | chr1:204447165-204449222 | Adipose_Nuclei | SE_01898 | chr1:204446732-204449955 | Aorta | SE_03188 | chr1:204445701-204449764 | Brain_Angular_Gyrus | SE_03975 | chr1:204443311-204451730 | Brain_Anterior_Caudate | SE_04850 | chr1:204441602-204452008 | Brain_Cingulate_Gyrus | SE_05834 | chr1:204441572-204454041 | Brain_Hippocampus_Middle | SE_06778 | chr1:204441694-204452486 | Brain_Hippocampus_Middle_150 | SE_07775 | chr1:204441566-204452208 | Brain_Inferior_Temporal_Lobe | SE_10905 | chr1:204440571-204455347 | CD20 | SE_24481 | chr1:204446396-204446926 | Colon_Crypt_2 | SE_24481 | chr1:204447117-204447620 | Colon_Crypt_2 | SE_24481 | chr1:204447850-204448210 | Colon_Crypt_2 | SE_25125 | chr1:204446211-204447705 | Colon_Crypt_3 | SE_25125 | chr1:204447777-204450200 | Colon_Crypt_3 | SE_25573 | chr1:204447782-204451557 | DND41 | SE_26688 | chr1:204446142-204447580 | Esophagus | SE_26688 | chr1:204447747-204450316 | Esophagus | SE_31610 | chr1:204446257-204447742 | Gastric | SE_31610 | chr1:204447799-204450438 | Gastric | SE_37407 | chr1:204442628-204450806 | HSMMtube | SE_42225 | chr1:204446187-204447730 | Lung | SE_42225 | chr1:204447736-204452375 | Lung | SE_49909 | chr1:204444472-204450053 | RPMI-8402 | SE_50149 | chr1:204447708-204450485 | Sigmoid_Colon | SE_52421 | chr1:204446127-204447357 | Small_Intestine | SE_52421 | chr1:204447689-204449720 | Small_Intestine | SE_58430 | chr1:204415099-204506026 | Ly1 | SE_59794 | chr1:204415680-204491493 | Ly4 | SE_61475 | chr1:204430067-204500813 | Toledo | SE_62377 | chr1:204415291-204492168 | Tonsil | SE_65868 | chr1:204446405-204446982 | Pancreatic_islets | SE_65868 | chr1:204448014-204448665 | Pancreatic_islets |
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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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| Number: 3 | ID | Chromosome | Start | End |
GH01I204477 | chr1 | 204446360 | 204447003 | GH01I204478 | chr1 | 204447118 | 204447620 | GH01I204479 | chr1 | 204447921 | 204451603 |
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Enhancer Sequence | AGTCTTCAAG GGCTACTAGG GATTCTGTAT AAAAACAAAT AGCCATGTCG GTCCCTTGAA 60 AGAGGAAGGG TAGATCAGGG CCTGCGTCTC TGCTACTCTG CAGCCCATCC AGGGAGAGAT 120 GGCTGGGGCC AATGCCACTA TGTCACACAA CTCTAGGGGG CACCCCACAC ATTGTATTCT 180 ATGTGAATGA TACCCCCGAC CACAAAAATG AAAACCATGT GAATGGTGCC TCCTGGAGTT 240 ATACACCTTG GTGGTTCAGG CTGCGTTCTC TCCTAATGTC CACCTCTTAG AAAACAGATG 300 GAAATCGTCC AGAAGGTCTG TTACAGCCAG TTTTCTTTCA CCACCTGCCT GCAATAATTG 360 TTAACATTTC TCCACATTTG CTCTCTTTCT TGCTCTGCTT TACCATTTAA AAGTAAGATG 420 CCCTTTGCAA AGTGTTTGTA AGAAACACTT TGCCTCTAAA AACTTCAGCC TGAATCTCTA 480 AGAGCAAGGG CATTCTCCTA TGTAAAACAC AATGCCATGA GCACACCCAC AAAACTTAAC 540 ATTGACAACA ATAATATTAT CTAATGCACA CTCCACATTT GAGTGACCGC AATTGTCATC 600 TGCGAAGCTT TAAAAATATA CACATTCCCG ACCTCTCCTC TGGAAGTTCT GACTCAGTAG 660 GGTGAGTCCC TGGATGCTGG ATGCTTCAGT AGCCCCTAAA GTGATTCAAA TGTGCAGCCA 720 GGTTTGACCC CACAGAAGAG GGTTTCAGAA CTCTCAGGAA GACAAGAAGA CCTGGGTAGA 780 GGCACCCCAA AAAGCACCAG TCAGCTGAAG AAACAAGAGG ACATGCCTAT GGCCAAGCAG 840 GTCGGTGCCA GGGTCTGAGC TGCACCAGGC ACCAAACTCA GTCTCACAGC TGCCCACAGA 900 TGGCTGAGGG CTAGCCGGGG AGGAAATGGG GTCAGGACAG AGTGACACAA TGGTTCAGAG 960 TCAAAGGATG GAAAGAAAGG AGAGGGCACT CCCTCCAGTG GAGCTGGCTC TGTTTAGTCC 1020 CTGTGCCAGA GAGGGAGGAG CCCAGGGGCC ACCACTGGAG CCAGTGGGTG GTGAGGGTTC 1080 CTGCTGTCTT GCTGGAAGGC ACCCTAACAG AATTGTTCTC CTTGGGACTG GGAGAATCTA 1140 GAGGGGTCTG GGTCATCTCT TCCCCATACC CTGAGCCACA GATTGGATCC CAAAGGGTGT 1200 TGAGTACCAG CTACATGCCA GGCCAGGCAC ATACATATCT AAAGACTACA AGTATTCAGA 1260 TGACTATGGC ACAATTCCAG GGAGCTTACA ATCTAGCAAA GGTGGCAGAC ACATACATAA 1320 AGAATTCAAT CCCCTCTTGG GGTGTAAAGC AGGAAGCAAG AAGGTACTGC ATGTCTTGGA 1380 CCATCTTCAG TGGGCAGGGA AAATGGAAAG CTCTCAAGCA AGGCGGTGAA GAATATGCAG 1440 GGTTTCAAGC CCCCAGTCTT GGGCATCCTG ATTTTCAGTA GATTTTACTA AGGGAAGAGA 1500 CTCAGCTCTA GGACTTCCCC AGGAAGGGAC CCTCAGCACT TCCCCTAAGG ACAGGCAGGG 1560 TCAGGGAGTC AGAGGCCATT AGGACTTAAA CCCTTTGGTG TCCAGGTTTT TCTCTTCAGA 1620 GAGGACCTCC ACTTCTGTCC ATCCCCCAGC ACCCACACTC ACCCATACCC CCAATCCCAC 1680 CTCCTTTGCA GCCAGGGACC CTGCCTCGCA TCTCACTCCA CACACATGCC GCTGGCTCCA 1740 ACTGCCCCTC CCACAGCCCG GCTCTAACAG GGAACATCAA CACACTGCCA GGAATCCGAC 1800 TCCTACAGCA GGGAGGTGTA TTAAGGTCAA GCAAGCCGGC TCCCCCAGCC TCCAACAGAT 1860 GTGCATCTGA TCCCTGCTTC CTTATGGAAA ACCCACAGGT TGTATACAGC TCTATAAGCT 1920 TTTTTGATGG CAGGTCTATT ACAGAATCAC ATGCATCCAT AAGGTCTTTC TCTTCTCTAG 1980 TGTGCGTGCC CTCTGGGTGC CTCTCATCTA GTTCCAAATG TGAGAAGACA AAATAACAGC 2040 TTGTGTTTTC TTCCCACTTA TACATCCCCT CTCTAGTGAC CTCTATAGCT AAACTAAAGC 2100 AGCCGCACAT GGTCTGGCAT TTCCTACCAG GACTTACTCT CCATTATTCT ACTCTCTGGG 2160 CATACCATAC CCTGGACTCT CCATTAATTT GAAGCCAAAG TGCACACAAG AGTTTAGTGG 2220 AAGTCTTTCT GGGTCCTAGA CAATCAGAGG GACAGAAGCT TGGAGCCTGT GGGACACAGC 2280 TACATAAAGT CAGGTCTGCA TGCACTGCTG ACTCCAACTC AGAGACCCCG ATTCTAGCTC 2340 AGAAACCATT TGGTCTCATG CACACACATA GAATCCTTGG AGATCATAGC TCCTGCTACA 2400 TACCCTGTAG ACTGTGGGCT CTGTGTTATG AGGAGACCAG GATGGAAGAG GTGAGGCAGC 2460 TTGTGGCTCC TCTAAAAACT TTCCTTCCTC TAGAGCTGGC AATTTTGATT GCAGGGTCAG 2520 GAACCAGAAG CTGGCAATCA ACTGAATGGA ACATTTGGCA AAGAAGGAAG AAAAGCTTTG 2580 GCAGTACGTG TATTTCTAAC CCAGGAATCA TCCCAGGAGC CAGAGCAGCC ACATCTCTGT 2640 CTGGTTCCTA CTTCCTGCTT CCTCCTCCCC TCTTCCCTCA CCCAAGAACC AATCCTTCTC 2700 ATCCAGTTCA CCCCAGGTTC CAAGGGCATG GTAGTTATGA GGGACTCCTC 2750
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