Tag | Content |
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EnhancerAtlas ID | HS104-05168 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:205261360-205264590 |
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) |
FOSL2 | MA0478.1 | chr1:205263880-205263891 | GGATGACTCAT | + | 6.62 | IRF2 | MA0051.1 | chr1:205263976-205263994 | GGAAAGAGAAAGGAAAAG | + | 6.03 | JUN(var.2) | MA0489.1 | chr1:205263882-205263896 | ATGACTCATCCCCC | - | 6.22 | JUNB | MA0490.1 | chr1:205263880-205263891 | GGATGACTCAT | + | 6.62 | PRDM1 | MA0508.2 | chr1:205262631-205262641 | GTGAAAGTGA | - | 6.02 | RREB1 | MA0073.1 | chr1:205261434-205261454 | GCCCACCCCACCCCCAACCA | + | 6.63 |
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| Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
SE_02431 | chr1:205262567-205264599 | Astrocytes | SE_05801 | chr1:205262462-205264469 | Brain_Hippocampus_Middle | SE_11085 | chr1:205260076-205262353 | CD20 | SE_11085 | chr1:205262547-205264187 | CD20 | SE_26974 | chr1:205262635-205264492 | Esophagus | SE_29391 | chr1:205262567-205264765 | Fetal_Intestine_Large | SE_32765 | chr1:205262511-205264574 | H1 | SE_38936 | chr1:205262243-205265794 | IMR90 | SE_46173 | chr1:205262329-205265260 | Osteoblasts | SE_50327 | chr1:205262518-205264578 | Sigmoid_Colon | SE_52983 | chr1:205262582-205264598 | Small_Intestine | SE_54130 | chr1:205262477-205264677 | Spleen | SE_55645 | chr1:205263252-205263684 | Thymus | SE_56704 | chr1:205262588-205264656 | u87 | SE_58462 | chr1:205242169-205295027 | Ly1 | SE_58967 | chr1:205242236-205295022 | Ly3 | SE_60263 | chr1:205242326-205284722 | Ly4 | SE_60576 | chr1:205242267-205294889 | DHL6 | SE_61365 | chr1:205242037-205294994 | HBL1 | SE_61423 | chr1:205183427-205322469 | Toledo | SE_62465 | chr1:205242393-205294944 | Tonsil | SE_65493 | chr1:205262566-205265065 | Pancreatic_islets | SE_68815 | chr1:205262515-205265189 | 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 | 205262860 | 205263030 | chr1 | 205262798 | 205264485 |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I205292 | chr1 | 205261271 | 205261570 | GH01I205293 | chr1 | 205262232 | 205274585 |
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Enhancer Sequence | TCAACCCTGC TAGGCGGAAA GACAGAATGG GTGAGCCTGG TGGGAGGCCA GGGTCAAGGA 60 GCCAGCCGTG TGCTGCCCAC CCCACCCCCA ACCATGACTG GCGAGGGAGG GAGTTGACCA 120 ACTCCACTCC TCACCCCTAC CTGGCATCTG TCTGCCTATT CTTTTTTTTC CCCCTTTTTG 180 TGGAGAATGG GGTCTTGAGA TATTGACCAG GCAGGTTTTG AACTCCTGGG CTCAAGCTAC 240 CTTCCGCCTC TGCCTCCCTA AGTGCTGGGA TTACAGGTGT GAGCCACCAC GCCCAGTCTG 300 TCTGCCCATT CTGACCCTCG TGGGCATTTC CAGCAAGGGC TGGGACAGCA AGGCTAACAT 360 TGCTTATGAG GAATGACTTG GGCTCTCAAA TATCTGCTCT ACTAACTCTG CCCCTGGGCC 420 CAGGCGTGCA GAGCCCCACA GCTGGGGGGC TTATTCCTTG ACTGACCAAT CCAGTGACGC 480 AAGAGTGGGG ACCGAAAACA GCCAGTTTTC AGTGTAGCCA CGTCAACACA AGCAGTCCCA 540 TGACAACCAG CTCCAGTGGA ACTGGGGCGT CTTACTACAC ACACCCTTGG CACACTCACC 600 TCTGTGCTGT TTTTTTTTTT TTTCTTTTTG AGATGGAGTT TTTGCTCATG TTGCCTAGGG 660 TGGAGGGCAA TGGTGCGATC TCGGCTTACC TCAACCTCTG CCTCCCGGGT TCAAGCAATT 720 CTCCTGCCTC AGCCTCTCGA GTAGCTGGGA TTACAGGCAT GTGCCTGGCT AATTTTGTAT 780 TTTTAGTAGA GACGGGGTTT CTCCGTGTTG GTCAGGCTGG TCTCGAACTC TCGACCTCAG 840 GTGATCCGCC CGCCTTGGCC TCCCAAAGTG CTAGGATTAT AGGCGTGAGC CACAGTGCCC 900 AGCCACCTCT GTGCTGTTAA CATCCATCCT GTAGGTGTTA GTTTATGGCC CCAACTTTAT 960 TATAAGTAAA TTCCTTGAAG GAGGGGACGT GCCTCAATTG CTTCTGTATT TTCCATGGCA 1020 CCTAGAACAA TAGTAAGGTC TTAATAAATG TTGATGTGTT TATTAGGGAA TGGGTTTTCA 1080 CTTGATTTAA CTATCAAGTT CCCCTTTATA AGGGGCTGGG GCCAGGAAAG CGGGTGGAGG 1140 CCCTTTATTA AACATTTATT GAGTACCTGT TCTCACTCCT TAGGTTTTCT CCAGTGATGT 1200 ATTGCTTAAA AAGCATGTTC ATGTGTTGTC TCATTTAATC CTTGCAGTAA TGTGATGGGT 1260 GTGAGCTGAC TGTGAAAGTG ACTCTCTAAG TCATTGCAAT GCACTCTGTG GGAAGAATGT 1320 GCTAGCCCAG CAAGGCTGTC TTTGTGATGT CCGATGTGTA CGTGCGTGGG GAGGCGCTCC 1380 CAAAAGCTGC GCTGGGGCAG GGTGTCCTGA ACGGCGTTAC CAGATGTATC TTGACAAAGA 1440 GGTTGGCACC ACCATGAAGA CCAATTCAAC CAGCTCTCCT AGCCCAGCTT CCATGCTCTT 1500 CAAGGAGACT TCCCACTGAA CTTCCGAATA CCCTTGTGTG AAACTGCCAC AGGCAGTGAA 1560 TGTGCTCATC AGCAAACCCA AGTATCTGGT TGGTTTGACA GGGGTTTTGT TATTCATTAG 1620 AAATGAATGA ATTGGCATGT TGGCTGAATC CATTCCTCTC CTAGAGCTCA GTGAGTCTGC 1680 TCCTGAGCCT CCTAGCCTGT TGATAAGCAA GGTTTCTGAG CAGCAAAGTG AGGCTGCTCA 1740 CTTTGGCAAA CAGGTCTTCA GGTGAGCCCG GCCACCATGT GAGGCCCTGT TGGCAGGCCA 1800 GGCTCTCCCC AGGCCCCACC TGGCCTCACC AATGGCTCTT GGATTCACAG AGGACTGCAC 1860 ATTGGACTGG GAGACAGGGC AAGCCAGGGG TCCCTTAGCA GAGAAGGGAT CCCTGCCAGT 1920 AACTAGCCTG CTGTGAGTAT GAAGTTGCCA CTTACCAAGG ACCCTCCTGA TGGACACAAC 1980 AAAGGCGATG GGTGATTGCT GCCAGGGCTC ATAAAGAGGT GATTCAGAAT CTAGCTGGGG 2040 GAACTTTGAA AGGTCATTGC ACCTTGACCC TAGCTTCCAG GCGGGACATG TGGTGAGTTC 2100 TGCTGCAATG GCTGGGTGCC CTCACAGGCC AGAGCTCAGG TTAATGCAGC TCAGAGCTCG 2160 AATTCTGATC ACAGGAAGAG AATGGTGAGG AGGATGGAGG CAGGGGTGCT GGCTGGGCCC 2220 AGAACACCAA AGGCAGAGCT GAACACTTCC ACTGGGAAGT GGGGGTTTTG GCCTCTTGGG 2280 CTGGGAAATT CCTGGCCGGC ACTGTCTGTT TATCAGGGAA GCTGAGTCAG ACTGAAACGT 2340 ATCTCCTAAA AAGCTCTGCT ATTTCTAGGA TTCCATCCGG TCAAAGCCAG CCTCCTCTTC 2400 CCTGGGGAAT TCCTTTGAGG GTGGAGAGAT AGAGGGGACA GACTGGCCTT TTCCTAGACA 2460 TGGAAACCTG AAATCTGAGT TTTTGCCCAT TTATGGACCT GAAATCCCCT CCCCCACCTA 2520 GGATGACTCA TCCCCCAGCT TGACCCAACT GCCCCTAGAG AGGGGAAAGG GTGAAACTGA 2580 GATGGTGGGA TTAGCTCAGG GAGGGGGTTG GAGGCTGGAA AGAGAAAGGA AAAGACAACT 2640 GAAAAGGATG GGGAATTCCT TTGCAAAGAG ATGGTGAGGA GAGGATTTCA GAGCCAAAAA 2700 GAGGCAGAAT GAGAAAGAGA GAAAGATTTT CATCCCAGAG GGAAGCTGCA TGCCTGGCAG 2760 AGTAAAAATC TTCCAGGTTA AGGTAGGTTC AGGCCCTCAC CTTGAGTAAA TTCTGGAACT 2820 TTAGTGTGAT CAGAGCCACT TGCCGTGCTT GTGAAAATGC AGAGATTCCC GTGCCCTCCC 2880 TGGGCTGTGA TCCGCTTCCA GGCTCCTTCA GGGATCTGAA GTAGGAAGTT CTGAAACACA 2940 GAAAGAGGAT TGACTGGGAA TCCTTCTCCC AACCTGGGGC CTCTGCTGTA TAAAGCGACT 3000 CACAACCCCT CTGCAGGTGC CAATGTCAGA GGCAGAGCCC TGGTCCAAGG GTGACGTTTC 3060 TAACATTCTT ATAAAAATCT GTGAAAGACT TTGGCCAGGC CCAGTGGCTC AAGCCTGTGA 3120 TCCCAGCACT TTAGGAGGCT GAGGCAGGTG GATCTCTTGA GGTGAGGAGT TCGAGACCAG 3180 CCTGGCCAAC ATGGCAAAAC CCGTCTCTAC TAAAAATACA AAAAAATTAG 3230
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