Tag | Content |
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EnhancerAtlas ID | HS048-03175 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:205262560-205265210 |
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 |
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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 | chr1:205262547-205264187 | 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_56704 | chr1:205264714-205265918 | 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: 1 | ID | Chromosome | Start | End |
GH01I205293 | chr1 | 205262232 | 205274585 |
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Enhancer Sequence | ATTGCTTAAA AAGCATGTTC ATGTGTTGTC TCATTTAATC CTTGCAGTAA TGTGATGGGT 60 GTGAGCTGAC TGTGAAAGTG ACTCTCTAAG TCATTGCAAT GCACTCTGTG GGAAGAATGT 120 GCTAGCCCAG CAAGGCTGTC TTTGTGATGT CCGATGTGTA CGTGCGTGGG GAGGCGCTCC 180 CAAAAGCTGC GCTGGGGCAG GGTGTCCTGA ACGGCGTTAC CAGATGTATC TTGACAAAGA 240 GGTTGGCACC ACCATGAAGA CCAATTCAAC CAGCTCTCCT AGCCCAGCTT CCATGCTCTT 300 CAAGGAGACT TCCCACTGAA CTTCCGAATA CCCTTGTGTG AAACTGCCAC AGGCAGTGAA 360 TGTGCTCATC AGCAAACCCA AGTATCTGGT TGGTTTGACA GGGGTTTTGT TATTCATTAG 420 AAATGAATGA ATTGGCATGT TGGCTGAATC CATTCCTCTC CTAGAGCTCA GTGAGTCTGC 480 TCCTGAGCCT CCTAGCCTGT TGATAAGCAA GGTTTCTGAG CAGCAAAGTG AGGCTGCTCA 540 CTTTGGCAAA CAGGTCTTCA GGTGAGCCCG GCCACCATGT GAGGCCCTGT TGGCAGGCCA 600 GGCTCTCCCC AGGCCCCACC TGGCCTCACC AATGGCTCTT GGATTCACAG AGGACTGCAC 660 ATTGGACTGG GAGACAGGGC AAGCCAGGGG TCCCTTAGCA GAGAAGGGAT CCCTGCCAGT 720 AACTAGCCTG CTGTGAGTAT GAAGTTGCCA CTTACCAAGG ACCCTCCTGA TGGACACAAC 780 AAAGGCGATG GGTGATTGCT GCCAGGGCTC ATAAAGAGGT GATTCAGAAT CTAGCTGGGG 840 GAACTTTGAA AGGTCATTGC ACCTTGACCC TAGCTTCCAG GCGGGACATG TGGTGAGTTC 900 TGCTGCAATG GCTGGGTGCC CTCACAGGCC AGAGCTCAGG TTAATGCAGC TCAGAGCTCG 960 AATTCTGATC ACAGGAAGAG AATGGTGAGG AGGATGGAGG CAGGGGTGCT GGCTGGGCCC 1020 AGAACACCAA AGGCAGAGCT GAACACTTCC ACTGGGAAGT GGGGGTTTTG GCCTCTTGGG 1080 CTGGGAAATT CCTGGCCGGC ACTGTCTGTT TATCAGGGAA GCTGAGTCAG ACTGAAACGT 1140 ATCTCCTAAA AAGCTCTGCT ATTTCTAGGA TTCCATCCGG TCAAAGCCAG CCTCCTCTTC 1200 CCTGGGGAAT TCCTTTGAGG GTGGAGAGAT AGAGGGGACA GACTGGCCTT TTCCTAGACA 1260 TGGAAACCTG AAATCTGAGT TTTTGCCCAT TTATGGACCT GAAATCCCCT CCCCCACCTA 1320 GGATGACTCA TCCCCCAGCT TGACCCAACT GCCCCTAGAG AGGGGAAAGG GTGAAACTGA 1380 GATGGTGGGA TTAGCTCAGG GAGGGGGTTG GAGGCTGGAA AGAGAAAGGA AAAGACAACT 1440 GAAAAGGATG GGGAATTCCT TTGCAAAGAG ATGGTGAGGA GAGGATTTCA GAGCCAAAAA 1500 GAGGCAGAAT GAGAAAGAGA GAAAGATTTT CATCCCAGAG GGAAGCTGCA TGCCTGGCAG 1560 AGTAAAAATC TTCCAGGTTA AGGTAGGTTC AGGCCCTCAC CTTGAGTAAA TTCTGGAACT 1620 TTAGTGTGAT CAGAGCCACT TGCCGTGCTT GTGAAAATGC AGAGATTCCC GTGCCCTCCC 1680 TGGGCTGTGA TCCGCTTCCA GGCTCCTTCA GGGATCTGAA GTAGGAAGTT CTGAAACACA 1740 GAAAGAGGAT TGACTGGGAA TCCTTCTCCC AACCTGGGGC CTCTGCTGTA TAAAGCGACT 1800 CACAACCCCT CTGCAGGTGC CAATGTCAGA GGCAGAGCCC TGGTCCAAGG GTGACGTTTC 1860 TAACATTCTT ATAAAAATCT GTGAAAGACT TTGGCCAGGC CCAGTGGCTC AAGCCTGTGA 1920 TCCCAGCACT TTAGGAGGCT GAGGCAGGTG GATCTCTTGA GGTGAGGAGT TCGAGACCAG 1980 CCTGGCCAAC ATGGCAAAAC CCGTCTCTAC TAAAAATACA AAAAAATTAG CTGGGTGTGG 2040 TGGCATGCAC CTGTAGTCCC AGCTACTGGA GGAGCAGGGG GGCGCTGAGG TGGAGGATCG 2100 CTTGTGCTCA GGAGGTCGAG GCTGCAGTAA GCTGAGATTG CACCATTGTA CTCCAGCCTG 2160 GGCCACAGAG TGAGATCCTG TGTCAAAAAA AAAAAAGACT TTTTATCGGA TGGAGAAAGC 2220 CAGTCCCCAC CAGGCCAAAT ATGCCTCCTC ATTGCAGCAC TGCCCACCTC CCCACATAAT 2280 CATATCAGAG AAGCTTTGGA AAGAACTGCT TTCCTAGTCA ATACAATCCT AGGATCTTTA 2340 CAGCCAGAAG GGACTTCTTC AGGTATCATC TGGCGGGATT TTTCACCTGA AGCAGAAATT 2400 CCTTCTAGCA ACAACCCCCA CATCTCTATC TCCAACCCAA ATCTCTCAAA CTCCAGGCTC 2460 CTCATACCAC TTATCTTTGC CTGGAGGCCT AAGTGCCTCT GACTTCACCT CACACCTCCT 2520 CCATCTGCAA GTCTTCCCCG ACCCAGCTAA TGGACACTCT ACCCTCCAAG TTTCTCAGGC 2580 CAGAGACCAT GGAGTGATTC TTGGTTTCTC TCTTTCTTTC ATACCCTACA TCTAATCCAT 2640 CAGGAAAGCC 2650
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