Tag | Content |
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EnhancerAtlas ID | HS052-32730 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr6:43765610-43768240 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr6:43766754-43766765 | GATGAGTCACA | - | 6.14 | JUND | MA0491.1 | chr6:43766754-43766765 | GATGAGTCACA | - | 6.14 | MAFK | MA0496.2 | chr6:43767999-43768018 | AAGGGCTGAGTCAGCTCAT | + | 6.07 | ZNF263 | MA0528.1 | chr6:43767721-43767742 | AGGGGAGGGAGAAAATGGAGA | + | 6.11 | ZNF263 | MA0528.1 | chr6:43767843-43767864 | AGAGGAGGGGAAAGAAGAGTG | + | 6.23 | ZNF263 | MA0528.1 | chr6:43767837-43767858 | TGAGGAAGAGGAGGGGAAAGA | + | 6.85 | ZNF263 | MA0528.1 | chr6:43767840-43767861 | GGAAGAGGAGGGGAAAGAAGA | + | 7.22 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_00396 | chr6:43766034-43772289 | Adipose_Nuclei | SE_24400 | chr6:43765933-43766752 | Colon_Crypt_2 | SE_24400 | chr6:43766795-43767748 | Colon_Crypt_2 | SE_27752 | chr6:43765702-43768484 | Fetal_Intestine | SE_28697 | chr6:43765598-43768460 | Fetal_Intestine_Large | SE_31486 | chr6:43766002-43767888 | Gastric | SE_33438 | chr6:43765653-43768930 | H2171 | SE_40829 | chr6:43763899-43769361 | Left_Ventricle | SE_42766 | chr6:43765308-43768215 | Lung | SE_47847 | chr6:43766267-43766705 | Pancreas | SE_47847 | chr6:43766778-43767806 | Pancreas | SE_48225 | chr6:43765401-43766793 | Psoas_Muscle | SE_48225 | chr6:43766826-43768247 | Psoas_Muscle | SE_48830 | chr6:43766682-43768391 | Right_Atrium | SE_51234 | chr6:43764754-43768479 | Skeletal_Muscle | SE_52639 | chr6:43765415-43768531 | Small_Intestine | SE_57095 | chr6:43764707-43766691 | VACO_400 | SE_57095 | chr6:43766746-43768372 | VACO_400 | SE_57428 | chr6:43766161-43766701 | VACO_503 | SE_57428 | chr6:43766737-43767591 | VACO_503 | SE_65246 | chr6:43762755-43768367 | Pancreatic_islets | SE_67049 | chr6:43765653-43768930 | H2171 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr6 | 43767400 | 43768215 | chr6 | 43765800 | 43766200 | chr6 | 43766474 | 43766976 | chr6 | 43767552 | 43768173 | chr6 | 43766213 | 43767293 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I043797 | chr6 | 43765547 | 43768568 |
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Enhancer Sequence | AGCCCCATCC TCAGGGAGCC CCACTCTGAG GGAGACACAG CCCCGTCCTA CGGGAGCCCC 60 AGTCTGAGCG AGGTTTAGCC CCATCCTCAG GGAGCCCCAG TCTGAGGGGA GACGCAGCCC 120 CGTCCTACGG GAGCCCCAGT CTGAGCGAGG TGCAGCCCCA TCCTCAGGGA GCCCCAGTCT 180 GAGGGGAGAC GCAGTCCCGT CCTCAGGGAA CCGCAGTCTG AGGGAGATGC AGCCCCGTCC 240 TCAGGAAGCC CCAGTCTGAG GGAGACGCAG CCCTGTCCTC AGGAAGCCCC ATTCTGAGGG 300 AGATGCAGCC CCATCCTCAG GGAGCCCCAG TCTGAGGGGA GGCACAGCCC TGACTCAGGG 360 AGCCCCAGTT TGAGGGGAGA CACAGCAGTG TCTTTAGGGA GCCCAGTCTG AGGGGAGACA 420 CAGCAGTGTC TTTAGGGAGG TCCCTTTAGG AGTTCAACCC CTTGGTCCTT CTTCTGAGGT 480 AGTGGGTTTT GTGGGGCACT GGAGGCCCAG AGTTGGCTGT TTGAGGAAGA GTCTTTCAGG 540 GCATTGCCAT TCTTTGTCAT TCTTTACTGT AGCCAGAGGT GTGGTGTGAT CTGAAGGGTC 600 CCGGGCAGGT GTCCTCCTTC CCCTCCACTG TGCCCACCAT CACCCTCCTA GTTCTTTCCC 660 TTCAATCATT CACCGTAGTC TGTAATCACC ATGCCCCACC TTAAATTAAG GTCTAGAAAG 720 GATCTTGGAG ACGTGTGAGT CCCAGATCAG AGGAGGGAAC TGAGGCCCCA AAAGAGAAGG 780 GGAGGAATCT TGTGTGAGGT CACCCAGGGA GTTAATAGCA GGGCCTAAAT CTCAGAGCAG 840 TGCTTTGGGC TTATGGAGAG ACTCTGGGAG ATGTGGGGCC ACCCAGCACA CATGTGAGCA 900 GAGAGGCGCT GTGAAGGAGT GTGTGTGTGT GTGCGTGTGT GTGTGTGTGC AGGGGTGAGT 960 GGGGTTAGGC GTCTGGGTCC CCTGTGAGCA GATGGGAGTT CATATGGGTG TCTGCTGCAA 1020 GGCGTCTGGC TATTTTCCTA TGTCACAGTG TGGGGTGGAG CAGGGAGGGA CAGGCCTGTA 1080 GCAGGGACAT CAGACTGGTC TTATGAGTCC TGGCCCAGCC CTCTTGAGAC CAAGGGCAGA 1140 GGGCGATGAG TCACAGATGA CTCAGGTGCT GGAGGCCACA GCCACGCATG GCACGTGACA 1200 GCCAAGGAGG GCCAGGTCTA TTTCTGGACC GGATAGACAG GTGACCCAGG AGGCTGACAC 1260 TGAAATCTCT CTTCCTAGAG GATAGGAGGG ATTCTATTCA CAGACTCAGA GCCTGGGCCC 1320 CTGGGATGGG GCTGAAAAGA CGGCCTGTGG GCTTACCTGT CCCTTGGAGC TTTGCTCCAC 1380 TGGCTGGTTG AGCTGTTACT TCAGTGGGGC AGGGCTGTCC TGAGCCATCC CCATTCTCCT 1440 GAAGATGTGC GGTTAGGGTC ACTCTCCACT GGGGATGAGT TCTCCCTGGC CCTTTGGATG 1500 CCAGCATCTA GCAGCAAAGC ACCCCTGCCC TGCCTTGGTA ATGCAGTGTC TGACCACAGA 1560 CAGCCCCTCT TCTTTGTCTG AGGCAAGGGA GCCAAATCCT TGACCTGCCA CTTGACCCCA 1620 AGGCCTAGGC CAGAAGATGA GGTAGTCTGG GGTGCAGACA GTGCCTTGGG TTCAAATCTC 1680 ACCCTGAGAC CTGGAGTTAC ATTGTTTCCT CTTGGGGCCT CAGTTCCATC CTCTGTACCC 1740 CGTGGGGGTT GTGCTTGAAG GCTCAGGGGT CCCCTCTAGC TGGCTCCTCA TCAGGCCTTG 1800 AAGGCTGGGC TGACGGCGAG GCCTTGAAGC TGCCTCCTCT CTCTTGCCTA TGTTTGAGGT 1860 GGGGGACTGG GGAGGGTTGG CTGAGGATAG AAAGTCCTGG CCTGGTAGGG GCATGCCTCA 1920 GGGTCCCCGG TCACCTGAAA CACAGTGATG ATTACAGGGT GAGCCTCTGG GACCAGACAC 1980 TGTAATCTGC TGCCCTCCTT CCTGCCAAGG GCCTACTGCA GCATTTCCTT CTGCTTTTCA 2040 CAACTGTTTT CTAAGAACCC CAGGAAGGCA GAGGCCTCAT CTCTGAGGGG TGCGGCAGAA 2100 GACTAAAGAA GAGGGGAGGG AGAAAATGGA GATGGTGAGA GAGGAAGGGA GAGAGGATGA 2160 AAGGATGAGG GAAAGGAGAT GCGTGAGGTG TGGTAGACAT CAGAAGGCTT TTCCCTGGTT 2220 GACAGTTTGA GGAAGAGGAG GGGAAAGAAG AGTGGGTGGG GTCATTCTCT GCCTCTAAGC 2280 TCCCAGCTTA GGTGCTCCTC CTCAGAAAGA CTGCCCTGAC CTCATTACCT AAAGTAGCAG 2340 CCTCCTCCCC ACCTCAGTCA CTTTCTATCA ATTGCTGCAT TTAATGAGGA AGGGCTGAGT 2400 CAGCTCATGT CACTTTTTGG CTCAAATCCC CGCAGTGGCT CCTGGTCTTC CTCAGACTAA 2460 AGACCAAAGT CCTTACGATG GCCTTCAAGG TCCTACATGA TTCCTTTCCA AGAACAGCAA 2520 GTGTGTTCTT CAAACACATC TGGCATACTC CTGACCCAGG GCCTTTGCAC AGCTTTCCCC 2580 CTCTGCCTGG AATGTTCTTT CTCCAGATAT CTGCAGGACT CACTCCCTTG 2630
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