Tag | Content |
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EnhancerAtlas ID | HS118-16134 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr6:43766180-43768350 |
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: 4 | Chromosome | Start | End |
chr6 | 43767400 | 43768215 | 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 | AGCCAGAGGT GTGGTGTGAT CTGAAGGGTC CCGGGCAGGT GTCCTCCTTC CCCTCCACTG 60 TGCCCACCAT CACCCTCCTA GTTCTTTCCC TTCAATCATT CACCGTAGTC TGTAATCACC 120 ATGCCCCACC TTAAATTAAG GTCTAGAAAG GATCTTGGAG ACGTGTGAGT CCCAGATCAG 180 AGGAGGGAAC TGAGGCCCCA AAAGAGAAGG GGAGGAATCT TGTGTGAGGT CACCCAGGGA 240 GTTAATAGCA GGGCCTAAAT CTCAGAGCAG TGCTTTGGGC TTATGGAGAG ACTCTGGGAG 300 ATGTGGGGCC ACCCAGCACA CATGTGAGCA GAGAGGCGCT GTGAAGGAGT GTGTGTGTGT 360 GTGCGTGTGT GTGTGTGTGC AGGGGTGAGT GGGGTTAGGC GTCTGGGTCC CCTGTGAGCA 420 GATGGGAGTT CATATGGGTG TCTGCTGCAA GGCGTCTGGC TATTTTCCTA TGTCACAGTG 480 TGGGGTGGAG CAGGGAGGGA CAGGCCTGTA GCAGGGACAT CAGACTGGTC TTATGAGTCC 540 TGGCCCAGCC CTCTTGAGAC CAAGGGCAGA GGGCGATGAG TCACAGATGA CTCAGGTGCT 600 GGAGGCCACA GCCACGCATG GCACGTGACA GCCAAGGAGG GCCAGGTCTA TTTCTGGACC 660 GGATAGACAG GTGACCCAGG AGGCTGACAC TGAAATCTCT CTTCCTAGAG GATAGGAGGG 720 ATTCTATTCA CAGACTCAGA GCCTGGGCCC CTGGGATGGG GCTGAAAAGA CGGCCTGTGG 780 GCTTACCTGT CCCTTGGAGC TTTGCTCCAC TGGCTGGTTG AGCTGTTACT TCAGTGGGGC 840 AGGGCTGTCC TGAGCCATCC CCATTCTCCT GAAGATGTGC GGTTAGGGTC ACTCTCCACT 900 GGGGATGAGT TCTCCCTGGC CCTTTGGATG CCAGCATCTA GCAGCAAAGC ACCCCTGCCC 960 TGCCTTGGTA ATGCAGTGTC TGACCACAGA CAGCCCCTCT TCTTTGTCTG AGGCAAGGGA 1020 GCCAAATCCT TGACCTGCCA CTTGACCCCA AGGCCTAGGC CAGAAGATGA GGTAGTCTGG 1080 GGTGCAGACA GTGCCTTGGG TTCAAATCTC ACCCTGAGAC CTGGAGTTAC ATTGTTTCCT 1140 CTTGGGGCCT CAGTTCCATC CTCTGTACCC CGTGGGGGTT GTGCTTGAAG GCTCAGGGGT 1200 CCCCTCTAGC TGGCTCCTCA TCAGGCCTTG AAGGCTGGGC TGACGGCGAG GCCTTGAAGC 1260 TGCCTCCTCT CTCTTGCCTA TGTTTGAGGT GGGGGACTGG GGAGGGTTGG CTGAGGATAG 1320 AAAGTCCTGG CCTGGTAGGG GCATGCCTCA GGGTCCCCGG TCACCTGAAA CACAGTGATG 1380 ATTACAGGGT GAGCCTCTGG GACCAGACAC TGTAATCTGC TGCCCTCCTT CCTGCCAAGG 1440 GCCTACTGCA GCATTTCCTT CTGCTTTTCA CAACTGTTTT CTAAGAACCC CAGGAAGGCA 1500 GAGGCCTCAT CTCTGAGGGG TGCGGCAGAA GACTAAAGAA GAGGGGAGGG AGAAAATGGA 1560 GATGGTGAGA GAGGAAGGGA GAGAGGATGA AAGGATGAGG GAAAGGAGAT GCGTGAGGTG 1620 TGGTAGACAT CAGAAGGCTT TTCCCTGGTT GACAGTTTGA GGAAGAGGAG GGGAAAGAAG 1680 AGTGGGTGGG GTCATTCTCT GCCTCTAAGC TCCCAGCTTA GGTGCTCCTC CTCAGAAAGA 1740 CTGCCCTGAC CTCATTACCT AAAGTAGCAG CCTCCTCCCC ACCTCAGTCA CTTTCTATCA 1800 ATTGCTGCAT TTAATGAGGA AGGGCTGAGT CAGCTCATGT CACTTTTTGG CTCAAATCCC 1860 CGCAGTGGCT CCTGGTCTTC CTCAGACTAA AGACCAAAGT CCTTACGATG GCCTTCAAGG 1920 TCCTACATGA TTCCTTTCCA AGAACAGCAA GTGTGTTCTT CAAACACATC TGGCATACTC 1980 CTGACCCAGG GCCTTTGCAC AGCTTTCCCC CTCTGCCTGG AATGTTCTTT CTCCAGATAT 2040 CTGCAGGACT CACTCCCTTG CCTTCTTCAA GTCTTTGCTC AAACATCGCC TTCTCAATGA 2100 GGCCTGCCCT GGGCATCCTA TTTAAAATGG CAATATTCTT CCTACACTCT CCAGCCCTCT 2160 TACCCTATAC 2170
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