Tag | Content |
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EnhancerAtlas ID | HS051-23606 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr6:43766190-43768360 |
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 | GTGGTGTGAT CTGAAGGGTC CCGGGCAGGT GTCCTCCTTC CCCTCCACTG TGCCCACCAT 60 CACCCTCCTA GTTCTTTCCC TTCAATCATT CACCGTAGTC TGTAATCACC ATGCCCCACC 120 TTAAATTAAG GTCTAGAAAG GATCTTGGAG ACGTGTGAGT CCCAGATCAG AGGAGGGAAC 180 TGAGGCCCCA AAAGAGAAGG GGAGGAATCT TGTGTGAGGT CACCCAGGGA GTTAATAGCA 240 GGGCCTAAAT CTCAGAGCAG TGCTTTGGGC TTATGGAGAG ACTCTGGGAG ATGTGGGGCC 300 ACCCAGCACA CATGTGAGCA GAGAGGCGCT GTGAAGGAGT GTGTGTGTGT GTGCGTGTGT 360 GTGTGTGTGC AGGGGTGAGT GGGGTTAGGC GTCTGGGTCC CCTGTGAGCA GATGGGAGTT 420 CATATGGGTG TCTGCTGCAA GGCGTCTGGC TATTTTCCTA TGTCACAGTG TGGGGTGGAG 480 CAGGGAGGGA CAGGCCTGTA GCAGGGACAT CAGACTGGTC TTATGAGTCC TGGCCCAGCC 540 CTCTTGAGAC CAAGGGCAGA GGGCGATGAG TCACAGATGA CTCAGGTGCT GGAGGCCACA 600 GCCACGCATG GCACGTGACA GCCAAGGAGG GCCAGGTCTA TTTCTGGACC GGATAGACAG 660 GTGACCCAGG AGGCTGACAC TGAAATCTCT CTTCCTAGAG GATAGGAGGG ATTCTATTCA 720 CAGACTCAGA GCCTGGGCCC CTGGGATGGG GCTGAAAAGA CGGCCTGTGG GCTTACCTGT 780 CCCTTGGAGC TTTGCTCCAC TGGCTGGTTG AGCTGTTACT TCAGTGGGGC AGGGCTGTCC 840 TGAGCCATCC CCATTCTCCT GAAGATGTGC GGTTAGGGTC ACTCTCCACT GGGGATGAGT 900 TCTCCCTGGC CCTTTGGATG CCAGCATCTA GCAGCAAAGC ACCCCTGCCC TGCCTTGGTA 960 ATGCAGTGTC TGACCACAGA CAGCCCCTCT TCTTTGTCTG AGGCAAGGGA GCCAAATCCT 1020 TGACCTGCCA CTTGACCCCA AGGCCTAGGC CAGAAGATGA GGTAGTCTGG GGTGCAGACA 1080 GTGCCTTGGG TTCAAATCTC ACCCTGAGAC CTGGAGTTAC ATTGTTTCCT CTTGGGGCCT 1140 CAGTTCCATC CTCTGTACCC CGTGGGGGTT GTGCTTGAAG GCTCAGGGGT CCCCTCTAGC 1200 TGGCTCCTCA TCAGGCCTTG AAGGCTGGGC TGACGGCGAG GCCTTGAAGC TGCCTCCTCT 1260 CTCTTGCCTA TGTTTGAGGT GGGGGACTGG GGAGGGTTGG CTGAGGATAG AAAGTCCTGG 1320 CCTGGTAGGG GCATGCCTCA GGGTCCCCGG TCACCTGAAA CACAGTGATG ATTACAGGGT 1380 GAGCCTCTGG GACCAGACAC TGTAATCTGC TGCCCTCCTT CCTGCCAAGG GCCTACTGCA 1440 GCATTTCCTT CTGCTTTTCA CAACTGTTTT CTAAGAACCC CAGGAAGGCA GAGGCCTCAT 1500 CTCTGAGGGG TGCGGCAGAA GACTAAAGAA GAGGGGAGGG AGAAAATGGA GATGGTGAGA 1560 GAGGAAGGGA GAGAGGATGA AAGGATGAGG GAAAGGAGAT GCGTGAGGTG TGGTAGACAT 1620 CAGAAGGCTT TTCCCTGGTT GACAGTTTGA GGAAGAGGAG GGGAAAGAAG AGTGGGTGGG 1680 GTCATTCTCT GCCTCTAAGC TCCCAGCTTA GGTGCTCCTC CTCAGAAAGA CTGCCCTGAC 1740 CTCATTACCT AAAGTAGCAG CCTCCTCCCC ACCTCAGTCA CTTTCTATCA ATTGCTGCAT 1800 TTAATGAGGA AGGGCTGAGT CAGCTCATGT CACTTTTTGG CTCAAATCCC CGCAGTGGCT 1860 CCTGGTCTTC CTCAGACTAA AGACCAAAGT CCTTACGATG GCCTTCAAGG TCCTACATGA 1920 TTCCTTTCCA AGAACAGCAA GTGTGTTCTT CAAACACATC TGGCATACTC CTGACCCAGG 1980 GCCTTTGCAC AGCTTTCCCC CTCTGCCTGG AATGTTCTTT CTCCAGATAT CTGCAGGACT 2040 CACTCCCTTG CCTTCTTCAA GTCTTTGCTC AAACATCGCC TTCTCAATGA GGCCTGCCCT 2100 GGGCATCCTA TTTAAAATGG CAATATTCTT CCTACACTCT CCAGCCCTCT TACCCTATAC 2160 TCTTTTATCT 2170
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