Tag | Content |
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EnhancerAtlas ID | HS116-27839 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr5:133902780-133906960 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr5:133905999-133906017 | CCTTCCCTCCTGTCTTCC | - | 6.64 | EWSR1-FLI1 | MA0149.1 | chr5:133906003-133906021 | CCCTCCTGTCTTCCTTCC | - | 7.31 | IRF1 | MA0050.2 | chr5:133904729-133904750 | TCTTTGTTTCAGTTTCTACTT | + | 6.62 | IRF1 | MA0050.2 | chr5:133904751-133904772 | TCTGAGTTTCAGTTTCTTTGT | + | 6.64 | IRF8 | MA0652.1 | chr5:133904755-133904769 | AGTTTCAGTTTCTT | - | 6.03 | IRF9 | MA0653.1 | chr5:133904755-133904770 | AGTTTCAGTTTCTTT | - | 7.05 | JUN | MA0488.1 | chr5:133906930-133906943 | ATGACCTCATCTT | - | 6.54 | JUND(var.2) | MA0492.1 | chr5:133906929-133906944 | TATGACCTCATCTTA | - | 7.07 | Nr2f6(var.2) | MA0728.1 | chr5:133903468-133903483 | TGACCTATTGCCCCC | - | 6.27 | RARA | MA0729.1 | chr5:133903465-133903483 | AAATGACCTATTGCCCCC | - | 6.29 | TCF3 | MA0522.2 | chr5:133903737-133903747 | AACACCTGCT | + | 6.02 | ZNF263 | MA0528.1 | chr5:133906426-133906447 | CCCTCCCTCTCTGGCTGCTCC | - | 6.02 | ZNF263 | MA0528.1 | chr5:133906003-133906024 | CCCTCCTGTCTTCCTTCCCCC | - | 6.1 | ZNF263 | MA0528.1 | chr5:133905999-133906020 | CCTTCCCTCCTGTCTTCCTTC | - | 6.27 | ZNF263 | MA0528.1 | chr5:133903525-133903546 | GAAGGAAGAGGTGGAGGTGGG | + | 6.66 |
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| Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
SE_00886 | chr5:133901746-133906938 | Adrenal_Gland | SE_06180 | chr5:133901587-133907397 | Brain_Hippocampus_Middle | SE_11045 | chr5:133902724-133905051 | CD20 | SE_11045 | chr5:133905058-133906758 | CD20 | SE_18783 | chr5:133903006-133905185 | CD4p_CD25-_Il17-_PMAstim_Th | SE_38826 | chr5:133902759-133905751 | HUVEC | SE_40774 | chr5:133902554-133908863 | Left_Ventricle | SE_42303 | chr5:133901455-133907017 | Lung | SE_48716 | chr5:133903254-133907061 | Right_Atrium | SE_52569 | chr5:133902698-133906025 | Small_Intestine | SE_53502 | chr5:133902462-133906158 | Spleen | SE_53502 | chr5:133906159-133907026 | Spleen | SE_65308 | chr5:133901494-133909997 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 133903269 | 133905854 | chr5 | 133903728 | 133903998 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I134566 | chr5 | 133902500 | 133906734 |
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Enhancer Sequence | TAGATGGGTA AACGCGGCTC CGTGGGGTGC TGGGCAAACA GAACAGAGGC ACGAAGGAGA 60 CAGGGTGGAC TCAAGGAACG GTGGAGTGGA AGGAAGAGGT GAAAGGGGCT GGTGGATCGC 120 ACGAGACTGG GCTGGTGGAT CACAGTGTGT CTGGAAGCTG CAGAAGTGCT AAGGAGGGAC 180 TGACATACTG TGGCTGGGAC TTGCACCCAA CACTCCCTGG AGGAGAAGTC CCAGAGTCTG 240 GAATGGGTGG GCTGGCTGAA AACCACCCCC AGCTGTGTGC TGGGAAACAG GTGACGGTGG 300 CTTGGTCCAG GGGGCTGAGT GAAATGAAGC AGGATTTCTG GATCCTTTTC CAGTCCTCTG 360 AACCCCACAG GCTGTTCTGG TCTCTCCTCT CTGGGACATT TCTAGGGTTC CAGAGCATAT 420 GGGACCGTGT CACAGTGTCT CCCCTGGGTT CAGACATACA TGCTCACCCT CTCCCTGGGT 480 CCTGTCAGGA AATAGCCCTG GGCAGGAGCA TGCAGGGAAC GTTGTGTGAC CCAAGGCGCC 540 TGCTTTTCTT ATCTGCATCG CAGTGGGCAA GGCTGTAAAA TGGGTAGAAC ATCTCCAGGG 600 GTGTTGTACT GTCAGGGAAG GGGCACTGGA CCCAGCTTCC CCAATCCCCT CCTTCCCACT 660 CATCTGCGCT GCCTGCTCAA GAGGGAAATG ACCTATTGCC CCCAGAGAGC CCTCACTGCC 720 TGGCAGCCAG CTTGCCACCA GGCCAGAAGG AAGAGGTGGA GGTGGGAGGA ACCAGATGTC 780 CCTGGCTCCA GCCAGGACAG AGGGCAAGGC TACCTACATT GCAGCCACCA CCTCCTGGCC 840 AGCCCAGCCT CCTGTCACAT GTGGCAGGGG CATCAGGTGT AAGACCTTCT GGGACCGAAG 900 CTGCTTCCAG AGTCTTCTTT AGGCCACCAT GTCTCCACCC GCTGGATCTC CAGTGGAAAC 960 ACCTGCTTTT ACTCCTACTG TTTCCCAAAC AACCCCTCAG AACTGACCTC TCTGTTCTGT 1020 GCTGGTCAGC CCATGTGTCT GTCCCTGGCT GGGTTGTCCA GGGAGGTCAA GGGCTTGACT 1080 CACTTATGTA GTCATCATCC TGGAAAAAGA GACTTGAGGA AGATCCTCCC AGCCCTGCTG 1140 AGCAGATGAG GAAACTGGGG CTCGGAGAGA CGAATAACAG GAAGTCTTAG AGGAACTCCA 1200 TTCCAAGGGT TTTGAGCTTG AATTTGGACC TCAGTCGGGG GCAGAAAAGG AGTTGTTGGC 1260 TTATTCTCTA TTCTGTAAAT TTCCTGGGCA AAAGCATCCC TTTTTCAGTC CCCTAATCTT 1320 CCCACCCCAG TGTTGGCTGG TTCAGGTGGA GCCTGGGGCT GAGGTTGGCG GGCTCTGGGG 1380 TTCCGGGGAA TGAGAGCTGC TGCAGAGACT CCTGCAGTGG GAGCCAGAAC ACTCCAGAGT 1440 CAGGTGTGAA CCGTCCCACT CCTCCTCTGG GAAGAGGAAG CAGGGCCAAT TTTGAAGTAT 1500 GTGCAGCCTC TTACGGCTCA GGGGGCCCTG TCAAATGCTG CTTTCTGAGC AGCCACCAAG 1560 CTGGGCTGGC GGGCACCAGC TTCAATGAGG GCAGGGGCAT GCACAGCCCT GGCAGGGCCG 1620 AGGAGGGACA ACCATGAGCC AAGCTGACCC CCATCAGCGG CCCAGCCTCA AGGCCTTTCC 1680 AGGTCACACA TTTGCAACTT GGGTGAATGA ACAGCGACAA GAACCCTGCC ACGGGGCAGG 1740 CTTTCTGCAA AGGCCCATGG TGGTTGGTGG CCTGGCCAGC GGGCCCAGTC TCGGACCGTG 1800 GCCCAGTGCC AGCAGCCGGG AGTATCCAGC CTGTAACTGG GCACTAAGCC AGCCTGGGCA 1860 GGAATCATCG GAAGATGGGG CAGGGCTTGA GGTCGAGGCC TTGGTAGCCT GACTTTGCAT 1920 CCAGTTCCTG CACTCCCAGC TCTATACCTT CTTTGTTTCA GTTTCTACTT CTCTGAGTTT 1980 CAGTTTCTTT GTCTGTAAAA TGGGAATAAG GATCAGACTG ACCTTGGGGT CACAGTGCAT 2040 GTGGGGGACA AAGCTTAGCA CAGTGCCCTC CATTGTTGGC CGTGATTGTT GTTACTGTCC 2100 TGGCCCCTCA GCATTTGGCT CTTAGAAGAA GGGAGGCCAG CCCGTGCGCT CTGAGGGTGG 2160 GCTCCACAGA GGACCAAAAG GGCAGGCCCA GTGCTAGGGC CTGGGAACCC AGCATCCTCC 2220 CAGATTGATT CGTTCCTCCT CAGCCAGGCA GGGGTTTTGC TGAGAGAAAC AGGAGCCGGG 2280 GCTGCTGCCG GCATGAAATC CCATTTTATG GTCAACCAGA TGTGCTTTCC TAAAATTTCA 2340 GCCTTGGGCC TCGGCCCCAG CGGACGCTCG GAAGGCATGG CCACTGCAGC CTCCCAGAGT 2400 TATTTACGGC TGACAAAAAT CGCAGCACTG TTGATCAGCC CGACAAGTGC CGGCTGGTGT 2460 CCCCTAGCAA CCGTGCTGAC AAGCAGGCTG TGCAGGGACT TGCTGCTTGT GGCTCTGGCT 2520 CTGGTCACCA GGAGTTTATT TGGGAGCCTG ACCTGGCCTG AGGAGGAGGC CAAGAGGGTG 2580 GAGGCGGCTC TGAGACACAC ACCTGCCCAG AGGATGATAT GGGACAACTT CCCAAGGAGG 2640 GAAAGGCTCA GAAGGAAGTG GGTCCTGGCC TCAGTGCCTG GATGGTGGTC CCTTTGGCCT 2700 CCCACCAAAG CCAACCTTGT CCTGGGCAGC TCCAGCCTGC AGACCTCTGG CTCTTCTGCC 2760 CCTGTGCCTT CCATCTCTAG GGCTCCCCCA ACCCATTAGT GCCCTTGCCT CACCCAAGCC 2820 CAGTCACCAC CTCCAGCTGC TCCCAGGTCA GTAGCCCAGA AATTGCCACA TCCTGCTCCG 2880 TGCCTGCAGT CTACTGCTCT CCCTGCTCAC TTGTCTCCCA GGCCCTCCAC CCTTCTTTGT 2940 CCTGCTTTCT TCACTCACTC CCTGTATGGC ACTGGCCTGC TATGCCCCAG CCCTTGTCCC 3000 TCACTGAGGC CAGAACCCTG GCAGAGCCTC ACCCAGTAAG AGCCACTCCC TCCACCAGGA 3060 GAAATCCCAT AGCGCTGAGC AGGGCAGTCC CTGCCGCACA CCCCACCTCA TACCTGCTGC 3120 CCACATGCTG AGCCCTGCCT CCCTCAGGAC AGCGTCCCCT CTGTCCTCAT ACCAGGGCCT 3180 CTAACTTCTG CCAGCCGAGC CTCTCGGTCC ATTCTCTTCC CTTCCCTCCT GTCTTCCTTC 3240 CCCCACAGGG GCTCTTTTCC AGCCCACACC TGCAGCTGAC GAGTCTGTCT TTTCTTCATC 3300 CCCTCTGCGG GTCCTTTTCC ACCAATATTT GAATCTGTTC AACCCTCTCT CATCTTCAAA 3360 AGCGAATCCT CCCTCCCTAT TTCCCTCTAG TCGTGGGTTC CTCCGCTCCC ACCCCCATCT 3420 CTCCTTTCCT GTCATCCCTC ATGGTATTTG CATCCTTGCT GCCCACTCTG GCCGGGTTTC 3480 CGCCACATCC CAGAGCCTGC CACCTGGGCT GCCTGCAGCC TCCCTGCCCA CCTCTCCATC 3540 CCCCGATCCT CTCAGCAGCG GCTGCCACAA TCAGACCTGC CCTTAGTCTT GGAGTCCTTT 3600 TTCTGTGATG CTCTGACCAG GTCCCCCCTG AGGTCCTGGT TTACCCCCCT CCCTCTCTGG 3660 CTGCTCCTTG GCCTCAATGG TCATCCATTG CTCTCCCCTG ACTGCTCACT CCCAGGGCTG 3720 GAGACCTCAG GCTCCACTGT CTTTCACGGC TGCCCACAGT TTTGCCCCAC GTGGGGGTGC 3780 TGGCTGCCCC TCCCTTTTGA GCTCCACACC AAGTCCCTTT TAAAGGCCAC CGGCATCTCA 3840 TGCCCAGCAT CCCTGTTAGT TTCCTAGGCC TGCCCGTGTG CCACCAGCTG GATGGTGAGA 3900 TTTATCCTCA TGGTTTTGGA GGCTGGAAGC CCAAGGTTGA GGTGTCAGCA GGATTAGTTC 3960 CTGCCGGAGG CTCTGCGGGG GAGTCTCTCC GTGCCTCCCA GCTTCTGGTG GTTGCCAGGA 4020 ATCTTTGCTG TTCCTTGGCC TGCGGACATC TGTCTGGCCT CTGCCTCTGC CAGGTCACAT 4080 GGCCTTCTCC CTGTAGGCAC CTGTGTCAGG ACTCCACTCA TAGTAGATCA AGGGCCCACC 4140 CTAATGTAGT ATGACCTCAT CTTAACTATT TATATCTACA 4180
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