| Tag | Content |
|---|
EnhancerAtlas ID | HS092-32229 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr5:133903220-133906100 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 | | 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 | chr5:133906003-133906024 | CCCTCCTGTCTTCCTTCCCCC | - | 6.1 | | ZNF263 | MA0528.1 | chr5:133905999-133906020 | CCTTCCCTCCTGTCTTCCTTC | - | 6.27 | | ZNF263 | MA0528.1 | chr5:133903525-133903546 | GAAGGAAGAGGTGGAGGTGGG | + | 6.66 |
|
| | Number of super-enhancer constituents: 12 | 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_65308 | chr5:133901494-133909997 | Pancreatic_islets |
|
| | 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 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I134566 | chr5 | 133902500 | 133906734 |
|
Enhancer Sequence | CCCCTGGGTT CAGACATACA TGCTCACCCT CTCCCTGGGT CCTGTCAGGA AATAGCCCTG 60
GGCAGGAGCA TGCAGGGAAC GTTGTGTGAC CCAAGGCGCC TGCTTTTCTT ATCTGCATCG 120
CAGTGGGCAA GGCTGTAAAA TGGGTAGAAC ATCTCCAGGG GTGTTGTACT GTCAGGGAAG 180
GGGCACTGGA CCCAGCTTCC CCAATCCCCT CCTTCCCACT CATCTGCGCT GCCTGCTCAA 240
GAGGGAAATG ACCTATTGCC CCCAGAGAGC CCTCACTGCC TGGCAGCCAG CTTGCCACCA 300
GGCCAGAAGG AAGAGGTGGA GGTGGGAGGA ACCAGATGTC CCTGGCTCCA GCCAGGACAG 360
AGGGCAAGGC TACCTACATT GCAGCCACCA CCTCCTGGCC AGCCCAGCCT CCTGTCACAT 420
GTGGCAGGGG CATCAGGTGT AAGACCTTCT GGGACCGAAG CTGCTTCCAG AGTCTTCTTT 480
AGGCCACCAT GTCTCCACCC GCTGGATCTC CAGTGGAAAC ACCTGCTTTT ACTCCTACTG 540
TTTCCCAAAC AACCCCTCAG AACTGACCTC TCTGTTCTGT GCTGGTCAGC CCATGTGTCT 600
GTCCCTGGCT GGGTTGTCCA GGGAGGTCAA GGGCTTGACT CACTTATGTA GTCATCATCC 660
TGGAAAAAGA GACTTGAGGA AGATCCTCCC AGCCCTGCTG AGCAGATGAG GAAACTGGGG 720
CTCGGAGAGA CGAATAACAG GAAGTCTTAG AGGAACTCCA TTCCAAGGGT TTTGAGCTTG 780
AATTTGGACC TCAGTCGGGG GCAGAAAAGG AGTTGTTGGC TTATTCTCTA TTCTGTAAAT 840
TTCCTGGGCA AAAGCATCCC TTTTTCAGTC CCCTAATCTT CCCACCCCAG TGTTGGCTGG 900
TTCAGGTGGA GCCTGGGGCT GAGGTTGGCG GGCTCTGGGG TTCCGGGGAA TGAGAGCTGC 960
TGCAGAGACT CCTGCAGTGG GAGCCAGAAC ACTCCAGAGT CAGGTGTGAA CCGTCCCACT 1020
CCTCCTCTGG GAAGAGGAAG CAGGGCCAAT TTTGAAGTAT GTGCAGCCTC TTACGGCTCA 1080
GGGGGCCCTG TCAAATGCTG CTTTCTGAGC AGCCACCAAG CTGGGCTGGC GGGCACCAGC 1140
TTCAATGAGG GCAGGGGCAT GCACAGCCCT GGCAGGGCCG AGGAGGGACA ACCATGAGCC 1200
AAGCTGACCC CCATCAGCGG CCCAGCCTCA AGGCCTTTCC AGGTCACACA TTTGCAACTT 1260
GGGTGAATGA ACAGCGACAA GAACCCTGCC ACGGGGCAGG CTTTCTGCAA AGGCCCATGG 1320
TGGTTGGTGG CCTGGCCAGC GGGCCCAGTC TCGGACCGTG GCCCAGTGCC AGCAGCCGGG 1380
AGTATCCAGC CTGTAACTGG GCACTAAGCC AGCCTGGGCA GGAATCATCG GAAGATGGGG 1440
CAGGGCTTGA GGTCGAGGCC TTGGTAGCCT GACTTTGCAT CCAGTTCCTG CACTCCCAGC 1500
TCTATACCTT CTTTGTTTCA GTTTCTACTT CTCTGAGTTT CAGTTTCTTT GTCTGTAAAA 1560
TGGGAATAAG GATCAGACTG ACCTTGGGGT CACAGTGCAT GTGGGGGACA AAGCTTAGCA 1620
CAGTGCCCTC CATTGTTGGC CGTGATTGTT GTTACTGTCC TGGCCCCTCA GCATTTGGCT 1680
CTTAGAAGAA GGGAGGCCAG CCCGTGCGCT CTGAGGGTGG GCTCCACAGA GGACCAAAAG 1740
GGCAGGCCCA GTGCTAGGGC CTGGGAACCC AGCATCCTCC CAGATTGATT CGTTCCTCCT 1800
CAGCCAGGCA GGGGTTTTGC TGAGAGAAAC AGGAGCCGGG GCTGCTGCCG GCATGAAATC 1860
CCATTTTATG GTCAACCAGA TGTGCTTTCC TAAAATTTCA GCCTTGGGCC TCGGCCCCAG 1920
CGGACGCTCG GAAGGCATGG CCACTGCAGC CTCCCAGAGT TATTTACGGC TGACAAAAAT 1980
CGCAGCACTG TTGATCAGCC CGACAAGTGC CGGCTGGTGT CCCCTAGCAA CCGTGCTGAC 2040
AAGCAGGCTG TGCAGGGACT TGCTGCTTGT GGCTCTGGCT CTGGTCACCA GGAGTTTATT 2100
TGGGAGCCTG ACCTGGCCTG AGGAGGAGGC CAAGAGGGTG GAGGCGGCTC TGAGACACAC 2160
ACCTGCCCAG AGGATGATAT GGGACAACTT CCCAAGGAGG GAAAGGCTCA GAAGGAAGTG 2220
GGTCCTGGCC TCAGTGCCTG GATGGTGGTC CCTTTGGCCT CCCACCAAAG CCAACCTTGT 2280
CCTGGGCAGC TCCAGCCTGC AGACCTCTGG CTCTTCTGCC CCTGTGCCTT CCATCTCTAG 2340
GGCTCCCCCA ACCCATTAGT GCCCTTGCCT CACCCAAGCC CAGTCACCAC CTCCAGCTGC 2400
TCCCAGGTCA GTAGCCCAGA AATTGCCACA TCCTGCTCCG TGCCTGCAGT CTACTGCTCT 2460
CCCTGCTCAC TTGTCTCCCA GGCCCTCCAC CCTTCTTTGT CCTGCTTTCT TCACTCACTC 2520
CCTGTATGGC ACTGGCCTGC TATGCCCCAG CCCTTGTCCC TCACTGAGGC CAGAACCCTG 2580
GCAGAGCCTC ACCCAGTAAG AGCCACTCCC TCCACCAGGA GAAATCCCAT AGCGCTGAGC 2640
AGGGCAGTCC CTGCCGCACA CCCCACCTCA TACCTGCTGC CCACATGCTG AGCCCTGCCT 2700
CCCTCAGGAC AGCGTCCCCT CTGTCCTCAT ACCAGGGCCT CTAACTTCTG CCAGCCGAGC 2760
CTCTCGGTCC ATTCTCTTCC CTTCCCTCCT GTCTTCCTTC CCCCACAGGG GCTCTTTTCC 2820
AGCCCACACC TGCAGCTGAC GAGTCTGTCT TTTCTTCATC CCCTCTGCGG GTCCTTTTCC 2880
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