| Tag | Content |
|---|
EnhancerAtlas ID | HS191-15352 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr16:88838410-88841370 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr16:88840520-88840534 | GGGTGGGCGTGGCC | - | 6.69 | | Klf12 | MA0742.1 | chr16:88840519-88840534 | TGGGTGGGCGTGGCC | - | 6.28 | | Nr2f6(var.2) | MA0728.1 | chr16:88838970-88838985 | GAGGTCAACAGATCA | + | 6.15 | | Nr5a2 | MA0505.1 | chr16:88839947-88839962 | GGGCTCAAGGCCACC | + | 6.07 | | PLAG1 | MA0163.1 | chr16:88839594-88839608 | CCCCCTCTGGCCCC | - | 6.18 | | SP1 | MA0079.4 | chr16:88840521-88840536 | GGTGGGCGTGGCCTG | - | 7.44 | | SP3 | MA0746.2 | chr16:88840521-88840534 | GGTGGGCGTGGCC | - | 7.52 | | SP4 | MA0685.1 | chr16:88840519-88840536 | TGGGTGGGCGTGGCCTG | - | 7.05 | | SP8 | MA0747.1 | chr16:88840521-88840533 | GGTGGGCGTGGC | - | 6.62 | | ZNF263 | MA0528.1 | chr16:88839763-88839784 | GGAGGAGGTGGGCAGGGGGAG | + | 6.08 |
|
| | Number of super-enhancer constituents: 15 | ID | Coordinate | Tissue/cell |
| SE_19495 | chr16:88839529-88840681 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20944 | chr16:88833062-88841844 | CD8_Memory_7pool | | SE_26909 | chr16:88838435-88840646 | Esophagus | | SE_26909 | chr16:88840699-88841897 | Esophagus | | SE_41570 | chr16:88838421-88839005 | LNCaP | | SE_41570 | chr16:88839199-88841823 | LNCaP | | SE_42993 | chr16:88839041-88841790 | Lung | | SE_45418 | chr16:88838420-88841550 | NHLF | | SE_47797 | chr16:88838526-88839006 | Pancreas | | SE_47797 | chr16:88839163-88840165 | Pancreas | | SE_50742 | chr16:88839023-88841254 | Sigmoid_Colon | | SE_53797 | chr16:88839090-88840673 | Spleen | | SE_54707 | chr16:88832832-88841883 | Stomach_Smooth_Muscle | | SE_56985 | chr16:88838441-88838803 | VACO_400 | | SE_56985 | chr16:88839162-88839582 | VACO_400 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I088766 | chr16 | 88833274 | 88841799 |
|
Enhancer Sequence | CCACCCGCGG CCCCAGGCCC TCCTGAGACT CTATGCCCGT CCACCCGCGG CCCCAGGCCC 60
ACCTGAGACT CTATGCCTGT CCACCCGCGG CCCCAGGCCC TCCTGAGACT CTGGTCAGGA 120
TGCCTGTCCA CCTGCGGCCC CAGGCCCTCC TGAGACTCTG GGCATGGCTG TCAGAATGAC 180
CATCCCTGGT GCCATTGAGA CCCCAGATCC AGCACCTGTG TCCAGCGCTG AAGTCCCAAG 240
TCTGTGTCCA AGCTCAGAAG GAGGGCCCAG AATCCCAGAC GTATCATGGC AGCAAGTGAG 300
CCGGGGGTTG GGACAGGTAA GCAGGCTCTT GTGGCTTAGC CACCAGCTCG GAATATACTT 360
TCCATGTGGA CATGAGGCCC AGGTGCCAAT AACCAACAGC CACGCTGGAG CTGAGGGCCC 420
TGGGAGCCTG CAGGCCCCAG CCCACAGGCA GGTGGCAGAG GGCACGGCTT CCTCCCTCAT 480
AAAAAGGCCC GTGCCTGGCA GGGCACAGTG GCTCACGCCT GTAATCCCAG CACTTTGGGA 540
GGCCGAGGCA AGCAGATCAC GAGGTCAACA GATCAAGACC ATCCTGGACA ACATGGTAAA 600
ACCCCGTCTC TACTAAAAAT ACAAAAATGA GCCGGGCGTG ATGGTGGGTG CCTGTAATCT 660
CAGCTACTGG GGAGGCTGAG GCAGGAGAAT CGCTTGAACC TGGGAGGCGA AGGTGGCAGT 720
GAGCTGAGAT CGTGCCACTG CATTCCAGCC TGGCCAAAGA GTGAGACTCT GTCAAAAAAA 780
AAAAAAAAAA GGCCTGTGCC CCCTCCTCCC TGTTCTCTGA GGGGGATGCC CGCCGCAGCC 840
CTGGCTCAGT CTTCATGTCA CCCCCTTGCA AATGTGCAAG CTCCTGAGGC CGCAGGCTGG 900
GGTGGGCCAT GGCAGGGCCA GCCTCCCCTC CAAACACCCA CGGGACACGT GAGTGGAGGC 960
ACATGGCTTC CAGCTGGCCC CAGGGGTGCC TGGAAGACTG TGTCAGCCTC TGGAATGTGA 1020
GGCGGCCTGT CTGTCCACCC AGAAGCTTCT GGCACTCCAG GGAGCTCGAG CTCGCTGTGC 1080
TCTGGAAGCA GCAATTACTC CTCCATCTGT CACCAGCGGC TCCAGCCAGC CCTCAGGTCC 1140
ACGTGCCTCC TTCCTCCTGG GTCTCATTGA TTCAGGCTGA GCCTCCCCCT CTGGCCCCCC 1200
AGTAACTCCC GGCGTCACGC CCAGGCCCTC GCTCAGGGGA TCTGAGTAGA GGGGAGGCCT 1260
GAGTCAGGAC AGCCCTCCAA GAGTGGGCAG CCAACGAGGG ACCCCCTGAA TAAAAACCGC 1320
AGAGGAGGTC TGCCCACCTG GCGTGGGGGC CAGGGAGGAG GTGGGCAGGG GGAGGGGCCT 1380
TGCCCGAGAC CAGAGGTGGC TGGGGGCCGA GGGTCGGCAG GAAGCCAGGC GACCGATGGG 1440
CGCAGCACAG ACTGCCTCCA CGTGGCCCTG CACAGCCTGG CCTCACTAGG GGAAGGGTGA 1500
AGACAGCAGC TGGCGCTTCC CCTCAAAAAA ACCCTGGGGG CTCAAGGCCA CCCCTGAGGT 1560
CTCCAGGCTC CTAGGAACAG GGCCTGACAG GGAAAAGGCT GACAGGCAGG TCGGGGGACT 1620
GGACAGCAGC TGCCTATTGG GTGACAGGCA GGTCGGGGGA GTGGACAGCA GCTGCCTACT 1680
GGGTGACAGG CAGGTCGGGG GAGTGGACAG CAGCTGCCTA CTGGGTGACA GGCAGGTCGG 1740
CGGAGTGGAC AGCAGCTGCC TACTGGGGGT GAGGGCTCCG GCCACCCTGC ACCCAGTGTC 1800
CTCCTGGGTG GTCTTAGGAA GAGGGTCACT CGACCCCAGC CCTCCAGTGC AGGGCCCCAC 1860
CGGAGCTTGC TCTGGGCACT TCTGGCCCTG CCAAAAGTCC CCTCAGGTGC CACCATCCCT 1920
GACCACCAAC ACCTCCCTGC AGGTCCCCCG AGTCCCTTCA GCACCGCAAG CCTCCTCCCC 1980
GCCACTGCTG ACCTTCAGAG ATTGGGGCCC CTCCAGGCCT CCCTCTCCCC TGGCTTGGAA 2040
GTTCTGTGCC CGGCGATAAG GTCTGGGATG CAGCTCCCAA CACAGCAGGA ACCGGTCACC 2100
AGGCAGGGCT GGGTGGGCGT GGCCTGAGCT TCTAAGCGCA TGACTGTCAC CTCCTCCTGG 2160
CCTCTGCCTG GGCCCCCTTC CCACCCACAG GATGGCGACG CCCAGTGACT CCCTGACCAG 2220
GCTGTAATAA TATAAACTAG AGGTCCAGCC TGGTGATACA TGCCTGTAAT CCCAGCTACT 2280
CAGGAGGCTG AGGCATGAGA ATCGCTTGAA CCCGGGAGGC GGAGTTTGCG ATGAGTCGAG 2340
ATTGTGCCAC TGCACACCAG CTTGGGCGAC AGAGCGAGAC TCTGTCTCGA TAAGTAAATA 2400
AATAAAAATA ACAATATAAA CTGGAGAAAG ACACCCGTGG GTGCTGAAGG GGAAAACAGG 2460
ACCCAGCTGT GATAGCCAGG ACAGCTCAGG GTCAAGGAGA CTCACTCCTG GGCTCCAGAG 2520
TCCCCAGCAG CAGCCTGGGC ACCTCTGTAT ACCACGTGGA GGAGAAACGG GTGGGCATCG 2580
CTGGCCCAGC TGCAGGTCTG AGTGGGGGTC CCAGGAAGCC TGAAAAGGAA GCCGGCAATC 2640
CCGCGCTGGA CCCATGAAGA AGGGCCGACC AGACAAGGAT GGGGCCCAAG GGCAAAGAGA 2700
CCGCTTGTCT TATGCCACAG TGGCTGGGGA GAGCACTCTT AGGGTACATG GGGTTCCCTG 2760
CAGGATTCCG CAAAAACAGG GCACCCCGGA GCCGGCTGCG CAGGAGCGAA CGGTGCCCAC 2820
ATGGTCTAAG ATACCTCAGC ACAGCCTCCT GGGCGCTGAA ACCACCCAGG CATTCAGAGA 2880
TGGTAATACC AGGCCTGGGA ATTAACCCCA GAGGAACCAG TCAAAGGAAG GAAAAACAGG 2940
CGCAAAGATA GTGGCTATGT 2960
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