| Tag | Content |
|---|
EnhancerAtlas ID | HS098-22785 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr16:88838360-88841260 |
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 | CTATGCCCGT CCACCCGCGG CCCCAGGCCC TCCTGAGACT CTATGCCCAT CCACCCGCGG 60
CCCCAGGCCC TCCTGAGACT CTATGCCCGT CCACCCGCGG CCCCAGGCCC ACCTGAGACT 120
CTATGCCTGT CCACCCGCGG CCCCAGGCCC TCCTGAGACT CTGGTCAGGA TGCCTGTCCA 180
CCTGCGGCCC CAGGCCCTCC TGAGACTCTG GGCATGGCTG TCAGAATGAC CATCCCTGGT 240
GCCATTGAGA CCCCAGATCC AGCACCTGTG TCCAGCGCTG AAGTCCCAAG TCTGTGTCCA 300
AGCTCAGAAG GAGGGCCCAG AATCCCAGAC GTATCATGGC AGCAAGTGAG CCGGGGGTTG 360
GGACAGGTAA GCAGGCTCTT GTGGCTTAGC CACCAGCTCG GAATATACTT TCCATGTGGA 420
CATGAGGCCC AGGTGCCAAT AACCAACAGC CACGCTGGAG CTGAGGGCCC TGGGAGCCTG 480
CAGGCCCCAG CCCACAGGCA GGTGGCAGAG GGCACGGCTT CCTCCCTCAT AAAAAGGCCC 540
GTGCCTGGCA GGGCACAGTG GCTCACGCCT GTAATCCCAG CACTTTGGGA GGCCGAGGCA 600
AGCAGATCAC GAGGTCAACA GATCAAGACC ATCCTGGACA ACATGGTAAA ACCCCGTCTC 660
TACTAAAAAT ACAAAAATGA GCCGGGCGTG ATGGTGGGTG CCTGTAATCT CAGCTACTGG 720
GGAGGCTGAG GCAGGAGAAT CGCTTGAACC TGGGAGGCGA AGGTGGCAGT GAGCTGAGAT 780
CGTGCCACTG CATTCCAGCC TGGCCAAAGA GTGAGACTCT GTCAAAAAAA AAAAAAAAAA 840
GGCCTGTGCC CCCTCCTCCC TGTTCTCTGA GGGGGATGCC CGCCGCAGCC CTGGCTCAGT 900
CTTCATGTCA CCCCCTTGCA AATGTGCAAG CTCCTGAGGC CGCAGGCTGG GGTGGGCCAT 960
GGCAGGGCCA GCCTCCCCTC CAAACACCCA CGGGACACGT GAGTGGAGGC ACATGGCTTC 1020
CAGCTGGCCC CAGGGGTGCC TGGAAGACTG TGTCAGCCTC TGGAATGTGA GGCGGCCTGT 1080
CTGTCCACCC AGAAGCTTCT GGCACTCCAG GGAGCTCGAG CTCGCTGTGC TCTGGAAGCA 1140
GCAATTACTC CTCCATCTGT CACCAGCGGC TCCAGCCAGC CCTCAGGTCC ACGTGCCTCC 1200
TTCCTCCTGG GTCTCATTGA TTCAGGCTGA GCCTCCCCCT CTGGCCCCCC AGTAACTCCC 1260
GGCGTCACGC CCAGGCCCTC GCTCAGGGGA TCTGAGTAGA GGGGAGGCCT GAGTCAGGAC 1320
AGCCCTCCAA GAGTGGGCAG CCAACGAGGG ACCCCCTGAA TAAAAACCGC AGAGGAGGTC 1380
TGCCCACCTG GCGTGGGGGC CAGGGAGGAG GTGGGCAGGG GGAGGGGCCT TGCCCGAGAC 1440
CAGAGGTGGC TGGGGGCCGA GGGTCGGCAG GAAGCCAGGC GACCGATGGG CGCAGCACAG 1500
ACTGCCTCCA CGTGGCCCTG CACAGCCTGG CCTCACTAGG GGAAGGGTGA AGACAGCAGC 1560
TGGCGCTTCC CCTCAAAAAA ACCCTGGGGG CTCAAGGCCA CCCCTGAGGT CTCCAGGCTC 1620
CTAGGAACAG GGCCTGACAG GGAAAAGGCT GACAGGCAGG TCGGGGGACT GGACAGCAGC 1680
TGCCTATTGG GTGACAGGCA GGTCGGGGGA GTGGACAGCA GCTGCCTACT GGGTGACAGG 1740
CAGGTCGGGG GAGTGGACAG CAGCTGCCTA CTGGGTGACA GGCAGGTCGG CGGAGTGGAC 1800
AGCAGCTGCC TACTGGGGGT GAGGGCTCCG GCCACCCTGC ACCCAGTGTC CTCCTGGGTG 1860
GTCTTAGGAA GAGGGTCACT CGACCCCAGC CCTCCAGTGC AGGGCCCCAC CGGAGCTTGC 1920
TCTGGGCACT TCTGGCCCTG CCAAAAGTCC CCTCAGGTGC CACCATCCCT GACCACCAAC 1980
ACCTCCCTGC AGGTCCCCCG AGTCCCTTCA GCACCGCAAG CCTCCTCCCC GCCACTGCTG 2040
ACCTTCAGAG ATTGGGGCCC CTCCAGGCCT CCCTCTCCCC TGGCTTGGAA GTTCTGTGCC 2100
CGGCGATAAG GTCTGGGATG CAGCTCCCAA CACAGCAGGA ACCGGTCACC AGGCAGGGCT 2160
GGGTGGGCGT GGCCTGAGCT TCTAAGCGCA TGACTGTCAC CTCCTCCTGG CCTCTGCCTG 2220
GGCCCCCTTC CCACCCACAG GATGGCGACG CCCAGTGACT CCCTGACCAG GCTGTAATAA 2280
TATAAACTAG AGGTCCAGCC TGGTGATACA TGCCTGTAAT CCCAGCTACT CAGGAGGCTG 2340
AGGCATGAGA ATCGCTTGAA CCCGGGAGGC GGAGTTTGCG ATGAGTCGAG ATTGTGCCAC 2400
TGCACACCAG CTTGGGCGAC AGAGCGAGAC TCTGTCTCGA TAAGTAAATA AATAAAAATA 2460
ACAATATAAA CTGGAGAAAG ACACCCGTGG GTGCTGAAGG GGAAAACAGG ACCCAGCTGT 2520
GATAGCCAGG ACAGCTCAGG GTCAAGGAGA CTCACTCCTG GGCTCCAGAG TCCCCAGCAG 2580
CAGCCTGGGC ACCTCTGTAT ACCACGTGGA GGAGAAACGG GTGGGCATCG CTGGCCCAGC 2640
TGCAGGTCTG AGTGGGGGTC CCAGGAAGCC TGAAAAGGAA GCCGGCAATC CCGCGCTGGA 2700
CCCATGAAGA AGGGCCGACC AGACAAGGAT GGGGCCCAAG GGCAAAGAGA CCGCTTGTCT 2760
TATGCCACAG TGGCTGGGGA GAGCACTCTT AGGGTACATG GGGTTCCCTG CAGGATTCCG 2820
CAAAAACAGG GCACCCCGGA GCCGGCTGCG CAGGAGCGAA CGGTGCCCAC ATGGTCTAAG 2880
ATACCTCAGC ACAGCCTCCT 2900
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