| Tag | Content |
|---|
EnhancerAtlas ID | HS112-06507 |
Organism | Homo sapiens |
Tissue/cell | KELLY |
Coordinate | chr17:79392620-79395370 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr17:79394296-79394311 | GGGTCAGACTGGCCT | + | 6.24 | | EWSR1-FLI1 | MA0149.1 | chr17:79393229-79393247 | TCCTCCTTCCTGCCTCCC | - | 6.08 | | EWSR1-FLI1 | MA0149.1 | chr17:79393233-79393251 | CCTTCCTGCCTCCCCTCC | - | 7.49 | | Myod1 | MA0499.1 | chr17:79394198-79394211 | TGCAGCTGTTCCC | + | 6.98 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_00395 | chr17:79390125-79398087 | Adipose_Nuclei | | SE_01010 | chr17:79392619-79395878 | Adrenal_Gland | | SE_01625 | chr17:79389351-79398706 | Aorta | | SE_05872 | chr17:79388722-79398913 | Brain_Hippocampus_Middle | | SE_26559 | chr17:79390386-79395974 | Esophagus | | SE_28164 | chr17:79392457-79394609 | Fetal_Intestine | | SE_29440 | chr17:79392485-79394550 | Fetal_Intestine_Large | | SE_29667 | chr17:79391361-79395846 | Fetal_Muscle | | SE_31439 | chr17:79390530-79395902 | Gastric | | SE_34246 | chr17:79391602-79395908 | HCT-116 | | SE_40858 | chr17:79390369-79395795 | Left_Ventricle | | SE_42181 | chr17:79390117-79398205 | Lung | | SE_44415 | chr17:79390147-79395782 | NHDF-Ad | | SE_47177 | chr17:79391538-79395537 | Panc1 | | SE_48277 | chr17:79391225-79395813 | Psoas_Muscle | | SE_48718 | chr17:79390442-79395880 | Right_Atrium | | SE_50245 | chr17:79389672-79395981 | Sigmoid_Colon | | SE_51344 | chr17:79390313-79398121 | Skeletal_Muscle | | SE_52635 | chr17:79390061-79395764 | Small_Intestine | | SE_53447 | chr17:79391260-79395889 | Spleen | | SE_54670 | chr17:79389831-79398114 | Stomach_Smooth_Muscle | | SE_56968 | chr17:79392274-79394812 | VACO_400 | | SE_65328 | chr17:79390158-79401315 | Pancreatic_islets | | SE_67997 | chr17:79358663-79398404 | TC32 | | SE_68398 | chr17:79359303-79407988 | TC71 |
|
| | 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 |
| GH17I081416 | chr17 | 79390540 | 79398129 |
|
Enhancer Sequence | GTGTGTGTGT GTAGCCACTC ATCCCAGACA TGTAGCACAG TCAGACCTTG TGTGTACACC 60
CATAGTCACG TGCATATGCC CAGAGACAGG TTTGCACAGA CACACCCCGT GAGTCACACA 120
CAGTCCCTCC CCTGCCTCTG TGCAAGTGTG AGTGTGTGCA AGTGTGAGTG TGTGCAAGTG 180
TGAGGTGCAC CCCACATCTC GAGTCTGGAC CACTAGTGAT TGCAGCCAGG GTGGGGGAAG 240
CATCACTGGG TTGTATCTGG GGGTTGAGCC TGCAAACACC TGCACACCCA GCATGCACCT 300
GCCTGTCTCC CAGCCACATC TGCACACTGG GGTGGCATGT GGCTGGGCCT CTAGCCCCTG 360
CCACAGCAGC TTCTGGTCTC CTGGTGCGGG CGGAGGTCCC AGAGTGGCCT CTCACCCCAG 420
GCAGAGCCTG GTCTCCCCAC CCCGTCCCTC ATTCCTCTTT CTGGGCAGCC AAATGGTCAG 480
ATGCTACACC CCTGCCTCCA AGCAGGCTGC ACCTCCCCTC TGCATCCACG CAGGAACCTG 540
TGCAGGGCGG CTTCCTCCCC GCGCTTTCCC GGAATGAGGA ATGTGGGGCA GGGCCAGCAG 600
GGGGGCTGCT CCTCCTTCCT GCCTCCCCTC CCGTCCTGCA CAGCTCCCTT GGGAGCCTGG 660
CTCGTGGGAA GTGTGCTTGG GACCGCCCAT CACTCCGTTC CCAGCCACTC CTGGTGTCCC 720
CCGCCTGGGC GGGCCCTGTG GGGAGCGGGG AAGGTGTGGA GCGGAAGCCA GTGCCGAGGG 780
AAGAGGGGAG CCTGAGTGGG TGTGGGTCGG GGGTGGGAGC TGACGCAGGC GGCGGGTGCA 840
GCCGCCAGAC TCGGAGCCGG GGAGGCCCAT GCCAGCAGCC CGGCAGCTGG GCTTCCGGAA 900
GCAGCGGGAG CCGGGAGCCT GGGAAGGGCC TCGCTGCTTC TCTGGAGCTG CCGCCATCTC 960
AACGAGGCGT TTTTTTTTTT TTTTTTTTTT ACAACCCATT TCACAGTTTC CAGAAAAGGA 1020
GGATGCTGTC TCGGCGGCTC ACTTAACTCA AAACAAATGC TCGCTCTGCC GGCTCCGCGC 1080
CCGCCTCTCC CGGCTCCCGG GCCCTGCCGT CCTCTTGTTC CGTCTGCCTT CAGTCTGGTG 1140
CCACAGGGCG GAGCAGGGTC AGCCTGGCAG GAGAGTGGGG TGGGGCACAG TGGGCACCTG 1200
GCCATCCGAT TGCCCAGGCC CAGCCTCTGC TGTGTGGGTC CTCGGGACCC TGGATGGGGG 1260
CTGCTGGCAC GGCTGCTGGA CCGACCCTTA CAGAGGGAGT GGCTCTCCGG GGAGTCCTGG 1320
GCTCCAGGGC CCCAGCATGC TCTGTACCCC TCAGGCTGCC CAGCATGTGT TGCCCTTCTT 1380
AGCCATCCAT GGCAAGGAGC CTGGAAGACA GGTTGGCAGG AGGCAGGCTA GTTCCCATCG 1440
GCTGTCCTGG CCACTTAGGG CCACCTCTGC TGTAAGCCCA TGTGGCCAGC TCTCACCTAC 1500
TGTGTGCCGG CCTCCCCACA CAGCACCCCT GGGCCGGGGC CAGGCTCACT GGGCACCGAG 1560
ACTCCAGCCC AGCTGTTGTG CAGCTGTTCC CCAGTCTTCC CGCTGCTGGG CCACCCTGGG 1620
ACAGCAGGTC CAGGCACAGC CTGCCTCCTG GTCTAGTTGG CTGGACCTTG GGCTCCGGGT 1680
CAGACTGGCC TCCCAGGGAT GGGGCTGTGC CCGAGGACCT GAGCCACCTG GGGGTGGCCA 1740
CAGCCCTCCT GGTGTTGCTG TCTCCCGAAA CCATTTCCTC AGCTAGCCGG CCGCCCAAGC 1800
CAGGCCTCTA CAGCATCTTG GGCAGAGCTG AGGTGGCCCT GGAGCTGGGG CCAGAGCCCG 1860
GTCTGGATCT AGAGCTGCAA ACCCGGCCTG GGCCGGCTGG GCAGTGGGGG CAGCCAACTG 1920
GAGGCCAGTG TGCAGTCCTC GGTGGCCCCG CTGACACCGC ATCCCGCTTA CTGTCCCTTC 1980
CCCAGGAACA TCCTAAACTC ATGCTGCCTC CTGTGATGAG AGCTGATGGG AAGCCTGGCA 2040
GAGCGGCCCC AGGCAGGCTC TGTGTGGGGC CAGGGTGCCC TGACCATGCA CGCGGGTGGG 2100
GACAGGCCGT GTTCAGCCCC CAGCGGAGCA CTTGGGGCTA TGGGCCTGGA CCAGCAACTT 2160
AGACTTGGTC ATGCTCCATC TCTTACCAGC CCCATGGCGG GCCCACGACC GACCTTGGGA 2220
GCATGATGGC ACTACGTCAC ATGAGTCTGA AGCCCCAGGT AGGGGAGGTG CCACTGCAGG 2280
CAGTGCCAGG ATGGGGCACT TGGTCTGAGG AGGTCTAGGT CAAGACCCCC TCCCTGGCCC 2340
CCAGCTGCCT CCGCCTGGGC TGGTAACCAC AGCACTTCCT TTGCCAAGAG GAAAGAGCCC 2400
TCAGCCCGGT TCCCGGCTGG CCTTGGCCCA CACGGTCTGG CCCTGGCTGG AGCCCAGGCT 2460
ACACTCGGCT CCCAGGCAGC TGAGGCACAG GCTCTGTCTG GGGTTGGCCA CTGGTCGGCG 2520
GGGGGGCTGG GGAGGTGGCA GCCTGGTCTG CCCACGGCTC TGCTGGCCAG TCACGGTGCC 2580
ATCCCCAAAC ACCGGGAGGC GGGGGTGACA GTAGAGGCGT GATGCTCTGT CCTGGGGTTT 2640
CCCGGGCTCC TCGGGAGCTG AGTGGGATAG GGAGGGCCTC AGGTGGCCGG CAGTCCCGTC 2700
CCCCACACTC GCAGGGGTCA CCACAGTAGT GACCACCTGG CAGGGCCTGC 2750
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