| Tag | Content |
|---|
EnhancerAtlas ID | HS007-07503 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr17:79392750-79395100 |
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 | CCTGCCTCTG TGCAAGTGTG AGTGTGTGCA AGTGTGAGTG TGTGCAAGTG TGAGGTGCAC 60
CCCACATCTC GAGTCTGGAC CACTAGTGAT TGCAGCCAGG GTGGGGGAAG CATCACTGGG 120
TTGTATCTGG GGGTTGAGCC TGCAAACACC TGCACACCCA GCATGCACCT GCCTGTCTCC 180
CAGCCACATC TGCACACTGG GGTGGCATGT GGCTGGGCCT CTAGCCCCTG CCACAGCAGC 240
TTCTGGTCTC CTGGTGCGGG CGGAGGTCCC AGAGTGGCCT CTCACCCCAG GCAGAGCCTG 300
GTCTCCCCAC CCCGTCCCTC ATTCCTCTTT CTGGGCAGCC AAATGGTCAG ATGCTACACC 360
CCTGCCTCCA AGCAGGCTGC ACCTCCCCTC TGCATCCACG CAGGAACCTG TGCAGGGCGG 420
CTTCCTCCCC GCGCTTTCCC GGAATGAGGA ATGTGGGGCA GGGCCAGCAG GGGGGCTGCT 480
CCTCCTTCCT GCCTCCCCTC CCGTCCTGCA CAGCTCCCTT GGGAGCCTGG CTCGTGGGAA 540
GTGTGCTTGG GACCGCCCAT CACTCCGTTC CCAGCCACTC CTGGTGTCCC CCGCCTGGGC 600
GGGCCCTGTG GGGAGCGGGG AAGGTGTGGA GCGGAAGCCA GTGCCGAGGG AAGAGGGGAG 660
CCTGAGTGGG TGTGGGTCGG GGGTGGGAGC TGACGCAGGC GGCGGGTGCA GCCGCCAGAC 720
TCGGAGCCGG GGAGGCCCAT GCCAGCAGCC CGGCAGCTGG GCTTCCGGAA GCAGCGGGAG 780
CCGGGAGCCT GGGAAGGGCC TCGCTGCTTC TCTGGAGCTG CCGCCATCTC AACGAGGCGT 840
TTTTTTTTTT TTTTTTTTTT ACAACCCATT TCACAGTTTC CAGAAAAGGA GGATGCTGTC 900
TCGGCGGCTC ACTTAACTCA AAACAAATGC TCGCTCTGCC GGCTCCGCGC CCGCCTCTCC 960
CGGCTCCCGG GCCCTGCCGT CCTCTTGTTC CGTCTGCCTT CAGTCTGGTG CCACAGGGCG 1020
GAGCAGGGTC AGCCTGGCAG GAGAGTGGGG TGGGGCACAG TGGGCACCTG GCCATCCGAT 1080
TGCCCAGGCC CAGCCTCTGC TGTGTGGGTC CTCGGGACCC TGGATGGGGG CTGCTGGCAC 1140
GGCTGCTGGA CCGACCCTTA CAGAGGGAGT GGCTCTCCGG GGAGTCCTGG GCTCCAGGGC 1200
CCCAGCATGC TCTGTACCCC TCAGGCTGCC CAGCATGTGT TGCCCTTCTT AGCCATCCAT 1260
GGCAAGGAGC CTGGAAGACA GGTTGGCAGG AGGCAGGCTA GTTCCCATCG GCTGTCCTGG 1320
CCACTTAGGG CCACCTCTGC TGTAAGCCCA TGTGGCCAGC TCTCACCTAC TGTGTGCCGG 1380
CCTCCCCACA CAGCACCCCT GGGCCGGGGC CAGGCTCACT GGGCACCGAG ACTCCAGCCC 1440
AGCTGTTGTG CAGCTGTTCC CCAGTCTTCC CGCTGCTGGG CCACCCTGGG ACAGCAGGTC 1500
CAGGCACAGC CTGCCTCCTG GTCTAGTTGG CTGGACCTTG GGCTCCGGGT CAGACTGGCC 1560
TCCCAGGGAT GGGGCTGTGC CCGAGGACCT GAGCCACCTG GGGGTGGCCA CAGCCCTCCT 1620
GGTGTTGCTG TCTCCCGAAA CCATTTCCTC AGCTAGCCGG CCGCCCAAGC CAGGCCTCTA 1680
CAGCATCTTG GGCAGAGCTG AGGTGGCCCT GGAGCTGGGG CCAGAGCCCG GTCTGGATCT 1740
AGAGCTGCAA ACCCGGCCTG GGCCGGCTGG GCAGTGGGGG CAGCCAACTG GAGGCCAGTG 1800
TGCAGTCCTC GGTGGCCCCG CTGACACCGC ATCCCGCTTA CTGTCCCTTC CCCAGGAACA 1860
TCCTAAACTC ATGCTGCCTC CTGTGATGAG AGCTGATGGG AAGCCTGGCA GAGCGGCCCC 1920
AGGCAGGCTC TGTGTGGGGC CAGGGTGCCC TGACCATGCA CGCGGGTGGG GACAGGCCGT 1980
GTTCAGCCCC CAGCGGAGCA CTTGGGGCTA TGGGCCTGGA CCAGCAACTT AGACTTGGTC 2040
ATGCTCCATC TCTTACCAGC CCCATGGCGG GCCCACGACC GACCTTGGGA GCATGATGGC 2100
ACTACGTCAC ATGAGTCTGA AGCCCCAGGT AGGGGAGGTG CCACTGCAGG CAGTGCCAGG 2160
ATGGGGCACT TGGTCTGAGG AGGTCTAGGT CAAGACCCCC TCCCTGGCCC CCAGCTGCCT 2220
CCGCCTGGGC TGGTAACCAC AGCACTTCCT TTGCCAAGAG GAAAGAGCCC TCAGCCCGGT 2280
TCCCGGCTGG CCTTGGCCCA CACGGTCTGG CCCTGGCTGG AGCCCAGGCT ACACTCGGCT 2340
CCCAGGCAGC 2350
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