| Tag | Content |
|---|
EnhancerAtlas ID | HS095-13350 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr17:79392200-79394650 |
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 | CTGCCCCAGG AGACGCAGCT CAGAACTGAG CAGCTGTGCC GGGTCAGGGT CTGGTTCCCA 60
TGCAGCAGTG GGCTGGGGGG CTGGAGCTGC AACTTGATGG AGATCTGAGG CCCCCCTCTA 120
CCACCAGTGG GCCGGGACAT GCCCCGACCC AGGGCAGCTG TTCATCCCGG TGCCGCTTCA 180
ATGCCACCTT TTGCACAGCG GAGGCCAAGA GCCCTTGCCA AGGTTCAGGT CAGTAAGTGG 240
ATAAGTCTGG TGGAGGCCTG AGCCCTGGGA AGCAGCATCT TTGAGGACTT GCCCAGCTGT 300
GTGGCTCCCA TGCCCGAGAA CAGAGTCTGC CAAGGTGCGC ACACCCACAG ACGTGTGTGT 360
GTGTACGTGT GTGTACGTGT GTGTGTACGT GTGTGCGTGT GTGTGTGTAC GTGTGTGTGT 420
GTGTGTGTGT GTAGCCACTC ATCCCAGACA TGTAGCACAG TCAGACCTTG TGTGTACACC 480
CATAGTCACG TGCATATGCC CAGAGACAGG TTTGCACAGA CACACCCCGT GAGTCACACA 540
CAGTCCCTCC CCTGCCTCTG TGCAAGTGTG AGTGTGTGCA AGTGTGAGTG TGTGCAAGTG 600
TGAGGTGCAC CCCACATCTC GAGTCTGGAC CACTAGTGAT TGCAGCCAGG GTGGGGGAAG 660
CATCACTGGG TTGTATCTGG GGGTTGAGCC TGCAAACACC TGCACACCCA GCATGCACCT 720
GCCTGTCTCC CAGCCACATC TGCACACTGG GGTGGCATGT GGCTGGGCCT CTAGCCCCTG 780
CCACAGCAGC TTCTGGTCTC CTGGTGCGGG CGGAGGTCCC AGAGTGGCCT CTCACCCCAG 840
GCAGAGCCTG GTCTCCCCAC CCCGTCCCTC ATTCCTCTTT CTGGGCAGCC AAATGGTCAG 900
ATGCTACACC CCTGCCTCCA AGCAGGCTGC ACCTCCCCTC TGCATCCACG CAGGAACCTG 960
TGCAGGGCGG CTTCCTCCCC GCGCTTTCCC GGAATGAGGA ATGTGGGGCA GGGCCAGCAG 1020
GGGGGCTGCT CCTCCTTCCT GCCTCCCCTC CCGTCCTGCA CAGCTCCCTT GGGAGCCTGG 1080
CTCGTGGGAA GTGTGCTTGG GACCGCCCAT CACTCCGTTC CCAGCCACTC CTGGTGTCCC 1140
CCGCCTGGGC GGGCCCTGTG GGGAGCGGGG AAGGTGTGGA GCGGAAGCCA GTGCCGAGGG 1200
AAGAGGGGAG CCTGAGTGGG TGTGGGTCGG GGGTGGGAGC TGACGCAGGC GGCGGGTGCA 1260
GCCGCCAGAC TCGGAGCCGG GGAGGCCCAT GCCAGCAGCC CGGCAGCTGG GCTTCCGGAA 1320
GCAGCGGGAG CCGGGAGCCT GGGAAGGGCC TCGCTGCTTC TCTGGAGCTG CCGCCATCTC 1380
AACGAGGCGT TTTTTTTTTT TTTTTTTTTT ACAACCCATT TCACAGTTTC CAGAAAAGGA 1440
GGATGCTGTC TCGGCGGCTC ACTTAACTCA AAACAAATGC TCGCTCTGCC GGCTCCGCGC 1500
CCGCCTCTCC CGGCTCCCGG GCCCTGCCGT CCTCTTGTTC CGTCTGCCTT CAGTCTGGTG 1560
CCACAGGGCG GAGCAGGGTC AGCCTGGCAG GAGAGTGGGG TGGGGCACAG TGGGCACCTG 1620
GCCATCCGAT TGCCCAGGCC CAGCCTCTGC TGTGTGGGTC CTCGGGACCC TGGATGGGGG 1680
CTGCTGGCAC GGCTGCTGGA CCGACCCTTA CAGAGGGAGT GGCTCTCCGG GGAGTCCTGG 1740
GCTCCAGGGC CCCAGCATGC TCTGTACCCC TCAGGCTGCC CAGCATGTGT TGCCCTTCTT 1800
AGCCATCCAT GGCAAGGAGC CTGGAAGACA GGTTGGCAGG AGGCAGGCTA GTTCCCATCG 1860
GCTGTCCTGG CCACTTAGGG CCACCTCTGC TGTAAGCCCA TGTGGCCAGC TCTCACCTAC 1920
TGTGTGCCGG CCTCCCCACA CAGCACCCCT GGGCCGGGGC CAGGCTCACT GGGCACCGAG 1980
ACTCCAGCCC AGCTGTTGTG CAGCTGTTCC CCAGTCTTCC CGCTGCTGGG CCACCCTGGG 2040
ACAGCAGGTC CAGGCACAGC CTGCCTCCTG GTCTAGTTGG CTGGACCTTG GGCTCCGGGT 2100
CAGACTGGCC TCCCAGGGAT GGGGCTGTGC CCGAGGACCT GAGCCACCTG GGGGTGGCCA 2160
CAGCCCTCCT GGTGTTGCTG TCTCCCGAAA CCATTTCCTC AGCTAGCCGG CCGCCCAAGC 2220
CAGGCCTCTA CAGCATCTTG GGCAGAGCTG AGGTGGCCCT GGAGCTGGGG CCAGAGCCCG 2280
GTCTGGATCT AGAGCTGCAA ACCCGGCCTG GGCCGGCTGG GCAGTGGGGG CAGCCAACTG 2340
GAGGCCAGTG TGCAGTCCTC GGTGGCCCCG CTGACACCGC ATCCCGCTTA CTGTCCCTTC 2400
CCCAGGAACA TCCTAAACTC ATGCTGCCTC CTGTGATGAG AGCTGATGGG 2450
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