| Tag | Content |
|---|
EnhancerAtlas ID | HS050-10904 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr11:2407020-2409390 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PLAG1 | MA0163.1 | chr11:2407703-2407717 | GTGGCCCTAGGGGG | + | 6.62 | | RREB1 | MA0073.1 | chr11:2408765-2408785 | CCACCCCCCAGCCCCCACCC | + | 6.02 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_01152 | chr11:2407457-2408719 | Adrenal_Gland | | SE_02091 | chr11:2407065-2409334 | Aorta | | SE_03032 | chr11:2407555-2408634 | Bladder | | SE_04400 | chr11:2405722-2413042 | Brain_Anterior_Caudate | | SE_05573 | chr11:2405785-2412981 | Brain_Cingulate_Gyrus | | SE_06164 | chr11:2398747-2415892 | Brain_Hippocampus_Middle | | SE_07349 | chr11:2405823-2413046 | Brain_Hippocampus_Middle_150 | | SE_08539 | chr11:2405824-2412470 | Brain_Inferior_Temporal_Lobe | | SE_09007 | chr11:2408080-2408397 | Brain_Mid_Frontal_Lobe | | SE_22977 | chr11:2405798-2411513 | CD8_primiary | | SE_26897 | chr11:2398408-2415129 | Esophagus | | SE_29923 | chr11:2407181-2407968 | Fetal_Muscle | | SE_31958 | chr11:2407217-2413608 | Gastric | | SE_38800 | chr11:2407754-2409050 | HUVEC | | SE_40846 | chr11:2405760-2414829 | Left_Ventricle | | SE_41958 | chr11:2406741-2409227 | LNCaP | | SE_42279 | chr11:2405609-2413782 | Lung | | SE_45268 | chr11:2407204-2409452 | NHLF | | SE_46903 | chr11:2407708-2408629 | Ovary | | SE_48723 | chr11:2405778-2409214 | Right_Atrium | | SE_50532 | chr11:2405760-2412981 | Sigmoid_Colon | | SE_52933 | chr11:2405757-2412812 | Small_Intestine | | SE_53501 | chr11:2397988-2412875 | Spleen | | SE_54770 | chr11:2405694-2415652 | Stomach_Smooth_Muscle | | SE_60561 | chr11:2398089-2423448 | DHL6 | | SE_61498 | chr11:2379166-2423231 | Toledo | | SE_62686 | chr11:2398060-2423320 | Tonsil | | SE_65362 | chr11:2398765-2416724 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTTCACCCGT TCACCGGTCA GTGGGCATAT GGGTTGTTTC AGTTTGGGGC ATTTACAAGA 60
AACGTGCTAG AACATTTGTG TACAAGTCTT GTGTGAACCT AAGTTCATTT CTCTTGGGTA 120
AATACCTGTG CGTGGAGCAG CTGGGTCATG TGGTGAATGT GGGTTTCACT GCTTAAGCAG 180
CAGTTTTACA TAACTGCCAA ACTGTTATTC AAGGTGGCTG GACCGTTTTA CAGCCCCCGT 240
TGTATGCGTC CCAGTTGCCT CCCCCAGCAG CATGTGGTGT GGTTGGTCTT TTTCGTGGCA 300
GCCAGTCCAC TGGGTGCGCT CGGCATGTGG CTGCAGCTTG ACCTGGGTTT CCTGGTCCCT 360
GGCAAGGTGG AGCATCTCTT CATGTGCTTT TTTGCTGTGT GTGGATCTTG CGGGGAAGGG 420
TCTGTTCCTG TTTTTTGCCC ATCTTTCAAA GATTGGGTTG CCAGTTTTCT TGCTGTTGAG 480
TTTGGAAAGC TCTGCATACG TTCAGGGCAC AGGTCCTTTA CCAGGCTCTG CCCCAGGTCT 540
TTCGGAGAGC AGGTGTCTTT CGCATTCCTG ACTCTGGGGA ACCTCTAGCC CTGCCACATG 600
GGGTTTGTTA TGGGGCAGGG GCACCTGTGC CTTTCCCACC ACGGGGCTTG GGGATTTGGT 660
GCTGCCATTG CCCTCCCTCG TAGGTGGCCC TAGGGGGGTC CCTCCGCCTC CGTTTCCTCA 720
TCCAGAAACC GGCAGTGACC ATCACCACCA TTGTTGTCAC CTAGCTCCAG CTCAAGGTCC 780
CTGCTGAAGG TCGGAGAGCT TGGCATGGCC CCGTTTGTCC ATGCTAGGGC TGGGAAGACC 840
AAGGCTCAGG TGAGGCCTCT GCCCAGTGCC TGGCACTCCT TCTTGCCCCA TTTTTCCACC 900
CAGGGTGGCT CCCGACTACT TCTGGTAGCC TCGGGGACAG TTGAGGTGGA CAGGCTGGCG 960
TCACCCCCAT TTCCGGCTGT CCCTCCCACC CCCTCCTGGC CCAGCTGTTC TGCCCTATTA 1020
AAAGTCACAT GGGCCCTCGG GTCCTTCCTG GTGTTGGCCC AGGCTCTTTC AGGCCCTGCA 1080
GGCCAGGACC AGCCTTCCCT GCAACCCTCG GCAGAGGCCT GGGGCCGGGG CTTGTCTAGG 1140
GGCAGCCTCC CCATACGGCC CTGGAGTCTG AACAGAAGCC CCTTCCCAGA GCACAGCAAG 1200
AAGCTGCAAC GTGGCCTGAA GTCCCACCAT TAGCAGGTTT GGGGTTTAGG CTGAGCTTTG 1260
CCATCACTAC CTTTCTGTTA GGACGGTATG CCCATTAGAT GGGATCATCC CCTCAGCGCC 1320
CAGGCTAGAG GAGGGGTGGT CCCTGCCCAG CCAGGGAGGG CTGGGGGTGG ATGGGCCTCT 1380
ACAGAGCAGC TTCCGAGCCA GGCACGGTTC CATGATCAGC TCTGTTTTAT AGAGGGGGAC 1440
ACTGAGGAAC CGGGAGCCTG GGGACCTTCC AGTGGCCCCA CAGCTCCTGT GGCTGAGTCA 1500
GGGTTTGTCA CCAGGCCTCT GTGGGGATGA GGCTCCCCCA TCCACCTGCC CCACTCTGTC 1560
CTGGAACAGC TCTCAAAACG GTCTCTGGAC CACAGTTTCA AAAGAAAATA AGCAATGTTT 1620
TCAAAGGCCC TGGAGGAAGC CAGAGTTACC ACGGCAACTC TCGGCCTCGC CACCTCCTCC 1680
CGCCAGGCTG CATCTGGAGC CAGCTCAGGA GGGCAGCAGG GTGAGGACAG CCAGGCTCTC 1740
TGGGGCCACC CCCCAGCCCC CACCCTTCCT GCCTCTCCTG CACTGTCCAC GGCCCTCCCT 1800
GTGCTCCCAC GGGTATAATG GGCACAGAAG AACCAGGAGC TGTCTGCCCC TGCAGGATTC 1860
TGGAAGCCAG GGGCCCCTGG CCTCCCTGGG GCCTTGTCAT GTGAGGGGCA CACGTGGGGT 1920
CCCAGCTGCC ACATGGCTTC CAGCGCTGCC CGCAGGTGTA TGTTGGGCCC TTGGTGACTC 1980
TAATGCACCT TCCACTCGGC ACAGAAGAGC TTCAGTCTGG GGCCTGGGCG GGGGAAGTAG 2040
GCTGCCATCC TCGCTAAACC AAAGTGTGAA AATTGAGTTG AAACTCCCAT AGGAGGGCAG 2100
GAGGCACAGC TCCTCAGAAG AAGGTCTGAG AAACCACAGC CCAGGTTGTT GTTTCGGGTG 2160
TGTGGAGAAG GTGCTCTGGC AGTCCTGCTA CAGGGGGACC ATCAACAGCC CCTTTGGGGT 2220
GAGAGCCCCG TGGCTGCTGG CACCAGCAGC CCCTATGAGG CTTATTTTAT TTTTGAGACA 2280
GGGTCTTGCT CTGTCACCGA GGCTGGAGTG CAGTGGCACA ATCATAACTC ACTGTAGCCT 2340
CAACCTCCTG AGCTCAAGCG ATCCTCCTGC 2370
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