| Tag | Content |
|---|
EnhancerAtlas ID | HS118-18889 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr8:142299810-142301040 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZBTB18 | MA0698.1 | chr8:142300322-142300335 | GCACATCTGGCTG | - | 6 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_32282 | chr8:142299590-142300157 | Gastric | | SE_32282 | chr8:142300226-142301049 | Gastric | | SE_41505 | chr8:142298211-142303409 | Left_Ventricle | | SE_42811 | chr8:142298458-142303236 | Lung | | SE_47600 | chr8:142299618-142300131 | Pancreas | | SE_47600 | chr8:142300551-142301037 | Pancreas | | SE_49311 | chr8:142298413-142300513 | Right_Atrium | | SE_49311 | chr8:142300527-142303341 | Right_Atrium | | SE_65316 | chr8:142298427-142303790 | Pancreatic_islets |
|
| | 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 |
| GH08I141288 | chr8 | 142298981 | 142302694 |
|
Enhancer Sequence | TGGCCTCTGC AGAGGGGGGC TCAGGGAGGC CTGGAGTGAG GGCTAGAGAA AGCCCATGGC 60
CCGGGGTCTT CCAGCCCAGC CCAGGGAGCA CTCCAGGTAA GGCAAGGCCT CACCACCCTC 120
CAAGTCCTCA GCACTAGGAG CCCACCAAGA GCCAACTCTG CCCTGGAGGC CCCGGACACT 180
GGAGCGAGGT GCCCCCAGCC CTACAGCTTC AGATCCCAGA TCTCAGTCCC CTACAAAGCA 240
TGCAGTCCCT CACCTCAGCA GGGAAAATGA GCTAGCAGAG AACTCCAACA CCCAGACATC 300
GCCCTACAAA GAACTTTAAA GAAGTAAAAA GCAAAAAACA TATTATGTTA CATTATGCTA 360
GACAGTACTA TCATTATACA TCATATGTAT AATTATACAT GTCCATATAT AATATATACA 420
CGTATGTATG TATATATTAT ACATGATCTA CATCTACGGT CATCTAACAC TGCACTGTAT 480
ATAAAGGAAT CTATTTTTTT TAAGTGCGTG GTGCACATCT GGCTGTGAGC TCACCACACG 540
TGCAGGTATC TGACCCCAGG CTCCTCTCCA GGACTCCTCG GCACCGGCAG AAAGGCCCCA 600
AGTGCCGCAG CTCCAAGCCC GGCCCTCCCA CTCAGGCTGG GCTCAGGGTT GAGAATTCCA 660
CCCGCCACTC CAACGCTGCC AAGTCTTATC TCTGCCACAT TTCTCAATGT GACATTGCAC 720
AATTCTTTTG GACAACCTTG ACTTTCCGTG GTGCTCACTG CTAATTTTAA CTACCTGATG 780
TTTCCCCACA AAGTAAATAT GAGGTGTTCA TGCCACCACC ATGGCAGCGT TCCAGTCACT 840
CTGCAAATTC GGCCAGTTTC GGTCATGACA ACGACATGAA ACACAACAAC CCAGGCGTGA 900
GGACAGCCAC CCTTGGGATT TATCTCCACT GGGGATGAAA CCAGGCCGCC CTCCTCCAGG 960
GCTGCCAAAC ACAGCTCCCA TGAACGACCA GGTCAAGCAC GTTGTCCTTG GGTCCAGAGA 1020
CAGACCAGGC AGCCCACGCT GCGTGTGGTC TTACCCTACG GTCCAGAGAC TGCAGGGATG 1080
TGGCGGGGGG GCCTGGGGAG GATCTTTCCT GGACACACAT AAACAACACC TAAATTGTTT 1140
TGTTTTGTTT TGTTTGAGAC TGGGTCTCAC TCTGTCACCC GGGCTGGAGT GCAGTGGTGC 1200
GATCTCAGCT CACTGTAACC TCCGCCTCCT 1230
|
