| Tag | Content |
|---|
EnhancerAtlas ID | HS105-59554 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr4:6697270-6698610 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr4:6698591-6698606 | GCTGACCTTGAGCCT | - | 6.9 | | Stat6 | MA0520.1 | chr4:6698282-6698297 | CATTTCCTGAGAACA | + | 7.08 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_32360 | chr4:6693831-6699251 | Gastric |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGCTCGGGGT GTTCTGATAA TGATCAAAGT ATGAGAATTG AACCCATGAG GACTTTGATC 60
CAAGATACTG GGGTGTGGGG AGGGGCAGGC ACAGGTGTCC TGGGAACACA CTTTGAGAAG 120
CAATGGCAAA GCTGGGGGTC CAGCTAATGT GTTACATTAG AATCACCTCG GGGAGGCCCT 180
GGGTGCCCTT CTCAGCCCTC CCTCCGGAGG CTGCTGAAGC CCAGCAAAGC CGGAGTCAGA 240
GAACAATGTC CGCCTGAGGG CAGGGCTGGG CTGGGCTGGC CTTCTGGCCC TATCTGCTCC 300
GTGCCCAACC CAGCGCCCCG CACAGTCGGA GCTTTGTAAA TACGAGGTGA CTGTCTGCCT 360
ACAAACTTTG TAAACATCAC TTGAAATGGC CGCAGGGTAT TGTGACATGG CCATACCACT 420
ATTTGTTTGC TATTGAATTT GTACTTCCCT GCCTTACTTT TGCTATTGCA AACCATGCTG 480
TCACTAAGGT CTTCATGCAC ACAGTTGTGT CTTGGTCAGA TGATATGTTT CTACCAATTT 540
TAATTGTGTT TCTTTCCACC TGGACACACA GCTCTCTGGC CCAGGGCTGG GTCATCAGCA 600
CACCCTGCTG CTGCTGTTCA GATCTGCATC CTGGTCCCGC TTGGTCCCAC AGTGAGAACG 660
CTTTGCTATC ACATGGGCAG GCTCTGAGAG CCCTGCCGGC CTGGCCTTCT CAAAGAAGAC 720
CTGAGAGCTT GGGACCCAAG CAGAGAGGAA GAACAGGGCT CAGGGTGCTT GCTCCATGCT 780
CGCTCCACAC CTGGGGCTCA ACCCTGGCTT TCCCCGGCTC CCTGTGTGAC TTCAGGGCAG 840
GTCCCTTGGG CCCTCTGGGC CTTATCATCT TCATCTGTAA CAGGGCGATG CCTCTGCCGT 900
GTCTGGTGGT GTTGAGGAGT TCCTGTTTGT GTAAGCAGCT AGTTCAGTGC CAGCACGAGA 960
TGGGAGGCCC ATGAAGTTAG CAGTGCACAA AAAATAGAGC AAAGACTGGA TGCATTTCCT 1020
GAGAACAACC ATCACTGTAA AGCACTTTAC AAATCCAAAG ACAACCCCCG GCAAAAACTC 1080
AAAATGAAAC TCCCTCTCGC AGAGCACAAT TCCAATTCGC TCTAAAAACA TTACAAGTTA 1140
GTTCATGTCA TGCCAGATAG CTGAAGGCAG CTCACAAGTT CTTAAGGCCA GGAATGCCAT 1200
GTGTCTGCTA TGCACAGCTG GCCCTGGCCC TGACAGCAAA GGTGACGCAG ATGTGGGTGC 1260
CCTGCTCCTG CCCAGCAGCA GTGCTTGGTG GAGGCTGAGG CCCTGCACAG GCACCCTCAC 1320
TGCTGACCTT GAGCCTCTCT 1340
|
