| Tag | Content |
|---|
EnhancerAtlas ID | HS184-22497 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr4:6697320-6698610 |
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 | GACTTTGATC CAAGATACTG GGGTGTGGGG AGGGGCAGGC ACAGGTGTCC TGGGAACACA 60
CTTTGAGAAG CAATGGCAAA GCTGGGGGTC CAGCTAATGT GTTACATTAG AATCACCTCG 120
GGGAGGCCCT GGGTGCCCTT CTCAGCCCTC CCTCCGGAGG CTGCTGAAGC CCAGCAAAGC 180
CGGAGTCAGA GAACAATGTC CGCCTGAGGG CAGGGCTGGG CTGGGCTGGC CTTCTGGCCC 240
TATCTGCTCC GTGCCCAACC CAGCGCCCCG CACAGTCGGA GCTTTGTAAA TACGAGGTGA 300
CTGTCTGCCT ACAAACTTTG TAAACATCAC TTGAAATGGC CGCAGGGTAT TGTGACATGG 360
CCATACCACT ATTTGTTTGC TATTGAATTT GTACTTCCCT GCCTTACTTT TGCTATTGCA 420
AACCATGCTG TCACTAAGGT CTTCATGCAC ACAGTTGTGT CTTGGTCAGA TGATATGTTT 480
CTACCAATTT TAATTGTGTT TCTTTCCACC TGGACACACA GCTCTCTGGC CCAGGGCTGG 540
GTCATCAGCA CACCCTGCTG CTGCTGTTCA GATCTGCATC CTGGTCCCGC TTGGTCCCAC 600
AGTGAGAACG CTTTGCTATC ACATGGGCAG GCTCTGAGAG CCCTGCCGGC CTGGCCTTCT 660
CAAAGAAGAC CTGAGAGCTT GGGACCCAAG CAGAGAGGAA GAACAGGGCT CAGGGTGCTT 720
GCTCCATGCT CGCTCCACAC CTGGGGCTCA ACCCTGGCTT TCCCCGGCTC CCTGTGTGAC 780
TTCAGGGCAG GTCCCTTGGG CCCTCTGGGC CTTATCATCT TCATCTGTAA CAGGGCGATG 840
CCTCTGCCGT GTCTGGTGGT GTTGAGGAGT TCCTGTTTGT GTAAGCAGCT AGTTCAGTGC 900
CAGCACGAGA TGGGAGGCCC ATGAAGTTAG CAGTGCACAA AAAATAGAGC AAAGACTGGA 960
TGCATTTCCT GAGAACAACC ATCACTGTAA AGCACTTTAC AAATCCAAAG ACAACCCCCG 1020
GCAAAAACTC AAAATGAAAC TCCCTCTCGC AGAGCACAAT TCCAATTCGC TCTAAAAACA 1080
TTACAAGTTA GTTCATGTCA TGCCAGATAG CTGAAGGCAG CTCACAAGTT CTTAAGGCCA 1140
GGAATGCCAT GTGTCTGCTA TGCACAGCTG GCCCTGGCCC TGACAGCAAA GGTGACGCAG 1200
ATGTGGGTGC CCTGCTCCTG CCCAGCAGCA GTGCTTGGTG GAGGCTGAGG CCCTGCACAG 1260
GCACCCTCAC TGCTGACCTT GAGCCTCTCT 1290
|
