| Tag | Content |
|---|
EnhancerAtlas ID | HS118-13823 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr4:6696950-6698610 |
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 | TCAAAGTGCT GTGATTACAG GCGTGAGCCC CGACACCTGG CCTAGTTCTA TTTTCTAAAT 60
GTGAATTCTG TAAAGATATC TTTTAAAAAT AAAGTTCTGT TTTTGGTAGA AAATGTAAAA 120
ATAGATAAAT ATGGAGGGAA GAAATCCCCC CTGGAATACA GACGCTTCCT CTCCCTTCCA 180
GCCTTTTCCC CATATGAACA TTGCTGTGAG TGAGATTTAC ATGCAATGTA ATTTCTTTTT 240
GAGCTTAACA TTACAACATA AATTCTCAAA CTCTGATGTT CATTAAACAC CCCAGCCCCA 300
TCCTGGGAAC TTGGGCTTGG GGCTCGGGGT GTTCTGATAA TGATCAAAGT ATGAGAATTG 360
AACCCATGAG GACTTTGATC CAAGATACTG GGGTGTGGGG AGGGGCAGGC ACAGGTGTCC 420
TGGGAACACA CTTTGAGAAG CAATGGCAAA GCTGGGGGTC CAGCTAATGT GTTACATTAG 480
AATCACCTCG GGGAGGCCCT GGGTGCCCTT CTCAGCCCTC CCTCCGGAGG CTGCTGAAGC 540
CCAGCAAAGC CGGAGTCAGA GAACAATGTC CGCCTGAGGG CAGGGCTGGG CTGGGCTGGC 600
CTTCTGGCCC TATCTGCTCC GTGCCCAACC CAGCGCCCCG CACAGTCGGA GCTTTGTAAA 660
TACGAGGTGA CTGTCTGCCT ACAAACTTTG TAAACATCAC TTGAAATGGC CGCAGGGTAT 720
TGTGACATGG CCATACCACT ATTTGTTTGC TATTGAATTT GTACTTCCCT GCCTTACTTT 780
TGCTATTGCA AACCATGCTG TCACTAAGGT CTTCATGCAC ACAGTTGTGT CTTGGTCAGA 840
TGATATGTTT CTACCAATTT TAATTGTGTT TCTTTCCACC TGGACACACA GCTCTCTGGC 900
CCAGGGCTGG GTCATCAGCA CACCCTGCTG CTGCTGTTCA GATCTGCATC CTGGTCCCGC 960
TTGGTCCCAC AGTGAGAACG CTTTGCTATC ACATGGGCAG GCTCTGAGAG CCCTGCCGGC 1020
CTGGCCTTCT CAAAGAAGAC CTGAGAGCTT GGGACCCAAG CAGAGAGGAA GAACAGGGCT 1080
CAGGGTGCTT GCTCCATGCT CGCTCCACAC CTGGGGCTCA ACCCTGGCTT TCCCCGGCTC 1140
CCTGTGTGAC TTCAGGGCAG GTCCCTTGGG CCCTCTGGGC CTTATCATCT TCATCTGTAA 1200
CAGGGCGATG CCTCTGCCGT GTCTGGTGGT GTTGAGGAGT TCCTGTTTGT GTAAGCAGCT 1260
AGTTCAGTGC CAGCACGAGA TGGGAGGCCC ATGAAGTTAG CAGTGCACAA AAAATAGAGC 1320
AAAGACTGGA TGCATTTCCT GAGAACAACC ATCACTGTAA AGCACTTTAC AAATCCAAAG 1380
ACAACCCCCG GCAAAAACTC AAAATGAAAC TCCCTCTCGC AGAGCACAAT TCCAATTCGC 1440
TCTAAAAACA TTACAAGTTA GTTCATGTCA TGCCAGATAG CTGAAGGCAG CTCACAAGTT 1500
CTTAAGGCCA GGAATGCCAT GTGTCTGCTA TGCACAGCTG GCCCTGGCCC TGACAGCAAA 1560
GGTGACGCAG ATGTGGGTGC CCTGCTCCTG CCCAGCAGCA GTGCTTGGTG GAGGCTGAGG 1620
CCCTGCACAG GCACCCTCAC TGCTGACCTT GAGCCTCTCT 1660
|
