| Tag | Content |
|---|
EnhancerAtlas ID | HS044-00676 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr1:117017540-117018890 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr1:117017850-117017860 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr1:117017850-117017860 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr1:117017850-117017860 | AATGGAAAAT | - | 6.02 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_27848 | chr1:117013898-117021408 | Fetal_Intestine | | SE_28774 | chr1:117013873-117021547 | Fetal_Intestine_Large | | SE_41250 | chr1:117016870-117021350 | Left_Ventricle | | SE_47846 | chr1:117017467-117019346 | Pancreas | | SE_50584 | chr1:117016337-117019459 | Sigmoid_Colon | | SE_52493 | chr1:117016317-117021272 | Small_Intestine |
|
| | 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 |
| GH01I116471 | chr1 | 117014027 | 117021401 |
|
Enhancer Sequence | GAAAGGACCT CTGTGCTCCC AGCCTCCCCG TGTTACAGCT GAGGAGTAGA GGGCCAAGGC 60
ATCTAGTGGC TTCCCCAAGG TTCTCCAGGC TGCTGTGGAG GCAGAGCCAT GGCCACGGCC 120
CTGGCCTCCT GGCACTCAGG CCTAACAGCT TCCATCAGGC TGTACCACTG AGATTATCAT 180
CATCAGTGAT GATGGTGCCA TTAACAGCCA TGGCCACCAC TATCTGGTTT TTTAGCACCA 240
GCCACCCTGG CAGCCATCTT CATTTTGTGA CTTGAAGAAA GCACTGCCCT GGTCATGTGA 300
GCACAAGAGG AATGGAAAAT TCCAGGTCAG GGAACAACAC ACCCTCCAGG CATCCTTCTC 360
CACCAGCCCT GCCTTCAGAG GCACCAGGCC CTTTTGTCCC ACCACCAGTT AATATTTCAC 420
TTGGGTGAGA CTTTAGAGAA CAAAGAACAC AAAGCTGGCC TTGAGGGGCC AAAGGTAAGC 480
AGCCCATGGT TCCCGATTCG GCTCATAAAT AAGAACAGGG CAAATGTACT TTGGATAAGG 540
ACGCGCTCAG CCTCCCGCAG AACAGCTGGG GAAGCTATTC ATAGGAAAGC GTGCTATTTG 600
CGTCTGCCTG GCATTTGAAT GAGGCTCACC TAACTGTGCC TGCCCTCCCC ACAGATGTGA 660
GTCACGCTCC CCACTCACGA GTGAGGAGTG GCCAGGGGCA AAGGAGAATT GCTTCTCGGC 720
TCAGCTGAGA GAACTGTGGG GGCCAGGAGC GGCACTGCCA AGGATATCTC CCTCCCCCGG 780
GCAGGGAGGG CCTCCAACTG AGGACACTTA TTCTGTAGTG ATAGAGCCTG ATTCCCCTCC 840
ATGTGAGAGA GGTGCCTCCT TGGACCCTGC TACTTTGTCC CTTGGCCCTT GGTCAAGCAA 900
AGGGGACAAT TCTCAGCCCC CAACCCCTTG CCGGTGGCTT TGACTATCTT CTCACATCTC 960
CAGTACTCGG GGAAAGCCAG TCAGAGCAGC GTGGGAGGCC AGTTCTAGTG TCACGCTGCC 1020
ATCCTCCAAG TTCTACTGGT CCCTGGTCTC TAATTGCAAA GCTTACGTGC TGTGGAGGTG 1080
AAGTGGGGGT GATCCCTCCC CCTTAAGCAG CACTGCCCAC TTCTGAAGGT CATCCACCAA 1140
TGCTCCTGCC TCCTGTAGCA TCCAGTGAAG TTCTGGGCTG GTTCTGAGCC GAGGGTGTGC 1200
CGGAAGCAGG GCTCATTATG GTCCAAAATA ACCTTGGGAG GTCAAGCCCA GGCCTGGGCA 1260
TCCCTCATCC AAGGAGCCCT GATGGGGGGG TCTCTCAGGG CCTAGCCGAA GAGTCAGTTC 1320
CGCTCCATAG CAGCACTGAT GGTTCAGGTC 1350
|
