Tag | Content |
---|
EnhancerAtlas ID | HS105-55385 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr3:48191930-48194120 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROG1 | MA0623.2 | chr3:48193784-48193794 | GACATATGTC | + | 6.02 | NEUROG1 | MA0623.2 | chr3:48193784-48193794 | GACATATGTC | - | 6.02 | NFAT5 | MA0606.1 | chr3:48193388-48193398 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr3:48193388-48193398 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr3:48193388-48193398 | AATGGAAAAT | - | 6.02 | Stat6 | MA0520.1 | chr3:48192488-48192503 | AGTTCTGTGGAAAAA | - | 6.16 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 48192359 | 48193930 | chr3 | 48192537 | 48194056 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH03I048150 | chr3 | 48192003 | 48193992 |
|
Enhancer Sequence | GTTTACAAGA ATGAATCAGA GGGCAGATGC ATTGGCTCAT TCCTATAATC TCGGCACTTT 60 GGGAGGCTGA GGTGGGAGGA TCACTTGAGG CCAGGAGATT GAGACCTGTC TGGGCAACAT 120 AGGGAGATCT TTGTCTCTAC AAAAAAAATT TTAAAAAAAC ATTAGCTGGG TGTGATGGTG 180 TGCATCTATA GTCCCAGCTA CTCAGAGCGA AACCCTATTC CCCATCCCCA ACCCTCCTAA 240 AAAGAATAAG TCTGTGGAAG GCTGGGAGCA GTGGCTCATG CCTGTAATCC CAGCACTTTG 300 GGAGGCTGAG GCAGGCGGAT CACCTGAGGT CAGGAGTTTG AGACCAGCCT GGACAACATG 360 GTGAAACCCC TGTCTCTACG AAAAATACAA AAATTAGCCA GGAGTGGTGG CAGGTGCCTA 420 TAATCCCAGC TACTCAGGAG GCTGAGGCAG GAGCATCGCT TGAACCTGGG AGGCGGAGGT 480 TGTGGTGAGC CGAGATCCTG CTACTGCACT CCAGCCTGGG CAACAAGAGT GAGACTCTGT 540 CTCCAAAAAA GAAAAAAGAG TTCTGTGGAA AAAGAAAGGC ATTCCCTGCA GGTGTCAGCA 600 AAGGTAAGGA GGTCCCAAAG AACAGGAATA GTGAGGAGTC CTTGGGGGAG GATGGGGAGG 660 TTGCCCAAGC TCATCCTTTA TACTTGAGAC CTCTGGTCCA GAGAAGTGAA GTGTTCTGCT 720 CAGTGTCACA CCACTGGTCA GGGGCAGACC GGAATCAGAA AGTAGGCCTT ATTTCTTCAT 780 CAGAGTCTAG GAAGCCGCCA GGGGAAAGAG GCTGTGCTTT AGAAGGTTAA GGCCTATGAT 840 CCACCCTGCG TCACCCAAAG TAAACTAGGA AGGAAGTGTA AATAAACCCC ACAAAGATCG 900 GACATTTTTC CATGATGACC ACATTGATGC ATTTATTAAA AATACAAAAT GCTAATAATC 960 CAAACCAGCC CTCTTCCCTT TTTTCCCCTT TGGGAGCCCT TGCACTGTGG TGCATGAAAC 1020 ACATGCTTGA ACTAGGCCAT TGGGAACTGC GGCTTGGACA AGGAACAGCC ACAGCTTTTC 1080 CTGTACTCAG AGCAGGCAAA GTGCCATTAA ATGCAGCTGG AAGCCAGGGC AGGGGAAGGG 1140 GTGGGAAGCT CCTGGAGAGC CCCCAGCTCC TCCCAGTTAC TGACTGGCTC TGGAGGAGAG 1200 GAGCTAGAAG GCCGAGATAC CTGAGGAGAC AAACCTGGGG CACCACTGCC ACCTGATGTC 1260 TTCCTATGGC CATTGCAGTG GTCACAGCCC CAAGCCCCGT GGCAGCCTGG CAGCAGAGTG 1320 AAACAAGAGG GCAAAGAAAG CCTATCGGTG GAAGTTTTTA TTTACCCTTG ACGGTGGGTA 1380 CTCCCAGACA GTGGGTATGT CTGAAATACT TCATATTGAA GAAAGACATC CATATTGAAA 1440 AACTAAACAG AAAACATAAA TGGAAAATGA ATCAACATAT ACAAAGTAGC CACAGTATGG 1500 AGGTGCGGAT TTGACTTTGC CTGCGGAAGA GCTGTCCTGC TCTGGCCAGC ACTGGAAGGG 1560 ACTCTGCCTC CTCTGTTCTG GGAGCGTGCA AGCAGGAACT CTGGACTGGG CTTTGCACAA 1620 CTTCCAGGAG TCATTGCTTA GAAATCAGAA TGACCAAGAT CTTAAGGTCT TAGAATCATC 1680 TAGGTAATCC ACCCCCATCC CAGCTGCCAG GTCACAGTCA CACAGAGGCT GAGCACGCCC 1740 AATGCCATGC CCAATGCCAC CCAGTCTTCC CCTGCTGCTG TTTCTGCCTC GCCTCCCTGT 1800 CCTTCCCCTA CCCTACCCTA GCGTGGGCAG GCTTTGTGTC CCAAGGTCAC CAGTGACATA 1860 TGTCCCACCA CAGGCAGCCG AGCTTAACCC TATCACTGAG ACCTCCTTGT GGCTGCTCCC 1920 TACCCCTCCC TGCCTGGCTT CCTGGCATCC TGCCTCTAAC CTCTCTCTCT GCTTCCCTGT 1980 CTTCTACATT GGTAGAACTG CCACTTGGAT ACGTGTGACA ACTTGCTGTC ACCAGCCTGG 2040 ATATTTCTCT GGAGCACTCC TCACATTCAA CACTTGACCA CTCAGGCATC GGGACAGTCA 2100 CTGCCCAGAT CCCCCCGTCC ACATAGGAGC TCAGCATGAC AGCCCCTCTT TTTTATTTAA 2160 TTTACTTATT TCAATTTTTA TTTTTATAGA 2190
|