| Tag | Content |
|---|
EnhancerAtlas ID | HS101-12171 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr13:33384870-33387270 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX3 | MA0684.1 | chr13:33385526-33385536 | TTTGCGGTTT | - | 6.02 |
|
| | 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 |
| GH13I032811 | chr13 | 33385539 | 33385738 |
|
Enhancer Sequence | TTGTCTTTTC AATTTCTTCA TGTTGTCCTT TGAAGCACAA AAGTTGTTAG TTTTAATGAA 60
GTTTACCTAT CTTTTCTTTT GTGCTTTTGG CATCCTATCT AGTACCATGG CGACCTACCA 120
TGGTTCAGAC CAATGGGAAC CACCCCTTTT GACACTTATA GCTGTGTGGG TTATCTTAGA 180
AAAGCAGGGC TAGACCAGGT GCGGTGGCTT ACGCCTGTAA TCCCAGCACT TTGGGAGGCT 240
AAGGCAGGCG GATCATGAGG TCGAGAGATC AAGACCATCC TGCCCAACAC GGTGAAACCT 300
GTCTCTACTA AAAATACGAA AACTTAGCTG GATGTGGTGG TGTGCACCTG TAGTCCCAGC 360
TACTCAGGAA GCTGAGGCAG GAGGATTGCT TGAACCCGGG AGGCGGAGGT TGCAGTAAGC 420
CAAGATCGTG CCACTGCACT CCAACCTGGA GACAGTGAGG ATCTGTCTCA AAAAAAAAAA 480
AAAAGAAAAG AAAAGAAAAG AAAAGCACAG CTGGCCATCA CCAGGGTCCC CTGCAGGTCC 540
CCCAGGTCAG GCAGTTATTT ATCACAGTAC TTGGATGGGT TTTAACCACA GAACTCTATA 600
AAGTCACAGA AAAATTACTT CAATGTGACA GAACCCAAAC TAGGAAATAA GATCTCTTTG 660
CGGTTTATGT TACACACACA CACATACTCT CTCAACCATA ATTAGACACA GCAAACCATA 720
AATAAGATGC AGCGGGGTTC ACATGTCACC TTCCATCTCT CTCATGAGAG AGCTGGAGGG 780
CGCCTTCGTC AGTGTGGATC CTGTCCAGCC TGCTCCTCTG TGAGCTCCCT GACGTGGGAG 840
CAGTGCTGTT CTGTGCTGAT CTCGCCCAGC AAGTTGCTTC CTCCTTTTGA GACTTTGTTG 900
TCATTTGTCT TGGCCTCCAC TTACTCTCGA TCTGTGTTCA CTGAATCAAC CACCCAGGGC 960
TGTTGCTAGT GTCACATAAC CTGGGAATGG CTTTACAAAC AAAACAACAC CCATTCCTGG 1020
GACCTGCTGC TCCTTTCTAG TCTCTGACCT GCAATCAGCT GCCTCTCTAT TGCATCCCTG 1080
CTTTAGCCAC AGGAAGGGTG CTTTGTATTC AGCATCTTTT TTCTTTAATT AAACAAAAAC 1140
AAAACTTCTG AATTGGATCT TCTGTTGTAG GGAAATGCAA TGTGTGTCAT TCCTGGGGGA 1200
CACTCCAGTG GGCATCTCTG CAGCTCCTGC AGCCGGCAGT GCTCACTCAT TACTGCATGT 1260
CTACTGCGGC ACAGGTGGGA CAGGGACCCC ACGGGGCCTG AGAATCACGT AGTAGGTCTT 1320
CAGCAAAGGC TGACTGAATG AGTACAGGTT ACTGATGGAA ACTGAGATCC TTAGAAATGG 1380
AGTAACTCTC TCTAGAGACA GAGGACGAAC TAAGTGGCCT TTTCTAAGTG AGTACTCATC 1440
AACCTTTGGG GGAACAGATA CCCAGTTTCA TTATAATTCA CTTTTCAATT TATTGGAAAT 1500
ACTGAATTTA TTATTCAGTT TATTGATGAA ATGGAAGTAA CAGTCCCCTG CAGTGTGTGT 1560
ATGTGTGTGT TTGCTGAAGG AGGTGGCCAT GTATTTAATG GTAAATTTCA GTATCCAGAG 1620
CATTTCCTGC TTTTAGTTTT GATTTTCTTT TATGTTACTA GATACGTTCT TAACGTGATC 1680
TTAATGTAGT TAAGTTAGCT TATAACGGCT ACGGGATAAA ATAGGCTCCT AGACAGCACA 1740
TTATAATGCC CCTTCTGAGA AAAGAATTAC AGCAAAAGCT GGACCCAATT GTAATAACAT 1800
TAAACTTATA AAAGCATGAA ATTGCTTCAT AGGGTGTACA TGAATTAATA TCTTCTTTGC 1860
ACTGGTGGTT TTCCCATATA GTACATCACT CAGGCTCAGC AACACACAAG TATGCTTTTG 1920
TACCAGCGAA GATTGCATTG CAAAGCTGTA TCATCTACTG GAAAAAAAAA GAATAAAAAA 1980
GGAAAAGAAA TACCCAGAAT AGTTTGGGCT GGTCCAGGAG TGAAGGACAC TTTAAAGATT 2040
GCCTTTCTCC TGAACTCCTA CCCTGCTCTC TGCCCTTTCT TGTGGACTGA TGGCCTTTCA 2100
TGAGTTGGCA GGACTTACCT ATCTTGATCT TCTGGTCCCA TGTAAAACGC ACGTTCTTAT 2160
ATCCAGAGGA TCAGAGCCAG CCTAGACAGC CCAACACCAT GCAGACAACC GTGCCATGGA 2220
CACTTCAACT CAACTGCAAT GTCGATTTGT TTGCAAAGAT GAGCCAGTAC TGTAAATGTC 2280
AAGCAACATT GCTCTGTGCA GCAGAGTCAG CCATCTTTGA ACTCACCAGA AAGTACCTAT 2340
GAGACTTGCG GACTTTTGAG CATATTACAT TGATCATGTT GAAAGGTAGA GGCAAAAAGA 2400
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