| Tag | Content |
|---|
EnhancerAtlas ID | HS101-35608 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr5:131693050-131694950 |
Target genes | | Number: 16 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr5:131694771-131694792 | ATTTCCTTTCCCTTTCAGTTT | + | 6.84 | | Sox3 | MA0514.1 | chr5:131694730-131694740 | CCTTTGTTTT | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_25154 | chr5:131693184-131693520 | Colon_Crypt_3 | | SE_25154 | chr5:131693653-131695507 | Colon_Crypt_3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr5 | 131693684 | 131693784 | | chr5 | 131693910 | 131694525 | | chr5 | 131693745 | 131694100 | | chr5 | 131694113 | 131694404 | | chr5 | 131694495 | 131694889 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I132357 | chr5 | 131693240 | 131695295 |
|
Enhancer Sequence | AGGGCATGGT GGTGGATGCC TGTAAGCCCA GCTACTTGGG AGGCTGAGGC AGGAGAACTG 60
CTTGAACCTG GGAGGCAGAG GTTGCAGTGA GCCGAAATCA TGCCATTGTA CTCCAGCCTG 120
GGCAACACAG CAAGACTCCA TCTCAAAAAA AGGAAAAAAA GAAAGAACGT AGACTAAGGT 180
ATTAACAGTA GGTATGTTTG GATGGTCAGA TTATAGATGA CTTCTGTTTT ATTTTTTCCA 240
GATTTCCATA CTTTACAAAT GCTTCATATA TTACTTTTAT AATCATAAAG CAGTTAAAAA 300
ATAAAAACTT ACTGAGTGTT GACTAAGTGC CAGGTCTTCA GAAGCATAGA TGAAGAGCAT 360
GAAGAATGCA AATTCATGCA TCAGGCTGGG CATGGTGGCT CAAGCCAGTA ATCCCAGCCC 420
TTTGGGAGGC CAAGGCAGGT GGATCACTTG AGGTCAGGAG CTCAAGACCA TCCTGGCCAA 480
CACGGTGAAA CCCTGTCTCT ACTAAAAAAA TACAAAATTT AGCCAGGCAT GGTAGCGGGT 540
GCCTGTAATC CCAGCTACTT GAGAGGCTGA GGCAGGAGAA TCACTTGAAC CAGGGAAGCG 600
GAGGTTGCAG TGAGCCAAGA TCACACCACT GCACTCTAGC CCGGGTGACA GAGTGAGACT 660
CTGTCTCAAA AAAAAAAAAA AAAAATTCTT GCATCAGTGG GCTTAGTCTA GCCTGGTTAT 720
AAACTCCTGC TTGTGGCCTT AGCAACTTGC CCAGTGCTCC CCTGGGGCTT AGCCCTGTGG 780
AGGCTGAAAC CCAGGTCAAA GTCATGTTCT CCAATCCAGA GCTGGGTGTC TCTCTCACTT 840
CCTTTGAGCA GCAATCACCT CTACCCTGAT TTAGACCAAG CCAAGCTTGC TATGCTGAGG 900
TAACTTAGCT TATCACCAAG GTTATATTTA ACAGACTGCT GAAAGGATTA TAAAAAATTA 960
TGGGGATTTG AACTATCACC CAATGCCTCC GTCTGTTGAC ACAGACAAGT TTAAAGCTTG 1020
ATTTTGTGAA CCTTGAGATG ATCTTCCTCC AGCACTGCAA ATGTAATCCT TCTCATCTAA 1080
AACTCCCATT CTAATGCCCT ACTGTGCTCC TGCCCCTGCA GAGCCCTCCA GCTCACCCTC 1140
CTGCAGTTGT CTTCTCTGTG ACTGAGTCCT CTGCAACACA TATTCCATTG TAGACATGCA 1200
ACTCTCCTCT TTCAAGTACA TCCCTGGTTG TTCTCTCCAT CTCCTTTCCT TGATAGAGAT 1260
CTGGCTTCTT TCTGAGCACT CCACTAGCCT CATGGCTCTG TCTCTCAAAG GAAGGCTACT 1320
CATTTTGCAC TATCCATGAT CCTGGAAGAC AAGAGCTGAG CAGGCTCTCA GCATTCTCCT 1380
TGCTTCCCAC TGCCATTTCT AAATCATAAC TCCTTCACCT TCACATACAT AAAAGACCTG 1440
CTCAGGTTTG TGCTGTGCCC TCCTGGTTGC TGTTACCAAC ATCTGCCTGG TTGGTTATCC 1500
ACATTCTGTG AGCTCTCTGA CACCCAGCCC AAGGTGCTGG TGACTTTTGT GCTCAGGAAG 1560
ATGAGTAGTG CTACACCTTA GCCTCGCAGT ACTTGACCTT CACCTATACT TCACACTCTT 1620
GCTGCTGAGG ACACACCCTG GGCCTCTCAT CAGTCACAAC AGCTCCATCT CACTCTAGGA 1680
CCTTTGTTTT CCTCCCAACT CTTCAGCTCT CACCTGATAT CATTTCCTTT CCCTTTCAGT 1740
TTATACCTTG TGATCCCTCC AGCCCATTCA TACTCTTGCC ACTACCCCAG TCCTTTTGTT 1800
TACTAGTCTT GCAAAGGCTA AGCTCACAAT AAGTCAAACC ATTTTACTCT TCACTCTCAA 1860
TCCAGGATGC TGACTTAAGA TACAAGAAAG AAGGGGGGCT 1900
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