| Tag | Content |
|---|
EnhancerAtlas ID | HS101-03356 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:182764510-182765750 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr1:182764845-182764859 | TACTTCCCCTTTCC | - | 6.22 | | SPIC | MA0687.1 | chr1:182764845-182764859 | TACTTCCCCTTTCC | - | 6.49 | | Stat4 | MA0518.1 | chr1:182765135-182765149 | CGTTTTCCTGGAAG | - | 6.23 | | TBX21 | MA0690.1 | chr1:182765288-182765298 | AAGGTGTGAA | + | 6.02 | | TBX2 | MA0688.1 | chr1:182765288-182765299 | AAGGTGTGAAA | + | 6.62 | | TFAP4 | MA0691.1 | chr1:182764881-182764891 | ATCAGCTGTT | - | 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 |
| GH01I182793 | chr1 | 182762991 | 182765483 |
|
Enhancer Sequence | GTCAAAAAGT TTGAACTGCC TTTATGTCAT AAGGCAGAGG CAAAAGGAAG ATGTATTTAG 60
TACACCTTTT ACAAGGGACT TTCTTTTTGG TCTTCTGTTG CTGAATTTAT AAACGTTCAT 120
CTTACCCTTT TAAAGGAGAT GAAATTTCTC ATGTCTTTTA GTATTCTCCT TCAAAGTTGG 180
CCATTTTGCA GTTCTACCTT AGAGACTCTC CAATGAGTCC AAGACTTCTG GCTTCTAAGA 240
TCCATGAAAA ATCACGTCCT TACTAGGTCT AAATAAGATT CTTGCTGATA CGGCATTTAG 300
ATTACTCAGC TGGTTAATAA TAATTTTTTT TCTGTTACTT CCCCTTTCCA CAAGTTTTAA 360
GAAAGACTGG CATCAGCTGT TTCTCAATGC ATCAGTCACT TGTTCGCAGA TCAAACAGAA 420
GACATGTGAT TGCATGAATC GGCAGGATTT ACTTCCTGTT ACAGAGTGAG ATCCTTTCTG 480
TAATCTCCTA ACACTGCATC TGGTCCATAC TACTTTAACC TTTTAATAAG ACCCCTCTTA 540
TCCTGGAAGT GGCTTCTTAA AACAGTCTTG TTTGTTCATC AGGGACCCAC GGACAATGTC 600
AGTGTGTTCT TCCTCCCTGT TTTGCCGTTT TCCTGGAAGG CCAGATCCCA TGATAGAGAT 660
AACTAAAATG ACTTTTTCTG GATCTTTTTC CGTTTCCCAA AAATCTGTGG TCCTGCTGCA 720
TCCATTTTAC TATTTTCTCA TCAATTCTGC GTTTTTCTTC TAGGAACCTT ACTTTCCTAA 780
GGTGTGAAAT CAAAAAAAAA AAAAAAAAAA AGAATGCATT ATGTGTAGGC TCTTTAAGAA 840
ATAAATAGTG TAGGTCAGTG TATAGCACAG AGTAGGCATG TGAGCCATGT TAGTTCCCTT 900
TTCTCCCACC ACCTGCTTCA TCAAACATTC CTGTAGGTAT AAAGTAGCTT TGGAACACCC 960
ACCAAGAACA CGTAGGCTTT AATGTACTTA CCCACAAGGG AATCTGCACT TCTGGCATGT 1020
TTCTAAGACA TGAGATGGAA GGAAGGGGCA CATGGAATCT AATACCTGGA AATACTGCCA 1080
GGTGACCTGC CATTGTGGGA GTTCTCCTAA CCTGGCATGT ACATATACAT ATCCTCCATA 1140
ATTCTGAGTG GCTGAACAAG GACTATTTCC CTATATCCTT TTTTCTTCTC AATTCCAATG 1200
AAAGCTCAGT AACAATTCAG CTTTCTGCAT ATAAGTTGAT 1240
|
