| Tag | Content |
|---|
EnhancerAtlas ID | HS180-43940 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr6:170677740-170679110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mecom | MA0029.1 | chr6:170678218-170678232 | GAGATAAGATAGAA | + | 6.24 | | NFYB | MA0502.1 | chr6:170678033-170678048 | CCATGAGCCAATCAG | + | 6.71 | | RUNX1 | MA0002.2 | chr6:170677824-170677835 | AAACCACAGAC | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 170678356 | 170678505 | | chr6 | 170678545 | 170679105 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I170369 | chr6 | 170678267 | 170679432 |
|
Enhancer Sequence | ATAAAAATTT GGTGAATGAA TGAATAGTAG ATGTACTGGT CAGTTTGGGC TGCCATAACA 60
AAACACCACG GACTGGGTGG CCTAAAACCA CAGACATTCC CTTCTCAGTG TTTTGGAAAC 120
TTGATGTCCA AGATCCATGT GCCAGCAGCT CTGCTGTCTG CCGGGGCTGG GGGGGGGGCT 180
CCCTCCTGGC TTGCAGGCAG CCAGTTTCTC ACTATGTCCT CATAGGTTGG AGAGCAGAGA 240
GCAGTCTCCT GAGGGCACTC ACCTGCTTTG GTAGGGTGCC CCCCACCCCC CCACCATGAG 300
CCAATCAGCT CTCATAGGCC CCCACCTCCA ATTACCATCC CATTGGGGAT TTAGCCTTCA 360
GCATAAGAAA TTTTGGAAGG ACGTATTTGC CCGTAGCAGT AGAAATAGAA ATCTTGAATG 420
TTTTACTGGG CTTCTGTAAA CACAGAAGAT GACTGATGAG TCCCTCAGCA GCTTAAATGA 480
GATAAGATAG AAATGAACAA AGCAAAAGAA AGCAAATGAA CAAAGCAAAA GAAATTAGTA 540
TTCATATTTT TCCTCACTTT TATTCTCTCT TGTGCACATA GACTTTCCAG TATTTATCCA 600
GAATTTTCAC AGGCCAAGAG AGAAGAGAGG TTTGTGGCTG CGTTTGAACC TAGGAAAGGA 660
CTTTGAGAAC TCAGGATGCC TGGAACCAGC TGTGCAGTGC GTCTGCCTCC TGGACTTGGC 720
AGCAGGGCCC CACTTTCACT GACTTTGCCC ATAGTCCTCA TAATTGTAGT AGGTGTCTCC 780
TGCTACAGAT CTTGATACGT GTTTGAGAAA ATGTGATCTC TATGAGGAAG CAAGAAAAGG 840
TAAGAAGGAC TATAGCAGAA AGCAGAGAAT TCCGAGTCCA GTTTGGAGAG AGTGAGGAAG 900
TCAACTGGAA AGGTCTCTCA TGATAAAGGT TCCAGGTGTT GCCAGCAGTG CTGGGGCAGG 960
CCCCGGGGCT GAACCCGCCA CTGGATGTAG CCTGTGGCAC TCCTCGGGTG ACCTTTGCCT 1020
CAGCAAACTT AGGGTAGTTT TTTTTTTTTT TTTTTTCCTG CTCCCATACC TGACTCCTAG 1080
ATAGGAGGTT TCTCTTGTCC TGGAGAATCT TAAGAGAAGT ATGTCTATGT TCTTGGAATC 1140
AGGAGAGCTC AGTTACTTGG GGGTGGAAAC TGAGTCTTTT ATAATTTCCA TGGAACCTTT 1200
GCACCTTGTA GGTACTCAAT AATTAATTGT CAGTTTGCTG AATATGTCCA TAAATCTTAT 1260
ACTTAAGAGT TTATGCTATA ATGCTGGTAG ATGGATTTTA TCTTCGTGAA TAAGAATCTT 1320
TCACATGTAA CTTATTTTTC TACAGCAGAA GCAAATTTCA GGATGTAATT 1370
|
