| Tag | Content |
|---|
EnhancerAtlas ID | HS050-27811 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr17:10671740-10673160 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFF | MA0495.3 | chr17:10672300-10672315 | ATGCTGAGTGAGCAC | - | 6.04 | | SOX10 | MA0442.2 | chr17:10672688-10672699 | TGCTTTGTTTT | - | 6.02 | | STAT1 | MA0137.3 | chr17:10671911-10671922 | TTTCCCAGAAA | - | 6.02 | | STAT3 | MA0144.2 | chr17:10671911-10671922 | TTTCCCAGAAA | - | 6.32 |
|
| | 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 |
| GH17I010768 | chr17 | 10672260 | 10672535 |
|
Enhancer Sequence | CTCTGGCACT CCGCAGTGAT CACCTATAGG AAAACATGGA GTATCAGAAT ATTGGTCTCT 60
CAGGAACCTG GCTTTGTGGG GTGGTTTGAG GCAGTAGTTG CCCCTTCATA TGTGCACCCA 120
GGCCCCTGCC AGACAGGTAA TCACATTGCC TCCTCCTTGT GGCAGATTAT ATTTCCCAGA 180
AAGTGCCTGC AACAATACTT CCAGTCCCAT ATGTGCTTCT AGAGCCGGTC ACTCTCTCAG 240
TTTAAAGGTG GAGTCTATTT CCCTTCCCCT TAAGACTGCC TCAGTGGTTA GACTATGGCA 300
AGAAAGATAT CATGTGACTT CCAAGACAAA TCCTAAAAGG CAACACAGCT TCCACCTGGC 360
TCTTTCTATT TTGAGCCACT TACCTATGGA ACACCAGCCA CCATGTTGGA AGGAAGCCCA 420
GGTGACATGG AGAAGCATCT GTGAGTGCTC TGGCAGGCAC GCCAGCTTGA ATCTCAGCCA 480
TCAGCCAGCA TCAACCACCA GATGCGTGAG AGAGAGCCTT CACATGACTT CAGGCCTCAG 540
CCTGCAAGCT GTCCCAGCTT ATGCTGAGTG AGCACAGACA ACCTATCCCT GCTGAGCCCT 600
GTCCAGTCTG CAGATTTCTG AGCAAAATAA ATGATGTTAT TGTTTTAAGC CACTGAGTTT 660
TGGCATAGTT TGTTATGCAG CCATAGTAAC TGGAATATCC TGAATTCATT GTTTCCAGTA 720
CAGCCCATTA TGCTCACACA CAGGGCTGCC CACCCAGGTT GTTGCTCAGC ACAGGCTCTG 780
GGCTCACTTG GTCCAGAGCT AAGGGCTGTG TTAGCCTGAA GAGGTGCCTT TTTGTAAGTG 840
GTCTTGCCCG GAGAGCACCA TTTCCTTTTT CCTACAGGGG TACTGCATGG GCTAGCTGCC 900
TCCCTGCTCA CAGATATTAA GATTCTAGAA CATGTTTGTT GTTGTTGTTG CTTTGTTTTT 960
GTTTTTAGAG CCAGGATTTT GCTTCGTTGC CCAGGCTGGA GTATGGTGGT GCTATCATAA 1020
CCCACTGTAA CCTCACACTG CTGGTCTCAA GTGATCCTCC TGCCCCAGTC TCTCGAGTAG 1080
CTAGGACTAC AGGGATGTAC CTCCACACTT GGCTAATTTA TTTTTTATTT TTTGTAGAGA 1140
TGGGGTCTTG CTGTATTACC CAGGCTGGTC TTGAACTCCT GGTCTCAGGT GCTTCTCCCA 1200
CCTCGGCCTC CCAAAGTGTT GGGATTACAG GTGTGAGTCA CTGCACCCAC CCAGAGTGTT 1260
TTTCTTAGTG TTGAGTAAAA CCTCCACTCT TTAATTTCCA TTCACTTGTC CTAATTCTAT 1320
TGTCTGGGTG TCATGTGGAA TTAATCTGGT TTCTTTCTGG TGTCTTGATG GTCGAAGATG 1380
TCACTCATGA TCTCCCTGAA CTTTCACCTT GTCTTGGCTA 1420
|
