| Tag | Content |
|---|
EnhancerAtlas ID | HS050-00921 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:19120160-19121430 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF9 | MA0653.1 | chr1:19120720-19120735 | AAAGAAACTGAAACA | + | 6.12 | | PHOX2A | MA0713.1 | chr1:19121352-19121363 | TAATTCAATTA | + | 6.14 | | Phox2b | MA0681.1 | chr1:19121352-19121363 | TAATTCAATTA | + | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 19120562 | 19120930 | | chr1 | 19121141 | 19121402 | | chr1 | 19120665 | 19121099 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I018794 | chr1 | 19121121 | 19121310 |
|
Enhancer Sequence | GATTGTCAGC CCCAGTCTAG AGGACATTAA ATCATCCTAA GCTCCCTATT TACCCCCGAC 60
CCTCACGCCA ATTCCTTCCT CTTTTCATCT TCAACTTAAC AAGTGTTGTC TGATCACAGC 120
CTATGGGCCA AGGGCTGGGG ATGCTACAGG GAATAAGATA CGGTTCCCGG CTGTAGATAG 180
TCAGTGTTCT CTGGGCCTCA GTTTCTCATC TGCAGAACGG GGCACCAATC CCTCCCTGGA 240
TGGCTTCATG GAGCGACTGT GAGGATCCTG GAGGGTCGTT AATGTGGGCA TAGTGGGAAA 300
GCAGTTGGTG CAGAGAATAG ATCACCCAAC ACAGAGTCAG GGTGCCTGGG TTCAAGTCCC 360
GGTATAGCCA CCGGCAAGCT GAGGGGCTGC AGGCAAATTA CTGCTTCTCC CTGAGCCTGT 420
CTTCTCGCTG CAAAGTGGGG AGAGCAGACA TAACCTAAAT AATATCTATT TGTCAAGCAC 480
TTACATGTGC CGGGCACTGT TCCAAGCTCT TCGGAAGACA TGAGTTAATT TAAGCTCCAC 540
AACCTCCCGT TTCGTAGATG AAAGAAACTG AAACACAAGA GGTCAAATAA CAGGCCCAAG 600
GCCACACAGC CAGGCAGTCT GGCTCCAGTA CCTGCTCTCC TAAGCCCCTT GCTCCGGCAT 660
CTCTCACCAC CCATCCATGA GCACCTCGGC CCAATCAGGC ATCTCTCCGC CTCCCCAGAG 720
TTCACGCAAA ACAAATGCCT CTATAATGCT CTCTCAGAGT CCACGGCAAC CAGGTCTCAT 780
TTTATTTTTA CCTTTCTTGG TATGTGTTTC TGTCTTTTGG TTTGGTTTTA AGCATCAGAC 840
AGGAAACTCT ATCAGGGCAA TTGCTATGCC TCCCCCATCC GGTAGCTCCC TCAAACAGGG 900
GCTGATCTCC CCATCATTCT GGGGGTTCCC CAGAGTGAGG ACAGGAGGGG AGCTCTGGGT 960
CTCATGGCAG TTTTTCCACC GGCCTGTTCT TAACCTCCCC AGTTCCCATC GGAGGCCCAG 1020
CCCTTCCTGG AGCCATCTGG TCTACCTCCT CAGGGGCACC ACCTGCAGGA TGATTCTCTC 1080
CAGCCGCCTT GGGGAAATGA ATATGGTAAT ACCCTTTCCT AAATTACTGT CGTAGTTGGC 1140
TGAATGTGAG AAACCTAGAG CTGGGGGCAT TGGCAGCTCA AGTGCTAAGA GTTAATTCAA 1200
TTAGCCAGAG CACAGAAAGC TTGGGCCTGC TGTCTGCCTG CAGCACAGAC CAGCAGGCTT 1260
CCGGGGCACT 1270
|
