| Tag | Content |
|---|
EnhancerAtlas ID | HS041-00512 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr1:19120270-19121460 |
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 | TGATCACAGC CTATGGGCCA AGGGCTGGGG ATGCTACAGG GAATAAGATA CGGTTCCCGG 60
CTGTAGATAG TCAGTGTTCT CTGGGCCTCA GTTTCTCATC TGCAGAACGG GGCACCAATC 120
CCTCCCTGGA TGGCTTCATG GAGCGACTGT GAGGATCCTG GAGGGTCGTT AATGTGGGCA 180
TAGTGGGAAA GCAGTTGGTG CAGAGAATAG ATCACCCAAC ACAGAGTCAG GGTGCCTGGG 240
TTCAAGTCCC GGTATAGCCA CCGGCAAGCT GAGGGGCTGC AGGCAAATTA CTGCTTCTCC 300
CTGAGCCTGT CTTCTCGCTG CAAAGTGGGG AGAGCAGACA TAACCTAAAT AATATCTATT 360
TGTCAAGCAC TTACATGTGC CGGGCACTGT TCCAAGCTCT TCGGAAGACA TGAGTTAATT 420
TAAGCTCCAC AACCTCCCGT TTCGTAGATG AAAGAAACTG AAACACAAGA GGTCAAATAA 480
CAGGCCCAAG GCCACACAGC CAGGCAGTCT GGCTCCAGTA CCTGCTCTCC TAAGCCCCTT 540
GCTCCGGCAT CTCTCACCAC CCATCCATGA GCACCTCGGC CCAATCAGGC ATCTCTCCGC 600
CTCCCCAGAG TTCACGCAAA ACAAATGCCT CTATAATGCT CTCTCAGAGT CCACGGCAAC 660
CAGGTCTCAT TTTATTTTTA CCTTTCTTGG TATGTGTTTC TGTCTTTTGG TTTGGTTTTA 720
AGCATCAGAC AGGAAACTCT ATCAGGGCAA TTGCTATGCC TCCCCCATCC GGTAGCTCCC 780
TCAAACAGGG GCTGATCTCC CCATCATTCT GGGGGTTCCC CAGAGTGAGG ACAGGAGGGG 840
AGCTCTGGGT CTCATGGCAG TTTTTCCACC GGCCTGTTCT TAACCTCCCC AGTTCCCATC 900
GGAGGCCCAG CCCTTCCTGG AGCCATCTGG TCTACCTCCT CAGGGGCACC ACCTGCAGGA 960
TGATTCTCTC CAGCCGCCTT GGGGAAATGA ATATGGTAAT ACCCTTTCCT AAATTACTGT 1020
CGTAGTTGGC TGAATGTGAG AAACCTAGAG CTGGGGGCAT TGGCAGCTCA AGTGCTAAGA 1080
GTTAATTCAA TTAGCCAGAG CACAGAAAGC TTGGGCCTGC TGTCTGCCTG CAGCACAGAC 1140
CAGCAGGCTT CCGGGGCACT TTCCACACCT CTGAAATCTC AGCTCCCCTT 1190
|
