| Tag | Content |
|---|
EnhancerAtlas ID | HS042-00764 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr1:19120580-19121530 |
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: 2 | Chromosome | Start | End |
| chr1 | 19121141 | 19121402 | | chr1 | 19120665 | 19121099 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I018794 | chr1 | 19121121 | 19121310 |
|
Enhancer Sequence | CTTCTCGCTG CAAAGTGGGG AGAGCAGACA TAACCTAAAT AATATCTATT TGTCAAGCAC 60
TTACATGTGC CGGGCACTGT TCCAAGCTCT TCGGAAGACA TGAGTTAATT TAAGCTCCAC 120
AACCTCCCGT TTCGTAGATG AAAGAAACTG AAACACAAGA GGTCAAATAA CAGGCCCAAG 180
GCCACACAGC CAGGCAGTCT GGCTCCAGTA CCTGCTCTCC TAAGCCCCTT GCTCCGGCAT 240
CTCTCACCAC CCATCCATGA GCACCTCGGC CCAATCAGGC ATCTCTCCGC CTCCCCAGAG 300
TTCACGCAAA ACAAATGCCT CTATAATGCT CTCTCAGAGT CCACGGCAAC CAGGTCTCAT 360
TTTATTTTTA CCTTTCTTGG TATGTGTTTC TGTCTTTTGG TTTGGTTTTA AGCATCAGAC 420
AGGAAACTCT ATCAGGGCAA TTGCTATGCC TCCCCCATCC GGTAGCTCCC TCAAACAGGG 480
GCTGATCTCC CCATCATTCT GGGGGTTCCC CAGAGTGAGG ACAGGAGGGG AGCTCTGGGT 540
CTCATGGCAG TTTTTCCACC GGCCTGTTCT TAACCTCCCC AGTTCCCATC GGAGGCCCAG 600
CCCTTCCTGG AGCCATCTGG TCTACCTCCT CAGGGGCACC ACCTGCAGGA TGATTCTCTC 660
CAGCCGCCTT GGGGAAATGA ATATGGTAAT ACCCTTTCCT AAATTACTGT CGTAGTTGGC 720
TGAATGTGAG AAACCTAGAG CTGGGGGCAT TGGCAGCTCA AGTGCTAAGA GTTAATTCAA 780
TTAGCCAGAG CACAGAAAGC TTGGGCCTGC TGTCTGCCTG CAGCACAGAC CAGCAGGCTT 840
CCGGGGCACT TTCCACACCT CTGAAATCTC AGCTCCCCTT CCACACCCCA TGTGGCTTTC 900
CCAGTCTTCC CTTATCCAAA ACTAAGGCTT AGATTAGGAC AAATACCTAA 950
|
