| Tag | Content |
|---|
EnhancerAtlas ID | HS018-12889 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr2:113847060-113848190 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr2:113848033-113848044 | TCTGATTGGCC | - | 6.02 |
|
| | 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 |
| GH02I113090 | chr2 | 113847761 | 113847860 |
|
Enhancer Sequence | GGTTTATTCA TTTAAAAAGT AACTATCAAG CACCTGCTCT GTGCATGATA CTGTTTTGGG 60
CGTTGAGATG CATCTGTGAA TAACACATAG TAAGGAATTT ACATTCTAGC GGTAGGAGAC 120
AGAGAATAAA TGCCTGAGCA AATACATACT CAATATAAAT TTGGATAGTG ATACAGGCTG 180
TGCAGAAAAA ATATCTGCTA TTAGATGAAC AGTGAAGGTG AGCAGAGAAA GTGGAGGTTT 240
GCTACAAATT GTGTTCTCCA AAGGAAATGG AGAGTGCTGT GGGAGTTGTG TTGACAGTAA 300
CCCTAGATAG ATTTTATTGT ATTAATGCTT GCTAGAATAA ATAGCTCTAC TGAATAGCAG 360
ATGGAGGAAA GCACACTGGG CTTTGCAAAT CATCACTGTG ATGCATGTAA TTTTGCAGCA 420
CTGCCAGGGT TTCTCACAGC AACTCATTCC CATTGTGGCC CCTTAGGGAA AGCTGTGACC 480
AGTGCAAGAT CTCTCCTACC TGCATGACCT CAGGGCCAGC AACAGACAAT TGCAACTCCT 540
GCCCACAGAC TCCATGGGTC AGGGAACCAC TGGAAAGCAA AGCAGACACT TGCTGTATCA 600
GGGTTGGAGG AAGCCTTTGA GGCCCTTTGC ATGCAGCTCA GAGAGGAATG GCATTCTCAG 660
GTTGAGCAAA GGGAAGTGGC TAGCACTTCA GACATGACAC TCATTGAAGC TTGGAGGAGA 720
CTTTTTTAGG GCAAAGAAAG GGAAGTTTTA TTTCACTCAT GGTTAGTAAA CATAAGACAT 780
GTACATTCTT AATACATCTC CAAATAACAT TAGAGGAAGA CCAGGAACAA TGCTGAGGGG 840
ATAGAGCTAT AACCGACTGG GGTGAGAAGT GGGGGCATTT GGGAAGGGTG AGAAGTGGGG 900
GCATTTGGGA AAGAGTCCTC ATTCCAAGTG GCCTCAAGGT CAGTATCTGG GCTCCTGTGA 960
TTCTCTCTGA TGCTCTGATT GGCCACTGCA TTGGAAATGC CACTCAGGCT CAGATTGGTG 1020
CCCTCCTTGT GTGTTTTTTC TTTATCACAT ATCCTACAGT CCACTTTCCT GATTCTCTCC 1080
TAACATGTGC CTCTTCTTGA GATCAAGAGG AAGATATTAT TTTCTAGTTA 1130
|
