| Tag | Content |
|---|
EnhancerAtlas ID | HS018-12234 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr2:46717110-46718600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr2:46717976-46717991 | AATCCAAAAATAGAA | + | 7.64 | | PLAG1 | MA0163.1 | chr2:46718008-46718022 | CCCCCTTGAGCCTC | - | 6.35 | | ZNF263 | MA0528.1 | chr2:46718157-46718178 | GGTGGAGGAGGTGGGGAGGGC | + | 6.03 |
|
| | 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 |
| GH02I046490 | chr2 | 46717233 | 46718477 |
|
Enhancer Sequence | TCAGAGGGCT TTTTAGGCTC TTAAGAGTGA AGTGGAGGAT GGGTTTCGGA CTTGCAAATT 60
TCTTACACTT AAGTAGGAGG GGATTACAGA TAGCTTCAGG AGGTAGGCAT TTTTGTTCCT 120
CAAAGAGAGC AAAGGGGTGG CATCAAAAGG CCTGAGCTCG TGGGGCAAAT CCTACAAAGG 180
GCCACGAGTC AGAGAGATGT CAGTCCCTCA CAGGGTTATA GTGACAATTA GTGAGATAAC 240
AAGGTGGAGG CTGGTGGTGA ATAAGAAGCT ACACAGATGA GAGGTATCAG CCAGAGCAGG 300
GAAGGGAAGT GACTGCTAAC CTGAATTTCA AGAACTGGGA GAGGTGGGGA GGTCCGGCTC 360
CTGAATTTGT GGGCCCAGTG CAAGAGGACA ATGCAGTGTC CCATCATGAA TTCCACGACG 420
GTGACAGCAG AGCATTAAGC CATGTGGAGA GCCCCCACTG AGAGCAGGGC CCTGTGCCAC 480
TGCCCTGGCG GTGGATGACG GAGACCCCAG GGTTAAGGGG CTTTTGTGGT GCCTCTCAAA 540
TCTCACCCAG AGAGTGACTA TCCTTGGCCT GTACTCCATC AACAGGAGGG AGGGAGGGAG 600
CAGGCTCTGT GCATTTTGCA GGGGCAGGGA CCGTTGGAGC AGGCCATTGG AGGAAGGAGT 660
CTGGTGGCCC CAGGGCAAGT GGCCCCTGCA TGCCTTCCAG CTCTGGGCGC AGAGTCTGCC 720
TGCAGAGGCG CCTCTTCACA AGCAGGTCAC GCTCTAGGCT TCCAGCTGCT AATCACAGGG 780
GCTCTCCAGC TTGGGTGCAT TTCCTCCCTC TGCTCCTGGC TTCCGCCCCA GTCCCATTCA 840
GCTGATCATT CTCCGCTGGG CTAGAAAATC CAAAAATAGA AGAAAGCTAC ACTTTTTACC 900
CCCTTGAGCC TCTTGTATCA AATGACACAG TCACTTTGCC TCAAACTTTT CATCAAAGCA 960
GCCTTTGTAA GGTCCTGGGG CAGAAAGCAG GCCTTGGAAG ACAGCCACCA GGAAGCCATG 1020
CAGAAAGTGC TGAGCAGGGG GACCCTTGGT GGAGGAGGTG GGGAGGGCAG GGTTTCAGGA 1080
GCTTCCCTCT GCCCCAGAAA GAGCCAGTGA CAGACACTTG CTACCATGGG GCAGCTCTTC 1140
TCTGAGCACC AGCTCTAGCT TCAGGTCTTG GAAGTGCAAG AGCAGCAAAT AGTGTGGCTG 1200
CACAGACCAC CCATTGCCAG GGTTCAACAA CCAGACCACA GAGCTCAATC AGTGATTAAG 1260
GAGCAATGAT TGATCAATCA AATAAACAGA AGGAGTGTAA GAGACGATCT GAGAAAGGCT 1320
CTGTGAGCTA AAGCATTCTG TGACGGCTTC TTGAAAAGGA AGCTCACCCT TGCCGAATAC 1380
CTAGGATGTA TTGTACCCTG TCCAACACTC TCATGTCATC TATTTTATCC CATAGCCCTC 1440
CATGAAGGAG CACTGGTACG CACTAGATTA ATCTGCCCAG GCTGCTCTAA 1490
|
