| Tag | Content |
|---|
EnhancerAtlas ID | HS182-09249 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr17:26827220-26828720 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr17:26827295-26827313 | TGAAGGAGGGAGGGAAGG | + | 6.75 | | PRDM1 | MA0508.2 | chr17:26827892-26827902 | GTGAAAGTGA | - | 6.02 | | RREB1 | MA0073.1 | chr17:26828074-26828094 | CCCCCACCGACCCCCCCACC | + | 6.95 | | ZNF263 | MA0528.1 | chr17:26827300-26827321 | GAGGGAGGGAAGGGTGGAGGA | + | 7.21 | | ZNF263 | MA0528.1 | chr17:26827296-26827317 | GAAGGAGGGAGGGAAGGGTGG | + | 7.49 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 26827971 | 26828324 | | chr17 | 26828227 | 26828489 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH17I028499 | chr17 | 26826742 | 26827406 | | GH17I028500 | chr17 | 26827971 | 26828324 |
|
Enhancer Sequence | CCCCAGAGTA GGCTCCTTGG GGGCGCAGGC CATGACTTCC TATCTCCTCA CAGTCTTGGA 60
GGGGAGGCTG CTTTCTGAAG GAGGGAGGGA AGGGTGGAGG AAGCTAGGGA GTGTTGGGTC 120
AGGGGTCGAG TAGAACTGGG TGGGTGAAGT TCTGGTGGAG TACCAGTCTC CAACCCTGCA 180
GCCTCCACCC CAGTTTGGCA AGGGAAGGGG AAGGGGGTGT GCAGAGGAGA AGGCAAGGAA 240
GGGAACAGAG CAGCCTAGTT GGAAAGAATG TGACGGGGAC TCAGAAGAGT GCTCTGAAGG 300
GTGGAAAGAC CCACAAATGT GTGTACGTGG AGTCACAGAT CCTTGGGTAC CCACAGAACC 360
CATAGACACA TGCACAGACA TGGATACCCG GGAACACACA GTTACACACA TTCACACACA 420
AACACTCATG CATACAACAT TACAGGCTCT CACAGCCTGA AAGACACACA GGACCACCCC 480
CAGAAACACA CACAGACATA CACAGCCACA GCCACCTGTA CACACACAGT CGCTCAGACG 540
CCTCCGCACC CCGTGTCAGA CCTGAGTGTT CTCGCTGCAT GTGGCTACCC ACATTTAGAC 600
ACAGATTCTG GCACGGACAT ACCCAGTAGC ACATTACAGC TCCACAGACT TCAGGCGCAC 660
CCATGGTGAC ACGTGAAAGT GAGAACACAA ATGTAAATAC GTACACACTC ATGCAGAGGT 720
ACACATGTAC TTACACAGAC ACTGACACCA GTGAAAACAC ACACACCCCA GCATTGCTTC 780
TCCCACCTCC ACAGCAGGAG GGATTAAGAC AAGAGGTGAG AAGCCCTCCC CACCCAGCAG 840
GACTCTGTGT TCCTCCCCCA CCGACCCCCC CACCAAGCTC TCAGATTGGA AACTCCCTGG 900
ATTTCCCAGG GGGTCAGCCA ACCAGAACAG GCTCAGACCT CGGCCCAGCT GCCCCGCCAC 960
ACGCCCTCCA CAGCTCTGGG TGCTTCTCCA TCAGCCACAG CCAATGAGCT GTCTGCTCTT 1020
CCCCAGGAAG CTCACCCTAA TTAACCCCAG ATCTCCCCAC CCCTTCTTTG ACATGTGGTC 1080
CCTGGGCCTC AGGGCCTCAT GGCAGCTTTG CTTGGGCCCT GTTCCTCTGT GGATGTTCTT 1140
CAGTGTCTTG CACACCAGTG GAGTGAGACT TGGAAAGCAG CAGGCTCAAA TCTTGGGAAC 1200
TCACTTTGGA AAAGCAAGTC CAGCCTGCAT GAGCGGAAGC AGACAGAAGA TGGCCAATCC 1260
AGATGCAGGG TTCAGGAAGG GGTCCCCCTC CTCCATCACA TTGGGGCTCC CAAGGGTGGG 1320
CACATGCTCT TCCTTCTTCC TAGCGTCCCT AGGGTCTTTC CCCAGACTGA AGCATAGCAG 1380
ACATGGGCCC CAGGGATTTC CATCCCCAGC CAGGGCTGTT TTCTGGCCCA AAGCAGCCCA 1440
GCCCTGGGCA CAGCTCAGCA GCATACAGTG AACTGCTTCT GACCTCCAGT ATTCAGAGGG 1500
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