| Tag | Content |
|---|
EnhancerAtlas ID | HS019-06886 |
Organism | Homo sapiens |
Tissue/cell | CD20+ |
Coordinate | chr17:28546770-28548630 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr17:28546803-28546814 | AGCTGTGATTT | - | 6.14 | | Nr2f6(var.2) | MA0728.1 | chr17:28548213-28548228 | TGAACTCCTGACCTC | - | 6.22 |
|
| | 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 |
| GH17I030219 | chr17 | 28546062 | 28547978 |
|
Enhancer Sequence | TGCAGCCTGA GTTTTTAGCC TAAAGGGTGG ATCAGCTGTG ATTTTCCCTA ATTTTCCCTG 60
CTGTAAAATG CTCTGAACCC AGAAACCTGA GGTCTGTGCA AATCAGAAAG GTCCATGTAA 120
TTTACAGTCA CACTGGGTAA ACCCGGCTCG AGAATAAAAC CATGTGTTCT CGTGATGGCC 180
TTCCTCCAAA GAGTTTGCTT GATCAGCTTT ACGCTGGGGA ATGAGTGTCG GGGAAATGTC 240
ACCAGTGACC CAGCCCCTTA CATAATGCCC AGGCTAAAGG TGAGTCCTCT GGAGCAGGAG 300
ATAAGGTGAT TATGACTTTT GCTCCTCCTA GGCAGGAAGC GCTGAGCTTC CCAGGGGCCC 360
CCTGGAACTA CCTTTGCAAC TACATGGACA GAAATCTTTA AAAGAGAGTA AATCCAGGCC 420
ACTCTGTGTT AGGTCACGGG AGAAGTGAGG GTGACACAAA TGGATGATCC CCAAACCTCT 480
TTGTAGCTGC CCTCCCAAAT CTGTTGTCAG AGTTCCCATG AAAATCAAGC TTGACGCATC 540
TGACACCCAC TTCTTGTTAT TTTCTTGTGC TGATAACAAG TCCAGAGGCC CCAAACCCAT 600
TCACTTTTCC CCACTGCTCT GCTCTCCCCC AGGTTCCCAT CTTCATGCCT ACAGTCAGCT 660
ACTATTTTTT ATAATCTACA AGTTAACTAC TTGAGAGGCT TTAGGGGTAC AAGGAACAAG 720
ATAGGGCCTC TGGCCTCAAA AATCTAACAT CCCAGGAGGA GATAGGAGGG CCAGCCATGC 780
GTGGTTTGAG GTTGGTATTA ATGTCATGCT GTGGATCTAA TCCAGCTTAA ATTCTGCCCA 840
GACTGGTAAT TAAGATTTAG GACTTAACGC TGATGCCCTT CTCTGACCTC ACACAGGTCC 900
AAAGGATCAG AAGCATCTGG GACTCTGAAG CCACCTCCAA ATTTTCCCTT ACGCAGGCCT 960
ACCCTCGTGG ACTCTTCCCA GCAGAACTTG CCAGCAGGAG TGAAGGGACT CAGCACAGGG 1020
CTGACGGCCA TTCCCTCACT TCTGGCTGGG GGAGGACAGA GCCTGGAGAA TGCAGGATGA 1080
GAAGGAGGCC CTTCAATAAA TGGAGCGCTA ATGATGCTGG AGATCTGTGA GGTCAGGTTT 1140
GGGAGGGCTT CACCCAGCTT CACAACCCGG AGAGCCTCAG ACACGCTGTC TTCAGCTTTT 1200
GGCTTGCTGG AGATTTGACT TTTTTTTTTT TTTTTTTTTT TTGAGACAGA GTCTCGCTCT 1260
GTCGCCTAGG CTGGAGTGCA GTGGTGCCAT CTCGGCTCAC TGCAACCTCC ACCTCCCAGG 1320
TTCAAGTGAT TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG ACTACAGGCG CCCACCACCA 1380
TACCCAGCTA ATTTTTATAT TTTTAGTGGA GACGGGGTTT TGCCATGTTG GTCAGGCTGG 1440
TCTTGAACTC CTGACCTCAG GTGATCCACC TGCCTCAGCC TCCCAAAGTG CTGGGATTAC 1500
AGGTGTGAGC CACCACGCCT GGCGAGATTT GACTTTTCTA CCAGCTCGAA AGTCTAAGTC 1560
ATCATGTTCC TAGTCTTACG CCAGTGAAGA CTGAAAAGAC ATAATCTGTC TTCTGGCCTC 1620
TCAAGAGGAC CTACAGCCCA TCCCAGGTCA CAGCCCACCC GGGTCACAGC CCACCCCAGG 1680
TCACAGCCCA CCCGGGTCAC AGCCCACCCC AGGTCACAGC CCACCCGGGT CACAGCCCAT 1740
CCCAGGTCAC AGCCCACCCC AGGTCGCAGC CCACCCGGGT CACAGCCCAC CCCGGGTCAC 1800
AGCCCACTCC GGGTCACAGC CCACCCTGGG TCACAGCCTC TACTCGCAGC CTGTGATACT 1860
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