| Tag | Content |
|---|
EnhancerAtlas ID | HS019-06553 | Organism | Homo sapiens | Tissue/cell | CD20+ | Coordinate | chr16:88681050-88682740 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr16:88681137-88681148 | ATTGACCTTGA | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 88681563 | 88681625 | | chr16 | 88682590 | 88682673 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH16I088615 | chr16 | 88682152 | 88687648 |
| Enhancer Sequence | TATTTCAGAT GTTTTTAATC CTTTTATGTT ACAGTAATCT CTAAGTTATT TTGAAGTTTA 60
CATGGTCATC CAAACGGGGA AACCGTCATT GACCTTGACA TTGTGCCGCC TTCTTCAGCC 120
TTTCAAGCCC TTTTGGATAG AAGCCCTTCC CCTACAGCAC ACACAGTATT TTCAGTGTGC 180
ACTCAGCCTA AGGCTGCCTT CTCCCCTGAG ACCCCACTGC AAAGGTGCAG CCCAGCACCC 240
CGTGCACACA CCCCCAGCCG CTCCCTCTGC CCAGATGGGC TGCCCCCATT TCCTCCATTC 300
CGTCTGCCTG GACGGGCTGC CCCACCTCCT GTTCCCTCTG CCCAGATGGG CTGCCCCCAC 360
CTCCTCCATT CCCTCTGCGT TTGACAGGCT GCCCCCACCT GCTCCGTTCC CTCTGCCTGG 420
ACGGGCTGCC CCCACCTGCT CCGTTCCCTC TGCCTGGACG GGCTGCCCCC ACCTGCTCCG 480
TTCCCTCTGC CTGGACGGGC TGCCCCCACC TCCTCCATTC CCTCTGCCTT TGACAGGCTG 540
CCCCCACCTC CTCCGTTCCC TCTGCCTTTG ACAGGCTGCC CCCACCTCCT CCGTTCCCTC 600
TGCCCGGACG GGCTGCCTCT ACCTCCTCCA GGGTTTTGCT CAGATTCCTC TGCACAGGGA 660
AGTCTCCCCA TCCCCTCCTG CTTGCCAGCC TGCTTTCTTG TTCCTCATGG CCCTCAGTGC 720
CCATCTGGAG CCCTTGCAGC AGATGGTCCT GGGGCACCAC CGTCTGCCCT GCTCCCCGTT 780
GCAGCCTCTG TGCCTGTCCC AGAGTCCCGC ACAGGTTGGT GCTTACCCAC ATTTGGGGGT 840
GCTGTCCGTG AGTTTTGGAT TTGGTATCAG CCTGCATTTT TACCTGCATG TCATAATTGA 900
TTGTTACAGG GTTGCTAAAA TTGCACATTG ATTTCTACAA ACAGAACCAG CTGAGTCTGC 960
TTTCCAGATT CACAAAATAG GGGTTTTCAC GCCACCCAGA TCATTGGTTT TAGAAGCAGA 1020
GACATAGAAA GGCAGTGATA TCCACGTGGA AGGTCACTGT GCTGTGTGGC TCTGGGTTTA 1080
TGAGTCCGTC AGCATGTCCA CTTTGGTGGC TTATGGGCAC ACGTGCCTGG CCACAGACCC 1140
CCTTCCCCAG CCCCTAGTCA TGTATTCTGC CTGTTTCTAA GCAGCCGGGG GCTCTTCCCA 1200
GTCAGGAGTC TGTAATTCCA ACTCAGGGAT GTTTTCTGTG TACAAGAATG TACTTCTGGA 1260
GTACGCGTTA GAGGGCCGCC ATGCCTAAGG TTGCTGTGTT CCTCTGCTGT GGCCCGCACT 1320
TTAGTGACCC GCGGAATGGG AGGGCAGATT CCCGACTGCT GTGCCCGTCT CCTGTGTGCT 1380
CAGCCTCCCC AGAGGAAAGC GGGTGACGGA TCCCAGGAGG CTTGGAGAGG GTAACTCTGC 1440
CAGCATGGCC ACCAGGCAGC AGGTTGCCAT CGCCAGCCCC TGAGCCCTCA GCTTCACAGA 1500
GGAGTCTTAC ATTCAGGAAG GGACTGGGAG GTGCTCAGAC GTTGTCTGGC CTGATCTGGG 1560
CTCACAGCTA GGGTTCAGGA AACTCTGTAC TAAATGAGTT TTTCTTAAAA TCAAACACAG 1620
CTGCTCTCAC CAAACTGGGC CGAGCCGCTC TTCCCACCTG TTTCTGACCT GGTTCATTTC 1680
CCTTCTGCGA 1690
|
| |
|
|
|
