| Tag | Content |
|---|
EnhancerAtlas ID | HS019-09550 | Organism | Homo sapiens | Tissue/cell | CD20+ | Coordinate | chr2:113603230-113604460 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr2:113603249-113603263 | CCCGCCTCGGCCTC | + | 6.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTCCTCACCT TGTGATCCGC CCGCCTCGGC CTCCCAAAGT GCTGGGATTA CAGGCATGAG 60
CCACCGCGCC CAGCCAGACC TCTTGAGTCT TAAACTCCTC TGTAGTTCCA GCCACCCTTT 120
AGCACATGAC TCTGTTAATT TTGTTCTCAC TGTCTGAAAT CATCTCCTGT CCACTCTTGA 180
CTGACAGGTC TCTGCACTAG CCCACTGCTT AATCAGAGTA GGTCCCTGTC AACTTATTCA 240
TATTGTGTCC CCATGCCAGT GTGGATGATT AAAATTGTTG AGTGGAGGCT GATCAGATGA 300
GCCATCTCCT TCCAAGTCCT CACTTGCTGG CTCCTGTCTT AGTTTTAGTC CCCATTCTTC 360
AAAGAACGTG AGCCCTGGAA AGTATTTTAG TCATTTAGTT CAGTGCCTTT GGATGGGAGG 420
ATCACATCCC TGGGTCCCGT CCTGCAGACT GTTTTGCTCT AGCTGACTAG GCAGGATTCC 480
CTGCCTTCTC TCACTTCTGC ATGGGACTTC CTTCTGAAAT TGCTGCTCAG TCAAGAGAAT 540
GACCTTCCCC AACATAATCC TACTCCACAG GGACTTAAAG GTGTGTCAGA GATCTCTTGC 600
TCATCTTTCT GGCCAGGTGC CAACGTCAGT TTATAGCCAA GGGACAAGAC TAGTTAGCAG 660
ATCAGGCAGG TCTTAGACCC CAGCGTAAGT GCCAGACTTC TAGCTGCAGT TGTTCCTGCC 720
CACACTGGGC GTTCAGGTGG AGAGAGGGCA TGGCACTACA CTGAGCTCTC GGCGAAACCC 780
AGGACTCTGA AATCTCGGTG TCAGCCCCAG GCCACTCTCT TCAGCAGAAC TTCAGTCAGT 840
CCTGTCACTA GGAGATGGGA CCCTGCCTGA TTGCATTCTT ACAAATGGCT ACATTGACAA 900
GGGGACTAGA CTTGACTGAG TGGAGATTGG GGGAAAAGGA AATAAGCCCT CAGTGCTTTC 960
TCTGAGCACA TCACCCTTGC TGGCTTAGCA TCTATTGTTT GTCAGAAGAC TTAGCTATTA 1020
TCTTGGCAAA TATTCTCTGC TTGACCAAAT TTTAGTCAGG CTCCTGAACC TTCTCCCAGG 1080
CACATTTGTA CACTTTCTTG TAAACTCCTT TTTTAGCAAG AACCTTCTAT GTTCAATATC 1140
TGATCACCCT TGAAATCTCA CTGGATTCCC CATCCTCCAC CATCCCCAAA GTGGTGTCCA 1200
ATCACCCTGT CCTGTCTTCA GCAAGGATCC 1230
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