Tag | Content |
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EnhancerAtlas ID | HS018-13444 | Organism | Homo sapiens | Tissue/cell | CD19+ | Coordinate | chr2:202869710-202870750 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr2:202870376-202870391 | TGACCTTTTGAGTTC | - | 6.03 | SPI1 | MA0080.4 | chr2:202870098-202870112 | TACTTCCTCTTTCA | - | 6.23 | SPIC | MA0687.1 | chr2:202870098-202870112 | TACTTCCTCTTTCA | - | 6.96 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAAAACAATA GATAAATAAA TGATATAAAT AAAAACAAGT GTAAACCCAG AGAGCTTATT 60 TGCTGATCAC TGTGCAACAT TAGCCAGTGG AAGGCTTTTA TCTGTAACAT GTATACTATG 120 TATATACTGT TTAGTCGTGA GCCATAACAT CAAACATTGA CTGATACATA TGTGCCGGAT 180 TCTGTGAATT GCTTCCCTGG CCCCAAACAG CCTCAGTTGC ACCAAATCTG AAATGCATCC 240 TGCCAAGCAT TTTCCCCCTA ATTGTTTTAA CACAGGATAT TTTCAGGAAA AGCTTATCCA 300 CCCATTTCTA ATTCCATTAC AGTTCGCCCC CTTAAGATGT TACCTTGCCC AAGCTAATTC 360 TATCAAAAAA AAAAAAAAAA AAACTTTTTA CTTCCTCTTT CAAGGTTTCA CTACTTTGCA 420 AACAGGTGGT CCATCAAAAC AGCTGCCCAT GCCCTCCTCC TCAACTCATG TTTGATTCAA 480 GCTCAGAAGG AGCTTTGTTT AAGCACTCAG ACTCCTGGAG AGGTTGGAAA ACACACCAGC 540 CCGGGATCAG GAGGAGAGAA CTGAAGCAAG CACTGAACTT TCTAACAACT CAAACCTAAT 600 CTTTCCCTCT CTCCTTATAG GATCAAATGG AAATTGCAAA GGTCATATGC AATAACTCAT 660 TCAAGCTGAC CTTTTGAGTT CAAGAGAAAC TAGGATGACA AGATAGAAGT GTGGCTTTTA 720 GACAGAGGGC CATCCTGCCT GGGGACATCA ACAGATCTTG GTAGCTTTAT TTTAGAACTA 780 GAAAGAATGG CAGGAGAAGC AACGAGCATC CTCATTAAAG CTGATTTACT GGAGAGACTC 840 AAAATCCTCC TTTCCTCTTT GGTATCACCC AAGTCACTCA TGCCAATTTG TGAAGCTGCA 900 CATCATTATT TTAATTGTCT GCAGCCCTTG GGTGAGTTTT AATCATCTCA GTGGCCTGGT 960 GGCTACAAGC AGGGCTCTGG ACACTACAGT GAAGAGTTTT CACAGGCACA TTTGGTGTCC 1020 ACCAATTCAG ATGGGACCAA 1040
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