Tag | Content |
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EnhancerAtlas ID | HS018-13627 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr2:231121570-231123450 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata1 | MA0035.3 | chr2:231121938-231121949 | AGAGATAAGGA | - | 6.02 | NEUROD2 | MA0668.1 | chr2:231122813-231122823 | ACCATATGGC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr2:231122265-231122280 | GAGGTCAGGAGTTCA | + | 6.22 | Nr5a2 | MA0505.1 | chr2:231122273-231122288 | GAGTTCAAGGCCAGC | + | 8.25 | RARA | MA0729.1 | chr2:231122265-231122283 | GAGGTCAGGAGTTCAAGG | + | 6.73 | RREB1 | MA0073.1 | chr2:231121806-231121826 | GGGCATGGGTTGGGGTGGGG | - | 6.11 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I230257 | chr2 | 231121973 | 231123143 |
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Enhancer Sequence | ACTTTCCATT ATGTCATTGG ATCATGCAGT GGTTTTTCAG AGTACTCTGA TAGGTGTTAT 60 AATTTTACTC ACAAAAACCT CAAGACTTAG ATAGGGAAGG TGCTGTTATT GCTGTTTTAA 120 GGAGCCAGAA ACACAGAAAT GCATGTGACA CGGGTGTTTG ATAAGACCCA AGAAAAAAGA 180 AAGAGCAGAG ACCAGTGTCC TGGATGACTC CTTACAGGCT TTCAGTTCTA TGAGGTGGGC 240 ATGGGTTGGG GTGGGGTCTC ATAGTCTGAG TCCAATGTGG ATGCCCAAAG GGTTTTTAGG 300 AATCCAAGAG ACTCTACCAG GGTTCAATGG AAAGAGACTT TTATCTAACA AATAAAGAAA 360 GATTAGGGAG AGATAAGGAA ACATTATCAA GAGTTGGAAA ATACTTGAAT GTAATCTACG 420 ATACGAGATA GGAGATATCC AGAAAAATAG AGCCAGAAAA GAGAAACAGA GAGGCAATAT 480 GAAAAGTATA TGTAGCACAT CACTGAAGGA GGAAGAGACA GTAAGGGAGA GGAGATGTTA 540 AGAAGAGAAA GTCCAGAAAG CCGAAAAGAA CCATAGATGC CGTCATAGAG TAATAAAAAG 600 ATATCACTAG TAGAAGGGGC TATCACTTAG GCTGGGTGCA GTGGGTCACC CCTGTAATCC 660 CAGCAATTTG GGAGGCCAAG GCAGGTGGAT CACTTGAGGT CAGGAGTTCA AGGCCAGCCG 720 GGCCAACATG GCAAAACCCC ATCTCTACTA AAAATACAAA AATTAGCTGG TTGTGGTCGA 780 GCACACCTGT AGTCCCAGCT ACTCGGGAGG CTGAAACAAG AGAGTTGCTT GAACCCGGGA 840 TGTGGAGGTT GCAGTCAGCT GAGATCACAT CACTGCACTC CAGCCTGGTG ACAGAGCAAG 900 ATTCCATCTC AGAAGAAAAA AAGAAAAAAT AAGGGGCCAC CACTTAATAT CAAACGAAAG 960 GCTGAATTTA TTGTTCAGTT AAGGGATAGT TGTGCTTGTG GGTCAGTTTC TCTGAACAGA 1020 GAACGTTTGT GGAAGTGTGG ATCTCGGTGA CTGGCGGCCT TCAAAAGTGA GATTTGTTAG 1080 TGGTTAGCTG ACCTTTAGTG AAAGCAGGGT CACTGGAGTG TGGCTGTTAC TGACTGTCTG 1140 ACTTTCAGAA GCATGGGGAA GTCAATGGTT GGCTGGCTTT CAGAGGCCTG TGTACTGGCC 1200 AGAAGCTATT GTTGATTAAT TGGGATGATT CTGGTTGTTA TTGACCATAT GGCCAAACAA 1260 TAATGAGTTT TCCTAGAAGT GTAGCAACTT TCAATTATCA GTTTCCCCTT TAGGAAATCT 1320 CTCATCTAAA GCTGCAGGAG GCACCATCAA GTATTTTCCC CATCCAAGAT GTCTTTTCTG 1380 GAAGAGGACC CTGGAAACAA AATCCTAGGA TTCCCCTTCA CTGAGTAGGA GTTATAGAGT 1440 TGCTAGATTG AGAGTGTTAT CCTTGCAAAG GATGACATAA GAAAAAGTAA TGATGTTTTA 1500 CAATACGTTA ATGGAATGGC AGACAACTGT TGAAAGTTTT TAATTAGCAG CAGAATTGTG 1560 CTGCTTGCAA TACTATCCTA TTTATTCCCT TTTGCTCCAA GAATACTCAC CAGCCACCCT 1620 TGTGGCTGCA GCGTTTATCC CAAGTAAATT TGCCATGAAA TATCTTGCTT TTATTATTAT 1680 TTTCACATCA CTCTAATATA TTGACTTTGG AAACAAAAGA CATTCTTCTA ATTATAGCAT 1740 TCTGGTTTTA GTAGTGGTAT TTCCATTTAC AAAATACAGT AATTGTTGAT CACTGAAAAT 1800 GTCAAATCCT GGAAAACGTG GCTTTCCCAC ATGTGCTGTT AACATTGTTA CTGAACAATT 1860 GTTGGCCGAA GATTCATTTG 1880
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