| Tag | Content |
|---|
EnhancerAtlas ID | HS018-00955 | Organism | Homo sapiens | Tissue/cell | CD19+ | Coordinate | chr1:93363240-93364680 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:93363667-93363679 | AAACAAACAAAC | - | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr1:93363439-93363454 | GAGGTCAGGAGTTCA | + | 6.22 | | PRDM1 | MA0508.2 | chr1:93363795-93363805 | GTGAAAGTGA | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCATTGACCC ATTGGTCACT CAGGAGCATG CTGTTTAATT TCCTGTTTGT AACATATCAG 60
AAGTTCCTTT TTTTTTTTTT AAAGAGACAA GGTGTATTAA TTTGTTTTGT GTCACTATAA 120
AGGAATACCT GAGGCTAGAT AATGTATAAA AACAAAAAAA AGGATTACAC TTTGGGATGC 180
CAAAGCAGGT GGATCGCTTG AGGTCAGGAG TTCAAGACCA GCCTGGCTAA TGTGGTGAAA 240
CCTTATCTCT ACTAAAAATA CAAAAATTAG CCATGCGTGG TGGCGTGCAC CTATAGTCTC 300
AGCTACTTGG GAGGCTGAGG CAGAAGAATT GCTTGAATCT GGGAGATGGA GGTTGAAGTG 360
GGTCAAGATT GTGTCACTGC ACTCTAGCCT GGGCAACAGA GCGAGACTCC ATCTCAAAAA 420
AAACAAAAAA CAAACAAACA AAAAAAACAA GAGGTTTAAT TGGCTCATGG TTCTGCAGGC 480
TGTACAAGGT ACAAGAAGCA TGGTGCCAAC ATCTGCTCAG CTTCTGATGA GGGCCTTCAG 540
CAACTTACAG TCATGGTGAA AGTGACAGGG AGCCAGCCTG TCACATGGTG AAGAGAGCAA 600
CGGGGGAAGG GGGAAGTGCT ACACACTTTT AAACAACCAG ATCTCACATG AACTCAGAGC 660
AATAACCCAC TCATCACCAA GGGGATGGTG CTAAGCCATT CATGAGAGAT CCACCCCCAT 720
GATCCAAACA CCTCCCACCA GACCCCATCT CCAATAATGG GGATTACATT TCAACATGAG 780
ATTTGGAGGG GACAAACATT CAAACCATAT CACAAAACAT ATCACCTTGT CATCCAGGAT 840
AGAGTGCGGT GGTATGAACA TAGTCACTGC AGCCTTGAAC TACTGGGCTC AAGGGATTCT 900
CTGATCTCAG CCTCCTGAGT AGCTGGGACT ATAGGTGTGA ACCACCATAC CTTGCTAATT 960
TTTATTTGTT TACGGTTTTT GTAGAGATGA GGTCTTGTTT TGTTGCCCAG GCTGGTTTCA 1020
AACTCTTGGC TTCAAGTGAT CCTTCTGCCT TGACTTCCCA AAGTGCTGGG ATTACAGGTA 1080
TGAGTCTGTC TTATTTAGAG ATAGGGTCTC ACTCTGTCAC CCAGGCTGGA GTGCACTGGC 1140
ACAATCATGG CTCACTGCAG CCTTGACCTC CTGGGCTCAA GCAACCCTCC CACTTCACCT 1200
TCCCGAGTAG CTGCGACCAC AGACATGTGC CACCATGCCT GGCTATTTTG CTTTTTAATG 1260
TTTTTGTATA GACGGGGGTC ACCCTATGTT GCCCAGGCTA ACCTCAAACT CCTGGATTCA 1320
AATATCCTCC CATGTCAGCC TCTCAAAGTG TTGGGATTAC AGGCATGAGC AATTGCACTT 1380
GGCCTAAAAT GTACTTTATA TTCATTTCTG TTGTTGATTT TCTGTCTAGA TGATCTATCC 1440
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