Tag | Content |
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EnhancerAtlas ID | HS018-15165 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr22:36887240-36889670 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr22:36889614-36889629 | GGGTCTCTGTGACCT | - | 6.45 | IRF1 | MA0050.2 | chr22:36887435-36887456 | GAGTGGTTTCTTTTTCTTTTT | + | 6.15 | Nr2f6(var.2) | MA0728.1 | chr22:36887670-36887685 | TGAACTCCTGACCTC | - | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 36889168 | 36889263 | chr22 | 36888044 | 36888199 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I036493 | chr22 | 36889448 | 36890490 |
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Enhancer Sequence | AACCAAAAGA AGCCATGCAA AGAGAGAAGC TACTGAAAGG AACAACCGCT AGGTCTGGGA 60 GTTCCTCGTG GGAATGAGAA TGAAGGTAGG GAAAGCGGGT GACATAGTTT GGGTCTGTGT 120 CCCCGCCCAA ATCTCATGTT GAAATGCAAT CTCTAATGCT GGAGGTGGGG CTGCTGGGAG 180 GTGACTGCAT CACAGGAGTG GTTTCTTTTT CTTTTTTTTT CTTGAGGCAG AGTCTCCCTC 240 TGTTGCCCAG GCAGGCTGGA GTACAGTGGC ACGATCCCAG CTCACTACAA CCTCTGCCTT 300 CTGGGTTCAA GTGATTCTCC TGCCTCAGCC TCCCCAGTAG CTGAGACTAC AGGTGCCCGC 360 CACCACGCTC AGCTAATTTT TGTGTTTTTT AAGTAGGGAG AGGGTTTCAC CATGTTGGCC 420 TGGCTTGTCT TGAACTCCTG ACCTCAAGCT ATCTGCCTTT CTCGGCCTCC CAAAGTGCTG 480 GGATTACAGG CGTGATCCAG CATCCAGAAA TAGATGCTGC CATGCGTCCA TACAGCCTGC 540 AGAACTGTGA GCCAATTAAA CCTGTTTCTT TATAAATTAC AGTCTCAGGT ATTTCTTTAT 600 AGCAATGTGA GAACAGACTA ATACAGTGAG AAAAAGTCAT TTAGCCAAGT ACTTATAAGA 660 CTTTAAACAA ACAGAAGAGC TGACACAGAT ATGGGCTCAG CCTTCTGAGG GAGTTAGAGA 720 CAAGGGCAGA CAGAGTGTCA GGAATGGGCT GGAGTCCTTC TGTAACTCTG AGCGAGCCTT 780 CTTGCCTCCC TGAGCCCCTC TATCTCAAGT GAAAAATGGG CACAGCACAA AGGATGTCGT 840 GAGGCTTCCA TGGGTGACCA GGCTGAAAGG TGCTCCAGAA ATATGACTTC CTGTTTATTT 900 CTGACTCTTA GCATGGAGGC CCCTGGGAGG CCAGGCCATG GCAAGCCTCT CCAAGCGGGT 960 AAGAGAGCAG ATGAGGAAGA GGACAGCGGG AAGACTGGGA GGGCAGCAAG GTGGCTGTTT 1020 GGCAGGCACC ACCTTCTGAC AACATCATCC CTTCTGCAGG GGGCTCAGAT GCTCAGCAGA 1080 ATCTGGGGCC AGCACTAACA GCTGCACATC AGCTACAGTA ACAGAGGGAC GGCTGCCACT 1140 ATGCCAGCTG GCCGCCTGCT GGGCGGATTC TCTCCAGTCC AAGGCAGCAG CACACAGTGG 1200 CCTGTACAGT CAAACAGTGT CTAGAAAGTG GGAGACAGGA GGCTAAAGGG CCTGGGACAA 1260 TGCATTGGTG GGACCCACAA CTCAGGGTGG GAATTCACTC CCTCACACAC CCTGGCATTT 1320 TTGTTGTTGT TGGTTTTGAG ATGGAGTCTC GCTCTGTTGC CCAGGCTGGA GTGCAGTGGC 1380 ATGATCTCGG GTCACTGCAA CATCCGCCTT CCGGGTTCAA GCGATTCTCC TGCCTCAGCC 1440 TCCCGAGTAG GTAGCTGGGA TTACAGGCAC CCACCACTGC CCCCAGCTAA TTTTTCTACT 1500 TTTAGTAGAA ATGGGGTTTC ACCATGTTGG CCAGGGCTGG TCTCGAACTC CTGACCTCAG 1560 GTGATCCACC CACCTCGGCC TCCCAAAGTG TTGAGATTAC AGGCGTGAGC CACTGCACCT 1620 GGCCTAAAAG TGTATTTCTT GAGAAGGTGT GCATTTGCTT CTGTGATTTC TATAGCTCAA 1680 TGATCTCATG AAGTTTGGCC CCAAATTTAC ATAAGCAGGG CCTACTGGTT GAATATTTTC 1740 AGAGATTTTT CTCTCCCACT CTATCTAGGG CCAAAACCAT GCATGTCATC TATCTCCTCC 1800 TTTGGAGGGT TTTGGCTCCC AGCTTCCCTA CTGAGATCCA AGCTTTATTG GAGTGTCTCT 1860 AAACAGGCCT CCCATCCTGC TCCAGCTCTG TCTTCCCACC CATACCTGGC CCTGGCGCCT 1920 TCCCATGGCG CCTGGCCCTG CTAATCCTTT TGAAAAGACA TATTATCAGC TGGGTGCGGT 1980 GGCTCACACT TGTAATCCCA ACACTTCAGC AGGCTGAGGC AGGCGGATCA CGAGGTCAGT 2040 TCGAGACCAG CCTGGCCAAT ATGGTGAAAC CCCATCTCTA CTAAAAAATA AAAAAATTAG 2100 TTGGGCATGG TGGCATGTGC CTGTAGTCCC AGCTTCTTGG GAGGCTGAGG CAGGAGAATC 2160 GCTTGAACCC GGGAGGCGGA GGTTGTAGTG AGCTGAGATT GCGCCACTAC ACTCCAGCCT 2220 GGGCAACAGA GCGAGACTCC ATCTCAAAAA AAAAAAAAAG AAGACATATT ATCCATTATT 2280 TTTAGGTGAG TTGTAATTTA ACCCACGGCA TTGTCGGGAA CAGTAGTCTG GGGTTTGGAT 2340 TTCCAGATAT GGGTCCTGAA ACTCCACGGG TCTTGGGTCT CTGTGACCTT TCTTCAACCT 2400 GGAGCTCAGA CCCTTTGTCT TTCTGGGAGC 2430
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