Tag | Content |
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EnhancerAtlas ID | HS018-20767 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr6:158691440-158692850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr6:158692259-158692280 | GTTTTGTTTCATTTTCAATTG | + | 6.69 | Nr2f6(var.2) | MA0728.1 | chr6:158691965-158691980 | GAGGTCAGGAGGTCA | + | 7.19 | RARA | MA0729.1 | chr6:158691965-158691983 | GAGGTCAGGAGGTCAAGA | + | 6.22 | ZNF263 | MA0528.1 | chr6:158692382-158692403 | TGAGGAGGAAGGGCAAGGAGA | + | 7.11 |
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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 |
GH06I158270 | chr6 | 158691618 | 158692775 |
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Enhancer Sequence | TTGAAGTTGG TTTATTTTGC CCATCTTCTC TCACTGTGTA GGGTGCTTCT CGGGGCTAGG 60 GACTGGACTT CGATGAGTTT TGCATTGTCA GCACCCGGCC TGTTCGGCCT GTGGTGGGCA 120 CTCACTAAGT GTCTCTGGTA CCGGGGCCGG TGATGGGCAC TCAGTTAGCG TCTCTGGCCT 180 GAGTGTTGCT TGGCTGCTTT CCTGGTTTGA CACTGCACTT TAGACTATTG CAGCTAAAAT 240 TAACACACAT CATCTGTTGA TGTGATGCTT GCCTCCTTTT AAGCTTTTCT CAAGCTTTCA 300 AAATTTCTTC CTGAAGTTTT TCCTTCACAG ATGAAATTGC TCCTGAATTA GAGGTGATTT 360 ACTCCAGGCT TCCTTGTGCT TAAATGTGGC AACTTTCAAG GCTGCCTTCA TTTTTGCCTC 420 AGAGTTTATA AAGCAGCTTA GTGTGAATAG ATGCTGTAGG GCCGGGCACA GTGGCCCATG 480 CCTGTAATCC CAGCACTTTG GGAGGCTGAG GCAGGTTGAT CACCTGAGGT CAGGAGGTCA 540 AGACCAGCCT GGCCAACATG GTGAAACCCT GTCTCTATTA AAAATACAAA AATTACCCAG 600 GCATGGTGGC AGGTGCCTAT AATCCCAGAT ACATGGGAGG CTGAGGCAGG AGAATGGCTT 660 GAACCCAGGA GGTGGAGGTT GCAGTTAGCC GAGATCGCGC CACTGTACTC CAGCCTGGGT 720 GACAAAGTGA GACTCTGTCT CAAAAAAAAA AAAAAAAAAA AGATGCTGTA CTGAGTTTAT 780 TTAATATAAG CAGTTTTATG TTAGTCACTG CTCTGTTGAG TTTTGTTTCA TTTTCAATTG 840 TTGCTTCTCA TGTGGTAATG AAGAAAGCAT TTAAAGGCCA AGTTAAGTGG GTGCCTAACC 900 AAAATAGGTC CAGCTTCCTC AAGTTGTGTC ATGACTTGTT GATGAGGAGG AAGGGCAAGG 960 AGACATCTAA CTCTCACAGG CTTTGTCTCT TGTAGCTCAG ATAGGGTTTC TTTAATCCAT 1020 TTTAGAATTT TTTTTTTTTT TTTGAGATAG GTTCTTGCTC TGCCACCCAG GCTGGAGTGC 1080 AGTGTGCCAT CATAACTTGC TGCAGCCTCA AACTCCTGGG CTCAGGCGAT CCTCCCACCT 1140 CAGCCTCTGA GTAGCTGGGG CTACAGGCGG GTCACCACAT TTGGCAAATT TTTAAATTTT 1200 TTGTAGAGAT GGGGTCTCAC TCTGTTCCCC AGGCTAGTCT CAAACTCCTG AGTTCAAGCC 1260 ATCCTCCTGC CTTGGATTCC CAAAGTGCTG GGATTACAGG CATGAGCCAC CACGCCTGGC 1320 CCCACATTAA AAATTTTGAA ACGGTAGCTT TGATTCAGGT GTAACTGTCC TCCTAAAGAA 1380 AAATAAAATG TTCTGAGAAG TTTTAGTTTA 1410
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