Tag | Content |
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EnhancerAtlas ID | HS108-21337 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr2:3634140-3635570 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr2:3635275-3635289 | CTGAGTCATCTTCT | - | 6.53 | Zfx | MA0146.2 | chr2:3634388-3634402 | GAGGCCGAGGCGGG | - | 6.01 |
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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: 2 | ID | Chromosome | Start | End |
GH02I003583 | chr2 | 3631437 | 3634339 | GH02I003587 | chr2 | 3634643 | 3636301 |
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Enhancer Sequence | GTCCTCCACG GGCAGAGGGG ATGGCTGCCC AAAGGACATG ATGTGATGGG CCTGGCCTGG 60 GCACACTGTG CTCCACACCC CACTTCAGAC AATAGAGGCA GATTCACCAT GAGGCCAATA 120 AAGATCCGGC TGGAGAGGCC TTAGCATTGA GTTCTGTGGT CATATATTTG TATAAAATTA 180 GCACAAATAA AATATTAAGC ACAATGGGCC GGGTGCGGTG GCTCACGCCT GTAATCCCAG 240 CACTTTGGGA GGCCGAGGCG GGCGGATCAC GAGGTCAGGA GATCGAGACC ATCCTGGCTA 300 ACACGGTGAA ACCCCGTCTC TACTAAAAAT ACAAAAAATT AGCTGGGCGT GGTGGCGGGC 360 GCCTGTAGTC CCAGCTGCTT GGGAGGCTGA GGCAGGAGAA TGACGTGAAC CCAGGAGGTG 420 GAGCTTGCAG TGAGCCGAGA TCGCGCCACT GCACTCCAGC CTGGGCGACA GAGCCAGACT 480 CTGTCTCAAA AAAAAAAAAA AAAAAAGCAC AATGAGTGAA GACCGCTGTC TGGTTCCTCT 540 GTCACAGCCT CCTGCTGAGT GGTGCCGATG CGGCCCAGGC ATCTTTGCAT CCTGCTGAGG 600 GTTTCCCCAC CTTGGCACTG TTAGCTTTTA GGGCTGGAGA GCTCTGTGCT GTGGGGCCAT 660 CCCATGCATT GTAGAATGTT TAGCAGCCTC CCTGTCCTCT CCCACTAGAA GCCAGTACCA 720 TGTCCCCAGT TGTGACAACT AAAAATGTCT CCTGCACATT GTCAAATGTC CCTGAGCCCG 780 AGGGGTGGGG AGAACAAACT GACGTTGAGT TGGGGTTATA TTATTTTGGA TTTCAGCTGG 840 ATATGCTGGG TGGTTCATGG TGCAGGAGGA GGTCATGAGC TACAAATTGG TCAGTGGTGT 900 GGTCATTTCA AAGACTAGGA TTACTCTGAA CAAAACAAAC CAAAACCCAA TCGTTGAGAT 960 GCCTGAAATC AAACACCTAG TATATGAAAG AAAACTGATA GAGGTTTCCC CAGACTTGAC 1020 AGCTATCCAA AAACTGTTCA TGGCGTCACT GATAAAGGCT TGTGGAGCTG AAGTAAACTG 1080 TTTTGAAGCT ACCAATAAGA AGATATTTAA ATAACCATGC AAGAAAGAGC AAATACTGAG 1140 TCATCTTCTG TTCTCTTTGT AGAAATTTGT GTTCACGGGA GCAGGCAATG AAAGAATATA 1200 CAGCCAAATA ATATAAAAAC GTAAGGGCTG GGCTGGGTGC GATGGTTCAC ATCTGTACTC 1260 CCAGCACTTT GGGAGGCCGA GGTGGGTGGA TCATGAAGTC AGAAGAGCGA GACCATCCTG 1320 GCTAACACGG TGAAACCCCG TCTCTACTAA AATACATAAA ATTAGCCGGG TGTGGTGGCG 1380 GGCGCCTGTA GTCCCAGCTA CTCAGGAGGC TGAGGCAGAA GAATCGCTTG 1430
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