Tag | Content |
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EnhancerAtlas ID | HS059-02760 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:153821110-153823110 |
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) |
Foxd3 | MA0041.1 | chr1:153821438-153821450 | AAACAAACAAAC | - | 6.32 | Nr2f6(var.2) | MA0728.1 | chr1:153821211-153821226 | GAGGTCAGGAGTTCA | + | 6.22 | Nr2f6(var.2) | MA0728.1 | chr1:153822326-153822341 | TGAACTCCTGACCTC | - | 6.22 | SOX10 | MA0442.2 | chr1:153821425-153821436 | AAAACAAAGCA | + | 6.02 | Zfx | MA0146.2 | chr1:153821189-153821203 | 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: 1 | ID | Chromosome | Start | End |
GH01I153848 | chr1 | 153821114 | 153823003 |
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Enhancer Sequence | AATTGCCTAA CATCTCCATT TGGGTGTTGT CTTAGTCCAT TATGCATGGT GGCTAACGCC 60 TGTACTTCAA GCACTTTGGG AGGCCGAGGC GGGTGGATCA TGAGGTCAGG AGTTCAAGAA 120 CAGCCTGGTC AAGATGGTGA AACCCCGTCC CTACTGAAAG TACAAAAAAA TTAGCCAGGT 180 GTGGTGGTGG GTGCCTGTAA TCCCAGCTAC TCAGAAGGCT GAGGCAGAGA ACTGCTTGAA 240 CCCGGGAGGC AGAGGTTGCA GTGAGCCAAT ATCGCGCCAC TGCACTCTGG CCTGGGCAAC 300 AGCGAGACTC ATCTCAAAAC AAAGCAAAAA ACAAACAAAC CCCCCCCCTC CCCCAGACTG 360 GGTAATTTAT ATAGGGGTAT GTGGGTGTGT GTGTTCTGTT TTGTTTTGTT TAGAGATGGA 420 GTCTCTCCAT GTTGCCAAAC TCCTTGAGCT CAAATGATCC TCCCACCTCA GCATCCCAGG 480 TAGCTGGGGC TATGGGTGTA TGTCACCGTA CCCAGCTTTG GGCACTTTAT AATGACCAGA 540 AGTTTATTGG CTATTTATTG GCACACAGTT CCAGAAGTTG GGAAGCCTAA CATCAAGGTA 600 CTGGCATGTG GTGAAGACCT TCTTGCCATC TAATAACATA GCAGATGGCA AAGAGAGGGT 660 GCCCTTTTAT AACAACATTA ATCCCACCCA TGAGGGTAAA GCCCTAACAA CTTAATCACT 720 TCTTAAAGGT CCCACTTCTT AATATTATTA CAATGTCAAT TAAATTTCAA CATGAATTTT 780 GGAGGGACAA ACATTCACAA GATAGCAGAT ATCTAACAGG CATTTTATAA TCTTATGTCC 840 AAAATTGTTT CTTCCCCTAC TGTTACACAT CTTAGCAAAT GACACCACTA TTCAAACCAA 900 ACACTTGGAG TCATTCTTAG TTCCTCTTTC TCATACCCAC ATGCATTCTA TCTGTAAACT 960 CTATCAGCAT TACCTTCCAA ATATATTTTA AATTTGACCT TGTTTTTTCT TTTTTTGAGA 1020 CAGTTTCACT CTTTCACCCA GGCTGCAGTA CAGTGGCGTG ATCTTGGCTC ACTGCAACCC 1080 CCTCCTTCCG GTTTCAAGCG ATTCTCCTGC CTCAGCCTCC TGAGTAGCTG GGATTACAGA 1140 CATGTGCCAC CTCACCCAGC TAATGTTTTG TATTTTTAGC AGAGGTTAGG TCTCACCATG 1200 TTGGCCAGGC TGGTCTTGAA CTCCTGACCT CAGGTGATCC GCCTGGCTTG GCCTCCCAAA 1260 GTGCTGGGAT TACAGGCATG AGCTACCATG CCTGGCTGTA TTTAATCCTT TTAAATGCAC 1320 TTATTCTATG GTCTATAGTC AATGAACTGG AGATCTAGTC CTGAGAGGTA GTGTATCTGT 1380 GACTCTTATT CATGGTAAAT GAGCTGTTTT CTTATTTTTT GTCACTTTTG ATTATGAGCC 1440 TTGTCACAAT CAAGTGGGTT ATTCAGTGGG ATTTTATCTG TTAGAATCCT GTGTGGCTTA 1500 AACTGTGGAT CTGTTCCTCC AGAGTAGCTT TACATATGCT TCCGCTGGTT ACCCCAAGGG 1560 TATTATACAG GGTCCTGAAT AATTTTTTTA TATTCATTTC CCAGTTTGGG GATCTCAGAC 1620 CAAGCTGGTG ATAATAATTT AAACCCACAC AAATAAGCCC ATACTTAATT ATTTTTCCTT 1680 TTTAGGACAG AGTCTCACTC TGTTGCCCAG GCTGCAATGC AGTGGCACAA ACTTGGCTCA 1740 CTGCAGCCTT CACCTCCCGG GTTCAAGTGA TCCTCCTGCC TCAGCCTCCT GAGTAGCTGG 1800 GATTACAGGC ATCCGCCACC ATACCCAGCT AATTTTTGTA TTTTCAGTAG AGACCAGGTA 1860 TCACTATGTT GGCGAGGGTG GTCTCGAACT CCTGACCTCA AGTGATCCGC CCACATCAGC 1920 CTCCCAAAAT GCTGGGATTA CAGGTGTGAG CCACTGCGCT CAGCCTAATA AGCCCATACT 1980 TAATTTTTAA AAAATTGTTT 2000
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