Tag | Content |
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EnhancerAtlas ID | HS127-29860 | Organism | Homo sapiens | Tissue/cell | Macrophage | Coordinate | chr8:11638120-11639630 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxa2 | MA0047.2 | chr8:11639196-11639208 | TGTTTACTTTGC | + | 6.27 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr8 | 11638684 | 11638961 | chr8 | 11638232 | 11638660 |
| Enhancer Sequence | GCCTCAAGCG ATCGCCTACC TCCGCCTCCC AAAGTGCTGG GATTACAGGC GTGAGCCACC 60 ATGCTTGGCC CCAGTTTTTA TAATCTATGA ATGTTGAGAT CAACATTTTA TGCATAAGAC 120 TCTATCTAGG TTTAGGATAT GTCCTCAGTG TCAATTCCCA GAGGAGTAAT TGCTGGTCAG 180 AGGGAATGCA TATTCTTAGG GCTGTACATT TTTCTGGCCT TAGGAAAGTG CTAGCTGAGC 240 TGAAATCTCA TGAATGTTAG GTCGTTTGTG TACTTCTTAT CAATGTAATG AAGCTTTTGC 300 ACAGAAAGTC TGTTTGTTTT TGTGACATGT GTTGCCAGTA TTGTTTCAAG TCTGTCCTCT 360 GTCCTTTGAT TGTGCTTATG ATGTCTCTTG GCATTTGGGA TTTTAAATTT TTATATCATC 420 AACGGTGGGT ATTTTTCTTG GTTGCTTGTA GGTTTCCCCT TTTGCTAAAA AAAGGCCCCT 480 TCTGCCCCCA GAGAAAGTCA CATGCCTTCT ATTTTCTGAA GTTTTATAAC TTGTAAAAAT 540 GTTTAGAAGT GTAGTCTTTA TTTGTGTGGC CTGACGTAGG TACCATAGGA TGCTATGGGC 600 TGTAAAAATA ACTCGGAGTA GCTTCTGTGG TCTGGAGATT TTGGGCTCAC ATGACTGGAA 660 GTTCAGAAGG AGGGTGGGCT TTGGGGCTGC CGTTCCAAGG TTCTGGCTTC CTGTTTTTGT 720 GATTCTCCTG GCTTTGCACT TTCCACGCAT TGGTTTTCTC CTTAGACCAG CAGCAAGAGG 780 CTACTGCAGC TCCAGGATTT TATTCACACC AAAAAATCCA GAAGAAGAGC AGATCATTTT 840 TAGAAGTTCA GATGAGGAAA CTTTCCTTAG AACCCCCAGC AAACCTGTCA TCATCAGGAG 900 CCTGCCCTTT GCTGAGTCCT GGATTAGTCA CCAGCTGGAG GCATTGAAAT GTGCTCCCCG 960 AAGGAGGCTC ACCCCTAGGT TTTCAGATAT AGTGCCGTAG AGTGAATGTG TATCATGCCA 1020 TTATTTTTAA ATCTCTTTTT ACCTGGTTAG GTCTCTTTTC TCATGTACCT GTTTTATGTT 1080 TACTTTGCTT TGTCTCTTTT TTCTTTAATA GGCTGGCCTG AGTTTATCTA CTTTGTTGGT 1140 CTTTGAAATA AATACTATTA GCTTGCCAGG TATAATACTG ACTCCTGTCT GTAATCCCAG 1200 CACTTTGGGA GGCTGAGACA GGAGGATCAC TTGAGCCCAG GAGTAAGAGA CTAGCCTGGG 1260 CAACATAGTG AAGACCCTGT TTGTACAAAA AAATAAAATA AAATTAACCG GGTGTGGGGG 1320 TGCATACCTG TAGTCCCAGT TACTTGGGAG GCTGAAGTGG GAGGGTAGTT TGAGCCAGGG 1380 AGGTTGAGAC TGCAGTGAGC TGTGATTGTG CCACTATACT CCAGCCTGGG CAACAGAGCA 1440 AGACCCTATT TCCAAATAAA TAAATAAATA AAATTAGCTT TATATATCCT TTCTATATGG 1500 AAAGGGTATA 1510
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