| Tag | Content |
|---|
EnhancerAtlas ID | HS127-26132 | Organism | Homo sapiens | Tissue/cell | Macrophage | Coordinate | chr6:5830990-5832600 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr6:5831375-5831385 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr6:5831375-5831385 | GGCACGTGCC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH06I005831 | chr6 | 5831297 | 5833432 |
| Enhancer Sequence | ATGGGACAAT AAATATAAAA TGCTCAGCAC AAAACTTAGT CTATGGTCAG TGCTCAACAA 60
ATATCAGTCA CTGATAATAG TAGAACCACC TGGAAATGAC ACTGTCATTT CCAGGCCCTC 120
ATGAGGATTC TCATTTACTC GTCATACTAG CCCTGCAAAA TGGACACTAT TGCTTCCGTT 180
ATACAGATGA GGAAACTGAG GCTCAGAGAA GCTAAGTAAC TTCTTCAAAG TTGCCCAGGC 240
TGGGCGCGGT GCCTCATGCC TGTAATCCCA GCACTTTGGG AGGCCAAGGC AGGCAGATTA 300
CTTGAGGGGA GGAGTTTGAG AACAGCCTGG CCAACATGAC AAAACCCCCT CTCTACCAAA 360
AATATAAAAA TTAGCCAGGC GTGGTGGCAC GTGCCTATAG TCCCAGCTAC TCAGGAGGCT 420
GAGGCAGGAG AATTGCTTGA ACCAGGGAGG AAGGGGTTGA GCATGCCACT GCACTTCAGC 480
CTGGGCAATA GAGCAAGACT CTGTCTCAAA AAAAAATAAA AAAATAAAAA AGTTGCCCAG 540
TGACAGAGCC AAGTCTTGCT TTACAAGCCT AGGCTCGCTC TCCTACACTA ACTACCTGGC 600
CCCATGCTGC CCAGTCCTGG GCTGGCTGCA GGAGGCTGCT GCATTACCCA CCTCAAACCA 660
CACAAGCACT GGCAGTAACA AGAGGCCGTA GAGAACCTAG AGTTCTCCAG TGGGTGTGGT 720
TCTCTGGCTG CCGTGGGCTG CCAGGGATCC CTTAGATCAC AGACTCCACA GTTCTTTCTT 780
GCCACCTCCA GAAGTGAGGC TGCAGCCCCA TGAGCCAGGC AGCAGGAAGG GAGGAAGTCT 840
CGCTTCTTGC CAGACACATT GTTTAACTGC AACAGTCAGT TCTCCAAAAA CTCTGCCGGA 900
AGTCCACCCC GGAAACTCAA GGGAGGAAAC TGACTGCCTT CTTGGGGTTT TCTTAACTGT 960
GCTTCGTTTT TCTGCTCTGC AGGAAAGATG CAACCTGGGC CAGAGGCCCC TGGAGGCTGT 1020
GCCTGACCCC AGACAGATCA GACAAACCCG AGCAGCCATT AGCAGCTGCA TGGACTCCTT 1080
TGCACTGTGG GGCTGCTCCT GGGGTGCAAG ATGTCTTTGT GTGTGTATGG GGTTCGGGGG 1140
CTGGGCTGGC TGACTTGCAA AGGACACGCT GTGGCCCAGC CCTGGGCAGC ATCCAGCCTG 1200
CTTAGGTGGC CTTCTGGGGG CTTGGCTAAA GACACTGAGG CCTTTCTCTG TTTCACCTCC 1260
TTGTGCCAAC TTGGCTGTGT GTGAATAAAG GAATCACAAG CACACGCCTC TCTGAGTTCA 1320
CACTTGTGTA AAGTTGGACT GAAGAGCTTG GTGAATCAAA GTTCAAGAAG GGTGACTTTG 1380
CCGGACATGG TGGCTCACTC CTGTAATCCC AACATTTTGG GAGGCTGACG GGGAGCAGAT 1440
CACTTGAACC CAGGAGTTCA AGACCAGCTT GGACAACACA GAAAGACCCT GTCTCTACAA 1500
AAAAATTTAA AAATTAGCTA GGTGTGGTGA GGTGTGCCTG TATTTGCAGC TACTCTGGAG 1560
GCTGAGGTGG GAGGATTGCT TGAGACTGGG AGGTTGAGGC TGCAGTGAGC 1610
|
| |
|
|
|
