Tag | Content |
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EnhancerAtlas ID | HS073-00255 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr1:25466180-25467330 |
Target genes | |
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) |
EWSR1-FLI1 | MA0149.1 | chr1:25467070-25467088 | GGAAGGAAGCCCGGCAGG | + | 6.35 | Foxd3 | MA0041.1 | chr1:25466199-25466211 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr1:25466203-25466215 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr1:25466207-25466219 | GTTTGTTTGTTT | + | 6.32 |
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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 |
GH01I025140 | chr1 | 25466725 | 25467101 |
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Enhancer Sequence | TGTTTTTTTT GTTTTTTTTG TTTGTTTGTT TGTTTGTTTT GAGACAGGAT CTAGCTCCAT 60 TACCCAGCCC AGATCTAGCT CTGTCCGCCG AATGGTGTGA TCACAGCTCA CTGCAGCCTC 120 AGCTTCAACT GCCTGGACTT AAGCGATCCT CCCACCTCAG CCTCCTGAGA AGCTAGGACC 180 AGAGCCATCC ACCCATGCCA AGCTAATTTT TAAATTTTTT TGCAGAAACG AGGTCTCACT 240 ATGTTGCCCA GGCTAGTCTT GAACTCCTGG GCTCAAGCGA TCGTCCCACC TCAGCCTCCC 300 AGAGTGTTGG GATTACAGGC ATGAGCCACC GTGCCTGACC AAGATCTTTA AATAGTAATA 360 AAACAGACAT TTATTAAGTG CATCTCATGT GCTGTGCGCT GTTCCAAGTG CCTACACTCC 420 CCATCTCAGT TAAGCACACA CCACCCCACG GGCAGGCAGC TGCTATCATT ATCCCTTTCT 480 CATGGTGGGG AAGTGAAGAT CAGAAAGGCT GAATAACTTG CTCAAGATCA CAAGTCTGGA 540 CTTGACTGCA GGCCTGGCTG ATCCCAGAGC CCAGATCAAG AGTCTCCCCT GGTGCCTCTC 600 CCCTAAAACC ACCTCAGAAA CCCCCTGGTG TGTAACTCTA AACCATGCCT GCGGCAAACT 660 CAGCCCATTT CCTCTTCTCG CATCTTAAGC CCAGATGGGG TCTGAGTGAC ACTTATCTCA 720 TACCCTGTCA TAGAGCTGGA GCCCCACAGG AATGTGGAAC TCCCCATGGA CAGAGGGCAG 780 GAGGAAGTGA CCGCCGGCCC GAAGGGGGCT TGGTCCACTG GGTCCAAAGG TGCCGTCTGG 840 CCCTGGCTGC CACATGCCTC GTGTCCACAA AGCAGAAGTC ACAGGGACAG GGAAGGAAGC 900 CCGGCAGGCA GACTGTCATC ACAGGTGGTG TGTCCTCCTA TCCAGGGACA AGCAGAACTA 960 GCCAAGATTG CCTTCTCCAC GCAGCCTCTC CTGATTCCAC ACTTGTGACT TCATGTTCCC 1020 AGAGCGCTGT GCTGGCACGT GTGCTATGAT CTTGACTCTG TATGCACCCC GACGCCCAGC 1080 TACAAGCAGC TCTACCCTTA CCTAACCTTT AAATTGCTCG ATTGCCTCAT CTGTAAAAAC 1140 AGGGATGTTA 1150
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