| Tag | Content |
|---|
EnhancerAtlas ID | HS059-00772 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:25465590-25467480 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 | | ZNF263 | MA0528.1 | chr1:25465786-25465807 | TCCTCCCCTCCAGCCTCCCTC | - | 6.43 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 25466725 | 25467101 | | chr1 | 25465800 | 25467400 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I025140 | chr1 | 25466725 | 25467101 |
|
Enhancer Sequence | TCGGGACTTG TTTAGACCCC AAGGACTGAT GATGGAGCAG AAGCTACTCG TCCCCAGGCA 60
ACCAGGGGAG AGCTTTGGCC TGGGCCCCTC CGATTTTCAG CCAAGCTGCT GGTGTCTTCC 120
TCCCCTGAAG GTTCACCAAC TACAGGAGAA GGAAGAGGCC TTAAAGCCCT GCAAAGGCCA 180
TCTCTCCAGC TTCATCTCCT CCCCTCCAGC CTCCCTCTCC TCTAAGGCCA ACACATAGTA 240
CTGCTTTCCG TTCTTAGAAT GCGTCACACT TTCCCTCCTT TGCAAGTGCA GTTCCCTTTG 300
CCTGGAACAT CATTCCCTCA GTCACCTCTC ACTCCCGGTC CTCTTGCTAA CTCCTACCCT 360
TCCTGCACGC CTAGGCTTAA TCCTGGGAAA CCATTTGCCA CCCCCTTCCG CAAAAAGGCA 420
CAGGCTCCTG CTGCCAGTGC CTGGAGAGCT CCTTGTGTCC CACCCCAGCC CAGAGCATGT 480
CAAAAAGAAG AGATGAATGC CAATTTCCCA TAGTGTGGTC CACTGCTTCC ATTTTTGAGG 540
CAGAAAGTAA TGAGCAGTGG GTATCTAATG TGCCCTTAAA TATCTTTTTT TGTTTTTTTT 600
GTTTTTTTTG TTTGTTTGTT TGTTTGTTTT GAGACAGGAT CTAGCTCCAT TACCCAGCCC 660
AGATCTAGCT CTGTCCGCCG AATGGTGTGA TCACAGCTCA CTGCAGCCTC AGCTTCAACT 720
GCCTGGACTT AAGCGATCCT CCCACCTCAG CCTCCTGAGA AGCTAGGACC AGAGCCATCC 780
ACCCATGCCA AGCTAATTTT TAAATTTTTT TGCAGAAACG AGGTCTCACT ATGTTGCCCA 840
GGCTAGTCTT GAACTCCTGG GCTCAAGCGA TCGTCCCACC TCAGCCTCCC AGAGTGTTGG 900
GATTACAGGC ATGAGCCACC GTGCCTGACC AAGATCTTTA AATAGTAATA AAACAGACAT 960
TTATTAAGTG CATCTCATGT GCTGTGCGCT GTTCCAAGTG CCTACACTCC CCATCTCAGT 1020
TAAGCACACA CCACCCCACG GGCAGGCAGC TGCTATCATT ATCCCTTTCT CATGGTGGGG 1080
AAGTGAAGAT CAGAAAGGCT GAATAACTTG CTCAAGATCA CAAGTCTGGA CTTGACTGCA 1140
GGCCTGGCTG ATCCCAGAGC CCAGATCAAG AGTCTCCCCT GGTGCCTCTC CCCTAAAACC 1200
ACCTCAGAAA CCCCCTGGTG TGTAACTCTA AACCATGCCT GCGGCAAACT CAGCCCATTT 1260
CCTCTTCTCG CATCTTAAGC CCAGATGGGG TCTGAGTGAC ACTTATCTCA TACCCTGTCA 1320
TAGAGCTGGA GCCCCACAGG AATGTGGAAC TCCCCATGGA CAGAGGGCAG GAGGAAGTGA 1380
CCGCCGGCCC GAAGGGGGCT TGGTCCACTG GGTCCAAAGG TGCCGTCTGG CCCTGGCTGC 1440
CACATGCCTC GTGTCCACAA AGCAGAAGTC ACAGGGACAG GGAAGGAAGC CCGGCAGGCA 1500
GACTGTCATC ACAGGTGGTG TGTCCTCCTA TCCAGGGACA AGCAGAACTA GCCAAGATTG 1560
CCTTCTCCAC GCAGCCTCTC CTGATTCCAC ACTTGTGACT TCATGTTCCC AGAGCGCTGT 1620
GCTGGCACGT GTGCTATGAT CTTGACTCTG TATGCACCCC GACGCCCAGC TACAAGCAGC 1680
TCTACCCTTA CCTAACCTTT AAATTGCTCG ATTGCCTCAT CTGTAAAAAC AGGGATGTTA 1740
ATAGCACCTG TTTCACGGGG TTATTGGAAG GTGTGTGTAC ATACACACAC ACACACACAC 1800
TCATCAATAT AGATGAGTAT AGATTGTGTG TATGTATACA TGCTTAGAAC AATTCCTGGC 1860
ATATAGTAAG TGCTTAATGA ACATTACCTA 1890
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