| Tag | Content |
|---|
EnhancerAtlas ID | HS063-00088 |
Organism | Homo sapiens |
Tissue/cell | GM18505 |
Coordinate | chr1:25465730-25467490 |
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 | TACAGGAGAA GGAAGAGGCC TTAAAGCCCT GCAAAGGCCA TCTCTCCAGC TTCATCTCCT 60
CCCCTCCAGC CTCCCTCTCC TCTAAGGCCA ACACATAGTA CTGCTTTCCG TTCTTAGAAT 120
GCGTCACACT TTCCCTCCTT TGCAAGTGCA GTTCCCTTTG CCTGGAACAT CATTCCCTCA 180
GTCACCTCTC ACTCCCGGTC CTCTTGCTAA CTCCTACCCT TCCTGCACGC CTAGGCTTAA 240
TCCTGGGAAA CCATTTGCCA CCCCCTTCCG CAAAAAGGCA CAGGCTCCTG CTGCCAGTGC 300
CTGGAGAGCT CCTTGTGTCC CACCCCAGCC CAGAGCATGT CAAAAAGAAG AGATGAATGC 360
CAATTTCCCA TAGTGTGGTC CACTGCTTCC ATTTTTGAGG CAGAAAGTAA TGAGCAGTGG 420
GTATCTAATG TGCCCTTAAA TATCTTTTTT TGTTTTTTTT GTTTTTTTTG TTTGTTTGTT 480
TGTTTGTTTT GAGACAGGAT CTAGCTCCAT TACCCAGCCC AGATCTAGCT CTGTCCGCCG 540
AATGGTGTGA TCACAGCTCA CTGCAGCCTC AGCTTCAACT GCCTGGACTT AAGCGATCCT 600
CCCACCTCAG CCTCCTGAGA AGCTAGGACC AGAGCCATCC ACCCATGCCA AGCTAATTTT 660
TAAATTTTTT TGCAGAAACG AGGTCTCACT ATGTTGCCCA GGCTAGTCTT GAACTCCTGG 720
GCTCAAGCGA TCGTCCCACC TCAGCCTCCC AGAGTGTTGG GATTACAGGC ATGAGCCACC 780
GTGCCTGACC AAGATCTTTA AATAGTAATA AAACAGACAT TTATTAAGTG CATCTCATGT 840
GCTGTGCGCT GTTCCAAGTG CCTACACTCC CCATCTCAGT TAAGCACACA CCACCCCACG 900
GGCAGGCAGC TGCTATCATT ATCCCTTTCT CATGGTGGGG AAGTGAAGAT CAGAAAGGCT 960
GAATAACTTG CTCAAGATCA CAAGTCTGGA CTTGACTGCA GGCCTGGCTG ATCCCAGAGC 1020
CCAGATCAAG AGTCTCCCCT GGTGCCTCTC CCCTAAAACC ACCTCAGAAA CCCCCTGGTG 1080
TGTAACTCTA AACCATGCCT GCGGCAAACT CAGCCCATTT CCTCTTCTCG CATCTTAAGC 1140
CCAGATGGGG TCTGAGTGAC ACTTATCTCA TACCCTGTCA TAGAGCTGGA GCCCCACAGG 1200
AATGTGGAAC TCCCCATGGA CAGAGGGCAG GAGGAAGTGA CCGCCGGCCC GAAGGGGGCT 1260
TGGTCCACTG GGTCCAAAGG TGCCGTCTGG CCCTGGCTGC CACATGCCTC GTGTCCACAA 1320
AGCAGAAGTC ACAGGGACAG GGAAGGAAGC CCGGCAGGCA GACTGTCATC ACAGGTGGTG 1380
TGTCCTCCTA TCCAGGGACA AGCAGAACTA GCCAAGATTG CCTTCTCCAC GCAGCCTCTC 1440
CTGATTCCAC ACTTGTGACT TCATGTTCCC AGAGCGCTGT GCTGGCACGT GTGCTATGAT 1500
CTTGACTCTG TATGCACCCC GACGCCCAGC TACAAGCAGC TCTACCCTTA CCTAACCTTT 1560
AAATTGCTCG ATTGCCTCAT CTGTAAAAAC AGGGATGTTA ATAGCACCTG TTTCACGGGG 1620
TTATTGGAAG GTGTGTGTAC ATACACACAC ACACACACAC TCATCAATAT AGATGAGTAT 1680
AGATTGTGTG TATGTATACA TGCTTAGAAC AATTCCTGGC ATATAGTAAG TGCTTAATGA 1740
ACATTACCTA TTCTTATTCA 1760
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