| Tag | Content |
|---|
EnhancerAtlas ID | HS064-00243 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr1:25465640-25467420 |
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 | TCCCCAGGCA ACCAGGGGAG AGCTTTGGCC TGGGCCCCTC CGATTTTCAG CCAAGCTGCT 60
GGTGTCTTCC TCCCCTGAAG GTTCACCAAC TACAGGAGAA GGAAGAGGCC TTAAAGCCCT 120
GCAAAGGCCA TCTCTCCAGC TTCATCTCCT CCCCTCCAGC CTCCCTCTCC TCTAAGGCCA 180
ACACATAGTA CTGCTTTCCG TTCTTAGAAT GCGTCACACT TTCCCTCCTT TGCAAGTGCA 240
GTTCCCTTTG CCTGGAACAT CATTCCCTCA GTCACCTCTC ACTCCCGGTC CTCTTGCTAA 300
CTCCTACCCT TCCTGCACGC CTAGGCTTAA TCCTGGGAAA CCATTTGCCA CCCCCTTCCG 360
CAAAAAGGCA CAGGCTCCTG CTGCCAGTGC CTGGAGAGCT CCTTGTGTCC CACCCCAGCC 420
CAGAGCATGT CAAAAAGAAG AGATGAATGC CAATTTCCCA TAGTGTGGTC CACTGCTTCC 480
ATTTTTGAGG CAGAAAGTAA TGAGCAGTGG GTATCTAATG TGCCCTTAAA TATCTTTTTT 540
TGTTTTTTTT GTTTTTTTTG TTTGTTTGTT TGTTTGTTTT GAGACAGGAT CTAGCTCCAT 600
TACCCAGCCC AGATCTAGCT CTGTCCGCCG AATGGTGTGA TCACAGCTCA CTGCAGCCTC 660
AGCTTCAACT GCCTGGACTT AAGCGATCCT CCCACCTCAG CCTCCTGAGA AGCTAGGACC 720
AGAGCCATCC ACCCATGCCA AGCTAATTTT TAAATTTTTT TGCAGAAACG AGGTCTCACT 780
ATGTTGCCCA GGCTAGTCTT GAACTCCTGG GCTCAAGCGA TCGTCCCACC TCAGCCTCCC 840
AGAGTGTTGG GATTACAGGC ATGAGCCACC GTGCCTGACC AAGATCTTTA AATAGTAATA 900
AAACAGACAT TTATTAAGTG CATCTCATGT GCTGTGCGCT GTTCCAAGTG CCTACACTCC 960
CCATCTCAGT TAAGCACACA CCACCCCACG GGCAGGCAGC TGCTATCATT ATCCCTTTCT 1020
CATGGTGGGG AAGTGAAGAT CAGAAAGGCT GAATAACTTG CTCAAGATCA CAAGTCTGGA 1080
CTTGACTGCA GGCCTGGCTG ATCCCAGAGC CCAGATCAAG AGTCTCCCCT GGTGCCTCTC 1140
CCCTAAAACC ACCTCAGAAA CCCCCTGGTG TGTAACTCTA AACCATGCCT GCGGCAAACT 1200
CAGCCCATTT CCTCTTCTCG CATCTTAAGC CCAGATGGGG TCTGAGTGAC ACTTATCTCA 1260
TACCCTGTCA TAGAGCTGGA GCCCCACAGG AATGTGGAAC TCCCCATGGA CAGAGGGCAG 1320
GAGGAAGTGA CCGCCGGCCC GAAGGGGGCT TGGTCCACTG GGTCCAAAGG TGCCGTCTGG 1380
CCCTGGCTGC CACATGCCTC GTGTCCACAA AGCAGAAGTC ACAGGGACAG GGAAGGAAGC 1440
CCGGCAGGCA GACTGTCATC ACAGGTGGTG TGTCCTCCTA TCCAGGGACA AGCAGAACTA 1500
GCCAAGATTG CCTTCTCCAC GCAGCCTCTC CTGATTCCAC ACTTGTGACT TCATGTTCCC 1560
AGAGCGCTGT GCTGGCACGT GTGCTATGAT CTTGACTCTG TATGCACCCC GACGCCCAGC 1620
TACAAGCAGC TCTACCCTTA CCTAACCTTT AAATTGCTCG ATTGCCTCAT CTGTAAAAAC 1680
AGGGATGTTA ATAGCACCTG TTTCACGGGG TTATTGGAAG GTGTGTGTAC ATACACACAC 1740
ACACACACAC TCATCAATAT AGATGAGTAT AGATTGTGTG 1780
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