| Tag | Content |
|---|
EnhancerAtlas ID | HS060-00607 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr1:25465660-25467320 |
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: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I025140 | chr1 | 25466725 | 25467101 |
|
Enhancer Sequence | AGCTTTGGCC TGGGCCCCTC CGATTTTCAG CCAAGCTGCT GGTGTCTTCC TCCCCTGAAG 60
GTTCACCAAC TACAGGAGAA GGAAGAGGCC TTAAAGCCCT GCAAAGGCCA TCTCTCCAGC 120
TTCATCTCCT CCCCTCCAGC CTCCCTCTCC TCTAAGGCCA ACACATAGTA CTGCTTTCCG 180
TTCTTAGAAT GCGTCACACT TTCCCTCCTT TGCAAGTGCA GTTCCCTTTG CCTGGAACAT 240
CATTCCCTCA GTCACCTCTC ACTCCCGGTC CTCTTGCTAA CTCCTACCCT TCCTGCACGC 300
CTAGGCTTAA TCCTGGGAAA CCATTTGCCA CCCCCTTCCG CAAAAAGGCA CAGGCTCCTG 360
CTGCCAGTGC CTGGAGAGCT CCTTGTGTCC CACCCCAGCC CAGAGCATGT CAAAAAGAAG 420
AGATGAATGC CAATTTCCCA TAGTGTGGTC CACTGCTTCC ATTTTTGAGG CAGAAAGTAA 480
TGAGCAGTGG GTATCTAATG TGCCCTTAAA TATCTTTTTT TGTTTTTTTT GTTTTTTTTG 540
TTTGTTTGTT TGTTTGTTTT GAGACAGGAT CTAGCTCCAT TACCCAGCCC AGATCTAGCT 600
CTGTCCGCCG AATGGTGTGA TCACAGCTCA CTGCAGCCTC AGCTTCAACT GCCTGGACTT 660
AAGCGATCCT CCCACCTCAG CCTCCTGAGA AGCTAGGACC AGAGCCATCC ACCCATGCCA 720
AGCTAATTTT TAAATTTTTT TGCAGAAACG AGGTCTCACT ATGTTGCCCA GGCTAGTCTT 780
GAACTCCTGG GCTCAAGCGA TCGTCCCACC TCAGCCTCCC AGAGTGTTGG GATTACAGGC 840
ATGAGCCACC GTGCCTGACC AAGATCTTTA AATAGTAATA AAACAGACAT TTATTAAGTG 900
CATCTCATGT GCTGTGCGCT GTTCCAAGTG CCTACACTCC CCATCTCAGT TAAGCACACA 960
CCACCCCACG GGCAGGCAGC TGCTATCATT ATCCCTTTCT CATGGTGGGG AAGTGAAGAT 1020
CAGAAAGGCT GAATAACTTG CTCAAGATCA CAAGTCTGGA CTTGACTGCA GGCCTGGCTG 1080
ATCCCAGAGC CCAGATCAAG AGTCTCCCCT GGTGCCTCTC CCCTAAAACC ACCTCAGAAA 1140
CCCCCTGGTG TGTAACTCTA AACCATGCCT GCGGCAAACT CAGCCCATTT CCTCTTCTCG 1200
CATCTTAAGC CCAGATGGGG TCTGAGTGAC ACTTATCTCA TACCCTGTCA TAGAGCTGGA 1260
GCCCCACAGG AATGTGGAAC TCCCCATGGA CAGAGGGCAG GAGGAAGTGA CCGCCGGCCC 1320
GAAGGGGGCT TGGTCCACTG GGTCCAAAGG TGCCGTCTGG CCCTGGCTGC CACATGCCTC 1380
GTGTCCACAA AGCAGAAGTC ACAGGGACAG GGAAGGAAGC CCGGCAGGCA GACTGTCATC 1440
ACAGGTGGTG TGTCCTCCTA TCCAGGGACA AGCAGAACTA GCCAAGATTG CCTTCTCCAC 1500
GCAGCCTCTC CTGATTCCAC ACTTGTGACT TCATGTTCCC AGAGCGCTGT GCTGGCACGT 1560
GTGCTATGAT CTTGACTCTG TATGCACCCC GACGCCCAGC TACAAGCAGC TCTACCCTTA 1620
CCTAACCTTT AAATTGCTCG ATTGCCTCAT CTGTAAAAAC 1660
|
