| Tag | Content |
|---|
EnhancerAtlas ID | HS041-00705 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr1:25466110-25467240 |
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 |
|
| | 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 | CACTGCTTCC ATTTTTGAGG CAGAAAGTAA TGAGCAGTGG GTATCTAATG TGCCCTTAAA 60
TATCTTTTTT TGTTTTTTTT GTTTTTTTTG TTTGTTTGTT TGTTTGTTTT GAGACAGGAT 120
CTAGCTCCAT TACCCAGCCC AGATCTAGCT CTGTCCGCCG AATGGTGTGA TCACAGCTCA 180
CTGCAGCCTC AGCTTCAACT GCCTGGACTT AAGCGATCCT CCCACCTCAG CCTCCTGAGA 240
AGCTAGGACC AGAGCCATCC ACCCATGCCA AGCTAATTTT TAAATTTTTT TGCAGAAACG 300
AGGTCTCACT ATGTTGCCCA GGCTAGTCTT GAACTCCTGG GCTCAAGCGA TCGTCCCACC 360
TCAGCCTCCC AGAGTGTTGG GATTACAGGC ATGAGCCACC GTGCCTGACC AAGATCTTTA 420
AATAGTAATA AAACAGACAT TTATTAAGTG CATCTCATGT GCTGTGCGCT GTTCCAAGTG 480
CCTACACTCC CCATCTCAGT TAAGCACACA CCACCCCACG GGCAGGCAGC TGCTATCATT 540
ATCCCTTTCT CATGGTGGGG AAGTGAAGAT CAGAAAGGCT GAATAACTTG CTCAAGATCA 600
CAAGTCTGGA CTTGACTGCA GGCCTGGCTG ATCCCAGAGC CCAGATCAAG AGTCTCCCCT 660
GGTGCCTCTC CCCTAAAACC ACCTCAGAAA CCCCCTGGTG TGTAACTCTA AACCATGCCT 720
GCGGCAAACT CAGCCCATTT CCTCTTCTCG CATCTTAAGC CCAGATGGGG TCTGAGTGAC 780
ACTTATCTCA TACCCTGTCA TAGAGCTGGA GCCCCACAGG AATGTGGAAC TCCCCATGGA 840
CAGAGGGCAG GAGGAAGTGA CCGCCGGCCC GAAGGGGGCT TGGTCCACTG GGTCCAAAGG 900
TGCCGTCTGG CCCTGGCTGC CACATGCCTC GTGTCCACAA AGCAGAAGTC ACAGGGACAG 960
GGAAGGAAGC CCGGCAGGCA GACTGTCATC ACAGGTGGTG TGTCCTCCTA TCCAGGGACA 1020
AGCAGAACTA GCCAAGATTG CCTTCTCCAC GCAGCCTCTC CTGATTCCAC ACTTGTGACT 1080
TCATGTTCCC AGAGCGCTGT GCTGGCACGT GTGCTATGAT CTTGACTCTG 1130
|
