| Tag | Content |
|---|
EnhancerAtlas ID | HS041-04920 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr12:31232490-31234020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Atoh1 | MA0461.2 | chr12:31232586-31232596 | AACATATGTT | + | 6.02 | | Atoh1 | MA0461.2 | chr12:31232586-31232596 | AACATATGTT | - | 6.02 | | IRF1 | MA0050.2 | chr12:31233585-31233606 | TACTCCTTCCACTTTCTTTTT | + | 6.19 | | Sox3 | MA0514.1 | chr12:31233434-31233444 | CCTTTGTTTT | + | 6.02 |
|
| | 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 |
| GH12I031079 | chr12 | 31232433 | 31233808 |
|
Enhancer Sequence | GGACAAGGGC TGCTCCCTTA TGGCTGCTCC GTTATGACCT CCTTTACCCT TGAAGGCCAG 60
ATCTGTAGTA GAGTCACATG GCGGGGTTAG GATTTCAACA TATGTTTGTT TGTTAAGATG 120
GGCAGTCTCA CTATGTGGCC CAGGCTGGTC TCGAACTCAA GCGATCCTCC CCTCTCAGCC 180
TCCCAAGTAC CTGGTGGCTG GCAAGATCCA AGATTACTGG TGCACACCAC CATACACAGC 240
TTCTTTTGTT TTGTTTTTGT TCTTTAAAAA CATTTTTTTA ACATGCATTT TGGTGGGGAT 300
ACAATTCAGT CCACAGCAGT GACCAATTCC ATTTTTACCT TGGAGCCCTC CTGGAATCCT 360
CCATCCTTTC CCTGTCATTT GAATTAGTTG CTCCTCAGAC TGACTTGACA GATTTCAGCA 420
TGAGTGTTAA TGGGGACAGA CGGCCGCACC CACACCACAT CAGGGTATAC GTCCGTTTGG 480
AGGCTTTCCT CAAACGTCTG GCAGCCCTGG ACTGCCTGTG TATGCTGAAG AACAGGGCAC 540
AGAAAGGCTG AGTCTGCAGG GCACTGGCTG TGGCTGCCAG GCTGGGCTCC TTTGTTGGGG 600
GCCTCCAGTT GCCAGCACAT CTGTGGGATT TTCCCTAGAG TCTTCAGTCT CTCCAGAGCA 660
GGTGCCTCTG AGCCCTGGCC CAGCAGGTAC AGACGCTGAA GCCCAATAGC CGGTCTTCCG 720
GGAGGTGGTC TGGGGAAGGG GATCCAGGTG GAGAGTCCCC CTCAGTGCCT GCTTTCAGCC 780
TGGCCCTCCT CCCCCTCCCT CTTGCCTCCT CAATCTGCCG GTTGCCTCCA GGGCTCTCCT 840
AGCTCAGCTT CCACTTAGAG CCCACTTCCT GTCTTCTGCA AGGAGCAGGA GCAGGGATTG 900
CAACCTGAGA ATCTAATTGT TCTTAAAAAG AATTTCAACC CGTCCCTTTG TTTTCAGTGG 960
CCTGCTGTGT TCCTACCACT TCCTGAGTCT TTCTGAGAAT GAGTGGGGGA GATCTCTGGG 1020
GACACTTGGG CTTGAGTGTC TCTGCCGAAA TCACTTCCAT GTCTCTGCCT TCTTTCCCTC 1080
TCTCCTAAAA CATATTACTC CTTCCACTTT CTTTTTGTGG GTGTAAGCCT CCATATTACT 1140
TTGGTTAATT TTAGTGTGCT TTGGAACACA GATGAGTGCA TGTTCATTCT GCCTTGTTTA 1200
ATTTTAGAGA CAGGGTGTTG CTCTGTTGCC CAGGGCCGAG TGCAGTGTTA AGATCATGGT 1260
TTACTGCAGC CTCAACCTTC TGGCAACAAG TGATCTTCCC ACGTCAGCCT CCTGAGCAGC 1320
TGGGACTACA GGTGTGCACC ATCACACCTA GCTAATTTTT TAATTTGTAG AAATGAGATC 1380
TCACTATGCT GCTCAGGCCG GTGGTCTTAA ACCCCTAGGC TCAAGCAATC CTCCCTCCTT 1440
GGCCTCCCAT AGTGCTGAGA TTACAGGCAT GAGCCACTGT ACCTGACCCC TTTCACCTTG 1500
TTTAGCCTGA CAACCCATCT TCTCCCTCTC 1530
|
