| Tag | Content |
|---|
EnhancerAtlas ID | HS026-32221 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr8:10493570-10495140 |
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 | chr8:10494014-10494032 | CCCGCCTTCTTCCCTTCC | - | 6.19 |
|
| | 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 |
| GH08I010636 | chr8 | 10493587 | 10494886 |
|
Enhancer Sequence | ATGCTAAAAT GCTGTTTTGG TGTGGATGAG TTGCTTCACC TCTCTGGACT TCAGTTCCCT 60
CATCTGTCAA ATGACTTATT TGCAACGCAG TTGGACTCCA CAATGCTTAT GGGCCTTGCC 120
ATCGCTCAGA CTTTCTGGGT CTATAACAAG AGTTCCAGGA CACCCAATAT CTTGGCTTTA 180
AAGAAGGGTT CTGGGGGCAT CTGGGGCCGG TGACTCTTGC TTTGTCCAGC ATGAAGGCGT 240
CAACAAGAGG CAAAGGGAAA AGGAGCCGGT CTGCAGGCGG CCAGACCCGT CAGCATCCCA 300
GGGCTAGCCT TTGGCAGCTG TGAAGCCTTG GAGGAATGAA TCAACCTCTC TGAGCCAGTC 360
ACCATCCTCG GTAAAATGGA GACATCGCAT CTGCCCTGTG GGGCTGTAGT GGGATTGACT 420
GAGCCTCGCC TGTGCAGTTG AGGCCCCGCC TTCTTCCCTT CCCCCTCGAA TGGCAACCCA 480
GGCCCTGGCC TGACCACCAA GAGGACTCTC CTTCACAACG GCCTCCTCGG ATGAAAGGCG 540
TGGGGGCAAC AGGAAGAACT GTTGTTTTAA CTGCTCTCAG CTTCCTCCTT TTGTCTCGGG 600
CATGATAAAC AAGCCTATTC CCCCAAGCCA CAGCTGCTAA TCCAGCTGCA GGAGGGCAGC 660
GGTCAAGCAA TCAGACATGC TCTTCGCTGG GATTAGGTTA CTCCCAGCCG GGCCTGACCC 720
CTCCCCTGCC CAGCAGCAGA TCAGAACCGA CTCCCTCCTG GCTATCCCTG GGGCTGCTGG 780
GTTCGGATGC CCTGGGAAGC TGCAGGTCAC CTGGATGGAA CTGGAGTGAC AAGGACTGTG 840
GCCAGTCTGT CACACAGCTC CCTGACACAA CTCCCAGGCC TGGCCCAGCC TTAGAACCTT 900
CCCTGCCCTG AGGCCCTGAC AGCAGGGCTC TACGTGGGGC CACTCTGCAG TGTACAAAGC 960
ATCGTCACTC ACTCTCTCAG GTGGGCCTTG CAGTAGGCTG GTGAGGGAGA GAGACAGGCT 1020
GAGATTTAGA GAAAAAGAAT GCAAGGTTCG CTCAGGGCCA TAGAGCAGGC AAGGAGACAG 1080
CTGAGCCTTC CTGGTCAGGT TCCCGGACTC AAACTCAATG CTCACAGCAA GGCTGCCTCT 1140
CCCCACGTAG TAAGGGGCGT CCCCTTCACA GTCCCCAACC TCCCAGGCTT GGCCGCGGAA 1200
TGCGCAGAGT GGCAAGGTCC TCTCACCCCA GAGCAGAGCA CAGGATTTCC TCCAGTATTT 1260
ATCAAATGCA CCACAATTAA GCCAATTAGG CAAAAAGACT TAATGAGGAC CTCCTGTGTG 1320
TGATGTCAGT GTAGGGGCCA GAAAACTCCT CTAAGCCTTT TTTGGCATTA AATGAAGGAA 1380
TAAACATAGC AATAAAAAAT AAAAGCCGGC CACGGTGGCA TATGTCTAAA GTCCCACCTA 1440
CTCTGGAGGC TGAGGCGGGA GGATCACTTG AGCCCAGCAG TTCAAATGTA GCCTGGGCAA 1500
CAGAGTGAGA CCCCATCTCC AAAAACAATA AAATACATAA AAAAATTAAG AAAACTCCCC 1560
ATTTATAGTC 1570
|
