| Tag | Content |
|---|
EnhancerAtlas ID | HS034-28251 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr7:98759760-98760750 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr7:98759885-98759900 | TGAACTCCTGACCTC | - | 6.22 | | TBX21 | MA0690.1 | chr7:98760066-98760076 | TTCACACCTT | - | 6.02 | | TBX2 | MA0688.1 | chr7:98760065-98760076 | ATTCACACCTT | - | 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 |
| GH07I099162 | chr7 | 98759810 | 98760910 |
|
Enhancer Sequence | TGGGTTCAAG TGATTCTCCA ACCTTGCCTC CCGAGTAACT GGGATTACAG GCATGTGCCA 60
CCATACCCAG CTAATTTTGT ATTTTTAGCA GAGACAGGGT CTCACTATGT TGGCCAGGCT 120
GGTCTTGAAC TCCTGACCTC AGGTGATCTA CCTGCCTTGG CCTCCCAAAG TGCTGGGATT 180
ACAGGCATGA GCCACCATGC CCAGCTGAGA ATTGCATTCT TTGAGGTACA TTACAATTTC 240
TGGGCAAATG CAAAAGGTCA AAGTTGTTCC AGTTCAGTGT TCACACCGTA AACCAACCTA 300
TAGCCATTCA CACCTTCCTT CCTCTTTGTT GCCTCACCAG TCGTCCCAAC TCCCCGAGTC 360
TAAGCAGGTG GGCACCCAGC CAGAAGGTGA CTAACACCAT CTCTTTGCAC CCAGACCATA 420
TACCAAAGGC AAATTGCTCC TTTTTTTAAA CCTTGCTAGG CAAGTCAGTA TTAGTATCTT 480
CAAACTACAA AGGCTGCTTT GTCATGCAAA GAGAAGGAAA AAAAGAGGTT GACAGTATTT 540
TGAGCCAACA AGGTTAGATC ACTCGGACAA CAGTGACTAA GCTCAACAGG GCTTCCAGCT 600
CTTTTAATTA AAAAAATTTT TTCTCAAAGA CCTATCTTTG TAAACCATCT CACCTTTCCA 660
CCTCCCTTCA ACTACAATCT ACGAATAGGG GGAAAAATGC TTTAAGATGT TGAAAAAGAA 720
TCTGTATTCC AATCAGATTC TTTGAAAAAA AGTATATGTA AGGCTGGACA CGGTAGCTCA 780
CGCCTGTAAT CCCAACACTT TGGGAGGCTG ACACAGGCAG ATCAACTGAG GTCGGGAGTT 840
CAAGACCAGC CTGATCAACA TGGAGAAACC CTAGCTCTAC TAAAAATACA AAAATTAGCT 900
GGATGTGGTG GCACACTCCT ATAATCCCAG CTACTCGGGA AGCTGAGGCA GGAGGATCAC 960
TTGAACCTGG GAGGCGGAGG TTGCAGTGAG 990
|
