| Tag | Content |
|---|
EnhancerAtlas ID | HS106-02066 |
Organism | Homo sapiens |
Tissue/cell | iPSC |
Coordinate | chr7:98759840-98760670 |
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 | ATTTTTAGCA GAGACAGGGT CTCACTATGT TGGCCAGGCT GGTCTTGAAC TCCTGACCTC 60
AGGTGATCTA CCTGCCTTGG CCTCCCAAAG TGCTGGGATT ACAGGCATGA GCCACCATGC 120
CCAGCTGAGA ATTGCATTCT TTGAGGTACA TTACAATTTC TGGGCAAATG CAAAAGGTCA 180
AAGTTGTTCC AGTTCAGTGT TCACACCGTA AACCAACCTA TAGCCATTCA CACCTTCCTT 240
CCTCTTTGTT GCCTCACCAG TCGTCCCAAC TCCCCGAGTC TAAGCAGGTG GGCACCCAGC 300
CAGAAGGTGA CTAACACCAT CTCTTTGCAC CCAGACCATA TACCAAAGGC AAATTGCTCC 360
TTTTTTTAAA CCTTGCTAGG CAAGTCAGTA TTAGTATCTT CAAACTACAA AGGCTGCTTT 420
GTCATGCAAA GAGAAGGAAA AAAAGAGGTT GACAGTATTT TGAGCCAACA AGGTTAGATC 480
ACTCGGACAA CAGTGACTAA GCTCAACAGG GCTTCCAGCT CTTTTAATTA AAAAAATTTT 540
TTCTCAAAGA CCTATCTTTG TAAACCATCT CACCTTTCCA CCTCCCTTCA ACTACAATCT 600
ACGAATAGGG GGAAAAATGC TTTAAGATGT TGAAAAAGAA TCTGTATTCC AATCAGATTC 660
TTTGAAAAAA AGTATATGTA AGGCTGGACA CGGTAGCTCA CGCCTGTAAT CCCAACACTT 720
TGGGAGGCTG ACACAGGCAG ATCAACTGAG GTCGGGAGTT CAAGACCAGC CTGATCAACA 780
TGGAGAAACC CTAGCTCTAC TAAAAATACA AAAATTAGCT GGATGTGGTG 830
|
