| Tag | Content |
|---|
EnhancerAtlas ID | HS150-10161 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr7:98759770-98760530 |
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 | TGATTCTCCA ACCTTGCCTC CCGAGTAACT GGGATTACAG GCATGTGCCA CCATACCCAG 60
CTAATTTTGT ATTTTTAGCA GAGACAGGGT CTCACTATGT TGGCCAGGCT GGTCTTGAAC 120
TCCTGACCTC AGGTGATCTA CCTGCCTTGG CCTCCCAAAG TGCTGGGATT ACAGGCATGA 180
GCCACCATGC CCAGCTGAGA ATTGCATTCT TTGAGGTACA TTACAATTTC TGGGCAAATG 240
CAAAAGGTCA AAGTTGTTCC AGTTCAGTGT TCACACCGTA AACCAACCTA TAGCCATTCA 300
CACCTTCCTT CCTCTTTGTT GCCTCACCAG TCGTCCCAAC TCCCCGAGTC TAAGCAGGTG 360
GGCACCCAGC CAGAAGGTGA CTAACACCAT CTCTTTGCAC CCAGACCATA TACCAAAGGC 420
AAATTGCTCC TTTTTTTAAA CCTTGCTAGG CAAGTCAGTA TTAGTATCTT CAAACTACAA 480
AGGCTGCTTT GTCATGCAAA GAGAAGGAAA AAAAGAGGTT GACAGTATTT TGAGCCAACA 540
AGGTTAGATC ACTCGGACAA CAGTGACTAA GCTCAACAGG GCTTCCAGCT CTTTTAATTA 600
AAAAAATTTT TTCTCAAAGA CCTATCTTTG TAAACCATCT CACCTTTCCA CCTCCCTTCA 660
ACTACAATCT ACGAATAGGG GGAAAAATGC TTTAAGATGT TGAAAAAGAA TCTGTATTCC 720
AATCAGATTC TTTGAAAAAA AGTATATGTA AGGCTGGACA 760
|
