| Tag | Content |
|---|
EnhancerAtlas ID | HS145-24211 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr7:98759850-98760530 |
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 | GAGACAGGGT CTCACTATGT TGGCCAGGCT GGTCTTGAAC TCCTGACCTC AGGTGATCTA 60
CCTGCCTTGG CCTCCCAAAG TGCTGGGATT ACAGGCATGA GCCACCATGC CCAGCTGAGA 120
ATTGCATTCT TTGAGGTACA TTACAATTTC TGGGCAAATG CAAAAGGTCA AAGTTGTTCC 180
AGTTCAGTGT TCACACCGTA AACCAACCTA TAGCCATTCA CACCTTCCTT CCTCTTTGTT 240
GCCTCACCAG TCGTCCCAAC TCCCCGAGTC TAAGCAGGTG GGCACCCAGC CAGAAGGTGA 300
CTAACACCAT CTCTTTGCAC CCAGACCATA TACCAAAGGC AAATTGCTCC TTTTTTTAAA 360
CCTTGCTAGG CAAGTCAGTA TTAGTATCTT CAAACTACAA AGGCTGCTTT GTCATGCAAA 420
GAGAAGGAAA AAAAGAGGTT GACAGTATTT TGAGCCAACA AGGTTAGATC ACTCGGACAA 480
CAGTGACTAA GCTCAACAGG GCTTCCAGCT CTTTTAATTA AAAAAATTTT TTCTCAAAGA 540
CCTATCTTTG TAAACCATCT CACCTTTCCA CCTCCCTTCA ACTACAATCT ACGAATAGGG 600
GGAAAAATGC TTTAAGATGT TGAAAAAGAA TCTGTATTCC AATCAGATTC TTTGAAAAAA 660
AGTATATGTA AGGCTGGACA 680
|
