| Tag | Content |
|---|
EnhancerAtlas ID | HS093-07955 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr12:123889830-123890800 |
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 | chr12:123889936-123889951 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGGCTCAAAG AATTCTCCTC CCTCAGCCTC CAGAGTAGCC CAGCTAATTT TTTTTTTCTG 60
TATTTTTAGT AGAGGTGGAG TTTTGCCACA TTGGCCAAGC TGGTCTTGAA CTCCTGACCT 120
CAGACGATCC ACCCGCCTTG GCCTTCCAAA GTGCTAGGAT TACAGGTGTG AGCCACTGCG 180
CTCGGGCTGT TGTTGCCTTT TTTCAAAGCT GTGATGCAAT TATCGCCTGC TTCCTTTTTT 240
TTTTTTTTTT TTTTTTTTTT GAATCTCGAT CTGTCGCCCA AGCTGGAGTG CAGTGGCACA 300
ATCTTGGCTC ACTGCAACCT CCACCTCCCG GGTTCAAGGT ATTCTGTCTC AGCCTCCCAC 360
GTAACTGGGA TTACAGGTGT GCGTCACCAC GCCCAGCTAA TTCTTATATA TTTTTTTAGT 420
AGAGACAGGG TTTCATTATG TTGGCCAGGC TGGTCTGACC TCATATGGTC TGCCTGCCTT 480
AGCCTCCCAA AGTTCTGGGA TTACAGATGT GAGCCACTGC GCCTGGCCCC AGCTTCCCTT 540
TTTTTTTTTC TTTTGAGACG GAGTCTCGTT CTGTCACCCA GGCTGGAGTG CAGTGGTGCA 600
ATCTTGGCTT ACTGCAACCT CCACCTCCCA GGTTCAAGCG ATTCTCCTGC CTCAGCCTCC 660
TGAGTAGCTG GGACTACACA CACATGCCAC CATGCCTGGC TAATTTTTTG TATTTTTAGT 720
AGAGATGGAG TTTCACTGTG TTAGCCAGGA TGGTCTCAAT CTCCTAACCT TGTGACCTGC 780
CCACCTTGGC CTCCCAAAGT GCTGGGATTA CAGGCATGAG CCACTGTGGC CCCAGCTTCC 840
CATTTTTAAT CTTTGGAATT GGAGCTGTCC TGGATGTTAT CTCATCCAAG GGGAGAAGTG 900
GGCTAGTCAC ATGAAAACCT GTTAAGCAGC TCACCTGGCT CTCCTTCAGG GCATTTGGCC 960
AGAGCAGCTC 970
|
