| Tag | Content |
|---|
EnhancerAtlas ID | HS108-01673 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:46813000-46814260 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr1:46813314-46813326 | ATCTGTTTACTT | - | 6.74 | | FOXP2 | MA0593.1 | chr1:46813315-46813326 | TCTGTTTACTT | - | 6.32 | | IRF1 | MA0050.2 | chr1:46813521-46813542 | TTTGACTTTCTTTTTTTTTTT | + | 6.6 | | Nr2f6(var.2) | MA0728.1 | chr1:46814168-46814183 | GAGGTCAGGAGTTCA | + | 6.22 | | Zfx | MA0146.2 | chr1:46813795-46813809 | CCCGCCTAGGCCTC | + | 6.24 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 46813215 | 46813520 | | chr1 | 46813799 | 46814097 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I046347 | chr1 | 46813381 | 46814118 |
|
Enhancer Sequence | TCAGGAGGCT GAGGCAGGAG AATTGCTTGA ACCCGGGAAG TGGAGGTTAC AATGAGCTGA 60
GATCCTGCCA CTGCACTCCA GCCTTGGCGA CAGAGTGAAA CCCTGTCTCA CACACACACA 120
AAAAAAGAAT ATGGTAGGTT CTCTAGTCCC AAAGTCAGAG TGGAGGGTAG TACTTACTTT 180
CTAAGCTTGT GTATTTTTTC ATTAGTTCCT CTCTTTCTCT GTCAATTGGT CAAGAAAGAT 240
TGCTGAGCAA GTTCTCTGAA GTCAGATTGA AGTAGGGCTC TGATCAGTTG ATCACATGAT 300
ACACACTCCT CTTCATCTGT TTACTTTTCC TCTAAGATTA AGCCCATTTC TTTAGCCTAC 360
CAACTAAAAT GATAAGATCT GCCTGCAGCC ACCATTTATA TGCTTTATAT GTCACTCTTC 420
TAGGCTTTAT GTGCTTTAAC CTTACTCTGC TACTCTCTGT TGCCTTTGCT CTTGTTAAAT 480
TTTCTCCCTG GAATTCCCTC ACCCTTGGCT GTCCAAATCC TTTTGACTTT CTTTTTTTTT 540
TTCTTTCTTT TTTTTTCTCT TTTTTTCGAG ATGGAGTCTC ACTCTGTCAC CCAGGTTGGA 600
GTGCAGTGGC ACGACCTCGG CTCACTGCAA GCTCCGCCTC CTGGGTTCAC GCCATTCTCC 660
TGCCTCAGCC TCCCTACTAG CTAGGACTAC AGGCGCCCAC CACCACGCCC AGCTAATTTG 720
TTTTTGTACT TTTAGTAGAG ACAGGGTTTC ACCCTGTTAG CCAGGATGGT CTCAATCTCC 780
TGACCTTGTG ATCTGCCCGC CTAGGCCTCC CAAATTGCTG GGATTACAGG CATGAGCCAC 840
CGCGCCCGGC CCCTTGTGTC AAGTACTCAC TTCAGCCATC CACTGGCTGA TATCCTGCCT 900
GCCCAGTCAT CCTTTTGACT TTCAAGCCTC AGCTCAAGTG TGCCACCTCC TGGACGTCTG 960
TCCTTACGAC CTCTGCTGGC CGGTTCAGAA ATGATGCCTG TCTCCTACGC TCCCACAGCA 1020
TGGGTATCGC CCTTGCAACA TTAGCCTTGC CTTAGGGCTT TACTAGTTAT ATATCTTCTC 1080
CCTCTTAAAG ATGATGGATT CTGGCCGGGC ACGGTGGCTC ACGCCTATAA TTCCAGCACT 1140
TTGGAAGGCT GAGGCGGGTG GATCACCTGA GGTCAGGAGT TCAAGACAAG CCTGGCTAAC 1200
ATGGTAAAAC CCCGTTTCTA TTAAAAATAC AAAAAATTAG CCGGGCCTGG TGGTGGGCTA 1260
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