| Tag | Content |
|---|
EnhancerAtlas ID | HS108-01870 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:55487490-55488440 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:55487917-55487936 | TGGCGCCCTCTGCTGGTCT | - | 7.51 | | EWSR1-FLI1 | MA0149.1 | chr1:55488016-55488034 | TATTCCTTCCTTCCTCCC | - | 7.54 | | EWSR1-FLI1 | MA0149.1 | chr1:55488020-55488038 | CCTTCCTTCCTCCCTTCC | - | 9.6 | | ZNF263 | MA0528.1 | chr1:55488012-55488033 | TCCCTATTCCTTCCTTCCTCC | - | 6.04 | | ZNF263 | MA0528.1 | chr1:55488004-55488025 | TCCCTCTCTCCCTATTCCTTC | - | 6.08 |
|
| | 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 |
| GH01I055021 | chr1 | 55487341 | 55488393 |
|
Enhancer Sequence | GCGTGCTGGT CATGACCCTC TTTTGTTCAG AATCTCCCAG AGTCCCCTAA CCTCAGGAGA 60
GGGCCATGCC TTGGCCTCGA GAGGCGTTAA AAACCAGCCT CCCATCTCAG TGTCTCCAGC 120
TGGGCCATGC ACTGCTTCCT ACCACCATTA TAACTGGACC ACAGATCCCG AGCTGCCACC 180
TCCAGGAAGC CGGCCCGGAT TCAGTGCCCA TCTGACTGAG TTCCCGCAGC ACCTAGCCTG 240
TCCCTTCTGT GAGACTTGGC TCCTCTTGCC TCCTATCACA GTCGCCTGTG CTCTCATCTG 300
CCTCCCTGTG GACTCTGAGG ATGAGGCGAG GGCTGATTCA GCTCAGGGGT GAGAGCAGGT 360
GCCAGCAGCT TATGGGCTGG GCCGGGCCTG GGCAGTGGGC AGGCCGTGGG CTCAGATGAC 420
AGGTACCTGG CGCCCTCTGC TGGTCTAGCT GGGCAAGGCT GCTGCTCCAG AGTGGCCGGA 480
AGCTTCCTGG GAGAGGCCTG GTTCTCTGGG CCTGTCCCTC TCTCCCTATT CCTTCCTTCC 540
TCCCTTCCTG AAACTGCGTC CTCCAAATCC TGCTCCAGCA CCAGCAACCC CCTGCTTTTC 600
AACAGCCTCT GGCAGCGTTT CGGTCCCTTT CTGGCCTTGA CTGGAAGGCC CCTGTCCCCC 660
AAGGACACTG CTGCCGTCCC TGCAGTCCTT TCCCCCCGCC TGAGAGGGGT AGGGTCTCCT 720
TGCTCTCAGT GCCCCACTCT CTGGATCATT GTCCTTCTCT CCTCCATAAA CGCAGTCATG 780
CGCCACACAG CAATGTTTCA GGCAACGACA GACCACATAC ATGACAGTGG TTCCATAAGA 840
TTACAACAGA GCTGAGAAAC TCCTGTCACC TCGCTTAGAG ACGTCATAGC TGTCAGGCCT 900
CTGAGCCCAA GCCAAGCCAT CGCATCCCCT GTGACTTGCA CGTATACGCC 950
|
